DS4A - (1971) Physical Constants of Hydrocarbons C1 To C10

-~ -_
Physical
Constants
• of Hydrocarbon
and
~ Non-Hydrocarbon
C Compounds
- -~-
DS 48
Physical Constants
of Hydrocarbon
and Non-
Hydrocarbon
Compounds
2nd Edition
Compiled by
ASTM COMMITIEE D-2
ON PETROLEUM PRODUCTS AND
LUBRICANTS AND THE AMERICAN
PDROLEUM INSTITUTE'$ REFINING
DEPARTMENT TECHNICAL DATA
COMMITIEE, WHO WORKED WITH THE
DEPARTMENT OF CHEMICAL
ENGINEERING OF THE PENNSYLVANIA
STATE UNIVERSITY
ASTM Data Series DS 4B

(Revision of Data Series DS 4A)
ASTM Publication Code Number (PCN): 05-004020-12
~~l~ 1916 Race St., Philadelphia, PA 19103

Library of Congress Cataloging-in-Publication Data
Physical constants of hydrocarbon and non-hydrocarbon compounds I compiled by

ASTM Committee D-2 on Petroleum Products and Lubricants and the American
Petroleum Institute's Refining Department Technical Data Committee, who worked
with the Department of Chemical Engineering of the Pennsylvania State University.
- 2nd ed. (ASTM data series ; OS 4B)
Rev. ed. of: Physical constants of hydrocarbons C 1 to Cw I prepared by ASTM
Committee D-2 on Petroleum Products and Lubricants. 1971.
"ASTM publication code number (PCN): 05-004020-12."
Includes bibliographical references (p. ) .
ISBN 0-8031-1428-1
1. Hydrocarbons-Tables. I. ASTM Committee D-2 on Petroleum Products and
Lubricants. II. American Petroleum Institute. Refining Dept. Technical Data
Committee. III. Pennsylvania State University. Dept. of Chemical Engineering.
IV. ASTM Committee D-2 on Petroleum Products and Lubricants. Physical
constants of hydrocarbons C 1 to Cw. V. Series: ASTM data series publication;
OS 4B.
TA401.P48 1991
660'. 8 l----dc20 91-12453
CIP
Copyright © 1988 American Petroleum Institute
Printed in Ann Arbor, MI/May 1991

Foreword
This publication updates the 1971 Edition of the ASTM Data Series DS 4A titled
Physical Constants ofHydrocarbons C 1 TO C 10. This new edition includes all of Chapter
1 from the American Petroleum lnstitute's Publication 999, Technical Data Book-
Petroleum Refining. This edition is broader in scope, and includes Hydrocarbons Cl
to C30 as well as Non-hydrocarbons.
This book has been made available through a joint arrangement between ASTM
Committee D-2 on Petroleum Products and Lubricants, and The American Petroleum
Institute's Refining Department Technical Data Committee, who worked with the
Department of Chemical Engineering of The Pennsylvania State University.
PREFACE
The first major revision of Chapter 1 since 1970 was undertaken during 1985 and
1986. While the previous tables were almost entirely compiled from the work of The
Thermodynamics Research Center at Texas A&M University, the new tables were
compiled from a variety of sources as discussed in the introduction. Common high
molecular weight hydrocarbons and representative nonhydrocarbons were added
while excessive numbers of isomers of hydrocarbons were eliminated. With the
publication of the metric edition of the Technical Data Book-Petroleum Refining,
sets of tables in metric units were deleted from this edition. With the concurrent
computerization of the Technical Data Book, the pure component data are now
available in a form for computer retrieval.
A compound index containing synonyms was added to aid in retrieval of informa-
tion. The constants and conversion factors also were updated to the currently
accepted values with complete S.I. unit inclusion and elimination of little used
conversion factors.
Major work on this chapter was carried out and directed by Jill Schnitzer,
Research Assistant in Chemical Engineering, under the supervision of Dr. Thomas
E. Daubert, Principal Investigator. The chapter advisory committee for the Tech-
nical Data Committee included Calvin F. Spencer, Chairman, of M. W. Kellogg
Company, Carl Sutton of Gas Processors Association, Sheldon J. Kramer of
Amoco Oil Company, and Costa Tsonopoulos of Exxon Research and Engineering
Company.
Thomas E. Daubert
Ronald P. Danner
Department of Chemical Engineering
The Pennsylvania State University
University Park, PA 16802
June 1987
CHAPTER 1
GENERAL DATA
PAGE
1-0 Introduction ................................................. . 1-1
lA Fundamental Constants and Conversion Factors .................. . 1-2

lAl Fundamental Constants .................................... . 1-2
Table lAl.1 Fundamental Constants .................. . 1-2
1A2 Conversion Factors ........................................ . 1-4

Table 1A2.l Length Conversions ..................... . 1-4
Table 1A2.2 Area Conversions ....................... . 1-4
Table 1A2.3 Volume Conversions .................... . 1-5
Table 1A2.4 Liquid Volume Conversions .............. . 1-5
Table 1A2.5 Mass Conversions ....................... . 1--6
Table 1A2.6 Density Conversions ..................... . 1--6
Table 1A2.7 Pressure Conversions .................... . 1-7
Table 1A2.8 Flow Conversions ....................... . 1-7
Table 1A2.9 Kinematic Viscosity Conversions .......... . 1-8
Table 1A2.10 Absolute Viscosity Conversions ........... . 1-8
Table 1A2.11 Energy Conversions ..................... . 1-9
Table 1A2.12 Power Conversions ...................... . 1-10
Table 1A2.13 Specific Energy Conversions .............. . 1-10
Table 1A2.14 Specific Energy per Degree Conversions ... . 1-11
Table 1A2.15 Heat Flux Conversions .................. . 1-11
Table 1A2.16 Heat Transfer Coefficient Conversions ..... . 1-12
Table 1A2.17 Thermal Conductivity Conversions ........ . 1-12
1B Letter Symbols Used in Chemical Engineering ................... . 1-13

lBl Letter Symbols for the Principal Concepts Used in
Chemical Engineering ...................................... . 1-13
Table lB 1.1 Letter Symbols for the Principal Concepts
Used in Chemical Engineering ............ . 1-13
Table lBl.2 Alphabetical Index of Symbols Used in
Chemical Engineering ................... . 1-17
lC Property Definitions .......................................... . 1-19

Table lCO.l Index of Compounds .................... . 1-25
lCl Hydrocarbons-Primary Properties .......................... . 1-52
Table lCl.1 Paraffins ............................... . 1-52
Table lCl.2 Cycloparaffins .......................... . 1-58
Table lCl.3 Monoolefins and Diolefins ............... . 1-66
Table lCl.4 Cycloolefins and Acetylenes .............. . 1-74
1987 v
Table lCl.5 Benzene Derivatives...................... 1-76
Table lCl.6 Condensed Ring Aromatics and Derivatives. 1-82
1C2 Hydrocarbons-Secondary Properties ........................ . 1-86

Table 1C2.l Paraffins ............................... . 1-86
Table 1C2.2 Cycloparaffins .......................... . 1-92
Table 1C2.3 Monoolefins and Diolefins ............... . 1-100
Table 1C2.4 Cycloolefins and Acetylenes .............. . 1-108
Table 1C2.5 Benzene Derivatives ..................... . 1-110
Table 1C2.6 Condensed Ring Aromatics and Derivatives. 1-116
1C3 Nonhydrocarbons-Primary Properties ....................... . 1-120

Table 1C3.1 Acids .................................. . 1-120
Table 1C3.2 Alcohols and Phenols ................... . 1-120
Table 1C3.3 Aldehydes ............................. . 1-120
Table 1C3.4 Amines ....... ·.· ....................... . 1-122
Table 1C3.5 Other Nitrogen-Containing Compounds ... . 1-122
Table 1C3.6 Esters ................................. . 1-122
Table 1C3.7 Ethers ................................. . 1-124
Table 1C3.8 Gases ................................. . 1-124
Table 1C3.9 Halogenated Compounds ................ . 1-126
Table 1C3.10 Ketones ................................ . 1-126
Table 1C3. ll Sulfur-Containing Compounds ............ . 1-128
Table 1C3.12 Miscellaneous .......................... . 1-128
1C4 Nonhydrocarbons-Secondary Properties ..................... . 1-130

Table 1C4.l Acids .................................. . 1-130
Table 1C4.2 Alcohols and Phenols ................... . 1-130
Table 1C4.3 Aldehydes ............................. . 1-130
Table 1C4.4 Amines ................................ . 1-131
Table 1C4.5 Other Nitrogen-Containing Compounds ... . 1-131
Table 1C4.6 Esters ................................. . 1-131
Table 1C4.7 Ethers ................................. . 1-132
Table 1C4.8 Gases ................................. . 1-132
Table 1C4.9 Halogenated Compounds ................ . 1-133
Table 1C4.10 Ketones ................................ . 1-133
Table 1C4.11 Sulfur-Containing Compounds ............ . 1-134
Table 1C4.12 Miscellaneous .......................... . 1-134
1C5 Key to References ......................................... . 1-136

Table 1C5.1 Key to References-Hydrocarbons ........ . 1-136
Table 1C5.2 Key to References-Nonhydrocarbons ..... . 1-164
Bibliography ..................................................... . 1-175
vi 1987
CHAPTER 1
GENERAL DATA
Revised Chapter 1 to First (1966), Second (1970),

Third (1977), and Fourth (1982) Editions
DS4B-EB/May 1988
CHAPTER 1
GENERAL DATA
1-0 INTRODUCTION data were made using current Data Book procedures.
Predictions of nonhydrocarbon data were made using
Pure component properties are required for nearly all
DIPPR Compilation (50) procedures.
of the procedures in the API Technical Data Book. This
In addition to the data tables (Sections lCl through
chapter provides a compilation of properties for many
1C4), other information of general importance is
hydrocarbon plus selected nonhydrocarbon compounds.
presented in this chapter. Section lA is a list of con-
The compounds and properties chosen for inclusion
stants and conversion factors and Section lB is a list of
here are those deemed most useful in petroleum refin-
letter symbols and their definitions. Section lC is a
ing and associated industries. Further information on
compilation of property definitions and other pertinent
some hydrocarbons and many nonhydrocarbons may be
information on the properties in the data tables. Note
found in the Design Institute for Physical Properties
that codes in the data tables indicate whether data are
Re~earch (DIPPR) Data Compilation: Tables of Prop-
predicted (P), extrapolated (T), experimental (no
erties of Pure Compounds (50). The majority of data for
code), or if it is unknown whether the source is pre-
the compounds presented here was taken from the
dicted or experimental (S). Codes such as C, G, K, and
following sources (in order of priority).
N indicate further descriptive information for experi-
1. GPA 2145-86 (82). mental data. The key to these codes is given after Table
2. API Monograph Series (10--21). 1C4. Section 1C5 is the reference key for the properties
3. DIPPR Compilation (50). in the data tables.
4. TRC Tables (181-189, 210). The physical property data contained in Tables 1Cl.1
5. Current API Technical Data Book-Petroleum through 1C4.12 also are available in computer readable
Refining (51). form on tape or disk. The data are identical except that
the number of significant digits may be different.
Unless otherwise indicated, predictions of hydrocarbon
1987 1-1
Copyright © 1988 by ASTM International www.astm.org

1A1.1 DS4B-EB/May 1988
TABLE 1A1.1
FUNDAMENTAL CONSTANTS*
Basic Constants
Name Symbol Value Units
8
Velocity of light (vacuum) 2.997925 x 10 m per sec
Avogadro constant 6.02214 x 1023 molecules per g-mole
Planck constant 6.6261 x 10- 27 (ergs) (sec) per molecule
Faraday constant 96,485.3 coulombs per mole
Absolute temperature of the "ice" point:
oc 273.15 K
32 F 491.67 deg R
Pressure-volume product for 1 mole of
a gas at 0 C (32 F) and zero pressure
(ideal gas) 2,271.11 joules per g-mole
22.4141 (liters) (atm) per g-mole
2.27111 x 106 (cum) (Pa) per kg-mole
359.039 (cu ft) (atm) per lb-mol
5,276.42 (cu ft) (psia) per lb-mol
Derived Constants
F
Electronic charge e =NA 1.60218 x 10- 19 coulombs
R = (pvy;.~oc
Gas constant 8.3145 joules per (g-mole) (K)
To c
1.9872 g-cal per (g-mole) (K)
1.9859 Btu per (lb-mole) (deg R)
82.058 (cu cm) (atm) per (g-mole) (K)
1,545.4 ft-lb (force] per (lb-mole) (deg R)
10.732 (psia) (cu ft) per (lb-mole) (deg R)
62.364 (mm Hg) (liter) per (g-mole) (K)
0.084786 (kg per sq cm) (liter) per (g-mole) (K)
0.73024 (atm) (cu ft) per (lb-mole) (deg R)
554.99 (mm Hg) (cu ft) per (lb-mole) (deg R)
8,314.5 (Pa) (cum) per (kg-mol) (K)
Boltzmann constant 1.38066 x 10- 16 ergs per (molecule) (K)
Second radiation constant 1.43877 cm-deg C
Defined Constants
Standard gravity go 980.665 cm per sec per sec
32.174 ft per sec per sec
Standard atmosphere atm 1,013,250 dynes per sq cm
14.696 psi a
101,325 pascals
mmHg 1
Standard millimeter of mercury pressure atm
760
Calorie (thermochemical) cal 4.1840 joules
4.1840 x 107 ergs
Calorie (International Steam Tables) caln; I.T. cal 4.1868 joules
Liter 1,000 cu cm
1-2 1987

1A1 .1
TABLE 1A1.1 (Continued)
Conversion Factors-Engineering Units Vs. Metric Units

Name Value Units
1 in. =2.54 cm Definition: in. = U.S. inch
1 ft = 30.48 cm Definiton: U.S. foot (1 ft= 12 in.)
1 lb = 453.59237 g Definition: lb= avoirdupois pound
1 gal = 231 cu in. Definition: gal= U.S. gallon
= 0.133680555 cu ft
= 3,785.43449 cu cm
= 3. 785412 liters
1 l.T. cal = 1 mt . watt-hr Definition: l.T. =International Steam
860
Tables
= 4.18674 joules
= 4.18605 int joules
= 1. 000654 cal Definition: cal = thermochemical calorie
1
1 Btu per lb = 1. l.T. cal per g Definition: Btu= l.T. British thermal
8
unit
1 Btu = 251.996 l.T. cal
= 1,055.040 joules
= 1,054.866 int joules
= 0.293018 int watt-hr
= 252.161 cal Definition: cal= thermochemical calorie
= 0.293067 abs watt-hr
1 hp = 550 ft-lb [force] per sec
= 745.701 watts (abs)
= 745.578 int watts
1 erg = 1 dyne-cm
Mathematical Constants
1T= 3.14159
e (base of natural logarithms) = 2. 71828
natural logarithm (base e), log. 10 =In 10 = 2.30258509
Temperature Conversions
C = (F - 32)/1.8
F= 1.8 C + 32
K = C + 273.15
R = F + 459.67
R = 1.8 K
Where:
C = degrees centigrade
F = degrees Fahrenheit
K =kelvins
R = degrees Rankine
•Values taken from, or derived from, those given in Natl. Bur. Std. (U.S.), CO DATA Bull. No. 63 (1986).
1987 1-3
1A2.1-1A2.2
TABLE 1A2.1
LENGTH CONVERSIONS
To convert the numerical value of a property expressed in one of the units in the left-hand
column of the table to the numerical value expressed in one of the units in the top row of the
table, multiply the former value by the factor in the block common to both units.
Units-+ Milli- Centi- Kilo-

! Inches Feet Yards Miles Microns meters meters Meters meters
1.5783 2.5400
Inches 1 0.083333 0.027778 x 10- 5 25,400 25.400 2.54 0.0254 x 10- 5
1.8939 3.0480 3.0480
Feet 12 1 0.33333 x 10- 4 304.80 30.480 0.30480
x 105 x 10- 4
5.6818 9.1440 9.1440
Yards 36 3 1 x 10- 4 914.40 91.440 0.91440
x 105 x 10- 4
1.6093 1.6093 1.6093 1.6093
Miles 63,360 5,280 1,760 1 1.6093
x 109 x 106 x 105 x 103
3.9370 3.2808 1.0936 6.2137 10-3 10-4 10-6 10-9
Microns x 10- 5 x 10-6 x 10-6 x 10- 10 1
3.9370 3.2808 1.0936 6.2137 103 10-6

Millimeters x 10- 2 x 10-3 x 10- 3 x 10- 1 1 0.1 0.001
6.2137 104 10-5

Centimeters 0.39370 0.032808 0.010936 x 10-6 10 1 0.01
6.2137 106
Meters 39.370 3.2808 1.0936 x 10- 4 1,000 100 1 0.001
3.9370 3.2808 1.0936 109 106 105

Kilometers 0.62137 1,000 1
x 104 x 103 x 103
TABLE 1A2.2
AREA CONVERSIONS
Units-+ Square Square Square

! Inches Square Feet Square Yards Acres Centimeters Meters
Square Inches 1 6.9444 x 10- 3 7.7160 x 10- 4 1.5942 x 10- 1 6.4516 6.4516 x 10- 4
Square Feet 144 1 0.11111 2.2957 x 10- 5 929.03 9.2903 x 10- 2
Square Yards 1,296 9 1 2.0661 x 10- 4 8,361.3 0.83613
Acres 6.2726 x 106 43,560 4,840 1 4.0469 x 10 7 4.0469 x 103
Square 1.0764 x 10- 3 1.1960 x 10- 4 2.4711 10-s_ 10-4

0.15500 X 1
Centimeters
Square Meters 1,550 10.764 1.1960 2.4711 x 10- 4 104 1
1-4 1987
1A2.3-1A2.4
TABLE 1A2.3
VOLUME CONVERSIONS
Units-+
Cubic Inches Cubic Feet Cubic Yards Cubic Centimeters Cubic Meters
!
5.7870 2.1433 1.6387
Cubic Inches 1 x 10-• x 10- 5 16.387 x 10- 5
3.7037 2.8317 2.8317
Cubic Feet 1,728 1 x 10- 2 x 10 4 x 10- 2
7.6455
Cubic Yards 46,656 27 1 0.76455
x 105
6.1023 3.5315 1.3080 10-6
Cubic Centimeters x 10- 2 x 10- 5 x 10- 6 1
Cubic Meters 61,023 35.315 1.3080 106 1
TABLE 1A2.4
LIQUID VOLUME CONVERSIONS
Fluid Cubic
Units-+ Quarts Gallons Imperial Barrels Cubic Cubic Cubic
Ounces Liters Centi-
! (U.S.)
(U.S.) (U.S.) Gallons (Oil) Inches Feet
meters
Meters
Fluid Ounces 7.8125 6.5053 1.8601 1.0444 2.9574

1 0.03125 x 10- 3 x 10- 3 x 10-• 1.8047 x 10- 3 0.029574 29.574 x 10- 5
(U.S.)
Quarts 5.9524 9.4635
32 1 0.25 0.20817 x 10- 3 57.75 0.033420 0.94635 946.35
(U.S.) x 10-•
Gallons 3.7854
128 4 1 0.83267 0.023809 231 0.13368 3.7854 3,785.4 x 10- 3
(U.S.)
Imperial 4.5461
153.72 4.8038 1.20095 1 0.028594 277.42 0.16054 4.5461 4,546.1 x 10- 3
Gallons
1.5899
Barrels (Oil) 5,376 168 42 34.973 1 9,702 5.6146 158.99 0.15899
x 105
4.3290 3.6047 1.0307 1 5.7870 1.6387
Cubic Inches 0.55411 0.017316 x 10- 3 x 10-• 0.016387 16.387
x 10- 3 x 104 x 10- 5
Cubic Feet 957.51 29.922 7.4805 6.2289 0.17811 1,728 1 28.317 28,317 0.028317
6.2898 1 x 10- 3
Liters 33.814 1.0567 0.26417 0.21997 x 10- 3 61.024 0.035315 1 1,000
Cubic 1.0567 2.6417 2.1997 6.2898 3.5315 1 x 10- 6

0.033814 x 10- 3 x 10-• x 10-• x 10- 6 0.061024 x 10- 5 0.001 1
Centimeters
Cubic
33,814. 1,056.7 264.17 219.97 6.2898 61,024. 35.315 1,000 1x106 1
Meters
Note: According to ASME Guides SI-1 (22) and SI-4 (23),

1ml=1 cu cm.
1987 1-5
1A2.5-1A2.6
TABLE 1A2.5
MASS CONVERSIONS
Units-+ Ounces Pounds Ounces Pounds Tons Tons Metric

Grains Grams Kilograms
! (Avoir)* (Avoir)* (Troy)t (Troy)t (Short)t (Long)§ Tons
2.2857 1.4286 2.0833 1.7361 7.1428 6.3776 6.4799 6.4799
Grains 1 x 10- 3 x 10- 4 x 10- 3 x 10- 4 x 10- 8 x 10- 8 0.064799 X 10- 5 x 10- 8
Ounces 3.125 2.7902 2.8350
437.5 1 0.0625 0.91146 0.075955 X 10- 5 X 10- 5
28.350 0.028350 x 10- 5
(Avoir)*
Pounds 5 x 10- 4 4.4643 4.5359
7,000 16 1 14.583 1.2153 x 10- 4 453.59 0.45359 x 10- 4
(Avoir)*
Ounces 3.4285 3.0612 3.1103
480 1.0971 0.068571 1 0.083333 x 10- 5 x 10- 5 31.103 0.031103 X 10- 5
(Troy)t
Pounds 4.1143 3.6735 3.7324
5,760 13.166 0.82286 12 1 x 10- 4 x 10- 4 373.24 0.37324 x 10- 4
(Troy)t
Tons 1.4000 9.0718 9.0718
32,000 2,000 29,167 2,430.6 1 0.89286 0.90718
(Short)t x 107 x 105 x 102
Tons 1.5680 1.0160 1.0160
35,840 2,240 32,667 2,722.2 1.1200 1 1.0160
(Long)§ x 107 x 106 x 103
2.2046 2.6792 1.1023 9.8421 10-3 10-6
Grams 15.432 0.035274 x 10- 3 0.032151 x 10-3 x 10- 6 x 10- 1 1
1.5432 1.1023 9.8421 10-3

Kilograms 35.274 2.2046 32.151 2.6792 x 10- 3 x 10- 4 1,000 1
x 104
1.5432 3.5274 2.2046 3.2151 2.6792 106
Metric Tons 1.1023 0.98421 1,000 1
x 107 x 104 x 103 x 104 x 103
•Used for ordinary commodities. t Common in the United States and Canada.
t Used for drugs, jewels, precious metals. § Common in England.
TABLE 1A2.6
DENSITY CONVERSIONS
Units-+ _g_ lb lb
--
lb ~
--
! cu cm cu in. cu ft gal (U.S.) cum
_g_
1 0.036127 62.428 8.3454 1000
cu cm
lb
-- 27.680 1 1,728 231 27,680
cum.
lb
-- 0.016018 5.7870 x 10- 4 1 0.13368 16.018
cu ft
lb
0.11983 4.3290 x 10- 3 7.4805 1 119.83
gal (U.S.)
~ 0.001 3.6127 x 10- 5 0.062428 0.0083454 1
cum
1-6 1987
1A2.7-1A2.8
TABLE 1A2.7
PRESSURE CONVERSIONS
Units-+ dynes Atmos- ~ mm Hg* in. Hg* lb [force] ft HiO

i sq cm Bars pheres sq cm at 0 C at 32 F sq in. at 39.2 F Pascals
dyns 10-6 0.986923 1.01972 7.5006 2.9530 1.4504 3.3457
1 x 10- 6 x 10- 6 x 10-• X 10- 5 x 10- 5 X 10- 5 0.10000
sq cm
Bars 106 1 0.986923 1.01972 750.06 29.530 14.504 33.457 1x105
1.01325 1.01325
Atmospheres 1.01325 1 1.0332 760 29.921 14.696 33.900
x 106 x 1Q5
~ 980,670 0.98067 0.96784 1 735.56 28.959 14.223 32.809 98,066.5

sq cm
1.3332 1.31579 1.3595
mm Hg* at 0 C 1,333.2 x 10- 3 x 10- 3 x 10- 3 1 0.03937 0.019337 0.044605 133.32
in. Hg at 32 F 33,864 0.033864 0.033421 0.03453 25.400 1 0.49116 1.1330 3,386.4
lb [force] •
68.948 0.068948 0.068046 0.070307 51.715 2.0360 1 2.3066 6,894.7
sq in.
ft HiO at 39.2 F 29,889 0.029889 0.029499 0.030479 22.419 0.88265 0.43352 1 2,988.98
10- 5 9.86923 1.01972 7.5006 2.9530 1.4504 3.3456

Pascals 10.000 lX
x 10- 6 x 10- 5 x 10- 3 x 10-• x 10-• x 10-• 1
• 1 Torr = 1 mm Hg.
TABLE 1A2.8
FLOW CONVERSIONS
Units-+ gal (U.S.) gal (U.S.) cu ft cu ft bbl (42) bbl (42) liters cum
-- -- -- --
i min hr sec min hr day sec hr
gal (U.S.) 2.2280
1 60 x 10- 3 0.13368 1.4286 34.286 0.063090 0.22712
mm
gal (U.S.) 3.7133 2.2280 1.0515 3.7854
0.016667 1 X 10- 5 x 10- 3 0.023810 0.57143 x 10- 3 x 10- 3
hr
cu ft 2.6930 1.5388
-- 448.83 1 60 641.20 28.317 101.94
sec x 104 x 104
cu ft
-- 7.4805 448.83 0.016667 1 10.686 256.47 0.47195 1.6990
min
bbl (42) 1.5596
0.70000 42 x 10- 3 0.093576 1 24 0.044163 0.15899
hr
bbl (42) 6.4984 3.8990 1.8401 6.6245
0.029167 1.7500 x 10- 5 x 10- 3 0.041667 1 x 10- 3 x 10- 3
day
liters
-- 15.850 951.02 0.035315 2.1189 22.643 543.44 1 3.6
sec
cum
-- 4.4029 264.17 0.0098096 0.58858 6.2898 150.96 0.27778 1
hr
1987 1-7
1A2.9-1A2.10
TABLE 1A2.9
KINEMATIC VISCOSITY CONVERSIONS
sq cm sq cm x 102
sq ft sq ft sq m
Units-. sec sec
hr sec hr
! (Stokes) (Centistokes)
sq ft
1 2.778 x 10-• 9.290 x 10- 2 0.2581 25.81
hr
sq ft
3,600 1 3.345 x 102 929 9.29 x 104
sec
sq m
10.76 2.990 x 10- 3 1 2.778 277.8
hr
sq cm
sec 3.875 1.076 x 10- 3 0.3600 1 100
(Stokes)
sq cm x 102 3.875 x 10- 2 1.076 x 10- 5 3.600 x 10- 3 0.0100 1
sec
(Centistokes)
TABLE 1A2.10
ABSOLUTE VISCOSITY CONVERSIONS
lb [force]-sec __g_x 102

Units-. --
lb lb
-- sec-cm ~
sec-ft hr-ft sq ft hr-m
! (Centipoises)*
lb
-- 1 3,600 0.03108 1,488 5,357
sec-ft
lb
-- 2.778 x 10-• 1 8.634 x 10- 6 0.4134 1.488
hr-ft
lb [force]-sec
32.17 1.158 x 105 1 47,880 1.724X 105
sq ft
__g_x 102 6.720 x 10-• 2.419 2.089 x 10- 5 1 3.600
sec-cm
(Centipoises)*
~ 1.867 x 10-• 0.6720 5.801x10- 6 0.2778 1
hr-m
• 1 poise= 100 centipoises = 1--g-. Kinematic viscosity, in centistokes, times density (-g-) at same temperature equals
sec-cm cu cm
centipoises.
1-8
1A2.11
TABLE 1A2.11
ENERGY CONVERSIONS
Centi-
Inter- British Absolute Foot- cu ft-lb [force) Liter
Units~ Absolute I.T. Horsepower- grade
national Calories Thermal Kilowatt- Pounds Atmos-
l Joules
Joules
Calories
Units Hours
Hours
[Force] sq m. pheres
Heat
Units
Absolute 9.4783 2.7778 3.7251 5.1220 9.8690 5.2657
0.99984 0.23901 0.23885 x 10-• x 10- 7 x 10- 7 0.73756 x 10- 3 x 10- 3 x 10-•
Joules 1
International 9.4799 2.7782 3.7257 5.1228 9.8706 5.2666
1.0002 1 0.23905 0.23889 x 10-• x 10- 7 x 10- 7 0.73768 x 10- 3 x 10- 3 x 10-•
Joules
3.9657 1.1622 1.5586 2.1430 4.1292 2.2032
Calories 4.1840 4.1833 1 0.99935 x 10- 3 x 10- 6 x 10- 6 3.0860 x 10- 2 x 10- 2 x 10- 3
3.9683 1.1630 1.5596 2.1444 4.1319 2.2046
I. T. Calories 4.1867 4.1861 1.0007 1 x 10- 3 x 10- 6 x 10- 6 3.0880 x 10- 2 x ·10- 2 x 10- 3
British
2.9307 3.9301
Thermal 1,055.0 1,054.9 252.16 252.00 1 x 10-• x 10-• 778.16 5.4039 10.412 0.55556
Units
Absolute
3.6000 3.5994 8.6042 8.5986 2.6552
Kilowatt- 3,412.2 1 1.3410 18,439 35,528 1,895.7
x 106 x 106 x 105 x 105 x 1D6
Hours
Horsepower- 2.6845 2.6841 6.4162 6.4120 1.9800
2,544.5 0.74570 1 13,750 26,494 1,413.6
Hours x 106 x 106 x 105 x 105 x 1D6
Foot-Pounds 1.2851 3.7662 5.0505 6.9444 1.3381 7.1394
1.3558 1.3556 0.32405 0.32384 x 10- 3 x 10- 7 x 10- 7 1 x 10- 3 x 10- 2 x 10-•
[Force]
cu ft-lb [force] 5.4233 7.2727
195.24 195.21 46.663 46.633 0.18505 x 10- 5 x 10- 5 144 1 1.9268 0.10281
sq in.
Liter 2.8147 3.7745 5.3356
101.33 101.31 24.218 24.202 0.096042 x 10- 5 x 10- 5 74.735 5.1900 1 x 10- 2
Atmospheres
Centigrade 5.2752 7.0741
1,899.1 1,898.8 453.89 453.59 1.8 x 10-• x 10-• 1,400.7 9.7269 18.742 1
Heat Units
1987 1-9
1A2.12-1A2.13
TABLE 1A2.12
POWER CONVERSIONS
Btu Btu ft-lb ft-lb Metric cal

- Horse- Watts LT. cal joules (abs)
Units-+ - - Horse- - --
min hr sec mm power (Absolute) sec sec sec
! power
Btu
- 1 60.00 12.969 778.16 0.023580 0.023908 17.584 4.2027 4.1999 17.584
min
Btu 3.9301 3.9846
- 0.016667 1 0.21615 12.969 x 10-• x 10-• 0.29307 0.070045 0.069999 0.29307
hr
ft-lb 7.7105 1.8182 1.8434
- x 10- 2 4.6263 1 60.00 x 10- 3 x 10- 3 1.3558 0.32405 0.32384 1.3558
sec
ft-lb 1.2851 3.0303 3.0723 5.4008 5.3973
- x 10- 3 0.77105 0.016667 1 x 10- 5 x 10- 5 0.022597 x 10- 3 0.022597
min x 10- 3
Horsepower 42.408 2,544.5 550.00 33,000 1 1.0139 745.70 178.23 178.11 745.70
Metric
41.828 2,509.7 542.48 32,549 0.98632 1 735.50 175.79 175.67 735.50
Horsepower
Watts 1.3410 1.3596
0.056869 3.4122 0.73756 44.254 x 10- 3 x 10- 3 1 0.23901 0.23885 1
(Absolute)
-cal
sec
0.23794 14.277 3.0860 185.16
5.6108
x 10- 3
5.6886
x 10- 3 4.1840 1 0.99935 4.1840
IT. cal 5.6145 5.6924
-- 0.23810 14.286 3.0880 185.28 x 10- 3 x 10- 3 4.1867 1.0007 1 4.1867
sec
joules (abs) 1.3410 1.3596
0.056869 3.4122 0.73756 44.254 x 10- 3 x 10- 3 1 0.23901 0.23885 1
sec
Notes:
One boiler horsepower= 33,471.9 Btu per hr.
One standard commercial ton of refrigeration= 288,000 Btu per day.
TABLE 1A2.13
SPECIFIC ENERGY CONVERSIONS

joules (abs) joules (int) cal LT. cal Btu

Units-+ - ---
g g g g lb
!
joules (abs)
1 0.99984 0.23901 0.23885 0.42993
g
joules (int)
1.0002 1 0.23905 0.23889 0.43000
g
cal
- 4.1840 4.1833 1 0.99935 1.7988
g
LT. cal
--- 4.1867 4.1861 1.0007 1 1.8
g
Btu
2.3260 2.3256 0.55592 0.55556 1
lb
1-10 1987
1A2.14-1A2.15
TABLE 1A2.14
SPECIFIC ENERGY PER DEGREE CONVERSIONS
joules (abs) joules (int) cal I.T. cal Btu

Units~ - ~--
g-K g-K g-K g-K lb-deg F

i
joules (abs)
1 0.99984 0.23901 0.23885 0.23885
g-K
joules (int)
1.0002 1 0.23905 0.23889 0.23889
g-K
cal
- 4.1840 4.1833 1 0.99935 0.99935
g-K
l.T. cal
--- 4.1867 4.1861 1.0007 1 1
g
Btu
4.1867 4.1861 1.0007 1 1
lb-deg F
TABLE 1A2.15
HEAT FLUX CONVERSIONS
Btu cal kg-cal watts (abs) joules (abs)

Units~
hr-sq ft sec-sq cm hr-sq m sq cm sec-sq m
i
Btu
1 7.5397 X 10-s 2.714 3.1546 x 10-4 3.1546
hr-sq ft
cal
13,263. 1 36,000 4.1840 41,840
sec-sq cm
kg-cal
0.3684 2. 7778 x 10-5 1 1.1622 x 10-4 1.1622
hr-sq m
watts (abs)
3,170.0 0.23901 8,604.2 1 10,000
sq cm
joules (abs) 1 x 10-4
0.31700 2.3901 x -5 0.86042 1
sec-sq m
1987 1-11
1A2.16-1A2.17
TABLE 1A2.16
HEAT TRANSFER COEFFICIENT CONVERSIONS
Btu cal kg-cal watts (abs) joules (abs)

Units-+
hr-sq ft-deg F sec-sq cm-K hr-sq m-K sq cm-K sec-sq m-K
!
Btu
1 1.3571 x 10-4 4.8857 5.6783 x 10-4 5.6783
hr-sq ft-deg F
cal
7,368.4 1 36,000 4.1840 41,840
sec-sq cm-K
kg-cal
0.20468 2. 7778 x 10-5 1 1.1622 x 10-4 1.1622
hr-sq m-K
watts (abs)
1,761.1 0.23901 8,604.2 1 10,000
sq cm-K
joules (abs)
0.17611 2.3901 x 10-5 0.86042 1x10-4 1
sec-sq m-K
TABLE 1A2.17
THERMAL CONDUCTIVITY CONVERSIONS
Btu Btu cal kg-cal watts (abs) joules (abs)
Units-+
! hr - sq ft - degFper in. hr - sq ft - deg F perft sec - sq cm - K per cm hr - sq m - K perm sq cm - K per cm sec - sq m - K perm
Btu
1 0.08333 3.4471 x 10- 4 0.12410 1.4423 x 10 0.14423
hr - sq ft - deg F perin.
Btu
12.000 1 4.1366 x 10- 3 1.4892 0.017307 1.7307
hr- sq ft - degFperft
cal
2,901.0 241.75 1 360 4.1840 418.40
sec-sqcm - K per cm
kg-cal
8.0582 0.67152 2.7778 x 10- 3 1 0.011622 1.1622
hr-sqm- Kperm
watts (abs)
693.35 57.779 0.23901 86.042 1 100
sq cm - Kpercm
joules (abs)
6.9335 0.5778 2.3901 x 10- 3 0.86042 0.01 1
sec -sq m - kperm
1-12 1987
DS4B-EB/May 1988
181 .1
TABLE 1B1.1
LETTER SYMBOLS FOR THE PRINCIPAL CONCEPTS USED IN CHEMICAL ENGINEERING
The letter symbols for the concepts most widely used in chemical engineering are listed on
the following pages.
A letter symbol is a single letter used to represent a primary concept for a physical
quantity, and it may be used with a subscript or superscript. A subscript may designate a place
in space or time, a system of units, or a constant or reference value. A superscript may
designate a dimensionless form, a reference or equilibrium value, a sequence in time or
space, or a mathematical identification (average value, derivative, tensor index). The sym-
bols are listed under categories which are basic to all operations and processes. An alphabet-
ical listing of the symbols is given in Table lBl.2.
The list has been adapted from the official tables of the American Institute of Chemical
Engineers and of the American National Standards Institute. Suitable modifications have
been made in the units to conform with the editorial policies of the American Petroleum
Institute. Several additions have been made for symbols used frequently in this book. Listing
is alphabetical by concept within each category. Illustrative units or definitions are supplied
where appropraite.
General Concepts
Symbol Unit or Definition Symbol Unit or Definition
Acceleration . . . . . . . . a ft per sec per sec Newton law of motion,
Of gravity ......... g ft per sec per sec conversion factor in gc gc = ma/F, (lb) (ft per sec
Acentric factor . . . . . . w per sec) per lb [force]
Base of natural Number
logarithms . . . . . . . . e In general. ........ N
Coefficient. . . . . . . . . . C Of moles ......... n
Difference, finite . . . . ~ Pressure ............ p lb [force] per sq ft; atm; lb
Differential operator . d [force] per sq in. (abs)
Partial............ a Quantity, in general. . Q
Efficiency . . . . . . . . . . . 11 Radius of gyration . . . R
Energy, dimension. . . E Btu; ft-lb [force] Ratio, in general. . . . . R
Enthalpy ............ H Btu Refractive index . . . . . n
Entropy ............ S Btu per deg R Resistance . . . . . . . . . . R
Force ............... F lb [force] Shear stress . . . . . . . . . T lb [force] per sq ft
Fugacity Coefficient. . <!> Temperature
Function............ <!>, lji, X Absolute .......... T K; deg R
Gas constant, Dimension of. . . . . . 0
universal. . . . . . . . . . R To distinguish, use Ro In general. . . . . . . . . T, t deg C; deg F
Gibbs free energy. . . . G, F G =H-TS, Btu Temperature
Heat ............... Q Btu difference,
Helmholtz free energy A A= U - TS, Btu logarithmic mean . . 0 deg F
Internal energy . . . . . . U Btu Time
Mass, dimension of .. m lb Dimension of.. . . . . T sec
Mechanical equivalent In general. ..... : . . t, T sec; hr
of heat. J ft-lb [force] per Btu Watson characteri-
Moment of inertia . . . I lb-ft2 zation factor . . . . . . K
Work ............... W Btu
Geometrical Concepts
Angle . . . . . . . . . . . . . . ex, 0, <I> In general. . . . . . . . . A sq ft
In x,y plane....... a Projected . . . . . . . . . AP sq ft
In y,z plane....... <!> Surface
In z,x plane....... 0 Per unit mass.... Aw, s sq ft per lb
Solid angle . . . . . . . . w Per unit volume. . A., a sq ft per cu ft
Area Linear dimension
Cross-section . . . . . . S sq ft Breadth .......... b ft
Fraction free cross- Diameter ......... D ft
section . . . . . . . . . O' Distance along
path ............ s, x ft
1987 1-13

181.1
TABLE 181 .1 (Continued)
General Concepts--(continued)
Height above Mean free path ... . >.. cm; ft
datum plane. . . . . Z ft Radius .......... . r ft
Height equivalent . . . . H ft (Use subscript p for Thickness
equilibrium stage and In general. ..... . B ft
t for transfer unit.) Of film ........ . Br ft
Hydraulic radius . . . rH ft; sq ft per ft Wavelength ...... . >.. cm; ft
Lateral distance Other
from datum Particle-shape
plane ........... Y ft factor ......... . <l>s
Length, distance or Volume
dimension of . . . . L ft Fraction voids .... . f.
Longitudinal dis- Humid volume ... . VH cu ft per lb dry air
tance from datum In general. ....... . v cu ft
plane ........... X ft
Intensive Properties
Absorptivity for At constant
radiation. . . . . . . . . . a volume ......... Cv Btu per (lb) (deg F)
Activity ............. a Heat capacities, ratio
Activity coefficient, of ................ "Y
molal basis . . . . . . . . "Y Helmholtz free
Coefficient of energy ............ A Btu per lb
expansion Humid heat ......... c, Btu per (lb dry air) (deg F)
Linear .......... a ft per ft per deg F Internal energy ...... u Btu per lb
Volumetric. . . . . . 13 cu ft per cu ft per deg F Latent heat, phase
Compressibility change ........... >.. Btu per lb
factor . . . . . . . . . . . . z z ==pVIRT Molecular weight .... MW
Density............. p lb per cu ft Reflectivity for
Diffusivity radiation .......... p
Molecular, Surface tension ...... O' lb [force] per ft
volumetric . . . . . . . . Dv, B cu ft per (hr) (ft); sq ft Thermal
per hr conductivity ....... k Btu per (hr) (sq ft) (deg F
Thermal .......... a a== klcp, sq ft per hr per ft)
Emissivity ratio for Transmissivity of
radiation. . . . . . . . . . 1;, radiation .......... T
Enthalpy............ H Btu per lb Vapor pressure ...... p* lb [force] per sq ft; atm; lb
Entropy ............ S Btu per (lb) (deg R) [force] per sq in. (abs)
Fugacity ............ f lb [force] per sq ft; atm Viscosity
Gibbs free energy. . . . G, F Btu per lb Absolute or coeffi-
Heat capacity . . . . . . . c Btu per (lb) (deg F) cient of ......... µ lb per (sec) (ft)
At constant Kinematic ......... v sq ft per sec
pressure . . . . . . . . cP Btu per (lb) (deg F) Volume, per mole v cu ft per lb-mole
Symbols for Concentrations

Absorption factor. . . . A A== L/KV At saturation. . . . . . H,, Y* lb per lb dry air
Concentration, mass At wet-bulb
or moles per unit temperature . . . . . H w, Y w lb per lb dry air
volume ........... c lb per cu ft; lb-moles per Mass concentration of
cu ft particles . . . . . . . . . . cP lb per cu ft
Fraction Moisture content
By volumes . . . . . . . Xv Equilibrium water
By weight. . . . . . . . . Xw to bone dry
Cumulative beyond stock . . . . . . . . . . . x· lb per lb dry stock
a given size . . . . . <!> Free water to bone-
Humidity . . . . . . . . . . . H, Y H lb per lb dry air dry stock . . . . . . . X lb per dry stock
At adiabatic satura- Total water to bone-
tion temperature. H., Y. lb per lb dry air dry stock . . . . . . . XT lb per lb dry stock
1-14 1987
181 .1
Symbols for Concentrations---(continued)
Mole or mass fraction Relative distribution
In heavy or extract of two components
phase ........... x Between two
In light or raffinate phases in
phase........... y equilibrium . . . o:
Mole or mass ratio Between
In heavy or extract successive
phase ........... X stages . . . . . . . . p Pn = (y/yJn
In light or raffinate (x/x;)n+I
Relative humidity. . . . HR, RH
phase ........... Y
Slope of equilibrium
Number concentration
curve ............. m m = dy*ldx
of particles. . . . . . . . nP number per cu ft
Stripping factor. . . . . . S S = KVIL
Phase equilibrium
ratio ............. K K = y*/x
Symbols for Rate Concepts
Mass transfer Quantity per unit time,
coefficient unit area
Individual. . . . . . . k lb-moles per (hr) (sq ft) Emissive power,
(driving force) total.......... W Btu per (hr) (sq ft)
Gas film ........ kG To define driving force, Mass velocity,
Liquid film. . . . . . kL use subscript: average ...... ,. G G = w/S, lb per (sec) (sq ft)
Overall........... K c for lb-moles per cu ft Vapor or
Gas film basis . . . KG p for atm light
Liquid film basis . KL x for mole fraction phase ..... G, G lb per (hr) (sq ft)
Quantity per unit Liquid or
time, in general. . . . q heavy
Angular velocity . w phase ..... L, L lb per (hr) (sq ft)
Feed rate . . . . . . . F lb per hr; lb-moles per hr Radiation, in-
Frequency . . . . . . f, N1 tensity of . . . . . I Btu per (hr) (sq ft)
Friction velocity. . u* u* = (gcT..,p) 112 , ft per sec Velocity
Heat transfer Nominal, basis
rate . . . . . . . . . . q Btu per hr total cross-
Heavy or extract section of
phase rate . . . . L lb per hr; lb-moles per hr packed
Heavy or extract vessel . . . . . . v, ft per sec
product rate. . . B lb per hr; lb-moles per hr Volumetric
Light or raffinate average . . . . . . . V, V cu ft per (sec) (sq ft); ft
phase rate . . . . V lb per hr; lb-moles per hr per sec
Light or raffinate Quantity per unit
product rate... D lb per hr; lb-moles per hr time, unit volume
Mass rate of flow . . w lb per sec; lb per hr Quantity reacted
Molal rate of per unit time,
transfer......... N lb-moles per hr reactor
Power ............ P ft-lb [force] per sec volume ....... NR mole per (sec) (cu ft)
Revolutions per unit Space velocity,
time ............ n volumetric . . . . A cu ft per (sec) (cu ft)
Velocity Quantity per unit
In general. . . . . . . u ft per sec time, unit area, unit
Instantaneous, driving force, in
local general........... k
Longitudinal Eddy diffusivity. . BE sq ft per hr
(x) com- Eddy viscosity... VE sq ft per hr
ponent of. u ft per sec Eddy thermal
Lateral (y) diffusivity . . . . . o:E sq ft per hr
component Heat transfer
of ........ v ft per sec coefficient
Normal (z) Individual. . . h Btu per (hr) (sq ft) (deg F)
component Overall..... U Btu per (hr) (sq ft) (deg F)
of ........ w ft per se<.: Stefan-Boltzmann
Volumetric rate constant . . . . . . . . . . u 0.173 x 10-s Btu per (hr)
of flow ..... q cu ft per sec; cu ft per hr (sq ft) (deg R)4
1987 1-15
181 .1
TABLE 181.1 (Continued)
Modifying Signs for Principal Symbols
Concept Remarks Superscript Subscript Concept Remarks Superscript Subscript
Average value Written over (Bar) Partial molal Written over (Bar)
symbol quantity small
Dimensionless Follows symbol + (Plus) capitals
form Sequence in time
Equilibrium Follows symbol * (Asterisk) or space Follows symbol ' (Prime) 1. 2. 3, etc.
value " (Double
Fluctuating Usually applied prime)
0
component to local ' (Prime) Standard state Follows symbol (Degree)
velocity First derivative
Initial or refer- with respect to Written over (Dot)
ence value Follows symbol o (Zero) time symbol
Modified form Follows symbol ' (Prime) Second deriva- Written over ··(Double
" (Double tive with re- symbol dot)
prime) spect to time
Molal quantity Written over - (Tilde)
symbol
Dimensionless Numbers Used in Chemical Engineering
Condensation Peclet number....... Np, Lucp Lu DV

--or-·-
number ........... Nco k 0. , 0.
Prandtl number...... Np, cµ. v

Euler number . . . . . . . N Eu gcp, gcPP k or~
pu2, G2
Fanning friction gcpD (~P1)
Prandtl velocity ratio . u + u
f u*
factor ............ 2G2(~L)
Reynolds number.... NR,
Fourier number...... NFo kt o.t µ. µ.
cpL 2 or L 2
Reynolds number, ru* p
Froude number . . . . . . N Fr u2 u2 local ............. y µ.
aL 'gL
Schmidt number . . . . . Nsc µ.
Graetz number...... Na, cLG LV
--or- pDv
k 0.
L 3p2pg ~t L3pg ~t Sherwood number . . . Nsh kcL . (

Grashof number ..... Na,
2 or - - 2 - R or ]M NR,)(N,c)
113
h µ.(c µ. )
213
v Stanton number . . . . . Ns, h h
Heat transfer factor. . jH 213
cG k or (Ns,) (Np,) cpu 'cG
Vapor condensation L 3p2g>.
Lewis number . . . . . . . N Le k 0.
--or- number ........... Nev kµ.~t
Mass transfer factor . . jM

~pD(v )~; Weber number . . . . . . Nw, Lu 2 p. DG 2
~ P~v ,
gcrr gcprr
Nusselt number. . . . . . N Nu hL hD
k , k
Note: Pounds mass is abbreviated as lb and pounds force as lb(force]
1-16 1987
181 .1
TABLE 1B1.2
ALPHABETICAL INDEX OF SYMBOLS USED IN CHEMICAL ENGINEERING
Primary Concept Subscript Concept Primary Concept Subscript Concept

a Acceleration Acoustic Generalized
Activity Adiabatic component
Area, alternate for Arithmetic Interface
Surface per unit volume Internal or inner
A Absorption factor Absolute I Intensity of radiation
Area Area basis Moment of inertia
Helmholtz free energy Component A
j Transfer factor Generalized
b Breadth Baffle component
Base
Normal boiling point J Mechanical equivalent of heat
B Heavy product rate Black body k Mass transfer coefficient, indi-

Thickness Boiling point vidual
Component B Quantity per unit time, unit
area, unit driving force, in
c Concentration, mass or moles Concentration basis general
per unit volume Contraction Thermal conductivity
Specific heat, heat capacity Conversion factor
Critical K Watson characterization fac!or
Cutoff size Mass transfer coefficient,
overall
c Coefficient Component C Phase concentration ratio
d Differential operation Discharge L Heavy or extract phase rate Liquid
Disperse Length Liquid film basis
Drop Mass velocity of liquid or heavy
Dry phase
D Diameter Component D m Mass Mass
Diffusivity Distillate Dimension of Mean
Light or raffinate product rate In general
e Base of natural logarithms Effective Slope of equilibrium curve
Exit M Mass basis
E Energy Component E Molecular
Dimension of Eddy MW Molecular weight
In general Entrainment
n Number concentration Generalized stage
f Frequency Film Number of moles number
Friction factor, Fanning Fluid Refractive index
Fugacity Frequency Revolutions per unit time
Friction
N Molal rate
F Feed rate Feed Number, in general
Force
Gibbs free energy 0 Initial
Outer
g Acceleration of gravity Gage
Gravity 0 Overall
Vapor p Pressure Constant pressure
G Gibbs free energy Vapor Particle
Mass velocity Vapor film basis Plate or stages
In general Pressure basis
Of vapor Projected
p Power
h Individual coefficient of heat Heat
transfer Heated pc Pseudocritical
H Enthalpy Heat basis q Quantity per unit time, in gen- Rate basis
Height equivalent Humidity era)
Humidity Hydraulic Rate of heat flow
Rate of volumetric flow
1987 1-17
181.2

Q Heat y Mass or mole ratio in light or
Quantity, in general raffinate phase
r Radius Radius or radial z Compressibility factor
Reduced
z Height above datum plane
R Gas constant Radiation
Ratio, in general Reactor volume basis Cl Absorptivity for radiation
Reflux ratio Relative value Angle
Resistance Angle in x,y, plane
Coefficient of linear expansion
Radius of gyration Relative distribution of two
s Distance along path Saturation components between two
Specific surface Shape phases at equilibrium
Stress Thermal diffusivity
Surface basis Coefficient of volumetric
s Cross-section Cross-section basis expansion
Entropy Solid Relative distribution of two
Stripping factor Solvent components between succes-
sive stages
Temperature Tangential
Time Terminal Activity coefficient, molal
Transfer unit or units basis
Ratio of heat capacities
T Absolute temperature Constant temperature
Temperature, in general Total Differential operator, partial
u Longitudinal component of Upper Diffusivity, volumetric Film basis

local velocity Difference, finite
Velocity, in general
E Emissivity ratio for radiation
u Heat transfer coefficient, Fraction voids
overall T] Efficiency
Internal energy
0 Angle
v Lateral component of local Constant volume Angle in z,x plane
velocity Velocity basis Temperature, dimension of
Nominal velocity Volumetric
Specific volume Log mean temperature differ-
ence
v Light or raffinate phase rate Vapor
Volume, in general Latent heat of phase change
Volumetric average velocity Mean free path
Wavelength
w Mass flow rate Mass basis
Normal component of local Wet bulb A Volumetric space velocity
velocity µ Viscosity, absolute At constant viscosity
w Work v Viscosity, kinematic
Total emissive power
p Density Density basis
x Distance along path Mole fraction basis Reflectivity for radiation
Fraction
Mole or mass fraction in heavy u Fraction free cross-section
or extract phase Stefan-Boltzmann constant
Surface tension
x Longitudinal distance from Mole ratio basis
datum plane T Shear stress
Mole or mass ratio in heavy or Time, alternate for
extract phase Transmissivity for radiation
y Mole or mass fraction in light Angle
or raffinate phase Angle in y,z plane
Fraction cumulative, larger
y Humidity than a given size
Lateral distance from datum Function
plane Fugacity coefficient
Particle factor
1-18 1987
DS4B-EB/May 1988
1C
TABLE 1B1 .2 (Continued)
Function w Acentric factor

Angular frequency
Function
Angular velocity
Solid angle
Greek Alphabet
A a Alpha I Iota p p Rho

B 13 Beta K K Kappa l a Sigma
r 'I Gamma A >.. Lambda T T Tau
~ 8, a Delta M µ Mu y \) Upsilon
Epsilon N Nu Phi
E
z
H
t:
{
TJ
Zeta
Eta
-
0
v
~
0
Xi
Omicron
<I>
x
'I'
<1>
x Chi
Psi
e e Theta TI 7T Pi n "'
w Omega
SECTION 1C. PROPERTY DEFINITIONS
The data in Chapter 1 are divided into four main tables, as listed below:
lCl Hydrocarbons-Primary Properties
1C2 Hydrocarbons-Secondary Properties
1C3 Nonhydrocarbons-Primary Properties
1C4 Nonhydrocarbons-Secondary Properties
A list of properties included in the data tables as well as a definition of the property and
any other pertinent information follows.
1. Compound name.
2. Chemical formula.
PRIMARY TABLE PROPERTIES

3. Molecular weight (MW) based on IUPAC "Atomic Weights of the Elements," 1986 (102).
4. Boiling point at one atmosphere in degrees Fahrenheit.
5. Freezing point in air at one atmosphere in degrees Fahrenheit.
6. Critical properties.
The conditions of equilibrium for coexisting vapor and liquid phases of a pure substance
are defined on a pressure-temperature diagram by the vapor pressure curve. This curve starts
at the triple point, where vapor, liquid, and solid phases are in equilibrium, and ends at the
critical point. As the critical point is approached by the coexisting phases, their properties
approach each other until they become identical at the critical temperature and pressure,
where a single homogeneous phase is present.
Values of critical temperature in degrees Fahrenheit, pressure in pounds per square inch
absolute, volume in cubic feet per pound, and compressibility factor are given.
Further information on critical properties is given in Chapter 4.
7. Acentric Factor
The acentric factor is calculated from the definition:
w =-log P:.01 -1.000
Where:
w = acentric factor.
P:, 01 =the reduced vapor pressure at a reduced temperature, T,, of 0.7, P*f Pc
P* =vapor pressure, in pounds per square inch absolute.
Pc= critical pressure, in pounds per square inch absolute.
1-19

1C
T, =reduced temperature, TITc.

T= temperature, in degree Rankine.
Tc= critical temperature, in degrees Rankine.
When vapor pressure data were not available at T, = 0.7, Procedure 2Al.1 was used.
Further information on the acentric factor is given in Chapter 2.
8. Density of Liquids
.. . p(60 F, lb/gal)
Spec1f1c gravity, 60 F/60 F = p( water, F lb/ l)
60 , ga
p(60 F, lb/gal)
sp gr= 8.33718
Where:
p = liquid density.
Liquid densities at 60 F are given in pounds per gallon at one atmosphere when 60 F is
below the normal boiling point or at saturation pressure when 60 F is at or above the normal
boiling point. For compounds that are solid at 60 F, the liquid density is the liquid value
extrapolated back to 60 F.
Densities at other temperatures can be calculated from the density at 60 F by
p(T deg F) ~ 1 + [ V1 (:1

aT
F)
p
(T - 60)
l
Where:
T =temperature, in degrees Fahrenheit.
t (~i) P =coefficient of expansion, in degrees Fahrenheit- 1 •
API gravity is defined as:
de API = l 4 1. 5 - 131.5
g sp gr
Further information on liquid density is given in Chapter 6.
9. Refractive Index of Liquids
Values of the refractive index, nv, of the air saturated hydrocarbon relative to air at the
sodium D-line (5892.6A) are reported at 77 F.
10. Vapor Pressure
Vapor pressure is the pressure at which the vapor phase of a substance is in equilibrium
with the liquid phase of that substance at a specified temperature. Values of vapor pressure
at 100 degrees F are reported in units of pounds per square inch absolute.
Further information on vapor pressure is given in Chapter 5.
11. Heat Capacity of the Liquid and Gas
Heat capacities at constant pressure are reported for the liquid and ideal gas at 60 F and
1 atm pressure. These are related to the enthalpy by:
The observed heat capacity for a saturated liquid or vapor is C,. This may be converted to
the heat capacity at constant pressure by:
av) dP*
+ C,
Cp = T ( aT P dT
Where:
dP*ldT =the temperature derivative of the vapor pressure, in pounds per square inch
absolute per degree Rankine.
When values of the ideal gas heat capacity calculated from spectroscopic data were not
available, they were predicted by the second order method of Benson using the CHETAH
program (180). Heat capacities are reported in units of British thermal units per pound-
degree F. For compounds where the normal boiling point is below 60 F, liquid heat capacity
is reported at the saturation pressure.
Further information on heat capacity is given in Chapter 7.
1-20 1987
1C
12. Viscosity of Liquids

The kinematic viscosity in centistokes is reported at 100 F and 210 F and 1 atmosphere
pressure. The kinematic viscosity, v, is related to the absolute viscosity, µ,by:
µ(poise)
v (stokes)= ( )
p gm /cu cm
Where:
p = liquid density.
Further information on viscosity is given in Chapter 11.
13. Heat of Vaporization

The heat of vaporization, ~. is defined as the enthalpy of the real gas at the equilibrium
vapor pressure, minus the enthalpy of the liquid at the same pressure and temperature. When
experimental data were not available, ~ was predicted at the normal boiling point by the
Clapeyron Equation:
~ = ( d:;) T(V 8 - VL) (1441778)

Where:
~=latent heat of vaporization, in Btu/lb.
P* = pure substance vapor pressure, in psia.
T =temperature, in degrees Rankine.
V8 =specific volume of saturated vapor, in ft3/lb.
VL =specific volume of saturated liquid, in ft3/lb.
144/778 = conversion factor.
The heat of vaporization is reported in units of Btu/lb.
Further information on heat of vaporization is given in Chapter 7.
14. Net Heat of Combustion of the Liquid
Hydrocarbons:
The net heat of combustion at 77 F, !:..He, is the change in enthalpy for the reaction:
C.Hb (liquid, 77 F, 1 atm) + (a + ~) 02 (gas, 77 F, 1 atm) =

b
a C02 (gas, 77 F, 1 atm) + 2 HzO (gas, 77 F, 1 atm)
Net heat of combustion is related to gross heat of combustion by the relationship:

b
!:..He (net, Btu/lb)= !:..He (gross, Btu/lb)+ 2~w
Where:
~w =heat of vaporization of water at 77 F and saturation pressure= 1,050.0 Btu/lb (108).
For compounds which are gaseous at 77 F and 1 atm (i.e., C1 to C5 hydrocarbons), the net
heat of combustion of the vapor is given. This is related to the net heat of combustion of the
liquid as follows:
!:..He (vapor)= !:..He (liquid) - ~
Where:
~=heat of vaporization at 77 F, in Btu/lb.
Nonhydrocarbons:
For nonhydrocarbons, the standard combustion products are:
C02 (gas)
HzO (gas)
Fz (gas)
Ch (gas)
Br2 (gas)
Iz (gas)
S02 (gas)
Nz (gas)
Net heats of combustion for nonhydrocarbons are calculated from the change in enthalpy
upon reaction to these standard products.
1987 1-21
1C
For compounds where the heat of formation was not available, the net heat of formation
was predicted by the second order method of Benson using the CHETAH program (180)
after which the heat of combustion as calculated from the definition.
Net heat of combustion at 77 Fis reported in units of British thermal units per pound. The
heat of combustion is defined as the heat evolved; therefore, the values for heat of com-
bustion in this chapter are positive.
Further information on heat of combustion is given in Chapter 14.
15. Surface Tension of the Liquid
Surface tension is the tension exhibited by the free surface of a liquid.
The liquid surface tension at 77 F is reported in units of dynes per centimeter.
Further information on surface tension is given in Chapter 10.
SECONDARY TABLE PROPERTIES

16. Search Number
This number is for compound identification and is used only with the computerized version
of the data tables.
17. Solubility Parameter
The solubility parameter is defined by:
= (AUvap)112
8 V.!o
Where:
Auv•p =internal energy change on vaporization to the ideal gas, in cal/mol.
..!'.:.,!,,=liquid molar volume at 25 C, in cm 3/mol.
An approximation of the internal energy change yields:
_('A.
8- - - -
v_b_
RT) 112
Where:
'A. = heat of vaporization at 25 C, in cal/mol.
.!'.:_!, = liquid molar volume at 25 C, in cm 3/mol.
R =gas constant = 1. 9872 cal/mol · K.
T =absolute temperature, 298.15 in kelvins.
The above equation was used to calculate solubility parameters in units of (cal/cm 3) 112 •
18. Flash Point Temperature
The flash point of a liquid or solid is the lowest temperature at which sufficient vapor is
given off through evaporation or sublimation to form an ignitable mixture with the air near
the surface of the liquid or in the vessel used. Flash point temperatures are given in degrees
Fahrenheit.
19. Heat of Formation
Heat of formation of a hydrocarbon, C.Hb, in the ideal gas state is reported at 77 Fin units
of British thermal units per pound. Heats of formation of the hydrocarbon in the liquid state
are related to those in the ideal gas state by the following equation:
AHji" (Btu/lb)= fl.HJ"' (Btu/lb) - 'A. (Btu/lb)
Where:
'A.= the heat of vaporization at 77 F.
To derive a liquid heat of formation of a hydrocarbon, C.Hb, from a heat of combustion,
the following equations, which neglect pressure corrections, can be used:
AH}'q (Btu/lb)= AHc (net, Btu/lb)
MW (C02) b MW (H20)
+a MW (C.Hb) AH1 (C02, gas) + 2 MW (C.Hb) AH1 (H20, gas)
AH}'q (Btu/lb)= fl.He (net, Btu/lb) - M~4(~~~b) (44) a - M:~~·~Hb) (18) ~
1-22 1987
1C
Where:
fl.He= net heat of combustion, in British thermal units per pound.
MW = molecular weight, in pound per pound mole.
ll.H1 = heat of formation at 77 F
-3844.28 Btu/lb= heat of formation of C02 gas, in British thermal units per pound.
- 5770.9 =heat of formation of liquid H20, in British thermal units per pound
(108).
The heats of formation of nonhydrocarbons are obtained using the same techniques with
standard products of combustion as given earlier. Values are taken from DIPPR Compilation
where available.
For compounds where heats of formation were not derived from experimental data, heats
of formation were predicted by the second order method of Benson using the CHETAH
program (180).
20. Gibbs Free Energy of Formation
The Gibbs free energy of formation for the ideal gas state is reported at 77 F in units of
British thermal units per pound.
21. Heat of Fusion
The heat of fusion is reported at 77 F in units of British thermal units per pound.
22. Flammability Limits
Lower and upper limits of flammability are reported as volume percent in a mixture with
air.
When experimental data were not available, lower flammability limits were predicted by
the method of Shebeko et al. (191), and upper flammability limits were predicted by the
DIPPR Compilation method (50).
SECONDARY TABLES-HYDROCARBONS ONLY

23. Coefficient of Expansion
The coefficient of expansion is calculated by the definition:
13 = .!.
V
(av)
aT P
1
Values are reported at 60 F in units of (deg F)- •
24. Aniline Point

The aniline point of a petroleum product is the critical solution temperature of a mixture
of equal volumes of aniline and the hydrocarbon. It is the lowest temperature at which a
petroleum product is completely miscible with an equal volume of freshly distilled aniline.
The aniline point is reported in degrees Fahrenheit.
25. ASTM Octane Numbers
The octane number of a motor fuel indicates its relative tendency to knock under specified
conditions of laboratory engine operation. It is equal to the percentage of iso-octane in the
reference fuel whose knock characteristics equal those of the sample under test.
Octane numbers are reported for both the motor method and the research method of
testing, and for both clear and solutions with 3 ml TEL per gallon added.
26. Watson K Factor
The Watson characterization factor, K, is defined by the equation:
(MeABP) 113
K=~--~-
sp gr
Where:
MeABP =mean average boiling point, the normal boiling point for a pure component, in
degrees Rankine.
Further information on the Watson characterization factor is given in Chapter 2.
1987 1-23
1C0.1
TABLE 1C0.1
INDEX OF COMPOUNDS
COMPOUND TABLE ENTRY NAME TABLE SEQUENCE NUMBER
ACENAPHTHALENE ACENAPHTHALENE 471

ACENAPHTHENE ACENAPHTHENE 472
AC ENAPHTHY LENE ACENAPHTHALENE 471
ACETALDEHYDE ACETALDEHYDE 729
ACETENE ETHYLENE 192
ACETIC ACID ACETIC ACID 701

ACETIC ALOEHYDE ACETALDEHYDE 729
ACETIC ETHER ETHYL ACETATE 755
ACETIOIN ETHYL ACETATE 755
ACETONE ACETONE 821
ACE TON ITRI LE AC ETON ITRI LE 744

ACETOXYETHANE ETHYL ACETATE 755
1-ACETOXYETHYLENE VINYL ACETATE 757
1-ACETOXYPROPANE n-PROPYL ACETATE 759
ACETYLENE ACETYLENE 322
ACRALDEHYOE ACROLEIN 732

ACRI DINE ACRI DINE 751
ACROLEIN ACROLEIN 732
ACRYLIC ALDEHYDE ACROLEIN 732
ADAKANE 12 n-DODECANE 74
AETHYLIS CHLORIDUM ETHYL CHLORIOE 818

AIR AIR 770
ALGOFRENE TYPE 2 DICHLORODIFLUOROMETHANE 800
ALLENE PROPADIENE 290
ALLYLENE METHYLACETYLENE 323
ALLYL ALOEHYDE ACROLEIN 732

ALLYLIC ALCOHOL ACETONE 821
AMINIC ACID FORMIC ACID 700
AMINOBENZENE ANILINE 747
1-AMINOBUTANE n-BUTYLAMINE 739
2-AMINOBUTANE sac-BUTYLAMINE 741

AMINOETHANE ETHYLAMINE 736
1-AMINOETHANE ETHYLAMINE 738
2-AMINOETHANOL MONOETHANOLAMINE 853
bata-AMINOETHYL ALCOHOL MONOETHANOLAMINE 853
2-AMINOISOBUTANE tart-BUTYLAMINE 742

AMINOMETHANE METHYLAMINE 735
1-AMIN0-2-METHYLPROPANE ISOBUTYLAMINE 740
2-AMIN0-2-METHYLPROPANE tart-BUTYLAMINE 742
AMINOPHEN ANILINE 747
1-AMINOPROPANE 1,2-PROPYLENE GLYCOL 850

2-AMINOPROPANE ISOPROPYLAMINE 738
AMMONIA AMMONIA 771
AMYL ACETATE n-PENTYL ACETATE 762
n-AMYL ACETATE n-PENTYL ACETATE 762
AMYL ACETIC ESTER n-PENTYL ACETATE 762

AMYL ACETIC ETHER n-PENTYL ACETATE 762
AMYL ALCOHOL 1-PENTANOL 717
n-AMYL ALCOHOL 1-PENTANOL 717
sac-AMYL ALCOHOL 2-PENTANOL 718
1987 1-25
1C0.1
TABLE 1C0.1 (Continued)
tart-AMYL ALCOHOL 2-METHYL-2-BUTANOL 72D

tert-n-AMYL ALCOHOL 2-METHYL-2-BUTANOL 720
AMY LENE 2-METHYL-2-BUTENE 203
alpha.beta-AMYLENE 2-METHYL-2-BUTENE 203
cis.beta-AMYLENE cis-2-PENTENE i99
trans,beta-AMYLENE trans-2-PENTENE 200

AMYLENE HYDRATE 2-METHYL-2-BUTANOL 720
AMYL HYDROSULFIDE i-PENTANETHIOL 84i
n-AMYL MERCAPTAN i-PENTANETHIOL 84i
AMYL SULFHYDRATE i-PENTANETHIOL 84i
AMYL THIOALCOHOL i-PENTANETHIOL 84i

ANILINE ANILINE 747
ANHYOROL ETHANOL 1io
ANHYOROUS HYDROBROMIC ACID HYDROGEN BROMIDE 782
ANHYDROUS HYDROFLUORIC ACID HYDROGEN FLUORIDE 785
ANTHRACENE ANTHRACENE 474

ARCTON 9 TRICHLOROFLUOROMETHANE soi
AREGINAL ETHYL FORMATE 754
ARGON ARGON 772
ARTIC METHYL CHLORIDE 809
AZABENZENE PYRIDINE 748

9-AZAFLUORENE DI BENZOPYRROLE 750
i-AZAINDENE INDOLE 748
i-AZANAPHTHALENE QUINOLINE 749
AZINE PYRIDINE 746
i-BENZAZOLE INDOLE 748

BENZENE BENZENE 335
BENZENE.HYOROXY- PHENOL 724
8ENZENOFORM CARBON TETRACHLORIDE 802
BENZENOL PHENOL 724
BENZINOFORM CARBON TETRACHLORIDE 802

BENZO (JK) FLUORENE, IDRYL FLUORANTHENE 477
BENZOL BENZENE 335
BENZOLENE BENZENE 335
BENZO (a) PHENATHRENE CHRYSENE 478
i,2-BENZOPHENANTHRENE CHRYSENE 478

BENZOPHENOL PHENOL 724
BENZOPYRROLE IN DOLE 748
BI BENZENE INDOLE 748
BICARBURET of HYDROGEN BENZENE 335
c1s-BICYCL0[4.4,0]DECANE cis-DECAHYDRONAPHTHAENE ia4

trans-8ICYCL0[4.4,0]DECANE trans-DECAHYDRONAPHTHALENE ia5
BICYCLOHEXYL BICYCLOHEXYL ia3
i.i-BICYCLOHEXYL BICYCLOHEXYL ia3
BICYCLOPENTADIENE DICYCLOPENTADIENE 3i9
BI ETHYLENE i ,3-BUTADIENE 292

BIHEXYL n-DODECANE 74
BIISOPROPYL 2,3-DIMETHYLBUTANE i3
BI METHYL ETHANE 2
BI PHENYL BI PHENYL 398
i.1'-BIPHENYL BI PHENYL 396

BISCYCLOPENTADIENE OICYCLOPENTAOIENE 319
BIS[ETHOXY(i-ETHANOL)]ETHER TETRAETHYLENE GLYCOL 852
BIS(2-HYDROXYLETHYL) AMINE DIETHANOLAMINE 854
BIVINYL i. 3-BUTADI ENE 292
1-26 1987
1C0.1
BROMINE BROMINE 773

BUTADIENE 1,3-BUTADIENE 292
BUTA-i.3-DIENE 1,3-BUTADIENE 292
1 • 2-BUTADI ENE 1,2-BUTADIENE 29i
1 ,3-BUTADIENE 1, 3-BUTADIENE 292
alpha,garrma-BUTADIENE 1.3-BUTADIENE 292

BUT AL n-BUTYRALDEHYDE 73i
BUTALDEHYDE n-BUTYRALDEHYDE 73i
n-BUTANAL n-BUTYRALDEHYDE 73i
BUTANALDEHYDE n-BUTYRALDEHYDE 73i
sec-BUTANAMINE sec-BUTYLAMINE 74i

1-BUTANE ISOBUTANE 5
n-BUTANE n-BUTANE 4
BUTANECARBOXYLIC ACID n-PENTANOIC ACID 705
BUTANE. 2-HYDROXY sec-BUTANOL 7i5
n-BUTANETHIOL n-BUTANETHIOL 834

tert-BUTANETHIOL tert-BUTANETHIOL 835
2-BUTANETHIOL 2-BUTANETHIOL 836
n-BUTANOIC ACID n-BUTYRIC ACID 703
n-BUTANOL n-BUTANOL 7i3
sec-BUTANOL sec-BUTANOL 7i5

t-BUTANOL tert-BUTANOL 7i6
tert-BUTANOL tert-BUTANOL 7i6
n-BUTAN-1-0L n-BUTANOL 7i3
BUTAN-2-0L sec-BUTANOL 7i5
BUTANOL-2 sec-BUTANOL 1i5

2-BUTANONE METHYL ETHYL KETONE 822
trans-2-BUTENAL trans-CROTONALDEHYDE 733
c1s-2-BUTENE c1s-2-BUTENE i95
trans-2-BUTENE trans-2-BUTENE i96
i-BUTENE i-BUTENE i94

alpha-BUTENE i-BUTENE i94
BUTENYNE VINYLACETYLENE 328
BUTEN-3-YNE VINYLACETYLENE 326
n-BUTYL ACETATE n-BUTYL ACETATE 76i
i-BUTYL ACETATE n-BUTYL ACETATE 76i

n-BUTYL ALCOHOL n-BUTANOL 7i3
2-BUTYL ALCOHOL sec-BUTANOL 7i5
BUTYL ALDEHYDE n-BUTYRALDEHYDE 73i
n-BUTYL ALDEHYDE n-BUTYRALDEHYDE 73i
n-BUTYLAMINE n-BUTYLAMINE 739

sec-BUTYLAMINE sec-BUTYLAMI NE 74i
tert-BUTYLAMINE tert-BUTYLAMINE 742
i-BUTYLAMINE n-BUTYLAMINE 739
i-BUTYLBENZENE n-BUTYLBENZENE 349
n-BUTYLBENZENE n-BUTYLBENZENE 349

sec-BUTYLBENZENE sec-BUTYLBENZENE 35i
tert-BUTYLBENZENE tert-BUTYLBENZENE 352
n-BUTYLCARBINOL i-PENTANOL 7H
sec-BUTYLCARBINOL 2-METHYL-1-BUTANOL 7i9
tert-BUTYLCARBINOL 2,2-DIMETHYL-i-PROPANOL 722

n-BUTYLCYCLOHEXANE n-BUTYLCYCLOHEXANE i58
sec-BUTYLCYCLOHEXANE sec-BUTYLCYCLOHEXANE i6o
tert-BUTYLCYCLOHEXANE tert-BUTYLCYCLOHEXANE i6i
n-BUTYLCYCLOPENTANE n-BUTYLCYCLOPENTANE i24
1987 1-27
1C0.1
COMPOUND TABLE ENTRY NAllE TABLE SEQUENCE NUllBER
BUTYLENE HYDRATE sec-BUTANOL 715

BUTYLENE OXIDE TETRAHYDROFURAN 76B
BUTYL ETHANOATE n-BUTYL ACETATE 761
BUTYL ETHYLENE TETRAHYDROFURAN 76B
BUTYL HYDROXIDE n-BUTANOL 713
tart-BUTYL HYOROXIOE tert-BUTANOL 716

n-BUTYL llERCAPTAN n-BUTANETHIOL B34
tart-BUTYL llERCAPTAN tert-BUTANETHIOL B35
1-n-BUTYLNAPHTHALENE 1-n-BUTYLNAPHTHALENE 436
2-n-BUTYLNAPHTHALENE 2-n-BUTYLNAPHTHALENE 437
1-n-BUTYL-1,2,3,4-TETRAHYDRONAPHTHALENE 1-n-BUTYL-1,2,3,4-TETRAHYDRONAPHTHALENE 454

6-n-BUTYL-1,2,3,4-TETRAHYDRONAPHTHALENE 6-n-BUTYL-1,2,3,4-TETRAHYDRONAPHTHALENE 455
BUTYRAL n-BUTYRALDEHYDE 731
BUTYRALDEHYDE n-BUTYRALDEHYDE 731
n-BUTYRALDEHYDE n-BUTYRALDEHYDE 731
n-BUTYRIC ACID n-BUTYRIC ACID 703

BUTYRIC ALDEHYDE n-BUTYRALDEHYDE 731
BUTYRYALDEHYDE n-BUTYRALOEHYDE 731
CAMPHOR TAR NAPHTHALENE 427
CAPRYLENE 1-DCTENE 257
CARBAZOLE DIBENZOPYRROLE 750

CARBINAllINE llETHYLAllINE 735
CARBINOL METHANOL 709
CARBOLIC ACID PHENOL 724
CARBONA CARBON TETRACHLORIDE BD2
CARBON BISULFIDE CARBON DISULFIDE B31

CARBON CHLORIDE CARBON TETRACHLORIDE B02
CARBON DIOXIDE CARBON DIOXIDE 775
CARBON DISULFIDE CARBON DISULFIDE 831
CARBON llDNDXIDE CARBON llDNDXIDE 774
CARBON OXIDE CARBON MONOXIDE 774

CARBON DXYSULFIDE CARBONYL SULFIDE 776
CARBON SULFIDE CARBON DISULFIDE B31
CARBON TETRACHLORIDE CARBON TETRACHLORIDE BD2
CARBON TETRAFLUORIDE CARBON TETRAFLUORIDE B03
CARBON TRIFLORIOE TRIFLUOROllETHANE B07

CARBONIC ANHYDRIDE CARBON DIOXIDE 775
CARBONIC OXIDE CARBON MONOXIDE 774
CARBONYL DIAllIDE UREA 743
CARBONYL SULFIDE CARBONYL SULFIDE 776
CARBDXYETHANE PROPIDNIC ACID 702

CAUSTIC SODA SODIUll HYDROXIDE B47
CETANE n-HEXADECANE 7B
CHI NOLI NE QUI NOLI NE 749
CHLORINE CHLORINE 777
CHLORODIFLUOROMETHANE CHLORODIFLUOROMETHANE B04

CHLOROETHANE ETHYL CHLORIDE B1B
CHLOROETHENE VINYL CHLORIDE B11
CHLOROETHYLENE VINYL CHLORIDE B11
CHLOROFORM CHLOROFORM B06
CHLOROllETHANE llETHYL CHLORIDE B09

CHLOROT~IFLUOROllETHANE CHLOROTRIFLUOROllETHANE 799
CHRYSENE CHRYSENE 47B
CINNAllENE STYRENE 3B4
CINNAllINDL STYRENE 3B4
1-28 1987
1C0.1
COM POU NO TABLE. ENTRY NAME. TABLE SEQUENCE NUMBER
CINNAMOL STYRENE 3B4

COAL NAPHTHA BENZENE 335
m-CRESOL m-CRESOL 726
o-CRESOL o-CRESOL 725
p-CRESOL p-CRESOL 727
2-CRESOL o-CRESOL 725

3-CRESOL m-CRESOL 726
4-CRESOL p-CRESOL 727
m-CRESYLIC ACIO m-CRESOL 726
o-CRESYLIC ACIO o-CRESOL 725
p-CRE.SYLIC 11.ClO 'P-CRE.SOL 727

CROTONAL trans-CROTONALOEHYOE 733
trans-CROTONALOEHYOE trans-CROTONALOEHYOE 733
CROTONIC ALOEHYOE trans-CROTONALOEHYOE 733
CROTONYLENE OIMETHYLACETYLENE 324
CROTYLALOEHYOE trans-CROTONALOEHYOE 733

CUl&E.NE. tSOPROPYlSENIENE 342
psl-CUMENE 1.2,4-TRIMETHYLBENZENE 347
CYCLOBUTANE CYCLOBUTANE 98
CYCLOHEPTANE CYCLOHEPTANE 179
CYCLOHEXANE CYCLOHEXANE 146

CYCLOHEXATRIENE BENZENE 335
CYCLOHEXENE C'ICLOHEXENE 31S
CYCLOHEXYLBENZENE CYCLOHEXYLBENZENE 383
CYCLOHEXYLMETHANE METHYLCYCLOHEXANE 147
CYCLON HYDROGEN CYANIDE 7B4

CYCLONONANE CYCLONONANE 181
CYCLOOCTANE CYCLOOCTANE 1BO
CYClOPEN'Tll.OlENE C'ICLOPENiADlENE 31B
CYCLOPENTAOIENE OIMER DICYCLOPENTAD!ENE 319
1,3-CYCLOPENTADIENE, DIMER D!CYCLOPENTADIENE 319

CYCLOPENTANE CYCLOPENTANE 101
CYCLOPENTENE CYCLOPENTENE 310
CYCLOPROPANE CYCLOPROPANE 93
CYClOiEi~AMEiHYLENE OXIDE TEiRAH'IDROFURAN 768
m-CYMENE m-CYMENE 357

o-CYMENE o-CYMENE 356
p-CYMENE p-CYMENE 358
CYMOL p-CYMENE 358
cls-DECAHYDRONAPHTHALENE cls-DECAHYDRONAPHTHALENE 184
trans-DECAHYDRONAPHTHALENE trans-DECAHYDRONAPHTHALENE 185

cls-DECALIN cls-DECAHYDRONAPHTHALENE 184
trans-DECALIN trans-DECAHYDRONAPHTHALENE 185
n-DECANE n-DECANE 62
1-DECENE 1-DECENE 279
n-DECYLBENIENE n-DEC'ILBENZENE 376

n-DECYLCYCLOHEXANE n-DECYLCYCLOHEXANE 168
n-DECYLCYCLOPENTANE n-DECYLCYCLOPENTANE 135
1-n-DECYLNAPHTHALENE 1-n-DECYLNAPHTHALENE 445
1-n-DECYL-1,2,3,4-TETRAHYDRONAPHTHALENE 1-n-DECYL-1,2,3,4-TETRAHYDRONAPHTHALENE 462
1-DECYNE 1-DECYNE 334

DELPHINIC ACID 3-METHYLBUTYRIC ACID 707
DEVOTON METHYL ACETATE 753
DIBENZAL (els) cls-1,2-DIPHENYLETHENE 420
DIBENZAL, (E form) trans-1,2-DIPHENYLETHENE 421
1987 1-29
1C0.1
DIBENZOFURAN DIBENZOFURAN 769

OIBENZOPYRROLE DIBENZOPYRROLE 7SO
DIBENZO (B.O) PYRROLE DIBENZOPYRROLE 7SO
DIBENZYLIDNE. (E form) c1s-1.2-DIPHENYLETHENE 420
OICHLORODIFLUOROMETHANE DICHLORODIFLUOROMETHANE BOO
OICHLOROFLUOROMETHANE DICHLOROFLUOROMETHANE BOS

1,1-0ICHLOROETHANE 1,1-DICHLOROETHANE B1S
1,2-DICHLOROETHANE 1,2-DICHLOROETHANE B16
DICHLOROMETHANE DICHLOROMETHANE BOB
DICHLOROMONOFLUOROMETHANE DICHLOROFLUOROMETHANE BOS
1,2-0ICHLOROPROPANE 1,2-DICHLOROPROPANE B20

alpha,beta-DICHLOROPROPANE 1,2-DICHLOROPROPANE B20
DICYCLOHEXANE BICYCLOHEXYL 1B3
DICYCLOPENTADIENE DICYCLOPENTADIENE 319
OIETHANOLAMINE DIETHANOLAMINE BS4
N.N-DIETHANOLMETHYLAMINE METHYL OIETHANOLAMINE 8S6

m-DIETHYLBENZENE m-DIETHYLBENZENE 360
o-DIETHYL8ENZENE o-DIETHYLBENZENE 3S9
p-OIETHYL8ENZENE p-OIETHYLBENZENE 361
1,2-DIETHYL8ENZENE o-DIETHYL8ENZENE 3S9
1,3-DIETHYL8ENZENE m-DIETHYLBENZENE 360

1,4-DIETHYLBENZENE p-DIETHYLBENZENE 361
01 1-DIETHYLCYCLOPENTANE 1,1-DIETHYLCYCLOPENTANE 127
cis-1,2-DIETHYLCYCLOPENTANE cis-1,2-DIETHYLCYCLOPENTANE 128
DIETHYLDIMETHYLMETHANE 2,3-DIMETHYLPENTANE 19
DIETHYLENE GLYCOL DIETHYLENE GLYCOL 8S1

DIETHYLENE OXIDE TETRAHYDROFURAN 768
DIETHYL ETHER DIETHYL ETHER 76S
DIETHYL KETONE DIETHYL KETONE 823
DIETHYL OXIDE DIETHYL ETHER 76S
3,3-DIETHYLPENTANE 3,3-DIETHYLPENTANE SS
OIETHYLSULFIDE 3-THIAPENTANE 838
DIETHYLTHIOETHER 3-THIAPENTANE 838
DICHLORODIFLUOROMETHANE DICHLORODIFLUOROMETHANE 800
1,1-DIFLUOROETHANE 1,1-DIFLUOROETHANE 817
DIGLYCOLAMINE DIGLYCOLAMINE 8SS

DIHEXYL n-DODECANE 74
1,2-DIHYDROACENAPHTHALENE ACENAPHTHENE 472
DIHYDROBUTADIENE SULFONE SULFOLANE 862
DIHYDROGEN OXIDE WATER 84S
2,3-DIHYDROINDENE 2,3-DIHYDROINDENE 466

2,2'-DIHYDROXYDIETHYLAMINE 3-THIAPENTANE 838
beta,beta'-DIHYDROXYDIETHYL ETHER DIETHYLENE GLYCOL 8S1
DI(2-HYDROXETHYL) AMINE DIETHANOLAMINE 8S4
1,2-DIHYDROXYPROPANE 1,2-PROPYLENE GLYCOL 8SO
DIISOBUTYL 2,2,3,3-TETRAMETHYLBUTANE 40
DIISOPROPANOLAMINE DII SOPROPYLAMI NE 8S8
DIMETHYL ETHANE 2
DIMETHYLACETIC ACID 2-METHYLPROPIONIC ACID 704
DIMETHYLACETONE DIETHYL KETONE 823
DIMETHYLACETYLENE DIMETHYLACETYLENE 324

m-DIMETHYLBENZENE m-XYLENE 339
o-DIMETHYLBENZENE a-XYLENE 338
p-DIMETHYLBENZENE p-XYLENE 340
1,2-DIMETHYLBENZENE a-XYLENE 338
1-30 1987
1C0.1
1,3-0IMETHYLBENZENE m-XYLENE 339

1,4-DIMETHYLBENZENE p-XYLENE 340
2,3-DIMETHYL-1,3-BUTADIENE 2,3-0IMETHYL-1,3-BUTADIENE 300
2,2-DIMETHYLBUTANE 2,2-DIMETHYLBUTANE 12
2,3-DIMETHYLBUTANE 2,3-0IMETHYLBUTANE 13
1,3-DIMETHYL BUTANOL 4-METHYL-2-PENTANOL 723

2,3-DIMETHYL-1-BUTENE 2.3-DIMETHYL-1-BUTENE 218
2,3-DIMETHYL-2-BUTENE 2,3-DIMETHYL-2-BUTENE 220
3,3-DIMETHYL-1-BUTENE 3.3-DIMETHYL-1-BUTENE 219
DIMETHYLCARBINOL ISOPROPANOL 712
1,1-DIMETHYLCYCLOHEXANE 1,1-DIMETHYLCYCLOHEXANE 149

cls-1,2-DIMETHYLCYCLOHEXANE c1s-1,2-DIMETHYLCYCLOHEXANE 150
trans-1,2-DIMETHYLCYCLOHEXANE trans-1.2-DIMETHYLCYCLOHEXANE 151
cls-1,3-0IMETHYLCYCLOHEXANE c1s-1,3-DIMETHYLCYCLOHEXANE 152
trans-1,3-DIMETHYLCYCLOHEXANE trans-1,3-DIMETHYLCYCLOHEXANE 153
cls-1,4-DIMETHYLCYCLOHEXANE c1s-1.4-DIMETHYLCYCLOHEXANE 154

trans-1.4-DIMETHYLCYCLOHEXANE trans-1 ,4-DIMETHYLCYCLOHEXANE 155
1,1-DIMETHYLCYCLOPENTANE 1.1-DIMETHYLCYCLOPENTANE 104
cls-1,2-DIMETHYLCYCLOPENTANE c1s-1,2-DIMETHYLCYCLOPENTANE 105
trans-1,2-DIMETHYLCYCLOPENTANE trans-1.2-DIMETHYLCYCLOPENTANE 106
cls-1,3-DIMETHYLCYCLOPENTANE c1s-1,3-DIMETHYLCYCLOPENTANE 107

trans-1,3-DIMETHYLCYCLOPENTANE trans-1,3-DIMETHYLCYCLOPENTANE 108
cls-1,2-DIMETHYLCYCLOPROPANE cls-1,2-DIMETHYLCYCLOPROPANE 96
trans-1,2-DIMETHYLCYCLOPROPANE trans-1,2-DIMETHYLCYCLOPROPANE 97
DIMETHYLDISULFIDE 2,3-DITHIABUTANE 829
DIMETHYLENEMETHANE PROPADIENE 290

1,1-DIMETHYLETHANETHIOL tert-BUTANETHIOL 835
1,1-DIMETHYLETHANOL tert-BUTANOL 716
DIMETHYL ETHER DIMETHYL ETHER 763
DIMETHYL ETHER of POLYETHYLENE GLYCOL SELEXOL 863
1,1-DIMETHYLETHYLAMINE tert-BUTYLAMINE 742

DI(1-METHYLETHYL)AMINE DIISOPROPANOLAMINE 858
(1,1-DIMETHYLETHYL) BENZENE tert-BUTYLBENZENE 352
1,2-DIMETHYL-3-ETHYLBENZENE 1,2-DIMETHYL-3-ETHYLBENZENE 362
1,2-DIMETHYL-4-ETHYLBENZENE 1.2-DIMETHYL-4-ETHYLBENZENE 363
1,3-DIMETHYL-2-ETHYLBENZENE 1.3-DIMETHYL-2-ETHYL8ENZENE 364

1,3-0IMETHYL-4-ETHYLBENZENE 1,3-0IMETHYL-4-ETHYLBENZENE 365
1,3-DIMETHYL-5-ETHYLBENZENE 1,3-DIMETHYL-5-ETHYL~ENZENE 366
1.4-DIMETHYL-2-ETHYLBENZENE 1,4-DIMETHYL-2-ETHYLBENZENE 367
DIMETHYL ETHYL CARBINOL 2-METHYL-2-BUTANOL 720
1,1-DIMETHYLETHYLCYCLOHEXANE tert-BUTYLCYCLOHEXANE 161

1,1-DIMETHYL-2-ETHYLCYCLOPENTANE 1,1-DIMETHYL-2-ETHYLCYCLOPENTANE 129
cls-1,2-DIMETHYLETHYLENE cls-2-BUTENE 195
trans-1,2-DIMETHYLETHYLENE trans-2-BUTENE 196
2,2-DIMETHYL-3-ETHYLPENTANE 2.2-DIMETHYL-3-ETHYLPENTANE 56
2,4-DIMETHYL-3-ETHYLPENTANE 2,4-DIMETHYL-3-ETHYLPENTANE 57
OIMETHYLETHYNE DIMETHYLACETYLENE 324
OIMETHYLFORMALDEHYDE ACETONE 821
DIMETHYL FORMAMIDE N,N-DIMETHYLFORMAMIDE 859
N,N-DIMETHYLFORMAMIDE N,N-DIMETHYLFORMAMIDE 859
2,6-DIMETHYL-1.5-HEPTADIENE 2,6-DIMETHYL-1,5-HEPTADIENE 308

2,2-DIMETHYLHEPTANE 2,2-DIMETHYLHEPTANE 46
2,6-DIMETHYLHEPTANE 2,6-DIMETHYLHEPTANE 47
2,2-DIMETHYLHEXANE 2,2-DIMETHYLHEXANE 28
1987 1-31
1C0.1
3,3-0IMETHYLHEXANE 3,3-DIMETHYLHEXANE 32
c1s-2,2-DIMETHYL-3-HEXENE cis-2,2-DIMETHYL-3-HEXENE 274
2,3-DIMETHYL-1-HEXENE 2,3-DIMETHYL-1-HEXENE 272

2,3-DIMETHYL-2-HEXENE 2,3-DIMETHYL-2-HEXENE 273
2,4-DIMETHYL-3-ISOPROPYL PENTANE 2,4-DIMETHYL-3-ISDPRDPYL PENTANE 72
DIMETHYLKETAL ACETONE 821
DIMETHYL KETONE ACETONE 821
N,N-DIMETHYLMETHANAMIDE N,N-DIMETHYLFDRMAMIOE 859

DIMETHYLMETHANE PROPANE 3
6,6-DIMETHYL-2-METHYLENE8ICYCL0(3,1,1)HEPTANE beta-PIN ENE 321
2,4-DIMETHYL-3-(1-METHYLETHYL)PENTANE 2,4-DIMETHYL-3-ISOPROPYLPENTANE 72
DIMETHYL MONOSULFIDE DIMETHYL SULFIDE 829
1,2-DIMETHYLNAPHTHALENE 1,2-DIMETHYLNAPHTHALENE 432

1,4-DIMETHYLNAPHTHALENE 1,4-DIMETHYLNAPHTHALENE 433
3,7-DIMETHYL-1,6-0CTADIENE 3,7-DIMETHYL-1,6-DCTADIENE 309
2,7-DIMETHYLOCTANE 2,7-DIMETHYLOCTANE 67
2,2-DIMETHYLPENTANE 2,2-DIMETHYLPENTANE 1B
2,3-0IMETHYLPENTANE 2,3-DIMETHYLPENTANE 19
2,4-DIMETHYLPENTANE 2,4-DIMETHYLPENTANE 20
3,3-0IMETHYLPENTANE 3,3-DIMETHYLPENTANE 21
2,3-DIMETHYL-1-PENTENE 2,3-DIMETHYL-1-PENTENE 244

c1s-3,4-DIMETHYL-2-PENTENE cis-3,4-DIMETHYL-2-PENTENE 251
trans-3,4-DIMETHYL-2-PENTENE trans-3,4-DIMETHYL-2-PENTENE 252

c1s-4,4-DIMETHYL-2-PENTENE c1s-4,4-DIMETHYL-2-PENTENE 253
trans-4,4-DIMETHYL-2-PENTENE trans-4,4-DIMETHYL-2-PENTENE 254
2,2-DIMETHYLPROPANE NEOPENTANE 8
2,2-DIMETHYL-1-PROPANOL 2,2-DIMETHYL-1-PROPANOL 722

DIMETHYL SULFIDE DIMETHYL SULFIDE 829
DIMETHYLSULFOXIDE DIMETHYL SULFDXIDE 861
DIMETHYLSULPHOXIDE DIMETHYL SULFOXIDE 861
2,2-DIMETHYL-1,2,3,4-TETRAHYDRONAPHTHALENE 2,2-DIMETHYL-1,2,3,4-TETRAHYDRONAPHTHALENE 449

DIMETHYL THIOETHER DIMETHYL SULFIDE 829
DINITROGEN MONOXIDE NITROUS OXIDE 791
DINITROGEN OXIDE NITROUS OXIDE 791
OINITROGEN TETRAOXIDE NITROGEN TETRAOXIDE 793

1,1-DIOXIOE TETRAHYDROTHIOFURAN SULFOLANE 862
OIOXOTHIOLAN SULFDLANE 862
DI PHENYL BIPHENYL 396
DIPHENYLACETYLENE DIPHENYLACETYLENE 423
1,2-DIPHENYLBENZENE 1,2-DIPHENYLBENZENE 424

1,3-DIPHENYL8ENZENE 1,3-DIPHENYLBENZENE 425
1,4-DIPHENYL8ENZENE 1,4-DIPHENYLBENZENE 426
p-DIPHENYL8ENZENE 1,4-DIPHENYLBENZENE 426
1,1-0IPHENYL8UTANE 1,1-DIPHENYLBUTANE 407
1-32 1987
1C0.1
1,1-DIPHENYLDECANE 1,1-DIPHENYLDECANE 413

1,1-DIPHENYLDODECANE 1,1-DIPHENYLDODECANE 415
DIPHENYLENEIMINE DIBENZOPYRROLE 750
DIPHENYLENIMIDE DIBENZOPYRROLE 750
1,1-DIPHENYLETHANE 1,1-DIPHENYLETHANE 403
1,2-DIPHENYLETHANE 1,2-DIPHENYLETHANE 404

1,2-DIPHENYLETHENE (Z FORM) cis-1,2-0IPHENYLETHENE 420
cis-1,2-DIPHENYLETHENE cis-1,2-DIPHENYLETHENE 420
trans-1,2-DIPHENYLETHENE trans-1,2-DIPHENYLETHENE 421
DIPHENYLETHYNE DIPHENYLACETYLENE 423
1,1-DIPHENYLHEPTANE 1,1-DIPHENYLHEPTANE 410

1,1-DIPHENYLHEXADECANE 1,1-DIPHENYLHEXADECANE 419
1,1-DIPHENYLHEXANE 1,1-DIPHENYLHEXANE 409
DIPHENYLMETHANE DIPHENYLMETHANE 402
1,1-DIPHENYLNONANE 1,1-DIPHENYLNONANE 412
1,1-DIPHENYLOCTANE 1,1-DIPHENYLOCTANE 411

1,1-DIPHENYLPENTADECANE 1,1-DIPHENYLPENTADECANE 418
1,1-DIPHENYLPENTANE 1,1-DIPHENYLPENTANE 408
1,1-DIPHENYLPROPANE 1,1-DIPHENYLPROPANE 405
1,2-DIPHENYLPROPANE 1,2-0IPHENYLPROPANE 406
1,1-DIPHENYLTETRADECANE 1,1-DIPHENYLTETRADECANE 417

1,1-DIPHENYLTRIDECANE 1,1-DIPHENYLTRIDECANE 416
1,1-DIPHENYLUNDECANE 1,1-DIPHENYLUNDECANE 414
DIPROPYLMETHANE n-HEPTANE 14
2,3-DITHIABUTANE 2,3-DITHIABUTANE 828
DITHIOCARBONIC ANHYDRIDE CARBON DISULFIDE 831

DI VINYL 1,3-BUTADIENE 292
n-DOCOSANE n-DOCOSANE 84
n-DODECANE n-DODECANE 74
DODECANE n-DODECANE 74
1-DODECENE 1-DODECENE 281

n-DODECYLBENZENE n-DOOECYLBENZENE 378
n-DODECYLCYCLOHEXANE n-DODECYCLCYCLOHEXANE 170
n-DODECYLCYCLOPENTANE n-DODECYLCYCLOPENTANE 137
DRY ICE CARBON DIOXIDE 775
n-EICOSANE n-EICOSANE 82
1-EICOSENE 1-EICOSENE 289
n-EICOSYLCYCLOHEXANE n-EICOSYLCYCLOHEXANE 178
n-EICOSYLCYCLOPENTANE n-EICOSYLCYCLOPENTANE 145
1,4-EPOXYBUTANE TETRAHYDROFURAN 768
ERYTHRENE 1 , 3-BUTADI ENE 292

ETHANAL AC ET ALDEHYDE 729
ETHANE ETHANE 2
ETHANECARBOXYLIC ACID PROPIDNIC ACID 7D2
ETHAN EN ITRI LE AC ETON ITRI LE 744
ETHANETHIDL ETHYL MERCAPTAN 831

ETHANOIC ACID ACETIC ACID 701
ETHANOL ETHANOL 710
ETHANOLAMINE MONOETHANOLAMINE 853
beta-ETHANOLAMINE MONOETHANOLAMINE 853
ETHENE ETHYLENE 192

ETHENYL ACETATE VINYL ACETATE 757
ETHENYL BENZENE STYRENE 384
1-ETHENYL ETHANOATE VINYL ACETATE 757
ETHER DIETHYL ETHER 765
1987 1-33
1C0.1
ETHER HYDROCHLORIC ETHYL CHLORIDE 818

ETHER MURIATIC ETHYL CHLORIOE 818
ETHINE ACETYLENE 322
ETHOXYETHANE DIETHYL ETHER 765
ETHYL ACETATE ETHYL ACETATE 755
ETHYL ACETIC ACIO n-8UTYRIC ACID 703

ETHYL ACETIC ESTER ETHYL ACETATE 755
ETHYLACETONE METHYL-n-PROPYL KETONE 825
ETHYLACETYLENE ETHYLACETYLENE 325
ETHYL ALCOHOL ETHANOL 710
ETHYL ALDEHYDE AC ET ALDEHYDE 729

ETHYLAMINE ETHYLAMINE 736
ETHYLBENZENE ETHYLBENZENE 337
ETHYLBENZOL ETHYLBENZENE 337
1-ETHYL-[c1s-8ICYCL0[4.4.0)0ECANE) 9-ETHYL-[c1s-DECAHYORONAPHTHALENE) 190
1-ETHYL-[trans-BICYCL0[4.4.0)DECANE 9-ETHYL-[trans-DECAHYDRONAPHTHALENE) 191

2-ETHYL-[c1s-BICYCL0[4.4.0)DECANE) 1-ETHYL-[cls-OECAHYDRONAPHTHALENE) 188
2-ETHYL-[trans-BICYCL0[4.4.0)DECANE) 1-ETHYL-[trans-DECAHYDRONAPHTHALENE) 189
2-ETHYL-1-8UTENE 2-ETHYL-1-BUTENE 217
ETHYL CARBINOL n-PROPANOL 711
ETHYL CHLORIDE ETHYL CHLORIDE 818

ETHYLCYCLOBUTANE ETHYLCYCLOBUTANE 100
ETHYLCYCLOHEPTANE ETHYLCYCLOHEPTANE 182
ETHYLCYCLOHEXANE ETHYLCYCLOHEXANE 148
1-ETHYLCYCLOHEXENE 1-ETHYLCYCLOHEXENE 317
ETHYLCYCLOPENTANE ETHYLCYCLOPENTANE 103

1-ETHYLCYCLOPENTENE 1-ETHYLCYCLOPENTENE 312
3-ETHYLCYCLOPENTENE 3-ETHYLCYCLOPENTENE 313
ETHYLCYCLOPROPANE ETHYLCYCLOPROPANE 95
1-ETHYL-cls-DECAHYDRONAPHTHALENE 1-ETHYL-cls-DECAHYDRONAPHTHALENE 188
1-ETHYL-trans-DECAHYDRONAPHTHALENE 1-ETHYL-trans-DECAHYDRONAPHTHALENE 189

9-ETHYL-cls-DECAHYDRONAPHTHALENE 9-ETHYL-cls-DECAHYDRONAPHTHALENE 190
9-ETHYL-trans-DECAHYDRONAPHTHALENE 9-ETHYL-trans-OECAHYORONAPHTHALENE 191
1-ETHYL-2.3-DIMETHYLBENZENE 1.2-DIMETHYL-3-ETHYLBENZENE 362
ETHYLDIMETHYLMETHANE ISOPENTANE 7
ETHYLENE ETHYLENE 192

ETHYLENE CHLORIDE 1.2-DICHLOROETHANE 816
ETHYLENE DICHLORIDE 1.2-DICHLOROETHANE 816
ETHYLENE DIGLYCOL DIETHYLENE GLYCOL 851
ETHYLENE FLUORIDE 1.1-DIFLUOROETHANE 817
ETHYL ETHANOATE ETHYL ACETATE 755

1-ETHYL-2-ETHENYL BENZENE 1-ETHYL-2-ETHENYL BENZENE 392
ETHYL ETHER DIETHYL ETHER 765
ETHYLETHYLENE 1-BUTENE 194

ETHYLETHYNE ETHYLACETYLENE 325
ETHYL FLUORIDE ETHYL FLUORIDE 819
ETHYL FORMATE ETHYL FORMATE 754
ETHYLFORMIC ACID PROPIONIC ACID 702
ETHYLFORMIC ESTER ETHYL FORMATE 754

3-ETHYLHEPTANE 3-ETHYLHEPTANE 45
3-ETHYLHEXANE 3-ETHYLHEXANE 27
2-ETHYL-1-HEXENE 2-ETHYL-1-HEXENE 269
1-34 1987
1C0.1
COllPOUNO TABLE ENTRY NAME TABLE SEQUENCE NUMBER

ETHYL HYDRATE ETHANOL 710
ETHYL HYORIOE ETHANE 2
ETHYL HYDROSULFIDE ETHYL MERCAPTAN 830
ETHYL HYDROXIDE ETHANOL 710
ETHYLIC ACID ACETIC AC ID 701

1,1'-ETHYLIDENEBISBENZENE 1,1-DIPHENYLETHANE 403
ETHYLIDENE CHLORIDE 1,1-DICHLOROETHANE B15
ETHYLIOENE DICHLORIDE 1,1-DICHLOROETHANE B15
ETHYLIDENE DIFLUORIDE 1,1-DIFLUOROETHANE B17
ETHYLIDENE FLUORIDE 1,1-DIFLUOROETHANE B17

ETHYL KETONE DIETHYL KETONE B23
ETHYL MERCAPTAN ETHYL MERCAPTAN B30
ETHYL METHANOATE ETHYL FORMATE 754
o-ETHYLMETHYLBENZENE o-ETHYLTOLUENE 343
p-ETHYLMETHYLBENZENE p-ETHYLTOLUENE 345

1-ETHYL-2-llETHYLBENZENE o-ETHYLTOLUENE 343
1-ETHYL-3-llETHYLBENZENE m-ETHYLTOLUENE 344
1-ETHYL-4-llETHYLBENZENE p-ETHYLTOLUENE 345
ETHYL METHYL CARBINOL sec-BUTANOL 715
ETHYL METHYL ETHER llETHYL ETHYL ETHER 764

ETHYL METHYL KETONE llETHYL ETHYL KETONE B22
1-ETHYLNAPHTHALENE 1-ETHYLNAPHTHALENE 430
2-ETHYLNAPHTHALENE 2-ETHYLNAPHTHALENE 431
ETHYLOLAllINE MONOETHANOLAMINE B53
3-ETHYLPENTANE 3-ETHYLPENTANE 17
2-ETHYL-1-PENTENE 2-ETHYL-1-PENTENE 241
1-ETHYL-4-PHENYLBENZENE 1-ETHYL-4-PHENYLBENZENE 400
ETHYL PROPIONYL DIETHYL KETONE B23

ETHYLPROPYL SULFIDE 3-THIAHEXANE B40
alpna-ETHYLSTYRENE 2-PHENYL-1-BUTENE 395
ETHYL SULFHYDRATE ETHYL MERCAPTAN 830
ETHYL SULFIDE 3-THIAPENTANE B3B
1-ETHYL-1,2,3,4-TETRAHYDRONAPHTHALENE 1-ETHYL-1,2,3,4-TETRAHYDRONAPHTHALENE 44B

ETHYL THIOALCOHOL ETHYL MERCAPTAN B30
ETHYL THIOETHANE 3-THIAPENTANE B3B
2-ETHYL TOLUENE o-ETHYLTOLUENE 343
4-ETHYL TOLUENE p-ETHYLTOLUENE 345
m-ETHYLTOLUENE m-ETHYLTOLUENE 344

o-ETHYLTOLUENE o-ETHYLTOLUENE 343
p-ETHYLTOLUENE p-ETHYLTOLUENE 345
ETHYNE ACETYLENE 322
ETHYNYLETHENE VINYLACETYLENE 326
FLUORANTHENE FLUORANTHENE 477

FLUORENE FLUORENE 473
FLUORHYDRIC ACID HYDROGEN FLUORIDE 7B5
FLUORINE FLUORINE 77B
FLUOROCARBON 11 TRICHLOROFLUOROMETHANE B01
FLUOROCARBON 12 OICHLORODIFLUOROMETHANE 800

FLUORODICHLOROMETHANE DICHLOROFLUOROMETHANE B05
FLUOROETHANE ETHYL FLUORIDE B19
FLUOROFORM TRIFLUOROMETHANE B07
FLUOROMETHANE METHYL FLUORIDE B10
1987 1-35
1C0.1
FLUOROTRICHLOROMETHANE TRICHLOROFLUOROMETHANE Bai

FORMALDEHYDE FORMALDEHYDE 72B
FORMIC ACID FORMIC ACID 700
FORMIC ALOEHYDE FORMALDEHYOE 72B
FORMIC ANAMMONIDE HYDROGEN CYANIDE 7B4
FORMOL FORMALDEHYDE 72B

FORMONITRILE HYDROGEN CYANIDE 7B4
FORMYLDIMETHYLAMINE N,N-DIMETHYLFORMAMIDE B59
FORMYLIC ACID FORMIC ACID 700
FORMYL TRICHLDRIDE CHLOROFORM B06
FREON io CARBON TETRACHLORIDE B02

FREON ii TRICHLOROFLUOROMETHANE Bai
FREON i2 DICHLORODIFLUOROMETHANE BOO
FREON i4 CARBON TETRAFLUORIDE B03
FREON 20 CHLOROFORM B06
FREON 2i DICHLOROFLUOROMETHANE BOS

FREON 23 TRIFLUOROMETHANE B07
FREON 30 DICHLOROMETHANE BOB
FREON i43 i,i,i-TRIFLUOROETHANE Bi4
FREON i52A i,i-DIFLUOROETHANE BH
2-FURALDEHYOE FURFURAL B49

2-FURANALDEHYDE FURFURAL B49
2-FURANCARBONAL FURFURAL B49
FURANIDINE TETRAHYDROFURAN 768
FURFURAL FURFURAL B49
FURFURALDEHYDE FURFURAL B49

FUROL FURFURAL B49
2-FURYLMETHANAL FURFURAL B49
GENETRON i2 DICHLORODIFLUOROMETHANE BOO
GENE TRON ioo i,i-DIFLUOROETHANE BH
GENETRON i52A i,i-DIFLUOROETHANE BH

GLACIAL ACETIC ACID ACETIC ACID 70i
HALON DICHLOROOIFLUOROMETHANE BOO
HALON i4 CARBON TETRAFLUORIDE B03
HELIUM HELIUM-4 7BO
HELIUM-3 HELIUM-3 779

HELIUM-4 HELIUM-4 7BO
a-HELIUM HELIUM-4 7BO
p-HELIUM HELIUM-4 7BO
HENOECANE n-UNDECANE 73
n-HENEICOSANE n-HENEICOSANE B3
n-HEPTACOSANE n-HEPTACOSANE B9
n-HEPTADECANE n-HEPTADECANE 79
i-HEPTADECENE i-HEPTADECENE 2B6
n-HEPTADECYLCYCLOHEXANE n-HEPTADECYLCYCLOHEXANE HS
n-HEPTAOECYLCYCLOPENTANE n-HEPTADECYCLCYCLOPENTANE i42

n-HEPTANE n-HEPTANE i4
i-HEPTANETHIOL i-HEPTANETHIOL B44
i-HEPTENE i-HEPTENE 22i
i-n-HEPTENE i-HEPTENE 22i
n-HEPT-i-ENE i-HEPTENE 22i

c1s-2-HEPTENE c1s-2-HEPTENE 222
trans-2-HEPTENE trans-2-HEPTENE 223
c1s-3-HEPTENE c1s-3-HEPTENE 224
trans-3-HEPTENE trans-3-HEPTENE 225
1-36 1987
1C0.1
COllPOUNO TABLE ENTRY NAME TABLE SEQUENCE NUMBER
n-HEPTYLBENZENE n-HEPTYLBENZENE 373

n-HEPTYLCYCLOHEXANE n-HEPTYLCYCLOHEXANE 165
n-HEPTYLCYCLOPENTANE n-HEPTYLCYCLOPENTANE 132
HEPTYL HYDRIDE n-HEPTANE 14
1-n-HEPTYLNAPHTHALENE 1-n-HEPTYLNAPHTHALENE 441
1-n-HEPTYL-1 2 3 4-TETRAHYORONAPHTHALENE
0 0 0 1-n-HEPTYL-1 2,3,4-TETRAHYDRONAPHTHALENE
0
459
1-HEPTYNE 1-HEPTYNE 331
alpha-HEPTYLENE 1-HEPTENE 221
n-HEXACOSANE n-HEXACOSANE 88
n-HEXAOECANE n-HEXAOECANE 78
1-HEXADECENE 1-HEXADECENE 285

n-HEXAOECYLBENZENE n-HEXYLDECYLBENZENE 382
n-HEXADECYLCYCLOHEXANE n-HEXADECYLCYCLOHEXANE 174
n-HEXAOECYLCYCLDPENTANE n-HEXADECYLCYCLOPENTANE 141
1 2-HEXADIENE
0 1,2-HEXADIENE 301
1 5-HEXADIENE
0 1 5-HEXADI ENE
0
302
2,3-HEXAOIENE 2. 3-HEXADI ENE 303
HEXAHYDROBENZENE CYCLOHEXANE 146
HEXAHYDROTOLUENE METHYLCYCLOHEXANE 147
HEXAMETHYLENE CYCLOHEXANE 146
HEXANAPHTHENE CYCLOHEXANE 146

n-HEXANE n-HEXANE 9
1-HEXANETHIDL 1-HEXANETHIOL 843
n-HEXANOIC ACID n-HEXANDIC ACID 708
2-HEXANONE METHYL-N-BUTYL KEONE 825
HEX ENE 1-HEXENE 204

1-HEXENE 1-HEXENE 204
n-HEXENE 1-HEXENE 204
cls-2-HEXENE cis-2-HEXENE 205
trans-2-HEXENE trans-2-HEXENE 206
cls-3-HEXENE cls-3-HEXENE 207

trans-3-HEXENE trans-3-HEXENE 208
n-HEXYLBENZENE n-HEXYLBENZENE 372
n-HEXYLCYCLOHEXANE n-HEXYLCYCLOHEXANE 164
n-HEXYLCYCLOPENTANE n-HEXYLCYCLOPENTANE 131
1-n-HEXYLNAPHTHALENE 1-n-HEXYLNAPHTHALENE 439

2-n-HEXYLNAPHTHALENE 2-n-HEXYLNAPHTHALENE 440
1-n-HEXYL-1 2 3 4-TETRAHYORONAPHTHALENE
0 0 0 1-n-HEXYL-1 2 3 4-TETRAHYDRONAPHTHALENE
0 0 0 458
1-HEXYNE 1-HEXYNE 330
HYDROCHLORIC ACID. ANHYDROUS HYDROGEN CHLORIOE 783
HYDROCHLORIC ETHER ETHYL CHLORIDE 818

HYDROFURAN TETRAHYDROFURAN 768
HYDROGEN HYDROGEN 781
HYDROGEN BROMIDE HYDROGEN BROMIDE 782
HYDROGENCARBOXYLIC ACID FORMIC ACID 700
HYDROGEN CHLORIDE HYOROGEN CHLORIOE 783

HYOROGEN CYANIDE HYDROGEN CYANIDE 784
HYDROGEN FLUORIDE HYDROGEN FLUORIDE 785
HYDROGEN SULFIDE HYDROGEN SULFIDE 786
HYDROXYB ENZ ENE PHENOL 724
1-HYDROXYBUTANE n-8UTANOL 713

2-HYDROXYBUTANE sec-BUTANOL 715
beta-HYDROXYETHYLAMINE MONOETHANOLAMINE 853
b1s(2-HYDROXYETHYL)ETHER OIETHYLENE GLYCOL 851
HYDROXYMETHANE METHANOL 709
1987 1-37
1C0.1
1-HYOROXY-2-METHYLBENZENE o-CRESOL 725

1-HYDROXY-3-METHYLBENZENE m-CRESOL 726
1-HYDROXY-4-METHYLBENZENE p-CRESOL 727
1-HYDROXYMETHYLPROPANE ISOBUTANOL 714
1-HYOROXYPROPANE n-PROPANOL 711
2-HYOROXYPROPANE ISOPROPANOL 712

3-HYDROXYPROPENE ACETONE 821
2-HYOROXYTOLUENE o-CRESOL 725
4-HYDROXYTOLUENE p-CRESOL 727
m-HYDROXYTOLUENE m-CRESOL 726
o-HYOROXYTOLUENE o-CRESOL 725

p-HYDROXYTOLUENE p-CRESOL 727
HYPONITROUS ACID ANHYDRIDE NITROUS OXIDE 791
ICOSANE n-EICOSANE 82
2,2'-IMINODIETHANOL DIETHANOLAMINE 854
INDENE INDENE 463

IN DOLE INDOLE 748
INOONAPHTHENE INDENE 463
1-ISOAMYLENE 2-METHYL-1-8UTENE 201
alpha-ISOAMYLENE 3-METHYL-1-BUTENE 202
Deta-ISOAMYLENE 2-METHYL-2-BUTENE 203

ganma-ISOAMYLENE 2-METHYL-1-BUTENE 201
ISOAMYLHYDRIDE ISOPENTANE 7
ISOBUTANE ISOBUTANE 5
ISOBUTANOL ISOBUTANOL 714
ISOBUTENAL METHACROLEIN 734

ISOBUTENE I SOBUTENE 197
ISOBUTYL ALCOHOL ISOBUTANOL 714
ISOBUTYLAMINE ISOBUTYLAMINE 740
ISOBUTYLBENZENE ISOBUTYLBENZENE 350
IS08UTYLCYCLOHEXANE ISOBUTYLCYCLOHEXANE 159

ISOBUTYLCYCLOPENTANE ISOBUTYLCYCLOPENTANE 125
IS08UTYLENE ISOBUTENE 197
ISOBUTYL METHYL CARBINOL 4-METHYL-2-PENTANOL 723
ISOBUTYLMETHYLMETHANOL 4-METHYL-2-PENTANOL 723
IS08UTYLTRIMETHYLETHANE 2,2,4-TRIMETHYLPENTANE 37
ISOBUTYRIC ACID 2-METHYLPROPIONIC ACID 704
!SOCUMENE n-PROPYLBENZENE 341
ISODIPHENYLBENZENE 1,3-DIPHENYLBENZENE 425
ISOHEPTANE 2-METHYLHEXANE 15
ISOHEXANE 2-METHYLPENTANE 10
ISOOCTANE 2-METHYLHEPTANE 24
!SOPENTAOIENE 2-METHYL-1,3-8UTAD!ENE 299
ISOPENTANE ISOPENTANE 7
ISOPENTANOIC ACID 3-METHYLBUTYRIC ACID 707
ISOPRENE 2-METHYL-1,3-BUTADIENE 299

ISOPROPANOL ISOPROPANOL 712
ISOPROPENYLBENZENE 2-PROPENYLBENZENE 387
ISOPROPYL ACETATE ISOPROPYL ACETATE 760
ISOPROPYL ACETIC ACID 2-PROPENYL BENZENE 387
ISOPROPYL ALCOHOL I SOPROPANO L 712

ISOPROPYLAMINE ISOPROPYLAMINE 738
ISOPROPYL8ENZENE ISOPROPYLBENZENE 342
ISOPROPYLBENZOL ISOPROPYLBENZENE 342
ISOPROPYL CARBINOL ISOBUTANOL 714
1-38 1987
1C0.1
COMPOUNO TABLE ENTRY NAME TABLE SEQUENCE NUMBER
ISOPROPYLCYCLOHEXANE ISOPROPYLCYCLOHEXANE 157

ISOPROPYLCYCLOPENTANE ISOPROPYLCYCLOPENTANE 110
ISOPROPYLETHYLENE 3-METHYL-1-BUTENE 202
ISOPROPYLFORMIC ACIO 2-METHYLBUTYRIC ACID 706
1-ISOPROPYL-2-METHYL BENZENE o-CYMENE 356
1-ISOPROPYL-3-METHYL BENZENE m-CYMENE 357

1-ISOPROPYL-4-METHYL BENZENE p-CYMENE 358
4-ISOPROPYL-1-METHYL BENZENE p-CYMENE 358
ISOPROPYLTOLUENE p-CYMENE 358
m-ISOPROPYLTOLUENE m-CYMENE 357
o-ISOPROPYLTOLUENE o-CYMENE 358

p-ISOPROPYLTOLUENE p-CYMENE 358
ISOVALERIC ACID ISOPROPYLBENZENE 342
KAR SAN FORMALDEHYDE 728
KELENE ETHYL CHLORIDE 818
KETONE PROPANE ACETONE 821

beta-KETOPRDPANE ACETONE 821
KRYPTON KRYPTON 787
LAURYLBENZENE n-DODECYLBENZENE 378
LEMON ENE BI PHENYL 396
LUPROSIL PROPIONIC ACID 702

MERCAPTOETHANE ETHYL MERCAPTAN 830
MERCAPTOMETHANE METHYL MERCAPTAN 827
MESITYLENE 1,3,5-TRIMETHYLBENZENE 348
METACETONE DIETHYL KETONE 823
METHACROLEIN METHACRDLEIN 734

METHACRYLALDEHYDE METHACROLEIN 734
METHACRYLIC ALDEHYDE METHACROLEIN 734
METHALDEHYDE FORMALDEHYDE 728
METHANAL FORMALDEHYDE 72B
METHANE METHANE 1
METHANE CARBOXYLIC ACID ACETIC ACID 701
METHANE DICHLORIDE DICHLOROMETHANE 808
METHANE TETRACHLORIDE CARBON TETRACHLORIDE 802
METHANETHIDL METHYL MERCAPTAN 828
METHANE TRICHLORIDE CHLOROFORM 806

METHANOIC ACID FORMIC ACID 700
METHANOL METHANOL 709
METHENYL TRICHLORIDE CHLOROFORM 806
METHYLACETALDEHYDE n-PROPIONALDEHYDE 730
METHYL ACETATE METHYL ACETATE 753

METHYLACETIC ACID PROPIONIC ACID 702
METHYLACETYLENE METHYLACETYLENE 323
METHYLACROLEIN METHACROLEIN 734
2-METHYLACRDLEIN METHACROLEIN 734
alpha-METHYLACROLEIN METHACROLEIN 734

METHYL ACRYLALDEHYDE METHACROLEIN 734
METHYL ALCOHOL METHANOL 709
METHYL ALDEHYDE FORMALDEHYDE 728
METHYLALLENE 1,2-BUTADIENE 291
1-METHYLALLENE 1,2-BUTADIENE 291

METHYLAMINE METHYLAMINE 735
2-METHYL-1-AMINOPROPANE I SOBUTY LAM IN E 740
2-METHYL-2-AMINOPROPANE tert-BUTYLAMINE 742
METHYL AMYL ALCOHOL 4-METHYL-2-PENTANOL 723
1987 1-39
1C0.1
METHYL-tart-AMYL ETHER METHYL-tart-AMYL ETHER 767

1-METHYLAZACYCLOPENTANE-2-0NE N-METHYL-2-PYRROLIDONE B60
METHYLBENZENE TOLUENE 336
METHYLBENZOL TOLUENE 336
2-METHYL-[c1s-BICYCL0[4.4.0]DECANE] 1-METHYL-[cis-DECAHYDRONAPHTHALENE] 1B6
2-METHYL-[trans-BICYCL0[4.4.0]DECANE] 1-METHYL-[trans-DECAHYDRONAPHTHALENE] 1B7

beta-METHYL BIVINYL 2-METHYL-1.3-BUTAOIENE 299
cis-1-METHYL BUTADIENE cis-1.3-PENTADIENE 294
2-METHYL BUTADIENE 2-METHYL-1,3-BUTADIENE 299
2-METHYL-1,3-BUTADIENE 2-METHYL-1.3-BUTAOIENE 299
3-METHYL BUTADIENE 3-METHYL-1,2-BUTAOIENE 298

3-METHYL-1,2-BUTADIENE 3-METHYL-1,2-BUTADIENE 298
2-METHYL BUTANE ISOPENTANE 7
METHYL BUTANOATE METHYL n-BUTYRATE 758
2-METHYL BUTANDIC ACID 2-METHYLBUTYRIC ACID 706
3-METHYL BUTANOIC ACID 3-METHYLBUTYRIC ACID 7D7

2-METHYL-1-BUTANOL 2-METHYL-1-BUTANDL 719
2-METHYL BUTANOL-2 2-METHYL-2-BUTANOL 720
2-METHYL-2-BUTANOL 2-METHYL-2-BUTANOL 720
3-METHYLBUTAN-2-0L 3-METHYL-2-BUTANOL 721
3-METHYL-2-BUTANOL 3-METHYL-2-BUTANDL 721

2-METHYL-1-BUTENE 2-METHYL-1-BUTENE 201
2-METHYL-2-BUTENE 2-METHYL-2-BUTENE 2D3
METHYL-t-BUTYL ETHER METHYL-tert-BUTYL ETHER 766

METHYL-tart-BUTYL ETHER METHYL-tart-BUTYL ETHER 768
METHYL-n-BUTYL KETONE METHYL-n-BUTYL KETONE 826
METHYLBUTYL SULFIDE 2-THIAHEXANE 839
3-METHYL-1-BUTYNE 3-METHYL-1-BUTYNE 329
METHYL BUTYRATE METHYL n-BUTYRATE 758

METHYL n-BUTYRATE METHYL n-BUTYRATE 758
2-METHYLBUTYRIC ACID 2-METHYLBUTYRIC ACID 706
3-METHYLBUTYRIC ACID 3-METHYLBUTYRIC ACID 707
N-METHYL-gamma-BUTYROLACTAM N-METHYL-2-PYRROLIDONE 860
METHYL CARBINOL ETHANOL 710

METHYL CHLORIOE METHYL CHLORIDE 809
METHYLCYCLOBUTANE METHYLCYCLOBUTANE 99
METHYLCYCLOHEXANE METHYLCYCLDHEXANE 147
1-METHYLCYCLOHEXENE 1-METHYLCYCLOHEXENE 316
METHYLCYCLOPENTANE METHYLCYCLOPENTANE 102

1-METHYLCYCLOPENTENE 1-METHYLCYCLOPENTENE 311
METHYLCYCLOPROPANE METHYLCYCLOPROPANE 94
1-METHYL-cis-DECAHYDRONAPHTHALENE 1-METHYL-cis-DECAHYDRONAPHTHALENE 1BB
1-METHYL-trans-DECAHYDRONAPHTHALENE 1-METHYL-trans-DECAHYDRONAPHTHALENE 187
METHYL DIETHANOLAMINE METHYL DIETHANOLAMINE 856

N-METHYL DIETHANDLAMINE METHYL DIETHANOLAMINE 856
1-METHYL-2,3-DIHYDROINDENE 1-METHYL-2.3-DIHYDROINDENE 467
2-METHYL-2,3-DIHYDROINDENE 2-METHYL-2.3-DIHYOROINDENE 468
4-METHYL-2,3-0IHYDROINDENE 4-METHYL-2,3-DIHYOROINDENE 469
5-METHYL-2,3-0IHYDROINDENE 5-METHYL-2,3-DIHYOROINOENE 470

1-METHYL-1,1-DIMETHYLETHYLETHER METHYL-tart-BUTYL ETHER 768
METHYLENE BICHLORIDE DICHLOROMETHANE 808
METHYLENE CHLORIDE DICHLOROMETHANE 808
METHYLENE OICHLORIDE DICHLOROMETHANE 808
1-40 1987
1C0.1
METHYLENE GLYCOL 1,2-PROPYLENE GLYCOL 850

METHYLENE OXIOE FORMALOEHYOE 728
2-METHYLENEPROPANAL METHACROLE IN 734
4,7-METHYLENE-4,7,8,9-TETRAHYDROINOENE DICYCLOPENTAOIENE 319
METHYL ETHANOATE METHYL ACETATE 753
1-METHYL ETHANOL I SOPROPANOL 712

METHYL ETHENE PROPYLENE 193
1-METHYL-2-ETHENYL BENZENE 1-METHYL-2-ETHENYL BENZENE 388
METHYL ETHER OIMETHYL ETHER 763

1-METHYLETHYL ALCOHOL ISOPROPANOL 712
1-METHYLETHYLBENZENE ISOPROPYLBENZENE 342
4-METHYLETHYLBENZENE p-ETHYLTOLUENE 345
m-METHYLETHYLBENZENE m-ETHYLTOLUENE 344
o-METHYLETHYLBENZENE o-ETHYL TOLUENE 343

p-METHYLETHYLBENZENE p-ETHYLTOLUENE 345
1-METHYL-2-ETHYLBENZENE o-ETHYLTOLUENE 343
1-METHYL-3-ETHYLBENZENE m-ETHYLTOLUENE 344
1-METHYL-4-ETHYLBENZENE p-ETHYLTOLUENE 345
3-METHYL-2-ETHYL-1-BUTENE 3-METHYL-2-ETHYL-1-BUTENE 255

1-METHYLETHYLCYCLOHEXANE ISOPROPYLCYCLOHEXANE 157
1-METHYLETHYLCYCLOPENTANE ISOPROPYLCYCLOPENTANE 110
1-METHYL-1-ETHYLCYCLOPENTANE 1-METHYL-1-ETHYLCYCLOPENTANE 111
cls-1-METHYL-2-ETHYLCYCLOPENTANE cls-1-METHYL-2-ETHYLCYCLOPENTANE 112
trans-1-METHYL-2-ETHYLCYCLOPENTANE trans-1-METHYL-2-ETHYLCYCLOPENTANE 113

cls-1-METHYL-3-ETHYLCYCLOPENTANE cls-1-METHYL-3-ETHYLCYCLOPENTANE 114
trans-1-METHYL-3-ETHYLCYCLOPENTANE trans-1-METHYL-3-ETHYLCYCLOPENTANE 115
METHYLETHYLENE PROPYLENE 193
METHYLETHYLENE GLYCOL 1,2-PROPYLENE GLYCOL B50
1-METHYLETHYL ETHANOATE ISOPROPYL ACETATE 760

METHYL ETHYL ETHER METHYL ETHYL ETHER 764
METHYL ETHYL KETONE METHYL ETHYL KETONE 822
2-METHYL-3-ETHYLPENTANE 2-METHYL-3-ETHYLPENTANE 34
3-METHYL-3-ETHYLPENTANE 3-METHYL-3-ETHYLPENTANE 35
METHYLETHYL SULFIDE 2-THIABUTANE 832

METHYLETHYNE METHYLACETYLENE 323
METHYL FLUORIOE METHYL FLUORIOE 810
METHYL FLUOROFORM 1,1,1-TRIFLUOROETHANE B12
METHYL FORMATE METHYL FORMATE 752
2-METHYLHEPTANE 2-METHYLHEPTANE 24
2-METHYL-1-HEPTENE 2-METHYL-1-HEPTENE 264
trans-3-METHYL-3-HEPTENE trans-3-METHYL-3-HEPTENE 268

trans-6-METHYL-2-HEPTENE trans-6-METHYL-2-HEPTENE 267
2-METHYL-1,5-HEXAOIENE 2-METHYL-1,5-HEXADIENE 305
2-METHYL-2,4-H~XAOIENE 2-METHYL-2,4-HEXAOIENE 306
2-METHYLHEXANE 2-METHYLHEXANE 15
3-METHYLHEXANE 3-METHYLHEXANE 16
(3rs)-METHYLHEXANE 3-METHYLHEXANE 16
2-METHYL-1-HEXENE 2-METHYL-1-HEXENE 226
1987 1-41
1C0.1
COMPO UNO TABLE ENTRY NAME TABLE SEQUENCE NUMBER
cis-2-METHYL-3-HEXENE cis-2-METHYL-3-HEXENE 237

trans-2-METHYL-3-HEXENE trans-2-METHYL-3-HEXENE 23B
3-llETHYL-1-HEXENE 3-METHYL-1-HEXENE 227
trans-3-METHYL-2-HEXENE trans-3-METHYL-2-HEXENE 232
cis-3-llETHYL-3-HEXENE cis-3-METHYL-3-HEXENE 239


METHYL HYDRIDE METHANE 1
METHYL HYDROXIDE METHANOL 709
1-METHYL-4-HYDROXYBENZENE p-CRESOL 727

n-METHYLIMINODIETHANOL METHYL OIETHANOLAMINE 856
n-METHYL-2,2-IllINODIETHANOL METHYL OIETHANOLAMINE 856
2,2-(METHYLIMINO) DIETHANOL METHYL OIETHANOLAMINE 856
1-llETHYLINDENE 1-METHYLINOENE 464
2-METHYLINDENE 2-METHYLINOENE 465

METHYL ISOBUTYL CARBINOL 4-METHYL-2-PENTANOL 723
METHYL ISOBUTYL KETONE METHYL ISOBUTYL KETONE 824
p-METHYLISOPROPYLBENZENE p-CYMENE 358
1-METHYL-4-ISOPROPYLCYCLOHEXANE 1-METHYL-4-ISOPROPYLCYCLOHEXANE 162
METHYL KETONE ACETONE 821

METHYL MERCAPTAN METHYL MERCAPTAN 827
METHYL METHANE ETHANE 2
METHYL llETHANOATE METHYL FORMATE 752
1-METHYL-2-(1-METHYLETHYL)BENZENE o-CYMENE 356
1-METHYL-3-(1-METHYLETHYL)BENZENE m-CYMENE 357

1-METHYL-4-(1-METHYLETHYL)8ENZENE p-CYMENE 358
1-llETHYL-4-(1-llETHYLETHYL)CYCLOHEXANE 1-METHYL-4-ISOPROPYLCYCLOHEXANE 162
1-METHYL-4(4-METHYLPHENYL)-BENZENE 1-METHYL-4(4-METHYLPHENYL)-BENZENE 401
METHYL llONOSULFIDE DIMETHYL SULFIDE 829
1-llETHYLNAPHTHALENE 1-METHYLNAPHTHALENE 428

2-METHYLNAPHTHALENE 2-METHYLNAPHTHALENE 429
2-llETHYLNONANE 2-llETHYLNONANE 63
3-METHYLNONANE 3-METHYLNONANE 64
2-llETHYLOCTANE 2-METHYLOCTANE 42
3-METHYLOCTANE 3-METHYLOCTANE 43
4-METHYLOCTANE 4-METHYLOCTANE 44
METHYLOLPROPANE n-BUTANOL 713
3-llETHYL-1,2-PENTADIENE 3-METHYL-1,2-PENTADIENE 304

llETHYLPENTANE 2-METHYLPENTANE 10
2-llETHYLPENTANE 2-llETHYLPENTANE 10
3-llETHYLPENTANE 3-METHYLPENTANE 11
2-METHYL-4-PENTANOL 4-llETHYL-2-PENTANOL 723
4-METHYL-2-PENTANOL 4-METHYL-2-PENTANOL 723

4-METHYL-2-PENTANONE METHYL IS08UTYL KETONE 826
2-llETHYL-1-PENTENE 2-llETHYL-1-PENTENE 209
2-METHYL-2-PENTENE 2-METHYL-2-PENTENE 212
1-42 1987
1C0.1
cis-3-METHYL-2-PENTENE cis-3-METHYL-2-PENTENE 213

trans-3-METHYL-2-PENTENE trans-3-METHYL-2-PENTENE 214
cis-4-METHYL-2-PENTENE cis-4-METHYL-2-PENTENE 215
trans-4-METHYL-2-PENTENE trans-4-METHYL-2-PENTENE 216
METHYLPENTYL SULFIDE 2-THIAHEPTANE 842

2-METHYLPHENOL o-CRESOL 725
3-METHYLPHENOL m-CRESDL 726
4-METHYLPHENOL p-CRESOL 727
m-METHYLPHENOL m-CRESOL 726
o-METHYLPHENOL o-CRESOL 725

p-METHYLPHENOL p-CRESDL 727
1-METHYL-2-PHENYLBENZENE 1-METHYL-2-PHENYLBENZENE 397
1-METHYL-1-PHENYL-ETHYLENE 2-PROPENYLBENZENE 387

as-METHYLPHENYLETHYLENE 2-PROPENYLBENZENE 387
cis-METHYLPHENYL-ETHYLENE 2-PROPENYLBENZENE 387
o-METHYLPHENYLOL o-CRESOL 725
2-METHYL-1-PHENYLPROPANE ISOBUTYLBENZENE 350
2-METHYL-2-PHENYLPROPANE tert-BUTYLBENZENE 352

2-METHYL-1-PROPANAMINE ISOBUTYLBENZENE 740
2-METHYL-2-PROPANAMINE tert-BUTYLAMINE 742
2-METHYL PROPANE ISOBUTANE 5
2-METHYL-1-PROPANETHIOL 2-METHYL-1-PROPANETHIDL 837
2-METHYL PROPANOIC ACID 2-METHYLPROPIONIC ACID 704

METHYL PROPANOL ISOBUTANOL 714
1-METHYLPROPANOL sec-BUTANOL 715
2-METHYLPROPANOL ISOBUTANOL 714
2-METHYL PRDPAN-1-DL ISDBUTANDL 714
2-METHYL PROPAN-2-0L tert-BUTANOL 716

2-METHYL PROPANOL-1 ISOBUTANOL 714
2-METHYL PROPANOL-2 tert-BUTANOL 716
2-METHYL-2-PROPANOL tert-BUTANDL 716
2-METHYL PROPENAL METHACRDLEIN 734
1-METHYL-4-(trans-1-n-PROPENYL)BENZENE 1-METHYL-4-(trans-1-n-PROPENYL)BENZENE 391

2-METHYLPROPENE ISOBUTENE 197
2-METHYLPROPIONIC ACID 2-METHYLPROPIONIC ACID 704
alpha-METHYLPROPIONIC ACID 2-METHYLPRDPIONIC ACID 704
2-METHYLPROPYL ALCOHOL ISOBUTANOL 714
1-METHYLPROPYL BENZENE sec-BUTYLBENZENE 351

2-METHYLPROPYL BENZENE ISOBUTYLBENZENE 350
1-METHYL-2-n-PROPYLBENZENE 1-METHYL-2-n-PROPYLBENZENE 353
1-METHYL-3-n-PROPYLBENZENE 1-METHYL-3-n-PROPYLBENZENE 354
1-METHYL-4-n-PROPYLBENZENE 1-METHYL-4-n-PRDPYLBENZENE 355
2-METHYLPROPYLBENZENE ISDBUTYLBENZENE 350

METHYL PROPYL CARBINOL 2-PENTANDL 718
1-METHYLPROPYLCYCLOHEXANE sec-BUTYLCYCLOHEXANE 160
2-METHYLPROPYLCYCLOHEXANE ISOBUTYLCYCLOHEXANE 159
1-METHYL-1-n-PROPYLCYCLOPENTANE 1-METHYL-1-n-PROPYLCYCLOPENTANE 126
2-METHYLPROPYLCYCLOPENTANE ISOBUTYLCYCLOPENTANE 125

METHYL-n-PROPYL KETONE METHYL-n-PROPYL KETONE 825
1-METHYLPYRROLIDINONE N-METHYL-2-PYRRDLIDONE 860
N-METHYLPYRROLIDINONE N-METHYL-2-PYRROLIDONE 860
N-METHYL-alpha-PYRROLIDINDNE N-METHYL-2-PYRROLIDONE 860
1987 1-43
1C0.1
i-METHYLPYRROLIDONE N-METHYL-2-PYRROLIDONE 860

N-METHYLPYRROLIDONE N-METHYL-2-PYRROLIDONE 860
N-METHYL-2-PYRROLIDONE N-METHYL-2-PYRROLIDONE 880
N-METHYL-alpha-PYRROLIDONE N-METHYL-2-PYRROLIDONE 860
alpha-METHYLSTYRENE 2-PROPENYLBENZENE 387
cis,bata-METHYLSTYRENE cis-i-PROPENYLBENZENE 385

trans,bata-METHYLSTYRENE trans-i-PROPENYLBENZENE 386
m-METHYLSTYRENE i-METHYL-3-ETHENYLBENZENE 389
o-METHYLSTYRENE i-METHYL-2-ETHENYLBENZENE 388
p-METHYLSTYRENE i-METHYL-4-ETHENYLBENZENE 390
METHYL SULFHYORATE METHYL MERCAPTAN 827

METHYL SULFOXIDE OIMETHYL SULFOXIDE e6i
i-METHYL-i,2,3,4-TETRAHYORONAPHTHALENE i-METHYL-i,2,3,4-TETRAHYDRONAPHTHALENE 447
METHYL THIOALCOHOL METHYL MERCAPTAN 827
m-METHYLTOLUENE m-XYLENE 339
o-METHYLTOLUENE o-XYLENE 338

p-METHYLTOLUENE p-XYLENE 340
METHYL TRICHLORIDE CHLOROFORM 806
MONOBUTYLAMINE n-BUTYLAMINE 739
MONOCHLORETHANE ETHYL CHLORIDE eie
MONOCHLOROETHANE ETHYL CHLORIDE eie

MONOCHLOROETHYLENE VINYL CHLORIDE eii
MONOCHLOROMETHANE METHYL CHLORIDE 809
MONOCHLOROTRIFLUOROMETHANE CHLOROTRIFLUOROMETHANE 799
MONOETHANOLAMINE MONOETHANOLAMINE 853
MONOETHYLAMINE ETHYLAMINE 736

MONOFLUORODICHLOROMETHANE OICHLOROFLUOROMETHANE 805
MONOFLUOROTRICHLOROMETHANE TRICHLOROFLUOROMETHANE soi
MONOHYDROXYBENZENE PHENOL 724
MONOHYDROXYMETHANE METHANOL 709
MONOMETHYLAMINE METHYLAMINE 735

MONOPROPYLAMINE n-PROPYLAMINE 737
MONOPROPYLENE GLYCOL i,2-PROPYLENE GLYCOL 850
MONOYINYLACETYLENE VINYLACETYLENE 326
MORPHOLINE MORPHOLINE 745
NAPHTHALENE NAPHTHALENE 427

p-NAPHTHALENE ANTHRACENE 474
NAPHTHALENE-i,2,3,4-TETRAHYDRIDE i,2,3,4-TETRAHYDRONAPHTHALENE 446
NAPHTHA LINE NAPHTHALENE 427
i,2-(i,8-NAPHTHYLENE)BENZENE FLUORANTHENE 477
NEOAMYL ALCOHOL 2,2-0IMETHYL-i-PROPANOL 722

NEOHEXANE 2,2-0IMETHYL-i-PROPANOL 722
NEON NEON 788
NEOPENTANE NEOPENTANE 8
NEOPENTANOL 2,2-0IMETHYL-i-PROPANOL 722
NITRIC OXIDE NITRIC OXIDE 790

NITRIL0-2,2' ,2''-TRIETHANOL TRIETHANOLAMINE B57
2,2,2-NITRILOTRIETHANOL TRIETHANOLAMINE 857
2,2',2''-NITRILOTRIETHANOL TRIETHANOLAMINE 857
NITROGEN NITROGEN 789
NITROGEN DIOXIDE NITROGEN DIOXIDE 792

NITROGEN PEROXIDE NITROGEN TETROXIDE 793
NITROGEN TETROXIDE NITROGEN TETROXIDE 793
NITROUS OXIDE NITROUS OXIDE 79i
n-NONACOSANE n-NONACOSANE 91
1-44 1987
1C0.1
n-NONAOECANE n-NONAOECANE 81
1-NONADECENE 1-NONAOECENE 288
n-NONADECYLCYCLOHEXANE n-NONADECYLCYCLOHEXANE 177
n-NONAOECYLCYCLOPENTANE n-NONAOECYLCYCLOPENTANE 144
n-NONANE n-NONANE 41
1-NONENE 1-NONENE 278

n-NONYLBENZENE n-NONYLBENZENE 375
n-NONYLCYCLOHEXANE n-NONYLCYCLOHEXANE 167
n-NONYLCYCLOPENTANE n-NONYLCYCLOPENTANE 134
1-n-NONYLNAPHTHALENE 1-n-NONYLNAPHTHALENE 443
2-n-NONYLNAPHTHALENE 2-n-NONYLNAPHTHALENE 444

1-n-NONYL-1,2,3,4-TETRAHYDONAPHTHALENE 1-n-NONYL-1,2,3,4-TETRAHYDRONAPHTHALENE 461
1-NONYNE 1-NONYNE 333
NOPINENE beta-PIN ENE 321
n-OCTACOSANE n-OCTACOSANE 90
n-OCTADECANE n-OCTAOECANE 80
1-0CTADECENE 1-0CTADECENE 287
n-OCTADECYLCYCLOHEXANE n-OCTAOECYLCYCLOHEXANE 176
n-OCTAOECYLCYCLOPENTANE n-OCTAOECYLCYCLOPENTANE 143
2,6-0CTADIENE 2,6-0CTAOIENE 307
n-OCTANE n-OCTANE 23
1-0CTENE 1-0CTENE 257
cls-2-0CTENE cis-2-0CTENE 258
trans-2-0CTENE trans-2-0CTENE 259
cls-3-0CTENE cis-3-0CTENE 260
trans-3-0CTENE trans-3-0CTENE 261

cis-4-0CTENE ci s-4-0CTENE 262
trans-4-DCTENE trans-4-0CTENE 263
alpha-OCTENE 1-0CTENE 257
n-OCTYLBENZENE n-OCTYLBENZENE 374
n-OCTYLCYCLOHEXANE n-OCTYLCYCLOHEXANE 168

n-OCTYLCYCLOPENTANE n-OCTYLCYCLOPENTANE 133
1-n-OCTYLNAPHTHALENE 1-n-OCTYLNAPHTHALENE 442
1-n-OCTYL-1,2,3,4-TETRAHYORONAPHTHALENE 1-n-OCTYL-1,2,3,4-TETRAHYDRONAPHTHALENE 460
1-0CTYNE 1-0CTYNE 332
ORTHOCRESOL o-CRESOL 725

OXACYCLOPENTANE TETRAHYOROFURAN 768
3-0XAPENTANE-1,5-DIOL OIETHYLENE GLYCOL 851
OXOMETHANE FORMALDEHYDE 728
1,1'-0XYBISETHANE DIETHYL ETHER 765
2,2'-DXYBIS(ETHANOL) DI ETHYLENE GLYCOL 851

2,2'-DXYDIETHANOL DI ETHYLENE GLYCOL 851
OXYGEN OXYGEN 794
o-OXYTOLUENE o-CRESDL 725
p-OXYTOLUENE p-CRESOL 727
OZONE OZONE 795

PARANAPHTHALENE ANTHRACENE 474
n-PENTACOSANE n-PENTACOSANE 87
n-PENTAOECANE n-PENTAOECANE 77
1-PENTAOECENE 1-PENTAOECENE 284
n-PENTADECYLBENZENE n-PENTAOECYLBENZENE 381

n-PENTAOECYLCYCLOHEXANE n-PENTADECYLCYCLOHEXANE 173
n-PENTADECYLCYCLOPENTANE n-PENTAOECYLCYCLOPENTANE 140
1,2-PENTAOIENE 1,2-PENTAOIENE 293
cls-1,3-PENTAOIENE cis-1,3-PENTAOIENE 294
1987 1-45
1C0.1
trans-1,3-PENTADIENE trans-1,3-PENTADIENE 295

1,cis-3-PENTADIENE cis-1,3-PENTADIENE 294
1,trans-3-PENTADIENE trans-1,3-PENTADIENE 295
1,4-PENTADIENE 1,4-PENTADIENE 296
2,3-PENTADIENE 2,3-PENTADIENE 297
PENTAMETHYLENE CYCLOPENTANE 101

n-PENTANE n-PENTANE 6
tert-PENTANE NEOPENTANE 8
1-PENTANETHIOL 1-PENTANETHIOL 841
n-PENTANOIC ACID n-PENTANOIC ACID 705
PENTANOL-1 1-PENTANOL 717

PENTANOL-2 2-PENTANOL 718
PENTAN-1-0L 1-PENTANOL 717
n-PENTANDL 1-PENTANOL 717
1-PENTANOL 1-PENTANOL 717
2-PENTANDL 2-PENTANOL 718

1-PENTANDL ACETATE n-PENTYL ACETATE 762
2-PENTANONE METHYL-n-PROPYL KETONE 824
3-PENTANONE DIETHYL KETONE 823
PENTASOL 1-PENTANOL 717
1-PENTENE 1-PENTENE 198

cis-2-PENTENE cis-2-PENTENE 199
trans-2-PENTENE trans-2-PENTENE 200
R-PENTINE CYCLOPENTADIENE 318
PENTOLE CYCLDPENTADIENE 318
1-PENTYL ACETATE n-PENTYL ACETATE 762

n-PENTYL ACETATE n-PENTYL ACETATE 762
PENTYL ALCOHOL 1-PENTANOL 717
n-PENTYL ALCOHOL 1-PENTANOL 717
sec-PENTYL ALCOHOL 2-PENTANOL 718
n-PENTYLBENZENE n-PENTYLBENZENE 371

n-PENTYLCYCLOHEXANE n-PENTYLCYCLOHEXANE 163
n-PENTYLCYCLOPENTANE n-PENTYLCYCLOPENTANE 130
PENTYL ETHANOATE n-PENTYL ACETATE 762
1-n-PENTYLNAPHTHALENE 1-n-PENTYLNAPHTHALENE 438
1-n-PENTYL-1,2,3,4-TETRAHYORONAPHTHALENE 1-n-PENTYL-1,2,3,4-TETRAHYDRONAPHTHALENE 456

6-n-PENTYL-1,2,3,4-TETRAHYDRONAPHTHALENE 6-n-PENTYL-1,2,3,4-TETRAHYDRONAPHTHALENE 457
1-PENTYNE 1-PENTYNE 327
2-PENTYNE 2-PENTYNE 328
PERCHLOROMETHANE CARBON TETRACHLORIDE 802
PHENANTHRENE PHENANTHRENE 475

PHENOL PHENOL 724
PHENYLACETYLENE PHENYLACETYLENE 422
PHENYL ALCOHOL PHENOL 724
PHENYLBENZENE BI PHENYL 398
2-PHENYL BIPHENYL 1,2-DIPHENYLBENZENE 424

2-PHENYL-1-BUTENE 2-PHENYL-1-BUTENE 395
4-PHENYL DIPHENYL 1,4-0IPHENYLBENZENE 426
PHENYLETHYLENE STYRENE 384

PHENYLETHYNE PHENYLACETYLENE 422
PHENYLHYDRIDE BENZENE 335
1-PHENYLISOBUTANE ISOBUTYLBENZENE 350
PHENYLMETHANE TOLUENE 336
1-46 1987
1C0.1
2-PHENYL-2-METHYLPROPANE tert-BUTYLBENZENE 352

1-PHENYLPROPANE n-PROPYLBENZENE 341
cis-1-PHENYL-1-PROPENE cis-1-PROPENYLBENZENE 385
trans-1-PHENYL-1-PROPENE trans-1-PROPENYLBENZENE 386
2-PHENYLPROPENE 2-PROPENYLBENZENE 387
2-PHENYL-1-PROPENE 2-PROPENYLBENZENE 387

beta-PHENYLPROPENE 2-PROPENYLBENZENE 387
2-PHENYLPROPYLENE 2-PROPENYLBENZENE 387
beta-PHENYLPROPYLENE 2-PROPENYLBENZENE 387
PINENE alpha-PINENE 320
2-PINENE alpha-PINENE 320

2(10)-PINENE beta-PINENE 321
alpha-PINENE alpha-PINENE 320
beta-PINENE beta-PIN ENE 321
PRIMARY AMYL ALCOHOL 1-PENTANOL 717
PROPAOIENE PROPAOIENE 290

PROPALOEHYOE n-PROPIONALOEHYDE 730
PROPANAL n-PROPIONALDEHYDE 730
PROPANAMINE n-PROPYLAMINE 737
PROPANE PROPANE 3
n-PROPANE PROPANE 3
PROPANE CARBOXYLIC ACIO n-BUTYRIC ACID 703
1-PROPANE CARBOXYLIC ACIO n-BUTYRIC ACIO 703
1,2-PROPANEOIOL 1,2-PROPYLENE GLYCOL 850
PROPANE-1,2-DIOL 1,2-PROPYLENE GLYCOL B50
PROPANE, 2-HYDROXY ISOPROPANOL 712

1-PROPANETHIOL 1-PROPANETHIOL 833
PROPANOIC ACID PROPIONIC ACIO 702
PROPANOL n-PROPANOL 711
PROPANOL-1 n-PROPANOL 711
PROPAN-2-0L ISOPROPANOL 712

1-PROPANOL n-PROPANOL 711
n-PROPAN-1-0L n-PROPANOL 711
n-PROPANOL n-PROPANOL 711
2-PROPANOL ISOPROPANOL 712
n-PROPAN-2-0L ISOPROPANOL 712

sec-PROPANOL ISOPROPANOL 712
PROPANOL, 2-METHYL ISOBUTANOL 714
PROPANONE ACETONE B21
PROPENAL ACROLEIN 732
PROP-2-EN-1-AL ACROLEIN 732

PROP ENE PROPYLENE 193
2-PROPEN-1-0NE ACROLEIN 732
cis-1-PROPENYL BENZENE cis-1-PROPENYL BENZENE 385
trans-1-PROPENYL BENZENE trans-1-PROPENYL BENZENE 3B6
2-PROPENYL BENZENE 2-PROPENYL BENZENE 387

PROP I NE METHYLACETYLENE 323
PROPINOALOEHYDE n-PROPIONALDEHYDE 730
PROPIONAL n-PROPIONALOEHYDE 730
n-PROPIONALOEHiOE n-PROPIONALOEHYOE 730
PROPIONIC ACIO PROPIONIC ACIO 702

PROPIONIC ALDEHYDE n-PROPYL ACETATE 759
n-PROPYL ACETATE n-PROPYL ACETATE 759
PROPYL ALCOHOL n-PROPANOL 711
n-PROPYL ALCOHOL n-PROPANOL 711
1987 1-47
1C0.1
COM POU NO TABLE ENTRY NAME TABLE SEQUENCE NUMBER
sec-PROPYL ALCOHOL ISOPROPANOL 712

1-PROPYL ALCOHOL n-PROPANOL 711
PROPYL ALOEHYOE n-PROPIONALOEHYOE 730
n-PROPYLAMINE n-PROPYLAMINE 737
n-PROPYLBENZENE n-PROPYLBENZENE 341
PROPYL CAR8INOL n-BUTANOL 713

n-PROPYLCYCLOHEXANE n-PROPYLCYCLOHEXANE 156
n-PROPYLCYCLOPENTANE n-PROPYLCYCLOPENTANE 109
1-n-PROPYLCYCLOPENTENE 1-n-PROPYLCYCLOPENTENE 314
PROPYLENE PROPYLENE 193
PROPYLENE CARBONATE PROPYLENE CARBONATE B4B

PROPYLENE CHLORIOE 1,2-0ICHLOROPROPANE B20
PROPYLENE OICHLORIOE 1,2-0ICHLOROPROPANE B20
alpha,beta-PROPYLENE OICHLORIOE 1,2-0ICHLOROPROPANE B20
PROPYLENE GLYCOL 1,2-PROPYLENE GLYCOL B50
1,2-PROPYLENE GLYCOL 1,2-PROPYLENE GLYCOL B50

alpha-PROPYLENE GLYCOL 1,2-PROPYLENE GLYCOL B50
PROPYL ETHANOATE n-PROPYL ACETATE 759
PROPYLETHYLENE 1-PENTENE 19B
n-PROPYL FORMATE n-PROPYL FORMATE 756
PROPYL FORMIC ACIO n-BUTYRIC ACIO 703

PROPYL HYORIOE PROPANE 3
PROPYLIC ALOEHYOE n-PROPIONALOEHYOE 730
PROPYL METHANOATE n-PROPYL FORMATE 756
1-n-PROPYLNAPHTHALENE 1-n-PROPYLNAPHTHALENE 434
2-n-PROPYLNAPHTHALENE 2-n-PROPYLNAPHTHALENE 435

1-n-PROPYL-1,2,3,4-TETRAHYORONAPHTHALENE 1-n-PROPYL-1,2,3,4-TETRAHYORONAPHTHALENE 452
6-n-PROPYL-1,2,3,4-TETRAHYORONAPHTHALENE 6-n-PROPYL-1,2,3,4-TETRAHYORONAPHTHALENE 453
1-PROPYNE llETHYLACETYLENE 323
PRUSSIC ACIO HYOROGEN CYANIOE 7B4
PYRENE PYRENE 476

PYRIOINE PYRIOINE 746
PYROACETIC ACIO ACETONE B21
PYROPENTYLENE CYCLOPENTAOIENE 31B
PYRROLYLENE 1,3-BUTAOIENE 292
QUI NOLI NE QUINOLINE 749

SELEXOL SELEXOL B63
SKELLYSOLVE A n-PENTANE 6
SOOIUM HYORATE SOOIUll HYOORXIOE B47
SOOIUll HYOROXIOE SOOIUll HYOROXIOE B47
c1s-STILBENE c1s-1,2-0IPHENYLETHENE 420

trans-STI LBENE trans-1,2-0IPHENYLETHENE 421
STYRENE STYRENE 3B4
STYROL STYRENE 3B4
STYROLENE STYRENE 3B4
SULFOLANE SULFOLANE B62

SULFUR OIOXIOE SULFUR OIOXIOE 796
SULFUR TRIOXIOE SULFUR TRIOXIOE 797
SULFURIC ACIO SULFURIC ACIO B46
SULFURIC ANHYORIOE SULFUR TRIOXIOE 797
SULFUROUS ACIO ANHYORIOE SULFUR OIOXIOE 796

SULFUROUS ANHYORIOE SULFUR OIOXIOE 796
SULFUROUS OXIOE SULFUR OIOXIOE 796
SULPHURIC ACIO SULFURIC ACIO B46
m-TERPHENYL 1,3-0IPHENYLBENZENE 425
1-48 1987
1C0.1
o-TERPHENYL i.2-DIPHENYLBENZENE 424

p-TERPHENYL i,4-DIPHENYLBENZENE 426
TETRACHLOROCARBON CARBON TETRACHLORIDE 802
TETRACHLDROMETHANE CARBON TETRACHLORIDE 802
n-TETRACOSANE n-TETRACDSANE 86
n-TETRADECANE n-TETRADECANE 76
i-TETRADECENE i-TETRADECENE 283
n-TETRADECYLBENZENE n-TETRADECYLBENZENE 380
n-TETRADECYLCYCLOHEXANE n-TETRADECYLCYCLDHEXANE i72
n-TETRADECYLCYCLOPENTANE n-TETRAD£CYLCYCLOPENTANE i39
TETRAETHYLENE GLYCOL TETRAETHYLENE GLYCOL 852

TETRAETHYLMETHANE 3,3-DIETHYLPENTANE 55
TETRAFLUOROMETHANE CARBON TETRAFLUORIDE 803
TETRAHYDRO~URAN TETRAHYDROFURAN 768
i.2,3,4-TETRAHYDRONAPHTHALENE i.2,3,4-TETRAHYDRONAPHTHALENE 446
TETRALIN i,2,3.4-TETRAHYDRONAPHT~ALENE 446

i.2,3.4-TETRAMETHYL BENZENE i,2,3.4-TETRAMETHYL BENZENE 368
i.2.3,5-TETRAMETHYL BENZENE i.2,3,5-TETRAMETHYL BENZENE 369
i,2,4,5-TETRAMETHYL BENZENE i,2,4,5-TETRAMETHYL BENZENE 370
2.2,3,3-TETRAMETHYLBUTANE 2,2,3,3-TETRAMETHYLBUTANE 40
TETRAMETHYLENE CYCLOBUTANE 98
TETRAMETHYLE~E OXIDE TETRAHYDROFURAN 768
TETRAMETHYLENE SULFDNE SULFDLANE B62
2,2,3,3-TETRAMETHYLHEXANE 2.2.3,3-TETRAMETHYLHEXANE 70
2.2,5,5-TETRAMETHYLHEXANE 2.2,5,5-TETRAMETHYLHEXANE 7i
TETRAM~THYLMETHANE NEOPENTANE 8
2.2,3,3-TETRAMETHYLPENTANE 2.2.3.3-TETRAMETHYLPENTANE 58
2.2,3,4-TETRAMETHYLPENTANE 2.2,3,4-TETRAMETHYLPENTANE 59
2,2.4,4-TETRAMETHYLPENTANE 2,2,4.4-TETRAMETHYLPENTANE 60
2,3,3,4-TETRAMETHYLPENTANE 2,3,3 4-TETRAMETHYLPENTANE
0 6i
2-THIABUTANE 2-THIABUTANE 832

THIACYCLOPENTANE DIOXIDE SULFOLANE 862
2-THIAHEPTANE 2-THIAHEPTANE 842
2-THIAHEXANE 2-THIAHEXANE 839
3-THIAHEXANE 3-THIAHEXANE 840
3-THIAPENTANE 3-THIAPENTANE 838

2-THIAPROPANE DIMETHYL SULFIDE 829
THIOETHANOL ETHYL MERCAPTAN 830
THIOETHYL ALCOHOL ETHYL MERCAPTAN 830
THIOMETHYL ALCOHOL METHYL MERCAPTAN 827
TOLUENE TOLUENE 336

TOLUENE HEXAHYDRIDE METHYLCYCLDHEXANE i47
n-TRIACONTANE n-TRIACONTANE 92
TRIATOMIC OXYGEN OZONE 795
i,i,i-TRICHLOROETHANE i,i,i-TRICHLOROETHANE ei2
i.i,2-TRICHLOROETHANE i.i.2-TRICHLOROETHANE Si3

TRICHLOROFLUOROMETHANE TRICHLOROFLUOROMETHANE soi
TRICHLOROFORM CHLOROFORM 806
TRICHLOROMETHANE CHLOROFORM 806
n-TRICOSANE n-TRICOSANE 85
TRI DANE n-TRIDECYLBENZENE 379

n-TRIDECANE n-TRIDECANE 75
i-TRIDECENE i-TRIDECENE 282
n-TRIDECYLBENZENE n-TRIDECYLSENZENE 379
n-TRIDECYLCYCLOHEXANE n-TRIDECYLCYCLOHEXANE Hi
1987 1-49
1C0.1
n-TRIDECYLCYCLOPENTANE n-TRIDECYLCYCLOPENTANE 138

TRIETHANOLAMINE TRIETHANOLAMINE 857
TRIFLUOROCHLOROMETHANE CHLOROTRIFLUOROMETHANE 799
1,1,1-TRIFLUOROETHANE 1,1,1-TRIFLUOROETHANE 814
TRIFLUOROMETHANE TRIFLUOROMETHANE 807
TRIFLUOROMETHYL CHLORIOE CHLOROTRIFLUOROMETHANE 799

TRI(HYDROXYETHYL)AMINE TRIETHANOLAMINE 857
sym-TRIMETHYLBENZENE 1,3,5-TRIMETHYLSENZENE 348
1,2,3-TRIMETHYLBENZENE 1,2,3-TRIMETHYLBENZENE 346
1,2,4-TRIMETHYLBENZENE 1,2,4-TRIMETHYLSENZENE 347
1,3,5-TRIMETHYLSENZENE 1,3,5-TRIMETHYLBENZENE 348

2,2,3-TRIMETHYLBUTANE 2,2,3-TRIMETHYLBUTANE 22
2,3,3-TRIMETHYL-1-BUTENE 2,3,3-TRIMETHYL-1-BUTENE 256
TRIMETHYLCARBINOL tert-BUTANOL 716
1,1,2-TRIMETHYLCYCLOPENTANE 1,1,2-TRIMETHYLCYCLOPENTANE 116
1,1,3-TRIMETHYLCYCLOPENTANE 1.1,3-TRIMETHYLCYCLOPENTANE 117

1,c-2,c-3-TRIMETHYLCYCLOPENTANE 1,c-2,c-3-TRIMETHYLCYCLOPENTANE 118
1,c-2,c-4-TRIMETHYLCYCLOPENTANE 1,c-2,c-4-TRIMETHYLCYCLOPENTANE 121
1,c-2,t-3-TRIMETHYLCYCLOPENTANE 1,c-2,t-3-TRIMETHYLCYCLOPENTANE 119
1,c-2.t-4-TRIMETHYLCYCLOPENTANE 1,c-2,t-4-TRIMETHYLCYCLOPENTANE 122
1,t-2,c-3-TRIMETHYLCYCLOPENTANE 1,t-2,c-3-TRIMETHYLCYCLOPENTANE 120

1,t-2,c-4-TRIMETHYLCYCLOPENTANE 1.t-2,c-4-TRIMETHYLCYCLOPENTANE 123
TRI METHYLENE CYCLOPROPANE 93
3,3,4-TRIMETHYLHEPTANE 3.3.4-TRIMETHYLHEPTANE 68
3,3,5-TRIMETHYLHEPTANE 3,3,5-TRIMETHYLHEPTANE 69
2,2,3-TRIMETHYLHEXANE 2,2,3-TRIMETHYLHEXANE 48
2.2,5-TRIMETHYLHEXANE 2,2,5-TRIMETHYLHEXANE 50
2,3,5-TRIMETHYLHEXANE 2.3,5-TRIMETHYLHEXANE 52
2,4,4-TRIMETHYLHEXANE 2.4,4-TRIMETHYLHEXANE 53
3.3,4-TRIMETHYLHEXANE 3,3,4-TRIMETHYLHEXANE 54
TRIMETHYLMETHANOL tert-BUTANOL 716
2.2,3-TRIMETHYLPENTANE 2,2,3-TRIMETHYLPENTANE 36
2,2,4-TRIMETHYLPENTANE 2,2,4-TRIMETHYLPENTANE 37
2,3;3-TRIMETHYLPENTANE 2,3,3-TRIMETHYLPENTANE 38
2,3,4-TRIMETHYLPENTANE 2,3,4-TRIMETHYLPENTANE 39
2,3,3-TRIMETHYL-1-PENTENE 2,3,3-TRIMETHYL-1-PENTENE 275
TRIPTANE 2,2,3-TRIMETHYLBUTANE 22
n-UNDECANE n-UNDECANE 73
1-UNDECENE 1-UNDECENE 280
n-UNDECYL8ENZENE n-UNDECYLBENZENE 377
n-UNDECYLCYCLOHEXANE n-UNDECYLCYCLOHEXANE 169
n-UNOECYLCYCLPENTANE n-UNDECYLCYCLOPENTANE 136

UREA UREA 743
VALERIC ACID N-PENTANOIC ACID 705
VINEGAR ACID ACETIC ACID 701
VINYL ACETATE VINYL ACETATE 757
VINYLACETYLENE VINYLACETYLENE 326

VINYL BENZENE STYRENE 384
VINYL CHLORIDE VINYL CHLORIDE 811
VINYL ETHYLENE 1,3-BUTADIENE 292
WATER WATER 845
1-50 1987
1C0.1
XENON XENON 798

1,2-XYLENE a-XYLENE 338
1,3-XYLENE m-XYLENE 339
1,4-XYLENE p-XYLENE 340
m-XYLENE m-XYLENE 339
a-XYLENE a-XYLENE 338

p-XYLENE p-XYLENE 340
1987 1-51
1C1 .1
TABLE 1C1.1
PARAFFINS-PRIMARY PROPERTIES
Critical Constants
Bolling
Point
No. Compound Formula M.W. at l atm Fraazing Temp- Pressure VolUIMI Compres- A.centric
deg F Point era tu re psia cu ft alblllty Factor
in air deg P per lb Factor
at l
atm.
deg F
Pa,.afft na, C1 to C3
1
2
I METHANE
ETHANE
CH4
C2H5
18.04
30.07
-258. 73
-127.49
-43. 75
-298.44
-297 .04
z
z
-118.87
5g,g2
666.40
706.50
818.00
o.09g1
0.0788
0.0737
0. 2880
0. 2840
0.2800
0.0108
0.0990
0.1517
3 PROPANE C3H5 44 .10 -305. 73 E 208 .06
Pa,.afftne, C4H10
41 n-8UTANE C4H10 58.12 31.08 -217.05 305. 82 550.60 0.0704 0. 2743 o.ig31
5 IS08UTANE C4H10 58 .12 10. 78 -255. 28 274.48 527. 90 0.0724 0. 2820 0.1770
Pa,.aff1na, C5H12
81 n-PENTANE C5H12 72 .15 g8.92 -201 .51 385.80 488 .60 0.0693 0. 25go 0.2486
7 I SOPENTANE C5H12 72.15 82. 12 -255.82 35g, 10 4go.40 0.067g 0. 2700 0.2275
8 NEOPENTANE C5H12 72.15 49.10 2.17 321. 13 464.00 0.0874 o. 25go 0.1964
Paraffin•. C9H14
9 n-HEXANE C5H14 88.18 155. 72 -13g,55 453.60 438.go 0.0688 0.2640 0 .3047
,,
10 2-METHYLPENTANE
3-METHYLPENTANE
C5H14
C5H14
88.18
88. 18
140.47
145,g1
-244.83
-281. 22
435.83
448.30
438. 60
453.10
0.0681
0.0681
0. 2670
o. 2730
0.2781
0 .2773
12 2 ,2-0lMETHYLBUTANE C5H14 88.18 121 .52 -147. 77 p 420 .13 448.80 0 .0887 0.2720 0 .2339
13 2 .3-0IMETHYLIUTANE C5H14 88. 18 138.38 -199.37 p 440.29 453.50 0.0665 0. 2690 0.2478
Pa,..aff1ne, C7H1e
14 n-HEPTANE C7H15 100.20 209.18 -131. 05 512. 70 3g5, 80 o.08g1 0. 2630 o,34g4
15 2-METHYLHEXANE C7H15 100.20 1g4_og -180.89 4g5,oo 3g5, 50 0.0873 0.2610 0. 3282
18 3-METHYLHEXANE C7H15 100.20 1g1,33 -182. g2 503. 78 408 .11 0.0646 0. 2550 0.3218
17 3-ETHYLPENTANE C7H18 100. 20 200.25 -181. 48 513.48 41g. 28 0.0865 0. 2680 0.3094
18 2 ,2-0lMETHYLPENTANE C7H15 ioo.20 174 .55 -190.86 477 .23 402 .23 0 .0685 0. 2670 0 .287g
1g 2 ,3-0IMETHYLPENTANE C7H15 100.20 1g3,51 ... 507 .58 421. 78 0.0628 0. 2560 0. 2g23
20 2, 4-0IMETHYLPENTANE C7H15 100. 20 178,go -182.64 475,g5 3g5, g4 0.0868 0. 2650 o.3oi8
21 3 ,3-0IMETHYLPENTANE C7H15 100. 20 i88.gi -2io. 03 505. 85 427. 21 0.0662 0. 2730 0. 2672
22 2, 2, 3-TRIMETHYLBUTANE C7H15 100.20 177 ,5g -12.84 p 4g9, 44 428. 3g 0.0836 0.2660 0. 2503
Para ff t na. C5H15
23 n-OCTANE C5H15 114. 23 258.21 -70. 18 564. 22 360. 70 o.o6go 0. 25go 0_3g52
24 2-METHYLHEPTANE C5Hi9 114. 23 243. 76 -164.27 547 .68 360.35 0.0684 0.2610 0 .376g
25 3-METHYLHEPTANE C9H19 114.23 248.08 -184.go 554.94 39g,31 0.0651 0. 2520 0.3716
28 4-METHYLHEPTANE C5H15 114. 23 243.88 -185. 72 551 .46 368 .40 0.088g 0. 2595 0.3711
27 3-ETHYLHEXANE C5H15 114. 23 245. 36 ... 558.05 378.55 0.0838 0. 2530 0.3628
28 2, 2-0IMETHYLHEXANE C9H19 114. 23 224.31 -188. 12 52g,g7 395,g5 0.0670 0. 2850 0.3378
29 2 ,3-0IMETHYLHEXANE C9H15 114. 23 240.og ... 554.45 381.45 0.0657 0. 2630 0.3472
30 2, 4-0IMETHYLHEXANE C5H19 114.23 229,g7 ... 538.63 371. 30 0.0882 0. 2630 0.3436
31 2, 5-0IMETHYLHEXANE C5H15 114.23 228.40 -132.07 530.33 361. 14 0.0676 0.2820 0.3576
32 3, 3-0IMETHYLHEXANE C5H15 114. 23 233.55 -194.98 551.93 384.35 0.0821 0.2510 o.31g5
NOTE: See page 1-135 for Key to footnote codes.
1-52 1987
1C1 .1
API Denaity Refractive Vapor Heat Capacity Heat ot Net Heat ot Surface
specific Gravity ot the Indes Pressure at 60 P' and Con- vapor ha- Combustion Tenalon
Gravity at 60 F Liquid ot th• at 100 P' stant Preasure ltlnematlc tlon at ot Liquid ot th• No.
60/60 deg API at 60 F Liquid psia Btu/lb deg F Viscosity ot tb• Normal at 77 P' Liquid
lb/gal at 77 P' Liquid Bolling Btu/lb at 77 P'
cent ls tokes Point dyne/cm.
Ideal Liquid Btu/lb
Gas at l
atm. at 100 P' at 2l0 F
Psr"stt1na. c, to C3
0.3000 340.00 I 2.500 z 1.00040 5000.000 z

z
0.5267 ... ...
...
...
...
219.45 21501. v . ..
...
1
0.3582
0.5070 I 285. 78
147.60
2.970 F
4. 227 F
1 .00470
1. 28980
800.0000
188.6400
0.4078
0.3885
0.9723"Z
0.6200 0. 1858 T ...
211.14
183.01
20426. v
19918. v 7 .02 T
2
3
Perett1ns. C4H10
I
0.5840 110.791 4.869 F 1 .32594 51. 7060 0.3950 0.5701 0.2586 T 0.1675 T 165.93 19657. v 11 .87 T 4
0.5629 119.89 4.893 F 1.35140 72.5810 0.3867 0.5707 0.2773 T 0.1873 T 157. 23 19589. v 9.81 T 5
Psr"stt1na. C5H12
0.8311
92. 70 I 5.282 1. 35472 15.5740 0. 3882 0.5435 0.3397 T 0. 2647 T
...
153.57 19495. 15 .47 T 6
0.8247
0.5974 I 95.01
105.35
5.208
4.981
1.35088
1.33900
20.4450
38.6609
0.3844
0.3904
0.5378
0.5542
0.3175 T
... ...
147 .12
135.53
19304.
19369. v
14.45 T
10.89 T
7
8
Perett1na. C5H14
0.6838 81.68 5.534 1.37228 4.9597 0.3863 0.5318 0.4095 ... 143.94 19232. 17.98 T 9
0.8578 83.83 5.484 1.36873 8. 7537 0.3851 0.5288 0.3914 ... 139.40 19202. 16.87 T 10
0.8889 80.03 5.577 1 .37388 6.1323 0.3803 0.5188 0.3925 ... 143. 77 19214. 17 .58 T 11
0.8535 85.02 5.448 1.36595 9 .8564 0.3814 0.5137 0.4719 ... 131. 79 19162. 15.80 T 12
0.8870 80.63 5.581 1.37281 7 .4228 0.3747 0.5140 0.4443 ... 137. 13 19195. 16.87 T 13
Perett1na. C7H15
0.6882 74. ,, 5. 738 1 .38511 1.6201 0.3845 0.5285 0.5050 0.3521 T 136.00 19158. 19. 78 T 14
0.6823 75.88 5.689 1 .38227 2.2773 0.3808 0.5218 0.4764 ... 133. 72 19135. 18. 79 T 15
0.8928 72. 75 5. 778 1.38609 2.1281 0. 3787 0.5183 0.4479 ... 133.82 19148. 19.30 T 16
0. 7043 89.42 5.871 1.39084 2.0043 0.3854 0.5142 0.4410 ... 133.04 19156. 19.92 T 17
0.6821 75.98 5.688 1 .37955 3.4914 0. 3854 0.5167 0.5381 ... 125 .55 19097. 17 .53 T 18
0. 7024 69.95 5.858 1.38945 2. 3522 0.3751 0.5098 0.5330 ... 130.83 19140. 19.47 T 19
0.6764 77 .69 5.639 1 .37882 3. 2933 0.3885 0.5238 0.5265 ... 127 .84 19113. 17.64 T 20
0.6981 71. 78 5.804 1 .38842 2. 7688 0.3854 0.5013 0.5825 ... 127 .59 19121. 19. 07 T 21
0.6954 71.98 5. 797 1.38692 3.3720 0.3777 0.4991 0.8928 ... 124.33 19105. 18.99 T 22
Per"att1ns. C9H19
o. 7070 68.65 5.894 1 .39505 0.5369 0.3833 0.5238 0.6372 0.3995 129.52 19098. 21 .08 T 23
0. 7037 69.59 5.866 1.39257 0. 7677 0.3804 0. 5170 0.5588 0.3400 125.84 19080. 20.15 T 24
o. 7098 67 .88 5.917 1.39610 o. 7303 0. 3772 0.5138 0.5501 0.3348 128.11 19090. 20. 75 T 25
0.7210 64. 74 6.011 1 .39553 0. 7634 0. 3794 0.5151 0.5338 0.3294 127 .50 19093. 20. 54 T 26
0.7173 65. 77 5.980 1.39919 0. 7457 T 0.3860 T 0.5158 T 0.5335 T 0.3265 T 128.80 T 19097. 21.08 T 27
0. 7001 70.60 5.837 T 1.39104 1. 2201 T 0.3825 T 0.5064 T 0.8235 T 0.3780 T 121.82 T 19054. 19.15 T 28
o. 7162 68.07 5.971 1 .39880 0.8610 T 0.3723 T 0.5055 T 0.5830 T 0.3659 T 124.88 T 19089. 20. 53 T 29
a. 1011 70.18 5.850 1.39291 1 .0989 T 0.3897 T 0.5179 T o. 7057 T 0.4141 T 122.23 T 22460. 19.59 T 30
0.6983 71. 12 5.822 T 1.39004 1 .0974 T 0.3787 T 0.5113 T 0.5828 T 0.3703 T 123. 19 T 19060. 19.28 T 31
a. 1141 68.65 5.954 T 1. 39782 1 .0309 T 0.3867 T 0.5052 T 0.5858 T 0.3649 T 122.84 T 19071. 20.17 T 32
1987 1-53
1C1.1
Critical Constants
Boiling
Point
llO. compound Formula M,W, at l atm Free2in9 Temp- Preaeure Volume Compres- Acentr le
deg F Point erature P•ia cu ft sibility Factor
in air deg F per lb Factor
•t l
atm.
deg F
Pereff1ns. C9H1e
33 3 ,4-01 METHYLHEXANE C9H19 114.23 243.91 ... 564.17 390.15 0.0654 0. 2650 0.3361
34 2-METHY L-3-ETHYLPENT ANE C5H15 114.23 240.17 -174.91 560.93 391.60 0.0621 0. 2540 0. 3309
35 3-ME THYL-3-ETHYLPENTAN E C9H19 114. 23 244.67 -131 .57 579.03 407.56 0 .0638 0. 2670 0.3047
36 2, 2, 3-TRIMETHYLPENTANE C9H15 114. 23 229. 72 -170.07 554.63 395.91 0.0611 0. 2540 0. 2970
37 2, 2,4-TRIMETHYLPENTANE C9H15 114.23 210.63 -161 .27 519.46 372 .40 0.0656 0. 2660 0.3031
39 2, 3, 3-TRIMETHYLPENTANE C9H15 114.23 239.59 -149.67 572 .63 409.01 0. 0639 0. 2690 0. 2903
39 2, 3 ,4-TRIMETHYLPENTANE C9H19 114.23 236. 25 -164.56 559.67 395.95 0.0646 0. 2670 0.3161
40 2, 2, 3 ,3-TETRAMETHYLBUTANE C9H19 114. 23 223 .65 ... 562. 37 416.26 0.0646 0.2601 0.2171
Pereff 1ne. C9H20
41 n-NONANE C9H20 126.26 303.47 -64.29 610.68 331.90 0.0684 0. 2550 0.4368
42 2-METHYLOCTANE C9H20 129.26 299.90 -112 .67 596.48 332.13 0.0676 0.2540 0.4217
43 3-METHYLOCTANE C9H20 126.26 291.61 -161.68 602 .60 339.49 0.0661 0. 2520 0.4125
44 4-METHYLOCTANE C9H20 129.26 269. 39 -171. 76 599.10 339.46 0.0653 0.2510 0.4130
45 3-ETHYLHEPTANE C9H20 129.26 289.40 ... 610.07 352.44 0.0651 0.2564 0.3798
46 2, 2-0IMETHYLHEPTANE C9H20 126.26 270.94 -171 .40 579.67 p 339.95 p 0.0648 p 0. 2525 0.3922
47 2 ,6-0IMETHYLHEPTANE C9H20 129.26 275. 39 -153.22 576.21 320.53 0.0669 0. 2470 0.3955
48 2, 2 ,3-TRI METHYLHEXANE C9H20 129.26 272.49 ... 604.67 368 .40 0 .0629 0. 2602 0.3191
49 2, 2 ,4-TRIMETHYLHEXANE C9H20 129.26 258 .77 -164.00 573.99 343. 74 0.0642 0. 2552 0. 3437
50 2, 2 ,5-TRI METHYLHEXANE C9H20 129.29 255.36 -159.37 582.92 339.01 0.0648 0. 2560 0. 3567
51 2 ,3, 3-TRIMETHYLHEXANE C9H20 129.26 279.92 -179.24 619.07 375.65 0.0631 0. 2627 0.3124
52 2 ,3, 5-TRI METHYLHEXANE C9H20 126.26 268.41 -199.04 569.01 345.19 0.0645 0. 2636 0.9249
53 2 ,4,4-TRI METHYLHEXANE C9H20 129. 26 267.17 -172.09 599. 29 349 .54 0.0643 0. 2564 0. 3329
54 3 ,3 ,4-TRI METHYLHEXANE C9H20 129. 26 264.63 -150.16 626.99 366. 70 0.0617 0. 2639 0.3236
55 3, 3-01 ETHYLPENTANE C9H20 129. 26 295.14 -27 .56 639.42 397 .97 0.0591 0.2490 0.3391
56 2, 2-01 ME THYL-3-ETHYLPENTANE C9H20 129.26 272 .99 -147.06 601.54 p 373 .07 p 0.0636 p 0.2681 0.3369
57 2, 4-01 ME THYL-3-ETHYLPENTANE C9H20 129.26 276.04 -166.25 604.02 p 367.12 p 0.0639 p 0. 2637 0.3570
58 2, 2, 3, 3-TE TRAMETHYLPENTANE C9H20 129. 26 294.49 14.20 639.96 396. 79 0.0597 0. 2570 0. 2900
59 2, 2, 3 ,4-TETRAMETHYLPENTANE C9H20 129. 26 271.43 -195.96 606.20 371.91 0.0812 0. 2550 0.3106
60 2, 2, 4 ,4-TETRAMETHYLPENTANE C9H20 129.26 252.11 -97. 77 568. 76 342.42 0.0629 0. 2500 0.3159
81 2 ,3 ,3 ,4-TETRAMETHYLPENTANE C9H20 128.28 296. 79 -151.92 634.01 394.50 0.0609 0. 2626 0.3145
Peraf'1ne. C10H22
62 n-OECANE C10H22 142.29 345.46 -21. 36 652 .00 305. 20 0.0679 0.2490 0.4642
83 2-METHYLNONANE C10H22 142.29 332.60 -102.37 637.07 297 .33 0.0677 0. 2434 0.4636
64 3-METHYLNONANE C10H22 142.29 334.04 -120.64 644.99 310.39 0.0665 0. 2476 0.4565
65 4-METHYLNONANE C10H22 142.26 330. 26 -145.66 654.53 p 320.62 p 0. 0637 p 0.2431 0.4000
66 5-METHYLNONANE C10H22 142.29 329.19 -125.86 637.91 p 313.19 p 0.0659 p 0.2493 0.4613
67 2, 7-01 ME THYLOCTANE C10H22 142.29 319. 77 -65. 20 621.23 291.53 0.0669 0. 2393 0.4460
58 3, 3, 4-TRI METHYLHEPTANE C10H22 142.29 323.42 ... 670.19 359.69 0.0622 0. 2630 0.3431
69 3, 3, 5-TRIMETHYLHEPTANE C10H22 142.29 312.22 ... 637 .61 336,49 0 .0634 0. 2579 0.3953
70 2, 2, 3 ,3-TETRAMETHYLHEXANE C10H22 142 .28 320.56 -65. 20 661.73 364.04 0.0640 o. 2755 0.3668
1-54 1987
1C1 .1
API Density Refractive Vapor Heat Capacity Heat of Net Heat of Surface
Spec ltlc Gravity ot th• Index Pressure at 60 F and Con- Vapor iza- Combustion Tension
Gravity at 60 F Liquid ot tho at 100 F stant Pressure ltinema.tic t ion at ot Liquid ot the No.
60/60 deg API at 60 F Llquld psi a Stu/lb deg F Viscosity of th• Normal at 77 F Liquid
lb/gal at 77 F Llquld Bolling Stu/lb at 77 F
centistokes Point dyne/cm
Ideal Llquld Stu/lb
Gas at l
atm. at 100 F at 210 F
Paraffins, CsH1s
o. 7243 63.87 6.038 1 .40180 0. 7982 T 0.3678 T 0.4997 T 0.5736 T 0.3639 T 125. 37 T 19093. 21. 21 T 33
o. 7240 63.94 6.036 T , .40167 0 .8732 T 0.3810 T 0.5072 T 0.5286 T 0.3221 T 125. 19 T 19094. 21 .05 T 34
o. 1315 61 .93 6.099 , .40549 0.8391 0.3810 ... ... . .. . .. 19088. 21 .53 35
o. 1202 64.97 6.005 1 .40066 , . 1421 0.3799 o. 5021 0.6794 0.3981 121 .03 19073. 20. 22 T 38
0.6992 70.87 5.829 1 .38898 1. 7088 0.3810 0.4891 0.6033 o. 3703 116.75 19064. 18.32 T 37
o. 1301 62.31 6.087 , .40522 0.9666 o. 3780 0.5048 o. 1021 0.3623 121 .94 19077. 21.,, T 38
o. 1240 63.94 6.036 1 .40198 0.9769 0.3871 0.5096 0.6823 0.4053 122. 78 19080. 20.68 T 39
... ... ... ... 0.8265 0.3908 0.4466 p ... . .. 118. 26 22445. 20. 95 p 40
Pareff i na, C9H20
o. 1219 64.52 6.018 1.40311 o. 1195 o. 3825 o. 5213 o. 8010 o. 4697 124.36 19055. 22. 38 T 41
o. 1111 65.65 5.984 1 .40080 0.2512 o. 3796 o. 5065 0.6582 0.3865 122. 10 19037. 21 .44 T 42
o. 1250 63.68 6.044 , .40400 o. 2520 0.3770 0.4994 0.6514 0.3818 122 .02 19044. 21 .92 T 43
o. 7249 63. 70 6.043 1 .40390 o. 2132 0.3781 0,5005 0.6518 0.3820 121 .30 19041. 21 .92 T 44
0.7308 62. 12 8.093 1 .40700 o. 2865 ... ... ... . .. 120.00 19052. 22. 34 45
a. 114& 86.50 5.958 1 .39930 0.4298 0.3828 0.4558 p ... . .. ... 19011. 20.34 48
o. 1131 66.92 5.946 1. 39830 0.3686 ... ... . .. . .. 117.66 19019. 20.38 47
o. 7336 61 .39 6. 116 , .40820 0.4298 ... ... . .. . .. 114.97 19030. 21 .41 48
o. 1191 65. 12 6.000 , .40100 0.5748 ... ... . .. . .. 112.63 19029. 20.09 49
o. 1154 66.29 5.964 1 .39728 0.8209 0.3744 0.4871 1 .3067 o. 1108 112. 57 18993. 19.59 T 50
o. 7419 59.24 6. 185 , .41190 0.3835 ... ... ... ... . .. 19035. 21 .95 51
o. 1281 63.36 6.054 1 .40370 0.4539 ... ... . .. . .. 115. 31 19025. 20.82 52
o. 1218 62.91 6.068 , .40510 0.5121 ... ... . .. . .. 112.96 19038 . 20. 75 53
o. 7498 57. 22 6.251 , .41540 o. 3531 ... ... ... . .. . .. 19047 . 22. 79 54
o. 7587 55.00 6.328 1 .41837 o. 2925 0.3908 0.5090 1 .5876 0.8916 118. 27 19054. 23. 29 T 55
o. 7389 80.01 6. 160 , .41020 0.4298 ... ... ... . .. 114.64 19063. 21. 92 56
o. 7420 59. 21 6. 186 1.41150 o. 3835 ... ... ... . .. . .. 19073. 22. 34 57
o. 7807 54.52 6.342 , .42140 0.3613 0.3814 0.4954 0.8146 0.3802 115.57 19045. 22. 94 T 58
o. 7238 64.0S 6.032 , .41246 o. 1293 0.3886 0.4858 0.8119 0.3579 109.89 19053. 21 .57 T 59
o. 7238 64.06 6.032 , .40459 0.7293 0.3886 0.4858 0.8119 0.3579 109.07 19039. 19.91 T 60
o. 7588 54.99 6.326 1 .42003 0.3495 o. 3928 0.4557 p ... . .. ... 19046 . 22 .88 61
Paraff1ns, C10H22
o. 7342 61. 22 6. 121 1.40967 0.0609 0.3818 0.5203 1 .0130 0.5525 119.65 19019. 23. 37 T 62
o. 7308 62. 18 6.091 1 .40750 0.0852 0.3802 ... . .. . .. 116.64 19003. 20.56 0 63
o. 1315 60.35 6. 149 1 .41030 0.0850 0.3777 ... . .. . .. 116.64 19010. 21. 35 p 64
o. 7365 80.64 6. 140 1 .40950 0.0950 ... ... ... . .. . .. 19010. 22. 96 p 65
o. 7387 60.57 6. 142 1 .41000 0.0978 ... ... . .. . .. 115.43 19010 . 23. 00 p 68
o. 7285 82. 72 6.074 1 .40620 o. 1206 0.3778 ... ... . .. . .. 18987. 21 .59 67
o. 1801 54.52 6.342 1 .42130 o. 1401 ... ... . .. . .. 111 .50 19010. 26. 21 p 68
o. 7490 57 .95 6. 227 1 .41.410 o. 1142 ... ... ... . .. .. . 19008. 24. 32 p 69
o. 7684 52.88 6.408 1 .42800 o. 1584 ... ... . .. . .. 109.39 19011 . 27. 33 p 70
1987 1-55
1C1 .1
Cr 1 t ical Con•tanta
Boiling
Point
No. Compound Formula M.W. at l atm .rraazin9 Tamp- Preaaura Volume Comprea- Acantr ic
de9 F Point erature paia cu ft alblllty Factor
at l
atm.
dog F
Par·aff1na. C10H22
71
72 I 2. 2 • S. S-TETRAMETHVLHEXANE
2. 4- OlMETHVL-3-ISOPROPVL-
PENTANE
C10H22
c 10"22
142, 28
142.28
279.43
314.67
9.32
-11S.08
S88.8S
646.30 p
317 .83
34S.21 p
0.0643
0.0629 p
0. 2S90
0. 2604
0.3780
0.3707
Paraffins, C11 to C30
73 n-UNDECANE c 11"24 1S6.31 384.60 -14.07 690. 71 279.92 0. 068S 0. 2428 O.S362
74 n-OOOECANE C12H25 170,34 421.38 14. 75 72S.4S 2S8. 17 0.0683 0. 2362 0.S7S2
7S n-TRIOECANE C13H29 184.36 4SS .84 22 .30 7S7 .31 239.31 0.0682 0.2304 0.6188
76 n-TETRAOECANE C14H30 198,39 488.44 42.SS 794.66 208.SO 0.0680 0. 2090 O.S701
77 n-PENTADECANE C1sH32 212.42 S19.23 49.86 813.47 207 .40 0.0679 0.2190 0. 7083
78 n-HEXAOECANE C15H34 226,44 S48 .3S 64.68 838.49 194.3S 0.0678 0.2142 0. 7471
79 n- HEPTAOECANE C17H35 240.47 S7S.64 71 .S7 860.40 s 191 .00 s 0.0870 s 0.2170 0. 764S
80 n-OCTAOECANE C19H39 2S4 .so 601.34 82.69 881 .80 176. 00 s 0.0630 s 0.1980 0. 7946
81 n-NONAOECANE C19H40 268.S3 6S0.84 89.40 901.00 s 162.00 s 0.0670 0.2000 0.8196
82 n-ElCOSANE C20H42 282.SS 6S0.84 97 .S7 921 .00 s 182.00 s 0.0640 s 0. 1980 0.9119
83 n-HENEICOSANE C21 H44 296.S8 673. 70 104.90 947.48 p 168.38 p 0.0647 p 0. 2112 0.9221
84 n-OOCOSANE C22H45 310,61 69S .so 111 .90 98S.SO p 1S9. 72 p 0.0648 p 0. 209S 0.9S47
85 n-TRICOSANE C23H49 324.63 716.40 117. 70 982.67 p 1S3.S8 p 0.064S p 0 .2078 0.9887
88 n-TETRACOSANE C24Hso 338.66 736. 30 123.80 998.96 p 147 .89 p 0.0644 p 0.2082 1 .0188
87 n-PENTACOSANE C2sHs2 352 .69 7SS .40 128. 70 1014. 39 p 142.61 p 0.0644 p 0. 2047 1 .0498
88 n-HEXACOSANE C25H54 366. 71 774.00 133.SO 1029. 36 p 137. 70 p 0.0643 p 0.2033 1 .0834
89 n-HEPTACOSANE C27Hs5 380. 74 791 .80 138.20 1043.69 p 133. ,., p 0.0643 p 0.2019 1.1117
90 n-OCTACOSANE C29Hs9 394. 77 808.90 142.SO 10S7.32 p 128.81 p 0.0642 p 0.2008 1. 140S
91 n- NONACOSANE C29H90 408. 79 82S .40 148. 70 1070.26 p 124. 79 p 0.0642 p 0. 1994 1. 1686
92 n-TRlACONTANE C30H52 422 '82 841 .so 150.40 1083.22 p 121 .00 p 0. 0641 p 0. 1982 1. 1932
1-56 1987
1C1 .1
API Density Refractive Vapor Heat Capacity Heat ot Net Heat of Surtace
Specific Gravity ot the Index Pressure at 60 F and Con- Vapor iza- Combustion Tension
Gravity at 60 F Liquid ot th• at 100 F st ant Pressure JUnematic t ion at ot Liquid ot the No.
60/60 deg API at 60 F Liquid psia Btu/lb deg P Viscosity ot the Normal at 77 F Liquid
lb/gal at 77 F Liquid Boiling Btu/ lb at 77 F
cent is tokes Point dyne/cm
Ideal Liquid Btu/lb
Gas at l
Perafftns. C10H22
0. 7229 6.027 1 .40316 0.3453 ... ... . .. . .. . .. 18939. 21 .26 p 71
I
64.241
0. 7824 54.11 6.356 1 .42248 0. 1747 ... ... . .. . .. 108.48 19071 . 28.44 p 72
Pereff1ns. C11 to C30
0. 7445 58.56 8.207 1 .41507 0.0204 0.3833 0.5204 1 .2580 0.6394 116.95 18988. 24. 24 T 73
0. 7527 58.48 6.276 1 .41507 0.0071 0.3830 0.5210 1 .5446 0. 7467 112. 26 18964. 24.94 T 74
0. 7817 54. 28 8.351 1.42346 0.0031 0.3814 0.5212 1 .7546 0. 8299 107.96 18942. 25.55 T 75
0. 7833 53.87 6.364 1 .42685 0. 0009 0.3812 0.5228 2. 2511 0.9930 102.82 18925. 26. 32 T 76
0. 7722 51. 75 6.438 1 .42979 0.0002 0.3808 0.5241 2.4918 1 .0950 104.00 18909. 28.68 T 77
0. 7772 50.58 6.480 R 1 .43250 0.0001 0.3806 0.5246 T 2.9193 1 .2480 99. 72 18894. 27 .09 T 78
0. 7797 49.99 6.500 R 1 .43480 <.0001 0.3819 0.5236 T 3.5813 1. 4462 93.54 18883. 27 .52 T 79
o. 7820 49.45 8.519 R 1 .43890 R <.0001 0.3825 0.5212 T 4. 1314 1 .5974 89.20 18872. R 27 .97 T 80
0. 7889 48.31 8.581 R 1 .43880 R <.0001 0.3823 0.5011 T 4.8990 1. 7939 89. 78 18862. R 28. 22 T 81
0. 7924 47. 10 6.597 R 1 .44050 R <.0001 0.3821 ... 5. 3926 1.9846 89. 79 18854. R 28.54 T 82
0. 7954 48.41 6.831 R 1.44200 R ... . .. . .. . .. ... . .. 18999. v 27. 75 v 83
0. 7981 45. 79 8.854 R 1 .44340 R ... 0.3889 0.5166 v ... ... . .. 18992. v 27 .91 v 84
0.8004 45.28 8.873 R 1.44470 R ... 0.3816 0.5167 v ... ... . .. 18985. v 28.04 v 85
0.8025 44.82 8.890 R 1 .44590 R ... 0.3974 0.5166 v ... . .. . .. 18979. v 28. 14 v 86
0.8027 44. 79 8.892 R 1 .44700 R ... 0.3821 0.5164 v ... ... . .. 18973. v 28.29 v 87
0.8079 43.64 8. 738 R 1 .44800 R ... 0.3813 0.5180 v ... . .. . .. 18969. v ... 88
0.8088 43.50 8. 741 R 1 .44900 R ... 0.3805 0. 5158 v ... . .. . .. 18964. v 28.48 v 89
0.8101 43.17 8. 754 R 1 .44990 R ... 0.3815 0.5150 v ... ... . .. 18959. v 28.54 v 90
0.8120 42. 78 6. 770 R ... 1 .45080 R 0.3813 0.5144 v . .. ... . .. 18955. v 28.63 v 91
0.8132 42.50 8. 780 R ... ...
1.45150 R . .. . .. . .. . .. 18951. v 28.68 v 92
1987 1-57
1C1.2
TABLE 1C1.2
CYCLOPARAFFINS-PRIMARY PROPERTIES
Cr ltlcal Constant•
Bolling
Polnt
No. Compound Formula M.W. at l atm .Freezing Temp- Preeeure Volume Compree- Acentr le
deg F Point erature p•l• cu ft elblllty Factor
ln air deg F per lb Factor
at 1
atm.
deg r
A 1ky1eye1 opr"openee, C3 to C5
93 CYCLOPROPANE C3H5 42.08 -27 .04 -197 .36 258.57 808.60 0.0620 0.2745 a. 1349
94 YE THY LCYCLOPROPAN E C4H9 56. ,, 33.31 -287.14 874.87 p 659.29 p 0.0853 p a. 1983 a. 1510
95 E THYLCYCLOPROPANE C5H1Q 70. 13 98.67 -238.59 407 .82 p 589.04 p 0.0848 p a. 2119 a. 2110
98 c 1e-1, 2-0IMETNYLCYCLOPROPANE C5H10 70. 13 98.65 -221.57 410 .92 p 589.04 p 0.0848 p a. 2168 0.2410
97 trene-1, 2-0IMETHYLCYCLOPROPANE C5N10 70. 13 82. 78 -237 .23 ... ... ... ... . ..
A 1ky1 eye I obutenea, C4 to C5
CYCL08UTANE C4H5 56. 11 54.52 -131.31 B 368. 20 723 .00 0.0800 a. 2140 0.1866
10; I YETNYLCYCLOBUTANE
ETHYLCYCL08UTANE
C5H10
C5N12
70. 13
84.16
97.34
159.08
...
-224. 95
417 .45 p
488.55 p
808 .43 p
529.03 p
a .0624P
0.0625 p
a. 2828
a. 2133
a. 1930
a. 2250
A 1ky1eye1 opentenee, C5 to C7
101 CYCLOPENTANE C5N10 70. 13 120.67 -136.98 481.50 653.00 0.0590 a. 2130 a. 1943
102 YE THYLCYCLOPENTANE C5N12 84.18 161 .28 -224.42 499.35 548.90 a .0601 a. 2120 a. 2302
103 ETHYLCYCLOPENTANE C7N14 98.19 218.24 -211. 20 585.47 492 .80 0.0611 0.2690 0.2715
104 1. 1-0IWETHYLCYCLOPENTANE C7N14 98.19 190. 12 -93.63 525.00 500.00 0.0591 0.2746 0.2721
105 c 1a- 1. 2-0IWETNYLCYCLOPENTANE C7N14 98.19 211. 18 -85.01 551 .eo 499.66 0.0604 0.2710 0.2662
108 trena-1, 2-0IME TNYLCYCLOPENTANE C7N14 98. 19 197.38 -179.64 538.00 499.88 0.0587 0.2700 0.2898
107 cis-1 .3-0IWETNYLCYCLOPENTANE C7N14 98.19 195.39 -208.88 532.00 500.00 0.0591 a. 2121 a. 2131
108 tr"&ns-1. 3-0IMETHYLCYCLOPENTANE C7N14 98.19 197.10 -209. 15 538.00 500 .00 0.0591 0.2716 a. 2878
Alkylcyclopentenea, C9N19
109 n- PRO PY LC YC LO PENT ANE C9H15 112.21 287. 71 -179.21 625. 73 p 435. 11 p 0.0607 p a .2540 0.2719
110 I SOPROPYLCYCLOPENTANE C9H15 112.21 259.55 -168 .47 608.18 p 441 .03 p 0.0599 p a .2588 0.3029
111 1-ME TNYL-1-ETHYLCYCLOPEN TA.NE C5H19 112. 21 250. 74 -228.84 588.08 p 438.29 p 0.0811 p 0.2871 0.3305
112 c1 a-1-METNYL-2-ETNYL-
CYCLOPENTANE C5N15 112.21 262.49 -158. 71 605.43 p 438.29 p 0.0811 p 0.2628 0.3278
113 tr"ene-1-YETHYL-2-ETNYL-
CYCLOPENTANE c5•15 112 .21 250. 16 -158.87 587.26 p 438.29 p 0.0811 p 0.2873 a .3293
114 c1 e-1-METHYL-3·ETHYL-
CYCLOPENTANE C5H15 112 .21 250. 18 ... 588.98 p 438.29 p a .0611 P 0.2674 0.3280
115 tr"ene-1-YE TNYL-3-ETNYL-
CYCLOPENTANE c5•15 112.21 250. 18 ... 588.98 p 438.29 p a .0611p o. 2874 0.3291
118 1, 1.2-TRIMETNYLCYCLOPENTANE C5H15 112.21 238. 71 -8.95 587.37 p 438. 29 p 0.0811 p o. 2125 a .3324
117 1, 1.3-TRIYETNYLCYCLOPENTANE C5H15 112. 21 220 .81 -224.39 543.92 p 438 .29 p 0.0611 p o. 2789 0.3318
118 1,c-2.c-3-TRIMETHYL-
CYCLOPENTANE c5•18 112.21 253.40 -177.57 592.00 p 438.29 p 0.0811 p 0.2881 0.3307
119 1 .c-2.t-3-TRIWETNYL-
CYCLOPENTANE C9H15 112.21 243 .50 -189.60 577 .38 p 438.29 p 0.0611 p 0.2899 0.3325
120 1. t-2.c-3-TRIWETNYL-
CYCLOPENTANE c5•15 112.21 230.38 -170.87 558.57 p 438.29 p 0.0611 p a. 2749 0.3315
121 1,c-2.c-4-TRIMETNYL-
CYCLOPENTANE C9Ni5 112. 21 242.60 -208. 19 575.42 p 438. 29 p 0.0611 p 0.2704 0.3281
1-58 1987
1C1.2
TABLE 1C1 .2 (Continued)
API Density Retractlve vapor Keat Capac l ty Heat ot Ket Heat ot Surface
Specif le Cravlty ot th• Index Pressure at 60 l' and Con- Vaporl2a- Combustion Tension
Cravlty at 60 F Llquld of the at 100 F stant Pressure Kinematic tlon at of Llquld of the Ho.
60/60 de9 API at 60 l' Llquld psla Btu/lb de9 F Vlscos lty ot th• Normal at 77 F Llquld
lb/9al at 77 F Llquld Bollln9 Btu/lb at 77 F
cent ls tokes Point dyne/cm
Ideal Llquld Stu/lb
Gas at 1
A 1ky1 cycl opropenes, C3 to C5
0 .6338 91. 75 5.284 ... 145.4780 0.3064 ... 0. 2488 T ... 205.19 20018. y 12.99 T 93
... ... ... ... ... ... 0.3160 p ... .. . .. . 19657. v .. . 94
0.8891 73.85 5. 745 1. 37560 ... ... 0.3357 p ... ... 220 .14 19495. p 17 .58 p 95
0.8989 70.96 5.827 1. 38000 ... ... 0.3355 p ... ... 221.06 19440. p 18.62 p 96
0.6748 78.19 5 .817 ... ... ... ... ... ... ... .. . ... 97
A 1ky1 cycl obutenes, c4 to Cs
0.6999 5.835 1. 36200 34.0919 0. 2960 0.4562 0.3571 ... 183. 76 19676. y 16. 73 T 98
I
70.671
0 .6977 71. 30 5 .817 "38100 ... ... 0.3356 p ... .. . 222. 37 19457. p 16.38 p 99
0. 7327 61.61 6.109 1. 39940 ... ... 0.3427 p ... ... 207. 28 19354. p 19.58 p 100
A 1ky1eye1 opentanes, C5 to C7
0. 7603 54.61 6.338 1 .40363 9.9196 0. 2712 0 .4227 0.4927 ... 167 .09 18825. 21. 71 T 101
0. 7540 56.17 6.286 1,40700 4.5044 0.3001 0.4404 0.5648 ... 149.87 18768. 21.65 T 102
0. 7712 51 .98 8.429 1.41730 1.4066 0.3058 0 .4433 0.8199 0.3901 141.19 18758. 23.33 T 103
o. 7592 54.87 6.330 1 .41091 2 .5609 0.3180 0.3649 p ... ... ... 18721. 21. 24 104
0. 7771 50.59 6.478 T 1.41963 1.6484 T 0.3154 T 0.4502 T 0 .5698 T 0.3655 T 138.85 T 18750. 23 .62 T 105
0. 7561 55.83 8.304 T 1.40941 2. 1928 T 0.3170 T 0.4453 T 0.5870 T ... 138.80 T 18724. 21. 20 T 106
0. 7495 57. 28 6.249 1 .40633 2.2916 0.3170 0.3646 p ... ... ... 18729. 20. 22 p 107
0. 7535 58.29 6. 282 1 .40813 2. 2091 0.3170 0.3645 p ... ... ... 18738. 20 .65 p 108
A lky 1cycl opentenes, C9H15
0. 7811 49.88 6.512 1 .42389 0.4710 0.3145 0.4514 o. 7256 0.4613 132.54 18750. 24.42 T 109
0. 7808 49. 71 6.510 1.42350 0. 6011 0. 3157 0.3616 p ... ... ... 18873. p 23.89 110
o. 7854 48.68 8.548 1.42476 0. 7263 0. 2705 0. 3820 p ... ... ... 18863. p 24. 29 p 111
0. 7896 47. 7i 6.583 , ,42695 o. 5502 ... 0. 3755 p ... ... .. . 18873. p 24.83 p 112
o. 7734 51.46 6.448 1 .41950 0. 7227 ... 0.3760 p ... ... .. . 18873. p 22.81 p 113
o. 7712 51.97 6.430 1.41700 0. 7144 ... 0.3761 p ... .. . ... 18873. p 22 .50 p 114
0. 7712 51.97 6.430 , .41700 0. 7387 ... 0.3761 p ... ... .. . 18873. p 22.50 p 115
0. 7771 50.58 6.479 1 .42051 0. 9988 0.3604 o. 3767 p ... ... ... 18829. p 23. 24 p 116
o. 7528 58.47 6. 278 1.40870 1.3930 0.3604 0.3775 p ... ... .. . 18829. p 20.42 p 117
o. 7837 49.05 6.534 1 .42380 0. 6920 ... 0.3759 p ... .. . ... 18873. p 24.05 p 118
0. 7750 51.09 6.481 1.41940 0.8525 ... 0.3764 p ... ... ... 18840, p 22 .99 p 119
0. 7581 55.18 8.320 1.41140 1. 1388 ... 0.3770 p ... ... 133.37 p 18840. p 21.02 p 120
o. 7760 50.84 8.470 1. 42000 0.8499 ... 0.3764 p ... ... ... 1B840 . p 23.06 p 121
1987 1-59
1C1.2
Critical Constants
Bolling
Point
No. Cc.pound Formula M.W. at 1 atm Freeiing Temp- Pressure Volume Compres- Acentr ic
deg F Point erature psis cu tt slblllty Factor
in air deg p per lb Factor
at l
atm.
deg P
Alkylcyclopentsnes, C9H1s
122 1 ,c-2, t-4-TRIMETHVL-

CVCLOPENTANE C9H15 , 12 .21 242. 12 -206. 59 577.38 p 438.29 p a .as,, p 0.2699 0.3306
123 1,t-2,c-4-TR!METHVL-
CVCLOPENTANE C9H15 ,,2. 21 228. 72 -203 .40 555 .60 p 438. 29 p 0.0611 p 0.2757 0.3310
Alkylc:yclopentsnee, C9H1a
124 n-8UTV LCVCLOPENT A.NE C9H19 126. 24 313.88 -162.37 858.60 p 395.00 p 0.0813 p 0.2546 0.3280
125 I S08UTVLCVCLOPENTANE C9H19 126.24 298.31 -175.40 864. 12 p 422.39 p 0.0579 p 0.2561 0.2670
126 1-METHVL-1-n- PROPVL-
CVCLOPENTANE C9H19 126.24 294.80 ... 631 .02 p 395 .00 p 0.0613 p 0.2610 0.3760
127 1, 1-0I ETHVLCVCLOPENTANE C9H19 126.24 302 .90 ... 642. 72 p 395.00 p 0.0613 p 0.2583 0.3730
128 c is-1, 2-0IETHVLCVCLOPENTANE C9H19 126.24 308.41 -180.40 650. 70 p 395 .00 p 0.0813 p a. 2564 0.3730
129 1, 1-0IMETHVL-2-ETHVL-
CVCLOPENTANE C9H19 126.24 280 .40 ... 810.20 p 395.00 p 0.0613 p 0.2681 0.3730
Alkylc:yc:lopentenes. C10 to C25
130 n- PENTVLCVCLOPENT A.NE C10H20 140.27 356.90 -117 .40 899. 71 p 359 .46 p 0.0814 p 0.2490 0.4184
131 n- HEXVLCVCLOPENTANE C11H22 154.JO 397. 22 -99.40 737. 26 p 329. 77 p 0.0616 p a. 2439 0.4646
132 n- HEPTVLCVCLOPENTANE C12H24 168.32 435.02 -63.40 771 .62 p 304.61 p 0.0817 p a. 2394 0.5100
133 n-OCTV LCVC LOP ENT ANE C13H25 182 .35 470 .JO -47 .20 802 .90 p 283 .00 p o .0618 P a .2353 o .5525
134 n- NONV LCVCLOPENT A.NE C14H29 198.38 503 .60 -20.20 831 .92 p 264. 26 p 0.0819 p 0.2316 0.5956
135 n-DECV LCVCLOPENTANE C15H3Q 210.40 534.88 -7 .83 858.61 p 247 .84 p 0.0619 p 0.2283 0.6314
136 n-UNDECV LCVCLOPENTANE C19H32 224.43 564.44 14.00 883 .47 p 233.34 p 0.0620 p 0.2252 0.6741
137 n-DODECVLCVCLOPENT ANE C17H34 238 .48 592. 16 23.00 908.JJ p 220.43 p 0.0620 p 0.2225 a. 1183
138 n-TRIOECVLCVCLOPENTANE C19H35 252 .48 618.82 41.00 927 .93 p 208 .88 p 0.0621 p 0.2199 a. 7582
139 n- TE TRAOECV LCVCLOPENTANE C19H39 266.51 644.00 48.20 948.54 p 198.48 p a. 0521 o a. 2115 a. 7949
140 n- PENTAOECV LCVCLOPENTANE C20H40 280.54 667 .40 62.60 966.99 p 189.07 p 0.0622 p 0.2154 0.8395
141 n- HEXAOECVLCVCLOPENTANE C21H42 294.56 690.80 89.80 985. 78 p 180.50 p 0.0622 p 0.2133 0.8755
142 n- HEPTAOECV LCVCLOPENTANE C22H44 308.59 710.60 80.60 1000.42 p 172.68 p 0.0622 p 0.2117 0.9060
143 n-OCT AOECVLCVCLOPENTANE C23H45 322 .62 732. 20 86.00 1017.61 p 165.52 p 0.0623 p 0.2098 1 .0010
144 n- NONADECVLCVCLOPENTANE C24H49 336.64 752 .00 95.00 1032 .87 p 158 .92 p a. 0523 o 0.2081 0.9660
145 n- EICOSVLCVCLOPENTANE C25H5Q 350.67 770.00 100.40 1046.21 p 152 .83 p a. 0523 o 0.2067 1 .0750
A I ky I eye I ohexanea, c 6 sna C7
148
147
I CVCLOHEXANE
METHVLCVCLOHEXANE
C9H12
C7H14
84.18
98. 19
177 .33
213.68
43.80
-195.87
536. 70
570.27
591 .00
503 .48
o .0588
0.0800
0.2730
0.2690
0.2149
0.2350
A 1ky1 cycl ohexsnes, C9H19
148 ETHVLCVCLOHEXANE C9H19 112 .21 269.21 -168.38 838.80 440.88 0.0642 0.2700 0.2455
148 1, 1-0IMETHVLCVCLOHEXANE C9H19 112.21 247. 18 -28.29 804.40 428. 18 0.0642 0.2690 0.2326
150 c1a-1, 2-0IMETHVLCVCLOHEXANE C9H19 112.21 265.51 -58.04 631.40 428. 18 0.0657 0.2680 0.2324
151 trens-1, 2-0IMETHVLCVCLOHEXANE C9H19 112.21 256.01 -130. 19 613.40 428. 18 0.0657 0.2730 a. 2319
1-60 1987
1C1.2
API Deneity Refractive Vapor Heat Capacity Heat of Net Heat ot' Surtace
Specltic Gravity ot th• Index Preaeure at 60 r and Con- Vapor ha- Combuation Tension
Gravity at 60 r Liquid ot the •t ioo r stant Preeaure kinematic tion at ot Liquid ot' the No.
60/60 deq API at 60 F Liquid paia Btu/lb deq F Viacoaity ot' the Normal at 77 F Liquid
lb/901 •t 77 F Liquid Boiling Btu/lb •t 77 F
centhtokes Point dyne/cm
Ideal Liquid Btu/lb
GH •t l
atm. •t 100 F at 210 F
A 1ky1eye1 opentanae. C9H15
0. 7680 52. 74 6.403 1 .41812 0.8814 0.3719 0.3764 p ... . .. ... 18840. p 22. 18 p 122
0. 7518 56. 71 6.268 1.40812 1. 1825 ... 0.3771 p ... ... " . 18840. p 20.33 p 123
A 1ky1eye1 opentanea, C9H15
0.8103 43. 12 6.758 1 .42930 ... . .. 0.3861 p ... . .. 176. 13 18745 . 25.39 124
0. 7853 48.69 6.547 1.42730 ". . .. 0.3887 p ... . .. 170.32 18831. p 24.29 125
0.8036 44. 78 6.700 1 .43500 ... . .. 0.3888 p

". . .. 171. 17 18860. p 26.56 p 126
0.8072 43. 79 8.730 1 .43830 ." ... 0.3885 p
". " . 173.30 18860. p 28. 76 p 127
0.8004 45.29 8.673 1 .43300 " . . .. 0.3863 p ... . .. 174. 72 18869. p 26.20 p 128
0. 7928 46.97 8.810 1 .43000 ... . .. 0.3874 p ... . .. 167 .41 18831. p 25. 16 p 129
A I ky I eye I opentanaa. C10 to C25
0. 7954 48.41 6.631 1 .43360 " . 0.3304 0.3982 p 1. 1280 0.6200 . .. 18739. 26.30 130
0.8006 45.24 6.875 1 .43700 " . 0.3348 0.4058 p 1. 1450 0. 7300 . .. 18735. 26.90 131
0.8051 44.28 e. 112 1.44000 ... 0.3382 0.4150 p 1. 7480 0.8500 " . 18731. 27 .40 132
0.8088 43.45 e. 743 1 .44250 ... 0.3412 0.4239 p 2. 1300 0.9800 . .. 18728. 28.00 133
0.8121 42. 73 8.771 1 .44480 ... 0.3428 0.4328 p 2.5700 , .1200 103.61 18726. 28.60 134
0.8143 42. 27 6.789 1 .44859 ... 0.3452 0.4410 p 3.0500 1 .2700 . .. 18723. 28.89 135
0.8175 41.58 6.818 1 .44820 ... 0.3473 0.4493 p 3.6300 1.4400 97.48 18721. 28.47 p 136
0.8197 41. 12 6.834 1 .44970 ... 0.3492 0.4574 p 4.2500 1.6100 94.82 18720. 28. 70 p 137
0.8217 40. 70 8.851 1.45100 " . 0.3509 0.4654 p 4.9500 1. 7800 . .. 18718. 28.86 p 138
0.8235 40.32 8.866 1 .45220 ... 0.3524 0.4732 p 5. 7100 1.9800 " . 18717. 29.01 p 139
0.8252 39.97 8.880 R 1 .45330 ... 0.3537 ... 6.5800 2. 1900 . .. 18715. 29. 13 p 140
0.8287 39.67 8.892 R 1 .45430 ... 0.3550 ... ". ... . .. 18714. 29.23 p 141
0.8280 39.40 8.903 R 1 .45520 R ... ... ... ". . .. 116.53 18863. v 29.42 v 142
0.8293 39. 13 6.914 R 1 .45800 R ... ... ... " . . .. 114.07 18862. v 29.52 v 143
0.8303 38.93 8.922 R 1 .45860 R ... ... ... ... . .. 111 .66 18861. v 29.59 v 144
0.8315 38.88 6.932 R 1.45750 R " . . .. ... ... . .. 109.27 18860. v 29.66 v 145
A 1ky1 cyc1 ohexenea, Ce and C7
o. 7835
0. 7748 I 49. 10
51. 13
I 8.532
8.459
1.42354
1 .42058
3.2818
1 .8047
0.2892
0.3179
0.4301
0.4399
0.9407
o. 7660
...
0.4343
152.68
139.34
18676.
18642.
24.85 T
23 .30 T
146
147
A 1ky1 C)'CI oh•••n••. C5H1e
o. 7921 47.14 8.804 1.43073 0.4834 0.3274 0.4428 0.8834 0.5123 130.89 18661. 25.05 T 148
o. 7854 48.87 8.548 T 1 .42862 0.8193 T 0.3185 T 0.4356 T 0.8628 T 0.5043 T 124.30 T 18636. 23.65 T 149
0.8006 45.23 8.875 T 1 .43358 0.5397 T 0.3227 T 0.4382 T 1 .0733 T 0.6717 T 128.52 T 18663. 25. 19 T 150
o. 1503 49.85 8.505 T 1 .42470 o. 7080 T 0.3277 T 0.4358 T 0.8844 T 0.5043 T 125.86 T 18638. 23.57 T 151
1987 1-61
1C1.2
Critical Constants
Bolling
Point
No. Compound Formula M.W. at l atm l'r•••in9 T•mp- Pr•ssure Volume Compr•s- A.centric
dog r Point erature psla cu tt slblllty Factor
in air dog r per lb Factor
at 1
atm.
d•9 p
A I ky 1 eye I ohe1<snes, CeH16
152 Ci s-1, 3-0IMETHYLCYCLOHEXANE C5H15 112. 21 248.16 -104.03 604.40 426.16 0.0642 0. 2690 0. 2366
153 trsns-1, 3-0IMETHYLCYCLOHEXANE C5H15 112. 21 256.01 -130.19 617 .oo 426.18 0.0657 0.2720 0. 2335
154 cis-1,4-0IUETHYLCYCLOHEXANE C9H15 112 .21 255. 78 -125.38 617.00 s 426.16 0.0657 0. 2720 0.2311
155 trans-1, 4-0IMETHYLCYCLOHEXANE C9H15 112. 21 246.83 -34. 53 602.60 426.18 0.0642 0.2690 o. 2310
A 1ky I cyclohe1<snes, Cg ana C10
156 n- PROPYLCYCLOH EX.A.NE C9H19 126.24 314, 10 -138.82 690.80 407 .08 0.0605 0. 2520 0. 2595
157 I SOPROPYLCYCLOHEXANE C9H15 126.24 310.57 -128.90 684.90 p 516.39 p 0. 0529 p 0.2810 0.3675
158 n- BUTYLCYC LOH EX.A.NE C10H20 140.27 357. 70 -102.50 740.93 s 372. 75 s 0.0654 p 0. 2660 0.2743
159 I S08UTYLCYCLOH EXANE C10H20 140. 27 340. 32 ... 729.05 p 573.77P 0.0476 p 0.3006 0.4084
160 sec- SUTYLC YCLOH EXANE C10H20 140.27 354. 70 ... 710 .17 p 375.05 p 0.0593 p 0.2486 0.3520
161 ter t-BUTYLCYCLOHEXANE C10H20 140.27 340.83 -42. 09 702.39 p 382.91 p 0.0583 p 0.2510 0.3380
162 1-WETHYL-4- ISOPROPYL-
CYCLOHEXANE C10H20 140.27 339.30 ... 688.03 p 375.05 p 0.0593 p 0. 2534 o. 3530
A I ky I cycl ohe1<anes, C11 to C25
163 n-PENTYLCYCLOH EX.A.NE C11 H22 154.30 398.61 -71 .50 745.81 p 341.20 p 0.0605 p 0.2461 0.4498
164 n-H EXYLCYCLOHEXANE C12H24 168.32 436.46 -45 .40 779.81 p 314.30 p 0.0607 p 0.2413 0.4931
165 n-H f PTYLCYCLOHEXANE C13H25 182.35 472 .82 -22. 90 612. 16 p 291.32 p 0.0608 p o. 2359 0. 5280
166 n-OCTYLCYC LOHEXANE C14H29 196.36 506.48 -3.46 641.24 p 271.48 p 0.0610 p 0. 2329 0.5793
167 n- NONYLCYC LOH EX.A.NE C15H30 210,40 536. 70 13.64 868.66 p 254.16 p 0.0611 p 0. 2293 0.6205
168 n-OECYLCYC LOH EX.A.NE C15H32 224,43 567.66 28.89 892.56 p 236.94 p 0.0612 p o. 2263 o. eeoo
169 n- UNOECYLCYCLOHEXANE C17H34 236.46 595 .76 42.44 915.56 p 225.42 p 0.0613 p o. 2234 0.6988
170 n-OOOECYLCYCLOHEXANE C19H35 252.48 622. 22 54.50 936.91 p 213.35 p 0.0614 p 0. 2208 0. 7402
171 n-TRI OfCYLCYCLOHEXANf C19H39 266.51 647 .42 65.30 957 .oo p 202.50 p 0.0615 p 0.2183 o. 7749
172 n-TETRAOECYLCYC LOH EX.A.NE C20H40 260.54 671 .00 75. 20 975.43 p 192. 71 p 0.0616 p 0.2161 0.8115
173 n- PENT AOECYLCYCLOHEXANE C21H42 294.56 694.40 64.20 994.01 p 163.82 p 0.0616 p 0.2140 0.8506
174 n-HEXAOECYLCYCLOHEXANE C22H44 306.59 716.00 92.48 1010.66 p 175.71 p 0.0617 p 0.2120 0.8897
175 n- H EPTAOECYLCYCLOHEXANE C23H45 322. 62 735.80 100.04 1025.40 p 168. 29 p 0.0618 p 0. 2104 0.9168
176 n-OCTAOECYLCYCLOHfXANf C24H49 336.64 755.60 104.90 1040.47 p 161.47 p 0.0618 p o. 2oe1 0.9510
177 n-NONAOECYLCYCLOH EX.A.NE C25H50 350.67 773. 60 113.36 1053.63 p 155.18 p 0.0616 p 0. 2072 0.9887
178 n-EICOS YLCYCLOHEXANE C25H52 364.70 791.60 119.30 1067 .09 p 149.36 p 0. 0619 p o. 2055 1.0217
Cyclopsrsffins. C7 to C12
179 CYCLOHEPTANE C7H14 98. 19 245.62 17.60 628.00 557.00 0.0565 0.2741 0. 2430
160 CYCLOOCTANE C5H15 112.21 304.05 58.64 705. 20 517.00 0.0561 0. 2697 0. 2537
161 CYCLONONANE C9H19 126.24 353. 12 51.80 768.00 485.00 0.0561 0. 2700 0. 2680
162 ETHYLCYCLOHEPTANE C9H19 126.24 325 .99 ... 691.77 p 429.39 p 0.0566 p o. 2510 0.3520
183 81CYCLOHEXYL C 12H22 166.31 482. 27 38.53 848.93 p 371 .30 p 0.0576 p 0. 2530 0.4217
1-62 1987
1C1.2
API Density Refractive Vapor Heat Capacity Heat ot Net Heat ot Sur tac•
Specif le Gravity of the Index Pressure at 60 F and Con- vaporiza- Combustion Tension
Gravity at 60 P Liquid ot the at 100 F stant Pressure Kinematic tion at of Liquid ot the No.
60/60 de9 API at 60 F Liquid psi a Btu/lb de9 F Viscosity ot the Normal at 77 F Liquid
lb/gal at 77 F Liquid Boiling Btu/lb at 77 F
Ideal Liquid Btu/lb
Gas at l
Alky1cyclohexenes, C9H15
0. 7704 52. 17 6. 423 T 1 .42063 0.7819 T 0.3249 T 0.4360 T 0.8900 0.5135 T 125.37 T 18620. 22 .59 T 152
0. 7892 47 .ea 6.580 T 1 .42843 0.6509 T 0.3245 T 0.4435 T 0.6645 0.4496 T 127.38 T 18648. 24. 15 T 153
0. 7873 48.23 6.564 T , .42731 0.6605 T 0.3245 T 0.4422 T 0.8797 T 0.5040 T 126.97 T 18648. 23.94 T 154
0. 7670 52.98 6.395 T 1 .41853 0.8201 T 0.3251 T 0.4382 T 0. 7491 T 0.4724 T 124.43 T 18622. 22. 52 T 155
AlkylcycloheJCanes, Cg •nd Cio
0. 7981 45. 79 6.654 1.43476 0. 1700 0 .3376 0.4465 1 .0010 0. 5759 124,30 16663. 26.07 T 156
0.8064 43.97 6. 723 0. 1902 0.3750 o. 3615 p 16775. p 25.30 157
0.8034 44.64 6.698 , .43855 0.0575 0.3418 0.4523 1 .2539 0.6881 118.63 18668. 26.51 T 158
0.8161 41 .88 6.804 0.0907 o. 3665 p 18781. p 25.34 159
0 .8172 41 .65 6.613 , .44450 0.5143 p 167 .02 18781. p 26.99 160
0.8168 41. 75 6.609 1.44470 0. 3684 p 18746. p 26. 18 161
0.8586 33.30 7. 158 p 0. 3686 p 163.42 16754. p 33.68 p 162
A 1ky1eye1 ohexenes, c, 1 to C25
0.8077 43.69 6. 734 , .44160 0. 3450 0. 3726p 113. 78 18670. 27 .00 163
0.8115 42.66 6. 766 , .44410 0.3480 0. 3782p 18672. 27 .so 164
0.8112 42.94 6. 763 , .44630 0.3503 0.3836 p 16673. 27 .90 165
0.8177 41.55 6.817 1 .44830 0.3524 0. 3889p 102.50 18675. 26.40 166
0.8202 41.02 6.838 , .44990 0.3543 0.3942 p 18676. 28.90 167
0.8223 40.57 6.856 1 .45141 0.3556 0.3996 p 16677. 29.34 168
0.8244 40. 14 6.673 1 .45270 0.3572 0.4049 p 99. 71 18678. 28.98 p 169
0.8281 39.80 6.667 1 .45390 0.3583 0.4102 p 18678. 29. 16 p 170
0.6277 39.45 6.901 1 .45500 16679. 29.29 p 171
0.8291 39. 18 6.912 A 1 .45590 16680. 29.51 172
0.6303 36.93 6.922 1.45680 A 18680. 29.53 173
0.6316 36.66 8.933 1 .45760 A 16681. 29.61 v 174
0.6327 38.44 6.942 1.45630 A 16625. v 29.76 v 175
0.8337 38. 22 6.951 A 1.45900 A 16626. v 29 .83 v 176
0.8346 38.05 6.958 A 1 .45960 A 18826. v 29.89 v 177
0.6357 37 .81 6.967 A 1 .46020 R 16827. v 29.95 v 178
Cyclope.-eff1ns, C7 to C12
0.8144 42.24 6. 790 T 1 .44240 0.7926 T 0.2880 T 0.4309 T 1.4796 T 0.6081 T 146.89 T 16783. 26.99 T 179
0.6405 36.86 7.007 1 .45630 0.2218 0.2907 137 .54 16625. 29.30 180
0.6545 34.10 7. 124 1 .46440 0. 3795 129.95 16852. 34.95 p 181
0. 7992 45.55 6.863 0. 3603 p 180.56 18901. p 26.43 p 182
0.8900 27 .49 7.420 1 .47768 0.0054 0.3040 0.4212 2 .9175 115.08 18233. 32. 17 T 183
1987 1-63
1C1.2
Cr 1 tical Constanta
Bollln9
Point
Ho. Compound Formula M.W. at 1 atm l"reeaing Temp- Preaaur• Volume Compres- Acentr ic
deg P Point erature psi a cu rt slblllty Factor
in air deg F per lb Pact or
at l
atm.
de9 F
Oecahydronaphtha lenea. C10 to C12
184 ci s-DECAHYDRONAPHTHALENE C10H19 138.25 384.47 -45.36 804.38 470.27 0.0556 0.2670 0.2942
185 trana-OECAHYDAONAPHTHALENE C10H19 138.25 369.16 -22 .68 777 .02 411.49 0.0556 0. 2380 0.2536
186 1-WETHYL- [cis-DECAHYDRO-
NAPHTHALENE] C11H20 152. 28 469.40 ... 899.53 p 388 .28 p 0.0568 p 0.2303 0.3040
187 1-WETHYL- [trans-DECAHYDRO-
NAPHTHALENE] C11H20 152.28 455.00 ... 878.45 p 388.28 p 0.0568 p 0.2339 0.3040
188 1-ETHYL- (ci a·OECAHYDAO-
NAPHTHALENE] C12H22 166.31 500.00 ... 853.03 p 353 .82 p 0.0573 p 0.2395 0.3960
189 1-ETHYL· [trana-DECAHYDAO-
NAPHTHALENE] C12H22 166.31 491.00 ... 824.95 p 353.82 p 0.0573 p 0. 2447 0.3960
190 9-E THYL- ( ci a·OECAHYOAO-
NAPHTHALENE] C12H22 168.31 451 .00 ... 837. 77 p 353.82 p 0.0573 p 0.2423 0.3960
191 9-ETHYL- ( trana-OECAHYORO-
NAPHTHALENE] C12H22 168.31 437.00 ... 817.27 p 353.82 p 0.0573 p 0. 2482 0.3960
1-64 1987
1C1.2
API Deneity Ret'ractive Vapor Heat Capacity Heat ot Net Heat ot Surtace
Specltic Gravity or the Index Pressure at 60 F and Con- Vapor iza- Combustion Tena ion
Gravity at 60 P Liquid ot the at 100 F stant Pressure Kinematic tion at ot Liquid or th• No.
60/60 deg API at 60 F Liquid psi.a Btu/lb deg F Viscosity ot the Normal at 77 F Liquid
lb/gal at 77 F Liquid Bolling Btu/lb at 77 F
centhtokes Point dyne/cm
Ideal Liquid Btu/lb
Gas at l
Oecehydronephthe1enes. C10 to C12
0.9018 25.41 7.518 1 .47878 0.0354 0. 2766 0. 3908 2 .6582 , .0975 123. 77 18323. 184
0.8755 30.13 7.299 1.46715 0.0541 0. 2789 0.3861 1.8150 0.8519 120.10 18288. 185
1.0148 7 .96 8.459 p 0.3690 p 177. 77 52.83 p 186
1.46980 0.3694 p 174.57 49.28 p 187
0.3731 p 159.11 43. 75 p 188
0.3736 p 158.07 39. 74 p 189
0.8900 27 .49 7 .420 1 .47800 0.3732 p 159.89 31. 74 p 190
0.8648 32. 12 7. 210 1.46400 0.3739 p 156.99 28 .21 p 191
1987 1-65
1C1.3
TABLE 1C1.3
MONOOLEFINS AND DIOLEFINS-PRIMARY PROPERTIES
Cr 1 tlcal Constants
Bolling
Point
No. Compound Formula M.W. at l atm Freezing Temp- Pressure Volume Compres- Acentr ic
deg F Point erature psla cu t't slblllty Factor
at l
atm.
deg F
Monoolefins. C2 end C3
192
193 I ETHYLENE
PROPYLENE
C2H4
C3H5
2R.05
42.06
-154.68
-53.66
-272.47
-301.45
48.56
196.90
729.60
669.00
0.0737
0.0689
0. 2770
0. 2750
0.0652
0. 1424
Monoo 1ef i na. C4H5
194 1-6UTENE C4H5 56. 11 20.73 -301 .63 295.59 563.00 0.0665 0. 2760 0. 1667
195 cis-2-8UTENE C4H5 56. ,, 36. 70 -218.04 324.37 610.00 0.0668 0. 2720 0.2030
196 trens-2-8UTENE C4H5 56. ,, 33.56 -157 .99 311.66 595.00 0.0680 0. 2740 0.2162
197 IS06UTENE C4H9 56. ,, 19.58 -220.63 292.55 580.00 0.0682 0.2750 0.1693
Monoolefins. C5H10
198 1-PENTENE C5H10 70. 13 65.94 -265.40 376.93 51L41 0.0676 0. 2702 0. 2330
199 cte-2-PENTENE C5H10 70. 13 98.50 -240.50 397 .00 530.00 0.0690 0. 2790 0. 2406
200 trsna-2-PENTENE C5H10 70. 13 97 .44 -220.44 396.00 530.00 0.0690 0. 2790 0.2373
201 2-METHYL- 1-6UTENE C5•10 70. 13 66.09 -215.61 378.00 493.00 0.0667 0.2570 0 .2287
202 3-METHYL- 1-6UTENE C5H1Q 70. 13 68. ,, -271 .29 351 .00 510.00 0.0690 0. 2840 0. 2286
203 2-METHYL-2-6UTENE C5H10 70. 13 101 .42 -206.76 388. 00 493.00 0.0667 0.2537 0. 2767
Monoolefina. C5H12
204 1-HEXENE C5H12 84. 16 146.27 -219.67 447 .08 455.43 0.0673 0.2651 0. 2600
205 cia-2-HEXENE C5H12 64.16 156.00 -222.05 463. 73 p 458 .32 p 0.0683 p 0.2660 0.2722
208 trsna-2-HEXENE C5H12 64. 16 154. 17 -207.38 463. 73 p 456.32 p 0.0685 p 0. 2670 0.2613
207 cis·3-HEXENE C5H12 84. 16 151 .61 -216.07 454. 23 p 459.42 p 0 .0667 p 0.2631 0. 2906
208 trsna-3-HEXENE C5H12 64. 16 152. 76 -H2.H 455.72 p 459.42 p 0 .0667 p 0. 2628 0. 2879
209 2-METHYL- 1-PENTENE C5H12 84.16 143.80 -2'2.30 452.93 p 458.32 p 0.0683 p 0.2690 0. 2406
210 3-METHYL- 1-PENTENE C5H12 64.16 129.52 -243.40 431 .04 p 476.02 p 0.0652 p 0.2744 0. 2652
211 4-METHYL- 1- PENTENE C5H12 64.16 128.96 -244.53 433. 13 p 467.02 p 0.0657 p 0.2690 0. 2389
2'2 2-METHYL- 2- PENT ENE C5H12 84.16 153. 15 -211. 13 465.53 p 456.32 p 0.0691 p 0.2680 0. 2445
213 ci s-3-METHYL- 2-PENTENE C5H12 64. 16 153.66 -210.71 467 .65 p 476.02 p 0.0652 p 0. 2636 0. 2585
214 t rsna-3-METHYL- 2-PENTENE C9H12 64. 16 156.79 -2H .20 475.30 p 476.02 p 0.0652 p 0.2615 0. 2583
215 ct s-4-METHYL- 2-PENTENE C5H12 64.16 133.46 -210.73 438.53 p 467.02 p 0.0659 p 0.2690 0. 2442
216 trsns-4-METHYL-2- PEN TENE C5H12 64. 16 137 .46 -221 .44 442. 13 p 467 .02 p 0.0659 p 0. 2670 0. 2552
217 2-ETHYL- 1-6UTENE C5H12 64.16 148.43 -204. 75 481.93 p 456.32 p 0.0693 p 0. 2700 0. 2277
218 2•3-DIMETHYL-1-6UTENE C5H12 84. 16 132. 10 -251 .07 440.33 p 467 .02 p 0 .0664 p 0. 2700 0.2269
219 3. 3-DIMETHYL- 1-6UTENE C5H12 84.16 106. 25 -'75.36 404.10 476.81 p 0 .0635 p 0.2749 0.2266
220 2. 3-DIMETHYL-2-6UTENE C5H12 64.16 163.77 -101. 70 490.01 p 481 .63 p 0.0637 p 0.2533 0. 2268
Monoo 1ef ins. C7H14
221 1-HEPTENE C7H14 96.19 200.56 -161.98 507. 74 410.46 0.0673 0.2613 0.3310
222 cia-2-HEPTENE C7H14 96.19 209.14 ... 526.53 p 411.91 p 0.0692 p 0.2640 0.2942
223 trsne-2-HEPTENE C7H14 98. 19 208.31 -165.06 517 .84 p 413.42 p 0.0682 p 0.2581 0.3389
224 cia-3-HEPTENE C7H14 96.19 204.35 -213.95 521.33 p 4'1.91 p 0 .0687 p 0.2640 0.2949
225 trsne-3-HEPTENE C7H14 98. 19 204.21 -213.93 511 .84 p 413.42 p 0.0682 p 0.2577 0.3379
1-66 1987
1C1.3
API Density Retract iv• Vapor Heat Capacity Heat or Net Heat ot Surtace
Specltic Cravlty ot the Index Pressure at 60 F and Con- Vapor lza- Cornbust ion Tension
Gravity at 60 '/! Liquid or th• at 100 F st ant Preasure klnemat le t ion at ot Liquid or the No.
60/60 deg APl at 60 F Liquid psi a Btu/lb deg F Vlsco9lty ot th• Normal at 77 F Liquid
centhtokes Polnt dyne/cm
Ideal Liquid Btu/lb
GH at l
Monoo 1•'ins. C2 and C3
...
0.5210 I 1~:;0 I ...
4.343
1 .36320 J ...
1 .36250 L 227 .6070
0. 3648
0.3547
...
0.5737
. ..
...
...
...
206.34
188.92
20281. y
19675. y
. ..
6.88 T
192
193
1111onoole,1ns. C4H9
0.6005 i04. 14 5.006 1 .37770 " 63. 2775 0. 3554 0.5359 ... ... 171 .98 19468. y 12. 12 T 194
0.6286 93.61 5. 241 1 .38420 u 45. 7467 o. 3273 0.5323 0. 2710 ... 179. 53 19415. y 13.99 T 195
0.6112 100.02 5.095 1 .39320 u 49.8821 0.3661 ... 0. 2792 ... HS.51 19389. y 12. 72 T 196
0.6013 103.83 5.013 1.39260 u 64.5830 0.3710 0.5463 0. 2557 ... 170.21 19341. y 11 .69 T 197
Monoo 1•'1 ns. C5H10
0.6458 87 .60 5.384 1. 36835 19. 1808 0.3642 0.5194 ... ... 157 .57 19187. 15.46 T 198
0.6598 82.97 5.500 1. 37980 15. 1333 0.3369 0 .5079 ... ... 162.68 19146. 16.80 T 199
0.6524 85.39 5.439 1 .37610 15 .4392 0.3607 0.5253 ... ... 160.92 19119. 16.41 T 200
0.6563 84. 10 5.472 1. 37460 18.4107 0.3683 0.5264 ... . .. 156.83 19101. 15.40 T 201
0.6322 92.32 5. 271 , .36110 26.4036 0.3950 0.5212 ... ... 149.49 19158. 13.80 T 202
0.6683 80.24 5.571 1 .38420 14.3133 0.3491 0.5141 ... . .. 162.33 19057. 17.06 T 203
Monoole,1ns. C5H12
0.6769 77 .53 5.644 1. 38502 6.0069 0.3660 0.5116 0. 3423 ... 146.32 19105. 17 .89 T 204
0.6917 73.06 5. 767 T 1.39473 4.9069 T 0.3468 T 0.5000 T 0. 3828 T ... 147. 25 19046. 19. 10 T 205
0.6825 75.84 5.690 T 1. 39073 5. 0943 T 0. 3667 T 0.5189 T 0.3673 T ... 148.64 19037. 18.08 T 206
0.6848 75. 14 5. 709 1 .39189 5 .3780 ... 0.4399 p ... . .. 146.62 19071. 17 .50 p 207
0.6820 75.98 5.688 1 .39137 5. 2190 ... 0.4399 p ... ... ... 19035. 17. 21 p 208
0.6844 75. 25 5. 706 T 1 .38912 6. 3005 T 0. 3754 T 0.5191 T 0.3639 T ... 144.84 19015. 17 .58 T 209
0.6722 79.01 5.604 1 .38133 8.4430 ... 0.4404 p ... ... . .. 19075. 16.93 p 210
0. 6687 80. 11 5.575 T 1 .37974 8. 5168 T 0.3491 T 0.4947 T 0. 3585 T ... 140.04 19086. 15.92 T 211
0.6909 73 .32 5. 760 T 1. 39739 5.1762 T 0. 3493 T 0.4943 T 0.3465 T ... 147.64 18970. 17 .91 T 212
0.6980 71. 23 5.819 1. 39876 5. 1430 ... 0.4398 p ... ... 147. 26 18992. 19.35 p 213
0. 7024 69.95 5.856 1 .40166 4.6140 ... 0.4398 p ... ... ... 18992. 19.85 p 214
0.6741 78.40 5.620 1 .38498 7. 7463 0.3689 0.5151 0. 3207 ... 140.54 19030. 8. 74 T 215
0.6738 78.58 5.616 1. 38583 7. 1236 0.3920 0.5368 0. 3209 ... 142. 26 19006. 8. 73 T 218
0.6944 72.26 5. 790 T 1 .39380 5. 7044 T 0.3685 T 0.5065 T 0. 3448 T ... 144.81 19030. 18.62 T 217
0.6828 75. 72 5 .693 T 1.38729 7 .9752 T 0.3972 T 0.5334 T 0. 3473 T ... 140.34 18994. 17 .05 T 218
0.6584 83.42 5.489 1 .37313 13.0930 ... 0.4410 p ... ... ... 19028. 15.50 p 219
0. 7130 68.97 5.944 1.40952 4. 1630 ... 0. 4397 p ... ... 151.08 18956. 20. 19 T 220
111onoole,1ns, C7H14
0. 7015 70. 21 5.849 1 .39713 1 .9629 0.3679 0.5107 0.4318 0.3044 138.97 19202. y 19.81 T 221
0. 7114 67 .41 5.931 T 1 .40420 1 .6885 T 0.3486 T 0.4921 T 0.4458 T ... 136.43 19172. y 20.81 T 222
0. 7058 68.99 5.884 1 .40200 1. 7000 ... 0.4460 p ... . .. 135.58 19154. y 19.48 p 223
o. 1012 68.60 5.896 T 1 .40330 1 .8521 T 0.3458 T 0.4902 T 0.4488 T ... 138. 28 19172. y 19.93 T 224
0. 7028 69.88 5.858 1 .40170 1 .9000 ... 0.4460 p ... ... 135.58 19154. y 18. 75 p 225
1987 1-67
1C1.3
Cr 1t ical Constants
Bolling
Point
No. Compound Formula M.W. at l atm P'rff2in9 Temp- Preeaure Volume Compres- Acantr 1c
deg F Point eratura psia cu ft slblllty Factor
ia air deg F per lb Factor
at l
ata.
deg F
Wonooleftna. C7H14
226 2-WETHYL- 1 -HEX ENE C7H14 98. 19 197 .60 -153.11 508.37 p 416. 10 p 0.0649 p o. 2552 0.3114
227 3-WETHYL- 1-HEXENE C7H14 98. 19 183.02 ... 490. 23 p 428.05 p 0.0649 p o. 2675 o. 3078
228 4-WETHYL- 1-HEXENE C7H14 98. 19 188.11 -222.61 497. 77 p 428. 05 p 0.0649 p o. 2654 0.3074
229 5-WETHYL- 1 -HEXENE C7H14 98. 19 185.56 ... 490.62 p 416. 10 p 0.0649 p o. 2599 0.31,,
230 2-WETHYL-2-HEXENE C7H14 98. 19 203. 74 -202. 63 517 .41 p 416. 10 p 0.0649 p 0.2528 0.3128
231 c i s-3-METHYL-2-HE)(EN E C7H14 98. 19 207 .07 -181 .31 525. 78 p 428.05 p 0.0649 p 0.2578 0.3096
232 trana-3-WETHYL-2-HEXEN E C7H14 98. 19 203. 32 -200. 74 520.25 p 428.05 p 0.0649 p o. 2593 0.3091
233 ct a-4-WETHYL-2-HE)(ENE C7H14 98. 19 187 .36 ... 496.65 p 428 .05 p 0.0649 p 0.2657 0.3081
234 trana-4-METHYL-2- HEX ENE C7H14 98. 19 189.61 -194.24 499.96 p 428.05 p 0.0649 p 0.2648 0.3083
235 ct a-5-METHYL-2-HE)(ENE C7H14 98. 19 193. 10 ... 501. 75 p 416. 10 p 0.0649 p 0.2569 0.3120
236 t rane-5-WE THYL-2-H EX ENE C7H14 98. 19 190.60 -191 .81 498.06 p 416. 10 p 0.0649 p o. 2519 0.3113
237 ct a-2-WETHY L-3-H EX ENE C7H14 98. 19 186.80 ... 492 .46 p 416.10 p 0.0649 p o. 2594 0.3123
238 t rans-2-WETHYL-3- HEXENE C7H14 98.19 186.62 -222.81 492. 19 p 416. 10 p 0.0649 p o. 2595 o. 3112
239 c i a-3-WETHYL-3-HEXENE C7H14 98.19 203. 72 ... 520.83 p 428.05 p 0.0649 p 0.2592 o. 3067
240 trana-3-WETHY L-3-HEXENE C7H14 98. 19 200.38 ... 515 .88 p 428.05 p 0.0649 p 0.2605 0.3065
241 2-ETHYL-1-PENTENE C7H14 98. 19 201. 20 ... 517. 10 p 428.05 p 0.0649 p 0.2601 0.3127
242 3-ETHYL-1-PENTENE C7H14 98. 19 183.40 -197 .46 494.20 p 440.51 p 0.0649 p 0.2742 0.3030
243 3-ETHYL-2-PENTENE C7H14 98.19 204.82 ... 525 .97 p 440.51 p 0.0649 p o. 2653 0.3056
244 2.3-0IWETHYL-1 -PENTENE C7H14 98.19 183. 70 -209. 74 501. 26 p 443 .47 p 0.0636 p 0.2684 o. 2150
245 2 ,4-0IWETHYL-1-PENTENE C7H14 98. 19 178.90 -191 .31 487.09 p 418.81 p 0.0636 p 0.2573 o .2811
246 3. 3-0I WETHYL-1-PENTENE C7H14 98. 19 171 .46 -209.88 488.30 p 452. 52 p 0.0634 p o. 2110 o. 2599
247 3 ,4-0IWETHYL-1-PENTENE C7H14 98. 19 177 .44 ... 491 .90 p 443.47 p 0.0636 p o. 2111 o. 2154
248 4,4-0IWETHYL-1-PENTENE C7H14 98. 19 162.53 -213.88 467 .83 p 427. 11 p 0.0634 p o. 2512 0.2747
249 2.3-0IWETHYL-2-PENTENE C7H14 98. 19 207 .32 -180.89 536.54 p 443.47 p 0.0636 p o. 2589 0.2784
250 2 4-0IWETHYL-2-PENTENE
0 C7H14 98.19 181.94 -197 .86 491.59 p 418.81 p 0.0636 p 0.2561 0.2852
251 ct a-3 ,4-0I WETHYL-2-PENTENE C7H14 98. 19 192.65 -172. 11 514.62 p 443 .47 p 0.0636 p 0.2648 o. 2152
252 trana-3. 4-0I METHYL- 2-PENTENE C7H14 98.19 196. 70 -191 .82 520.68 p 443.47 p 0.0636 p 0.2631 o. 2114
253 cia-4 ,4-0I METHYL-2-PENTENE C7H14 98.19 176. 77 -211.83 489.06 p 427. 11 p 0.0634 p 0.2612 o. 2155
254 trana-4. 4-0I METHYL-2-PENTENE C7H14 98. 19 170. 13 -175 .42 479. 16 p 427. 11 p 0.0634 p 0.2640 0.2705
255 3-WETHYL-2-ETHYL- 1-BUTENE C7H14 98. 19 187 .46 ... 503.28 p 430.88 p 0.0636 p o. 2603 o. 2808
256 2,3,3-TAIMETHYL-1-BUTENE C7H14 98. 19 172. 20 -165. 73 496.40 p 455.59 p 0.0621 p o. 2109 o. 2394
Yonool efins, C9H19
257 1-0CTENE C9H15 112. 21 250.30 -151. 12 561 .02 371.30 0.0873 0.2561 0.3747
258 cts-2-0CTENE C9H15 112. 21 258. 15 -148.36 570.79 p 375 .46 p 0.0658 p o. 2506 0.3848
259 trans-2-0CTENE C9H15 112. 21 257 .00 -125 .88 578.93 p 374. 20 p 0.0891 p o. 2600 0.3384
260 cts-3-0CTENE C9H15 112. 21 253.22 ... 583. 72p 375 .48 p 0.0658 p o. 2524 0.3839
261 trans-3-0CTENE C9H15 112. 21 253 .94 -166.00 573 .53p 374. 20 p 0.0685 p 0.2600 0.3438
262 cis-4-0CTENE C9H15 112. 21 252.57 -181 .66 562. 78p 375.46 p 0.0658 p 0.2526 0.3882
263 trans-4-0CTENE C9H15 112. 21 252.05 -138.86 571. 73p 374. 20 p 0.0685 p o. 2900 0.3393
264 2-WETHYL- 1-HEPTENE C9H15 112. 21 246. 74 -130.00 554.41 p 375 .46 p 0.0658 p o. 2541 0.3855
265 3-WETHYL- 1 -HEPTEN E C9H15 112. 21 231 .80 ... 541.87 p 387. 28 p 0.0846 p 0.2813 0.3552
1-68 1987
1C1.3
API Density Refractive Vapor Heat Capacity Heat of Net Heat of Surface
Speclt'lc Gravity of the Index Pressure at 60 F' and Con- Vapor ha- Combustion Tension
Gravity at 60 P Liquid ot th• at 100 F stant Pressure Kinematic tlon at of Liquid ot the No.
60/60 deg API at 60 F Liquid psla Btu/lb deg F Vhcoslty of the Normal at 77 F Liquid
lb/gal at 77 F Liquid Boll Ing Btu/lb at 77 F
Ideal Liquid Btu/lb
cas at l
atm. at 100 F at 210 F'
0. 7074 68.52 5.898 1.400BO 2.1000 0.4460 p 135.56 19136. y 20.01 226
0.6959 71.83 5.802 1 .393BO 2 .8000 133. 73 19182. v 1B. 72 227
0. 7030 69. 78 5.B61 1 .39730 2 .5000 191B2. y 19.51 p 22B
0.6965 71.65 5.807 1.39400 2. 7000 19170. y 18. 78 p 229
0. 7126 67.07 5.941 1.40790 1.9000 19110. v 20. 24 p 230
0. 7203 64.95 6.005 1.41000 1.8000 19122. y 21. 14 p 231
0. 7188 65.35 5.993 1.40910 1.9000 19122. y 20.97 p 232
0. 7040 69.51 5.B69 1.39990 2 .6000 19153. v 19.26 p 233
0. 7013 70.26 5.847 1. 39980 2 .5000 19134. y 18.96 p 234
o. 7065 68. 79 5.890 1.40100 2 .3000 19141. v 19.47 235
0.6971 71.48 5.B12 1.39790 2 .4000 19123. y 18.50 23B
0.6981 71.20 5.820 1.39900 2. 2600 19141. v 1B.40 p 237
0.6941 72.36 5. 7B7 1.39740 2 .6000 19123. y 17 .84 p 23B
0. 7180 65.5B 5.986 1.40995 1.8010 0.4460 p 19122. y 20.41 p 239
0. 7144 66.57 5.956 1.40820 1. 9570 0.4460 p 19122. y 20.04 p 240
0. 7125 B7.10 5.940 , .40200 2 .0000 135.56 19147. v 20.5B p 241
0. 7005 70.51 5.840 1.39550 2 .BOOO 133. 73 19193. y 19.23 p 242
0. 7249 63.69 6.044 1.41220 1.BOOO 0.4460 p 135.56 19133. y 21. 70 p 243
0. 7097 67.BB 5.917 1.40060 2 .8000 19117. v 20. 2B p 244
0.6987 71.03 5.825 1.39577 3.1870 0.4462 p 127 .B7 19104. v 19.01 p 245
0.7019 70.09 5.852 1.395BO 3.5200 19142. v 19.38 p 246
0. 7022 70.02 5.B54 1.39650 3.1300 19152. y 19.42 p 247
0.6872 74.42 5. 729 1.3BB95 4.4850 0.4464 p 19121. v 17. 75 p 248
0. 7323 61. 74 6.105 1.41850 1.8000 190B8. y 22.61 249
0.6995 70. 78 5.832 1.40090 2.8690 0.4462 p 132.63 19079. y 18. 75 250
0. 71BO 65.5B 5.9BB 1.407BO 2 .3000 133. 73 19091. v 20.B7 p 251
0. 7212 64.69 6.013 1.41010 2. 2000 19091. v 21 .26 p 252
0. 7040 69.51 5.869 1.399B9 3.3510 0.4462 p 127 .69 19092. y 19.24 p 253
0.6935 72.53 5. 782 1.39525 3. 7050 0.4463 p 129.15 19073. y 18.09 p 254
0. 7178 65.B2 5.9B5 1.40244 2.6000 0.44B1 p 19117. v 20. 70 p 255
0. 7092 68.01 5.913 1.40007 3. 6820 19092. y 20.21 p 258
Monoolefins. C9H1e
0. 7193 65.21 5.997 1.40620 0.6561 0.368B 0.5059 0.5681 0.3599 131.75 19000. 21. 29 T 257
0. 7287 62.69 6.075 1.41250 0.6000 0.4530 p 19111. p 20.94 p 258
0. 7243 63.B5 6.039 1.41070 O.B100 0.4530 p 128.99 1B9B5. p 21. 70 T 259
0. 7257 63.49 6.050 1.41110 0.6800 19114. p 21 .41 p 260
0. 7194 B5.20 5 .998 T 1.41020 0.6439 T 0.3609 T 0.4998 0.5808 0.3517 T 129.01 189B5. p 20.BB 261
0. 7255 63.53 8.049 1.41240 0.6600 0.4530 19114. p 20.58 262
0. 7182 65.52 5 .98B T 1.40930 0.BB52 T 0.3609 T 0.4991 0.5B13 T 0.3528 T 129.17 189B5. p 20.67 T 2B3
0. 7248 63. 72 8.043 1.409BO 0.7500 0.4529 19102. p 21 .38 p 264
0. 7149 88.44 5.980 1.40400 1.0000 19127. p 20. 24 p 265
1987 1-69
1C1.3
Critical Constants
Boiling
Point
llo. Compound Formula M.W. at l atm Freezing Ts mp- Pressure Volume Compres- A.centric
deg F Point erature psia cu ft slblllty Factor
in air de9 F per lb Factor
at l
atm.
deg F
lilonoolefine. C9H15
266 4-METHYL-1-H EP TENE C9H15 ,,2. 21 23S.04 ... S46. S7 p 387.28 p 0.0646 p 0.2601 0. 3SSS
267 trans-6- ME THYL-2- HEPTENE C9H15 112.21 242.60 ... SS4.31 p 377 .64 p 0.0646 p 0. 2S17 0. 3S98
268 trsns-3- lllETHYL-3- HEPTENE C9H15 112.21 249.80 ... S87 .9S p 387.28 p 0.0646 p 0. 2S47 0. 3SS7
269 2-ETHYL-1-HEXENE C9H15 112.21 248.00 ... S73.S3 p 44S.27 p O.OS70 p 0. 2S70 0.3799
270 3-ETHYL-1-HEXENE C9H15 112.21 230.S4 ... S43. 27 p 397.29 p 0.0646 p 0. 2677 0.3S4S
271 4-ETHYL-1-HEXENE C9H15 112.21 23S.40 ... sso. 3S p 397.29 p 0.0646 p 0.26S9 0.3S24
272 2, 3-0IWETHYL-1-HEXENE CeH1e 112.21 230.90 ... SS0.02 p 399.85 p 0.083S p 0. 2628 0.3259
273 2. 3-0llllETHYL-2-HEXENE C9H15 112.21 251. 19 -175. 18 S79.69 p 399 .es P 0.083S p 0. 2SS3 0. 3272
274 cis-2, 2-0UETHYL-3-HEXENE C9H15 112.21 221. 77 -21S.23 S34. 94 p 388.S3 p 0.0634 p 0. 2S74 0.322S
27S 2 ,3,3-TRIMETHYL·1-PENTENE C9H15 112.21 226.96 -92. 20 S63.38 p 431.SS p 0.0822 p 0.2744 0.2731
276 2 4 4-TRUIETHYL-1 ·PENTENE
0 0 C9H15 112.21 214.S9 -136. 26 53S.73P 381.4S p 0.0664 p 0. 2660 0.289S
277 2 .4.4-TRUIETHYL-2-PENTENE C9H15 112.21 220.84 -1S9.39 S44. 73 p 381.4S p 0.0671 p 0. 2660 0.26SO
lllonoolefine. Cg to C20
278 1-NONENE C9H19 126.24 296. 36 -114.47 608.18 337 .94 0.0670 0.249S 0.4171
279 1 ·0ECENE C10H20 140.27 339.03 -87. 3S 6S0.66 308. 93 0.0667 0. 2272 0.464S
280 1-UNDECENE C1 iH22 154.30 378.81 -56.53 703. 13 p 292.98 p 0.0692 p 0.2S10 0.4489
281 1-000ECENE C12H24 168.32 416.04 -31.41 739.13 p 274.12 p 0.0690 p 0. 2470 0.4909
282 1-TRIOECENE C13H25 182.3S 4S1 .00 -9.S3 773.33 p 2S6. 72 p 0.0691 p 0.24SO 0.S280
283 1-TETRADECENE C14H29 196.38 483.98 8.87 807 .S3 p 240.78P 0.0700 p 0. 2430 O.S460
284 1-PENTADECENE C15H30 210.40 515. ,, 25.29 811.04 208.86 0.0888 0.2148 0.6633
28S 1-HEXADECENE C15H32 224.43 544. 77 39.42 p 865. 13 p 214.68 p 0.0704 p 0. 2380 0.6128
286 1-HEPTADECENE C17H34 238.46 S72.S9 52.16 ese. 74 182. 7S 0.066S 0. 2050 0. 7288
287 1 ·0CTADECENE C19H35 2S2.48 S98.68 63.68 913. 73 p 194.3S p 0.0704 p 0. 2340 0.6669
288 1-NONADECENE C19H39 266.S1 624. 38 74.12 899. 60 180.99 0.0665 0.19S6 0.8246
289 1-EICOSENE C20H40 280.S4 648. 32 83.48 9S8.73P 178.9S p 0.0702 p 0. 2290 0. 7340
Oiolsfins. C3 to C5
290 PROPADIENE C3H4 40.06 -30.10 -213.34 248.00 793.36 p 0.0648 p 0.2710 0.1S94
291 1, 2-BUTADIENE C4H5 54.09 S1 .S3 -213. 14 339.S3 p 652.67 p 0.0649 p 0. 2670 0.2509
292 1 ,3-BUTADIENE C4H5 S4.09 24.06 -164. OS 306.00 828.00 0.06S4 0. 2700 0.1932
293 1,2-PENTADIENE Cs He 68.12 112. 74 -21S. 07 42S.19 p SS1.04 p 0.0648 p 0.2S61 0. 2235
294 cis-1,3-PENTADIENE CsHe. 68.12 111.32 -221.48 436.S3 p S42.44 p 0.0649 p 0.2490 0.1470
29S trans- 1, 3-PENTAOIENE Cs He 68.12 107 .88 -12S.4S 440.33 p S42.44 p 0.0649 p 0.2480 0.1162
298 1 .4-PENTADIENE Cs He 68. 12 78. 74 -234.89 402. 53 p 542.44 p 0.0713 p o. 2850 0.0837
297 2,3-PENTADIENE C5H9 68.12 118.88 -194.17 434. 68 p SS1.04 p 0.0648 p 0. 2S34 0.2194
298 3-METHYL-1,2-BUTADIENE Cs He 68.12 10S.S3 -172.S2 421.47 p SSB.02 p 0.0629 p 0. 2S20 0.1923
299 2-METHYL-1,3-BUTADIENE CsHS 68.12 93.32 -230.71 411.S3 p SSB.40 p 0.0649 p 0.2640 0.1S83
01olefins. Ce to C10
... ... ... ... ...

I
300 2, 3-0IWETHYL-1 ,3-BUTADIENE C9H1Q 82.1S 1SS.80 -104.81
301 1 ,2-HEXAOIENE C9H10 82.1S 168.80 ... 487.81 p 488.44 p 0.0645 p o. 2534 0.2710
1-70 1987
1C1.3
API Density Refractive Vapor Heat Capacity Heat ot Net Heat ot Surface
Speclflc Gravity ot th• Index Pressure at 60 F and Con- Vapor iza- Combustion Tension
Gravity at 60 F Liquid of the at 100 F stant Pressure Kinematic tion at ot Liquid of the No.
60/60 de9 API at 60 P Llquld psi a Btu/lb deg F Viscosity ot the Normal at 77 F Liquid
Ideal Liquid Btu/lb
Gas at l
Monoolefins. C9H15
0. 7209 64.7g 6.010 1 .40800 o.g400 ... ... . .. . .. ... 23788 . p 20.g5 p 266
0. 7221 64.47 6.020 , .41000 0.8100 ... ... . .. . .. . .. 1gos1. p 20. 70 p 267
0. 732g 61 .SB 6. 110 1 .41600 0. 7000 ... ... . .. ... 140.59 p 1gos1. p 21 .SB P 268
0. 731S 61 ,g4 6.0gB T 1 .41320 0.728g T 0.36g1 T 0 .sogg T 0.546g T 0.34SO T 130. 70 1sg6s. p 2S.38 T 25g
0. 11g7 6S. 12 6.000 1 .40SOO 1 .0000 ... ... . .. ... . .. 19120. p 20. 74 p 270
0. 730S 62.21 6.ogo 1 .41000 0 ,g300 ... ... ... . .. ... 1g123 . p 22.01 p 271
0. 72SB 63.46 6.0S1 1 .4osgo 1 .0000 ... ... ... . .. . .. 21802 . p 21 .so p 272
0. 74S2 SB.38 6.213 , .42440 0.6800 ... ... ... . .. . .. 1goo3. p 23.SS p 273
0. 7171 6S.81 s.g1g 1 .40740 1.3ogo ... 0.4S28 p . .. . .. . .. 1gos2. p , , .93 p 274
0. 7398 5g, 76 6. 168 , .41510 , . 1000 ... ... . .. . .. . .. 1go22. p 23.21 p 27S
0. 11g3 65.22 S.gg7 T 1 .40600 1 .S607 T 0.37S3 T 0 .4g3s 0. 3684 T 0. 2S46 T 118. 71 1sg16. 19.25 T 276
0. 7260 63.40 6.0S3 T , .41350 1 .2880 T 0.3736 T o.soog 0.3648 T 0. 2S20 T 122.32 1sg29. 19.68 T 277
Monoolefins, Cg to C20
0. 7336 61 .38 6. 116 , .41333 0. 2200 0.3709 0.5212 o. 1009 0.4314 126.09 18964. 22.56 T 27B
0. 7447 58.51 6.209 , .41913 0.0738 0.3718 0 .S044 0.8852 O.S031 120.64 19g35, 23.SS T 27g
0. 7S41 S6. 13 6.287 1 .42383 0.0244 0.3724 O.S028 1 .01g5 o.sgog 11S. 72 18914. 24.40 T 280
0. 7630 53,g5 6.361 , .42782 O.OOB3 0.3730 0.5042 1 .3233 0.6807 ,,, . 77 18895. 25. 14 T 281
0. 7899 S2.30 6.418 , .43118 0.0034 0.373S 0.4886 1 .6032 0. 7871 106. 76 1887g. 2S. 7g T 282
0. 774g 51. ,, 6.480 , .43412 0.0011 0.3740 0 .4772 1 .g222 o.go40 103.80 1886S. 26. 3S T 283
0. 7802 4g.ss 6.505 1 .4366g ... ... O.S26g p . .. . .. 99.43 188S3. 26.87 284
0. 7847 48.83 6.S42 1 .43go7 0. 0002 0.3747 O.S110 2. 7227 1. 1666 g1 .07 18843. 27 .33 T 28S
0. 7900 47 .63 6.SB6 1.44100 ... ... ... ... ... . .. 1B834. 27. 71 286
0. 7g23 47. 10 6.BOS R 1 .44280 ... 0.37S3 0 .4766 3 .5276 1 .4278 88.47 18826. 28 .og T 287
0. 7958 46.30 6.63S R 1 .444SO ... ... . .. ... ... . .. 1ss1g . 28.40 288
0. 7gs1 4S.BO 6.8S4 T 1 .44590 R ... 0.37S4 T 0.4784 T 4. go50 T 1 .8462 T 87.62 18812. R 28. 73 T 2sg
D1olef1ns. C3 to Cs
0.5997 104.46 4,g99 1.41690 144.5430 0.3442 ... 0. 2280 . .. 221 .04 19921. y g.so T 290
0.6S78 83.68 S.482 1 .420SO 36. 7698 0. 346S O.S407 0. 27SS 0. 2248 1g2.48 1g557, y 1S. 78 T 291
0.6273 94.08 S.230 1 .42930 5g. 2g39 0. 3406 0.5341 0. 2033 0. 1274 178.67 1g153. y 13.41 T 2g2
0.6978 71 .34 5.816 , .4i773 ii .49iO ... 0.4340 p . .. . .. . .. i9427. p 1s.2g p 2g3
0.6864 71.68 5.806 , .43291 ,, .82,, 0.3213 O.S047 0. 2873 ... i68.49 18866. 18.33 T 294
0.681S 76. 13 S.682 1 .4268g 12. 7061 0.3533 0.S142 0. 2729 ... 167.6g 18825. 16. 75 T 295
0.6863 BO.BB S.SS5 T 1 .38542 21 .sg50 T 0.3367 T O.S066 ... ... 1S4.S7 1go33. 1S.S2 T 296
0. 7001 70.61 5.837 1 .42509 10. 1440 ... 0.4339 p ... ... . .. 14841. p 17 .57 p 297
0.8816 73. 10 s. 786 1 .415g2 13. 2oi1 ... 0.4342 p ... . .. . .. 16576. p 17 .61 p 2gs
0.6864 74.64 5.723 1 .41852 16.6788 0.35Bg O.S227 ... ... 161. 71 1goo3. 16.38 T 29g
Dio1ef1na. Cs to C10
o. 1314
0. 7198
I 62.00
65.09
I 6.osg
6.001
...
1 .42520
...
...
...
...
...
0.4396
. ..
. ..
. ..
. ..
...
214.g3
...
1BS71. p
. ..
20.00 p
300
301
1987 1-71
1C1.3
Cr ltlcal Con1tant1
Boiling
No. Compound Formula M.W.

Point
at l atm
deg F
Pree:zln9
Point
in air
'l'--
erature
deg F
Pre11ure
p•ia
Volume
cu rt
per lb
Compre1-
olblllty
Factor
Acentrlc
Factor
at l
atm.
deg F
01o1ef1ns, Ce to C10
302 1 ,5-HEXAOI ENE C5H10 82. 15 139.03 -221. 22 442.94 p 486.44 p 0.0645 p 0.2660 0. 2829
303 2, 3- HEXAOI ENE C5H10 82. 15 154.40 ... 468.11 p 486.44 p 0.0645 p 0. 2593 0. 2710
304 3-METHYL-1, 2-PENTAOI ENE C5H10 82. 15 158.00 ... 482.41 p 506.97 p 0.0629 p 0.2591 0. 2280
305 2-METHYL-1 ,5-HEXAOIENE C7H12 96.17 190.60 ... 779. 32 p 437.78 p 0.0829 p 0. 1992 0. 2880
306 2-METHYL-2 ,4-HEXAOI ENE C7H12 96.17 232. 70 ... 891. 79 p 437.78 p 0.0829 p o. 1e26 0. 2870
307 2,8-0CTAOIENE CeH14 110. 20 256. 10 ... 917. 13 p 392.86 p 0.0641 p 0. 1878 0.3700
308 2,8-0IYETHYL-1,5-HEPTAOIENE C9H15 124. 23 289.00 ... 998.98 p 370.57 p 0.0619 p O. 1822 0.3450
309 3, 7-0IMETHYL-1 ,6-0CTAOIENE C10H19 138.25 322.00 ... 1055.55 p 339.30 p 0.0620 p 0. 1788 0.4450
1-72 1987
1C1.3
API Density Refractive Vapor Heat Capacity Heat ot' Net Heat ot' Surface
Specific Gravity ot' the Index Pressure at 60 F and Con- Vaporiza- Cornhus t ion Tension
Gravity at 60 F Liquid ot' the at 100 F stant Pressure Kinematic tion at ot' Liquid ot' the No.
60/60 d~g API at 60 F Liquid psh Btu/lb deg F Viscosity ot' the Normal at 77 F Liquid
Ideal Liquid Btu/lb
Gas at l
Oioleftns, cs to t10
0.6970 71 .51 5.B11 , .40100 7 .0964 0.4401 p 19128. 17 .94 p 302

0.6849 75.10 5. 710 1. 39200 0.439B 209. 23 163B5. 15.5B p 303
o. 1191 65.12 6.000 1.42200 0.439B 210.51 19252. p 19.09 p 304
o. 7234 64. ,, 6.031 0.4473 p 252.B4 16271. p 20.52 p 305
o. 1490 57 .68 6.236 0.4490 p 279.B9 15650. p 22.65 p 306
o. 7473 57 .B6 6.230 0.4686 p 257. 14 18962. 14.69 p 307
o. 1112 51.97 6.430 0.471B p 241 .84 17379. 25. 11 p 30B
o. 7611 54.43 6.345 o .4859 P 231.30 1B906. p 23.46 p 309
1987 1-73
1C1.4
TABLE 1C1.4
CYCLOOLEFINS AND ACETYLENES-PRIMARY PROPERTIES
Cr it Leal Con et ants

Bolling
Polnt
No. C011pOund Formula M.W. at l atm Freezing Temp- Pressure Volume Compres- Acentr le
deg F Polnt er ature ps la cu tt sibllity Factor
ln air dog F per lb Factor
at l
atm.
deg F
Alkylcyclopentenes. C5 to c8
310 CYCLOPENTENE C5H5 68. 12 111 .64 -211. 14 452.93 p 694. 73 p 0.0564 p 0. 2730 0.1946
311 1 -METHYL-CYCLOPENTENE C5H10 82. 15 167 .88 -195. 75 522.43 p 599. 27 p 0.0592 p 0. 2765 0.2290
312 1-ETHYLCYCLOPENTENE C7H12 96.17 223. 39 -181 .12 581 .40 p 521. 15 p 0.0597 p 0.2680 0 .2370
313 3-ETHYLCYCLOPENTENE C7H12 96.17 207 .99 ... 581 .40 p 780.31 p 0.0473 p 0.3174 0.3110
314 1-n-PAOPYLCYCLOPENTENE C9H14 110.20 268. 16 ... 620.46 p 425.56 p 0.0600 p 0. 2429 0.3270
Alkylcyclohexenes. Cs to Cs
315 CYCLOHEXENE C5H10 82. 15 181 .36 -154 .32 549.05 630.92 p 0.0567 p 0. 2720 0.2142
316
317 I 1-METHYLCYCLOHEXENE
1-ETHYLCYCLOHEXENE
C7H12
C9H14
96.17
110.20
230.53
278. 59
-184. 72
-165.93
601 .61 p
648 .09 p
550 .36 p
483.59 p
0. 0580 p
0.0586 p
0. 2694
0. 2627
0 .2550
0 .2690
Cyclic Otolef1ns. C5 end C10
318
319
I CYCLOPENTADIENE
OICYCLOPENTADI ENE
C5H5
C10H12
66.10
132 .20
108. 70
337. 73 s
-121 .00
-72 .00
452.93 p
728.33 p
746.95 p
443.82 p
0.0545 p
0.0539 p
0.2750
0.2480
0.2118
0.2851
Cycl 1c Unaeturetes. C10H15
320
321
I olpha-PINENE
beta-PINENE
C10H15
C10H15
136.24
136.24
313.06
330.87
-83.20
-78. 77
677 .93 p
697. 73 p
400.31 p
400.31 p
0.0593 p
0.0595 p
0.2650
0.2610
0.2862
0.3252
Acetylenes, C2 to C4
322 ACETYLENE C2H2 26.04 -119.20 A -113.44 B 95.31 890.40 0.0695 0.2710 0. 1873
323 METHYLACETYLENE C3H4 40.06 -9.80 -152.86 264.63 816. 22 0.0656 0.2760 0.2161
324 DUETHYLACETYLENE C4H5 54.09 80.58 -26. 07 419.00 738.79P 0.0854 p 0. 2770 0. 1305
325 ETHYLACETYLENE C4H5 54.09 48.53 -194.30 374.90 683.13 p 0.0654 p 0.2700 0.0500
326 YINYLACETYLENE C4H4 52.08 41.18 ... 357 .53 p 704.89 p 0.0671 p 0.2810 0. 1182
Acety 1enea. C5 to C10
327 1-PENTYNE C5H5 68. 12 104.32 -158.26 429.96 p 585.50 p 0.0648 p 0.2707 0.1603
328 2-PENTYNE C5H5 68. 12 132.93 -164. 74 475.07 p 585.50 p 0. 0648 p 0.2576 0.1585
329 3-METHYL- 1-BUTYNE C5H5 68. 12 79.43 -129.46 ... ... . .. . .. . ..
330 1-HEXYNE C5H10 82. 15 160.39 -205.42 491.97 p 512.30 p 0.0645 p 0.2856 0.2320
331 1-HEPTYNE C7H12 96.17 211 .53 -113.62 545. 79 p 454.94 p 0.0642 p 0.2605 0.3030
332 1-0CTYNE C9H14 110.20 259. 18 -110. 74 594. 12 p 408.92 p 0.0641 p 0.2553 0.3240
333 1-NONYNE C9H15 124. 23 303.26 -58.00 837. 29 p 371.25 p 0.0639 p 0.2505 0.3480
334 1-0ECYNE C10H1s 138.25 345.20 -47. 20 877 .52 p 329.95 p 0.0838 p 0.2386 0.4340
1-74 1987
1C1.4
API oenllty Retract iv• Vapor Heat Capacity Heat of Net Heat ot Sur tac•
Specitic Gravity ot th• Index Pressure at 60 P and Con- Vaporiza- Combustion Tension
Gravity at 60 P Liquid ot th• at 100 F stant Pressure Kinematic tion at ot Liquid ot the No.
60/60 deg API at 60 F Liquid psi a Btu/lb deg F Viscosity ot the Normal at 77 F Liquid
lb/gal at 77 F Liquid Boilln9 Btu/lb at 77 F
Ideal Liquid Btu/lb
Gas at l
A I ky I cycl opentenes. c5 to c8
0. 7773 50.53 6.481 1.41940 , , . 7797 0. 2507 0.4197 0. 2656 0.2001 174.22 18552. 21 .51 T 310
0. 7854 48.66 6.54B 1.43020 ... ... 0. 4398 p . .. . .. 218. 78 18489. 22.21 p 311
0. 8030 44. 71 6.695 1 .43840 ... ... 0. 4459 p . .. . .. 203.86 1B541. 24. 56 p 312
0. 7878 48.,, 6.568 1.42910 ... ... 0.4460 p . .. . .. 214 .99 18581. 22.78 p 313
0.8061 44.03 6. 721 ... ... ... 0.4531 p . .. . .. 186.31 18560. 25. ,, p 314
A 1ky I eye I oheMenes. c6 to c8

0.8157
41.981
6.800 1 .44377 2.9899 0.2941 0.4222 0.6605 ... 162.81 18485. 26.09 T 315
... ... 0. 3480 p . .. . .. 25.43 p 316
I
0.8188 41. 78 6.808 1 .44784 207 .60 18438.
0.8269 39.62 6.894 1.45437 ... ... 0.3544 p . .. . .. ... 18471 . 27 .03 p 317
Cyclic Oiolefins. C5 end C10
... 18181. p 318

I
0.8041 44.481 6. 704 1.44290 13.0810 0.2601 0.4479 0. 3094 167 .54 32. 78 T
0.9712 14. 19 8.097 1.50610 0.1148 0.2696 0.4162 0.8146 0.4454 121.34 18053. p 30.69 T 319
Cyc I ic Unsetur-etes. C10H15
...
0.8620
0.8742 I 32.651
30.37
7. 187
7. 288
1.46320
I .47680
0. 1864
0.1219
0. 2384
... ...
1. 2793
1.4751
0.6626
0.667B
112.80
119.37
18461.
18493.
26.49 T
26.85 T
320
321
Acaty 1anes. C2 to C4
0.6150 98.60 3.481 ... ... 0.4000 ... ... . .. 275.46 20744. y 1.19 T 322
0. 6212 96.30 5.179 1.38630 119. 3520 0.3550 ... 0.2214 0. 1913 238. 73 19838. y 11.51 T 323
0.6959 71.84 5.802 1 .38930 21.4920 0.3379 0.5475 ... . .. 210.07 19226. 20. 15 T 324
0.8565 84.04 5.473 ... 41.0451 0.3521 0.5951 0. 2933 0. 2304 194.31 19590. 17 .06 T 325
... ... ... 1.41610 ... 0. 3282 . .. ... . .. 196.42 19319. p . .. 328
Acety Jenee, C5 to C10
0.8993 70.85 5.830 1 .38220 13.5000 0.3609 ... ... ... . .. 19256. 19.89 p 327
0. 7160 68. 14 5.989 1.40090 7 .6000 0.3383 ... ... ... . .. 19122. 21 .89 p 328
0.8720 79.10 5.590 ... ... 0. 3579 . .. ... . .. . .. 19223 . . .. 329
0. 7200 65.02 6.003 1. 39570 ... 0.3640 ... ... . .. 210.81 19159 . . .. 330
0. 7375 60.35 6. 149 1 .40600 ... ... ... . .. . .. 195.96 19090 . 22.20 331
0.7511 56.89 8.262 1 .41380 ... ... . .. . .. . .. ie4. i4 19039. 23.30 332
0. 7622 54.i4 8.355 1.41950 ... ... ... . .. . .. i74.26 19000. 24.50 333
0. 7712 51 .97 8.430 1 .42490 ... ... ... . .. . .. i64.64 18968 . 25. 40 334
1987 1-75
1C1.5
TABLE 1C1.5
BENZENE DERIVATIVES-PRIMARY PROPERTIES
Critical Constanta
Bolling
No. Compoond Formula M.W.

Point
at l atm
deg r
Freezing
Point
in air
T--
erature
deg F
Preesure
peia
Volume
cu ft
per lb
Compree-
elblllty
Pac tor
Acentric
Factor
at l
atm.
deg r
A 1 ky I benzene•. Ca and C7
I
335 BENZENE C6"6 7B. 11 176.1B 41 _g5 552. 22 710.40 0.0531 0.2710 0.210B
338 TOLUENE C7H9 g2, 14 231. 1 2 -13B.gB 605.55 5g5,go o.os4g o. 2540 0. 2641
A 1ky1 benzenes. CBH10
337 ETHYLBENZENE CBH10 106.17 277. 13 -138.gs 651. 24 523.50 0.0564 0. 2630 0.3036
338 o-XYLENE CBH10 106.17 2g1 _g7 -13.30 675.00 541.60 0.0557 o. 2530 0.3127
339 m-XYLENE CBH10 106.17 282.42 -54. 12 651 .02 513.60 0.0567 o. 2sgo 0.3260
340 p-XYLENE CBH10 106.17 281 .05 55.B6 54g_50 sog. 20 0.0572 0.2600 0.32sg
A 1ky1 benzenes, CgH12
341 n-PROPYLBENZENE CgH12 120. 1g 318.64 -147.06 69g_41 464. 10 0.05B6 0.2650 0. 3462
342 ISOPROPYLBENZENE CgH12 120. 19 306. 34 -140.B1 676.40 465.40 0.0570 D. 2620 0.3377
343 o-ETHYLTOLUENE CgH12 120. 1g 329.32 -113.44 712.40 4go.oo 0.0574 o. 268B 0.2932
344 m-ETHYL TOLUENE CgH12 120. 1g 322.39 -139,g9 687. 20 471 .00 0.0580 o. 2668 0.3221
345 p-ETHYL TOLUENE CgH12 1 20 ,ig 323.63 -BO. 16 5g2.60 45g_oo 0.05B4 o. 2663 0.3242
346 1, 2, 3-TRIMETHYLBENZENE CgH12 1 20 ,ig 34g_o1 -13.62 736.4B soo.gg 0.0552 o. 2sgo 0.3664
347 1, 2 ,4-TRIMETHYLBENZENE CgH12 120. 1g 336.BB -46,gg 70B. 76 468.BO 0.0573 o. 2sBo o,37g2
348 1, 3,5-TRIMETHYLBENZENE CgH12 120. 1g 32B .54 -48.45 687 .SB 453.52 0.0577 o. 2560 o,3g95
Alkylbenzenee. C10H14
34g n-BUTYLBENZENE C10H14 134.22 361.89 -126.35 p 729.32 4'B.6g o.osg3 0. 2610 0.3917
350 ISOBUTYLBENZENE C10H14 134. 22 343.02 -60.66 710.60 440.B8 0.0544 p 0. 25BO 0.3811
351 HC-BUTYL8ENZENE C10H14 134. 22 343_g5 -103.85 736.50 s 428.00 s o.osg3 p o. 2550 o. 21s6
352 tert-BUTYLBENZENE C10H14 134, 22 338.41 -72. 13 728. 33 s 430.80 s 0.0587 p 0. 2660 0.2672
353 1 - METHYL-2-n-PROPYLBENZ ENE C10H14 134, 22 364.87 -76.55 732.85 p 426. 28 p 0.0576 p 0.2574 0.4051
354 1- METHYL-3-n-PROPYLBENZ ENE C10H14 134.22 359.58 -116.64 71B .56 p 407 .01 p 0.0576 p 0.24B7 0.4098
355 1- METHYL-4-n-PROPYLBENZENE C10H14 134. 22 382.08 -82.85 722 ,ig p 407.01 p 0.0576 p o. 24BO 0.4094
356 o-CYMENE C10H14 134. 22 352.87 -g6, 77 731 _g3 p 424.g6 p 0.0584 p o. 2500 0.3372
357 m-CYMENE C10H14 134.22 347.09 -82. 74 122.g3 p 424,g6 p o.os1g p 0. 2600 0.3411
35B p-CYMENE C10H14 134.22 350. 7B -90.2B 71B.OO 411.49 0.05B7 p 0.2570 0.3722
35g o-DIETHYLBENZENE C10H14 134. 22 382. 1B -24.23 742. 73 p 417. 71 p 0.0599 p 0. 2600 o,33g5
360 m-DIETHYLBENZENE C10H14 134.22 357 .98 -11g.05 733.73 p 417. 71 p 0.0582 p o. 2sso 0_34g7
361 p-DIETHYLBENZENE C10H14 134.22 362. 75 -45.09 724.66 406.4g 0.0593 p o. 2sso 0.4035
362 1, 2-DIMETHYL-3-ETHYLBENZENE C10H14 134.22 381.04 -57 .06 764.33 p 417. 71 p 0.0605 p 0.2580 0.3621
363 1, 2-DIMETHYL-4-ETHYLBENZENE C10H14 134.22 373.06 -B8.47 739.58 p 418.41 p 0.0576 p 0. 2512 0.4141
364 1 ,3-DIMETHYL-2-ETHYLBENZENE C10H14 134.22 374. 18 2. 73 7•7 .54 p 438.51 p 0.0576 p 0.2616 0.40B4
365 1, 3-DIMETHYL-4-ETHYLBENZENE C10H14 134.22 370. 76 -81. 18 736. 27 p 418.41 p 0.0576 p o.251g 0.4147
366 1, 3-DIMETHYL-5-ETHYLBENZENE C10H14 134. 22 3B2.44 -11g, 7B 737. gB p 438 .51 p 0.0576 p o. 2B38 0.4140
387 1 ,4-DIMETHYL-2-ETHYLBENZENE C10H14 134. 22 368.29 -64.66 747 .56 p 418.41 p 0.0576 p o. 24g7 0.4013
368 1, 2,3,4-TETRAMETHYLBENZENE C10H14 134.22 401.07 20. 75 768.45 p 451 .26 p 0.0578 p 0. 2803 0.4127
369 1, 2, 3,5-TETRAMETHYLBENZENE C10H14 134.22 38B .40 -10.63 766.94 p 430.30 p 0.0576 p 0.252B 0.3943
370 1, 2,4,5-TETRAMETHYLBENZENE C10H14 134.22 3BB. 24 174.63 755.60 428. 18 0.0575 p 0. 2520 0.4349
1-76 1987
1C1.5
API Oenslty Refract lve Vapor Heat Capacity Heat of Net Heat of Surface
Speclf lc Cravlty of th• Index Pressure at 60 F and Con- Vapor lza- Combustlon Tens Lon
Gravlty at 60 F Llquld of th• at 100 F stant Pressure ltlnernatlc tion at of Liquld of the No.
60/60 deg API at 60 F Llquld psla Stu/lb deg F Vlscoslty of the Normal at 17 F Liquld
lb/gal at 77 F Liquld Boiling Stu/lb at 77 F
cent i stokes Point dyne/cm
Ideal Liquld Btu/lb
Gas at l
A I ky I benzenes. Cs and C7
0.8829
0.8743 I 28. 771
30.34
7 .361
7. 29g
, .49792
, .49413
3. 2122
, .0311
0. 2407
0. 2603
0.4106
0.4010
o.5g5g
0. 5605
...
0.342g
16g. 22
156. 75
17258.
17423.
28. 21 T
27 .93 T
335
336
A I ky I benzenes, C9H10
0 .8744 30.32 7. 2go 1 .4g320 0. 3732 0. 21g9 0.4052 0. 6537 o.3g71 145.44 175g5. 28.5g T 337
0.884g 28.40 7 .377 1 .502g5 0.2631 0. 2920 0.4133 0. 7415 0.4238 14g.05 17546. 2g.60 T 338
0.86g4 31.26 7 .248 , .49464 0.32g5 0.2787 0.4044 0. 5g34 0.3642 147. 14 17542. 28. 26 T 33g
0.8666 31. 78 7. 225 1 .4g325 0. 3473 0. 2774 0.4002 0.6152 0.3700 145.06 17546. 27. g2 T 340
A I ky I benzenes. C9H12
0 .8683 31 .45 7 .23g , .48951 0. 1418 0. 2g35 0.4190 o. 7g55 0.4524 137. 22 17721. 28.43 T 341
0.8685 31.43 7 .240 1 .488go 0. 1865 o.2g1g 0.4135 0. 7376 0.4367 136.17 17711. 27 .6g T 342
0.8847 28.43 7 .376 1 .50208 o. 1088 0. 3035 0.4133 0.8354 0.4201 136.17 175g2. 2g.66 T 343
0.8685 31 .43 7. 240 , .49406 0. 1264 o.2g13 0.4082 0. 7870 0.4215 135.68 17684. 28.54 T 344
0.8652 32.04 7 .213 1 .49244 0. 1249 0. 2g25 0.4067 0.6717 0.4184 136.52 17680. 28. 30 T 345
0 .0g95 25.gg 7 .491 1 .51150 0.0713 0. 29g2 0.4236 0.8317 o.3g7g 142.53 17649. 30. 75 T 346
0.8806 2g. 1g 7 .342 1 .50237 0.0942 0.3014 0.4205 0.8547 0.4383 13g.02 17637. 29. 19 T 347
0.8699 31. 17 7 .252 1 .49684 0. 1076 0. 2go9 0.4086 0.8449 0.4139 140.08 17631. 28.05 T 348
A I ky I benzenes. C1QH14
0.8860 31.go 7. 220 1 .48742 0.0465 0. 3025 0.4241 o.g433 0.5165 12g.33 17824. 28.63 T 34g
0 .8575 33.52 7. 149 1 .48400 0.0822 0. 2g79 0.4218 o.g882 0.5136 124.06 17803. 26.g8 T 350
0.8662 31.86 7 .221 1.48779 0.0767 0.3027 0.4054 o.g5o2 0.4997 125.30 17814. 28 .02 T 351
0 .8707 31.01 7 .25g 1.4g024 0.0919 0. 3053 0.4179 o. g135 0.5054 123. 14 17800. 27. 63 T 352
0.8780 2g.66 7 .320 1 .49750 ... . .. 0.3674 p ... . .. ... 177g5. 30.52 p 353
0.8653 32.03 7 .214 1 .49110 ... ... 0. 3676 • ... ...
. ..
... 17783. 28. 76 p 354
0.8829
0.8807
32.4g
2g.15
7 .194
7 .343
1 .48g8o
1 .4g830
...
0.0648
...
0. 3048
0. 3675 p
0.4164
...
o. 9740 o.5g73
...
126. 14
17786.
111g2.
28.47
31 .01 T
• 355
356
0.8653 32.03 7. 214 1 .49050 o.013g 0. 3006 0.4144 0.8063 0.5117 125. 25 17775. 28.88 T 357
0.8607 32.8g 7 .176 1 .48850 0.0648 0.2671 0.4146 0.8074 0.5120 127 .32 17777. 28.35 T 358
0.883g 28.5g 7 .369 1 .50106 0.0469 0.3165 0.4226 1.0676 0.5024 120.g2 17807. 2g. 77 T 35g
0.8683 31 .45 7 .23g 1 .49310 0.0505 0. 3060 0.4219 0.9746 0.5180 129. 20 17791. 29. 77 T 360
0.8663 31.85 7. 222 1 .4g245 0.0470 0. 3050 0.4220 o.g768 0.5202 130.00 17794. 28.47 T 361
0.8g68 26.33 7. 475 T 1 .5og50 0.0287 T 0.3168 T 0.4335 T 1 .078g T 0.4881 T 133.38 17769. 33 .82 T 362
0.8788 29.51 7 .327 1 .50090 ... ... 0.3672 •p ... ... . .. 17751. 30.65 p 363
0 .8948 26.64 7 .460 1 .50850 ... ... 0.3672 ... . .. ... 17770 . 32. g5 • 364
0.8808 29.16 7 .343 1 .50150 ... ... 0.3673 • ... . .. ... 17913. • 30.g1 p 365
0.8892 31.29 7. 247 1 .4g580 ... ... 0.3885 • ... . .. ... 17913. • 29.47 • 366
0.8816 29.00 7 .350 1 .50200 ... ... 0. 3667 • ... . .. ... 17913. • 31. 20 p 367
o.g094 24.09 7 .582 1.51810 ... ... ... ... . .. . .. 17738. 35. 25 p 368
o.0g45 26.68 7 .458 ... ...
1 .51070 ... ... ... . .. 17718. 32 .g8 p 369
0.8918 27. 20 7 .423 R... 1.50930
0.3245 ... ... 0.4g70 136.06 17643. R . .. 370
1987 1-77
1C1.5
Critical Constants
Bolling
Point
No. Compound Porm.ula M.W. at l atm Pree1in9 Temp- Pressure Volume Compres- Acentrlc
deg F Point erature psia cu ft slbillty Pact or
•t l
atm..
dog F
A 1k)'1 benzenes. C11 to C22
371 n-PENTYLBENZENE C11H15 148.25 401. 72 -103.00 764. 20 37B.OO 0.0594 0.2533 o. 4434
372 n-HEXYLBENZENE C12H1B 162.27 43B .9B -77.80 796. 73 p 345. 19 p 0.0610 p 0.2530 0.4784
373 n-HEPTYLBENZENE C13H20 176.30 474.9B -54.40 824. 70 319.00 0.0624 0.2546 0.5362
374 n-OCTYLBENZENE C14H22 190.33 507 .92 -32 .80 851.00 295.00 o .0630 0.2517 o .5838
375 n-NONYLBENZENE C15H24 204.36 53g .60 -11.20 874.00 275 .00 0.0636 0.2498 0.6387
376 n-OECYLBENZENE C15H25 218.38 568.20 6.12 928 .13 p 256. 72 p 0.0646 p 0.2459 0.5462
377 n-UNOECYLBENZENE C17H29 232.41 595. 76 23.00 916.00 242 .00 0.0645 0.2400 o. 1351
37B n-DODECYLBENZENE C19H30 246 .44 B21 .68 37 .40 934.00 229.00 0.0650 0.2424 o. 1a10
37g n-TRIOECYLBENZENE C19H32 260.46 646.34 50.00 949. 73 p 217.56 p 0.0652 p 0.2440 0.6144
380 n-TETRADECYLBENZENE C20H34 274.49 669.20 60.80 966.00 206.00 0.0656 0.2400 O.B921
381 n- PENTAOECYLBENZENE C21H35 288.52 690.BO 71 .60 981 .00 195.00 0.0624 0.2271 o. 945B
382 n-HEXAOECYLBENZ ENE C22H3B 302 .54 712.40 80.60 995.00 1B7 .00 0.0628 0.2276 0.9992
Crclohexrlbenzene. C12H15
383 I CYCLOHEXYLBENZENE C12H1B 160.26 484.22 44.58 B59. 73 p 417. 71 p 0.0531 p 0.2510 0.4505
A I kenr 1benzenes. c8 to c 10
384 STYRENE CB He 104. 15 293.25 -23. 13 706. 73 p 5BO. 15 p 0.0541 p 0.2810 0.2356
385 cis-1-PROPENYL BENZENE C9H10 118.18 333. 37 .7g,02 717 .60 p 487.02 p 0.0552 p 0.2515 0.3270
386 teens- 1-PROPENYL BENZENE C9H10 118. 18 352.87 -20. 7g 746.55 p 487 .02 p 0.0552 p 0.2455 0.3270
387 2-PROPENYL BENZENE C9H10 118. 18 329.90 -9. 76 722.93 p 487 .33 p 0.0579 p o. 2B30 0.3123
388 1-METHYL-2-ETHENYL BENZENE C9H10 118.18 337 .B6 -91 .43 725.85 p 502.99 p 0.0552 p 0.2579 0.3390
39g 1-METHYL-3-ETHENYL BENZENE C9H10 118. 18 340.BS -123 ,41 723 .18 p 476.B1 p 0.0552 p 0.2451 0.3830
390 1-METHYL-4-ETHENYL BENZENE C9H10 118 .1B 343.04 -29.47 726.39 p 476.B1 p 0.0552 p 0.2444 0. 3B30
391 1-lllETHYL-4-( tr"ens-
1-n-PROPENYL)BENZENE C10H12 132.20 393.80 -0.40 776.17 p 425.83 p 0.0580 p 0.2378 0.4080
392 1-ETHYL-2-ETHENYL BENZENE C10H12 132.20 35g, 14 -103.90 747 .25 p 446.63 p 0.0560 p 0.2554 0.4230
393 1-ETHYL-3-ETHENYL BENZENE C10H12 132.20 374.00 -149.80 747 .50 p 425.83 p 0.0560 p 0.2435 0.4030
394 1-ETHYL-4-ETHENYL BENZENE C10H12 132.20 378. 14 -57 .46 753 .49 p 425.83 p 0.0560 p 0.2423 0.4030
395 2-PHENYL- 1-BUTENE C10H12 132.20 359.60 ... 739.65 p 436.48 p 0.0551 p 0.2468 0.3490
Phenrlbenzenee. C12 to C14
398 Bl PHENYL C12H10 154.21 491 .00 158.56 961 .oo 558.00 0.0521 o. 2940 0.3659
397 1 ·METHYL-2-PHENYLSENZENE C13H12 168.24 491.54 ... 907 .65 p 429.69 p 0.0513 p o. 2529 0.4080
398 1 ·METHYL-3-PHENYLBENZENE C13H12 168.24 522.88 40.50 945.27 p 412.21 p 0.0513 p 0.2361 0.4610
399 1·METHYL-4-PH ENYLBENZEN E C13H12 168.24 518.00 118.00 93B.32 p 412.21 p 0.0513 p o. 2313 0.4610
400 1-ETHYL-4- PHENYLBENZENE C14H14 182.26 541.00 117.00 885.25 p 373.89 p 0.0522 p 0.2466 0.4910
401 1-METHYL-4(4-METHYLPHENYL) -
BENZENE C14H14 182.28 559 .00 250.00 968 .00 p 368.34 p 0.0522 p 0.2288 0.4830
01pnenylelkenee, C13 to C24
402 I OIPHENYLMETHANE C13H12 168.24 507 .69 77 .43 g22. 73 p 423.51 p 0.0521 p o. 2500 0.4811
1-78 1987
1C1.5
Al'I Density Refractive Vapor Heat Cape.cl ty Heat ot Net Heat ot Surface
Specltic Gravity ot the Index Pressure at 60 F and Con- Vapor iza- Cornbu st ion Tension
Gravity at 60 r Liquid ot the at 100 F stant Pressure kinematic t ion at of Liquid ot the No.
60/60 deg Al'I at 60 F Liquid psia Btu/lb dog F Viscosity ot the Normal at 77 F Liquid
lb/gal at 77 P' Liquid Boiling Btu/lb at 77 F
Ideal Liquid Btu/lb
Gas at l
atm. at 100 P' at 210 F
A 1ky l benzenes, C11 to C22
O.B6Z9 32.49 7. 194 1 .4B550 0.3711 p 17905. 29. 24 371

O.B621 32.64 7. 187 T 1. 48420 0.0062 T 0.3159 T 0.4204 T 1 .4467 T 0.7307T 119.08 17973. 30.04 T 372
O.B608 32. B7 7. 177 1.4BJ20 0.3756 p 1BOJO. 29.B6 373
O.B602 32.99 7. 172 1.48240 0.3767 p 105.B5 1B07B. 30. 10 374
O.B599 33.06 7. 169 1 .48170 0.3771 p 1B120. 30.40 375
O.B593 33. 17 7. 164 T 1 .48112 0.0001 T 0.3323 T 0.424B T 3.0B94 T 1.2107 T 102.41 1B156. 30.51 T 376
O.B587 33. 2B 7. 164 1 .48070 0.3765 p 96. 75 18188. 29. BJ P 377
0. B553 33.94 7. 130 1. 4BOJO <.0001 0.3371 0.4496 4. 2604 1. 534B 99. 09 18217. 29.59 T 37B
O.B589 33.25 7. 161 T 1 .4BOOO <.0001 0.3399 T 0.4562 T 4.9591 T 1. 7073 1B242. 30. 32 T 379
O.B587 33.29 7. 159 R. 1. 47970 0.3725 p 1B265. 29. 97 p JBO
O.B587 33. 29 7. 159 R. 1.47940 0.3706 p 1B2B5. 30.63 p JB1
O.B586 33.31 7. 158 R. 1.47920 R. 0. 3683 p 18304. R. 30.65 p JB2
CycloheJCylbenz.ene, C12H15
0.9473 I 17.BB I 7.B97 1. 52393 0.0032 o. 26B1 o. JB6B 1. 3777 0. 629B 126.52 17639. v B5. 60 T JBJ
Alkenylbenzenes, Ce to C10
0.90B7 24. 22 7.576 1 .54395 0. 2465 0. 2713 0.4113 0.6643 0. 3766 151. 18 17418. 30. B5 T JB4
0.9134 23.41 7 .615 1 .54020 0. 3626 p 19B.92 17726. '( 31. 77 p JB5
0.9063 24.62 7.556 1.547BO 0. 3624 p 204 .54 17711. 30.B2 p JB6
0.912B 23.56 7.60B 1 .535BO 0. 2B56 0.4016 0. 7330 0.4017 140.46 1752B. 31 .52 T JB7
0.9165 22. B9 7 .641 1 .54130 o. 3626 p 17715. '( 32 .66 p JBB
0.9164 22.91 7.640 1. 53B50 0.3625 p 17704. '( 32. 62 p JB9
0.9261 21. 29 7. 721 1. 53950 0. 3625 p 17701. 9 34. 03 p 390
0.9104 23.93 7 .590 1.54100 0.3667 p 192.47 177BJ. p 32. 27 p 391

0.9103 23.95 7.5B9 1. 53560 0.3673 p 1B6. 71 17B21. p 32. 76 p 392
O.B990 25.90 7 .495 1.53250 0.3672 p 186. 77 17821. p 32. 73 p 393
O.B989 2B. 26 7. 478 1 .534BO O.JB71 p 1BB.36 17821. p 30.B6 p 394
O.B960 2B.43 7 .470 1 .52620 0.3676 p 1B2. 19 17818. p 30. 71 p 395
Phenylbenzenee, C12 to C14
1 .5B72B 0. 2424 0.9906 136. 74 16816. 396

1 .0159 7. 7B B.470 1 .5B900 0.3747 p 173. 37 17156. p JB .69 p 397
1 .01B5 7 .44 8.491 1 .60160 0.3731 p 179.09 17156. p 39. 11 p 39B
1. 1009 -2 .97 9. 179 177. 18 17156. p 53.4B v 399
1 .0377 4.BB B.651 172B6. p 43.91 v 400
1. 1220 -5.39 9. 354 v 165.68 15573. p 60. 22 v 401
Oiphenylelkenee, C13 to C24
1.0104 I B.541 B.424 R 1.57520 R 0.0017 0. 2502 0. 3726 2. 2350 0.9319 123. 36 17029. 37.57 T 402
1987 1-79
1C1.5
Critical Constants
Bolling
Point
No. Compound Formula M.W. at l atm Freezing Temp- Pressure Volume Compres- Acantric
deg P Point erature psia cu ft sibility Pactor
at 1
atm.
dog F
Diphenylalkanes. C13 to C24
403 1, 1-0IPHEHYLETHANE C14H14 182. 26 522. 73 -0.31 935.33 p 388. 70 p 0.0531 p o. 2510 0.4497
404 1, 2-0IPHEHYLETHANE C14H14 182. 26 536.90 124. 14 944.33 p 384.35 p 0.0533 p o. 2480 0.4885
405 1, 1-0IPHEHVLPRQPAHE C15H16 196. 29 541 .80 56.66 937 .80 p 348. 29 p 0.0523 p o. 2386 0.5360
406 1, 2-0IPHEHVLPROPANE C15H15 196.29 542 .59 32.45 938.89 p 348. 29 p 0.0523 p o. 2384 0.5360
407 1, 1-0IPHENVLSUTAHE C15H19 210.32 561. 72 -13.36 944.69 p 320.52 p 0.0530 p o. 2312 0.5740
408 1, 1-0IPHEHVLPENTAHE C17H20 224. 35 586. 20 10.36 959.05 p 296.81 p 0.0537 p o. 2347 0.6240
409 1, 1-DIPHEHYLHEXANE C19H22 238. 37 609.85 11. 23 973. 27 p 276.36 p o .0542 P 0.2322 0.6730
410 1, 1-0IPHEHVLHEPTANE C19H24 252 .40 633. 20 55.40 987 .91 p 258.53 p 0.0547 p o. 2291 o. 1286
411 1, 1-DIPHENYLOCTAHE C20H25 266 .43 654.80 24.80 1001 .01 p 242 .85 p 0.0551 p o. 2215 0.8950
412 1, 1-0IPHENYLNONANE C 21 H29 280.45 674.60 59.00 1012.48 p 228.96 p 0.0555 p o. 2256 o. 1590
413 1, 1-0IPHEHVLOECAHE C22H30 294.48 692.60 37 .40 1022.29 p 216.56 p 0.0559 p o. 2240 0. 7210
414 1, 1-DI PHEHVLUHOECANE C 23H32 308.50 710.60 69.80 ... ... ... ... .. .
415 1, 1-0IPHENVLDOOECAHE C24H34 322 .53 726.80 50.00 1041.42 p 195.40 p 0.0565 p 0.2209 o. 1600
416 1, 1-0IPHENYLTRIOECAHE C25H35 336.56 743.00 80.60 1050.67 p 178.51 p 0.0592 p o. 2104 0.9330
417 1, 1-01 PHENYL TETRAOECAHE C25H39 350.59 757 .40 64.40 1058.13 p 163.75 p 0.0620 p o. 2009 1 .0032
418 1, 1-0IPHENYLPENTAOECAHE C27H40 364.61 771.80 91 .40 1066.06 p 150.72 p 0.0647 p o. 1921 0.9210
419 1, 1-0IPHEHYLHEXAOECANE C29H42 378 .64 784.40 78 .80 1072.18 p 139.20 p 0.0674 p o. 1941 0.8530
Oiphenylalkenea. C14H12
420
421
I cio-1 ,2-0IPHENYLETHENE
trana-1, 2-DIPHENYLETHENE
C14H12
C14H12
180.25
180. 25
503.33 p
583. 70
23.00
255.56
902.93 p
982.13 p
397 .40 p
397 .40 p
0.0508 p
0.0514 p
o. 2490
o. 2390
0.4708
0.6195
Phenylalkynee. Cs and C14
422
423
I PHENYLACETYLENE
01 PHENYLACETYLENE
C9H9
C14H10
102. 14
178. 23
287 .06
571. 73 s
-40.00
144.50
766. 35 p
1037.93 p
1796. 73 p
420.61 p
o .0214 P
o .0549 P
o. 382 2
o. 2560
0.5000
0.3836
01phenylbenzenee. C9H14
424 11 ,2-0IPHENYL9ENZENE C19H14 230.31 638.53 p 133. 16 1144.04 565.80 0.0523 0.3960 0.4671
425 1 ,3-0IPHENYL8ENZENE C19H14 230.31 710.33 p 188.33 1205.06 508.48 0.0534 o. 3500 0.5583
428 1 ,4-0IPHENYL9ENZENE C19H14 230.31 708.80 413.33 1207. 04 482.03 0.0530 o. 3290 0.5281
1-80 1987
1C1.5
API Density Refractive Vapor Heat Capacity Heat or Net Heat or Surt'ace
Specif le Gravity or th• Index Pressure at 60 F and Con- Vapor iza- Combustion Tension
Gra•ity at 60 F Liquid ot' the at 100 F stant Pressure Kinematic t ion at ot' Liquid ot' the No.
60/60 deg API at 60 F Liquid psia Btu/lb deg F Viscosity ot the Normal at 77 F Liquid
lb/gal at 77 F Liquid Boil im~ Btu/lb at 77 F
Ideal Liquid Btu/lb
Gas at l
Qi pheny I a 1 kanes, C13 to C24
1.0041 9.43 8.371 T , . 57020 0.0006 T 0.2600 T 0.3729 T 2.8955 T 1. 1536 T 118.89 17101. 36.99 T 403
1.57040 0. 2602 2.8516 1. 1430 120. 15 17086. 404
0.9910 ,, .29 8.262 ., .56200 0. 3769 37 .85 405
0.9817 12.63 8. 185 , .55620 0. 3769 H423. p 36.44 406
0.9793 12.98 8. 165 1 .55460 0.3776 147. 14 37. 17 p 407
0.9700 14.38 8.087 1 .54890 0. 3773 p 141.51 36. 74 p 408
0.9605 15.82 8.008 , .54280 0.3766 p 136.52 36.09 p 409
0.9542 16. 79 7 .955 , .53810 0. 3755 35. 77 410
0.9468 17.94 7 .894 1 .53360 0.3741 128.04 35.32 411
0.9413 18.82 7 .848 1 .52990 0.3724 p 124.20 35.01 412
0.9364 19.60 7 .807 1 .52660 0.3707 p 120.57 34. 74 413
0.9322 20.30 7. 772 R 1 .52380 414
0.9284 20.97 7. 740 1 .52130 0.3665 p ,,4. 17 34.31 p 415
0.9248 21 .51 7. 710 R 1 .51900 R 0.3643 114.36 40.51 416
0.9224 21 .91 7 .690 R 1 .51820 0. 3625 47. 71 417
0.9190 22 .47 7 .662 L51510 R 0.3607 v , 14. 27 56.40 v 418
0.9173 22. 75 7.648 1 .51400 R 0.3592 v 113.99 65. 73 v 419
Qi pheny 1a1 kenes, C14H12
1.0198
... I 7: 261
8.502 0.0004 0.2458
0. 2539
0. 3556 114,45
133.91
17166. p
H176. v
40.•3 T 420
421
Phenyhlkynes. Ce end C14
I 2~:~31
0.9320 7. 770 0.3570 p 265. 10 17684. p 32. 15 p 422
... 0.2451 1 .5824 122.89 17243. v 423
01pheny1 benzenes, C9H14
0. 2453 4.4334 109.35 16899. v 424

v
I I
0. 2453 3.8410 119 .64 16899. 425
0. 2453 118.41 16899. v 426
1987 1-81
1C1.6
TABLE 1C1.6
CONDENSED RING AROMATICS AND DERIVATIVES-PRIMARY PROPERTIES
Cr 1 t ic:al Constants
Boiling
Point
No. Compound Formula M.W. •t l atm rree2in9 Temp- Pressure Voluma Compres- Ac:entr le:
deg P' Point erature psia c:u t't sibllity ractor
in air deg P' per lb Factor
at l
atm.
deg P
Al ky I naphthalenes, C10 to C20
427 NAPHTHALENE C10H9 128.17 424. 30 176.52 887. 36 587.55 0.0516 0.2690 0.3019
428 1-METHYLNAPHTHALENE C11H10 142. 20 472.43 -22.86 930.00 529.39 p 0.0589 p 0. 2970 0.2921
429 2-METHYLNAPHTHALENE C11H10 142. 20 465.89 94.24 910.13 471.37 p 0.0571 p 0. 2600 0. 3459
430 1-ETHYLNAPHTHALfNE C12H12 156. 23 496.99 7 .14 936.63 p 481. 19 p 0.0533 p 0. 2878 0.4115
431 2-ETHYLNAPHTHALEN E C12H12 156. 23 496. 27 18.68 927.66 p 459.76P 0.0533 p 0.2573 0.4209
432 1,2-DIMETHYLNAPHTHALENE C12H12 156. 23 511 .34 30.20 959.63 p 494. 78 p 0.0533 p 0. 2707 0.4127
433 1 .4-DIMETHYLNAPHTHALENE C12H12 156.23 513.14 45. 79 962.15 p 508 .95 p 0.0533 p 0. 2780 0.4905
434 1-n-PAOPYLNAPHTHALENE C13H14 i7Q.25 523 .00 16. 75 947.66 p 430.14 p 0.0541 p 0. 2625 0.4565
435 2-n-PAOPY LNAPHTHALENE C13H14 170.25 524. 30 26.60 942.30 p 412.73 p 0.0541 p 0. 2528 0.4597
436 1-n-BUTYLNAPHTHALENE C14H15 184.28 552.90 -3.50 965.86 p 388. 77 p 0.0548 p 0. 2568 0.4810
437 2- n -BUTYL NA.PH THAL ENE C14H15 184.28 552. 20 23.00 958. 24 p 374.36 p 0.0548 p 0.2484 0.5010
438 1-n-PENTYLNAPHTHALENE C15H19 198.31 582.80 -11.85 985.30 p 354.60 p 0.0554 p 0.2511 ...
439 1-n-HEXYLNAPHTHALENE C15H20 212.33 611.60 -0.40 1004. 29 p 325.90 p 0.0559 p 0.2481 ...
440 2-n - HEXY LNA PH THAL ENE C19H20 212.33 613.40 22.10 1001.07 p 315.56 p 0.0559 p 0. 2388 ...
441 1-n-HEPTYLNAPHTHALENE C17H22 226. 38 638 .60 17 .60 1029.09 p 301.48 p 0.0583 p 0. 2405 ...
442 1-n-OCTYLNAPHTHALENE C19H24 240. 39 665.60 28.40 1040. 20 p 280.43 p 0.0567 p 0. 2374 ...
443 1-n-NONYLNAPHTHALENE C19H25 254.41 690.80 46.40 1077 .53 p 243.66 p 0.0642 p 0.2410 0.5781
444 2-n-NONYLNAPHTHAl ENE C19H25 254.41 696. 20 51.80 1070.68 p 255.27 p 0.0570 p 0. 2254 ...
- 445 1-n-DECYLNAPHTHALENE
Tatr•nydronapntn• 1anas. C10 to C20

C20H29 268.44 714.20 59.00 1086.53 p 229.16 p 0.0638 p 0. 2370 0.6415
446 1. 2 3 4-TETRAHYDRO-
0 0
NAPHTHALENE C10H12 132.20 405. 77 -32.35 836.60 478.63 0.0534 0. 2430 0.2859
447 1-METHYL- [ 1 2 3 4-TETRA-
0 0 0
HYORONAPHTHALENE] C11H14 146. 23 429.06 ... 835.25 p 443.42 p 0.0542 p 0.2531 ...
448 1-ETHYL- [ 1. 2. 3 4-TETRA-
0
HYORONAPHTHALENE] C12H15 160. 26 463. 23 ... 860.00 p 399.20 p 0.0550 p 0. 2484 ...
449 2. 2-DIMETHYL- [ 1. 2. 3 4-TETRA- 0
HYOAONAPHTHALENE] C12H15 160.26 446.00 ... 835.38 p 399.20 p 0.0550 p 0. 2532 ...
450 2 .8-DIMETHYL- [ 1. 2. 3 4-TETRA- 0
HYORONAPHTHALENE] C12H15 160. 26 460.40 68.00 850.93 p 392.66 p 0.0550 p 0.2461 ...
451 8. 7-0IMETHYL- [ 1. 2 ,3 ,4-TETAA-
HYORONAPHTHALENE J C12H15 160.26 485.60 50.00 888. 53 p 402.52 p 0.0550 p 0. 2452 ...
452 1-n-PAOPYL- [ 1 .2 ,3 ,4-TETAA-
HYDRONAPHTHALENE] C13H19 174.29 493 .52 ... 880. 36 p 362.96 p 0.0556 p 0. 2447 . ..
453 8-n-PR:OPYL- [ 1. 2 ,3 ,4-TETAA-
HYOAONAPHTHALENE] C13H19 174.29 505.40 ... 892.36 p 357 .52 p 0.0556 p 0. 2389 . ..
454 1-n-8UTYL- [ 1. 2. 3 ,4-TETAA-
HYOAONAPHTHALENE] C14H20 188.30 523 .63 ... ... . .. ... . .. . ..
455 8-n-SUTYL- [ 1. 2. 3 4-TETRA- 0
HYDRONAPHTHALENE J C14H20 188.30 537 .BO ... ... . .. ... . .. . ..

458 1-n-PENTYL- [1. 2 ,3 ,4-TETAA-
HYORONAPHTHALENE] C15H22 202. 33 553 .33 ... . .. ... ... . .. . ..
1-82 1987
1C1.6
API Dene lty Refractive vapor Heat Capacity Heat ot Net Heat of Surface
Specific Gravity ot th• Index Pressure at 60 P and Con- vapor lza- Combustion Tension
Gravity at 60 F Liquid ot the at 100 F stant Pressure Kinematic tion at of Liquid of the No.
60/60 dog API at 60 P Liquid psia Btu/lb deg F Viscosity of the Normal at 77 F Liquid
Ideal Liquid Btu/lb
Gas at l
Alkylnaphthalenes. C10 to C20
1 .93200 0. 2393 0. 7737 145.66 16707. 427

1 .0250 6.55 B.546 1.61512 0.0033 0. 2593 0.3703 2.,, 79 0.9919 138.53 16913. 39. 71 T 428
1.60190 v 0.0032 0. 2600 1 .8153 0.8332 139.92 16879. 35.45 T 429
1 .0121 B.30 B.438 1 .60400 0.3714 p 17259. p 37. 97 430
0.9963 10.53 B.306 1 .59770 0.3714 p 17887. p 36.60 431
, .0214 6.96 B.520 1 .61430 0.3709 p 17854. p 38.81 432
, .0177 7 .53 B.485 , .61140 0. 3708 17854. p 42.47 p 433
0.9937 10.89 B.285 , .59010 0 .3731 17966. p 36. 20 434
0.9808 12. 77 8., 77 1 .58500 0.3731 p 17966. 35.24 435
0 .9808 12. 77 B.177 1.57970 0.3740 p 16032. 35.24 436
0 .9934 10.95 B.282 1.57460 0.3740 p 18032. p 34.90 437
0 .9705 14.31 B.091 1.57040 0.3741 p 162.57 18089. p 34. 70 438
0.9614 15.69 B.015 , .56260 a. 3131 156. 17 18139. 34.40 439
0.9521 17. 12 7 .938 1 .56010 0.3736 155.94 18139. 33.54 440
0.9537 16.87 7 .951 1 .55650 0.3725 p 151 .26 18182. p 34. 18 441
0.9468 17 .94 7 .894 , .55060 0.3715 p 145.43 18220. 33 .84 442
0.9411 18.86 7 .846 T 1 .54550 < .0001 0.3111 T 0.4068 T 4.1431 T 1. 7046 T 96.84 17744. 35.59 T 443
0 .9428 18.59 7. 786 , .54420 0.4162 p 18254. 38.05 p 444
0 .9354 19. 78 7. 798 T 1 .54120 < .0001 0.3145 T 0.4134 T 4. 6966 T 1 .8501 T 95.57 T 17778. 35. 16 T 445
Tetl"ahydronaphthalenes, C10 to C20
0 .9748 13.65 8. 127 1 .53919 0.0174 0. 2697 0 .3852 1 .6628 0. 7672 137. 72 17423. 33. 16 T 446
0 .9623 15.54 B.023 1. 53330 0.3702 p 183.07 17684. p 34.96 p 447
0 .9569 16.37 7 .978 1 .52980 0.3727 p 173 .35 17785. p 35.55 p 448
a. 9404 18.97 7 .840 , .51800 0.3735 p 169.63 17183. p 32.89 p 449
0.9464 18.02 7 .890 , .52400 0.3728 v 172. 79 17743. v 33. 77 v 450
0.9584 16. 15 7.990 1 .53600 0.3718 p 179. 20 17733. p 35. 70 p 451
0.9480 17. 75 7 .904 1 .52550 0.3746 p 164.68 16817. p 35. 15 p 452
0.9401 19.01 7 .838 1 .52410 0.3740 p 167. 10 12417. p 34. 16 p 453
0 .9382 19.30 7 .822 454
0.9368 19.50 7 .810 455
0.9310 20.50 7. 762 458
1987 1-83
1C1.6
Critical Constants
Bolling
Point
No. Compound Formula M.W. at l atm Freezing Temp- Presaure VolUIDll Compres- Acentr le
deg F Point era tu re psi a cu ft slblllty Factor
in air deg F pet lb Factor
at l
atm..
deg F
Tetrahydr"onaphtha l enaa, C10 to C20
457 6-n-PENTYL- { 1, 2 ,3, 4-TETAA-

HYORONAPHTHALENE] C15H22 202. 33 566.60 ... ... ... ... ... . ..
458 1-n-HEXYL-( 1.2,3, 4-TETRA-
HYORONAPHTHALENE] C15H24 216.37 581 .00 ... g42.60 p 285.22 p 0.0570 p 0. 2340 ...
45g 1-n-HEPTYL- ( 1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] C17H25 23Q.3g 6Qg.eo ... g54. 40 p 266.20 p 0.057• p 0.2304 . ..
460 1-n-OCTYL- [ 1. 2. 3 0 4-TETRA-
HYORONAPHTHALENE] C19H29 244. 42 635.00 ... ge2. 08 p 24g.55 p 0.0577 p 0. 2276 . ..
461 1-n-NONYL- [ 1 0 2 0 3 0 4-TETRA-
HYORONAPHTHALENE] C1gH30 258.45 658.40 ... 1021.50 p 234.86 p 0.0580 p 0.2215 ...
462 1-n-OECYL- [ 1. 2. 3. 4-TETRA-
HYOROHAPHTHALEHE] C20H32 212 .47 681 .80 ... 1014.58 p 221 .81 p 0 .0583 p 0 .2225 . ..
Indenes, Cg to C10
483 INOENE CgH9 116.16 360.32 2g.30 776.g3 p 554.05 p 0.0507 p 0. 2460 0.3352
484
485 I 1-METHYLI NOE NE
2-METHYLINOENE
01hydro1ndenea, Cg to C10
C10H10
C10H10
130. 1g
130. 1g
39g .30
365.00
...
176.00
805.87 p
76g.64 p
501. 72 p
501. 72 p
0.0537 p
0.0537 p
0.2584
0. 2660
0.3370
0.3370
488 2, 3-DIHYDROINOENE C9H10 118.18 352. 13 -60.54 766. 24 p 541.59 p 0.0538 p o. 2608 ...
487 1-METHYL-2. 3-0IHYOROINOENE C10H12 132.20 375.08 ... 112.g5 p 476.99 p 0.0546 p 0.2603 . ..
468 2-METHYL-2. 3-0IHYOROINOENE C10H12 132.20 376.52 ... 775.og p 476.99 p 0.0546 p 0. 25g9 . ..
489 4-METHYL-2 0 3-0IHYOROI NOENE C10H12 132.20 3g5. 60 ... 814.53 p 4g1 .58 p 0.0546 p o.25g5 ...
470 5-METHYL-2 0 3-0IHYOROINOENE C10H12 132.20 401.go ... 7g9.04 p 467.60 p 0.0546 p 0.2501 . ..
Condensed R1ng Ar"omatics. C12 to c 18
471 ACE NAPHTHALENE C12H9 152. 1g 518.09 ... g55.g3 484.12 0.0505 0.2300 ...
472 ACENAPHTHENE C12H10 154. 21 531 .30 200. 14 ge6. 00 p 44g.e2 p 0.0540 p 0.2410 0.3811
473 FLUORENE C13H10 166. 22 567. 12 238.62 1106. 33 p 681.68 p 0.0385 p 0. 2600 0.3388
474 ANTHAACENE C14H10 178. 23 848. 18 41g.oo 1104.53 s 484.43 p o.04g9 s 0. 2560 0.5753
475 PHENANTHRENE C14H10 178.23 844.54 210.47 1104.98 420.81 p o.04g9 p 0. 2220 0.4858
478 PYRENE C15H10 202. 25 742.84 300.53 1225.13 p 378.55 p o.04gg p 0. 2110 0.5088
477 FLUOAANTHENE C19H10 202. 25 721.04 230.32 p ,,gg.g3 p 378.55 p 0.0577 p 0.2480 0.4g02
478 CHRYSENE C19H12 228. 2g 825.80 498.40 1302.53 p 348.84 p 0.0484 p 0. 2030 0.6040
NoTE: See page 1-135 for Key to footnote codes.
1-84 1987
1C1.6
API Density Refractive Vapor Heat Capacity Heat ot Net Heat ot Surface
Spec It le Gravity ot the Index Pressure at 60 F and Con- vaporiza- Combustion Tension
Gravity at 60 F Liquid ot the at 100 F stant Pressure kinematic tion at ot Liquid ot the No.
60/60 dog API at 60 F Liquid psi a Btu/lb deg F Viscosity ot the Normal at 77 F Liquid
cent i stokes Point dyne/cm
Ideal Liquid Btu/lb
Gas at l
Tetl"ahydl"onaphtha1enes, C10 to C20
o.g291 20.80 7. 762 457
o.g251 21 .45 7. 713 1 .51270 0. 3760 p 145. 73 18058. p 34.05 p 458
0. g203 22. 25 7 .673 1 .51010 0. 3753 p 141. 13 18106. p 33.86 p 45g
o.g151 22.95 7.638 1 .50800 0. 3742 p 136.62 18148. p 33. 67 p 460
o.g124 23.58 7 .607 1 .50610 0.3712 p 134.88 18185. p 33.53 p 461
o.g093 24.,, 7 .581 , .!.i0450 0.3711 p 128. 76 1821g. p 33 .44 p 462
Indenes, Cg to C10
, .0036
g.4g I 8.367 1 .57400 0 .0500 0. 2483 0.3782 1 .3577 0.6308 151 .58 17097. 19.09 T 463
0.975g
0. g1gg I 13.50
12.90
8. 136
8. 170
1.55870
1 .56270
0.3668
0. 3674
1g6.64
18g.54
15724. p
1g205. v
33. 24 p
33.86 R
464
465
Di hydl"oi ndenes, Cg to C10
o.g68g 14.54 8.078 1 .53580 0.3624 p 17428. p 33. 23 p 466

0. g4J7 18.44 7 .868 1 .52410 0.3672 p 18g.11 17560. p 31 .g3 p 467
o.g464 18.02 7 .8go 1.51g30 0.3671 p 18g.55 17560. p 32.31 468
o.g608 15. 78 8.010 1 .53220 0.3666 1g1.50 17538. p 34.34 45g
o.g4g5 17 .53 7 .g18 1 .53330 o. 3667 1753g. p 32. 74 p 470
Condensed Ring Al"omattcs, C12 to Cie
16522. 471
1 .64700 0. 2480 1 .3826 141.8g 16732. 472
1 .64700 0. 25g7 1 .0487 136.05 16618. 473
1 .55600 0. 2440 132. 16 16517. 474
1 .54800 0. 2454 1. 7867 131. 18 16486. 475
1. 77000 o. 22g7 123.39 16198. 476
1. 73goo 0. 244g 4. 9494 122.40 16357. 477
1. 78500 0. 2410 12g. 75 16345. 478
1987 1-85
1C2.1
TABLE 1C2.1
PARAFFINS-SECONDARY PROPERTIES
Flash Ideal Gas Ideal Gas Heat ot

Search Solubility Point Heat of Gibbs Free Fusion
No. Compound Formula Number Parameter Temperature Formation Energy of at 77 deg F
(Cal/cm3) 11 2 deg F at 77 F Formation Btu/lb
Btu/lb at 77 F
Btu/lb
Paraffins, C1 to C3
~I
METHANE CH4 1 5.6BO ... -1997.37 -1352.22 25. 23
ETHANE C2H5 2 6.050 ... -119B.BB -456.B2 40.88
PROPANE C3H9 3 6.400 ... -1020.61 -237 .89 34.35
Paraffins, C4H10
:I n-BUTANE
IS08UTANE
C4H10
C4H10
5
4
6. 768
6.376
...
...
-929 .42
-998.54
-122.49
-158.59
34.48
33.58
Paraffins. C5H12
!I 7 7 .059 -40. 00 -874. 22 -52. 26 50.06

n-PENTANE C5H12
ISOPENTANE C5H12 8 6. 775 ... -915.86 -82 .59 30.69
NEOPENTANE C5H12 9 6.219 ... -1001 .50 - 100. 23 18. 75
Paraffins. C5H14
9 n-HEXANE C5H14
,, 7 .32B -7.00 -B32. 85 -0.75 65.25
12 7.049 -29. 47 p
,,10 2-ME THVLPENTANE
3-METHVLPENTANE
C5H14
C5H14 13 7. 270 -24.07 p
-871.47
-B58. 35
-25.64
-15.81
31. 27
26.46
12 2, 2-01 METHYL8UTANE C5H14 14 6. 730 -54. 00 -921. 31 -42.50 2.89
13 2, 3-01 METHYL8UTANE C5H14 15 7 .017 -20. 00 -881. 99 -14.47 3.99
Paraffins. C7H15
14 n-HEPTANE C7H15 17 7 .433 25.00 -805. 13 34.97 60. 23

15 2-METHVLHEXANE C7H15 18 7.301 ... -835.46 14.33 39.40
16 3-METHVLHEXANE C7H15 19 7.347 25.00 -820. 92 21 .80 ...
17 3-ETHYLPENTANE C7H15 20 7 .355 ... -812.34 48.83 40.97
18 2, 2-01 METHYLPENTANE C7H15 21 6.945 ... -883.04 2.36 24.99
19 2, 3-01 METHYLPENTANE C7H15 22 7. 274 ... -832.80 24.50 ...
20 2,4-0IMETHYLPENTANE C7H15 23 7 .020 10.00 -865. 28 14.59 29.37
21 3. 3-01 METHYLPENTANE C7H15 24 7. 105 ... -B57. 21 21 .07 30.32
22 2, 2, 3-TRI METHYL8UTANE C7H15 25 6.965 ... -877. 12 20.08 9.70
Paraffina. C9H19
23 n-OCTANE C9H19 27 7 .506 56.00 -785.94 59.92 78.06

24 2-METHYLHEPTANE C9H19 28 7 .373 ... -810.52 43.92 44.70
25 3- METHVLHEPTANE C9H19 29 7 .487 ... -799.83 47 .99 43.76
26 4- METHVLHEPTANE C9H19 30 7 .517 ... -797. 76 59. 13 40. 79
27 3-ETHYLHEXANE C9H19 31 7 .432 ... -793. 05 63.34 ...
28 2, 2-0 I METHYLHEXANE C9H19 32 7. 168 ... -845.33 39.29 25.51
29 2, 3-0 I METHYLHEXANE C9H19 33 7 .341 41 .60 -804. 68 58.30 ...
30 2, 4-01 METHYLHEXANE C9H19 34 7. 163 50.00 -825. 16 42. 72 ...
31 2, 5-01 METHYLHEXANE C9H19 35 7. 207 ... -837. 46 36.36 48. 75
32 3, 3-01 METHYLHEXANE C9H19 36 7. 276 ... -827.98 50.40 26. 77
1-86 1987
1C2.1
ASTM Octane Numbers

Coettlcient Aniline Flammability Watson
ot Expa.ns ion Point Limits, Volume It Factor No.
Percent in
deg F Motor Method Research Method Air Mixture
1 (av 1 0 357 0 908
v (lT p
With With Lower upper
at 60 F Clear 3 ml Clear 3 ml
par deg F TEL TEL
per gal per gal
Para.ff ins. C1 to C3
... ... ... ... ... ... 5.00 15.00 19.5 1

...
0.001520 E I ...
... I
+.05
97. 1 K I ...
...
+1 .6 K
+1 .8 K
. ..
. ..
2.90
2.00
13.00
9.50
19.4
14. 7
2
3
Pa.r-affins. C4H10
0.001170 181 .6 89.6 +0.4 K 93.8 +0.4 K 1 .50 9.00 13.5 4

0.001190 I 225. 7 I 97.6 I ... +O. 1 K . .. 1 .80 a.so 13.8 5
Pa.r-a.ff;ns. C5H12
0.000870 159.3 62.6 84.2 61. 7 86.0 1 .40 8.30 13.0 6

0.000900 170.6 90.3 ... ... , .a 8.00 13. 1 7
I I I
92.3 K 1 .30
0.001040 216.0 80.2 99.9 85.5 +O. 1 K 1 .40 7 .50 13.4 8
Par-affins. C5H14
0 .000750 155.5 26.0 65.2 24.8 65.3 1 .10 7. 70 12.8 9

0.000780 164.8 73.5 91. 1 73.4 93. 1 1 .20 7 .oo 12.8 10
0.000750 156. 7 74.3 91 .3 74.5 93.4 1 .20 p 7 .oo p 12.6 11
0.000780 178.2 93.4 +2.1 K 91 .8 +0.6 K 1 .20 7.00 12.8 12
0 .000750 161 .4 94.3 +1.8 K +O .3 K ... 1 .20 7 .oo 12.6 13
Par-a.ff i na.. C7H15
0.000690 157.5 a.a 46.9 0.0 43.5 1.00 7 .00 12. 7 14

0.000680 165.2 46.4 74.5 42.4 73.2 1.00 s 6.00 s 12. 7 15
0.000690 158.9 55.8 81 .0 52.0 74. 7 1 .00 p 7 .oo p 12.5 16
0.000700 150.3 69.3 88.0 65.0 85.0 1 .00 p 7 .00 p 12.4 17
0.000720 171. 7 95.6 +2.4 K 92.8 +0.4 K 1 .02 p 6.03 p 12.6 18
0.000700 153.7 88.5 +O .3 K 91. 1 +0.3 K 1. 10 6. 70 12.4 19
0 .000720 173.8 83.8 99. 1 83. 1 96.6 1 .02 p 6.50 p 12. 7 20
0.000650 158.9 86.6 •0.6 K 80.8 97. 7 1 .00 p 7 .00 p 12.4 21
<.000001 162.0 +0., K +3., K +1 .8 K ... 1 .02 p 6. 13 p 12.4 22
Par-a.ff ins. C9H19
0.000620 159. 1 ... 28. 1 ... 24.8 0.80 6.50 12. 7 23

0,000610 165.0 23.0 60.8 20.6 57.8 0.98 p 5.80 p 12.6 24
0.000620 162.0 35.0 68.0 26.8 59.6 0.98 p 5.80 p 12.5 25
0.000660 160.9 39.0 70. 1 26. 7 61. 1 0.98 p 5.80 p 12.3 26
0.000630 155.7 52.4 80.0 33.5 61.1 0.89 p 5.80 p 12.4 27
0.000650 172.0 77.4 95.2 72.5 93.3 0.89 p 5.51 p 12.6 28
0.000630 159. 1 78.9 93. 7 71 .3 91. 7 0.89 p 5.88 p 12.4 29
0.000660 164.1 69.9 89.0 65.2 87.3 0.89 p 5.88 p 12.6 30
0.000650 172.4 55.7 82.9 55.2 81 .6 0.89 p 5.88 p 12.6 31
0,000620 182.0 83.4 100 75.5 94.6 0.89 p 5.51 p 12.4 32
1987 1-87
1C2.1

Search Solubility Point Heat ot Gibbs Free Fusion
No, Compound Formula Number Parameter Temperature Formation Energy ot at 77 deg F
(Cal/cml)l/ 2 deg F at 77 F Formation Btu/lb
Btu/lb at 77 F
Btu/lb
Paraffins, c5H15
33 3, 4-0!WETHYLHEXANE C5H15 37 7.400 ... -800.43 63.00 ...

34 2-WETHYL-3-ETHYLPENT AHE C5H15 38 7 .419 ... -800 .92 71.28 42.67
35 3-WETHYL-3-ETHYLPENTANE c5H18 39 7.321 ... -808.63 86.,, 40. 79
36 2, 2, 3-TR IWETHYLPENTANE c5H15 40 7. 221 29.93 p -827 .83 66.66 32.44
37 2. 2, 4-TRI WETHYLPENTANE c5H15 41 6.871 10.00 -843. 11 52.43 34.61
38 2, 3, 3-TRI WETHYLPENTANE C5H15 42 7.294 ... -822. 18 68.80 3.23
39 2. 3, 4-TRI WETHYLPENTANE C5H15 43 7.301 ... -817.93 71 .51 34.88
40 2, 2, 3, 3-TETRAWETHYLBUTANE C5H15 44 7. 794 ... -849.58 84.65 c 7 .67
Paraffins, C9H20
41 n-NONANE C9H20 46 7 .562 88.00 -767. 14 82. 79 51 .96

42 2-WETHYLOCTANE C9H20 91 7 .490 ... -790.57 67.38 60.34
43 3-WETHYLOCTANE C9H20 92 7.522 ... - 783. 37 68. 72 56.98
44 4-WETHYLOCTANE C9H20 93 7 .481 ... -788.41 65. 70 53.63
45 3-ETHYLHEPTANE C9H20 448 7.523 ... -775.86 83. 13 53.63
46 2,2-0!WETHYLHEPTANE C9H20 96 7 .214 ... -824.93 59.67 29.83
47 2, 6-0IWETHYLHEPTANE C9H20 447 7 .303 ... -813.87 61 .01 43.58
48 2, 2, 3-TRIWETHYLHEXANE C9H20 432 7 .253 ... -809.24 85.81 34.53
49 2, 2, 4-TRI WETHYLHEXANE C9H20 433 7.034 ... -815. 11 73. 74 39.22
50 2, 2, 5-TR! WETHYLHEXANE C9H20 47 7.055 55.00 -849.05 46.26 20. 78
51 2, 3, 3-TR! WETHYLHEXANE C9H20 434 7.314 ... -802 .07 93. 19 30.50
52 2, 3. 5-TRI WETHYLHEXANE C9H20 435 7 .218 ... -813.03 68. 72 33.52
53 2, 4, 4-TRI WETHYLHEXANE C9H20 436 7 .086 ... -804.32 83.80 37 .88
54 3,3,4-TRIWETHYLHEXANE C9H20 437 7.410 ... -789.03 99.55 27. 15
55 3, 3-0! ETHYLPENTANE C9H20 50 7 .448 ... -780.48 139. 78 33.82
56 2, 2-0!WETHYL-3-ETHYLPENTANE C9H20 430 7 .282 ... -775 .29 120 .00 34. 19
57 2, 4-0! WETHYL-3-ETHYLPENTANE C9H20 431 7 .333 ... -764.06 121 .34 24. 13
58 2, 2, 3, 3-TETRAWETHYLPENTANE C9H20 51 7.388 ... -794.80 125.37 7. 71
59 2, 2, 3, 4-TETRAMETHYLP ENTANE C9H20 52 7.310 ... -787 .62 117 .99 1.68
60 2, 2, 4 ,4-TETRAMETHYLPENTANE C9H20 53 6.924 ... -812.03 ,,4,31 32.51
61 2, 3, 3 ,4-TETRAWETHYLPENTANE C9H20 54 7.413 ... -792.12 90.17 30.17
Pal"'affins, C 10H22
62 n-OECANE C 10H22 56 7.556 ,,5 .00 -754.01 99.72 86. 72

63 2-WETHYLNONANE C 10H22 57 7 .577 ... -775.13 85.21 52.88
64 3-WETHYLNONANE C 10H22 58 7.614 ... -768 .69 86. 72 56.81
65 4-WETHYLNONANE C10H22 443 7 .592 ... -769.69 87.33 ...
66 5-WETHYLNONANE C10H22 444 7.595 ... -769.69 92. 16 ...
67 2, 7-DIWETHYLOCTANE C10H22 61 7 .431 ... - 796. 25 79. 77 52.28
68 3, 3, 4-TR! WETHYLHEPTANE C10H22 438 7.466 ... -778. 79 111.20 39.28
69 3, 3, 5-TR I WETHYLHEPTANE C10H22 439 7 .255 ... -785. 25 97.60 42.30
70 2, 2, 3, 3-TETRAWETHYLHEXANE C10H22 440 7 .387 ... -779.57 141 .72 37 .47
1-88 1987
1C2.1
ASTM Octane Numbers

Coettlcient Aniline Flannabllity Watson
ot Expansion Point Limits, Volume K Factor No.
I-~~~~~~~~-,~~~~~~~~~-! Percent in
1 (av)
v ar p
0 357 0 908
With With Lower Upper

per deg F TEL TEL
per gal per gal
Paraffins, C9H19
0.000630 154.4 81. 7 97. 1 76. 3 94.7 0.89P 5.88 p 12 .3 33

0.000630 153.0 88. 1 +O. 1 K 87 .3 100 0.89 p 5.88 p 12.3 34
0.000590 150.6 88.7 +O. 2 K 80.8 95.9 0.89 p 5.51 12. 2 35
0. 000630 159.4 99.9 +2 .0 K +1. 2 K 1 .00 p 5.59 12 .3 36
0.000650 175.0 100. +3.0 K 100. •3.0 K 1.10 12.5 37
0.000590 152.6 99.4 +2 .0 K +0.6 K 1 .00 p 5.59 12. 2 38
0.000630 154.9 95.9 +0.1 K +O. 2 K 1 .00 p 5.97 12 .2 39
0.89 p 5.31 p 12. 1 40
Paraffins, C9H20
0.000630 164. 7 0. 70 5.60 12.6 41

0.000630 164. 7 0.85 p 5.36 12. 7 42
0.000580 171 .5 0.85 p 5.36 12 .5 43
0.000590 167.0 0.85 p 5.36 12.5 44
0.000640 176.0 0.80 p 5.36 12.4 45
0.000720 60.5 83.5 50.3 77 .2 0.80 p 5. 12 12.6 46
0.000620 163.0 0.80 p 5.43 12.6 47
0.000550 162.0 0.80 p 5. 18 12.3 48
0.000580 172.0 0.80 p 5. 18 p 12.4 49
0.000580 180.9 0.80 p 5. 18 12 .5 50
0.000560 0.80 p 5. 18 12. 2 51
0.000630 169.0 0.80 p 5.49 12.4 52
0.000540 0.80 p 5. 18 12.4 53
0.000650 0.80 p 5. 18 12. 1 54
0. 000520 149.0 91 .6 +O. 1 K 84.0 97.1 0.70 5. 70 12.0 55
0.000550 99.5 +0.8 K +1.8 K >+6.0 K 0.80 P 5. 18 p 12. 2 56
0. 000560 96.6 +0.4 K •0.5 K +3.6 K 0.80 P 5.49 p 12. 2 57
0 .000520 154.0 95.0 99.4 +3.6 K >•4.o K a.ea 4.90 11 .9 58
0.000560 0.85 p 5. 25 12 .5 59
0.000540 167 .0 0.85 p 4.95 12.3 60
0.000570 0.80 4.90 12.0 61
0.000550 170.6 0. 70 5.40 12.6 62

0.000640 176.5 0. 72 p 5.04 p 12. 7 63
0.000640 172.9 0. 72 p 5.04 p 12.6 64
0.000600 172.9 0. 72 p 5.04 p 12.6 65
0.000600 172.2 0. 72 p 5.04 p 12.6 66
0.000590 174.2 0. 72 p 5. 10 12.6 67
0.000570 0. 72 p 4.89 12. 1 68
0.000560 158.0 88. 7 +O .2 K 86.4 100. 0.72P 4.89 12.3 69
0.000530 92.4 96. 7 +2.0 K +2.5 K 0.72 P 4. 70 12 .o 70
1987 1-89
1C2.1
Flash Ideal Gas Ideal Gas Heat of

( Cal/cm 3 ) 1 1 2 deg !' at 77 !' Format ion Btu/lb
Btu/lb at 77 !'
Btu/lb
Paf"affins. C10H22
71
72 I 2, 2. 5. 5-TETRAMETHYLHEXANE
2, 4-0IMETHYL-3- ISOPROPYL-
PENTANE
C10H22 441
442
6.922
7 .570
...
...
-863.88
-721. 77
58.02
188.55
29.61
1.81
C10H22
Paraffins, C11 to C30
73 n-UNDECANE C11H24 63 7 .818 149.00 -743 .07 113.46 60.76

74 n-DODECANE C12H25 64 7 .810 165.00 -733 .94 125.01 90.50
75 n-TRIOECANE C13H29 65 7.687 ... -726. 24 134.81 66.46
76 n-TETRAOECANE C14H30 66 7.814 212.00 -719.58 143.22 97.67
77 n-PENTAOECANE C15H32 67 8.045 ... -713.81 150.52 70.02
78 n-HEXAOECANE C15H34 68 7 .848 ... -710.40 155,97 101.31
79 n-HEPTAOECANE C17H35 69 7. 759 ... -704.31 162.57 72.34
80 n-OCTAOECANE C19H39 70 7. 742 ... -700.34 167.60 104.68
81 n- NONAOECAN E C19H40 71 7 .845 ... -696. 78 172.10 73.35
82 n-EICOSANE C20H42 73 7. 755 ... -693.59 176.15 106.32
83 n-HENE!COSANE C21H44 445 ... ... -631.57 p ... .. .
84 n-OOCOSANE C22H45 75 ... ... -690.09 p ... .. .
85 n-TRICOSANE C23H4B 76 ... ... -687. 71 p ... .. .
86 n-TETRACOSANE C24H50 77 ... ... -885.51 p ... . ..
87 n-PENTACOSANE C25H52 7B ... ... -683.49 p ... ...
88 n-HEXACOSANE C25H54 79 ... ... -681 .64 p .. . ...
89 n-HEPTACOSANE C27H55 80 ... ... -679.91 p .. . ...
90 n-OCTACOSANE C29H59 81 ... ... -878 .30 p ... .. .
91 n-NONACOSANE C29H50 82 ... ... -676.81 p ... ...
92 n•TR!ACONTANE C30H62 446 ... ... -875 ,42 p ... .. .
1-90 1987
1C2.1
ASTM Octene Numbers

Coefficient Aniline Fla...,,bility Watson
of Bxpans ion Point Lim~ ts, Volume It Factor No.
Percent in
d•9 I!' Motor Method Reseercb Method Air Mixture
l
v (av
1
0 357 D 908
ar p
Witb With Lover Upper
et 60 F Clear 3 ml Clear 3 ml
per de9 F TEL TEL
per 9al per gel
Pe,.eff, ns. CioH22
0.000830 181,0 0. 72 p 4, 70 p 7'
0 .000520 I ...
Parefftns. C11 to C30
0. 72 p 5.16 p 72
0.66 p 4, 78 p 12. 7 73
0.60 4.68 p 12. 7 74
0.56 p 4,67 p 12. 7 75
0.50 4, 75 p i2.9 76
0.49 p 4.93 p 12.9 77
0.48 p 5. 21 p i2.9 78
0.43 p 5.63 p 13.0 79
0.41 p 6.21 p 13.1 80
0.39 p 8.98 p 13. 1 8i
0.37 p 8.00 p 13, 1 82
0.35 p 9,37 p 13.1 83
0.33 p 11, 19 p 13.2 84
0.32 p 13,64 p 13.2 85
0.31 p 16.96 p 13.2 86
0.29 p 21 .53 p 13.3 87
0.28 p 27 .89 p 13.3 88
0.27 p 36 .86 p 13.3 89
0.26 p 49, 72 p 13.4 90
0.25 p 68.46 p 13.4 91
0.25 p 96. 19 p 13,4 92
1987 1-91
1C2.2
TABLE 1C2.2
CYCLOPARAFFINS-SECONDARY PROPERTIES
Flash Ideal Ga• Ideal Gas Heat ot

Search Solub1l1ty Point Heat of Gibbs Free Pus1on
No. Compound Formula Number Parameter Temperature Formation Energy ot at 77 de9 F
(Cal/cm 3 ) l / 2 de9 F at 77 F Formation Btu/lb
Btu/lb at 77 F
Btu/lb
Alkylcyclopropanes. C3 to C5
93 CYCLOPROPANE C3H5 101 7 .600 ... 546.06 1069.00 55.57

94 ME THYLCYCLOPROPANE C4H5 350 ... . .. 581. 70 p ... . ..
95 ETHYLCYCLOPROPANE C5H10 351 ... ... 322 .40 p . .. ...
96 cis- 1, 2-0! METHYLCYCLOPROPANE C5H10 352 ... ... 190.82 p ... . ..
97 trans- 1, 2-0!METHYLCYCLOPROPANE C5H10 356 ... ... . .. ... . ..
Alkylcyclobutanes, C4 to c6
CYCLOBUTANE C4H5 102 7 .910 -83.47 p 208. 71 848 .00 8.34
981
99 ME THYLCYCLOBUTANE C5H10 353 ... ... 154.92 p ... . ..
100 ETHYLCYCLOBUTANE C5H12 354 ... . .. 238.74 p ... ...
Alkylcyclopantanes, C5 to C7
101 CYCLOPENTANE C5H10 104 8. 156 ... -473.49 236.74 3. 73

102 ME THYLCYCLOPENTANE C5H12 105 7 .907 -17 .00 -545.03 182. 74 35.39
103 ETHYLCYCLOPENTANE C7H14 107 7 .988 95.00 -556.37 195.29 30.08
104 1,1-DIMETHYLCYCLOPENTANE C7H14 108 7.557 ... -605.46 170. 92 4. 72
105 c 1s-1 , 2-0IMETHYLCYCLOPENTANE C7H14 109 7.903 24.53 p -567 .17 200. 23 7 .26
106 trans- 1 , 2-0IME THYLCYCLOPENTANE C7H14 110 7. 705 13.73 p -598.50 167 .99 31 .38
107 c 1s-1, 3-0!ME THYLCYCLOPENTANE C7H14 111 7.572 ... -594.84 171 .65 32 .26
108 trans- 1 , 3-0!ME THYLCYCLOPENTANE C7H14 112 7 .609 ... -584.94 181 .55 31 .84
Alkylcyclopantanes, C5H15
109 n-PROPYLCYCLOPEN TANE C5H15 114 8.015 60.53 p -587 .32 201 .34 38.44
110 ISOPROPYLCYCLOPENTANE C5H15 115 ... ... -252.63 p . .. ...
111 1- METHYL- 1-ETHYLCYCLOPENTANE C5H15 116 ... . .. -301.53 p . .. ...
112 cis- 1-METHYL-2-ETHYL-
CYCLOPENTANE C5H15 357 ... ... -301 .53 p . .. ...
113 trans- 1-ME THYL-2-ETHYL-
CYCLOPENTANE C5H15 358 ... ... -301 .53 p . .. . ..
114 c 1s-1-METHYL-3-E THYL-
CYCLOPENTANE C5H15 359 ... . .. -301.53 p . .. ...
115 trans-1-METHYL-3-ETHYL-
CYCLOPENTANE C5H15 360 ... . .. -301 .53 p . .. ...
118 1, 1 ,2-TR!METHYLCYCLOPENTANE C5H15 118 ... ... -383. 76 p . .. . ..
117 1, 1 ,3-TRIMETHYLCYCLOPENTANE C5H15 119 ... ... -383.76 p ... . ..
118 1. c-2. c-3-TRI METHYL-
CYCLOPENTANE C5H15 361 ... ... -301. 53 p . .. . ..
119 1 ,c-2, t-3-TRIMETHYL-
CYCLOPENTANE C5H15 362 ... ... -383.78 p . .. ...
120 1, t-2 ,c-3-TR!METHYL-
CYCLOPENTANE C5H15 363 ... ... -383.78 p ... . ..
121 1 ,c-2,c-4-TRIMETHYL-
CYCLOPENTANE C5H15 364 ... . .. -383.76 p ... . ..
1-92 1987
1C2.2
ASTH Octane Numbers

Coefficient Aniline l"lannabillty Watson
ot Expansion Point Limits, Volurne k Factor No.
Percent in
deg I" Motor Method Research Method Air Mixture
1
v l¥rl p 0 357 0 908
l<lith With Lover Upper

at 60 I" Clear 3 ml Clear 3 ml
per deg F TEL TEL
per gal per gal
A 1ky I eye 1opropanes, C3 to C5
... . .. ... ... . .. ... 2.40 10.40 11.9 93

... ... 81 .2 87 .2 +0.2 K +0.4 K 1.86 p 11.42 p 9.3 94
0.000820 ... 83.8 87 .8 +0.2 K +O. 7 K 1.49 p 9.57 p 11.9 95
0. 000780 ... 84.3 86.6 +0.4 K +0.7 K 1.49 p 9. 79 p 11.8 96
... ... ... ... ... ... ... . .. . .. 97
A 1ky1 eye I obutanes. C4 to Cs
0. 000870 ... ... . .. . .. . .. 1 .80 p 11.10 p 11.4 98

... ... . .. . .. . ..
0. 000740
0. 000730 I 101.7
I 63.9 ... 41., ...
1.49 p
1. 20
9.57 p
7. 70
11.8
11.6
99
100
A 1ky1eye1 opentanes, C5 to C7
0.000700 62. 2 84.9 95.2 +O. 1 K +0.9 K 1.40 p 9.36 p 11.0 101
0.000710 91.4 80.0 93.0 91.3 +0.5 K 1.20 p 8. 35 p 11. 3 102
0.000670 98.1 61.2 80.7 67. 2 79.5 1. 10 6. 70 11.4 103
0.000660 113.0 89. 3 +O. 1 K 92. 3 +0.9 K 1.06 p 6. 78 p 11.4 104
0.000630 103.8 ... . .. . .. ... 1.06 p 7. 30 p 11. 3 105
0. 000660 116.1 ... . .. ... ... 1.06 p 7. 30 p 11.5 106
0.000650 ... 73. 1 86.8 79. 2 91. 2 1.06 p 7. 30 p 11.8 107
0.000660 121 .8 72.6 87. 1 80.6 93. 2 1.06 p 7. 30 p 11.6 108
Alkylcyclopentanes, C9H15
0.000580 112.0 28.1 60.5 31.2 59.8 0.95 6.42 p 11.5 109
0.000540 ... 76. 2 89.4 81., 94.3 0.93 p 6.42 p 11.5 110
0.000590 ... ... ... . .. . .. 0.93 p 6.10 p 11.4 111
0.000590 117.5 ... . .. ... ... 0.93 p 6.52 p 11.4 112
0.000580 126.0 ... . .. . .. ... 0.93 p 6.52 p 11.6 113
0.000580 ... 59.8 79.6 57 .6 79. 2 0.93 p 6.52 p 11.6 114
0.000580 ... 59.8 79.6 57 .6 79. 2 0.93 p 6.52 p 11.6 115

0.000630 ... ... ... . .. . .. 0.93 p 6.19 p 11.4 116
0.000660 ... 83.5 95.6 87. 7 +O. 1 K 0.93 p 6.19 p 11. 7 117
0.000590 105.8 ... . .. . .. ... 0.93 p 6.61 p 11.4 118
0.000580 105.8 ... . .. . .. ... 0.93 p 6.61 p 11.5 119
0.000660 105.8 ... ... . .. ... 0.93 p 6.61 p 11. 7 120
0.000830 ... ... . .. ... ... 0.93 p 8.61 p 11.5 121
1987 1-93
1C2.2
Plash Ideal Gas Ideal Gas Heat or

No. Compound Formula Number Parameter Temperature Formation Energy ot at 77 deg F
(Cal/cm 3 i l / 2 deg F at 77 F Formation Btu/lb
Btu/lb at 77 F
Btu/lb
A 1k:t I eye 1open tan es. C5H15
122 1, c-2, t-4-TRIYETHVL-

CVCLOPENTANE C5H15 120 ... ... -383. 78 p ... .. .
123 1, t-2, c-4-TR!YETHVL-
CVCLOPENTANE C5H15 365 ... ... -383. 76 p ... ...
A 1ky1eye1 opentanes. C9H15
124 n-8UTV LCVCLOPENTAN E C9H15 366 ... ... -573. 10 209. 03 38.53
125 I S08UTVLCVCLOPENTANE C9H15 367 ... ... -334. 00 p ... . ..
126 1-ME THVL- 1-n-PROPYL-
CVCLOPENTANE C9H15 368 ... . .. -338. 56 p . .. ...
127 1, 1-0IETHVLCVCLOPENTANE C9H15 369 ... ... -338. 56 p ... . ..
128 c is- 1, 2-0l ETHVLCVCLOPENTANE C9H15 370 ... ... -338.56 p ... ...
129 1, 1-0IMETHVL-2-ETHVL-
CVCLOPENTANE C9H15 371 ... ... -411.66 p ... .. .
A I ky I c ye 1open tanes. C10 to C25
130 n- PENT VLCVCLOPE NTAN E C10H20 123 8.068 ... -579.00 213.90 ...
131 n- HE XVLC VC LOPENTANE C11H22 124 8. 102 ... -583.71 217 .88 ...
132 n- HEPT VLCVCLOP ENTANE C12H24 125 8. 131 ... -587. 77 221 .22 ...
133 n-OCT VLC VCLOPENTANE C13H25 128 8. 157 ... -591. 08 224.02 ...
134 n-NONV LC VCLOPENTANE C14H25 127 8.176 ... -594.01 226. 43 ...
135 n-OECV LCVCLOPEN TANE C15H30 128 8. 193 ... -596.58 228.44 67 .69
136 n-UNDECV LC VCLOP ENTANE C15H32 129 8.208 ... -598. 72 230. 27 ...
137 n-DODECV LCVCLOPENTANE C17H34 130 8. 223 ... -600. 68 231 .88 ...
138 n-TRI DECVLCVCLOPENTANE C15H35 131 8.236 ... -602.38 233. 33 ...
139 n-TETRAOEC VLCVC LOP ENTAN E C 19H35 132 8. 248 ... -603 .94 234.61 ...
140 n-P ENTADEC VLC VC LOPE NTAN E C20H40 133 8. 257 ... -605. 35 235. 77 ...
141 n-H EXAOECVLCVCLOPE NTAN E C21H42 134 8.265 ... -606. 58 238.82 ...
142 n- HEPTAOECVLC VCLOPE NTAN E C22H44 373 ... ... -483. 70 p ... ...
143 n-OCTADEC VLCVCLOP ENTANE C23H45 374 ... ... -490. 27 p ... ...
144 n-NONAOEC VLCVC LOP EN TANE C24H45 375 ... ... -496. 29 p ... ...
145 n-EICOSVLCVCLDPENTANE C25H50 376 ... ... -501. 84 p ... . ..
A I ky I eye 1 ohexanes, C5 and C7
146
147
I CVCLOHEXANE
METHVLCVCLOHEXANE
C5H12
C7H14
137
138
8. 164
7 .954
-4,00
25.00
-629.02
-877. 64
162. 22
119.44
14.00
29.56
A 1 ky lcyc I ohexanes, C5H15
148 ETHVLCVCLOHEXANE C5H15 140 7 .998 95.00 -858.06 150.37 31.93

149 1,1-0lMETHYLCYCLOHEXANE C5H15 141 7.662 ... -693.49 134.98 7. 74
150 c 1s-1,2-0IYETHYLCVCLOHEXANE C5H15 142 7 .944 71,33 p -859.66 157 .90 6.30
151 trans-1, 2-DIMETHVLCVCLOHEXANE C5H15 143 7. 713 62.33 p -689.64 132.09 39.93
1-94 1987
1C2.2
ASTM Octane Numbers

Coefficient Aniline Flammability Watson
ot Expansion Point Limits, Volume IC Factor No.
Percent in
deg F Motor Method Researcn Method Air Mixture
1 (av J D 357 0 908
v ar P
With With Lower lipper
per deg F TEL TEL
per gal per gal
A I ky 1cycl opentanes, C9H15
0.000570 79.5 89.2 98.3 0.93 p 6.61 p 11 .6 122
0.000660 0.93 p 6.61 p 11 .8 123
Alkylcyclopentanes, C9H19
0.000540 119.7 -2.0 36. 7 -3.0 29.6 0.83 p 5.87 p 11. 2 124
0.000590 28 .2 58. 1 33.4 59.2 0.83 p 5.94 p 11 .6 125
0.000600 0.83 p 5.61 p 11 .3 126

0.000550 0.83 p 5.61 p 11 .3 127
0.000600 127 .2 0.83 p 5.61 p 11 .4 128
0.000690 0.83 p 5.68 p 11 .4 129
A I ky I cycl open tan es. C10 to C25
0.000550 0. 74 p 5.47 p 11. 7 130

0.68 p 5.20 p 11 .9 131
0.62 p 5.06 p 12.0 132
0.57 p 5.01 p 12. 1 133
0.53 p 5.07 p 12.2 134
0.50 p 5.24 p 12.2 135
0.47 p 5.53 p 12.3 136
0.44 p 5.95 p 12.4 137
0.41 p 6.53 p 12.5 138
0.39 p 7 .33 p 12.6 139
0.37 p 8.38 p 12. 7 140
0.35 p 9. 79 p 12.8 141
0.34 p 11 .67 p 12. 7 142
0.32 p 14.20 p 12.8 143
0.31 p 17.63 p 12.9 144
0.30 p 22.34 p 12.9 145
Alkylcyclohexanes, Cs and C7
77.2 97.4 146

I I
0.000680 87 .8 87.3 83.0 1 .30 8.00 11.0
0.000630 105.8 71. 1 86.2 74.8 88.2 1 .20 7. 18 p 11.3 147
A 1 ky I eye I ohexanes, C9H15
0.000540 110.8 40.8 65.4 45.6 65. 1 6.60 9.00 11 .4 148

0.000590 113. 7 85.9 95.7 87.3 98.0 0.93 p 6. 10 p 11.3 149
0.000550 107. 1 78.6 90.7 80.9 94.3 0.93 p 6.52 p 11.2 150
0.000580 118.9 78.7 90.8 80.9 94.5 0.93 p 6.52 p 11.5 151
1987 1-95
1C2.2
!"lash Ideal Gas Ideal Gas Heat o!

Search Solubility Point Heat o! Gibba l"rae l"usion
No. Compound Formula Number Parameter Temperature l"ormation Energy ot at 77 deg F
(Cal/cm 3 ) l/2 deg I" at 77 I" l"ormation Btu/lb
Btu/lb at 77 F
Btu/lb
A 1ky I eye 1ohexanes. C9H15
152 c1s-1, 3-01 WETHYLCYCLOHEXANE C9H15 144 7 .647 58. 73 p -707 .91 114.30 41 .46
153 trans- 1 ,3-0IMETHYLCYCLOHEXANE C9H15 145 7.842 ... -676.49 139.15 37.80
154 c1s-1, 4-01 ME THYLCYCLOHEXANE C9H15 146 7 .813 60.53 p -676.81 145.40 35.66
155 trans- 1 , 4-01 METHYLCYCLOHEXANE C9H15 147 7.578 53.33 p -707. 27 121 .51 47.25
A 1ky1eye1 ohexanes. C9 and C10
156 n-PROPYLCYCLOHEXANE C9H19 149 8.007 ... -658.31 161 .16 35.32
157 I SOPROPYLCYCLOHEXANE C9H19 150 ... ... -319.47 p . .. . ..
158 n-8UTYLCYCLOHEXANE C10H20 152 8.023 ... -653. 37 172.99 43.40
159 I SOBUTYLCYCLOHEXANE C10H20 386 ... ... -419.09 p ... . ..
160 sac-8UTYLCYC LOHEXANE C10H20 383 ... ... -350.99 p . .. . ..
181 tar t-8UTY LCYCLOH EXANE C10H20 384 ... ... -386.00 p . .. . ..
182 1 -WETHYL-4· l SOPROPYL-
CYCLOHEXANE C10H20 372 ... ... -416. 78 p . .. ...
-lkylcyclohexanes. C11 to c 26
163 n-PENTYLC YCLOH EXANE C11H22 167 8.067 ... -651 .44 180. 70 50. 13
164 n-H EXY LCYCLOH EXANE C12H24 168 8. 100 ... -649. 76 187. 13 56.64
165 n-H EPTYLC YCLOH EXANE C13H25 157 8. 126 ... -648.40 192.56 61. 16
166 n-OCTYLCYCLOH EXANE C14H29 169 8. 151 ... -647. 14 197 .21 65.95
167 n-NONY LCYCLOH EXAN E C15H30 170 8.170 ... -646. 17 201. 25 70. 11
188 n-OECYLCYC LOHE XANE C 15H32 158 8. 186 ... -645. 28 204. 70 74.01
169 n-UNOECYLCYC LO HEXANE C 17H34 171 8.200 ... -644.43 207. 82 76.94
170 n-OOOECYLCYC LO HEXANE C19H35 172 8. 216 ... -643. 77 210.60 78.08
171 n-TRIOEC YLCYCLOH EXANE C 19H39 173 8. 228 ... -643.09 213 .08 82.34
172 n-TETRAOECY LCYCLOH EX ANE C20H40 174 8.241 ... -842. 54 215.31 84.64
173 n-PENTAOECYLCYCLOHEXANE C21H42 377 ... ... -642.06 217. 34 . ..
174 n- HEXAOECYLCYCLOHEXANE C22H44 378 ... ... -641 .55 219.17 . ..
175 n-HEPTAOECYLCYC LOHEXANE C23H45 379 ... ... -499.80 p ... . ..
176 n-OCTAOECY LCYC LOH EXANE C24H49 380 ... ... -505.43 p ... . ..
177 n-NONAOECYLCYC LOHEXANE C25H50 381 ... . .. -510.61 p ... . ..
178 n-E I COSY LCYC LOHEXANE C25H52 382 ... . .. -515.38 p ... . ..
Cyclopsrsffina, C7 to C12
179 CYCLOHEPTANE C7H14 159 8.416 ... -521. 21 277 .55 8.24
180 CYCLOOCTANE C9H15 160 8.509 ... -481. 56 345. 14 9.23
181 CYCLONONANE C9H19 164 8.589 ... -455.97 . .. 6.58
182 ETHYLCYCLOHEPTANE C9H19 385 ... ... -122.97 p ... . ..
183 8ICYCLOHEXYL C 12H22 155 8.419 165.20 -703.17 110. 13 p ...
1-96 1987
1C2.2
ASTM Octane Numbers

Coet:t: Lcient Anlline Flammablllty Watson
of Expans Lon Polnt Llmits, Volume X Factor No.
Percent Ln
deg F Motor Method Research Method ALr Mixture
1 [av J D 357 D 908
v ar P
per deg F TEL TEL
per gal per gal
Alkylcyclohexanes, C5H15
0.000580 125. 1 71.0 71. 7 0.93 p 6.52 ,, .6 152

0.000590 115.3 64. 2 83.8 66.9 83.5 0.93 p 8.52 11 .3 153
0.000590 116.4 68. 2 85.0 67.2 84,7 0.93 p 6.52 p 11.4 154
0.000620 126.9 62.2 83.4 68.3 82 .8 0.93 p 8.52 p 11.6 155
Alkylcyclohexanes, Cg and C10
0.000500 121 .6 14.0 47. 7 17.8 42.8 0.95 5,87 11 .5 156

0.000500 120.0 61. 1 81.4 62.8 79.6 0.83 5.87 11 .4 157
0.000500 129.9 25.3 22 .5 0.85 5.47 11 .6 158
135.3 0. 74 p 5.53 11 .4 159
0. 74 p 5,47 11 .4 160
128.5 0. 74 p 5.47 11 .4 161
133. 7 0. 74 5.86 10.8 162
A 1 ky lcyc 1ohexanes. C11 to C25
0.68 p 5. 20 11 .8 163
0.62 p 5.06 11.9 164
0.57 5,01 p 12.0 165
0.53 5.07 p 12. 1 166
0.50 5. 24 12.2 167
0.47 p 5.53 12.3 168
0.44 p 5.95 12.4 169
0.41 6.53 12.4 170
0.39 p 7 .33 p 12.5 171
0.37 p 8.38 p 12.6 172
0.35 9. 79 12.8 173
0.34 11 .67 12. 7 174
0.32 14.20 12.8 175
0.31 17 .63 p 12.8 176
0.30 22.34 p 12.9 177
0.29 p 28.90 12.9 178
Cycloparaffins, C7 to C12
0.000610 40.2 65.3 38.8 59.8 1 .06 7 .05 p 10.9 179

0.000520 58.2 71.0 0.93 6.33 10.9 180
0.000530 0.83 5. 79 10.9 181
0.83 5.87 p 11 .5 182
0. 70 5. 10 10.9 183
1987 1-97
1C2.2

(Cal/cml)l/2 deg F at 77 F Formation Btu/lb
Btu/lb at 77 F
Btu/lb
Decahydronaphthalenes. C10 to C12
184 c i s-DECAHYORONAPHTHALENE C10H18 153 8.617 136.04 -526.29 265.95 29.51

185 tr ans-DECAHYDRONAPHTHAL ENE C10H19 154 8.332 136.04 -566. 50 228. 72 44.81
186 1-METHYL- ( ci s-OECAHYDRO-
NAPHTHALENE] C11H20 176 ... ... ... ... . ..
187 1 -METHYL- ( trans-OECAHYORO-
NAPHTHALENE] C11H20 177 ... . .. ... ... ...
188 1 -ETHYL- ( c i s-DECAHYORO-
NAPHTHALENE] C12H22 178 ... . .. ... ... ...
189 1-ETHVL- ( trans-DECAHYDRO-
NAPHTHALENE] C12H22 179 ... . .. ... ... ...
190 9-ETHYL- ( c i s-DECAHYDRO-
NAPHTHALENE] C12H22 180 ... . .. ... ... . ..
191 9-ETHYL- ( trans-OECAHYORO-
NAPHTHALENE] C1.2H22 181 ... . .. ... ... ...
1-98 1987
1C2.2
ASTM Octane Numbers

Coefficient Anllln• Flammability Watson
of Expans lon Point Limits, Volume It Pactor No.
r-~~~~~~~~..-~~~~~~~~~ Percent in
d•9 I!' Ho tor He thod Research Method Air Mixture
.!. (~) D 357 D 908
V ()T p
at 60 I!' Clear l ml Clear 3 ml
per deg I!' TEL TEL
per gal per gal
Decahydronaphthalenes. C10 to C12
0.000510 95.5 0.70 4.90 10.5 184

0.000550 95.5 0.70 4.90 10. 7 185
0. 70 p 5.72 p 9.6 186
0. 70 p 5. 72 p 187
0.64 p 5.52 p 188
0.64 p 5.52 p 189
0.64 p 5.28 p 10.9 190
0.64 p 5.28 p 11 .2 191
1987 1-99
1C2.3
TABLE 1C2.3
MONOOLEFINES AND DIOLEFINS-SECONDARY PROPERTIES
Flash Ideal Gas Ideal Gas Heat or

search Solubility Point Heat of Gibbs Free Fusion
(Cal/cml)l/ 2 deg F at 77 F Formation Btu/lb
Btu/lb at 77 F
Btu/lb
Monoo 1ef1 ns. C2 and C3
192
193 I ETHYLENE
PROPYLENE
C2H4
C3H5
201
202
6.080
6.313
...
-162.00
801.35
201.37
1048.83
640. 78
51.36
30.68
Monoolef1ns. C4H5
194 1-BUTENE C4H5 204 6.935 ... 0.96 547. 88 29.48

195 cis-2-8UTENE C4H5 205 7 .337 ... -53.54 501.87 56.01
196 trsna-2-SUTENE C4H5 206 7 .137 ... -85.60 485. 78 74. 76
197 I SOBUTENE C4H9 207 6.894 ... -129.52 444.97 45.45
198 1-PENTENE C5H10 209 7 .138 0.00 -128.25 486.31 35.60

199 cfs-2-PENTENE C5H10 210 7 .411 -50.00 p -172. 11 440.40 43.60
200 trans-2-PENTENE C5H1Q 211 7 .316 -54.67 p -194.68 426.67 51.20
201 2- METHYL-1-BUTENE C5H10 212 7.184 20.00 -222 .64 397 .82 48.50
202 3-METHYL-1-8UTENE C5H10 213 6.794 -79.87 p -177 .49 458.36 32.86
203 2-METHYL-2-BUTENE C5H1Q 214 7 .454 20.00 -260.85 365. 76 46.58
Monoolefins. C5H12
204 1-HEXENE C5H12 216 7 .356 ... -212.88 447.56 47.75

205 cls-2-HEXENE C5H12 217 7.488 ... -247 .08 409.52 45.25
206 trans-2-HEXENE C5H12 218 7 .500 ... -268.45 398.19 42.17
207 cts-3-HEXENE C5H12 219 7.427 ... -247 .08 420.20 42.13
208 trans-3-HEXENE C5H12 220 7 .450 ... -268.45 407.14 56.58
209 2-METHYL-1-PENTENE C5H12 221 7.365 ... -289.82 372. 76 35.91
210 3-METHYL-1-PENTENE C5H12 222 7 .006 ... -235.54 435. 75 18.38
211 4-METHYL-1-PENTENE C5H12 223 7 .078 ... -249. 21 437 .08 18.20
212 2-METHYL-2-PENTENE C5H12 224 7 .517 ... -319.75 349.89 41.04
213 c I s-3-METHYL-2-PENTENE C5H12 225 7.511 ... -306.07 362. 70 30. 24
214 trana-3-METHYL-2-PENTENE C5H12 226 7.633 ... -306.07 357 .59 39.33
215 c I s-4-METHY L-2-PENTEN E C5H12 227 7. 142 ... -283.41 393.27 37.62
216 tr ans-4-METHYL-2-PENTEN E C5H12 228 7 .203 ... -304. 79 379.81 36.55
217 2-ETHYL- 1-BUTENE C5H12 229 7 .432 ... -276. 15 395.62 38.69
218 2,3-DIMETHYL-1-8UTENE C5H12 230 7 .172 ... -315.90 372.54 27 .83
219 3, 3-DIMETHYL-1-8UTENE C5H12 231 6.664 ... -304.57 417 .42 5.47
220 2, 3-0IMETHYL-2-BUTENE C5H12 232 7.773 ... -340.05 353.09 . ..
Monoolefins. C7H14
221 1-HEPTENE C7H14 234 7.545 32.00 -272. 78 420.43 54.30

222 cfa-2-HEPTENE C7H14 235 7.512 ... -303 .00 390.58 p ...
223 trana-2-HEPTENE C7H14 236 7.538 ... -323.17 p ... 51.30
224 cta-3-HEPTENE C7H14 249 7 .599 ... -300.81 391 .45 p . ..
225 trana-3-HEPTENE C7H14 237 7.474 ... -319.89 p ... 45.80
1-100 1987
1C2.3
ASTM Octane Numbers

Coeff 1c1ent An1l1ne Flannability Watson
of Expansion Point Limits, Volume K Factor No.
Percent in
de9 r Motor Method Research Method Air Mixture
1 (av l o 357 o 908
v ar P
per de9 F TEL TEL
per gal per gal
Monool ef ins. C2 and C3
...
0.001890
I
Monoolefins. C4H9
...
...
75.6
84.9
. ..
...
+.03 K
+O. 2 K
...
...
2. 70
2.00
36.00
11.00
. ..
14.2
192
193
0.001160 ... so.a ... 97.4 . .. 1.60 9.30 13.0 194

0.000980 ... 83.5 ... 100. ... 1.60 9.70 12.6 195
0.001070 ... ... ... . .. ... 1.80 9.70 12.9 196
0.001200 58.8 ... ... ... ... 1.80 a.so 13.0 197
Monool ef ins. C5H1Q
0.000890 66.2 77 .1 82.9 90.9 98.6 1.50 8.70 12. 7 198

0.000870 64.4 ... . .. ... . .. 1.40 p 10.59 p 12.5 199
<.000001 64.4 ... . .. . .. ... 1.40 p 10.59 p 12.6 200
<. 000001 ... 81 .9 84.2 +0.2 K .. a.J K 1.40 10.59 p 12.5 201
<.000001 ... ... N ... N ... N .. . N 1.50 s ... 12.B 202
<. 000001 55.0 84.7 85.8 97 .3 99.2 1.40 10.09 p 12. 3 203
Monoolefins. C5H12
<.000001 73.0 63.4 76.3 76.4 91. 7 1.20 p 9.25 p 12.5 204
0.000730 78.8 ... ... ... ... 1.20 p 8.95 p 12.3 205
0.000720 78.8 so.a 83.2 92. 7 98.4 1. 20 p 8.95 p 12.5 206
0.000730 80.6 ... ... ... . .. 1.24 p 8.95 p 12.4 207
0.000770 80.6 80.1 82.3 94.0 ... 1. 24 p 8.95 p 12.5 208
0.000770 ... 81.5 85.2 94.2 99.8 1. 20 p 8.57 p 12.3 209
0.000750 ... 81. 2 82.2 96.0 +. 05 K 1.24 p 9.38 p 12.5 210
0.000790 ... 80.9 84.5 95. 7 +0.5 K 1. 20 p 9.38 p 12.5 211
0.000730 ... 83.0 85.0 91 .a 99.5 1.20 p 8.35 p 12.3 212
0.000740 ... . .. ... .. . ... 1.24 p 7.82 p 12. 2 213
0.000700 ... a1 .o 84.0 97. 2 100 1.24 p 7.82 p 12., 214
<.000001 ... 84.5 86.3 99. 7 +0.2 K 1.20 p 10.51 p 12.5 215
o.oooaoo ... 82.6 ... 98.0 + .02 K 1. 20 p 10.51 p 12.5 216
0.000740 ... 79.4 82.0 98.3 +0.3 K 1.20 p 8.95 p 12 .2 217
0.000770 ... 82.8 85.5 +0.1 K +O. 3 K 1.20 p 8.44 p 12.3 218
0.000900 ... 93.3 ... +1. 7 K ... 1.24 p 8.92 p 12.6 219
0.000710 ... 80.5 84.0 97.4 98.5 1.24 p 9.10 p 12.0 220
0.000700 81 .0 50.7 68.9 54.5 80.2 1.00 p 8.00 p 12.4 221

0.000670 ... ... .. . . .. ... 1.10 p 7.76 p 12.3 222
0.000660 ... 68.8 78.9 73.4 89.5 1.06 p 7. 76 p 12.4 223
0. 000710 94.8 ... ... 90.2 . .. 1. 10 p 7. 76 p 12.3 224
0.000700 94.8 79.3 84.6 89.8 98.2 1.06 p 7. 76 p 12.4 225
1987 1-101
1C2.3

Search Solubi Li ty Point Heat of Gibbs Pree Fusion
No. Compound Formula Number Parameter Temperature Format ion Energy of at 77 deg F
(Cal/cm 3 )l/2 deg F at 77 F Formation Btu/lb
Btu/lb at 77 F
Btu/lb
Wonoolef ins. C7H14
226 2-WETHYL-1-HEXENE C7H14 238 7.452 ... -333. 79 p . .. 56. 79

227 3-WETHYL- 1-HEXENE C7H14 456 7. 295 ... -278.47 p . .. . ..
228 4-WETHYL- 1-HEXENE C7H14 457 7.381 ... -309.43 p . .. 32.98
229 5-WETHYL- 1 -HEX ENE C7H14 458 7. 298 ... -309.43 p . .. . ..
230 2-WETHYL-2-HEXENE C7H14 459 7 .527 ... -385. 09 p . .. 40.30
231 c1 s-3-WETHYL-2-HEXENE C7H14 460 7 .568 ... -482. 56 p . .. 49.37
232 trans-3-WETHYL-2- HEX ENE C7H14 461 7 .561 ... -388. 57 p . .. . ..
233 c1 s-4-WETHYL-2-HEXENE C7H14 462 7.386 ... -364. 75 p . .. . ..
234 trans-4- METHYL- 2- HEX ENE C7H14 463 7.372 ... -364. 75 p . .. 31. 14
235 c h-5-WETH YL-2-HEXENE C7H14 464 7 .396 ... -417. 15 p . .. . ..
236 tr ans-5- METHYL- 2- HEX ENE C7H14 465 7 .349 ... -417.15 p . .. 27 .48
237 c1 s-2-WETHYL-3-HEXENE C7H14 466 7.314 ... -357.06 p . .. . ..
238 trana-2-WETHYL-3-HEXENE C7H14 467 7.285 ... -357.06 p . .. 23.82
239 c1s-3-WETHYL-3-HEXENE C7H14 239 7 .653 ... -381 .61 p . .. . ..
240 trans-3-WETHYL-3- HEX ENE C7H14 240 7.564 ... -381 .61 p . .. . ..
241 2-ETHYL- 1-PENTENE C7H14 468 7 .478 ... -330.31 p . .. . ..
242 3-ETHYL- 1-PENTENE C7H14 469 7.415 ... -305.76 p . .. 21.98
243 3-ETHYL-2-PENTENE C7H14 241 7.593 ... -385.09 p . .. . ..
244 2. 3-01METHYL-1-PENTENE C7H14 470 7.368 ... -375.38 p . .. 31. 14
245 2. 4-01METHYL-1 ·PENTENE C7H14 242 7. 177 ... -371.90 p . .. 38.47
246 3. 3-DI METHYL- 1 -PENTENE C7H14 471 7.230 ... -341.85 p . .. 32.98
247 3 • 4-DI METHYL- 1 -PENTENE C7H14 472 7. 280 ... -343.86 p . .. . ..
248 4 ,4-DI METHYL- 1-PENTENE C7H14 243 6.880 ... -359.99 p . .. 27 .48
249 2, 3-01 WETHYL ·2-PENTENE C7H14 473 7.632 ... -343.87 p . .. 38.47
250 2, 4-01 WETHYL-2-PENTENE C7H14 244 7.314 ... -418.98 p . .. 29.31
251 c1s-3.4-01 WETHYL-2-PENTENE C7H14 474 7 .460 ... -447 .01 p . .. 38.47
252 trana-3 ,4-01 WETHYL-2-PENTENE C7H14 475 7.526 ... -418.98 p . .. 38 .47
253 c1s-4,4-DIWETHYL-2-PENTENE C7H14 245 7. 136 ... -414. 77 p . .. 25.65
254 trana-4, 4· 01 WE THY L-2- PENT ENE C7H14 246 7.,,, ... -414. 77 p . .. 29.31
255 3-WETHYL-2-ETHYL- 1 -BUTENE C7H14 247 7. 387 ... -364. 20 p . .. . ..
256 2, 3, 3-TRIWETHYL- 1-BUTENE C7H14 476 7 .109 ... -418. 98 p . .. 3.48
Wonoolef tns. C8H15
257 1-0CTENE C8H16 250 7.645 70.00 -317. 73 400. 12 59.66

258 ch-2-0CTENE C8H16 276 ... . .. -362.12 p . .. . ..
259 trans-2-0CTENE C8H16 251 7.535 70.00 -365. 12 p 352.86 p ...
260 ch-3-0CTENE C8H16 477 7 .592 ... -359.06 p . .. . ..
261 trans-3-0CTENE C8H16 277 7.516 ... -362.44 p 353.25 p . ..
262 c1a-4-0CTENE c8H18 278 ... . .. -359. 07 p . .. . ..
263 trana-4-0CTENE C8H16 279 7.533 ... -382.44 p 380. 14 p . ..
264 2-WETHYL- 1-HEPTENE C8H16 252 ... . .. -371.42 p . .. . ..
265 3-WETHYL- 1-HEPTENE C8H16 487 ... . .. -493.09 p . .. . ..
1-102 1987
1C2.3
ASTM Octane Numbers

Coefficient Aniline P'lammabi l i ty Watson
Percent in
d•g F Motor Method Research Method Air Mixture
1 (av J
a 357 a 908
v ar P
With With Lover Upper
at 60 F Clear J ml Clear J ml
per deg F TEL TEL
per gal per gal
Monoolefins. C7H14
0.000710 ... 78.8 85.0 90.7 98.6 1 .06 p 7.68 p 12.3 226
0.000690 ... 71 .5 80.0 82. 2 94.B 1.06 p 8.10 p 12.4 227
0.000660 ... 74.0 83.6 86.4 96.B 1 .06 p B. 10 p 12.3 228
0.000700 ... 64.0 78.6 75.5 91 .8 1.06 p 8. 10 p 12.4 229
0.000670 ... 79.2 83.7 91 .6 98.4 1.06 p 7.46 p 12. 2 230
0.000720 ... ea.a 84.0 92.4 97 .4 1.06 p 7.46 p 12. 1 231
0.000670 ... 79.6 83.8 91.5 97 .4 1.06 p 7.46 p 12. 1 232
0.000700 ... ... ... 98.6 . .. 1.06 p 7 .87 p 12.3 233
0.000700 ... 83.0 85.B 96.B + .06 K 1 .06 p 7.46 p 12.3 234
0.000530 ... ... . .. . .. ... 1 .06 p 7.87 p 12.3 235
0.000700 ... 81 .0 85.0 94.4 +O., K 1.06 p 7 .87 p 12.4 236
0.000520 ... ... ... .. . ... 1 .06 p 7.87 p 12.4 237
0.000740 ... 82.0 85.7 97.9 +O., K 1 .06 p 7.87 p 12.5 238
0.000810 ... ... . .. 96.0 . .. 1 .06 p 7.46 p 12. 1 239
0.000760 ... 81.4 85. 1 96.4 98.B 1 .06 p 7.46 p 12. 2 240
0.000670 ... ... ... . .. . .. 1 .06 p 7. 76 p 12. 2 241
0.000700 ... 81 .6 84.2 95.6 + .05 K 1 .06 p 8. 10 p 12.3 242
0.000680 ... 80.6 84. 1 93.7 97.6 1 .06 p 7.46 p 12.0 243
0. 000710 ... 84.2 86.4 99.3 +O. 1 K 1 .06 p 7.87 p 12. 2 244
0. 000740 ... 84.6 87.3 99.2 +0.3 K 1 .06 p 7 .87 p 12.3 245
0.000660 ... 86. 1 87.3 +0.3 K +0.6 K 1 .06 p 7. 74 p 12 .2 246
0.000660 ... 80.9 ... 98.9 +O. 1 K 1.08 p 8.20 p 12. 3 247
0.000730 ... 85.4 87.7 +0.4 K +0.8 K 1 .06 p 7. 74 p 12.4 248
0.000690 ... 80.0 83.3 97 .5 99.5 1.06 p 7 .OB p 11 .9 249
0.000700 ... 85.3 86.4 100. +O. 1 K 1.06 p 8.03 p 12.3 250
0.000720 ... 82 .2 85. 1 96.0 99.5 1.06 p 7 .58 p 12. 1 251
0.000720 ... ... ... . .. . .. 1 .06 p 7.58 p 12.0 252
0.000700 ... 90.2 ... +0.5 K . .. 1 .06 p 7.87 p 12. 2 253
0. 000740 ... 90.9 94.5 +0.5 K +0.9 K 1.06 p 7.87 p 12.4 254
0.000710 ... 82.0 85.6 91 .a +O. 1 K 1 .06 p 7.87 p 12.0 255
0.000710 95.4 90.5 93. 7 +0.5 K + 1. 2 K 1 .06 p 7.48 p 12. 1 256
Monoolefins. CeH15
0.000580 90.5 34. 7 57.7 28.7 63.5 0.90 p 7.08 p 12.4 257
0.000640 101 .3 56.5 73.0 56.3 78.7 0.93 p 6.88 p 12.3 258
0.000630 101 .3 56.5 73.0 56.3 78.7 0.90 p 6.88 p 12.4 259
0.000540 ... ... ... . .. ... 0.93 p 6.88 p 12.3 260
0.000670 ... 68. 1 81. 2 72.5 89.4 0.90 p 6.88 p 12.4 261
0.000450 ... . .. ... ... ... 0.93 p 6.88 p 12 .3 262
0.000630 ... 74.3 84.2 73.3 91 .B 0.90 p 8.88 p 12.4 263
0.000830 ... 66.3 79.6 70.2 87 .9 0.93 p 6.64 p 12.3 264
0.000870 ... ... ... . .. . .. 0.93 p 7. 16 p 12.4 265
1987 1-103
1C2.3

No. Compound Formula Nwnber Parameter Temperature Formation Energy of at 77 deg F
(Cal/cm3)l/2 deg F at 77 I' Formation Btu/lb
Btu/lb at 77 I'
Btu/lb
Monool ef t ns, C5H15
266 4-METHYL-1-HEPTENE C5H15 488 ... ... -390. 81 p ... . ..

267 tr ans-6- ME TH YL- 2- HEPTENE C5H15 489 ... ... -608.98 p ... . ..
268 tr ans-3-ME TH YL-3- HEPTENE C5H15 490 ... ... -416.30 p ... . ..
269 2-E THYL- 1-HEXENE C5H15 258 7 .541 ... -371.64 p 349. 70 p ...
270 3-ETHYL- 1-HEXENE C5H15 479 ... ... -403.80 p . .. . ..
271 4-ETHYL- 1-HEXENE C9H15 480 ... ... -397.23 p ... ...
272 2, 3-0IMETHYL- 1-HEXENE C5H15 481 ... ... -394.66 p ... . ..
273 2, 3-0IMETHYL-2-HEXENE C5H15 482 ... . .. -621.65 p ... . ..
274 c i s-2, 2-0IMETHYL-3-HEXENE C5H15 253 ... ... -420. 29 p ... ...
275 2, 3, 3-TRIMETHYL- 1 -PENTENE C9H15 484 ... ... -512.96 p . .. ...
276 2, 4, 4-TRIMETHYL-1-PENTENE C5H15 256 7. 100 ... -422.97 332.56 p 33.58
277 2, 4, 4-TRIMETHYL-2-PENTENE C5H15 257 7.324 1. 13 -401. 90 358. 23 p 26.03
Monoo I ef t ns, Cg to C20
278 1-NONENE C9H18 259 7. 740 80.33 p -352.52 384.30 61 .57

279 1-0ECENE C10H20 260 7. 750 128.00 -380.48 371 .63 42.32
280 1-UNOECENE C11H22 261 7 .878 160.00 -403.36 361. 16 47.34
281 1-000ECENE C12H24 262 7.914 120. 00 -422. 35 350. 10 50.85
282 1-TRIOECENE C13H25 263 7. 760 175.00 s -438.48 341 .40 53.83
283 1-TETRAOECENE C14H25 264 7 .898 230. 00 -452. 13 335. 14 55.76
284 1-PENTAOECENE C15H30 265 7.994 ... -464.32 329. 72 60.42
285 1-HEXAOECENE C15H32 266 7. 783 ... -474. 73 328.85 57 .84
286 1-HEPTAOECENE C1 7H34 491 8.058 ... -483.91 324.67 56.61
287 1-0CTAOECENE C15H35 267 7 .515 ... -492. 16 320.95 55.51
288 1-NONAOECENE C19H35 492 8.093 ... -500.14 317. 63 54.04
289 1-EICOSENE C20H40 284 7 .870 ... -506.09 314.63 52.57
Otolef ins, C3 to C5
290 PROPAOIENE C3H4 301 7 .625 ... 2055. 53 2160. 02 ...

291 1, 2-8UTAOIENE C4H5 302 7 .851 ... 1297.90 1577. 30 55.34
292 1, 3-8UTAOI ENE C4H5 303 7. 260 ... 876. 71 1190. 10 63.46
293 1 ,2-PENTAOIENE C5H5 304 ... ... 887. 95 1294.44 ...
294 cis-1 ,3-PENTAOIENE C5H5 305 7 .830 ... 522.47 951 .91 35.59
295 toans-1, 3-PENTAOI ENE C5H5 306 7. 701 ... 478.63 921 .62 45.09
296 1 ,4-PENTAOIENE C5H5 307 7. 114 ... 871 .42 1079. 77 38.33
297 2,3-PENTAOIENE C5H5 308 ... ... 839.85 1257.20 ...
298 3-METHYL- 1, 2-8UTAOI ENE C5H5 311 ... . .. 814.67 1246 .54 . ..
299 2-METHYL- 1, 3-8UTAOI ENE C5H5 309 7 .496 -65.00 478.09 922.89 31 .08
Oiolefins, C5 to C10
300 2. 3-0IMETHYL-1, 3-8UTAOIENE 312 ... ... 221.59 p ... ...

I
C5H10
301 1 ,2-HEXAOIENE C5H10 630 ... ... -344.46 p ... . ..
1-104 1987
1C2.3
ASTM OCtane Numbers

Coefficient Anil lne Flammability Watson
of l!xpans ion Point Limits, Volume K Factor NO.
Percent in
deg r Motor Method Research Method Air Mixture
1 (av) D 357 0 908
v ar P
at 60 F Clear l ml Clear l ml
per deg F TEL TEL
per gal per gal
llfonoolefins. C5H15
0.000630 0.93 p 7. 16 p 12. 3 266

0.000540 65.5 80.5 71 .3 90.2 0.93 p 6.97 p 12.3 267
0.000640 0.93 p 6.64 p 12. 1 268
0.000640 0.90 p 6.88 p 12.2 269
0.000670 0.93 p 7. 16 p 12.3 270
0.000500 0.93 p 7. 16 p 12. 1 271
0.000680 83.6 88. 1 96.3 0.93 p 6.97 p 12. 2 272
0.000650 79.3 93. 1 97. 1 0.93 p 6.34 p 12.0 273
0.000630 88.0 +0.7 K 0.93 p 6.66 p 12. 3 274
0.000690 85.7 87. 2 +0.6 K +0.9 K 0.93 p 6.66 p 11.9 275
0.000630 86.5 88.8 +0.6 K +1 .0 K 0.90 p 6.28 p 12.2 276
0.000630 90.0 86.2 88.0 +0.3 K +0.6 K 0.90 p 6.40 p 12. 1 277
llonoolefins. C9 to C20
0.000590 100.4 0.80 p 6.41 p 12.4 278

0.000600 111 .4 0. 74 p 5.93 p 12.5 279
0.68 p 5.61 p 12. 5 280
0.62 p 5.42 p 12.5 281
0.57 p 5.35 p 12.6 282
0.53 p 5.39 p 12. 7 283
0.50 p 5.55 p 12. 7 284
0.47 p 5.84 p 12.8 285
0.44 p 6.26 p 12.8 286
0.41 p 6.86 p 12.9 287
0.39 p 7 .68 p 12.9 288
0.40 p 8. 77 p 13.0 289
Oiolafins. C3 to C5
2.10 12.6 290

0.000980 2.00 p 12.00 p 12. 2 291
0.001130 2.00 11.50 12.5 292
0.000830 1.59 p 11.9 293
0.000820 1.59 p 13.07 p 11.9 294
0.000850 1 .59 p 13.07 p 12. 1 295
0.000830 1.60 p 13. 12 p 12. 2 296
0.000830 1.59 p 11.9 297
0.000860 42.4 49.6 61 .0 71 .5 1.59 p 12.0 298
0.000860 81 .0 79.4 99. 1 98.8 2.00 9.00 12.0 299
Diolefins. Cs to C1Q
0.000720 I 1.31 p
11 .6
11 .9
300
301
1987 1-105
1C2.3

Search Solubility Point Heat ot Gibbs Pree Pus ion
(Cal/cml}l/ 2 deg F at 77 F Formation Btu/lb
Btu/lb at 77 F
Btu/lb
Oio1efins. Cs to C10
302 1,5-HEXAD!ENE C5H1Q 310 ... ... 441.90 p ... . ..

303 2,3-HEXADIENE C5H10 631 ... ... 1118.99 p ... ...
304 3-METHVL-1, 2-PENTADI ENE C5H10 632 ... ... 358.69 p ... ...
305 2-METHVL-1,5-HEXAO!ENE C7H12 633 ... ... 455. 26 p ... . ..
306 2-METHVL-2 ,4-HEXAO!ENE C7H12 634 ... ... 280. 38 p ... . ..
307 2,6-0CTADIENE C8H14 635 ... ... 180.21 p ... ...
308 2, 6-0!METHVL-1, 5-HEPTADI ENE C9H15 636 ... ... 32. 72 p ... . ..
309 3, 7-0!METHVL-1,6-0CTADIENE C10H18 637 ... ... -225. 75 p ... . ..
1-106 1987
1C2.3
ASTM Octane Numbers

Coett le lent Aniline Flammability Watson
ot l!:xpans ion Point Limits, Volume K Factor No.
Percent in
1 (av) D 357 D 908
v ar P
par deg F TEL TEL
per gal per gal
Oiolefi ns, c 6 to C10
0.000780 37.6 43.3 71. 1 80.7 1.31 p 10.91 p 12. 1 302

0.000850 1. 31 p 12. 4 303
0.000810 1 .31 p 11 .8 304
0.000710 1.11 p 9.23 p 12.0 305
0.000580 1.11 p 9.00 p 11 .8 306
0.000580 0.97 p 7 .97 p 12.0 307
0.000530 0.86 p 7.03 p 11 .8 308
0.000560 0. 77 p 6.31 p 12., 309
1987 1-107
1C2.4
TABLE 1C2.4
CYCLOOLEFINS AND ACETYLENES-SECONDARY PROPERTIES

(Cal/cm 3 ) l/2 deg F at 77 F Format ion Btu/lb
Btu/lb at 77 F
Btu/lb
A I ky I eye l opentenes. C5 to Ca
310 CYCLOPENTENE C5Ha 269 a.3a7 -20.00 201.a2 699. 26 21. 23

311 1 -ME THYL-CYCLOPENTENE CsH10 620 ... . .. 449. 13 p . .. . ..
312 1-ETHYLCYCLOPENTENE C7H12 621 ... ... -100.25 p . .. . ..
313 3-ETHYLCYCLOPENTENE C7H12 622 ... ... -195.65 p . .. . ..
314 1-n-PROPYLCYCLOPENTENE C9H14 623 ... ... -173.52 p . .. . ..
A 1ky1 c ye l ohexenes, Cs to Ca
315 CYCLOHEXENE CsH10 270 a.610 20.00 -2a.03 550.04 17. 24

271 ... ... -162.35 p . .. . ..
I
316 1 -ME THYLCYCLOHEXENE C7H12
317 1-E THYLCYCLOHEXENE C9H14 272 a.510 ... -219.3a p . .. . ..
Cyc 1 ic Diol ef ins. C5 and C10
... a50.72 1122.36 p . ..

I
31a eve LOPENTADI ENE C5Hs 315 a.274
319 DICYCLOPENTADIENE C10H12 316 a.613 90.00 409.a2 p 992. 21 p 1 .63
Cyclk Unsaturates. C10H16
320
321
I a I pha-PINENE
beta-PINENE
C10H16
C10H15
a40
a41
7 .a21
a. 197
91 .40
103.00
a9.31
122. 13
sa1 .65 p
...
...
. ..
Acety 1enes. C2 to C4
322 ACETYLENE C2H2 401 5.023 0.00 3743. 63 3453.91 62. 1a

323 METHYLACE TYL ENE C3H4 402 a. 165 ... 19ao. 16 201a. 14 . ..
324 DI METHYLACE TY LENE C4Hs 403 a.53a ... 1162.95 1472. 02 73. 39
325 ETHYLACETYLENE C4H6 404 7.a33 ... 1312.93 160a. 34 47. 92
326 VINYLACETYLENE C4H4 41a ... ... 2514. 70 2526. 10 . ..
Acety 1enes. C5 to C10
327 1-PENTYNE C5Ha 405 ... ... 911 .02 1324.50 . ..

32a 2-PENTYNE C5Ha 412 ... ... a13.31 1225. 50 . ..
329 3-METHYL-1-BUTYNE C5Ha 411 ... . .. aso.a5 1297.00 . ..
330 1 - HEXYNE CsH10 413 ... ... 647. 04 1144.54 . ..
331 1-HEPTYNE C7H12 414 ... ... 460.50 1014.79 . ..
332 1-0CTYNE CaH14 416 ... ... 321 .56 91a.36 . ..
333 1 -NONYNE C9H16 395 ... ... 213.a6 a43. 37 . ..
334 1 -OECYNE C10H1a 396 ... ... 12a. 16 7a3.97 . ..
1-108 1987
1C2.4
ASTN Octane Numbers

Coett le lent Aniline Flammability Watson
Percent in
de9 F Motor Method Research Method Air Mixture
1
v (E-J
ar P
D 357 D 90a

at 60 F Clear 3 ml Clear l ml
per de9 F TEL TEL
per gal per gal
Alkylcyclopentenes. C5 to Ca
0 .0001ao -14.0 69. 7 73.4 93.3 94.a 1 .59 p 12. 13 p 10.7 310
0 .ooosao 19.4 72.9 77. 1 93.6 97 .0 1 .31 p 9.a2 p 10.9 311
0.000650 34. 2 72.0 1a. 2 90.3 95. 7 1.11 p a.3a p ,, .0 312
0.000640 71 .4 76.6 90.a 96.5 1.11 p a. 71 p 11.1 313
0.000550 57 .6 0.97 p 7 .35 p 11. 2 314
Alkylcyclohexenes, C5 to Ca
0.000660 -4.0 63.0 sa. 1 a3.9 aa.4 1 .31 p 10.06 p 10.6 315
0.000660
0.000570 I I 72.0
70.5
75.6
75.4
a9.2
a5.0
92. 7
91.2
1 .11 p
0.97 p
a.3a p
7.35 p
10.a
10.9
316
317
Cyclic Oiolefins, C5 and C10
1. 71 p 14.61 p 10.3 31a

I I 1 .00 a.39 p 9.5 319
Cyc\ ic Unsaturates, C10H16
o.ao p 6.57 p 10.6 320

I o.ao p 6.67 p 10.6 321
Ac et y 1 en es, C2 to C4
2.50 ao.oo 16. 7 322

1. 70 57.2a p 12.3 323
o.oooa10 70.2 71 .5 a5.9 as.4 2.02 p 41 .a4 p 11. 7 324
2.02 p 32.93 p 12. 1 325
2.22 p 54.93 p 326
Ac et y 1en es, C5 to C10
o.oooa10 1 .59 p 22.33 p 11 .a 327

o.oooaoo 1 .59 p 25.32 p 11. 7 32a
329
0.000760 1 .31 p 16.61 p 11 .8 330
0.000690 1.11 p 10.ao p 11 .9 331
0.000610 51 .5 66. 1 50.5 75.9 0.97 p 10.91 p 11 .9 332
0 .000620 o.as p 9.39 p 12.0 333
0.0005ao o.a2 p a.35 p 12. 1 334
1987 1-109
1C2.5
TABLE 1C2.5
BENZENE DERIVATIVES-SECONDARY PROPERTIES
Pl uh Ideal Gas Ideal Gas Heat of

Search Solubility Point Heat of Gibbs PrH Pus ion
No. Compound Formula Number Parameter Temperature Formation Bnergy of at 77 deg P
(Cal/cml)l/2 deg P at 77 P Formation Btu/lb
Btu/lb at 77 P
Btu/lb
A 1ky l benzenes, c6 and C7
BENZENE 501 9.144 12.00 456.46 713.63 54.30

I
335 C5H5
336 TOLUENE C7H9 502 8.969 40.00 234.10 570.61 30.96
A1ky1 benzenes, C9H10
337 ETHVLBENZENE C9H10 504 B.821 59.00 120.64 528. 77 37 .19

338 a-XYLENE C9H10 505 9.018 83.00 76.92 494.36 55.06
339 m-XVLENE C9H10 506 B.842 77.00 70.14 481.28 46.85
340 p-XVLENE C9H10 507 B. 722 77 .00 73.01 491.09 69.30
Alkylbenzenes, C9H12
341 n-PROPVLBENZENE C9H12 509 8. 705 88.00 28.26 493.95 33. 15

342 I SOPROPVLBENZENE C9H12 510 B.561 111.00 14.07 496.82 27.85
343 o-ETHVL TOLUENE C9H12 511 B.804 ... 4.65 469.30 35.63
344 m-ETHVL TOLUENE C9H12 512 8. 726 ... -6.44 452. 27 27.24
345 p-ETHVL TOLUENE C9H12 513 B.723 107.60 p -11.45 465.40 47. 77
346 1, 2, 3-TRIMETHVLBENZENE C9H12 514 B.968 123.98 -33 .98 446.40 29.26
347 1, 2, 4-TRI METHVLBENZENE C9H12 515 8. 773 113.90 -49. 36 418.50 47. 19
348 1,3,5-TRIMETHVLBENZENE C9H12 516 8. 765 111.92 -56.87 422.44 34.03
Alkyl benzenes, C10H14
349 n-BUTVLBENZENE C10H14 518 B.530 160.00 -42 .09 465.86 35.94
350 I SOBUTVLBENZENE C10H14 519 B.308 131.00 -65 .15 448.44 40.07
351 sec-BUTVLBENZENE C10H14 520 B.520 128.00 -54. 13 465.10 31.49
352 tert-BUTVLBENZENE C10H14 521 8.422 140.00 -69. 28 480. 15 26.88
353 1-METHVL-2-n-PROPVLBENZENE C10H14 584 8.817 ... -63.36 451.64 47 .31
354 1 -METHV L-3-n-PROPV LBENZ ENE C10H14 585 8. 700 ... -77. 32 433 .06 33.91
355 1-METHVL-4-n-PROPVLBENZENE C10H14 586 B.675 ... -74. 12 442 .67 36.86
356 o-CVMENE C10H14 522 B.498 127.40 p -72 .62 451 .64 32.03
357 m-CVM6NE C10H14 523 B.374 122.00 p -91 .93 427 .94 43.82
358 p-CVMENE C10H14 524 8.495 117.00 -88.86 437 .23 30.94
359 o-OIETHVLBENZENE C10H14 525 B.684 135.00 -50.39 461.89 53. 74
360 m-OIETHVLBENZENE C10H14 526 8.639 133.00 -67. 27 441.07 35.13
361 p-01 ETHVLBENZENE C10H14 527 8.572 134.00 -65. 25 448.76 33.91
362 1 ,2-0IMETHVL-3-ETHVLBENZENE C10H14 580 B.948 149.00 p -82 .16 443.31 43.69
363 1, 2-0IMETHVL-4-ETHVLBENZENE C10H14 581 B.931 ... -102.79 408.0B 38.60
364 1 ,3-0IMETHVL-2-ETHVLBENZENE C10H14 582 9.008 ... -84.02 441. 71 47.11
365 1 ,3-0IMETHVL-4-ETHVLBENZENE C10H14 583 8.885 ... -98.86 411.92 41.41
366 1,3-0IMETHVL-5-ETHVLBENZENE C10H14 528 8.752 ... -113.39 p 407 .44 28.68
387 1, 4-0IMETHVL-2-E THVLBENZENE C10H14 529 B.837 ... -103.08 407. 76 48.65
368 1, 2, 3, 4-TETRAMETHVLBENZENE C10H14 530 9.367 ... -105.86 424.09 35.97
369 1, 2, 3, 5-TETRAMETHVLBENZENE C10H14 531 9.175 ... -129 .86 394 .30 34.32
370 1, 2 ,4, 5-TETRAMETHVLBENZENE C10H14 532 ... 130.00 -142.73 385 .34 67.28
1-110 1987
1C2.5
ASTM Octane Numbers

Coefficient Aniline Fla-bility Watson
of Bxpansion Point Limits, Volwne It Factor No.
Percent in
1 deg F Motor Method Research Method Air Mixture
(av) D 357 D 908
v (lT p
at 60 p Clear 3 ml Clear 3 ml
per deg P TEL Tl!L
per gal per gal
A 1ky I benzenes. Cs and C7
0.000660
0.000600 I -22 .0
-22 .0
+2.8 K
+O. 3 K
...
+1. 7 K
...
+S.B K
...
...
L40
, .20
1. io
1. io
9.7
io.,
33S
336
A I ky I benzenes, CaHio
0.000S40 -22 .o 97 .9 +0.2 K +0.8 K +0.8 K , .00 6. 70 io.3 337

0.000S50 -4.0 ioo. ioo. ... ... LOO 6.00 io.3 338
0.000540 -22 .0 +2.8 K +6.0 K +4.0 K +6.0 K i. io 7.00 io.4 339
0.000540 -22 .0 +1.2 K +5.1 K +3,4 K >+6.0 K i. io 7 .00 io.4 340
A 1ky I benzenes. C9Hi2
0.000540 -22 .0 98. 7 +2.0 K +1 .5 K +4.3 K a.ea p 8.S7 p io.6 34i

O.OOOS40 s.o 99.3 +0.5 K +2 .1 K +4.3 K a.ea 6.SO io.s 342
0.000500 ... 92., 92.9 +0.2 K +0.3 K 0.93 p B.S9 p i0.4 343
0 .OOOS40 ... ioo. ... +1 .8 K ... 0.93 p 6.89 p io.s 344
o. OOOS40 ... 97.0 ... .. . ... 0.93 p 6.89 p io. 1 34S
0.0004SO ... +.06 K +.OS K +0.S K +O .S K a.ea p 8.62 p io.4 346
0.000490 ... +0.6 K +0.6 K +1 .4 K +1 .5 K a.ea p B.82 p io.s 347
0.000540 -22 .0 +0.6 K ... >+6,0 K . .. 0.93 p 8.62 p io.6 348
A 1ky I benzenes, Ci0Hi4
0.000540 -22.0 94.S +0., K +0.4 K +LS K a.so s.ao io.a 349
0,000S30 ... 98.0 +0,3 K +LS K +3,0 K a.so 6.00 io.a 3SO
0.000S40 ... 9S. 7 +0., K +0.7 K +LS K a.so 6.90 io. 7 3Si
O,OOOS40 ... +a.a K ... >+3.0 K ... 0.70 s. 70 io.s 3S2
0.000490 ... 92 .2 9S. 7 +0.3 K +0.6 K 0.82 p 7. 74 p io. 7 3S3
0.000540 ... +.04 K +0.6 K +LS K +3.8 K 0.82 p 7. 74 p io.a 3S4
0.000540 ... ... ... ... ... 0.82 p 7. 74 p io.9 3SS
o.ooosso ... 96.0 97.7 +0.6 K +LS K 0.82 p 7,74 p io.s 3S6
0.000540 ... ... ... .. . .. . 0.82 p 7. 74 p io.a 3S7
0.000540 ... 97. 7 ... +1 .4 K .. . 0. 70 S.60 io.a 3SB
o.ooosoo ... . .. ... ... ... 0.82 p 7. 74 p io.s 3S9
O.OOOS40 ... 97 .0 +O. 2 K >+3.0 K >+3.0 K 0.82 p 7. 74 p io.a 360
O.OOOS40 ... 9S.2 99.3 +0.6 K +1 .6 K a.so s. io io.a 36,
O.OOOS60 ... 9i .9 93.3 +0.4 K +0.4 K a.so p 7. 73 p io.s 362
o.ooosso ... ... .. . ... ... 0.82 p 7. 73 p io.1 383
0.000560 ... ... .. . . .. ... 0.82 p 7. 73 p io.s 364
o.ooosso ... 9S.9 98.8 +0.6 K +L 2 K 0.82 p 7. 73 p io.1 36S
0.000S40 ... +0.2 K +0.8 K +2. 7 K >+6.0 K 0.82 p 7. 73 p io.a 366
0.000490 ... 96.0 98.9 +0.6 K +0.9 K 0.82 p 7,73 p io.s 387
0.0004SO ... +.02 K 99.7 K ..0.5 K +0.S K 0.82 p 7. 72 p io.s 368
o.ooosoo ... +0.2 K ... .. . ... 0.82 p 7. 72 p io.a 389
0.000440 ... ... . .. .. . ... 0.82 p 7. 72 p io.s 370
1987 1-111
1C2.5

Ro. Compound Formula Number Parameter Temperature Formation Energy ot at 77 deg F
Btu/lb at 77 F
Btu/lb
Alkyl benzenes. C11 to C22
371 n-PENTYLBENZENE C11H15 567 B.945 ... -9B .31 445.44 44. 19
372 n-HEXYLBENZENE C12H1B 56B 8.433 1B1.13 s -144.66 42B .94 48.77
373 n-HEPTYLBENZENE C13H20 549 B.499 ... -183.63 415.05 53.06
374 n-OCTYLSENZENE C14H22 569 B.493 ... -217.0B 403.20 56. 71
375 n-NONYLBENZENE C15H24 570 B.491 ... -245.72 392 .9B 60.74
378 n-OECYLBENZENE C15H25 554 8 .329 225.00 -270. 70 384. 10 64.25
377 n-UNOECYLBENZENE C17H2B 571 B.484 ... -292 .B4 376.26 67.34
378 n-OODECYLBENZENE C1BH30 574 8.370 2B5.00 -312.28 369.35 70.07
379 n-TRIOECYLBENZENE C19H32 572 B.294 ... -329.63 363. 14 72.52
380 n-TETRADECYLBENZEN E C20H34 573 B.477 ... -345.21 357. 58 74.71
381 n-PEN TAOECYLBEN ZENE C21H35 5BB B.475 ... ·359.42 352.56 76.69
3B2 n-HEXADECYLBEN ZEN E C22H3B 5B9 B.473 ... -372. 1B 348.01 78.48
Cycl ohexy 1benzene. C12H15
383 I CYCLOHEXYLBENZENE C12H15 557 9.053 210.00 -56. 12 p 491.74 p 40.97
A 1keny I benzene•, c8 to c10

384 STYRENE ca He 601 9.351 90.00 60B.29 BB2.56 45.20
385 c1s-1-PROPENYL BENZENE C9H10 646 ... ... 441 .40 789 .05 ...
386 trana-1-PROPENYL BENZENE C9H10 647 ... ... 426. 1B 777 .4B ...
387 2-PROPENYL BENZENE C9H10 613 B.B94 129.00 410.97 75B.63 ...
3BB 1-METHYL-2-ETHENYL BENZENE C9H10 602 9. 107 ... 430. 75 77B.39 ...
3B9 1-METHYL-3-ETHENYL BENZENE C9H10 603 9.025 ... 420.09 761 .34 ...
390 1-METHYL-4-ETHENYL BENZENE C9H10 604 9.043 ... 417 .05 746.69 ...
391 1-METHYL-4- ( trana-
1-n-PROPENYL )BENZENE C10H12 64B ... . .. 346.69 p . .. ...
392 1-ETHYL-2-ETHENYL BENZENE C10H12 605 ... ... 346.42 p ... ...
395 2-PHENYL- 1-BUTENE C10H12 690 ... ... 342.BB p . .. ...
Pheny 1benzenea, C12 to C14
39B BI PHENYL C12H10 55B ... 235.00 507 .65 760.B3 51. 79
397 1 -METHYL-2-PHENYLBENZENE C13H12 655 ... ... 1BB.29 p ... ...
39B 1 -METHYL-3-PHENYLBENZENE C13H12 656 ... 32.00 352.30 p ... ...
399 1 -METHYL-4-PHENYLBENZENE C13H12 657 ... ... 352.30 p . .. ...
400 1-ETHYL-4-PHENYLBENZENE C14H14 659 ... ... 349.5B p ... ...
401 1-METHYL-4(4-METHYLPHENYL) -
·BENZENE C14H14 65B ... . .. 325.20 p . .. ...
01pheny 1a I kanea, C13 to C24
402
I O!PHENYLMETHANE C13H12 563 9.0B1 266.00 393.53 712.96 p 4B.B2 s
1-112 1987
1C2.5
ASTM Octane Numbers

CO.fflclent Aniline Flammability Watson
of bpanslon Point Limits, Volume I<. Factor No.
Percent in
1(av) D 357 o 908
v ar P
at 60 P Clear 3 ml Clear 3 ml
per deg P TEL TEL
per gal per gal
A 1ky 1ben.zenes. C11 to C22
0. 74 7. 18 11 .0 371
0. 70 6.81 11. 2 372
0.62 p 6.62 ,, .4 373
0.57 p 6.59 11 .5 374
0.53 6. 70 11 .6 375
0.50 6.97 11 .8 376
0.46 p 7.41 12.0 377
0.44 p 8.06 12 .o 378
0.40 p 8.94 p 12.0 379
0.39 10. 14 p 12. 1 380
0.37 11. 75 p 12 .2 381
0.35 p 13.90 p 12 .3 382
Cyc 1ohex11 benzene. C12H15
I I 0.69 p 7 .28 p 10.3 383
A 1keny1 benzenes. c 8 to C10
0.000570 +0.2 +O. 1 K >+3.0 K +2.5 K 1. 10 6. 10 10.0 384

0.000570 91.7 +0.5 K +0.5 K 0.97 p 9.45 10. 1 385
0.000570 92. 1 91 .4 +0.4 K +0.4 K 0.97 p 9.45 p 10.3 386
0.000570 +O. 1 K 100. +2., K +1 .8 K 1 .90 6.10 10. 1 387
0.000520 0.97 p 9.45 p 10. 1 388
0.000480 0.97 9.45 p 10. 1 389
0.000520 0.97 9.45 p 10.0 390
0.000510 0.85 8.55 p 10.4 391

0.000510 0.85 10.3 392
0.000560 0.85 p 10.5 393
0.000560 0.85 10.5 394
0.000560 0.85 8.49 p 10.4 395
Pheny 1benzenes. C12 to C14
0.60 5.80 9.6 396

0.69 p 8. 76 9.7 397
0.69 8.76 9.8 398
0.69 8. 76 9.0 399
0.63 p 8.58 9.6 400
0.63 p 8.67 9.0 401
01pheny 1a1 kanes. C13 to C24
I I 0.69 p 8.66 p 9.8 402
1987 1-113
1C2.5
Flash Ideal Gas Ideal Gas Heat ot'

(Cal/cmli 11 2 deg F at 77 F Format ion Btu/lb
Btu/lb at 77 F
Btu/lb
Oiphenylalkanaa, C13 to C24
403 1,1-0IPHENYLETHANE C14H14 562 9.227 264.00 273.62 477 .31 p 41.45
404 1, 2-0IPHENYLETHANE C14H14 564 ... 264.00 337 .31 679.35 p 72.05
405 1, 1-0IPHENYLPROPANE C15H15 666 ... ... ... .. . ...
406 1, 2-0IPHENYLPROPANE C15H15 667 ... ... 254.30 p ... ...
407 1,1-0IPHENYLBUTANE C15H18' 668 ... ... ... .. . ...
408 1, 1-0IPHENYLPENTANE C17H20 669 ... ... ... ... ...
409 1,1-0IPHENYLHEXANE C19H22 670 ... ... ... .. . . ..
410 1, 1-0IPHENYLHEPTANE C19H24 671 ... ... . .. ... ...
411 1, 1-0IPHENYLOCTANE C20H25 672 ... ... ... ... ...
412 1, 1-0IPHENYLNONANE C21 H2e 673 ... ... ... ... ...
413 1, 1-0IPHENYLOECANE C22H30 674 ... ... ... .. . ...
414 1, 1-0IPHENYLUNOECANE C23H32 680 ... ... ... .. . .. .
415 1, 1-0IPHENYLOOOECANE C24H34 675 ... ... ... ... .. .
416 1,1-0IPHENYLTRIOECANE C25H35 676 ... ... . .. ... ...
417 1, 1-0IPHENYL TETRAOECANE C25H39 677 ... ... ... .. . ...
418 1, 1-0IPHENYLRENTAOECANE C27H40 678 ... ... ... ... ...
419 1, 1-0IPHENYLHEXAOECANE C29H42 679 ... ... ... . .. ...
01phany1alkenea. C14H12
... ...
420
421 I cls-1,2-0IPHENYLETHENE
trans-1,2-0IPHENYLETHENE
C14H12
C14H12
735
736
7.813
... ...
584.81 p
574 .83 p
876.75 p
862.67 p 66.38
Phsnylalkynsa, Ce and C14
422
423 I PHENYLACETYLENE
OIPHENYLACETYLENE
C9H5
C14H10
691
424
...
...
...
...
356.81 p
1037 .51 p
...
1229.68 p
...
51.63
Di phany 1benzenea, C9H14
424 1, 2-0IPHENYLBENZENE C19H14 561 ... 325.00 516.27 p 789 .57 p 32.09
425
426 I 1,3-0IPHENYLBENZENE
1 ,4-0IPHENYLBENZENE
C1eH14
C19H14
560
559
...
...
375.00
405.00
516.27 p
516.27 p
789.57 p
791.46 p
44.97
62.96
1-114 1987
1C2.5
ASTM Octane Numbers

Coefficient Aniline Flamrnabil i ty Watson
of Expaos ion Point Limits, Volume It. Factor No.
Percent in
1 deg F Motor Method Research Method Air Mixture
(!{) 0 357 D 908
v ar P
With With Lower Up par
per deg F TEL TEL
par gal par gal
Di pheny 1•1 kanes. C13 to C74
0.60 p 8 .31 9.9 403

0.63 p 8.50 P 404
0.58 p 8.60 P 10.1 405
0.58 p 8.60 P 10.2 406
0.54 p 8.85 P 10.3 407
0.50 p g.31 p 10.5 408
0.47 p 10.03 p 10.6 409
0.44 p 11.03 p 10.8 410
0.42 p 12.41 10.9 411
0.40 p 14. 27 11.1 412
0.38 p 16. 77 11.3 413
414
0.34 p 24.6g p 11.4 415
0.34 p 24.40 p 11.5 416
0.34 p 24.13 p 11.6 417
0.34 p 23 .88 p , , .7 418
0.34 p 23.65 p , , .7 419
Oipheny la lkenes, C14H12
I I
0.65 p
0.65 p
8.98
8 .98 P
9.7 420
421
Phenyl•lkynes, Ca and C14
0.000480
I I
1. 17 p
0.67 p
16.34 p
11.63 p
9. 1 422
423
01pheny1 benzenes, C8H14
0.51 p 12.04 9.6 424

0.51 p 12.04 g.1 425
I I 0.51 p 12.04 9.6 426
1987 1-115
1C2.6
TABLE 1C2.6
CONDENSED RING AROMATICS AND DERIVATIVES-SECONDARY PROPERTIES

No. Compound Formula Number Parameter Temperature Formation Energy ot at 77 deg I'
Btu/lb at 77 F
Btu/lb
A I ky 1naphtha1 enes. C10 to C20
427 NAPHTHALENE C10H9 701 ... 176.00 505.09 751.70 63.66

428 1-METHYLNAPHTHALENE C11H10 702 9.864 ... 353.31 658. 18 21 .00
429 2-M ETHYLNAPHTHALEN E C11H10 703 ... . .. 351 .04 653.49 36.66
430 1-ETHYLNAPHTHALENE C12H12 704 ... . .. 891 .29 p . .. . ..
431 2-ETHYLNAPH THAL ENE C12H12 755 ... . .. -2. 19 p . .. . ..
432 1, 2-0IMETHYLNAPHTHALENE C12H12 756 ... . .. 202. 07 p . .. . ..
433 1 ,4-0IMETHYLNAPHTHALENE C12H12 757 ... . .. 168.45 p . .. . ..
434 1-n-PROPYLNAPHTHALENE C13H14 758 ... ... 154.58 p . .. . ..
435 2-n-PROPYLNAPHTHALENE C13H14 765 ... ... -148.77 p ... . ..
438 1-n-BUTYLNAPHTHALENE C14H15 759 ... ... 119.87 p . .. . ..
437 2-n-8UTYLNAPHTHAL ENE C14H15 766 ... ... 119.87 p . .. . ..
438 1-n-PENTYLNAPHTHALEN E C15H19 760 ... . .. 63.59 p . .. . ..
439 1-n-HEXYLNAPHTHALENE C15H20 761 ... . .. 14. 74 p ... . ..
440 2- n- HEXYLNAPH THALEN E C15H20 767 ... ... 59.39 p . .. . ..
441 1-n-HEPTYLNAPHTHALENE C17H22 769 ... ... -153. 77 p ... . ..
442 1-n-OCTYLNAPHTHALENE C19H24 762 ... . .. -26.41 p . .. . ..
443 1-n-NONYLNAPHTHALENE C19H25 711 8.405 ... -80.27 p 478. 72 p . ..
444 2-n- NONYLNAPHTHALEN E C19H25 768 ... ... -24.96 p . .. . ..
445 1-n-OECYLNAPHTHALENE C20H29 712 8.410 ... -109.23 p 467.02 p . ..
Tetrahydronaphtha 1en es. C10 to C20
448 1, 2 ,3 ,4-TETRAHYORO-
NAPHTHALENE C10H12 706 9.545 160.00 86.54 543.41 40.49
447 1-METHYL-[1,2,3,4-TETRA-
HYORONAPHTHAL ENE] C11H14 775 ... ... -108.25 p . .. . ..
448 1-ETHYL- [ 1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] C12H15 776 ... ... -43.44 p . .. . ..
449 2, 2-0UETHYL-[ 1, 2,3 ,4-TETRA-
HYORONAPHTHALENE I C12H15 777 ... ... -102.59 p ... . ..
450 2,6-0UETHYL-[ 1, 2,3, 4-TETRA-
HYORONAPHTHALENE] C12H15 778 ... ... -48.83 p . .. . ..
451 6, 7-0IMETHYL- [ 1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] C12H15 779 ... ... -125. 26 p . .. . ..
452 1-n-PROPYL-[1,2,3,4-TETRA-
HYORONAPHTHAL ENE] C13H15 780 ... ... -186.81 p . .. . ..
453 , 6-n-PROPYL- [ 1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] C13H19 781 ... . .. -196. 72 p ... . ..
454 1-n-BUTYL-[1,2,3,4-TETRA-
HYORONAPHTHALENE] C14H20 787 ... . .. ... . .. . ..
455 6-n-8UTYL- [ 1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] C14H20 788 ... ... . .. . .. . ..
458 1-n-PENTYL-[1,2,3,4-TETRA-
HYORONAPHTHALENE] C15H22 789 ... ... . .. . .. . ..
1-116 1987
1C2.6
ASTM octane Numbers

Coefflclent Anlllne Flammability Watson
of Bxpans lon Point Limits, Volume K Pactor No.
Percent in
1 (av l deg P Motor Method Research Method Air Mixture
D 357 D 908
v ar P
With Wlth Lower Upper
at 60 F Clear l ml Clear l ml
per deg F TBL TEL
per gal per gal
A I ky I naphtha I enes, C10 to C20
0.000190 0.88 5.90 9.3 427

0.82 p 9.18 p 9.5 428
0.82 p 9.18 p 9.8 429
0. 74 p 8.56 p 9.7 430
0. 74 p 8.56 p 8.0 431
0. 74 p 8.68 p 9.8 432
0. 74 p 8.68 p 9.9 433
0.67 p 8.06 p 10.1 434
0.67 p 8.06 p 10.3 435
0.62 p 8.05 p 10.2 436
0.62 p 8.05 p 10.2 437
0.57 p 8.09 p 10.6 438
0.53 p 8.33 p 10.8 439
0.53 p 8.56 p 10.8 440
0.49 p 8.77 p 10.9 441
0.46 p 9.45 p 11.1 442
0.40 p 10.42 p 11.1 443
0.44 p 10.62 p 11.1 444
0.41 p 11. 73 p 11.3 445
Tetr"ahydr"onaphtha 1enes. C10 to C20
0.000430 -4.0 81.9 84.0 96.4 100. 0.84 5.00 9.8 446
0. 77 p 7. 73 p 10.1 447
0.69 p 7.29 p 10.3 448
0.69 p 7.06 p 10.4 449
7.29 p 10.4 450
7.22 p 10.4 451
7.04 p 10.5 452
6.97 p 10.6 453
10.6 454
10.7 455
10.8 456
1987 1-117
1C2.6
Flash Ideal Gae Ideal Gas Heat ot

Search Solubility Point Heat of Gibbs Pree Pue ion
No. Compound Formula Number Parameter Temperature Formation l!ner9y of at 77 de9 F
(Cal/cml)l/2 de9 F at 77 F Formation Btu/lb
Btu/lb at 77 F
Btu/lb
Tetrahydr"'onaphthe 1enes. C10 to C20
457 6-n-PENTYL- [ 1, 2, 3, 4-TETRA-

HYDRONAPHTHALENE] C15H22 7go ... ... ... . .. . ..
45B 1-n-HEXYL-( 1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] C15H24 7B2 ... ... -21g.05 p . .. . ..
45g 1-n-HEPTYL- [ 1 , 2, 3, 4-TETRA-
HYORONAPHTHALENE] C17H25 7B3 ... . .. -244. 3B p . .. . ..
460 1-n-OCTYL-[ 1, 2, 3, 4-TETRA-
HYDRONAPHTHALENE] c1BH2B 7B4 ... ... -266. 7B p . .. . ..
461 1-n-NONYL- [ 1, 2, 3 ,4-TETRA-
HYORONAPHTHALENE] C1gH30 7B5 ... ... -2Bg. 26 p . .. . ..
462 1-n-DECYL-[ 1, 2, 3 ,4-TETRA-
HYDRONAPHTHALENE] C20H32 7B6 ... ... -303.g5 p . .. . ..
Indene•. Cg to c 1o
463 INDENE CgHB B03 10.006 ... 604.32 B65.g5 37. 75
464
465 I 1-WETHYLI NDENE
2-WETHYLINOENE
C10H10
C10H10
723
724
...
...
. ..
...
2gB.03 p
413_g5 p
. ..
. ..
. ..
. ..
D1hyd,..o1ndenee. Cg to c 10
466 2, 3-DI HYDROINDENE CgH10 742 ... ... 545.52 p ... . ..

467 1-WETHYL-2, 3-DI HYDRO I NDENE C10H12 743 ... ... 10B.03 p . .. . ..
468 2-WETHYL-2, 3-DI HYDRO INDENE C 10H12 744 ... . .. H.14 p . .. . ..
45g 4-WETHYL-2, 3-DI HYDRO I NDENE C10H12 745 ... ... H.14 p . .. . ..
470 5-WETHYL-2, 3-DI HYDRO INDENE C 10H12 746 ... ... -3.67 p . .. . ..
Conde need R1ng Aroma t 1ca. C12 to C1B
471 ACENAPHTHALENE C12HB 764 ... . .. 733.33 g26. 55 1g.60

472 ACENAPHTHENE C12H10 BOB ... . .. 432. 13 725.42 5g_B3
473 FLUORENE C13H10 73B ... ... 4B3.41 750.34 50.64
474 ANTHRACENE C14H10 B04 ... 250 .00 555.04 BOO. 12 70.B5
475 PHENANTHRENE C14H10 B05 ... 340.00 4gg_55 743. 1g 3g_ 71
476 PYRENE C15H10 B07 ... 3go.oo 47B. 2B 5g5_ 10 36.go
477 FLUORANTHENE C15H10 717 ... ... 614.,, B20.94 3g_B1
47B CHRYSENE C1BH'2 B06 ... . .. 4g5_ 10 755.32 p 4g_34
1-118 1987
1C2.6
AS'l'll Octane Numbers

Coett icient Aniline Fla-..bllity Watson
of &xpans lon Point Limits, Volume K Factor No.
Percent in
de9 r Motor Method Research Method Air Mixture
1 (av) D 357 D 908
v ar P
at 60 r Clear 3 ml Clear 3 ml
per de9 r TEL TEL
per gal per gal
Tetrahydronapht~a 1enes. C10 to C20
10.g 457
7 .31 p 11.1 458
7.75 p 11.2 45g
8.3g p 11.4 460
g.2g p 11.5 461
10.48 p 11.6 462
Indanes, Cg to C10
0.000500 +O. 7 +0.4 +2.3 +1.4 K 1.01 p 10.2g p g.3 463

0.000240
0.000370 R I
01hydro1ndenea, Cg to C10
0.8g p
0.8g p
g.24 p
g.2g p
g.8
g.1
464
465
0.000420 8g.8 go.8 +0.3 +0.5 o.g1 p g.32 p g.8 466

0.000240 0.85 p 8.42 p 10.1 467
0.000530 0.85 p 8.42 p 10.1 468
o.0004go 0.85 p 8.3g p 10.0 45g
0.000530 0.85 p 8.3g p 10.0 470
Condenaed Ring Aromatics, C12 to C19
471
0. 76 p g.24 p 472
0. 71 p g.38 p 473
0.60 g.66 p 474
0.67 p g.66 p 475
0.60 p 11.13 p 476
0.60 p 11.13 p 477
0.53 p 12.82 p 478
1987 1-119
1C3.1-1 C3.3
TABLES 1C3.1-1C3.3
ACIDS, ALCOHOLS AND PHENOLS, AND ALDEHYDES.-PRIMARY PROPERTIES
Critical Constants
No. Compound Formula M,W, Boiling
Point
at Freezing Temp- Pressure Volume Compres- Acentr ic
l atm Point erature psia cu ft sibillty Factor
deg P in air dog P per lb Factor
at l
atm.
dog F
Table lCl.l Acids
700 FORMIC ACID CH202 48.03 2i3.01 47. 12 584.33 p 1071 .83 p 0.0435 p 0. 1g20 0.4730
701 ACETIC ACID C2H402 80.05 244.22 61 ,gg 607 .21 53g, 14 0.0456 0.2010 0.4824
702 PROPIONIC ACIO C3H502 74.08 28S.4g -5.26 624. 2g 5g5 .13 0.0480 0 .1830 0.5131
703 n-BUTYRIC ACID C4H502 88. 11 325,5g 22.64 670. 73 641.07P 0.0515 p 0. 2400 0.6041
704 2-METHYLPROPIONIC ACID C4H502 88.,, 310. 10 -so. g5 636.80 587.84 0.0531 0. 2340 0.6181
705 n-PENTANOIC ACID C5H1002 102. 13 365,go -2g.20 712. 13 552. 60 p 0.0527 p 0. 2370 0.626g
708 2-METHYL8UTVRIC ACID C5H1002 102. 13 350.60 ... 5g7. 73 p 564.20 p 0.0524 p 0. 2430 0.5892
707 3-METHYLBUTVRIC ACIO C5H1002 102. 13 347. 18 -20. 74 681 .53 564. 20 p 0.0527 p 0. 2480 0.6480
708 n-HEXANOIC ACID C5H1202 118. 18 402. 28 26.60 74Q,g3 p 485.88 p 0.0536 p 0. 2350 0.6701
Table lCJ.2 Alcohols and Phenols
709 METHANOL CH40 32.04 148.48 -143.82 462 ,g7 1174.21 0.058g 0.2240 0.5656
710 ETHANOL C2H50 48.07 172. g2 -173.38 45g,55 g25 .85 0.0580 0. 2480 0.6371
711 n-PROPANOL C3H50 80. 10 205,g5 -1g5, 16 506.41 74g. 7g 0.0582 0. 2530 0 .627g
712 ISOPROPANOL C3H50 60. 10 180.07 -126.17 p 455. 2g 5g1 .01 0.0587 o. 2480 0.668g
713 n-8UTANOL C4H100 74, 12 243. 7g -128.74 553 .60 640.01 o.o5g3 0. 2sgo Q,5g45
714 ISOBUTANOL C4H100 74, 12 225. 7g -162.40 526. 24 622 ,g6 0.0588 0. 2570 0.5885
715 Hc-8UTANOL C4H100 74, 12 211. 1g -174.46 505. 15 608. 27 0.057g 0. 2520 0.5711
718 te,.t-BUTANOL C4H100 74, 12 180.38 78. 48 p 451 ,4g 576.08 o.05g4 0. 2600 0.6158
717 1-PENTANOL C5H120 88. 15 280 .04 -107.66 p 5g5,40 562. 75 p o.o5g2 p 0. 2600 Q,5g35
718 2-PENTANOL C5H120 88. 15 248. 20 -gg .67 533 ,g3 p 562. 75 p o.o5g4 p 0. 2760 0.6746
719 2-METHYL- 1-8UTANOL C5H120 88. 15 283.68 -477 .65 557.33 p 562. 75 p 0 ,05g4 p 0. 2700 0.6784
720 2-METHYL-2-8UTANOL C5H120 88. 15 215.60 16. 16 521 .60 562. 75 p O,Q5g4 p 0. 2800 0.4831
721 3-METHYL-2-8UTANOL C5H120 88. 15 232. 70 ... 573. 53 p 574. 35 p o.05g4 p 0. 2710 0.3510
722 2. 2-0IMETHYL- 1-PROPANOL C5H120 88. 15 235. 58 129. 20 530.33 p 562. 75 p o.o5g4 p 0. 2770 0.6036
723 4- METHYL-2-PENTANOL C5H140 102. 18 25g .08 ... 574. 25 503. 28 p o.o5g6 p o. 2760 0. 5723
724 PHENOL C5H50 g4,,, 35g,31 105.64 p 75g ,g8 55g,05 Q_Q3go 0. 2430 0. 425g
725 o-CRESOL C7H50 108. 14 375.81 87 .87 p 7g5 ,g2 725_g5 0.0418 Q_ 2430 0.4335
728 m-CRESOL C7H50 108. 14 3g5,09 54.03 p 810.86 661 .37 0.0462 Q_ 2420 o,44g3
727 p-CRESOL C7H50 108. 14 3g5, 57 g4_6Q p 808. 70 746. g5 0.0410 0. 2440 0.5134
Table lCl.3 Aldehydes
728 FORMALOEHYOE CH20 30.03 -2. 38 -133.60 274.73 p g55. 24 p 0.0560 p 0. 2040 0.2816
72g ACETALDEHYOE C2H40 44,05 68. 72 -18g,40 370. 13 804,g6 p 0.0571 p 0. 2270 0.3187
730 n-PROPIONALDEHYDE C3H50 58.08 118.40 -112.00 433 - 13 p 675.88 p 0.0579 p 0. 2370 0.3015
731 n-8UTYAALDEHV0£ C4H50 72.,, 166.64 -141 .52 485. 33 p 580.15 p 0.0584 p 0. 2410 0. 3445
732 ACROLEIN C3H40 56.08 126.84 -125.86 451. 13 p 725. 1g p 0.0563 p 0. 2340 0.31g8
733 tr-ans-CAOTONALDEHYDE C4H50 70.09 21g,35 -105. 70 568.13 p 616.41 p 0.0571 p o. 2240 0. 3455
734 METHACROLEIN C4H50 10.og 154.40 -113.80 4g4,33 p 616.41 p 0.0571 p 0.2410 0. 2456
1-120 1987
1C3.1-1C3.3
TABLES 1C3.1-1C3.3 (Continued)
Spec Lt le API ty
Demi i Refractive Vapor Heat Capacity Kinematic Heat of Net Heat ot Sur race
Gravity Gravity of the IndelC Pressure at 60 F and Con- Viscosity of the vapor iza- Combustion Tens ion
60/60 at 60 F Liquid of the at 100 F st ant Pressure Liquid t ion at ot Liquid of the No.
de9 API at 60 F Liquid psia Btu/lb de9 F centistokes Normal at 77 F Liquid
lb/9al at 77 F Boiling Btu/lb at 77 F
Point dyne/cm
Ideal Liquid Btu/lb
Gas at l
atm. at 100 F I at 210 F
Table lCJ.l Acids
1 .2263 -16. ,, 10.223 T 1 .36930 1 .4862 T 0. 2321 T 0.5118 T 1 .0535 0.4959 205.37 T 1975. 37 .07 T 700
1 .0537 2. 79 8. 184 T 1 .36980 0.6045 0. 2505 T 0.4813 0.9043 T 0.4816 T 167 .01 T 5630. 26.99 T 701
0.9996 10.05 8. 334 T 1. 38430 0. 1549 T 0. 2816 T 0.4843 0.8861 T 0.5018 T 191.16 T 8096. 26. 20 T 702
0.9824 15.53 8.023 T 1 .39580 0.0457 T ... 0.4733 1 .2806 0.6260 221 .00 T 9790. 26.08 T 703
0.9558 16.54 7.969 T 1 .39080 0.0827 T ... 0.4628 T 1 .0870 0.5689 208.46 9760. p 24.61 T 704
0.9431 18.53 7 .863 T 1 .40600 0.0130 T 0.3145 T 0.4816 T 1. 7190 T 0. 7889 T 204. 33 T 11014. 26.81 T 705
... ... . .. . .. ... . .. ... . .. 0.6831 T 195.83 T 11282. p . .. 706
0.9352 19.81 7. 796 T 1 .40220 0.0227 T ... . .. 1. 7475 T 0.7422 T 181 .95 T 11009. 25 .04 T 707
0.9293 20. 76 7. 748 T 1 .41480 0.0027 T ... 0.5341 T 2. 4009 1 .0339 192.91 T 11950. 26. 78 T 708
Table lCJ.2 Alcohols and Phenols
0. 7985 46. 15 6.641 T 1 .32652 4.6124 T 0.3229 T 0.5913 T 0.5942 T 0 .3269 T 471 .48 T 8562. 22. 16 T 709
0. 7967 46. 10 6.643 1 .35941 2. 3113 T 0. 3322 T 0.5631 1. 1031 T 0.4600 T 367. 72 T 11530. 21 .99 T 710
0.8111 42 .96 6. 762 T 1. 38370 0.8764 T 0.3391 T 0.5590 T 1.8470 T 0.6154 T 296.03 T 13191. 23 .40 T 711
0. 7925 47 .05 6.607 T 1. 37520 1 .8414 T 0.3442 T 0.5937 1.8698 T ... 285.23 T 13092. 21 .DO T 712
0.8147 42. 19 8. 792 T 1 .39710 0.3201 T 0.3468 T 0.5512 2. 3817 T 0. 7337 T 250.78 T 14246. 24.41 T 713
0.8052 44.24 6. 713 T 1. 39380 0.4852 T 0.3443 T 0.5615 T 2 .8730 T 0. 7527 T 252. 12 T 14205. 22 .56 T 714
0.8144 42 .26 6. 789 T 1 .39490 o. 7956 T 0.3513 T 0.8057 2 .5109 0.5835 237.59 T 14156. 23. 02 T 715
0. 7910 47 .39 6.586 R 1. 38520 1. 7591 T 0.3560 T ... 3 .0822 0.5471 232.67 T 14059. 19.81 T 716
0. 8203 41 .DO 6.839 T 1 .40800 o. 1221 T 0.3520 T 0.5495 3.0666 T 0.8839 T 218.66 T 14927. 25. 30 T 717
0.8152 42 .08 6. 796 T 1 .40440 O. 2856 T ... . .. 2.7296T 0.6675 T 21,. 73 T 14883. 23.45 T 718
0.8223 40.57 6.856 T 1 .40880 0. 1620 T ... 0.5846 T 3. 3928 0.8320 218. 24 T 14934. 25.05 T 719
0.8144 42 .26 6. 789 T 1 .40240 0. 7359 T ... 0.6476 T 2. 7205 0.6277 195.63 T 14823. 22. 31 T 720
0.8232 40.39 6.863 T 1 .40750 0.4296 T ... 0.5374 T 2.6799 T 0.6102 T 200.46 T 14886. 24.67 T 721
... ... . .. 1 .39150 . .. . .. . .. ... 1 .0707 T 201 .68 T 15117. p . .. 722
0.8139 42 .36 6. 785 T 1 .40900 0.2308 T ... . .. 3. 1204 0.6986 174.40 T 15406. p 22 .63 T 723
... ... . .. 1 .54960 R 0.0252 T 0. 2552 . .. ... 1 .3317 216. 14 T 13346. . .. 724
... ... . .. 1 .54420 R 0.0159 o. 2760 T . .. 4.4238 1 .0066 181 .55 T 13984. . .. 725
1 .0380 4.82 8.654 T 1 .53960 0.0086 T 0.2671 T 0.4883 T 8. 1505 1 .2461 193.53 T 14026. 35. 76 T 726
... ... . .. 1 .53910 R 0.0081 0. 2671 T . .. 6. 8174 1.3584 197 .32 T 14005. . .. 727
Table lCJ'. 3 Aldehydes
... . .. ... . .. 110. 1540T 0.2792 T . .. ... ... 331 .67 T 7438. . .. 728
0. 7868 48.33 6.560 T 1 .32830 26.8811 T 0. 2906 T 0.5814 T ... . .. 240. 38 T 10780. 19.53 T 729
0 .8087 43 .47 6. 742 T 1 .35930 10. 1329T 0 .3268 T o .5250 T 0.3606 T ... 212 .00 T 12478. 22.57 T 730
0.8081 43.60 6. 737 T 1. 37660 3. 7806T 0. 3363 T 0.5291 T 0.4738 T 0.3087 T 189.53 T 13734. 24.21 T 731
0.8453 35.90 7 .047 T 1 .40170 8.6990 T ... 0.5143 T 0 .3622 T . .. 222.64 T 11914. p 23. 14 T 732
0.8584 33.34 7. 157 T 1 .43730 1. 1405T ... 0.6420 T 0.4904 T 0.3253 T 213.49 T 13222. 25.66 T 733
0.8518 34.61 7. 102 T 1 .41690 4.9871 T ... 0.4420 T 0.4678 T . .. 182.45 T 13217. p 23.41 T 734
1987 1-121
1C3.4-1C3.6
TABLES 1C3.4-1C3.6
AMINES, OTHER NITROGEN-CONTAINING COMPOUNDS,
AND ESTERS-PRIMARY PROPERTIES
er it ical Constants
No. Compound Formula M.W. Boiling
Point
at Freezing Temp- Pressure Volume Com.pres- Acentr ic
l atm Point erature psia cu ft sibillty Factor
deg F in air deg F per lb Factor
at l
atm.
deg F
Table lCJ.4 Amines

735 METHYLAMINE CH5N 31 .06 20.61 -136. 23 314.42 1oe1 .63 0.0794 p 0.3210 a. 2e13
738 ETHYLAMINE C2H7N 45.oe 61 .e4 -113.eo 361 .40 e15.63 0.0647 a. 2100 a. 2e51
737 n-PAOPYLAMI NE C3H9N 59.,, 119.30 -117 .40 434.e4 6e7. 77 0.0705 p a. 29eo 0.2957
738 ISOPAOPYLAMINE C3H9N 59. 11 90 .32 -139.36 389.66 65e .3e 0.0599 a. 2550 a. 21e5
739 n-eUTYLAMINE C4H11N 73. 14 171. 32 -56 .3e 497. 75 609. 16 0.06e6 p a. 2910 a. 3295
740 ISOBUTYLAMINE C4H11N 73. 14 153.91 -120. 2e 465.04 p 611 .34 p 0.06e5 p 0.30e5 a. 3627
741 Hc-8UTYLAMINE C4H11N 73. 14 145.40 -156.01 466 .07 5e0.15P 0.0679 p a. 2900 a. 2e15
742 tert-BUTYLAMINE C4H11N 73. 14 ,,, .92 -ee.53 411.35 556. 95 a .0642 a. 2eoo a. 214e
Table lCJ.5 Other Nitrogen-Containing Compounds

743 UREA CH4N20 60.06 400.73 p 210.ee 845.33 p 979.01 p o.o5e1 p a. 2440 ...
744 ACETONITA! LE C2H3N 41 .05 11e.ee -46.e9 522. 23 701 .00 ... a. 1e40 0.33e2
745 MORPHOLINE C4H9NO e1. 12 262. 40 26.42 652. 73 p 774.50 p 0.0507 p a. 2e10 0.3583
7<1e PYRIDINE C5H5N 79. 10 239.47 -42.92 656. 24 e11. 10 0.0514 a. 21eo 0. 23e9
747 ANILINE C5H7N 93. 13 364.01 21. 16 p 79e.53 770.07 0.0464 a. 2410 0.4041
748 INDOLE C9H7N 117. 15 4e7.40 32.95 g52_33 p 623. 66 p 0.05e9 p a. 2820 a. 3742
749 QUINOLINE C9H7N 129. 16 459.68 5. 1e g4e. 20 675 .ee p 0.05e2 p 0.3360 0.32e7
750 OIBENZOPYRROLE C12H9N 167. 21 670.49 472.64 115e.53 p 472.e2 p 0.0462 p a. 2100 0.493e
751 ACAIOINE C13H9N 179. 22 654 .ea 234. 14 1169.60 522. 14 0.04e5 a. 2600 0.4300
Table lCJ.6 Baters

752 METHYL FORMATE C2H402 60.05 e9. 15 -146. 20 417. 29 e10 .00 0.0459 a. 25so a. 2531
753 METHYL ACETATE C3H502 74.oe 134.49 -144.40 452.57 680.42 0.0493 a. 2540 0.3254
754 ETHYL FORMATE C3H502 74.oe 129. 76 -111. 2e 455. 45 687. 77 a .0495 a. 2510 a. 2e4g
755 ETHYL ACETATE C4He02 e8. 11 170. 71 -11e.39 4e2. 1e 555.51 0.0520 0.2520 0.3611
75e n-PROPYL FORMATE C4He02 ee.,, 177 .48 -135. 22 50e. 73 5e9.31 0.051e a. 2590 0.31eo
757 VINYL ACETATE C4H502 e6.09 162.50 -135.04 4e3.53 p 616.41 p 0.0502 p a. 2e30 a. 33e4
7!58 METHYL n-eUTYAATE C5H1002 102. 13 216.95 -122.44 53e .43 503. 7e 0.0533 a. 2560 0.3e07
759 n-PROPYL ACETATE C5H1002 102. 13 214. 70 -139.00 529. 25 4e7.91 0.0541 a. 2540 0.3941
760 I SOPAOPYL AC ETA TE C5H1002 102. 13 191 .30 -100. 12 50e. 73 p 519. 24 p 0.0527 p a. 2590 a. 3550
1e1 n-eUTYL ACETATE C5H1202 116. 16 25e .ea -100.30 5e2.eo 45e.32 p 0.0536 p a. 2550 0.4167
1e2 n-PENTYL ACETATE C7H1402 130.19 300. 20 -95.44 616.73P 406. ,, p 0.0544 p a. 2490 a. 4896
1-122 1987
1C3.4-1 C3.6
Specific API D•nsity Refractive Vapor Heat Capacity Kinematic Heat of Net Heat of Surface
Gravity Gravity ot the Index Pressure at 60 F and Con- Viscosity ot the Vapori:a- Combustion Tension
60/60 at 60 r Liquid ot the at 100 F stant Pressure Liquid t ion at ot Liquid ot the No.
deg API at 60 r Liquid psia Btu/lb deg F centi stokes Norr1.al at 77 F Liquid
lb/gal at 77 F Boiling Btu/lb at 77 F
Point dyne/cm
Ideal Liquid Btu/lb
Gas at l
Table lCl.4 Allines

0.8681 80.29 5.570 T 1,34910 78. 3092 a. 3782 T ... 0.2681 T ... 361.45 T 13498. 19.41 T 735
a. 6888 73.93 5. 743 1 .36270 32. 0617 a. 3756 T 0.6393 T ... ... 260.81 T 15138. 19.58 T 736
a. 7241 63.92 6.037 T 1.38510 9.9739 T a. 3748 T 0.6599 T 0.4615 T ... 214.83 T 15745. 22 .49 T 737
0.8949 72.14 5. 793 T 1.37110 18.1660 T ... a .6587 T 0.4208 a. 2903 205.31 T 15686. 17 .40 T 738
a. 7498 57. 27 6.249 T 1. 39870 3.1899 T a. 3778 T a. 5762 T 0.6637 ... 189.03 T 16320. 24. 76 T 739
a. 7387 60.04 6.159 T 1.39450 4.7487 T ... a. 5932 T 0.6357 T ... 180.61 T 16293. 21. 70 T 740
a. 7293 62.51 6.081 T 1. 39070 5.8590 T ... a. 5550 T 0. 5804 T ... 176.39 T 16262. 21.11 T 741
a .8987 71.02 5.825 T 1.37610 11.7379 T ... 0.6228 T 0. 5619 T ... 162.28 T 16187. 16.86 T 742
Table lCJ.5 Other Ritr09en-Containing Coapounds

0.2594 T 3896. 743
a. 1900 47 .62 6.586 T 1.34160 3.0641 T 0.2991 T 0.5278 T 0.4082 317 .31 T 12467. 28.66 T 744
1,0055 9. 23 8. 383 T 1.45212 0.3687 T 1.5816 0.6871 191,39 T 12140. p 37 .08 T 745
0.9898 11,49 8.250 T 1.50745 0. 7800 T 0.2142 T 0.3949 T a. 1519 0.4573 194.42 T 14523. 36. 72 T 746
1.0252 8.52 8.547 T 1. 58364 0.0255 T 0. 2689 T 0.4907 T 2.6604 0.8320 T 204. 15 T 14951. 42. 38 T 747
1.1100 -4,03 9.254 T 1 .63000 0.0008 T 0. 2360 T 5.0169 0.9236 T 178.42 T 14977. 41.63 T 748
1.0975 -2. 57 9.150 T 1.62480 0.0033 T 0.3595 T 2. 2751 T 0.8176 T 157 ,40 T 15126. 42 .53 T 749
151 .37 T 15262. 750
15362. 751
Table lCJ.6 Baters

0.9820 12.59 8.187 T 1 .34150 18.3474 T 0.2591 T 0.4648 T 0,3134 T ... 201,79 T 6593. 24. 24 T 752
0.9412 18.84 7 .847 T 1 .35890 7.1,,7 T 0. 2697 T 0.4538 T 0.3511 T 0.2228 T 177.66 T 8479. 24 .54 T 753
a .9295 20. 73 7. 750 T 1.35750 7 .9783 T 0.2728 T 0 ,4814 T 0 .3716 T ... 172 .87 T 8746. 23 .08 T 754
0.9053 24.80 7 .548 T 1.37040 3.2706 T 0.3027 T 0.4564 T 0.4238 a. 2558 157.48 T 10066. p 23. 24 T 755
0.9110 23.82 7 .595 T 1.37500 2 .8656 T 0.2901 T 0.4707 T 0.4783 T 0.2956 T 156.18 T 9959. 23. 95 T 756
0,9389 19.21 7. 827 T 1. 39340 3.9191 T 0.2669 0.4362 T 0. 3902 T ... 156.75 T 9733. p 23. 99 T 757
0,9038 25.07 7 .535 T 1. 38470 1. 2009 T ... ... 0.5276 T 0.3197 T 144,63 T 11335. p 24. 58 T 758
0.8938 28.85 7 .450 T 1. 38280 1. 2395 T ... ... 0.5483 0.3158 145.10 T 11421. p 23.88 T 759
0.8822 28.89 7 .355 T 1. 37500 2.1319 T ... 0.4606 T 0.5323 T ... 135 .66 T 11189. p 21. 28 T 760
0.8867 28.09 7 .392 T 1.39180 0.4547 T 0. 3184 T 0.4616 T 0.6908 T 0.3583 T 135.34 T 12150. p 24. 75 T 761
0.8816 29.00 7. 350 T 1 .40280 0.1501 T ... 0.4728 T 0.8073 T 0.4357 T 127 .28 T 12857. p 25.10 T 762
1987 1-123
1C3.7-1C3.8
TABLES 1C3.7-1C3.8
ETHERS AND GASES-PRIMARY PROPERTIES
Cr 1t !cal Constants
No. Compound Formula H.W, Boiling
Point
at Freezing Temp- Pressure Volume Compres- A.centric
1 atm Point erature psia cu rt slbillty Factor
deq F in air deq P per lb Factor
at l
atm.
deq F
Table 1C3.7 Ethers

763 DIMETHYL ETHER C2H50 46.07 -12. 71 -222.68 260.51 77B. B9 0.0591 a. 2144 a. 2036
764 METHYL ETHYL ETHER C3HBO 60. 10 45. 23 -171.67 p 32B. 37 637 .B1 0.05B9 a. 2610 a. 21B9
765 DIETHYL ETHER C4H1QO 74. 12 93.97 -177 .34 3BO. 39 527 .59 0.0605 a. 2B20 a. 2B46
766 METHYL-tert-BUTYL ETHER C5H120 BB.15 131 .36 -163.4B 435. 11 497 .4B 0.059B p a. 2130 a. 2674
7B7 METHYL- tert ... AMYL ETHER CBH140 102. 1B 1B7 .34 ... ... .. . ... ... ...
768 TETRAHYDROFURAN C4HBO 72.,, 14B. 73 -163. 30 512.60 752 .43 a .0497 a. 2590 a. 2254
789 DIBENZOFURAN C12HBO 168. 19 543.97 1B0.50 99B.60 464. 13 0.04650 a. 2300 0.4260
Table 1C3.8 Gases

770 AIR 2B.96 -317. B3 -353. 20 -221.31 546. 90 0.0510 D a. 3200 0.013B
771 AMMONl4 NH3 17 .03 -28 .17 -107.93 270. 50 1635.67 0.0682 0.2420 0,2520
772 ARGON 4r 39.95 -302.57 -30B. B2 -1BB.12 710.40 0.0299 a. 2910 ...
773 BROMINE Br2 159.B1 137. 75 1B.95 591 .BO 1499.00 0.0135 s a. 2B10 a. 1189
774 CARBON MONOXIDE co 2B.01 -312.61 -337. 00 -220.41 507 .45 a. 0532 a. 2950 a. 08B3
775 CARBON DIOXIDE C02 44.01 -109.26 T -69. B3 B7 .91 1071 .oo a .0342 a. 2140 a. 221B
77B CARBONYL SULFIDE cos B0.07 -5B. 27 -217 .B4 222 .17 920. B5 0.0360 a. 2120 a. 1041
777 CHLORINE Cl2 70.91 -29.25 -149.B5 291. 20 111B.37 0.02BO a. 2150 0.0890
77B FLUORINE F2 3B.OO -306. 76 -363.32 -199.91 756.40 a. 0219 a. 2880 a. 058B
779 HELi UM-3 He 3.02 -453. 91 -457. B5 -453.71 1B.97 0.3B51 a. 30BO ...
7BO HELIUM-4 He 4.00 -452 .07 -456.50 -450.31 33.00 a. 2293 a. 3020 ...
7B1 HYDROGEN H2 2.02 -422. 9B -434. 56 -399.B2 1BB. 11 0.5167 a. 3050 ...
7B2 HYDROGEN BROMIDE HBr B0.91 -B8 .OB -124. 26 194.00 1240.34 O.Q19B s a. 2B40 0.0693
783 HYDROGEN CHLORIDE HCI 36.4B -121. 00 - 173 .52 124. 70 1205 .07 a. 035B a. 2490 a. 1322
7B4 HYDROGEN CYANIDE HCN 27 .03 78. 26 B.17 3B2. 30 7B1 .B3 0.0B21 a. 1910 0.409B
7B5 HYDROGEN F LUORI OE HF 20.01 67. 14 -11B.05 370.40 940.54 a .0552 a. 1110 a. 3B2B
7B8 HYDROGEN SULFIDE H2S 34.0B -76.50 -121. BB E 212.45 1300.00 0.0463 a. 2B40 a .0B21
7B7 KRYPTON Kr B3.BO -244.03 -251.27 -B2.B4 797 .99 a. 0114 a. 2BBO 0.0013
788 NEON Ne 20. 1B -410.91 -415.4B -379. 75 3B4. 79 0.0331 0.3000 ...
7B9 NITROGEN N2 2B.Q1 -320.45 -346. 00 E -232.51 493. 10 0.0515 a. 2920 0.0403
790 NITRIC OXIDE NO 30.01 -241. 19 -257.BO -135.40 940.54 a. o3oB a. 2500 a. 5B4B
791 NITROUS OX I DE N20 44.01 -127.26 -131.48 97 .5B 1050.76 0.0354 a. 2140 a. 141B
792 NITROGEN DIOXIDE N02 46.01 69.53 s ,, .84 s 316. 76 s 1469.60 s O.Q2B7 s a. 2330 a. B4BB
793 NITROGEN TETRQXIDE N204 92.01 B4.33 ,, . 75 316,40 1469.60 0.0144 s a. 2330 ...
794 OXYGEN 02 32.00 -297. 33 E -361. B2 E -1B1 .43 731. 40 a. 0367 a. 2BBO 0.021B
795 OZONE 03 48.00 -168.34 -315.40 10. 13 B08. 28 a .0291 a. 2290 a. 1947
796 SULFUR DIOXIDE S02 64.06 13.96 -99.67 315.6B 1143.50 0.0305 a. 2690 a. 2451
797 SULFUR TRIOXIDE S03 B0.06 112.55 62.24 423. B6 119Q.3B 0.0254 a. 2560 0.4215
79B XENON Xe 131. 29 -162.62 -169. 22 61 .B6 B47 .OB 0.0144 a. 2B60 0.0115
Norn: See page 1-135 for Key to footnote codes.
1-124 1987
1C3.7-1C3.8
Spec it le I.PI Dansity Refractive Vapor Heat Capacity Kinematic Heat ot Net Heat ot Surface
Gravity Gravity ot the Index Pressure at 60 F and Con- Viscosity of the Vapor ha- Combustion Tension
60/60 at 60 F Liquid ot the at 100 F stant Pressure Liquid tion at ot Liquid ot the No,
deg I.PI at 60 F Liquid psia Btu/lb deg F centistokes Normal at 77 F Liquid
lb/gal at 77 F Boiling Stu/lb at 77 F
Point dyne/cm
Ideal Liquid Btu/lb
Gas at l
Table lCl.7 Ethers

0.8711 79.36 5.595 1. 29B40 122.2B20 T 0.3349 201 .23 T 12397. 11. 36 T 763
o.7050 69.20 5.B7B T , .34410 44,3934 T 0.3501 190 .61 T 13B17. 14.B2 T 764
o. 7199 65.08 6.002 T 1 .3°4954 16.4345 T 0.3553 T 0.5557 T 0. 2B67 0. 1BB7 157. 11 T 14521. 16.42 T 765
0. 7459 5B .21 6.21B T 1 .36630 7.972B T 0.3553 T 0.499B T 0 .4065 0. 2645 137 .41 T 15119. 19.09 T 766
1. 3BB4B 767
O.B90B 27 .34 7 .427 1 .40496 5.3515 T 0.244B 0.402B 0.4752 T 1B0.42 T 13B63. 24.9B T 7BB
1.60790 14562. 769
Table lCJ.8 Gases

O.B748 30.28 7.293 G 1. 00102 o. 2399 BB. 20 o. 770
0.8182 9B. 12 5. 13B 1.32500 211,4BBO 0.4969 T 1,143B 0. 1991 T 0. 1373 T 5BB.92 T 799B. p 21 .OB T 771
1.00026 0.1242 T 69.31 T 772
3. 13BO -B6.41 26. 162 1.64BOO 6.B966 0.0537 0.1144 0. 2B09 BO .61 0. 40.96 T 773
1. 00031 0. 24B4 90. 70 T 4344, 774
O.B180 41.48 6.B20 1.00041 0. 1991 O.B699 T 246. 47 o. 0 .57 T 775
1 ,0200 7.22 8.504 1.37B50 246.9570 T 0.1627 T 0.3221 T 134 .01 3924. 7 .B7 T 776
, .4274 -32.37 11.901 1.37B60 157.7630 0.113B T 123.7B T 0. 17 .32 T 777
1. 20000 0. 195B T 73. B2 T 0. 77B
1. 00002 779
1. 00003 1 . 2404 T B.95 T 7BO
1 .00013 1B9.B5 T 51469. p 7B1
1. 7B34 -52.16 14.B68 T 1.00056 473.1420 0.0B60 T 0.1B04 T 95. 97 T 367. 9. 20 T 7B2
0.8483 35. 70 7 .056 T 1.32B70 90B.B620 T 0.190B T 0. 0920 191. 15 T 337. 3.30 T 7B3
0,8944 72.27 5.7B9T 1.25940 22.7120 0.3139 T 0.6252 T 427. B7 T 9915. 17. 76 T 7B4
0.9681 14,96 8.054 T 1.15740 27.0445 T 0.3479 T 0.5951 T 3259. p B.40 7B5
0.8014 45.08 8.682 F 1. 005B5 394. 5900 0. 23B3 235 .63 77B5. p 9. 11 7B6
1 .00039 0 .0592 46,59 7B7
1. 00006 0. 2460 36.47 7BB
O.B094 43.32 8. 74B G 1. 20530 0. 24B3 B5.59 o. 7B9
1. 33050 0.2374 T 194. 16 T 1293. p 790
o. B175 41 .5B 6.B16 T 1. 19300 0. 2067 T 168.06 T B01. p 1.33 791
1. 40000 30. 7473 0.1905T 0. 2277 356. 20 309. p 792
1 .40000 20.4B01 0. 2066 0. 365 7 42. p 793
, . 1421 -7 .61 g. 522 G 1. 22100 0. 21B9 91 .59 o. 794
0. 1929 126. 61 127B. p 795
1 .3948 -30.04 11.627 1. 35700 BB.0205 T 0.1472 T 0. 2332 165.70 T 0. 21. 69 T 796
1.9269 -5B.07 16.065 1. 40520 10. 4563 0. 1492 T 0. 6396 214.69 T 531. p 33. OB T 797
, ,4151 -31.51 11.79B , .00064 0 .037B 41. 33 79B
1987 1-125
1C3.~1 C3.1 o
TABLES 1C3.~1C3.10
HALOGENATED COMPOUNDS AND KETONES-PRIMARY PROPERTIES
Critical Constants
Jlo. Compound l"ormula M.W. Boiling
Point
at Freezing Temp- Pressure Volume Compres- Acentr le
l atm Point &l'ature psia cu tt siblllty Factor
dog F in air deg P per lb !"actor
at l
atm.
deg P
~able lCl.9 Halogenated Compounds

799 CHLOROTRI FLUOROMETHAHE CCI F3 104.46 -114.54 -293 .80 83.86 572 .32 0 .0276 o. 2830 o. 1800
800 OICHLOROOI FLUOROMETHAHE CCl2F2 120.91 -21. 62 -252.40 233. 24 598. 27 0.0287 o. 2800 0.1796
801 TRI CHLOROF LUOROMETHAHE CC I 3F 137. 37 74.88 -168.00 388.49 639. 28 o. 0289 o. 2790 o. 1837
802 CARSON TETRACHLORIDE CCI 4 153.82 189.95 -9.08 541. 76 661 .32 0.0287 0. 2720 o. 1926
803 CARION TETRAFLUORIDE CF4 88.00 -198 .51 -298.46 -so. 17 542. 28 o. 0255 0. 2770 0. 1855
804 CHLOROOI FLUOROMETHANE CHC I F2 86.47 -4i .49 -251.36 205. 07 720. 98 0 .0308 0.2690 0.2192
805 DICHLOROF LUOROMETHA HE CHC I 2F 102.92 48.02 -211 .00 353 .17 751 .85 0.0305 0. 2710 0.2069
806 CHLOROFORM CHCl3 119.38 142. 12 -82. 34 505 .85 793 .58 0.0321 0. 2930 o. 2129
807 TRI FLUOROMETHANE CHF3 70.01 -115.89 •247. 32 78.33 701 .44 0 .0305 0. 2590 o. 2672
808 OICHLOROMETHAHE CH2C I 2 84.93 103.55 -139.25 458 .33 881. 76 0.0349 p 0. 2650 0. 1918
809 METHYL CHLORIOE CH3CI 50.49 -11 .60 -143.88 289.58 968. 76 0.0441 0. 2680 0. 1529
810 METHYL FLUORIDE CH3F 34.03 -108.99 -223. 24 112. 19 852. 37 0.0532 0.2510 o. 2125
811 VINYL CHLORIDE C2H3C I 62.50 7 .93 -244.82 317.93 p 822 .37 p 0.0459 p 0. 2830 o. 1005
812 I. I, 1-TRICHLOROETHAHE C2H3Cl3 133.40 165.35 -22. 72 521 .33 623. 11 0.0337 p 0. 2660 o. 2157
813 1, 1, 2-TRICHLOROETHAHE C2H3CI 3 133.40 236. 93 -33. 97 623.93 p 649.77 p 0.0337 p 0. 2520 0. 2598
814 1, 1, 1-TRIFLUOROETHAHE C 2H3F 3 84.04 -53. 32 -168.34 163.58 545 .07 o. 0370 0. 2530 0. 2529
815 1, 1-0ICHLOROETHAHE C2H4Cl2 98.96 135.14 -142.53 481. 73 734.80 0.0388 0. 2800 0. 2443
816 1, 2-DICHLOROETHAHE C2H4C12 98.96 182.20 -32. 19 550. 13 778.89 0.0358 0. 2530 0. 2876
817 1, 1-0IFLUOROETHAHE C2H4F2 66.05 -14.44 -178 .60 236. 21 652 .50 0.0439 0. 2530 o. 2629
818 ETHYL CHLORIOE C2H5C I 64.51 54.09 -213.52 368.96 764. 19 o. 0497 s 0. 2750 0.1905
819 ETHYL FLUORIDE C2H5F 48.06 -35 .86 -225. 76 215.89 729.22 0.0547 p 0. 2640 0. 2220
820 1,2-DICHLOROPROPAHE C3H5C1 2 112.99 205 .47 -148. 79 569.93 p 614.98 p 0.0413 p 0. 2590 0. 2513
~able lCl.10 Ketones

821 ACETONE C3H50 58.08 133. 32 -138.46 455.09 681 .89 0 .0576 0. 2330 0.3064
822 METHYL ETHYL KETOHE C4H90 72.,, 175.35 -124.01 p 504. 23 602 .54 0. 0593 0. 2490 0.3241
823 DIETHYL KETOHE C5H1DO 86.13 215.58 -38. 15 550.04 542. 28 0.0625 0. 2690 0. 3502
824 METHYL·n-PROPYL KETOHE C5H100 86. 13 216.16 -106.35 550. 27 535 .82 0.0560 0. 2380 o. 3458
825 METHYL-n-BUTYL KETOHE C5H120 100. 16 261 .86 -68 .44 597 .02 482 .03 0.0590 p 0. 2510 0.3967
826 METHYL ISDBUTYL KETOHE C5H120 100. 16 241. 70 -119.20 568.85 474.68 0.0590 p 0. 2540 0. 3887
1-126 1987
1C3.9-1C3.10
Specific API Density Refractive Vapor Heat Capacity Kinematic Heat of Net Heat of Surface
Gravity Gravity ot the Index Pressure at 60 F and Con- Viscosity of the Vapor iza- Combustion Tens 1011
60/60 at 60 P' Liquid ot the at 100 F stant Pressure Liquid tion at ot Liquid of the No.
deg API at 60 P' Liquid psia Btu/lb deg P' cent is tokes NorNL at 77 P' Liquid
lb/gal at 77 P' Boiling Btu/lb at 77 F
Point dyne/cm
Ideal Liquid Btu/lb
Gas at l
atm. at 100 F I at 210 E'
Table lCJ.9 Baloqenated Co•pounds

a. g939 12. 32 8.202 T 1. 1ggoo ... a. 1510 T ... . .. ... 64.22 T 12g4. p a. 26 T 799
1 .3422 -26.08 ,, . 1go 1. 28500 130.4sgo T a. 1421 T a. 2203 T a. 15g5 a. 1051 73. 27 T 34g. p 8. 79 T 800
1. 5002 -37. 18 12. 507 T 1. 37400 23.8160 T a. 1348 T 0.2080 T 0.2652 T a. 1g31T 78. 7 3 T 328. p 18.34 T 801
1 .6021 -43. 18 13.357 1.45730 3. 7775 a .1205 T a .2020 T 0 .48g3 T 0.2706 T 83 .41 T 721. 26 .2g T 802
... ... ... 1. 15100 ... a. 1630 T ... . .. . .. 57. 10 T 2637. p ... 803
1 .2304 -16.4g 10.258 T 1. 25600 207. 2300 T a. 1538 T o.2go1 0. 1643 T ... 100.40 T 327. p 7 .87 T 804
1.3g15 -2g.01 ,, .601 T 1. 35400 3g.9974 T a. 13g5 T a. 24g7 a. 2101 T 0. 1686 T 102.g1 T g66. p 20. 16 T 805
1.4997 -37. 15 12.503 T , .44310 6.4505 a. 12g4 T a. 2268 T a. 3211 ... 107 .27 T 1368. 26.68 T 806
0.8781 2g.55 7. 320 T 1 .21500 ... 0.1713 T a. 3617 ... . .. 102 .04 T 1og0. p 0.03 T 807
1 .3374 -25. 70 ,, . 150 T 1.42120 13.6516 T a. 1415 T 0.2816 T 0.2851 a. 2060 143.67 T 2601. 28. 77 T 808
o.g331 20. 14 7. 77g 1 .33620 118.5450 a. 10g0 T a. 3778 T 0. 1733 T 0.1224 T 183.50 T 5751. 15. 19 T 8Qg
0.6110 100.og 5.Qg4 1. 17400 755 .6g10 T a. 2603 T ... ... . .. 223.22 T 55g4. p 1 .82 T 810
o.g1gg 22. 31 7 .670 T 1. 36600 82 .6703 T a. 2001 T 0.3167 T 0. 1713 T a. 1231 T 157 .00 T 7g66. p 15.84 T 811
1 .346g -26.45 11. 22g T 1 .43130 4. 1052 T a. 1631 T a. 2567 a. 5119T a. 2964 T 96. 16 T 3142. p 25.02 T 812
1 .4513 -34.00 12.099 T 1 .46890 0.8535 T ... 0.2674 T 0.6218 T a .3350 T 111 .59 T 3106. p 33. 75 T 813
0.9915 , , . 21 8.266 T 1. 20600 253. 4820 T a. 2101 T ... ... . .. 9g.55 T 2067. p 5.43 T 814
1. 1838 -11 .g1 9.869 T 1 .41380 7 .3321 T a. 1012 T a .3036 0.3561 T ... 126 .99 T 4821. p 25.04 T 815
1. 2605 -19. 24 10.5Qg T , .44210 2. 7294 T a. is11 T a .3012 0.5341 T a. 2955 T 139. 73 T 4801. 32. 27 T 816
o.g221 21 .gs 7.888 T 1. 24340 124.1g4Q T a. 2403 T 0.3776 T 0.2473 ... 141 .46 T 4937. p 10.03 T 817
a. 9032 25. 17 7 .530 T 1 .36520 35.1432 T a. 2211 T 0.381g T 0.2649 T a. 2023 T 164.93 T 8563. 18. 27 T 818
a. 1301 62. 14 6.092 T 1. 26210 184.8570 T a. 2090 T ... ... . .. 178 .53 T 9930. p 9. 25 T 01g
1. 1630 -9.83 9.6g8 T 1 .43680 1 .8148 T 0.2031 T a. 3091 T 0.5664 T ... 121 .87 T 6486. p 30.08 T 820
Table lCl.10 Ketones

a. 7g73 45.g8 8.647 T 1 .35596 7 .5011 T 0.3000 T 0.5129 T 0.3546 T ... 220.53 T 12282. 23 .04 T 821
0.8100 43. 18 6. 753 1. 37640 3.2516 T 0.3382 T 0.5211 T 0.4403 T 0.2805 T 186. 15 T 13485. 23. g5 T 822
0.8194 41. 18 6.831 T 1 .39002 1 .3348 T 0.3526 T 0.5250 T 0.4873 ... ... 14377. 24. 56 T 823
0.8125 42 .65 6. 774 T 1 .38800 1 .3299 T a. 3346 T 0.5056 0.5184 T 0.3326 T 167 .05 T 14375. 23. 26 T 824
0.8162 41 .86 6.805 T 1 .3g870 0.4204 T a. 3462 T a. 5039 0.6228 T 0.3594 T 157 .21 T 14981. 25. 28 T 825
a. 0059 44. 11 6. 718 T 1. 3g330 a. 1501 T 0.3441 T 0.5007 T 0.6432 0.4617 153.74 T 14969. p 23. 50 T 826
1987 1-127
1C3.11-1C3.12
TABLES 1C3.11-1C3.12
SULFUR-CONTAINING COMPOUNDS AND
MISCELLANEOUS-PRIMARY PROPERTIES
Critical Constants
No. Compound !'or mu la H.W. Boiling
Point
at Freezing Temp- Pressure Volume Compres- Acentr le
l atm Point eratura psia cu ft slblllty Factor
deg F in air deg F per lb Factor
at l
atm.
deg F
Table lCJ.11 Sulfur Containing Compounds
827 CARBON OISULFIOE CS2 76. 13 115. 20 -168.83 533 .93 1146.29 a .0337 a. 2160 a. 1019
B2B METHYL MERCAPTAN CH4S 4B. 10 42. 72 -1B9.35 3B6. 24 1049. 29 a. 04B3 a. 2680 a. 14BB
829 2 0 3•01 THI ABUT ANE C2H5S2 94. 19 229 .54 -120.50 631. 13 p 777. 40 p a. 0429 p a. 2680 a. 2652
B30 QI METHYL SULFIDE C2H5S 62. 13 99.20 -144.B9 445 .BO B02. 00 0.051B a. 2660 0. 1B93
B31 ETHYL MERCAPTAN C2H5S 62. 13 95.01 -234.20 43B.BO 796. 26 a. 0534 0.2740 a. 1921
B32 2-THIABUTANE C3HBS 76. 16 151 .99 ... 500 .00 0.00 a. 0553 ... . ..
833 1 -PROPANETHI OL C3HBS 76. 16 153.90 ... . .. ... ... . .. ...
834 n-BUTANETHIOL C4H10S 90. 1B 209. 23 -176. 24 564.53 p 575.BO p a. 0545 p a. 25BO a. 2784
835 ter- t-BUT ANETHIOL C4H10S 90. 1B 147. 59 34.00 494. 33 p 5BB.B5 P a. 0545 p a. 2B30 a. 1901
836 2-BUTANETHIOL C4H10S 90. 1B 1B4.96 ... ... . .. ... ... ...
837 2-METHYL- 1-PROPANETHIOL C4H10S 90. 19 191. 10 ... . .. ... ... . .. ...
83B 3-THIAPENTANE C4H10S 90. 1B 197. 7B -155. ,, 543. 20 574.61 a .0564 a. 2120 a. 2936
B39 2-THIAHEXANE C5H125 104. 21 254. 16 ... . .. ... ... ... . ..
840 3-THIAHEXANE C5H12S 104. 21 245. 30 ... ... . .. ... ... . ..
841 1-PENTANETHIOL C5H12S 104. 21 259 .95 -104. 26 616. 73 p 503. 2B p 0.0552 p a. 2510 0.3211
842 2-THIAHEPTANE C5H14S 118. 24 293. 00 ... . .. ... ... ... ...
843 1-HEXANETHIOL C5H145 11B. 24 306.B1 ... . .. ... ... ... ...
844 1-HEPTANETHIOL C7H155 132. 26 350 .49 ... ... . .. ... ... ...
Table lCJ.12 Miscellaneous
845 WATER H20 18.02 212.00 32. 00 705. 16 319B.BO a. 0491 a. 2290 0.3449
846 SULFURIC ACID H2504 9B.07 63B.33 p 50.56 1205.33 p 92B. 24 p a. 02B9 a. 1410 0.B560
847 SODIUM HYOROX!OE NaOH 40.00 2534.33 p 613. 13 4616.33 p 3673.99 p a. 0Bo1 p a. 2200 ...
B46 PROPYLENE CARBONATE C3H5C03 102 .09 ... ... . .. ... . .. ... ...
849 FURFURAL C5H402 96.09 323.06 -33. 70 722 .93 p 799. 46 5 0.0420 p a. 2540 0.4442
850 1. 2-PROPYLENE GLYCOL C3HB02 76.09 369. 6B -76.00 667.13 p BB4. 73 p 0.0503 p a. 2Boo 1 .10B5
851 OIETHYLENE GLYCOL C4H1003 106. 12 473 .00 13. 19 764 .33 p 667.1B p 0.0471 p a. 2540 1. 200B
852 TETRAETHYLENE GLYCOL cBH1Bo5 194. 23 5B6. 13 23.00 B39 .93 p 375.65 p 0.0465 p a. 2430 1 .57B3
853 MONOETHANOLAMINE C2H7NO 61 .OB 339. BO 50.90 6BB. 73 p 996.41 p 0.0590 p a. 2910 a. 7966
854 OIETHANOLAMINE C4H11N02 105. 14 516.00 B2.40 B27. 33 p 474.27 p 0.0532 p a. 1920 1 .0463
855 OIGLYCOLAMINE H(OC2H4)2NH2 105. 14 ... ... ... ... . .. ... ...
B56 METHYL OIETHANOLAMINE C5H13N02 119. 16 476.60 s -5.BO S 760. 73 p 562. 75 p 0.0539 p a. 2160 1 .3017
857 TRI ETHANOLAMI NE C5H15N03 149. 19 643. 73 p 70. 16 956.93 p 355. 34 p 0.0507 P a. 1110 1. 100B
B5B OZ I50PROPANOLAMINE ( HOC3H5) 2NH 133. 19 ... ... ... . .. . .. ... ...
859 N. N-01 METHYLFORMAMI OE C3H7NO 73.09 307. 40 -76. 77 704.93 p 641.07 p 0.05B5 p a. 2190 a. 3724
860 N- METHYL-2-PYRROLI CONE C5H9NO 99. 13 395. 60 - 11. 20 B43.53 P 693. 2B p a. os11 p a. 2s10 0.3577
B61 OiMETHYL SULFOXIOE C2H505 78. 13 372. 20 65 .34 84 7., 3 p 819 .47 p a. 0465 p a. 2120 a. 2094
B62 SULFOLANE C4HB025 , 20., 7 545. 00 B1. 6B 1079.33 p 729. 54 p a. 0400 P a. 2120 a. 3463
863 5ELEXOL 2BO. 00 51B.OO s -20.00 s ... ... ... ... . ..
1-128 1987
1C3.11-1C3.12
Speclflc API Oensi ty Refractive Vapor Heat Capacity KLnema.tic Heat ot' Net Heat ot' Surface
Cravlty Cravlty ot th• Index Pressure at 60 P and Con- VLscos Lty ot the Vapor iza- Combustion Tension
60/60 at 60 F Liquld of the at 100 F stant Pressure Llquld t Lon at ot Liquld ot the No.
deq API at 60 F Llquld psia Btu/lb deq F cent is tokes Normal at 77 P Llquid
lb/qal at 77 F Boiling Btu/lb at 77 F
Point dyne/cm
Ideal Llquld Btu/lb
Gas at l
Table lCJ.11 Sulfur Containing Co•pounds

1. 2705 -20. 12 10.592 T 1 .62409 11 .0771 T 0. 1412 T 0.2388 T 0.2613 T 152.63 T 6236. p 31 .56 T 827
0 .8783 29.97 7 .306 T 44.2060 T 0.2458 l 227.70 l 10293. 23 .84 T 828
1 .0684 0.94 8 .907 T 1. 52297 1 .0429 T 0. 2351 T 0. 3682 0.4690 T 0.2643 T 156. 76 T 9329. 33.07 T 829
0. 8622 32.62 7. 188 T 1. 43228 15.0690 T 0. 2797 0.4503 T 186.20 T 12068. 24.17 T 830
0.8445 36.05 7 .041 T 1.42777 16. 1741 T 0. 2738 0.4490 185.93 T 12011. 22 .82 T 831
1. 43735 832
1 .43533 833
0.8470 35.56 7 .061 T 1 .44033 1 .6119 T 0.3061 T 0.4508 0.4742 T 156.28 T 14089. 25. 22 T 834
0.8056 44. 15 6. 716 T 1 .42004 5.8694 T 0.3133 T 0.4586 T 0.6518 T 136. 10 T 14014. 20.29 T 835
1 .43394 16559. 836
1 .43600 16553. 837
0.8420 36.55 7. 020 T 1 .44015 2.0397 T 0.3030 T 0.4489 0.4534 152.55 T 14115. p 24.66 T 838
, • 44524 17082. 839
1 .44350 16972. 840
0.8489 35.58 7 .060 T 1 .44435 0.5260 T 0.3165 T 0.4562 T 0. 6162 T 0.3741 T 145. 13 T 14711. 26.02 T 841
1 .44820 842
1 .44720 843
1 .44981 844
Table lCJ.12 Miscellaneous

1 .0000 10.00 8.337 1. 33250 0.9501 0.4446 .9997 0. 7136 970. 18 0. 72 .82 T 845
1 .8462 -54.86 15. 392 T 1. 41828 0. 1927 T 8.3370 T 52.39 T 846
1. 43300 0.2889 T 847
848
1. 1683 -10. 18 9. 723 T 1 .52345 0.0953 T 0.2381 T 0.3986 T 1. 1596 T 0. 7223 188.61 T 10066. 43.01 T 849
1 .0407 4.48 8.676 T , .43140 0.0076 T 0.3134 T 0.5857 T 19. 4434 T 2.8772 T 307 .81 T 9309. 35.47 T 850
1. 1225 -5.45 9.359 T 1 .44600 0.0005 T 0.5426 15.9800 2 .4251 249.40 T 8730. 48. 18 T 851
1. 1314 -8.43 9.432 T 1 .45700 0.0000 T 0.5087 T 22.3149 T 2.9372 T 173.36 T 9695. p 44. 13 T 852
1 .0220 8.95 8.521 T 1 .45210 0.0203 T 0.3265 T 13. 0208 T 2.1609 T 362.72T 9594. 48.32 T 853
1.47470 0.0000 T 0.3135 T 210.8330 T 9.1426 T 263.58 T 9857. 47, 25 T 854
855
1 .0387 4. 73 8.660 T 1 .46850 0.0000 T 45. 7244 T 4.9235 252.01 11040. p 38. 22 T 856
1 .48350 0 .0000 T 0.3135 T 220.1190 T 11 .3059 203. 70 10117. 45. 24 T 857
858
0.9542 16. 78 7.956 T 1 .42690 0. 1692 0.2979 T 0.4875 T 0. 7562 T 0.4694 T 229.17 T 10521. 34. 43 T 859
1 .0387 4.99 8.643 T 1 .46900 0.0164 1 .2668 T 0.5008 .T 193.94 T 12166. p 30. 25 T 860
, . 47730 0.0274 0 .2671 T 1. 4894 0.6808 234.96 T 8515. p 42. 75 T 861
1. 47800 0.0005 T 6.6668 T 2.1609 T 187.03 T 8515. p 85.49 T 882
863
1987 1-129
1C4.1-1 C4.3
TABLES 1C4.1-1C4.3
ACIDS, ALCOHOLS AND PHENOLS, AND
ALDEHYDES-SECONDARY PROPERTIES
Search Solubility !!'lash Ideal Gas Ideal Gas Heat ot nalllNlblllty

No. Compound !'ormula Number Parameter Point Heat of Gibbs !'re• !'u.sion Limits, Volume
(Cal/cml)l/ 2 Tempera tu re l"ormatlon !ner9y of at 77 1" Percent in
deg I!' at 77 1" l"ormatlon Btu/lb Air Mixture
Btu/lb at 77 F
Btu/lb
tower
I Upper
Table 1C4.l Acids

700 FORMIC ACIO CH202 1251 10.48 156.00 -3536.63 -3278. 68 118.62 18.00 57 .00
701 ACETIC ACIO C2H402 1252 B.97 109.00 -3094. 56 -2677.90 83.87 5.40 16.00
702 PROPIONIC ACID C3H502 1253 9.36 130.00 -2632. 21 -2128.21 p 61.87 2.90 p 14,BO P
703 n-BUTYRIC ACID C4H902 1256 9,91 161 .00 -2294.82 -1717.0B P 56.56 2.19 13.40
704 2-METHYLPROPIONIC ACID C4H902 1260 11 .83 170.00 -2362.40 p -1767 .32 p 24.50 2,00 9.20
705 n·PENTANOIC ACIO C5H1002 1258 10.92 204 .80 -2064. 19 -1443.92 p 59.62 1.60 p ...
708 2-METHYLBUTYRIC ACIO C5H1002 1257 ... ... -2096.33 p -1481.74P ... 1,60 p ...
707 3-METHYLBUTYRIC ACID C5H1002 1261 9.81 ... -2166.63 -1544.89 p 30.82 1,60 p ...
708 n-HEXANOIC ACIO C5H1202 1262 11.39 215.00 -1900.93 -1258 ,40 p 55. 75 1.30 p ...
Table 1C4.2 Alcohols and Phenols
709 METHANOL CH40 1101 14.43 5i .oo -2692.46 -2179.34 43.00 7 ,30 38.00
710 ETHANOL C2H50 1102 12 .92 55.00 -2187.78 -1566.94 46.02 4,30 19.00
711 n-PROPANOL C3H90 1103 12.01 59.00 -1834.28 -1157.50 38.43 2.00 12.00
712 ISOPROPANOL C3H90 1104 11.53 53.00 -1948. 92 -1240.41 38. 70 2,00 12.00
713 n-BUTANOL C4H1QO 1105 11.39 84.00 -1593. 21 -874 .62 54.36 1.40 11.20
714 ISOBUTANOL C4H100 1106 11.61 ei .oo -1642.71 -899.10 p 36.67 1, 70 10.90
715 sec-BUTANOL C4H100 1107 11.06 75.00 -1698.77 -973.64 34.63 1, 70 9.80
718 te•t-BUTANOL C4H 1QO 1108 10.51 5i .oo -1812.10 -1030.43 38.83 2 ,40 8.00
717 1-PENTANOL C5H120 1109 ,, .04 91 .00 -1457 .02 -712. 19 47. 75 1.20 10,00
718 2-PENTANOL C5H120 1110 10.59 94.00 -1530.48 -776.BB p 0.00 1,50 p ...
719 2-METHYL-1-BUTANOL C5H120 1112 10.89 1n.oo -1473.35 -715.54 p 0.00 1,40 9.00
720 2- METHYL-2-BUTANOL C5H120 1111 10.15 105.00 -1608.03 -806.05 21. 73 1.20 9.00
721 3-METHYL-2-BUTANOL C5H120 1124 10.56 103.00 -1532.52 -762 .60 p ... 1,50 p ...
722 2, 2-DI METHYL-1 ·PROPANOL C5H120 1113 9.42 96.60 -1556.20 p -757.81 p 0.00 1,50 p ...
723 4-llE7HYL-2-PEN7ANOL C5H140 1130 9.47 106.00 -1440. 77 p -654.99 p ... 1.00 5.50
724 PHENOL C5H50 1181 11. 78 175.00 -440. 37 -149.07 52.60 1.50 s ...
725 o·CRESOL C7H90 1182 , , .44 176 .00 -511.15 -131 .00 62.90 1,40 ...
728 m-CRESOL C7H90 1183 11. 77 2oi .oo -525 .98 -159. 74 42.57 1.10 ...
727 p·CRESOL C7H90 1184 11.65 2oi .oo -498 .35 -125.87 50.52 1.10 ...
Table 1C4.J Aldehydes
728 FORMALOEHYDE CH20 1001 , , . 70 -e6.e1 P -1659.48 -1573.57 s ... 7 .00 73.00
729 ACETALOEHYDE C2H40 1002 9.69 -36.00 -1621.89 -1258 .07 31.44 1.60 10.40
730 n-PROP IONALOEHYDE C3H50 1003 9.47 -n.oo -1376.84 -920 .86 ... 2.60 16.10
731 n-BUTYRALOEHYDE C4H90 1005 9.26 20.00 -1228.61 -see .oo 66.21 2.50 12.50
732 ACROLEIN C3H40 1034 9.95 -14.BO -621 .17 p -429.25 p ... 2.BO 31.00
733 t '°ns-CROTONALOEHYOE C4H50 1036 10.16 55.00 -635 ,47 -298.72 p ... 2. 10 15.50
734 METHACROLEIN C4H50 1037 9.20 35.60 -691.39 p -353.33 p ... 6.00 ...
1-130 1987
1C4.4-1C4.6
TABLES 1C4.4-1C4.6
AMINES, OTHER NITROGEN-CONTAINING COMPOUNDS, AND ESTERS--
SECONDARY PROPERTIES
Search Solubll i ty Flash Ideal Gas Ideal Gas Heat of Flarrvnability

No. Compound Formula Number Parameter Point Heat of Gibbs Free Fus ion Limits, Volume
(Cal/cml)l/2 Temperature Format ion Energy of at 77 F Percent in
daq F at 77 F Format ion Btu/lb Air Mixture
Btu/lb at 77 F
Btu/lb
Lower Upper
I
Table 1C4.4 Aaines
7J5 ~ETHYLA~INE CH5N 1701 11 .JO ... -J17. 98 444. 24 84.91 4.90 20. 70
7J6 ETHYLAMINE C2H7N 1704 9.53 -49. 27 p -438 .89 355. 50 ... 3.50 14.00
7J7 n-PROPYLAMINE C3H9N 171, 9.05 10.00 -526.46 289. 40 ... 2.00 10.40
7J8 ISOPROPYLAMINE CJH9N 1719 8.5J -J4.60 -609 .50 2J2. 2J p 5J. 27 2 .00 10.40
7J9 n-8UTYLAMINE C4H11N 1712 8.9J 10.00 -541.09 289. 24 s ... 1. 70 9.80
740 IS08UTYLAMINE C4H11N 1714 8.6J -0.04 -580. 78 270.99 p ... 1 .60 p ...
741 sec-SUTYLAMINE C4Hi1N 1726 8.45 -20 .00 -612.42 2J8 .82 ... 1.60 p . ..
742 tert-8UTYLAMI NE C4Hi1N 1727 7 .69 15.80 -704.65 169. 71 5. 18 1. 70 8.90
Table 1C4.5 Other Hitrogen--<:ontaining Compounds
74J UREA CH4N20 1877 ... ... -1758. 22 -109J.27 106.J3 s 5.60 p J5. JO p
744 ACETONITRILE C2HJN 1772 11.78 42 .00 775. 40 961 .55 p 9J.JJ 4.40 16.00
745 ~ORPHOLINE C4H9NO 1765 10. 79 100.00 -769.8J p 78.96 p 45.40 p 1.80 10.80
746 PYRIOINE C5H5N 1791 10.66 68.00 761 .82 10JJ.80 45.00 1 .80 12.40
747 ANILINE C5H7N 1792 11. 79 158.00 400.99 769.54 48.66 1. JO ,, .00
748 INDOLE c8 H7 N 2784 ,, .62 ... 574. 71 870.87 33.0J . .. ...
749 QUI NOLI NE C9H7N 1748 10.73 214.00 739. 95 976.95 J5.95 1 .00 p ...
750 018ENZOPYRROLE C12H9N 2789 10.18 ... 5J8. 92 928. 20 p 75.67 . .. ...
751 ACRIOINE C1JH9N 704 ... . .. 698.16 958.89 41.26 ... . ..
Table 1C4.6 Esters
752 ~ETHYL FORMATE C2H402 1301 10.02 -2.00 -2522.91 -2111.97 5J .92 5.90 20.00
75J METHYL ACETATE C3H502 1312 9.51 14.00 -2374.50 - 1866. 10 p ... J. 10 16.00
754 ETHYL FORMATE CJH602 1J02 9. 26 24.80 -2253 .55 -1759. 08 53 .42 2. 70 1J.50
755 ETHYL ACETATE C4H802 1313 8.99 24.00 -2161.30 -1597.60 51. 14 2. 20 ,, .40
756 n-PROPYL FORMATE C4H802 1303 8.97 27 .00 -1973.26 p -1424.3J p ... 2. 10 p ...
757 ~INYL ACETATE C4H502 1321 9.02 18.00 -1576. 71 -1142.35 ... 2.60 1J.40
758 ~ETHYL n-8UTYRATE C5H1002 1JJ2 8.8J 57 .00 -1897.22 -1285.16 ... 1.60 p ...
759 n-PROPYL ACETATE C5H1002 1J14 8.80 40.00 -1956.58 -1J48.72 ... 1.80 8.00
760 ISOPROPYL ACETATE C5H1002 1319 8.37 36.00 -2027. 72 -1404. 71 ... 1. 76 s 7. 20 s
781 n-8UTYL ACETATE C5H1202 1J15 8.60 72.00 -1796. 18 -1155.88 ... 1. 70 7.60
762 n-PENTYL ACETATE C7H1402 1J57 8.61 77 .00 -1669.J7 -1002.29 ... 1. 10 p ...
1987 1-131
1C4.7-1C4.8
TABLES 1C4.7-1C4.8
ETHERS AND GASES-SECONDARY PROPERTIES
Search Solubility Flash Ideal Gas Ideal Gas Heat ot: Flammability
No. Compound !'ormula Number Parameter Point Heat ot: Gibbs Free Fusion Limits, Volume
( Cal/cm 3 ) 11 2 Temperature Formation Energy ot: at 77 F Percent in
deg F at 77 F Format ion Btu/lb Air Mixture
Btu/lb at 77 F
Btu/lb
Lower
I Upper
Table 1C4.7 Ethers

783 OIMETHYL ETHER C2H50 1401 8.59 ... -1717.64 -1052.69 46.07 3.40 18.00
764 METHYL ETHYL ETHER C3H90 1407 8.31 -35 .00 - 1548 .42 -841. 71 ... 2.00 10. 10
785 DI ETHYL ETHER C4H100 1402 7 .59 -49. 00 -1462.40 -706. 20 41. 70 1 .90 48.00
788 METHYL- tart-BUTYL ETHER C5H120 1405 7 .39 -1B. 00 -1428.45 -611. 78 37. 07 2.00 15. 10
787 METHYL- tert-AllfYL ETHER C5H140 1400 ... ... ... . .. ... . .. . ..
768 TETRAHYDRDFURAN C4H90 1479 9.35 6.00 -1098.16 -475.08 50.92 2.00 11 .80
789 DIBENZOFURAN C12H90 705 ... ... a.co a.co a.co . .. ...
Table 1C4.8 Gases
770 AIR 915 6. 1B ... a.co a.co ... 5. 71 p . ..
771 AMMONIA NH3 1911 14. 28 ... -1158.70 -414.05 142.80 16.00 . ..
772 ARGON Ar 914 6.91 ... a.co a.co 12. 72 ... . ..
773 BROMINE Br2 922 11 .57 ... 83. 15 s 8.43 28.44 . .. . ..
774 CARBON MONOXIDE co 908 3. 13 ... -1696.50 -2105.32 s 12.91 12.50 74.00
775 CARBON DIOXIDE C02 909 7. 12 ... -3844. 28 -3852. 90 88. 11 ... . ..
776 CARBONYL SULFIDE cos 1893 8.89 ... -990. 59 -1185.50 s 33 .84 12.00 29.00
777 CHLORINE Cl2 918 9.85 ... a.co a. co 38.84 . .. . ..
778 FLUORINE F2 917 7 .42 ... 0.00 0.00 5. 77 . .. ...
779 HELi UM-3 He 923 ... ... . .. ... ... ... ...
780 HELi UM-4 He 913 0.60 ... a.co a.co 5.37 ... . ..
781 HYDROGEN H2 902 3. 25 ... a.co a.co 24.98 4.00 75.00
782 HYDROGEN BROMIDE HBr 1906 10. 19 ... - 193. 64 -2B4.23 12. 78 . .. . ..
783 HYDROGEN CHLORIDE HCI 1904 10. 70 ... -1088. 49 -1123. 77 23 .56 ... . ..
784 HYDROGEN CYANIDE HCN 1771 12. 12 0.00 2149.88 1983 .48 133. 72 6.00 41 .00
785 HYDROGEN FLUORIDE HF 1905 ... ... -5856. 93 -5901. 97 98.43 ... ...
788 HYDROGEN SULFIDE H2S 1922 8.80 ... -260. 28 -421. 90 29.98 4.30 45.50
787 KRYPTON Kr 920 7 .47 ... a.co a.co 8.41 ... . ..
788 NEON Ne 919 4.60 ... a.co a.co 6.99 ... . ..
789 NITROGEN N2 905 4.44 ... 0.00 a.co 11 .04 ... . ..
790 NITRIC OXIDE NO 912 11 .37 ... 1293. 10 1240.34 32.97 . .. . ..
791 NITROUS OXIDE N20 899 10. 20 ... B01 .47 1017.51 63 .88 . .. . ..
792 NITROGEN DIOXIDE N02 900 16.40 ... 309. 28 478. 85 ... . .. . ..
793 NITROGEN TETRDXIDE N204 906 ... ... 42 .42 456. 59 6B.46 . .. . ..
794 OXYGEN 02 901 4.00 ... a.co a.co 5.96 ... . ..
795 OZONE 03 924 9. 27 ... 1277.96 1461 .60 1B. 74 p . .. . ..
798 SULFUR DIOXIDE S02 910 6.00 ... - 1992. 24 -2014.54 49.67 ... . ..
797 SULFUR TRIOXIDE 503 911 15. 15 ... -2125. 10 -1992. 08 40.45 ... . ..
798 XENON Xe 959 7. 78 ... a.co a.co 7. 52 ... . ..
1-132 1987
1C4.9-1C4.10
TABLES 1C4.9-1C4.10
HALOGENATED COMPOUNDS AND KETONES-~ECONDARY PROPERTIES
Search Solubility Flash Ideal Gas Ideal Gas Heat of Flammability

No. Compound Form1,.1la Number Parameter Point Heat of Gibbs Free Futlon Limits, Volume
( Cal/cml) 11 2 Temperature Formation Energy of at 77 F Percent in
deg F at 77 F Formation Btu/lb Air Mixture
Btu(lb at 77 F
Btu/ lb
Lower Upper
I
Table 1C4.9 Halogenated Co•pounds
799 CHLOROTR IF LUO ROME f HANE CCI F3 1606 6.99 ... -2913.69 -2746.B2 ... ... . ..
BOO OICHLOROOI FLUOROMETHANE CC l 2F2 1601 7 .39 ... -174B.Q3 -1609.71 ... ... ...
B01 TRICHLOROF LUOROME f HANE CC l 3F 1602 7 .64 ... -903. 55 -7B0.46 21 .59 ... ...
B02 CARBON TETRACHLORlOE CC14 1501 B.59 ... -26B.26 -150.00 7 .09 . .. . ..
B03 CARBON TETRAFLUORlOE CF4 1616 6. 76 ... -455B.96 -4340. 7B 3.48 . .. . ..
B04 CHLOROOI FLUOROMETHANE CHCIF2 1604 B.44 ... -2394.44 -2240. 25 20.50 . .. . ..
B05 01 CH LOROF LUOROME THANE CHC 12f 1696 B.53 ... -11B3.22 -1056.04 ... ... . ..
B06 CHLOROFORM CHCl3 1521 9. 30 ... -371.SB -253.57 34. 36 ... . ..
B07 TRI FLUOROME THANE CHF3 1615 B.63 ... -4257. 16 -4045. 74 24.92 ... . ..
808 OlCHLOROllE.HIANE. C\12C\l is i i 9.96 24 .53 p -483 .52 -349. 14 l3.30 15.50 66.00
809 METHYL CHLORIOE CH3C\ 1502 9.64 ... -697. 93 -497. 73 55. 76 10.70 12.40
810 METHYL FLUOR ICE CH3F 1613 9.96 ... -3002.28 -2700.49 ... ... . ..
811 VINYL CHLORIOE C2H3C 1 1504 8. 74 -108.00 195. 71 288. 57 32.63 3.60 33.00
812 1 , 1, 1 -TRICHLOROETHANE C2H3Cl3 1527 8.46 ... -458.59 -245.54 7. 57 8.00 10.50
813 1, 1, 2-TRI CHLOROE THANE C2H3Cl3 1524 9.69 ... -469. 23 -268.45 36.41 8.60 p ...
814 1, 1, 1 -TRI FLUOROE THANE C2H3F3 1619 7.70 ... -3814. 17 -3469. 78 31 .68 . .. ...
815 1, 1-DICHLOROETHANE C2H4C l 2 1522 B.96 1Q.40 -565. 30 -31B.45 34. 19 5.40 11 .40
816 1 ,2-0ICHLOROETHANE C2H4C 1 2 1523 9.90 56.00 -563 .86 -321. 19 38. 35 6. 20 16.00
817 1, 1-01 FLUOROETHANE C2H4F2 1640 8.50 ... -3213.62 -2839.43 ... 3. 70 18.00
818 ETHYL CH LOR I OE C2H5C 1 1503 B. 67 -SB. 00 -74B. 11 -403. 18 29. 67 3.80 15.40
819 ETHYL FLUORIDE C2H5F 1617 B.56 ... -2354. 33 -1887.99 ... ... . ..
820 1 , 2-01 CHLOROPROPA~E C3H5C l 2 1526 8.99 60.00 -630.45 -316. 18 ... 3.40 14.50
Table 1C4.10 Ketones
821 ACE.TONE C3H50 1051 9.67 Q.00 -1607.42 -1130.46 42. 13 2 .60 12.80
822 llETH~L ETH~LKETOHE. C41<90 1052 9. 19 21.00 -1421. 21 -810.89 S0.32 1 .80 10.00
823 OIETHYL KETONE C5H100 1053 8.93 ss.oo -1289. 79 -674.16 p 57.87 1 .50 a.co
824 METHYL-n-PROPYL KETONE C5H100 1060 B.94 45.00 -1293. 77 -690. 64 53 .02 1 .so 8. 20
825 METHYL-n-SUTYL KETONE C5H120 1062 8.87 77 .00 -1201. 13 -558. 36 ... 1. 20 8.00
826 METHYL ISOSUTYL KETONE C5H120 1054 8. 71 60.00 -1238. 31 p -581 .00 p ... 1 .40 7 .50
1987 1-133
1C4.11-1C4.12
TABLES 1C4.11-1C4.12
SULFUR-CONTAINING COMPOUNDS AND
MISCELLANEOUS-SECONDARY PROPERTIES
Search Solublllty Flash Ideal Gas Ideal Gas Heat of Flamrnablllty

No. Compound Formula Number Parameter Point Heat of Gibbs Free Fusion Limits, Volume
(Cal/cml) l / 2 Temperature Format ion Energy of at 77 F Percent in
deg F at 77 F Formation Btu/lb Air Mixture
Btu/lb at 77 F
Btu/lb
Lower I Upper
Table 1C4.ll Sulfur Containing Compounds

827 CARBON OISULFIDE CS2 1938 9.98 -22 .00 661.11 377 .83 24.81 1.30 50.00
828 METHYL WERCAPTAN CH4S 1801 10.11 -63.67 p -202.00 -84.91 52. 77 3.90 21.80
829 2, 3-0ITHIABUTANE C2H5S2 1828 9.84 44.33 -107. 71 70.09 41.96 1.90 p
830 DIMETHYL SULF!OE C2H5S 1820 9.05 -29. 00 -257.38 50.96 55. 25 2 .20 19. 70
831 ETHYL WERCAPTAN C2H5S 1802 8.93 -55.00 p -318.45 -29. 53 34. 43 2 .80 18.00
832 2-THIABUTANE C3H9S 1815
833 1-PROPANETHIOL C3H9S 1808
834 n-8UTANETHI0L C4H10S 1841 8. 77 35.00 -419 .87 52.66 49.87
835 t••t-8UTANETHI OL C4H10S 1804 7. 72 -521.04 4.96 11 .83
836 2-BUTANfTHlOL C4H10S 1823
837 2-WETHYL- 1-PRQPANE THI OL C4H10S 1B25
838 3-THIAPENTANE C4H1QS 1818 8.56 14.00 -397. 93 84. 77 56. 75
839 2-THIAHEXANE C5H12S 1816
840 3-THIAHEXANE C5H12S 1817
841 1-PENTANETHIOL C5H12S 1827 8.62 64. 13 -452. 95 74,67 72.32
842 2-THIAHEPTANE C5H14S 1819
843 1-HEXANETHIOL C5H14S 1826
844 1 -HEPTANETHI OL C7H15S 1829
Table 1C4.12 Miscellaneous

845 NATER H20 1921 23.38 ... -5769. 34 -5453. 70 143. 23 ... ...
846 SULFURIC ACID H2S04 1901 12 .53 ... -3222.63 -2864.66 s 46.95 . .. ...
847 SOOI UM HYOROX I OE NaOH 1912 ... ... -2125. 69 -2154. 75 71.06 . .. .. .
848 PROPYLENE CARBONATE C3H5C03 1185 ... ... ... ... ... ... . ..
849 FURFURAL C5H402 1889 11 .56 140.00 -675. 83 -460.28 64.21 2. 10 19.30
850 ! , 2-PllOPYLEHE GLYCOL C3H90z 1211 14.43 210.00 -2315. 47 -1658. 71 p ... 2.60 12.50
851 QI ETHYLENE GLYCOL C4H1003 1202 13. 10 255 .00 -2313.75 -1657.31 p ... 2 .00 p ...
852 TETRAETHYLENE GLYCOL CBH1905 1204 12.81 385.00 -1953.04 p -1238.27 p ... 1.00 p ...
853 W0NOETHAN0LAWINE C2H7NO 1723 15. 25 185.00 -1479.42 - 752. 29 p 144.26 p 3. 10 p ...
854 QI ETHANOLAWI NE C4H11N02 1724 i4. 42 305.00 -1622.93 -875.43 p 102.66 1.80 p ...
855 OIGLYCOLAWINE H(OC2H4)2NH2 1728 ... ... ... . .. ... . .. . ..
858 METHYL OIETHANOLAWINE C5:<13N02 1722 i4.,, 260.00 -1370.99 p -609. 73 p ... ... . ..
857 TRI ETHANOLAWI NE C5H15N03 1725 13.36 355.00 -1619.77 -B64. 32 p 78. 36 p 1 .20 p ...
85B Oil SOPROPANOLAWI NE ( HQC3H5) 2NH 1730 ... ... ... . .. ... .. . .. .
859 N, N-OI WE THYLFORMAWI DE C3H7NQ 1B76 11.60 136.00 -1127.54 -519.99 p 95.02 2. 20 15.20
860 N-WE THYL-2-PYRROL!OONE C5H9NQ 1071 11.43 204. 00 -847,40 p -231 .68 p ... 2. 18 12.24
B61 DIMETHYL SULFOXIDE C2H50S 1844 12 .BB 190.00 -1150.96 -636.61 76.67 2.60 2B.50
862 SULFOLANE C4HB02S 1B45 12 .SB 350.00 -1395.34 p -926. 65 p 4.91 ... . ..
863 SELEXOL 1410 ... 304.0Q s ... ... ... ... .. .
1-134 1987
KEY TO FOOTNOTE CODES
A = Sublimation point temperature.

B = Pseudocritical value.
C = Absolute values from weights in vacuum.
D = Calculated from the definition.
E =At saturation pressure (triple point).
F =At saturation pressure and 60 F.
G = At boiling point.
H =Critical solution temperature instead of aniline point.
J =Evaluated at -148 F.
K =The + sign and the number following signify that the octane number of the compound
corresponds to that of 2,2,4-trimethylpentane with the indicated number of milliliters
of tetraethyl lead added.
L =Evaluated at -54 F.
M = Evaluated at -193.3 F.
N =Too volatile to run as a liquid in the CFR engine.
P =Predicted.
Q =Specific gravity - 119.2 F/60 F (sublimation point).
R = For the undercooled liquid below the normal freezing point.
S = Unknown whether predicted or experimental.
T = Extrapolated.
U =Evaluated at -13.27 F.
V =Predicted and extrapolated.
W = Sublimation temperature.
Y =Net heat of combustion of the gas.
Z =Estimated value.
a= Net heat of combustion of the solid.
1987 1-135
TABLE 1C5.1
......
I
KEY TO REFERENCES-HYDROCARBONS
(..>
O>
Key to References
Boiling Freezing Cr 1 tical Constants Density a.tractive Vapor Heat Capacity Vi9cosity of Heat of
No. Compound. Name Point Point at 60 F lade1: of Pressure at 60 F the Liquid vaporization No.
at l in air the Liquid at 100 F at Normal
atm at l atm at 77 F Boiling Point
Tamp- Pressure Volume Ideal Liquid at 100 F at 200 F

erature Gas at l
atm
, WE THANE 82 82 82 82 51 82 i0i 82 82 ... ... ... 82 ,

2 ETHANE 82 82 82 82 5i 82 136 82 82 82 ... ... 82 2
3 PROPANE 82 82 82 82 5i 82 136 82 82 82 i09 ... 82 3
4 n-BUTANE 82 82 82 82 189 82 189 82 82 ... 189 189 82 4
5 IS08UTANE 82 82 82 82 51 82 88 82 82 82 i09 i0s 82 5
6 n-PENTANE 82 82 82 82 226 82 5i 82 82 ... i09 i09 82 6

7 ISOPENTANE 82 82 82 82 51 82 5i 82 82 ... i09 ... 82 7
8 NEOPENTANE 5i 51 5i 5i 51 i09 5i i89 i09 ... ... ... i09 8
9 n-HEXANE 82 82 82 82 51 82 51 82 82 i89 i99 ... 82 9
10 2-METHYLPENTANE 5i 5i 5i 51 51 189 5i i09 i09 i09 ... ... 189 10
,, 3-ME THYLPENTANE 51 73 51 51 51 189 51 189 189 189 ... ... 189 11

12 2, 2-0IMETHYLBUTANE 51 (P) 51 51 51 189 51 189 189 189 ... ... 189 12
13 2, 3-DIMETHYLBUTANE 51 (P) 51 51 51 189 51 189 189 189 ... ... 189 13
14 n-HEPTANE 82 82 82 82 51 82 51 82 82 189 189 189 82 14
15 2-ME THYLHEXANE 51 51 51 51 51 189 51 189 189 189 ... ... 189 15
16 3-METHYLHEXANE 51 171 51 51 51 189 51 189 189 ... ... ... 189 16

17 3-ETHYLPENTANE 51 51 51 51 51 189 51 189 189 189 ... ... 189 17
18 2, 2-DIMETHYLPENTANE 51 51 5i 51 51 189 51 189 189 189 ... ... 189 18
19 2, 3-0llllE THYLPENTANE 51 ... 51 51 51 189 51 189 189 189 ... .. . 189 19
20 2, 4-0llllETHYLPENTANE 51 51 51 51 51 189 51 189 189 189 ... ... 189 20
2i 3, 3-DIMETHYLPENTANE 51 51 51 51 51 189 51 189 189 189 ... ... 189 2i

22 2, 2, 3-TAUETHYLBUTANE 51 (P) 51 51 51 189 51 189 189 189 ... ... 189 22
23 n-OCTANE 82 82 82 82 51 82 51 82 82 189 189 189 82 23
24 2-ME THYLHEPTANE 51 51 51 51 51 189 51 189 189 189 ... ... 189 24
25 3-M ETHYLH EPT AN E 51 51 51 51 51 189 51 189 189 189 ... ... 189 25
26 4-llETHrLHEPTANE 51 51 51 189 189 189 51 189 189 189 ... ... 189 26
27 3-ETHYLHEXANE 51 ... 189 189 189 189 51 189 189 ... .. . ... 189 27
28 2, 2-DUETHYLHEXANE 51 51 189 189 189 189 51 189 189 ... ... ... 189 28
29 2, 3-DIMETHYLHEXANE 51 ... 189 189 189 189 51 189 189 ... ... ... 189 29
30 2 ,4-DIME THYLHEXANE 51 ... 189 189 189 189 51 189 189 ... ... .. . 189 30
31 2, 5-DUE THYLHEXANE 51 51 189 189 189 189 51 189 189 ... ... ... 189 31
32 3, 3-DIMETHYLHEXANE 51 51 189 189 189 189 51 189 189 ... ... ... 189 32
33 3, 4-0llllE THYLHEXANE 51 ... 189 189 189 189 51 189 189 ... ... .. . i89 33
34 2-MfTHYL-3-E THYLPENTANE 51 51 189 189 189 189 51 189 189 ... ... ... 189 34
35 3-ME THYL-3-E THY LPENTANE 189 189 10i 181 181 189 189 189 189 ... ... ... ... 35
36 2, 2, 3-TAIMETHYLPENTANE 51 51 5i 51 51 189 51 i09 189 ... ... ... 189 36

37 2, 2, 4-TAIMETHYLPENTANE 51 51 51 51 51 189 51 189 189 189 ... ... 189 37
36 2, 3, 3-TAIMETHYLPENTANE 51 51 189 189 189 189 51 189 i09 189 ... ... 189 38
39 2, 3 ,4-TAUETHYLPENTANE 51 51 189 189 189 189 51 189 189 189 ... ... 189 39
(P) Pt"edicted o,. calculated by pt"ojact staf'f',

...... TABLE 1C5.1 (Continued)
<O
a>
......
Aniline ASTH Octane Numbers Flanmablllty

Net Heat of Surface Flash Heat ot Gibbs Free Heat ot Coett1c1ent Point Limits, No.
No. Combustion Tension Point Formation Energy ot Fusion ot Expansion
of Liquid ot the Temp- at n F Format ion at 77 F at 60 F Motor Method Research Method Volume Percent
at 77 P Liquid erature at 11 P ln Air Hlxture
at n P
Clear With 3 Clear WI th 3 Lover Upper
ml TEL ml TEL
per gal per gal
1 189 ... . .. 187 187 189 ... ... ... ... ... ... 82 82 1
2 189 ... ... 187 187 189 ... . .. 82 ... ... 82 82 82 2
J 189 189 ... 187 187 189 51 ... 82 ... . .. 82 82 82 J
4 189 189 ... 187 181 189 51 51 82 51 51 82 82 82 4
5 189 189 ... 187 187 189 51 51 82 ... ... 82 82 82 5
6 189 189 209 187 187 189 51 51 82 51 51 82 82 82 6

7 189 189 ... 187 187 189 51 51 82 ... 51 82 82 82 7
8 189 189 ... 187 187 189 51 51 51 51 51 51 209 209 8
9 189 189 209 187 187 189 51 51 82 51 51 82 82 82 9
10 189 189 (P) 187 187 189 51 51 51 51 51 51 209 209 10
,, 189 189 (P) 187 187 7J 51 51 51 51 51 51 191 50 ,,

12 189 189 209 187 187 189 51 51 51 51 51 51 209 209 12
1J 189 189 209 187 187 189 51 51 51 51 ... 51 209 209 1J
14 189 189 209 187 187 189 51 51 82 51 51 82 82 82 14
15 189 189 ... 187 187 189 51 51 51 51 51 51 177 177 15
16 189 189 171 187 187 ... 51 51 51 51 51 51 51 51 16

17 189 189 ... 187 187 189 51 51 51 51 51 51 51 51 17
18 189 189 ... 187 187 189 51 51 51 51 51 51 191 49 18
19 189 189 ... 187 187 ... 51 51 51 51 51 51 209 209 19
20 189 189 209 187 187 189 51 51 51 51 51 51 191 49 20
21 189 189 ... 187 187 189 51 51 51 51 51 51 51 51 21

22 189 189 ... 184 184 189 51 51 51 51 ... 51 191 49 22
2J 189 189 209 187 187 204 51 51 ... 51 51 ... 82 82 2J
24 189 189 ... 187 187 189 51 51 51 51 51 51 51 49 24
25 189 189 ... 187 187 189 51 51 51 51 51 51 51 49 25
26 189 189 ... 187 187 18':· 51 51 51 51 51 51 51 49 26

27 189 189 ... 187 T87 ... 51 51 51 51 51 51 191 49 27
28 189 189 ... 187 187 189 51 51 51 51 51 51 191 49 28
29 189 189 177 187 187 ... 51 51 51 51 51 51 191 49 29
JO 189 189 177 187 187 ... 51 51 51 51 51 51 191 49 JO
J1 189 189 ... 187 187 189 51 51 51 51 51 51 191 49 J1

J2 189 189 ... 1 l7 187 189 51 51 51 51 51 51 191 49 J2
JJ 189 189 ... H7 187 . .. 51 51 51 51 51 51 191 49 JJ
J4 189 189 ... 187 187 189 51 51 51 51 51 51 191 49 J4
J5 189 189 ... ,~9 189 . .. 51 51 51 51 51 51 191 49 J5
J6 189 189 (P) 187 187 iqg 51 51 51 51 ... 51 51 49 J6

J7 189 189 209 187 187 •39 51 51 51 51 51 51 209 ... J7
J8 189 189 ... 187 187 189 51 51 51 51 ... 51 51 49 J8
J9 189 189 ... 187 187 189 51 51 51 51 . .. 51 51 49 J9
(P) Predicted or calculated by project staff.
......
' (")
c.:> 01
......
TABLE 1C5.1 (Continued) 0
U1
Boiling Pr•••ln9 Cr 1 tlcal Constant• Density Refractive Vapor Heat Capacity Vhco•lty of Heat of
llO. co.pound Ila• Point Point at 60 r Ind.es of Pre11ur• at 60 r the Liquid Vapor 1 sat lon Ho.
at l in alr the Liquid at 100 r at Nor•l
atm at l atm at 77 r Boiling Point
Temp- Pressure Volume Ideal Liquid at 100 r at 200 F

erature Gas at l
atm
40 2, 2, 3 ,3-TETRAMETHYLSUTANE 189 ... 189 189 189 ... ... 189 181 180 ... .. . 51 40
41 n-NONANE 82 82 82 82 51 82 51 82 82 189 189 189 82 41
42 2-METHYLOCTANE 51 51 51 51 51 ... 51 189 189 ... ... .. . ... 42
43 3-METHYLOCTANE 51 51 51 51 51 ... 51 189 189 ... ... ... .. . 43
44 4-METNYLOCTANE 51 51 51 51 51 ... 51 189 189 ... ... .. . .. . 44
45 3-ETHYLHEPTANE 189 ... 189 189 189 189 189 189 ... ... ... .. . 189 45
46 2, 2-0IMETNYLHEPTANE 189 189 (Pl (Pl (Pl 189 189 189 189 180 ... ... ... 46
47 2 0 6-DIMETNYLNEPTANE 189 189 189 189 189 189 189 189 ... ... ... ... 189 47
48 2, 2. 3-TA:IWETNYLHEXANE 189 ... 189 189 189 189 189 189 ... ... .. . ... 189 48
49 2, 2 0 4-TRIWETHYLHEXANE 189 189 189 189 189 189 189 189 ... ... ... .. . 189 49
50 2. 2 .S-TRIWETNYLHEXANE 51 51 51 51 51 ... 51 189 189 ... ... ... . .. 50

51 2 .3. 3-TRIWETHYLHEXANE 189 189 189 189 189 189 189 189 ... ... ... ... ... 51
52 2, 3 ,5-TRIWETHYLHEXANE 189 189 189 189 189 189 189 189 ... ... ... ... 189 52
53 2 ,4 ,4-TRIMETHYLHEXANE 189 189 189 189 189 189 189 189 ... ... ... ... 189 53
54 3, 3 ,4-TRIMETHYLHEXANE 189 189 189 189 189 189 189 189 ... ... ... .. . ... 54
55 3 ,3-01 ETHYLPENTANE 51 51 51 51 51 ... 51 189 189 189 ... ... .. . 55

56 2, 2-01 ME TNYL-3-ETHYLPENTAN E 189 189 (Pl (Pl (Pl 189 189 189 ... ... ... ... 189 56
57 2, 4-01 WETNYL-3-E THYLPENT AME 189 189 (Pl (Pl (Pl 189 189 189 ... ... ... ... . .. 57
58 2, 2 ,3, 3-TETRAMETHYLPENTANE 51 51 51 51 51 ... 51 189 189 189 ... .. . ... 58
59 2, 2 ,3 ,4-TETRAMETNYLPENTANE 51 51 51 51 51 ... 51 189 189 ... ... ... ... 59
60 2, 2 ,4 ,4-TETRAMETHYLPENTANE 51 51 51 51 51 ... 51 189 189 189 ... ... ... 60

61 2, 3 ,3 ,4-TETRAMETHYLPENTANE 189 189 189 189 189 189 189 189 189 180 ... ... ... 61
62 n-OECANE 82 82 82 82 51 82 51 82 82 189 189 189 82 62
83 2-WETNYLNONANE 189 189 189 189 189 189 189 189 189 ... ... ... 189 63
64 3-METHYLNONANE 189 189 189 189 189 189 189 189 189 ... ... ... 189 64
85 •-WETNYLNONANE 189 189 (Pl (Pl (Pl 189 189 189 ... ... ... ... .. . 65
66 5-WETHYLNONANE 189 189 (Pl (Pl (Pl 189 189 189 ... ... ... ... 189 66
87 2. 7-01 METHYLOCTANE 189 189 189 189 189 189 189 189 189 ... ... ... . .. 67
66 3 ,3 ,4-TRIMETHYLHEPTANE 189 ... 189 189 189 189 189 189 ... ... ... .. . 189 68
69 3 ,3 ,5-TRIMETNYLHEPTANE 189 ... 189 189 189 189 189 189 ... ... ... .. . ... 69
70 2, 2 ,3, 3-TETRAMETNYLNEXANE 189 189 189 189 189 189 189 189 ... ... ... ... 189 70
71 2 ,2 ,5 ,5-TETRAMETNYLHEXANE 189 189 189 189 189 189 189 189 ... ... ... ... ... 71
72 2, 4-01 METNYL-3· I SOPROPYL-
PENTANE 189 189 (Pl (Pl (Pl 189 189 189 ... ... ... ... 189 72
73 n-UNDECANE 189 189 189 189 189 189 189 ... 189 ... 189 189 189 73
74 n-OODECANE 189 189 189 189 189 189 189 ... 189 ... 189 189 189 74
75 n-TRIOECANE 189 189 189 189 189 189 181 ... 189 ... 189 189 189 75
76 n-TETRAOECANE 189 189 154 154 189 189 181 ... 189 ... 189 189 189 78
77 n- PENT ADE CANE 189 189 189 189 189 189 181 ... 189 ... 189 189 189 77
<O
00
......
Anlllne ASTM Octane Number• rla-.oblllty

Het Heat ot Surtace Flash Heat of Clbba Free Heat of Coet't' le lent Point Limit•, No.
No. Combu•tion T•n•lon Point Format ion Ener9y ot Fu• ion of Ex pans ion
of Liquid or th• Teqi- at 77 F Foru.t !.on at 77 F at 60 F Motor Method R•••arch Method Volu.me Percent
at 77 r Liquid erature at 77 r in Air Mixture
at 77 r
Clear With l Clear With 3 Lover Upper
ml TEL ml TEL
per gal per CJ•l
40 189 (P) 189 189 191 49 40

41 189 189 209 189 189 189 51 51 82 82 41
42 189 189 189 186 189 51 51 51 49 42
43 189 189 189 186 189 51 51 51 49 43
44 189 189 186 188 189 51 51 51 49 44
45 189 189 189 189 51 51 191 49 45

46 189 189 189 189 51 51 51 51 51 191 49 46
47 189 189 189 189 51 51 191 49 47
48 189 189 189 189 51 51 191 49 48
49 189 189 189 189 51 51 191 49 49
50 189 189 209 204 204 189 51 51 191 49 50

51 189 189 189 189 51 191 49 51
52 189 189 189 189 51 51 191 49 52
53 189 189 189 189 51 191 49 53
54 189 189 189 189 51 191 49 54
55 189 189 189 188 74 51 51 51 51 51 51 209 209 55

58 189 189 189 189 51 51 51 51 51 191 49 56
57 189 189 189 189 51 51 51 51 51 191 49 57
58 189 189 189 186 189 51 51 51 51 51 51 177 177 58
59 189 189 189 186 189 51 51 49 59
60 189 189 189 186 189 51 51 51 49 60

61 189 189 189 189 51 81
82 189 189 209 189 189 189 51 51 82 82 82
63 189 (P) 189 189 51 51 191 49 63
64 189 (P) 189 189 51 51 191 49 64
85 189 (P) 189 189 51 51 191 49 65

66 189 (P) 189 189 51 51 191 49 66
67 189 181 189 189 51 51 191 49 87
68 189 (P) 189 189 51 191 49 68
69 189 (P) 189 189 51 51 51 51 51 51 191 49 89
70 189 (P) 189 189 51 51 51 51 51 191 49 70

71 189 (P) 189 189 51 51 191 49 71
72 189 (P) 189 189 51 191 49 72

73 189 189 209 189 189 189 191 49 73
74 189 189 209 189 189 189 209 49 74
75 189 189 189 189 204 191 49 75

76 189 189 209 189 189 204 209 49 76
77 189 189 189 189 204 191 49 77
(P) :i: Pl"edicted OI" c•lculated by project •taff .

.....
.....
I
~
.....
I TABLE 1C5.1 (Continued)
~
Bolling P'ree:1in9 Critical Conatanta Oen•ity Retract iv• vapor Heat Capacity Viacosity ot Heat ot
llo. ~und Na ... Point Point at 60 r Inde• ot Pr•••ure at 60 r the Liquid vapor 12at1on No.
at l in air the Liquid at lOD r at Horu.l
atm at l atm at 77 r Bolling Point
Temp- Preaaure Volume Ideal Liquid at lDO r at 200 r

erature Gas at l
at•
78 n-HEXADECANE 189 189 189 189 189 189 181 ... 189 ... 189 189 189 78
79 n-HEPTADECANE 51 51 51 51 51 189 51 ... 189 ... 189 189 189 79
80 n-OCTADECANE 51 51 51 51 51 189 181 ... 189 ... 189 189 189 80
81 n-NONADECANE 189 51 51 51 51 189 51 ... 189 ... 189 189 189 81
82 n-EICOSANE 51 51 51 51 51 51 51 ... 189 ... 189 189 189 82
83 n-HENEIC05ANE 181 181 (P) (P) (P) 189 181 ... ... ... ... ... . .. 83
84 n-DOC05ANE 189 189 (Pl (P) (P) 189 181 ... 189 180 ... . .. ... 84
85 n-TRICOSANE 189 189 (P) (P) (P) 9 189 ... 181 180 ... ... ... 85
88 n- TE TRACOSAN E 189 189 (Pl (P) (Pl 9 181 ... 181 180 ... ... . .. 86
87 n-PENTAC05ANE 189 189 (P) (P) (P) 189 181 ... 181 180 ... ... ... 87
88 n-HEXACOSANE 189 189 (Pl (P) (P) 9 189 ... 181 180 ... ... ... 88
89 n-HEPTAC05ANE 189 189 (Pl (P) (P) 189 189 ... 181 180 ... . .. . .. 89
90 n-OCTAC05ANE 189 189 (P) (P) (P) 9 189 ... 181 180 ... ... . .. 90
91 n-NONACOSANE 189 189 (P) (P) (P) 189 189 ... 181 180 ... ... ... 91
92 n-TRIACONTANE 189 189 (P) (P) (P) 189 189 ... ... ... ... ... ... 92
93 CYCLOPROPANE 51 51 51 189 189 ... ... 189 ... ... ... ... . .. 93
94 METHYLCYCLOPROPANE 189 189 (P) (P) (P) ... ... ... ... 180 ... . .. . .. 94
95 ETHYLCYCLOPROPANE 189 189 (P) (P) (P) 189 189 ... ... 180 ... ... ... 95
98 cia- 1, 2-DIMETHYLCYCLOPROPANE 189 189 (P) (P) (P) 189 189 ... ... 180 ... ... ... 96
97 trana-1. 2-DilllETHYLCYCLOPROPANE 189 189 ... ... ... 51 ... ... ... ... ... ... . .. 97
88 CYCL08UTANE 51 51 51 51 51 ... 51 189 ... ... ... ... . .. 98

99 METHYLCYCL08UTANE 189 ... (P) (P) (P) 189 189 ... ... 180 ... ... . .. 99
100 ETHYLCYCL08UTANE 189 189 (P) (P) (P) 189 189 ... ... 180 ... ... ... 100
101 CYCLOPENTANE 51 51 51 51 51 189 51 189 189 ... 189 . .. 189 101
102 METHYLCYCLOPENT ANE 51 51 51 51 51 189 51 189 189 ... 189 ... 188 102
103 ETHYLCYCLOPENTANE 51 51 51 51 51 189 51 189 189 ... 189 189 189 103
104 1, 1-DUETHYLCYCLOPENTANE 189 189 189 189 189 189 189 189 189 180 ... ... . .. 104
105 cia-1, 2-DUETHYLCYCLOPENTANE 51 51 51 51 51 ... 51 ... 189 ... ... ... 189 105
108 tran9- 1•2-0illlETHYLCYCLOPENT ANE 51 51 51 51 51 ... 51 ... 189 ... ... . .. 189 106
107 cia- 1. 3-DUETHYLCYCLOPENTANE 189 189 189 189 189 189 189 189 189 180 ... ... ... 107
108 trana-1,3-DilllETHYLCYCLOPENTANE 189 189 189 189 189 189 189 189 189 180 ... ... ... 108
109 n-PROPYLCYCLOPENT ANE 51 51 51 51 51 189 51 189 189 ... 189 189 ... 109
110 I50PROPYLCYCLOPENTANE 189 189 (P) (P) (P) 189 189 189 181 180 ... ... ... 110
111 1-METHYL- 1- ETHYLCYCLOPENT ANE 189 189 (P) (P) (P) 189 189 189 181 180 ... ... ... 111
112 ci•- 1-lllETHYL-2-ETHYL-
CYCLOPENTANE 189 189 (P) (Pl (P) 189 189 189 ... 180 ... ... . .. 112
113 tr9na-1-lllETHYL-2-ETHYL-
CYCLOPENTANE 189 51 (P) (P) (P) 189 189 189 ... 180 ... ... . .. 113
114 cia- 1-METHYL-3-ETHYL-
CYCLOPENTANE 189 ... (P) (P) (P) 189 189 189 ... 180 ... ... ... 114
(P) Predicted or ca 1cu1 ated by project staff.

Aniline ASTM Octane Numbers Flammability

Net Heat of Surface Flash Meat of Gibbs Free Meat of Coefficient Point Limits, No.
No. Combustion Tension Point Formation Energy of Fusion of Expansion
ot Liquid of the Temp- at 77 P' Formation at 77 F at 60 F Motor Method Research Method Volume Percent
at 77 F Liquid erature at 77 F in Air Mixture
at 71 P'
Clear With J Clear With J Lower Upper
ml TEL rnl TEL
per gal per gal
78 189 189 204 204 204 191 49 78

79 189 189 189 186 189 191 49 79
80 189 189 189 186 189 191 49 80
81 189 189 189 189 189 191 49 81
82 189 189 189 186 189 191 49 82
83 180 51 (P) 191 49 83

84 180 51 (P) 191 49 84
85 180 51 (P) 191 49 85
86 180 51 (P) 191 49 86
87 180 51 (P) 191 49 87
88 180 (P) 191 49 88

89 180 51 (P) 191 49 89
90 180 51 (P) 191 49 90
91 180 51 (P) 191 49 91
92 180 51 (P) 191 49 92
93 189 189 189 189 189 51 51 93

94 180 (P) 51 51 51 51 191 49 94
95 180 (P) (P) 51 51 51 51 51 191 49 95
96 180 (P) (P) 51 51 51 51 51 191 49 96
97 97
98 189 189 (P) 181 181 189 51 51 49 98

99 180 (P) (P) 51 191 49 99
100 180 (P) (P) 51 51 51 51 100
101 189 189 189 189 189 51 51 51 51 51 51 51 49 101
102 189 189 171 189 189 189 51 51 51 51 51 51 51 51 102
103 189 189 177 189 189 189 51 51 51 51 51 51 51 51 103

104 189 189 189 189 51 51 51 51 51 51 191 49 104
105 189 189 62 189 189 189 51 51 191 49 105
106 189 189 62 189 189 51 51 191 49 106
107 189 (P) 189 189 51 51 51 51 51 191 49 107
108 189 (P) 189 189 51 51 51 51 51 51 191 49 108

109 189 189 (P) 189 189 189 51 51 51 51 51 51 51 49 109
110 180 189 (P) 51 51 51 51 51 191 49 110
111 180 (P) (P) 51 191 49 111
112 180 (P) (P) 51 51 191 49 112
113 180 (P) (P) 51 51 191 49 113
114 180 (P) (P) 51 51 51 51 51 191 49 114
(P) = Pred~c'teO or calculated by project staff.

......
I
.j:>.
......
I TABLE 1CS.1 (Continued)
.......
.i:..
I\)
Boiling Freexing Critical Com1tants Oan91ty Refractive Vapor Heat Capacity Viscosity ot Heat of
No. Compound Name Point Point at 60 F Index of Pressure at 60 F the Liquid Vapor 1 zat ion No.
at l in air the Liquid at 100 F at Normal
atm at l atm at 77 F Boiling Point
Temp- Pressure Volume Ideal Liquid at 100 F at 200 F

erature Gas at l
atm
115 tr-ans- 1-METHYL-3- ETHYL-

CYCLOPENTANE 189 ... (Pl (Pl (Pl 189 189 189 ... 180 ... ... .. . 115
116 1, 1, 2-TRIMETHYLCYCLOPENTANE 189 189 (Pl (Pl (Pl 189 189 189 181 180 ... ... ... 116
117 1, 1, 3-TRIMETHYLCYCLOPENTANE 189 189 (Pl (Pl {Pl 189 189 189 181 180 ... ... ... 117
118 1,c-2,c-3-TRUIETHYL-
CYCLOPENTANE 189 189 {Pl {Pl {Pl 189 189 189 ... 180 ... ... .. . 118
119 1 ,c-2,t-3-TRIMETHYL-
CYCLOPENTANE 189 189 {Pl {Pl {Pl 189 189 189 ... 180 ... ... .. . 119
120 1 ,t-2,c-3-TRIMETHYL-
CYCLOPENTANE 189 189 {Pl {Pl {Pl 189 189 189 ... 180 ... ... 51 120
121 , ,c-2,c-4-TRUIETHYL-
CYCLOPENTANE 189 51 {Pl {Pl {Pl 189 189 189 ... 180 ... .. . ... 121
122 1 ,c-2, t-4-TRUIETHYL-
CYCLOPENTANE 189 189 (Pl {Pl {Pl 189 189 189 181 180 ... ... ... 122
123 1,t-2,c-4-TRUIETHYL-
CYCLOPENTANE 189 189 (Pl {Pl {Pl 189 189 189 ... 180 ... .. . ... 123
124 n-BUTYLCYCLOPENT ANE 189 189 (Pl {Pl {Pl 189 189 ... ... 180 ... .. . 51 124
125 I SOBUTYLCYCLOPENTANE 189 189 (Pl {Pl {Pl 189 189 ... ... 180 ... ... .. . 125
128 1 -METHYL-1-n-PROPYL-
CYCLOPENT ANE 189 ... {Pl {Pl {Pl 189 189 ... ... 180 ... .. . .. . 126
127 1, 1-DIETHYLCYCLOPENTANE 189 ... {Pl {Pl {Pl 189 189 ... ... 180 ... ... .. . 127
128 c is-1, 2-0I ETHYLCYCLOPENTANE 189 189 {Pl {Pl {Pl 189 189 ... ... 180 ... ... .. . 128
129 1, 1-0IMETHYL-2-ETHYL-
CYCLOPENTANE 189 ... {Pl {Pl {Pl 189 189 ... ... 180 ... ... .. . 129
130 n- PENT YLCYC LOP ENTAN E 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 ... 130
131 n-HEXYLCYC LOPENT ANE 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 ... 131
132 n-HEPTYLCYCLOPENT ANE 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 ... 132
133 n-OCTYLCYC LOPENTANE 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 ... 133
134 n-NONYLCYC LO PENT ANE 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 189 134
135 n-DECYLCYC LO PENT ANE 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 ... 135
138 n-UNOECYLCYC LOP ENT ANE 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 189 136
137 n- DOOECYLCYC LOP ENT ANE 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 189 137
138 n-TRI DECYLCYCLOPEN TANE 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 ... 138
139 n-TETRADECYLCYCLOPENT ANE 189 189 {Pl {Pl {Pl 189 189 ... 189 180 189 189 ... 139
140 n-PENT AOECYLCYCLOPENT ANE 189 189 {Pl {Pl {Pl 189 189 ... 189 ... 189 189 ... 140
141 n-HEXADECYLCYCLOPENT ANE 189 189 {Pl {Pl {Pl 189 189 ... 189 ... ... ... ... 141
142 n-HEPT AOECYLCYCLOPENT ANE 189 189 (Pl {Pl {Pl 189 189 ... ... ... ... ... ... 142
143 n-OCT AOECYLCYCLOPENT ANE 189 189 (Pl {Pl {Pl 189 189 ... ... ... . .. ... ... 143
144 n-NONAOECYLCYCLOPENT ANE 189 189 (Pl {Pl {Pl 189 189 ... ... ... ... ... .. . 144
( P) Pr-adictad or- cs I cu I a tad by pr-ojact staff.

..... TABLE 1C5.1 (Continued)
<O
CX>
......
Aniline ASTM OCtane Numbers Fia....abil ity

Met Heat of Surface P'la1h Heat of Gibbs Free Heat of Coefficient Point Limits, No.
llo. Combustion Tension Point Format ion !ner9y of Fusion ot Exp.ans ion
ot Liquid ot the Temp- at 77 P Formation at 77 r at 60 P llOtor Met hod Research Method volume Percent
at 77 r Liquid erature at 77 r in Air Mixture
at 77 r
Clear With 3 Clear With 3 Lover Upper
ml TEL ml TEL
per gal per gal
115 180 (P) (P) 51 51 51 51 51 191 49 115

116 180 (P) (P) 51 191 49 116
117 180 (P) (P) 51 51 51 51 51 191 49 117
118 180 (P) (P) 51 51 191 49 118
119 180 (P) (P) 51 51 191 49 119
120 180 (P) (P) 51 51 191 49 120
121 180 (P) (P) 51 191 49 121
122 180 (P) (P) 51 51 51 51 191 49 122
123 180 (P) (P) 51 191 49 123

124 189 189 189 189 51 51 51 51 51 51 191 49 124
125 180 189 (P) 51 51 51 51 51 191 49 125
126 180 (P) (P) 51 191 49 126

127 180 (P) (P) 51 191 49 127
128 180 (P) (P) 51 51 191 49 128
129 180 (P) (P) 51 191 49 129
130 189 189 189 189 51 191 49 130

131 189 189 189 189 191 49 131
132 189 189 189 189 191 49 132
133 189 189 189 189 191 49 133
134 189 189 189 189 191 49 134
135 189 189 189 189 191 49 135

136 189 (P) 189 189 191 49 136
137 189 (P) 189 189 191 49 137
138 189 (P) 189 189 191 49 138
139 189 (P) 189 189 191 49 139
140 189 (P) 189 189 191 49 140

141 189 (P) 189 189 191 49 141
142 180 51 (P) 191 49 142
143 180 51 (P) 191 49 143
144 180 51 (P) 191 49 144
(P) = Predicted or calculated by project staff .
.....
.....
I
~
(,.)
.... TABLE 1C5.1 (Continued)
....
I
Bolling Pree1in9 Critical Constants Oenaity Retract iv• Vapor Heat Capacity Viscosity ot' Heat ot'
No. Compound Name Point Point at 60 r Index ot' Presaure at 60 r the Liquid Vaporhation No.
at l in air the Liquid at 100 P at Normal
atm at l atm at 77 r Boilin9 Point
Temp- Pres au re Volume Ida al Liquid at 100 F at 200 F

erature Gaa at l
atm
145 n-E ICOSYLCYCLOPENTANE 189 189 {P) (Pl (P) 189 189 ... ... ... ... ... . .. 145
146 CYCLOHEXANE 51 51 51 51 51 189 51 189 189 ... 189 ... 189 148
147 WETHYLCYCLOHEXANE 51 51 51 51 51 189 189 189 189 ... 189 189 189 147
148 ETHYLCYCLOHEXANE 51 51 51 51 51 189 51 189 189 ... 189 189 189 148
149 1, 1-0IWETHYLCYCLOHEXANE 51 51 51 51 51 ... 51 189 189 ... ... ... 189 149
150 c1s-1, 2-0IWETHYLCYCLOHEXANE 51 51 51 51 51 ... 51 189 189 . .. ... . .. 189 150

151 tr"ena-1, 2-0IWETHYLCYCLOHEXANE 51 51 51 51 51 ... 51 189 189 . .. ... . .. 189 151
152 c1s·1,3-0IWETHYLCYCLOHEXANE 189 189 51 51 51 ... 51 189 189 ... . .. . .. 189 152
153 tr"ans-1, 3-0IWETHYLCYCLOHEXANE 51 51 189 51 51 ... 51 189 189 ... ... . .. 189 153
154 c1s-1 ,4-0IWETHYLCYCLOHEXANE 189 189 51 51 51 ... 51 189 189 ... ... . .. 189 154
155 trans-1 ,4-0IWETHYLCYCLOHEXANE 51 51 51 51 51 ... 51 189 189 ... ... ... 189 155
158 n-PROPY LCYCLOHEXANE 51 51 51 51 51 189 51 189 189 ... 189 189 ... 158
157 I SOPROPYLCYCLOHEXANE 189 189 (P) (P) (P) 189 ... 34 181 180 ... ... ... 157
158 n-SUTYLCYCLOH EXANE 51 51 51 198 172 189 51 189 189 ... 189 ... ... 156
159 I S08UTYLCYCLOHEXANE 181 ... (P) (P) (P) 220 ... 34 . .. 180 ... ... . .. 159
160 sec-BUTYLCYCLOH EXANE 181 ... (P) {P) (P) 220 51 ... ... 180 ... . .. . .. 160
161 ter t-SUTYLCYCLOH EXANE 181 51 (P) (P) (P) 220 51 ... ... 180 . .. ... ... 161
162 1-WETHYL-4- I SOPROPYL-
CYCLOHEXANE 181 ... (P) (P) (P) (P) ... . .. ... 180 ... . .. ... 162
183 n-PENTYLCYC LOHEXANE 189 189 (P) (P) (P) 189 189 ... 189 180 ... . .. 189 163
164 n-HEXY LCYCLOHEXANE 189 189 (P) (P) (P) 189 189 ... 189 180 . .. ... ... 164
185 n-HEPTYLCYC LOHEXANE 189 189 (P) (P) (P) 189 189 ... 189 180 ... . .. ... 165
188 n-OCTY LCYCLOHEXANE 189 189 (P) (P) {P) 189 189 ... 189 180 ... ... 189 188
167 n-NONY LCYCLOHEXANE 189 189 (P) (P) (P) 189 189 ... 189 180 ... . .. ... 167
168 n-OECY LCYCLOHEXANE 189 189 (P) (P) (P) 189 189 ... 189 180 ... . .. ... 168
189 n-UNOECYLCYCLOHEXAN E 189 189 (P) (P) (P) 189 189 ... 189 180 ... ... 189 169
170 n-OOOECY LCYCLOHEXAN E 189 189 (P) (P) (P) 189 189 ... 189 180 . .. ... . .. 170
171 n-TRI OECYLCYCLOHEXANE 189 189 (P) (P) (P) 189 189 ... ... ... ... ... . .. 171
172 n-TE TRAOECY LCYC LOH EXANE 189 189 {P) (P) (P) 189 189 ... ... ... . .. ... ... 172
173 n-PENTAOECY LCYC LOH EXANE 189 189 (P) (P) (P) 189 189 ... ... ... . .. ... ... 173
174 n-HEXAOECY LCYCLOHEXANE 189 189 (P) (P) (P) 189 189 ... ... ... ... ... . .. 174
175 n-HEPTAOECY LCYCLOHEXANE 189 189 (P) (P) (P) 189 189 ... ... . .. . .. ... ... 175
178 n-OCT AOECYLCYCLOHEXAN E 189 189 (P) (P) (P) 189 189 ... ... ... . .. ... ... 176
177 n - NONAO EC YLC YC LOH EXAN E 189 189 (P) (P) (P) 189 189 ... ... ... . .. . .. ... 177
178 n-E ICOSYLCYCLOHEXANE 189 189 (P) (P) (P) 9 189 ... ... ... ... . .. . .. 178
179 CYCLOHEPTANE 189 189 189 189 189 ... 51 189 . .. ... . .. ... ... 179
180 CYCLOOCTANE 189 189 169 189 189 189 189 189 181 ... ... . .. 189 180
181 CYCLONONANE 189 189 189 189 189 189 189 ... 181 ... ... . .. 189 181
182 E THYLCYCLOHEPTANE 181 ... (P) (P) (P) 181 ... ... ... 180 . .. ... ... 182
183 81CvCLOHEXYL 171 171 150 130 172 ... 171 ... ... ... ... ... . .. 183
(P) Pradicted or calculated by project staff.
co
())
-....!
TABLE 1CS.1 (Continued)
Aniline ASTH Octane Numbers P'lal'lllTlability

Net Heat ot' Sur race Flash Heat ot' • Gibbs Free Heat ot' Coat't'icient Point Limits, No.
No. Combustion Tension Point Formation Energy ot' P'usion ot' Expansion
ot' Liquid ot' the Temp- at 77 F Formation at 77 F at 60 F Motor Method Research Method Volume Percent
at 77 f' Liquid erature at 77 F in Air Mixture
at 77 F
Clear With 3 Clear With 1 Lower Upper
ml TEL ml TEL
per 9al per gal
145 180 51 (P) 191 49 145

146 189 189 209 189 189 22~ 51 51 51 51 51 51 209 209 146
147 189 189 209 189 189 189 51 51 51 51 51 51 209 49 147
148 189 189 209 189 189 189 51 51 51 51 51 51 209 209 148
149 189 189 189 189 204 51 51 51 51 51 51 191 49 149
150 189 189 62 189 189 189 51 51 51 51 51 51 191 49 150

151 189 189 62 189 189 189 51 51 51 51 51 51 191 49 151
152 189 189 62 189 189 189 51 51 51 51 191 49 152
153 189 189 189 189 189 51 51 51 51 51 51 191 49 153
154 189 189 62 189 189 189 51 51 51 51 51 51 191 49 154
155 189 189 62 189 189 189 51 51 51 51 51 51 191 49 155

156 189 189 189 189 189 51 51 51 51 51 51 51 49 156
157 180 189 (P) 51 51 51 51 51 51 191 49 157
158 189 189 189 189 189 51 51 51 51 51 49 158
159 180 189 (P) 51 191 49 159
160 180 189 (P) 191 49 160

161 180 189 (P) 51 191 49 161
162 180 (P) (P) 51 191 49 162

163 189 189 189 189 191 49 163
164 189 189 189 189 191 49 164
165 189 189 189 189 191 49 165

166 189 189 189 189 191 49 166
167 189 189 189 189 191 49 167
168 189 189 189 189 191 49 168
169 189 (P) 189 189 191 49 169
170 189 (P) 189 189 191 49 170

171 189 (P) 189 189 191 49 171
172 189 (P) 189 189 191 49 172
173 189 51 189 189 191 49 173
174 189 51 189 189 191 49 174
175 180 51 (P) 191 49 175

176 180 51 (P) 191 49 176
177 180 51 (P) 191 49 177
178 180 51 (P) 191 49 178
179 189 181 181 189 51 51 51 51 51 191 49 179
180 189 180 181 204 51 51 51 191 49 180

181 189 (P) 181 51 191 49 181
182 180 (P) (P) 191 49 182
183 161 148 161 (P) 148 148 183
(P) =Predicted or calculated by project staff.
......
'
~
01
.....
I
Bolling Frsezln9 Cr 1t lcal Conetants Osnslty Rertactlvs Vapor Hsat Capacity Viscosity ot. Heat or
No. Compound Name Point Point at 60 F Ind.sic or PresaLlr• at 60 F the Liquid Vaporization No.
at l ln air ths Liquid at 100 F at Normal
atlft at l atm. at 77 F Bollin9 Point
Temp- Preaaure Volume Ideal Liquid at 100 F at 200 F

eraturs Gas at l
atm
184 c 1 s- DECAHVORONAPHTHA LENE. 14 14 14 14 14 ... 14 ... ... ... ... . .. ... 184
185 t,.sne-OECAHVDRONAPHTHALENE 14 14 14 14 14 ... 14 ... ... ... ... . .. . .. 185
188 1-WETHVL- (c 1a· OECAHVORO-
NAPHTHALENE] 189 ... (Pl (Pl (Pl (Pl ... . .. ... 180 ... . .. . .. 186
187 1 ·lllETHVL-(trsna-OECAHVORO-
NAPHTHALENE] 189 ... (Pl (Pl (Pl . .. 189 ... ... 180 ... . .. . .. 187
188 1-ETHVL- (c 1 s-OECAHVORO-
NAPHTHALENE] 189 ... (Pl (Pl (Pl ... ... ... ... 180 ... . .. . .. 188
189 1-ETHVL-{ tr"sns-DE.CAHVORO-

NAPHTHALENE] 189 ... (Pl (Pl (Pl ... ... ... ... 180 ... . .. . .. 189
190 9· ETHVL-(c 1a-OECAHVORO-
NAPHTHALENE] 51 ... (Pl (Pl (Pl 51 51 ... ... 180 ... . .. ... 190
191 9-ETHVL- { tr"sne-oe.CAHVDRO-
NAPHTHALENE] 51 ... (Pl (Pl (Pl 51 51 ... ... 180 ... ... . .. 191
192 ETHYLENE 51 51 51 51 51 ... 68 ... 189 ... ... . .. 189 192
193 PROPYLENE 51 51 51 51 51 189 68 189 189 189 ... . .. 189 193
194 1-SUTENE 51 51 51 51 51 189 136 189 189 189 ... . .. 189 194
195 c1a·2-8UTENE 51 51 51 51 51 189 136 189 189 189 ... . .. 189 195
198 tr"sna-2-BUTENE 51 51 51 51 51 189 136 189 189 ... ... . .. 189 196
197 IS08UTENE 51 51 51 51 51 189 134 189 189 ... ... . .. 189 197
198 1·PENTENE 51 51 189 189 189 189 51 189 189 189 ... . .. 189 198
199 cia-2-PENTENE 51 51 51 51 51 189 51 189 189 189 ... . .. 189 199

200 tr"sns-2-PENTENE. 51 51 51 51 51 189 51 189 189 189 ... . .. 189 200
201 2·WETHVL-1 ·8UTENE 51 51 189 189 189 189 51 189 189 189 ... . .. 189 201
202 3·WETHVL· 1-8UTENE 51 51 51 51 51 189 51 189 189 189 ... . .. 189 202
203 2-WETHVL-2-8UTENE 51 51 189 189 189 189 51 189 189 189 ... . .. 189 203
204 1 ·HEXENE 51 51 189 189 189 189 189 189 189 ... 189 ... . .. 204
205 cia-2-HEXENE 51 51 150 130 172 ... 51 189 189 ... ... ... 51 205
208 tr"sna-2-HEXENE 51 51 150 130 172 ... 51 189 189 . .. ... ... 51 206
207 ch-3-HEXENE 189 189 (Pl (Pl (Pl 189 189 189 ... 180 ... ... 189 207
208 tr"ena-3-HEXENE 189 189 (Pl (Pl (Pl 189 189 189 ... 180 ... ... . .. 208
209 2-WETHVL-1-PENTENE 51 51 150 130 172 ... 51 189 ... . .. ... . .. . .. 209
210 3-METHVL-1-PENTENE 189 189 (Pl (Pl (Pl 189 189 189 ... 180 ... . .. ... 210
211 4-METHVL-1 ·PENTENE 51 51 150 130 172 ... 51 189 ... . .. ... ... 51 211
212 2- lllETHVL • 2- PENT ENE 51 51 150 130 172 ... 51 189 ... . .. . .. ... 51 212
213 c 1a-3-METHVL·2-PfNTENE 189 189 (Pl (Pl (Pl 189 189 189 ... 180 ... ... 189 213
214 tr" sna-3-111 ETHVL-2· PEN TEN E 189 189 (Pl (Pl (Pl 189 189 189 ... 180 ... ... . .. 214
215 ci a-4-METHVL-2-PE.NTENE 51 51 150 130 172 ... 51 189 189 ... ... ... . .. 215
218 tr"ena-4-METHVL- 2- PENT ENE 51 51 150 130 172 ... 51 189 189 ... ... ... . .. 216
CP) Pr"ed1 ctea o,.. cs 1cu1 st ea by pr"oject stsff'.

Aniline ASTM Octane Numben Flammability

Net Heat ot' Surface Fla1h Heat or Gibb1 Free Heat ot' Coet't le ient Point Limit1, No.
No. Coll'lbu1tion Ten1ion Point Format ion Energy ot' FU!I ion ot' Ex pans ion
ot ~iquid or th• Temp- at 77 F Formation at 77 F at 60 F Motor Method Research Method Volume Percent
at 77 F ~iquid erature at 77 F in Air Mixture
at 77 F
Clear With l Clear with l Lower Upper
ml TEL ml TE~
per gal per gal
184 14 14 14 14 14 51 51 209 209 184

185 14 14 14 14 14 51 51 209 209 185
186 51 191 49 188
187 51 191 49 187
188 51 191 49 188
189 51 191 49 189
190 51 191 49 190
191 51 191 49 191

192 189 189 189 189 51 51 229 229 192
193 189 189 221 186 189 189 51 51 51 221 221 193
194 189 189 189 189 189 51 51 51 209 209 194

195 189 189 189 189 189 51 51 51 136 136 195
196 189 189 189 189 189 51 209 209 196
197 189 189 189 189 189 51 51 209 209 197
198 189 189 209 189 189 189 51 51 51 51 51 51 209 209 198
199 189 189 171 189 189 189 51 51 51 49 199

200 189 189 (P) 189 189 189 51 51 51 49 200
201 189 189 209 189 189 189 51 51 51 51 51 51 49 201
202 189 189 (P) 189 189 189 51 51 51 51 51 134 202
203 189 189 209 189 189 189 51 51 51 51 51 51 51 49 203
204 189 189 189 189 189 51 51 51 51 51 51 51 49 204

205 189 51 51 189 51 51 191 49 205
208 189 51 51 189 51 51 51 51 51 51 191 49 206
207 189 51 189 189 51 51 191 49 207
208 189 51 189 189 51 51 51 51 51 191 49 208
209 189 51 51 189 51 51 51 51 51 191 49 209

210 189 51 189 189 51 51 51 51 51 191 49 210
211 189 51 51 189 51 51 51 51 51 191 49 211
212 189 51 51 189 51 51 51 51 51 191 49 212
213 189 51 189 189 51 191 49 213
214 189 51 189 189 51 51 51 51 51 191 49 214

215 189 189 189 189 51 51 51 51 51 51 49 215
216 189 189 189 189 51 51 51 51 51 49 216
(P) =Predicted or calculated by project 1taff.

.....
I
Boiling Freezing Cr 1tical Constants Density Rat'ractiva Vapor H•at Capacity Viscosity or Heat of
No. Compound Na11111 Point Point at 60 r Indax of' Praasure at 60 r tha Liquid Vapor hat ion No.
at l in air the Liquid at 100 r at Normal
atm at l atm at 77 r Boiling Point
Temp- Prasaure Volwne Idaal Liquid at lOO r at 200 r

eratura Gu at l
atm
217 2- ETHYL- 1 -BUTENE 51 51 150 130 172 ... 51 189 ... . .. ... ... 51 217
218 2. 3-0IWETHYL- 1-BUTENE 51 51 150 130 172 ... 51 189 ... . .. ... ... 51 218
219 3. 3-0IWETHYL- 1-BUTENE 189 189 (P) (P) (P) 189 189 189 ... 180 ... ... . .. 219
220 2. 3-0IWETHYL-2-BUTENE 189 189 (P) (P) (P) 189 189 189 ... 180 ... ... 51 220
221 1-HEPTENE 51 51 189 189 189 189 189 189 189 ... 189 189 ... 221
222 Ci a-2-HEPTENE 51 ... 150 130 172 ... 51 189 ... . .. ... ... 51 222
223 tr"ana-2-HEPTENE 189 189 (P) (P) (P) 189 189 189 ... 180 . .. ... 189 223
224 ch-3-HEPTENE 51 51 150 130 172 ... 51 189 ... . .. ... ... . .. 224
225 tr-ana-3-HEPTENE 189 189 (P) (P) (P) 189 189 189 ... 180 ... ... 189 225
226 2- ME THVL- 1 - HEXENE 189 189 (P) (P) (P) 189 189 189 ... 180 . .. ... 189 226
227 3-WE THY L- 1- HEXENE 189 ... (P) (P) (P) 189 189 189 ... . .. ... . .. 189 227
228 4-METHVL- 1 ·HEXENE 189 189 (P) (P) (P) 189 189 189 ... . .. ... ... . .. 228
229 5-WETHYL- 1-HEXENE 189 ... (P) (P) (P) 189 189 189 ... . .. ... ... . .. 229
230 2-WETHYL-2- HEXEN E 189 189 (P) (P) (P) 189 189 189 ... ... ... . .. . .. 230
231 C 1 s-3-METHVL-2-HEXENE 189 189 (P) (P) (P) 189 189 189 ... . .. ... ... . .. 231
232 trana -3- Iii ETHVL-2-H EXEN E 189 189 (P) (P) (P) 189 189 189 ... . .. ... ... . .. 232
233 c 1 a-4-WETHVL-2-HEXENE 189 ... (P) (P) (P) 189 189 189 ... . .. ... ... . .. 233
234 tr"ana-4-METHVL-2-HEXENE 189 189 (P) (P) (P) 189 189 189 ... ... ... . .. . .. 234
235 ct a-5-WETHVL-2-HEXENE 189 ... (P) (P) (P) 189 189 189 ... ... ... . .. . .. 235
238 tr-ana-5- ME THVL-2- HEXENE 189 189 (P) (P) (P) 189 189 189 ... ... ... . .. . .. 236
237 c1s-2-METHYL-3-HEXENE 189 ... (P) (P) (P) 189 189 189 ... . .. ... ... . .. 237
238 tr"ana-2-WETHVL·J-HEXENE 189 189 (P) (P) (P) 189 189 189 ... ... ... ... . .. 238
239 c1 a-3-METHVL-3-HEXENE 189 ... (P) (P) (P) 189 189 189 ... 180 ... . .. . .. 239
240 trana-3-WETHVL-3- HEXENE 189 ... (P) (P) (P) 189 189 189 ... 180 ... ... . .. 240
241 2-ETHYL- 1-PENTENE 189 ... (P) (P) (P) 189 189 189 ... . .. . .. ... 189 241
242 3-ETHVL- 1 - PENT ENE 189 189 (P) (P) (P) 189 189 189 ... ... . .. ... 189 242
243 3-ETHYL-2- PENTEME 189 ... (P) (P) (P) 189 189 189 ... 180 ... ... 189 243
244 2. 3- DIMETHYL- 1-?ENTENE 189 189 (P) (P) (P) 189 189 189 ... ... ... ... . .. 244
245 2, 4-DIWETHYL-1-PENTENE 189 189 (P) (P) (P) 189 189 189 ... 180 ... . .. 189 245
246 3, 3-0IWE THYL- 1-PENTENE 189 189 (P) (P) (P) 189 189 189 ... ... ... ... . .. 246
247 3. 4-0I METHYL- 1-PENTENE 189 ... (P) (P) (P) 189 189 189 ... . .. ... ... . .. 247
248 4, 4-0IWETHYL- 1-?ENTENE 189 189 (P) (P) (P) 189 189 189 ... 180 ... ... . .. 248
249 2 ,3-0IWETHYL-2-PENTENE 189 189 (P) (P) (P) 189 189 189 ... . .. ... ... . .. 249
250 2. 4- DI WET HYL-2- PENTENE 189 189 (P) (P) (P) 189 189 189 ... 180 . .. ... 189 250
251 c1 a-3 ,4-DI WETHYL-2- PENTENE 189 189 (P) (P) (P) 189 189 189 ... . .. ... ... 189 251
252 tr"ana-3 ,4-DI WETHYL-2-PENTENE 189 189 (P) (P) (P) 189 189 189 ... ... ... . .. ... 252
253 c1 a-4 ,4-0I METHYL -2-PENTENE 189 189 (P) (P) (P) 189 189 189 ... 180 ... . .. 189 253
254 tr"ans-4 ,4- DIWETHYL-2-PENTENE 189 189 (P) (P) (P) 189 189 189 ... 180 . .. ... 189 254
255 3-WE THYL-2- ETHYL - 1 - BUT ENE 189 ... (P) (P) (P) 189 189 189 ... 180 ... ... . .. 255
(P) Pr"e<Sictea or calculated by grol•ct staff.

Anlline ASTM Octane Numbers r11 ...... bility

Net Heat ot Surface Flash Heat ot Gibbs Free Heat ot Coetticient Point Limits, No.
No. Combustion Tension Point Formation Energy ot Fusion ot !xpan!lion
ot Liquid ot the Temp- at 77 F Formation at 77 F at 60 F Motor Method Research Method Volume Percent
at 11 F Llquld erature at 11 F in Air Mlxture
at 77 F
Clear With l Clear With l Lover Upper
ml TEL ml TEL
per gal per gal
217 189 51 51 189 51 51 51 51 51 191 49 217

218 189 51 51 189 51 51 51 51 51 191 49 218
219 189 51 189 189 51 51 51 191 49 219
220 189 51 51 51 51 51 51 51 191 49 220
221 189 117 189 189 189 51 51 51 51 51 51 51 49 221
222 189 161 (P) 51 191 49 222

223 189 51 (P) 51 51 51 51 51 191 49 223
224 189 161 (P) 51 51 51 191 49 224
225 189 51 (P) 51 51 51 51 51 51 191 49 225
226 189 51 (P) 51 51 51 51 51 191 49 226
227 189 51 (P) 51 51 51 51 51 191 49 227

228 189 51 (P) 51 51 51 51 51 191 49 228
229 189 51 (P) 51 51 51 51 51 191 49 229
230 189 51 (P) 51 51 51 51 51 191 49 230
231 189 51 (P) 51 51 51 51 51 191 49 231
232 189 51 (P) 51 51 51 51 51 191 49 232

233 189 51 (P) 51 51 191 49 233
234 189 51 (P) 51 51 51 51 51 191 49 234
235 189 51 (P) 51 191 49 235
236 189 51 (P) 51 51 51 51 51 191 49 236
237 189 51 (P) 51 191 49 237

238 189 51 (P) 51 51 51 51 51 191 49 238
239 189 51 (P) 51 51 191 49 239
240 189 51 (P) 51 51 51 51 51 191 49 240
241 189 51 (P) 51 191 49 241
242 189 51 (P) 51 51 51 51 51 191 49 242

243 189 51 (P) 51 51 51 51 51 191 49 243
244 189 51 (P) 51 51 51 51 51 191 49 244
245 189 51 (P) 51 51 51 51 51 191 49 245
246 189 51 (P) 51 51 51 51 51 191 49 246
247 189 51 180 51 51 51 51 191 49 247

248 189 51 (P) 51 51 51 51 51 191 49 248
249 189 51 (P) 51 51 51 51 51 191 49 249
250 189 51 (P) 51 51 51 51 51 191 49 250
251 189 51 (P) 51 51 51 51 51 191 49 251
252 189 51 (P) 51 191 49 252

253 189 51 (P) 51 51 51 191 49 253
254 189 51 (P) 51 51 51 51 51 191 49 254
255 189 51 (P) 51 51 51 51 51 191 49 255
(P) = Prec1cted or calculated by project staff.
'
......
~
.....
I
Bolling Freezing Cr 1ti cal Constants Oensity Retract iv• Vapor Keat Capacity Viscosity ot Keat of
No. Compound Name Point Point at 60 r Index ot Pressure at 60 r the Liquid Vapor 1:mat ion No.
at l in air the Liquid at lOO r at Normal
Temp- Pressure Volume Ideal Liquid at lOO r at 200 r

erature Gu at l
atm
256 2, 3, 3-TRIWETHYL-1- BUTENE 189 189 (Pl (Pl (Pl 189 189 189 ... ... ... ... . .. 256
257 1-0CTENE 51 51 189 189 189 189 51 189 189 ... 189 189 ... 257
258 ch-2-0CTENE 189 189 (Pl (Pl (Pl 189 189 189 ... 180 ... ... . .. 258
259 tr-sns-2-0CTENE 51 51 150 130 172 189 51 189 ... 180 ... ... 51 259
280 cts-3-0CTENE 189 ... (Pl (Pl (Pl 189 189 189 ... ... ... . .. . .. 280
281 trsns-3-0CTENE 51 51 150 130 172 ... 51 189 ... ... ... . .. . .. 261
282 cta-4-0CTENE 189 189 (Pl (Pl (Pl 189 189 189 ... 180 ... ... . .. 262
283 trsns-4-0CTENE 51 51 150 130 172 ... 51 189 ... ... ... ... . .. 263
284 2-WE THYL- 1-HEPTENE 189 189 (Pl (Pl (Pl 189 189 189 ... 180 ... ... . .. 264
265 3-METHYL- 1-HEPTENE 189 ... (Pl (Pl (Pl 189 189 189 ... ... . .. . .. . .. 265
268 4-WE THYL- 1 -HEPTENE 189 ... (Pl (Pl (Pl 189 189 189 ... ... ... . .. . .. 268
267 tr-sns-6- ME THYL-2 ... HEP TENE 189 ... (Pl (Pl (Pl 189 189 189 ... ... ... . .. . .. 267
268 tr-sns- 3- ME THYL-3 ... HEPTENE 189 ... (Pl (Pl (Pl 189 189 199 ... . .. ... . .. 51 268
269 2- ETHYL- 1 -HEXENE 51 ... 150 130 172 ... 51 189 . .. ... ... . .. . .. 269
270 3-ETHYL- 1 -HEXENE 189 ... (Pl (Pl (Pl 189 189 189 ... . .. ... ... . .. 270
271 4-ETHYL- 1- HEXENE 189 ... (Pl (Pl (Pl 189 189 189 ... ... . .. . .. . .. 271
272 2, 3- OI METHYL- 1 - Hf XENE 189 ... (Pl (Pl (Pl 189 189 189 ... ... ... . .. . .. 272
273 2, 3- OIWETHYL-2-HEXENE 189 189 (Pl (Pl (Pl 189 189 189 ... ... ... ... . .. 273
274 ci s- 2, 2-0I WETHYL-3-HEXENE 189 189 (Pl (Pl (Pl 189 189 189 ... 180 ... ... . .. 274
275 2, 3, 3-TRI WETHYL-1-PENTENE 189 189 (Pl (Pl (Pl 189 189 189 ... . .. ... ... . .. 275
276 2, 4, 4-TRI METHYL- 1-PENTENE 51 51 150 130 172 ... 51 189 . .. ... ... ... . .. 276
277 2, 4, 4- TRI WETHYL-2-PENTENE 51 51 150 130 172 ... 51 189 ... ... . .. ... 51 277
278 1-NONENE 189 189 189 189 189 189 51 189 189 ... 189, 189 . .. 278
279 1-0ECENE 51 51 189 189 189 189 51 189 189 ... 189 189 ... 279
280 1-UNOECENE 51 51 150 130 172 189 51 189 189 ... 189 189 ... 280
281 1-000ECENE 51 51 150 130 172 189 51 189 189 ... 189 189 ... 281
282 1-TRIOECENE 51 51 150 130 172 189 51 189 189 ... 189 189 ... 282
283 1-TETRAOECENE 51 51 150 130 172 189 51 189 189 ... 189 189 . .. 283
284 1-PENTAOECENE 189 189 189 189 189 189 189 ... ... 180 ... ... 189 284
285 1-HEXAOECENE 51 (Pl 150 130 172 189 51 189 189 ... 189 189 ... 285
286 i-HEPTAOECENE 189 189 189 189 189 9 189 ... . .. ... ... ... . .. 286
287 1-0CTAOECENE 51 51 150 130 172 189 51 ... 189 ... 189 189 .. . 287
288 1-NONAOECENE 189 189 189 189 189 189 189 ... ... . .. ... ... .. . 288
289 1-EICOSENE 51 51 150 130 172 189 189 ... ... . .. 189 189 ... 289
290 PROPAOIENE 51 51 51 51 51 ... 68 189 189 ... ... ... . .. 290
291 1, 2-BUTAOI ENE 51 51 51 51 51 ... 68 189 189 ... ... . .. .. . 291

292 1 ,3-8UTAOIENE 51 51 51 51 51 ... 30 189 189 ... ... ... . .. 292
293 1. 2-PENTAOIENE 189 189 (Pl (Pl (Pl 189 189 189 ... 180 . .. ... . .. 293
294 cta-i ,3-PENTAOIENE 189 189 150 130 51 ... 51 189 189 ... . .. ... .. . 294
(P) Pr-acttcted or- cslculatad by project staff.

Anlllne ASTM Octane Numbers Fla .... blllty

Net Meat ot Surface Flash Heat ot Clbb1 Free Heat of Coett le lent Point Limits, No.
No. Combustion Tens ion Point Formation Energy or Fuelon of Bxpans lon
ot Liquid of the Temp- at 77 r rormtlon at 77 r at 60 r Motor Method Research Method Volume Percent
at 77 r Llquld erature at 71 r in Air Mixture
at 77 r
Clear With 3 Clear With l Lover Uppar
ml TEL ml TEL
per gal per gal
256 169 51 (P) 51 51 51 51 51 51 191 49 256

257 169 209 169 169 169 51 51 51 51 51 51 51 49 257
256 160 51 (P) 51 51 51 51 51 51 191 49 256
259 160 146 170 (P) 51 51 51 51 51 51 191 49 259
260 160 51 (P) 51 191 49 260
261 160 170 (P) 51 51 51 51 51 191 49 261

262 160 51 (P) 51 191 49 262
263 160 170 (P) 51 51 51 51 51 191 49 263
264 160 51 (P) 51 51 51 51 51 191 49 264
265 160 51 (P) 51 191 49 265
266 160 51 (P) 51 191 49 266

267 160 51 (P) 51 51 51 51 51 191 49 267
266 160 51 (P) 51 191 49 268
269 160 170 (P) 51 191 49 269
270 160 51 .(P) 51 191 49 270
271 160 51 (P) 51 191 49 271

272 160 51 (P) 51 51 51 51 191 49 272
273 160 51 (P) 51 51 51 51 191 49 273
274 160 51 160 51 51 51 191 49 274
275 160 51 (P) 51 51 51 51 51 191 49 275
276 169 161 (P) 160 51 51 51 51 51 191 49 276

277 161 199 161 (P) 160 51 51 51 51 51 51 191 49 277
276 169 (P) 169 169 169 51 51 191 49 276
279 169 177 169 169 139 51 51 191 49 279
260 169 221 169 169 139 191 49 260
261 169 221 204 204 139 191 49 261

262 169 221 169 169 169 191 49 262
263 169 146 169 169 169 191 49 263
264 169 169 169 169 191 49 264
265 169 169 169 139 191 49 265
266 169 169 169 169 191 49 266

267 169 169 169 169 191 49 267
266 169 169 169 169 191 49 266
269 169 169 169 169 191 49 269
290 169 169 169 177 290
291 169 169 169 204 51 51 51 291

292 169 169 169 135 51 209 209 292
293 160 51 169 169 51 191 293
294 51 143 143 143 51 191 49 294
(P) = Pred1ctad or celculatad Dy project steff.
......
I
()
01 01
......
I
TABLE 1C5.1 (Continued) (")
....... 01
01
I\)
Key to References
Bolling Freezing Critical Constants Density Ret'rect:lv• Vapor Heat Capacity Vlacoalty ot Heat of
No. Compound Name Point Point at 60 P lnde• of Pra•aure at 60 P tha Liquid Vaporization No.
at l ln air the Liquid at iOO F at Norm.al
1-~~~~~~--1~~~~~~~~--1

erature Gas at l
atm
295 trans- 1, 3-PENTAOI ENE 51 143 150 130 51 51 189 189 295
296 1 ,4-PENTAOI ENE 51 51 150 130 172 51 189 296
297 2,3-PENTAOIENE 189 189 (P) (P) (P) 189 189 189 180 297
298 3-METHYL- 1, 2-SUTAOI ENE 189 189 (P) (P) (P) 189 188 85 180 298
299 2-METHVL- 1, 3-BUTAOI ENE 51 51 51 51 51 189 189 189 299
300 2, 3-0UIETHYL- 1, 3-BUTAOI ENE 189 189 51 300

301 1 ,2-HEXAOIENE 189 (P) (P) (P) 189 189 301
302 1 ,5-HEXAOIENE 189 189 (P) (P) (P) 189 189 85 180 302
303 2,3-HEXAOIENE 189 (P) (P) (P) 189 189 180 303
304 3-METHVL- 1, 2-PENTAOIENE 189 (P) (P) (P) 189 189 180 304
305 2-METHYL- 1, 5-HEX.AOI ENE 51 (P) (Pl (P) 51 180 305

306 2-METHVL- 2, 4-HEXAOI ENE 51 (P) (P) (P) 51 180 306
307 2,6-0CTAOIENE 51 (P) (P) (P) 51 180 307
308 2, 6-0UIETHVL-1, 5-HEPTAOIENE 51 (P) (P) (P) 51 180 308
309 3, 7-01METHVL-1,6-0CTAOI ENE 51 (P) (P) (P) 51 180 309
310 CVCLOPENTENE 51 51 150 130 172 51 189 310

311 1-METHVL-CVCLQPENTENE 189 189 (P) (P) (P) 189 189 180 311
312 1-ETHVLCVCLOPENTENE 189 189 (P) (P) (P) 189 189 180 312
313 3- ETHYLCYC LOPENTENE 189 (P) (P) {P) 189 189 180 313
314 i-n-PROPYLCVCLQPENTENE 189 (P) (P) (P) 189 180 314
315 CVCLOHEXENE 51 51 204 130 172 51 189 315

316 i-METHVLCVCLOHEX.ENE 189 189 (P) (P) (P) 189 189 180 316
317 i- ETHVLCVCLOHEXENE 189 189 (P) (P) (P) 189 189 180 317
318 CVCLOPENTAOIENE 110 110 130 130 71 110 189 318
319 OICVCLOPENTAOI ENE 110 60 130 130 71 110 319
320 alpha-PINENE 34 171 150 130 172 171 320

321 beta-PINENE 34 171 150 130 172 171 321
322 ACETYLENE (P) 51 51 51 51 189 322
323 METHVLACETVLENE 51 51 51 51 51 83 189 189 323
324 DI METHVLACETVLENE 51 51 51 51 51 51 189 189 324
325 ETHVLACETVLENE 51 51 51 51 51 189 189 325

326 VINVLACETVLENE 220 150 130 172 220 326
327 i-PENTVNE 189 189 (P) (P) (P) 189 188 189 51 327
328 2- PENTVNE 189 189 (P) (P) (P) 189 189 189 51 328
329 3-METHVL- i-BUTVNE 189 189 51 51 329
330 1-HEXVNE 189 189 (P) (P) (P) 189 189 51 330
331 1-HEPTVNE 189 189 (P) (P) (P) 189 189 331
332 1-0CTVNE 189 189 (P) (P) (P) 189 188 332
333 1-NONVNE 189 189 (P) (P) (P) 189 189 333
334 1-0ECVNE 189 189 (P) (P) (P) 189 189 334
(P) =Predicted or calculated by project staff.

Key to References
Aniline ASTM OCtane Numbera Flammablllty
Net Beat ot Surface Flash Heat ot Gibb1 Free Heat ot Coefficient Point Limits, No.
No. COllbu•tion Tension Point Formation .Inergy ot P'uaion ot Expansion
ot Liquid ot th• Temp- at 77 F Formation at 77 F at 60 F Motor Method Research Method Volume Percent
at 77 F
Clear W1 th 3 Clear W1 th 3 Lower Upper
ml TEL ml TEL
per 9al par 9al
295 51 143 143 143 51 191 49 295

296 51 189 189 143 51 191 49 296
297 180 51 189 189 51 191 297
298 180 51 189 189 51 51 51 51 51 191 298
299 189 209 189 189 143 51 51 51 51 51 221 221 299
300 180 300

301 180 51 (P) 51 191 301
302 180 51 (P) 51 51 51 51 51 191 49 302
303 180 51 (P) 51 191 303
304 180 51 (P) 51 191 304
305 180 51 (P) 51 191 49 305

306 180 51 (P) 51 191 49 306
307 180 51 (P) 51 191 49 307
308 180 51 (P) 51 191 49 308
309 180 51 (P) 51 191 49 309
310 189 177 189 189 204 51 51 51 51 51 51 191 49 310

311 189 51 (P) 51 51 51 51 51 51 191 49 311
312 189 51 (P) 51 51 51 51 51 51 191 49 312
313 189 51 (P) 51 51 51 51 51 191 49 313
314 189 51 (P) 51 51 191 49 314
315 189 177 204 189 101 51 51 51 51 51 51 191 49 315

318 189 51 (P) 51 51 51 51 51 191 49 316
317 189 51 (P) 51 51 51 51 51 191 49 317
318 180 161 (P) 191 49 318
319 180 209 180 (P) 110 209 49 319
320 93 148 181 (P) 191 49 320

321 161 211 161 191 49 321
322 189 177 189 189 204 51 51 322
323 189 204 204 209 49 323
324 51 189 189 204 51 51 51 51 51 191 49 324
325 230 189 189 29 191 49 325

326 180 204 204 191 49 326
327 189 51 189 189 51 191 49 327
328 189 51 189 189 51 191 49 328
329 189 189 189 329
330 189 189 189 51 191 49 330

331 189 (P) 189 189 51 191 49 331
332 189 (P) 189 189 51 51 51 51 51 191 49 332
333 189 (P) 189 189 51 191 49 333
334 189 (P) 189 189 51 191 49 334
(P) = Predicted or calculatad by project staff.

'
......
01
w
Bollln9 Free'llnq Cr 1 t leal Con•tant• Oen9lty Refractive Vapor Heat Capacity Vlaeoalty of Heat of
llo. C011pOund Neme Point Point at 60 F Inde1 of Pr•s•ure at 60 F the Liquid Vapor hat ion No.
at l In air the Liquid at 100 F at Normal
atm et l a.tm at 77 F Bolling Point
Temp- Pre1eure Volume Ideal Liquid at 100 F at 200 F

erature Gaa at l
atm
335 BENZENE 51 51 51 51 51 ... 51 ... 189 189 189 ... 189 335
338 TOLUENE 51 51 51 51 51 ... 51 ... 189 188 189 189 189 336
337 ETHYLBENZENE 51 51 51 51 51 ... 51 ... 189 189 189 189 189 337
338 o-XYLENE 51 51 51 189 51 ... 51 ... 189 189 189 189 189 338
338 111-XYLENE 51 51 51 51 51 ... 51 ... 189 188 189 189 189 339
340 p-XYLENE 51 188 51 51 51 ... 51 ... 189 189 189 189 189 340
341 n-PROPYLBENZENE 51 51 51 51 51 ... 51 ... 189 189 189 189 189 341
342 I SOPROPYLBENZENE 189 51 51 51 51 ... 51 ... 189 ... 189 189 189 342
343 o-ETHYLTOLUENE 51 51 51 ... ... ... 51 ... 189 ... .. . ... 189 343
344 m-ETHYLTOLUENE 51 51 51 ... ... ... 51 ... 189 ... ... ... 189 344
345 p-ETHYLTOLUENE 51 51 51 51A 51• ... 51 ... 189 ... ... .. . 189 345
348 1, 2, 3-TRI METHYLBENZENE 51 51 51 51 51 ... 51 ... 189 189 ... .. . 189 346
347 1, 2 ,4-TRI METHYLBENZENE 51 51 51 51 51 ... 51 ... 189 189 ... ... 189 347
348 1 ,3,5-TRIMETHYLBENZENE 51 51 51 51 51 ... 51 ... 189 189 . .. .. . 189 348
349 n-BUTYLBENZENE 51 (P) 51 51 51 ... 51 ... 189 ... 189 189 .. . 349
350 I SOBUTYLBENZENE 51 51 51 51 172 ... 51 ... ... ... ... ... .. . 350
351 Hc-BUTYLBENZENE 51 51 51 51 172 ... 51 ... ... ... ... ... .. . 351
352 tert-BUTYLBENZENE 51 51 51 51 172 ... 51 ... ... ... ... ... .. . 352
353 1-METHYL-2- n-PROPYLBENZEN E 188 189 (P) (P) (P) 189 189 ... ... 180 ... ... ... 353
354 1-METHYL-3-n-PROPYLBENZEN E 188 189 (P) (P) (P) 189 189 ... ... 180 ... .. . ... 354
355 1-METHYL-4- n-PROPYLBEN ZEN E 189 189 (P) (P) (P) 189 188 ... ... 180 ... ... .. . 355
358 o-CYMENE 51 51 150 130 172 ... 51 ... ... ... ... ... .. . 356
357 m-CYMENE 51 51 150 130 172 ... 51 ... ... ... ... ... .. . 357
358 p-CYMENE 51 51 51 51 172 ... 51 ... ... ... ... ... .. . 358
359 o-01 ETHYLBENZENE 51 51 150 130 172 ... 51 ... ... ... ... ... .. . 359
360 m-01 ETHYLBENZENE 51 51 150 130 172 ... 51 189 ... .. . ... ... ... 360
361 p-01 ETHYLBENZENE 51 51 51 51 172 ... 51 189 ... ... ... ... .. . 361
382 1, 2-DIMETHYL-3-ETHYLBENZENE 51 51 150 130 172 ... 51 ... ... ... ... .. . 51 362
363 1, 2-DIMETHYL-4-ETHYLBENZENE 189 189 (P) (P) (P) 189 189 ... ... 180 ... ... .. . 363
364 1 ,3-DIMETHYL-2-ETHYLBENZENE 189 188 (P) (P) (P) 189 189 ... ... 180 ... ... ... 364
385 1 ,3-DIMETHYL-4-ETHYLBENZENE 189 189 (P) (P) (P) 189 189 ... ... 180 ... ... .. . 365
388 1 ,3-DIMETHYL-5-ETHYLBENZENE 189 189 (P) (P) (P) 189 189 ... ... 180 ... ... .. . 366
367 1 ,4-DIMETHYL-2-ETHYLBENZENE 189 189 (P) (P) (P) 189 189 ... ... 180 ... ... ... 367
368 1, 2, 3 ,4-TETRAMETHYLBENZENE 189 189 (P) (P) (P) 189 188 ... ... ... ... ... ... 368
388 1, 2, 3, 5-TETRAMETHYLBENZENE 188 189 (P) (P) (P) 189 189 ... ... ... ... .. . ... 369
370 1, 2 ,4, 5-TETRAMETHYLBENZENE 51 51 51 51 172 51 51 ... ... ... ... ... .. . 370
371 n-PENTYLBENZENE 189 189 189 189 189 189 189 ... ... 180 ... ... ... 371
372 n-HEXYLBENZENE 51 188 51 51 51 ... 188 ... ... .. . 189 189 ... 372
373 n-HEPTYLBENZENE 189 188 188 188 189 188 189 ... ... 180 ... ... .. . 373
(P) :11 Pr"ed1cted or celculeted by pr"oject eteff,

<O
CX>
--.I
Aniline ASTH Octane Numbers Flammability

Net Heat of Surface Flash Heat of Gibbs Free Heat of Coefficient Point Limits, No.
No. Combustion Tension Point Formation Energy of Fusion ot Expansion
ot Liquid ot th• Temp- at 77 F Formation at 77 F at 60 F Motor l'l•thod Research Method Volume Percent
at 17 F
ml TEL rnl TEL
per gal per gal
335 189 ... 209 189 189 189 51 51 51 ... . .. ... 209 209 335
336 189 ... 209 189 189 189 51 51 51 51 . .. 51 209 209 336
337 189 ... 209 204 189 189 51 51 51 51 51 51 209 209 337
338 189 ... 209 204 189 189 51 51 51 51 ... ... 209 209 338
339 189 ... 209 189 189 189 51 51 51 51 51 51 209 209 339
340 189 ... 209 61 61 189 51 51 51 51 51 51 209 209 340

341 189 ... 209 189 189 142 51 51 51 51 51 51 51 49 341
342 189 ... 209 204 189 189 51 51 51 51 51 51 51 51 342
343 189 ... . .. 188 189 189 51 ... 51 51 51 51 191 49 343
344 189 ... . .. 188 204 189 51 ... 51 . .. . .. 51 191 49 344
345 189 ... 62 188 189 189 51 ... 51 ... ... . .. 191 49 345
346 189 ... , 11 188 189 189 51 ... 51 51 51 51 51 49 346
347 189 ... 111 188 189 189 51 ... 51 51 51 51 51 49 347
348 189 ... 111 188 189 189 51 51 51 ... . .. 51 191 49 348
349 189 ... 209 188 189 204 51 51 51 51 51 51 209 209 349
350 189 ... 177 188 188 189 51 ... 51 51 51 51 177 177 350
351 189 ... 209 188 188 189 51 ... 51 51 51 51 209 209 351
352 189 ... 209 188 188 189 51 ... 51 ... . .. 51 209 209 352
353 189 (P) ... 189 181 ... 51 . .. 51 51 51 51 223 204 353
354 189 (P) ... 189 181 ... 51 . .. 51 51 51 51 223 204 354
355 189 (P) ... 189 181 ... 51 ... ... . .. . .. ... 223 204 355
356 189 ... 62 188 188 189 51 ... 51 51 51 51 191 49 356
357 189 ... 62 188 188 189 51 ... . .. ... . .. ... 191 49 357
358 189 ... 209 188 188 189 51 ... 51 ... . .. 51 221 221 358
359 189 189 148 188 188 189 51 ... ... ... . .. . .. 191 49 359
360 189 189 209 188 188 189 51 ... 51 51 51 51 191 49 360
361 189 189 148 188 188 189 51 ... 51 51 51 51 45 45 361
362 189 ... 62 188 188 189 51 ... 51 51 51 51 223 204 362
363 189 (P) ... 189 181 ... 51 ... ... ... . .. ... 223 204 363
364 189 (P) ... 189 181 ... 51 ... . .. ... . .. ... 223 204 364
365 180 (P) ... 189 181 ... 51 ... 51 51 51 51 223 204 365
366 180 (P) ... (P) 181 ... 51 ... 51 51 51 51 223 204 366
367 180 (P) ... 189 181 ... 51 . .. 51 51 51 51 223 204 367
368 189 (P) ... 189 181 ... 51 . .. 51 51 51 51 223 204 368
369 189 (P) ... 189 181 ... 51 . .. 51 ... . .. . .. 223 204 369
370 189 ... 148 188 188 189 51 ... ... ... ... . .. 191 49 370
371 189 189 ... 189 189 ... . .. ... ... ... . .. ... 223 204 371
372 189 ... 1 188 189 189 ... ... ... ... . .. ... 223 204 372
373 189 189 ... 189 189 ... ... ... ... ... . .. ... 223 204 373
(?) Predicted or calculated by project staff.
'
......
01
01
...... ......
TABLE 1C5.1 (Continued) (')
......
I
01 ~
m ......
Boil inq Freezing Cr it 1cal Constants Density Retract iv• Vapor Keat Capacity Viscosity ot Keat ot
No. Compound Name Point Point at 60 r Index ot Pressure at 60 F tho Liquid Vaporization No.
at l in air tho Liquid at lOO F at Normal
atm at l atm at 77 p Bo1lin9 Point
t-~~--.,..-~~--t~~~~-r-~~~--1
Temp- Pressure Volume Ideal Liquid at lOO r at 200 r

erature Gas at l
atm
374 n-OCTYLBENZENE 189 189 189 189 189 1B9 189 1BO 189 374
375 n-NONYLBENZENE 189 189 189 189 189 1B9 1B9 1BO 375
378 n-OECYLBENZENE 51 51 150 130 16B 51 189 189 378
377 n-UNOECYL8ENZENE 189 189 189 1B9 189 1B9 1B9 1BO 1B9 377
378 n·OOOECYL8ENZENE 51 51 51 51 51 51 1B9 1B9 1B9 378
379 n-TRIDECYLBENZENE 189 189 51 51 51 1B9 189 1B9 379

3BO n-TETRADECYLBEN ZEN E 189 1B9 1B9 1B9 1B9 189 189 1BO 380
3B1 n- PENTAOECV LBENZENE 1B9 189 1B9 189 189 1B9 191 180 3B1
3BZ n- HEXAOECVLBENZENE 1B9 1B9 1B9 1B9 189 1B9 1B9 1BO 3BZ
3B3 CYCLOHEXYLBENZENE 171 171 150 130 17Z 171 3B3
3B4 STYRENE 51 51 51 51 51 51 1B9 3B4

385 Ci s-i -PROPENVL BENZENE 189 189 (P) (P) (P) zzo 1B9 1BO 385
3B6 trans- i-PROPENYL BENZENE 189 189 (P) (P) (P) zzo 1B9 1BO 3B6
3B7 Z-PROPENYL BENZENE 1B9 189 150 130 17Z 1B9 1B9 3B7
388 1-lilETHYL-Z-ETHENVL BENZENE 189 189 (P) (P) (P) 1B9 1B9 1BO 388
3B9 1·METHVL·3-ETHENVL BENZENE 1B9 189 (P) (P) (P) 1B9 1B9 180 3B9
390 1-METHVL-4-ETHENVL BENZENE 1B9 1B9 (P) (P) (P) 1B9 1B9 180 390
391 1 -ME THVL-4- (trans-
-1- n-PROPENVL )BENZENE 1B9 1B9 (P) (P) (P) 1B9 1B9 1BO 391
39Z 1-ETHYL-2-ETHENYL BENZENE 1B9 189 (P) (P) (P) 1B9 189 1BO 39Z
393 1-ETHYL-3-ETHENYL BENZENE 189 189 (P) (P) (P) 1B9 1B9 1BO 393
394 1-ETHYL-4-ETHENVL BENZENE 1B9 1B9 (P) (P) (P) 1B9 1B9 1BO 394
395 2-PHENYL- 1-BUTENE 1B9 (P) (P) (P) 1B9 51 1BO 395
39B 8I PHENYL 51 51 51 51 51 21B 396
397 1 -ME THVL-Z-PHEN YL8ENZ ENE 51 (P) (P) (P) 51 51 1BO 397
39B 1 - METHYL-3-PHEN YLBENZ ENE 51 51 (P) (P) (P) 51 51 1BO 398
399 i - lilETHVL ·4· PHEN VLBEN ZEN E 51 51 (P) (P) (P) (P) 399
400 i-ETHVL-4-PHENVL8ENZENE 51 51 (P) (P) (P) (P) 400
401 i-METHVL-4(4·METHVLPHENVL) •
-BENZENE 51 51 (P) (P) (P) (P) 401
402 DI PHENVLMETHANE 51 51 150 130 17Z 51 40Z
403 i • i-OIPHENVLETHANE 51 51 150 130 168 51 403
404 i. Z-OIPHENVLETHANE 51 51 130 130 172 51 404

405 i. i-OIPHENVLPRQPANE 189 189 (P) (P) (P) 1B9 1B9 180 405
408 i. Z-DIPHENVLPRQPA.NE 189 189 (P) (P) (P) 189 189 180 406
407 i. i-OIPHENVLBUTANE 1B9 1B9 (P) (P) (P) 189 189 180 407
40B i. i-OIPHENVLPENTANE 189 189 (P) (P) (P) 1B9 1B9 1BO 408
409 i • i-OIPHENVLHEXANE 1B9 1B9 (P) (P) (P) 1B9 1B9 1BO 409
410 i • i-OI PHENVLHEPTA.NE 1B9 1B9 (P) (P) (P) 9 189 1BO 410
(P) = Pr-ed1ct•d or- calculstad by projact staff .
......
co
CX>
"""
Aniline ASTH Octane Numbers Flammability

Net Heat ot Surface Flash Heat ot Gibbs Pree Heat ot Coetticient Point Limits, No.
No. Combustion Tension Point Formation Energy ot Pus ion ot Expansion
ot Liquid ot the Temp- at 77 P Forl'ft4tion at 77 F at 60 F Motor Method Research Method Volume percent
at 17 P Liquid erature at 77 P in A.ir Mixture
at 71 F
ml TEL ml TEL
per gal per gal
374 189 189 189 189 223 204 374

375 189 189 189 189 223 204 375
376 189 177 188 189 189 223 204 376
377 189 (P) 189 189 223 204 377
378 189 177 189 189 189 191 49 378
379 189 188 189 189 223 204 379

380 189 (P) 189 189 223 204 380
381 189 (P) 189 189 223 204 381
382 189 (Pl 189 189 223 204 382
383 180 177 180 (P) 151 191 49 383
384 189 209 189 189 164 51 51 51 51 51 209 209 384

385 189 (P) 189 189 51 51 51 51 223 204 385
386 189 (P) 189 189 51 51 51 51 51 223 204 386
387 180 209 189 181 51 51 51 51 51 209 209 387
388 189 (P) 189 181 51 223 204 388
389 189 (P) 189 181 51 223 204 389

390 189 (P) 189 181 51 223 204 390
391 180 (P) (P) 51 223 204 391

392 180 (P) (P) 51 223 392
393 180 (P) (P) 51 223 393
394 180 (P) (P) 51 223 394

395 180 (P) (P) 51 223 204 395
396 230 209 204 204 204 209 209 396
397 180 (P) (P) 223 204 397
398 180 (P) 51 (P) 223 204 398
399 180 (P) (P) 223 204 399

400 180 (P) (P) 223 204 400
401 180 (P) (P) 223 204 401

402 189 177 51 (P) 46 191 49 402
403 161 177 161 (P) 190 223 204 403
404 51 177 51 (P) 190 191 49 404

405 (P) 223 204 405
406 180 (P) (P) 223 204 406
407 (P) 223 204 407
408 (P) 223 204 408
409 (P) 223 204 409

410 (P) 223 204 410
(P) =Predicted or calculated tJ~ project staff.
......
'
01
......
......
TABLE 1C5.1 (Continued) ()
......
I
~
&l ......
Boiling Jl'ree2in9 Critical Con.ttant• Dens! ty Rat uct: i ve vapor Heat Capacity Viscosity ot Heat ot
No. Compound Name Po1nt Point at 60 F Index ot Pressure at 60 F the L1qu1d Vaporhat1on Ho.
atl ina1r tho L1qu1d at 100 F at Normal
atm at l atm. at 77 F Boiling Point
t-~~~.--~~-;~~~~-r-~~~---i
Temp- Pressure Volume Ideal L1qu1d at 100 F at 200 F

erature Gas •t l
atm
411 1, 1-0IPHENYLOCTANE 189 189 (P) (P) (P) 189 189 180 411
412 1, 1-0IPHENYLNON.ANE 189 189 (P) (P) (P) 189 189 180 412
413 1, 1-0IPHENYLDEC.ANE 189 189 (P) (P) (P) 189 189 180 413
414 1, 1 -QI PHENYLUNOECANE 189 189 51 189 414
415 1, 1 -DI PHENYLOOOECANE 189 189 (P) (P) (P) 189 189 180 415
416 1, 1-0IPHENYLTRIOECANE 189 189 (P) (P) (P) 189 189 180 416
417 1, 1-DIPHENYL TETRADECANE 189 189 (P) (P) (P) 189 189 180 417
418 1, 1-0IPHENYLPENTAOECANE 189 189 (P) (P) (P) 189 189 180 418
419 1, 1-DIPHENYLHEXAOECANE 189 189 (P) (P) (P) 189 189 180 419
420 cis-1 ,2-0IPHENYLETHENE (P) 36 130 130 172 420
421 trans-1, 2-0IPHENYLETHENE 1 77 157 150 130 172 421

422 PHENVLAC ETVLENE 51 51 (P) (P) (P) 51 180 422
423 OI PHENYLACE TYL ENE 220 165 130 130 172 423
424 1 ,2-0IPHENYLBENZENE (P) 40 119 119 119 424
425 1 ,3-0IPHENYLBENZENE (P) 132 119 119 119 425
426 1 ,4-0IPHEN'l'LBENZENE 110 132 119 119 119 428

427 NAPHTHALENE 18 18 18 18 18 18 189 427
428 1-METHVLNAPHTHALENE 51 51 51 (P) 172 189 51 189 428
429 2-M ET HVL NAPHTHALENE 51 51 51 130 172 (P) 189 429
430 1 -ETHVLNAP11THA LENE 189 189 (P) (P) (P) 189 189 180 430
431 2- E THYLNAP11 THA LE NE 189 189 (P) (P) (P) 189 189 180 431
432 1 ,2-0IMETHVLNAPHTHALENE 189 189 (P) (P) (P) 189 189 180 432
433 1 ,4-0IMETHYLNAPHTHALENE 189 189 (P) (P) (P) 189 189 180 433
434 1 -n-PRQPYLNAPH THAL ENE 189 189 (P) (P) (P) 189 189 180 434
435 2- n- PROP YLNAPHTHALEN E 189 189 (P) (P) (P) 189 189 180 435
436 1 - n - BUTVLN.APH THAL ENE 189 189 (P) (P) (P) 189 189 180 438
437 2-n - BUTV LN.APHT H.ALENE 189 189 (P) (P) (P) 9 189 180 437
438 1 -n-PENTYLNAPHTHALENE 189 189 (P) (P) (P) 189 189 180 438
439 1 -n-HEXVLNAPHTHALENE 189 189 (P) (P) (P) 189 189 180 439
440 2- n- HEXV LN.A PH TH.A LE NE 189 189 (P) (P) (P) 189 189 180 440
441 1 - n- HEP T YLNAPH THA LENE 189 189 (P) (P) (P) 189 189 180 441
442 1-n-OCTYLNAPHTHALENE 189 189 (P) (P) (P) 189 189 180 442
443 1 -n- NONVLNAPHTHALENE 189 51 150 130 168 189 51 443
444 2-n- NONVLNAPHTHALENE 189 189 (P) (P) (P) 189 189 180 444
445 1 - n- OECYLNAPHT HAL ENE 189 51 150 130 166 189 51 445
446 1 ,2,3,4-TETRAHVORO-
NAPHTHALENE 21 21 21 21 21 21 189 446
447 1-METHVL-{1 ,2,J,4-TETRA-
HVORONAPHfHALENE J 189 (P) (P) (P) 189 189 180 447
(P) Pr-ed 1.ctied or cat cu 1ated by project •tat f.

Aniline ASTM Octane Numbers P'lammabili ty

Net Heat of Surface Flash Heat of Gibbs P'r•• Heat ot Coefficient Point Limits, No.
No. Combustion Tension Point Format ion !nergy of Fusion of Expansion
of Liquid of th• Temp- at 77 P' Formation at 77 F at 60 P' Motor Method Research Method Volume Percent
at 77 P' Liquid erature at 77 F in Air MiXture
at 77 P'
Clear With l Clear With l Lover Upper
ml TEL ml TEL
per gal per gal
411 (P) 223 204 411

412 (P) 223 204 412
413 (P) 223 204 413
414 414
415 (P) 223 204 415
418 (P) 223 204 416

417 (P) 223 204 417
418 (P) 223 204 418
419 (P) 223 204 419
420 180 180 (P) 191 49 420
421 180 180 (P) 72 191 49 421

422 180 (P) (P) 51 223 204 422
423 180 180 (P) 156 191 49 423
424 180 177 180 (P) 40 191 49 424
425 180 177 180 (P) 132 191 49 425
428 180 177 180 (P) 132 191 49 426

427 18 18 18 18 18 51 18 18 427
428 230 189 204 204 140 191 49 428
429 230 189 204 204 140 191 49 429
430 180 189 (P) 223 204 430
431 180 189 (P) 223 204 431

432 180 189 (P) 223 204 432
433 180 (P) (P) 223 204 433
434 180 189 (P) 223 204 434
435 180 189 (P) 223 204 435
438 180 189 (P) 223 204 436

437 180 189 (P) 223 204 437
438 180 189 (P) 223 204 438
439 180 189 (P) 223 204 439
440 180 189 (P) 223 204 440
441 180 189 (P) 223 204 441

442 180 189 (P) 223 204 442
443 180 170 (P) 223 204 443
444 180 (P) (P) 223 204 444
445 180 170 (P) 223 204 445
448 21 209 21 21 21 51 51 51 51 51 51 51 51 446
447 180 (P) (P) 223 204 447
(P) =Predicted or calculated by project staff .
......
......
I
(')
~ c.n
.....
I (")
~
O>
0
Key to References
Bolling Freezing Critical Constants Density Refractive Vapor Heat Capacity Vhcoslty of Heat of
No. Compound Na- Point Point at 60 F Index of Pressure at 60 F the Liquid Vaporization No.
at l In air th• Liquid at ioo r at Normal
atm at l atm at 77 P Boil in9 Point

eratura Gas at l
atm
448 1·ETHYL-[1, 2, 3 ,4-TETRA-

HYORONAPHTHALENE] 189 (P) (P) (P) 189 189 180 448
449 2, 2-01METHYL-[1, 2, 3, 4-TETRA-
HYORDNAPHTHALENE] 189 (P) (P) (P) 189 189 180 449
450 2, 6-01METHYL-[1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] 189 189 (P) (P) (P) 189 189 180 450
451 8, 7-01 METHYL- [ 1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] 189 189 (P) (P) (P) 189 189 180 451
452 1-n-PROPVL- [ 1, 2, 3, 4-TETRA-
HYDRONAPHTHALENE] 189 (P) (P) (P) 189 189 180 452
453 6-n-PROPYL- [ 1, 2, 3, 4-TETRA-

HVORONAPHTHALENE] 189 (P) (P) (P) 189 189 180 453
454 1-n- BUTYL- ( 1, 2, 3 ,4-TETRA-
HYORDNAPHTHALENE] 189 51 454
455 6-n-8UTYL-[ 1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] 189 51 455
456 1-n-PENTVL- [ 1, 2, 3, 4-TETRA-
HYORDNAPHTHALENE] 189 51 456
457 6-n-PENTYL- [ 1, 2, 3, 4-TETRA-
HYDRONAPHTHALENE] 189 51 457
458 1-n-HEXVL- [ 1, 2, 3 ,4-TETRA-

HYDRONAPHTHALENE] 189 ( P) (P) (P) 189 189 180 458
459 1-n-HEPTVL- [ 1, 2 ,3 ,4-TETRA-
HYORDNAPHTHALENE] 189 (P) (P) (P) 189 189 180 459
460 1-n-OCTVL- [ 1, 2 ,3, 4-TETRA-
461 1-n-NONYL- [ 1, 2, 3, 4-TETRA-
HYORONAPHTHALENE] 189 (P) (P) (P) 189 189 180 461
462 1-n-DECVL-[ 1, 2, 3 ,4-TETRA-
463 I NOE NE 16 16 150 130 16 16 463

464 1-METHYLINDENE 189 (P) (P) (P) 189 189 180 464
465 2-METHYLINDENE 189 189 (P) (P) (P) 189 189 180 465
468 2, 3-01 HYDRO! ND ENE 189 189 (P) (P) (P) 189 189 180 466
467 1-METHYL-2, 3-01 HYDRO! ND ENE 189 (P) (P) (P) 189 189 180 467
468 2-METHYL-2, 3-01 HYDRO! NO ENE 189 ( P) (P) (P) 189 189 180 468
469 4-METHYL-2, 3-DIHYDRO! NOE NE 189 (P) (P) (P) 189 189 180 469
470 5-METHYL-2, 3-D!HYORDI NO ENE 189 (P) (P) (P) 189 189 180 470
471 ACENAPHTHALENE 471
(P) = Pred1cted or calculated by project. staff.

co TABLE 1C5.1 (Continued)
CX>
'-I
ltey to Ref erencea

Aniline ASTH Octane Number J Flammability
Net Meat of Surface Fla ah Meat of Gibbs Free Meat of Coefficient Point Limits, No.
No. Combuation Teneion Point Formation Energy of Fusion of Expansion
of Liquid of th• Temp- at 77 'I' Format ion at 77 'I' at 60 'I' Motor Method Research Method Volume Percent
at 77 F Liquid eratur• at 77 'I' in-.Air HiXtur•
at 77 F
Clear iiith l Clear iiith l Lover Upper
ml TEL ml TEL
per gal per gal
448 180 (P) (P) 223 204 448
449 180 (P) (P) 223 204 449
450 180 (P) (P) 204 450
451 180 (P) (P) 204 451
452 180 (P) (P) 204 452
453 180 (P) (P) 204 453
454 454
455 455
456 456
457 457
458 180 (P) (P) 204 458
459 180 (P) (P) 204 459
460 180 (P) (P) 204 460
461 180 (P) (P) 204 461
462 180 (P) (P) 204 462
463 16 16 16 16 51 51 51 51 51 191 49 463

464 180 (P) (P) 51 223 204 464
465 180 (P) (P) 51 223 204 465
466 180 (P) (P) 51 51 51 51 51 223 204 466
467 180 (P) (P) 51 223 204 467
468 180 (P) (P) 51 223 204 468

469 180 (P) (P) 51 223 204 469
470 180 (P) (P) 51 223 204 470
471 471
(P) := Pred1cted or calculated by project staff.
'
...... (")
01
......
I
O'>
I\)
Bolling Freezing Critical Constante Density Refractive Vapor Heat Capacl ty Viscosity of Heat ot
llo. Compound Name Point Point at 60 I' Index of Preaaur• at iO F tho Liquid Vapor1 zatlon No.
at i in air tho Liquid at iOO F at Norm.al
atm at l atm at 77 F Bo1l 1ng Point
Temp- Pr ea.sure Volume Ideal Liquld at 100 F at 200 F

erature Gaa at i
atm
472 ACENAPHTHENE 10 (P) 10 10 172 10 472

473
474
FLUORENE
ANTHRACENE
194
,,,, ,,
75
,,
,,
194
,,
194
,,
172
,,
,,
10
,, 189
473
474
475 PNENANTHRENE 43 130 189 475
478 PYRENE 15 227 150 130 15 15 189 476
477 FLUORANTNENE 10 (P) 150 130 172 10 477

478 CHRYSENE 15 15 150 130 15 15 189 478
(P) = Predicted or celculated by project staff.
Aniline ASTM Octane Numbers Flannabllity

Gibbs Free Heat of Coeff lclent Point Limits, No.
Net Heat ot Surface Flash Heat of
No. Combuatlon Tention Point Formation Energy of Fualon of Expane lon
Formation at 77 F Motor Method Research Method Volume Percent
ot Llquld ot th• Temp- at 77 F at 60 F
at 77 r Liquid erature at 77 F in Air Mixture
at 77 F
Cleac With l Clear With l Lower Upper
ml TEL ml TEL
per g:al per gal
10 10 191 49 472
472 10 10
191 49 473
473
,,,,
10
,,
10
,,,,
10 10
,, 209 49 474
474
475
209
209 ,, ,, 191 49
49
475
476
209 196 196 15 191
476 15
10 10 191 49 477
477 10 10
(P) 15 191 49 478
478 15 15
<O
CX>
-....! (P) = Predicted or cslculated by project staff.
TABLE 1C5.2
KEY TO REFERENCES--NONHYDROCARBONS
1987 1-163
1C5.2
TABLE 1C5.2
KEY TO REFERENCES-NONHYDROCARBONS
Boiling l'ree:1in9 Critical Constants Dttnoity Refractive Vapor

No. Compound Name Point Point at 60 F Index of Pr••sure
at l in air the Liquid at 100 F
atm at l atm at 77 F
Temp- Preasure Volume

erature
700 FORMIC ACIO 182 182 130 3 71 210 182 210

701 ACETIC ACIO 182 182 6 182 182 210 182 210
702 PROPIONIC ACIO 182 182 4 4 4 210 182 210
703 n·8UTYRIC ACIO 182 182 119 130 71 210 182 210
704 2·METHYLPROP IONIC ACIO 189 189 119 119 119 210 88 210
705 n·PENTANOIC ACIO 182 182 182 130 71 210 182 210
708 2·METHYL8UTYRIC ACIO 58 ... 130 130 71 ... . .. . ..
707 3·METHYL8UTYRIC ACIO 202 206 182 130 71 210 171 210
708 n·HEXANOIC ACIO 182 182 130 130 71 ... 182 210
709 METHANOL 223 223 119 119 119 210 182 210
710 ETHANOL 223 223 223 223 223 210 223 210
711 n·PROPANOL 182 223 223 223 223 210 182 210
712 ISOPROPANOL 223 (P) 223 223 223 210 223 210
713 n·8UTAN0L 223 223 223 223 223 210 223 210
714 IS08UTANOL 182 202 223 223 119 210 223 210
715 aec-BUTANOL 182 182 182 182 182 210 182 210
716 tert-BUTANOL 182 (P) 223 223 119 51 223 210
717 1 ·PENTANOL 182 (P) 223 223 223 210 223 210
718 2·PENTAN0L 223 (P) 130 130 71 210 223 210
719 2·METHYL ·1 ·8UTANOL 223 110 130 130 71 210 223 210
720 2 ·METHYL· 2 ·8UTANOL 223 182 223 130 71 210 182 210
721 3-ME THYL ·2 ·8UTANOL 223 ... 130 130 71 210 223 210
722 2•2-0IMETHYL·1 ·PROPANOL 223 223 130 130 71 ... 110 . ..
723 4·METHYL • 2· PENTANOL 223 ... 127 130 71 210 182 210
724 PHENOL 28 (P) 122 122 122 ... 122 210
725 o·CRESOL 182 (P) 182 182 182 ... 120 210
726 m·CRESOL 120 (P) 120 120 120 210 120 210
727 p·CRESOL 120 (P) 120 120 120 ... 120 210
728 FORULOEHYOE 182 182 169 169 71 ... ... 210
729 ACETALOEHYOE 182 182 119 130 71 ... 182 210
730 n·PROPIONALOEHYOE 182 182 130 130 71 ... 182 210

731 n·8UTYRALDEHYOE 182 182 130 130 71 ... 182 210
732 ACROLEIN 171 202 130 130 71 ... 171 ...
733 tr-ans-C ROTONALDEHYOE 171 171 130 130 71 ... 171 . ..
734 METHACROLEIN 111 110 130 130 71 ... 110 . ..
735 METHYLAMINE 182 182 182 182 71 ... 182 ...

736 ETHYLAMINE 182 182 182 182 4 ... 182 ...
737 n-PRQPYLAMINE 182 182 182 182 71 ... 182 ...
738 ISOPROPYLAMINE 182 182 4 4 4 ... 182 ...
1-164 1987
1C5.2
Heat Capacity Viscosity ot Heat ot Net Heat ot eurt•c• !'luh Heat ot Gibbs Pree Heat of !'lanwnability
at 60 F th• Liquid Vapor i:lat ion Combuetion Tena ion Point Pormation Bnerqy ot Pus ion Limits No.
at Normal ot Liquid ot th• Temp- at 77 !' Formation at 77 F Volume Percent
Boiling Point at 77 F Liquid erature at 77 !' in Air Mixture
at 77 !' at 77 p
Ideal Liquid at 100 !' at 200 F
Gas at l Lower Upper
atm
... ... ... ... ... 230 . .. 209 204 204 204 177 177 700
... ... ... ... .. . 230 .. . 209 217 217 204 209 209 701
... ... ... ... ... 230 .. . 209 48 (Pl 133 221 221 702
... ... ... ... ... 230 .. . 209 46 (Pl 133 221 221 703
... ... ... ... . .. (Pl .. . 221 180 (Pl 171 148 148 704
... ... ... ... . .. 230 .. . 110 204 (Pl 171 191 ... 705
... ... ... ... .. . (Pl ... ... 170 (Pl ... 191 ... 706
... ... ... ... ... 181 ... .. . 161 (Pl 171 191 ... 707
... ... ... ... .. . 181 .. . 177 181 (Pl 171 191 ... 708
210 210 210 210 210 230 210 209 42 42 223 209 209 709
210 210 210 210 210 230 210 209 223 223 222 209 209 710
210 210 210 210 210 230 210 209 223 223 222 209 209 711
210 210 210 ... 210 230 210 209 223 223 182 209 209 712
210 210 210 210 210 230 210 171 223 223 223 209 209 713
210 210 210 210 210 230 210 209 223 (Pl 171 209 209 714
210 210 210 210 210 230 210 209 182 182 222 209 209 715
210 ... 210 210 210 230 210 209 223 223 223 209 209 716
210 210 210 210 210 230 210 209 223 223 223 209 209 717
... ... 210 210 210 230 210 209 223 (Pl ... 191 ... 718
... 210 210 210 210 230 210 209 182 (Pl ... 178 178 719
... 210 210 210 210 230 210 177 223 223 182 177 177 720
... 210 210 210 210 223 210 209 223 (Pl ... 191 ... 721
... ... ... 210 210 180 .. . 110 180 (Pl ... 191 ... 722
... ... ... ... ... (Pl 210 209 180 (Pl .. . 209 209 723
210 ... ... . .. 210 122 ... 209 125 125 182 212 ... 724
210 ... ... .. . 210 230 ... 209 120 120 120 209 ... 725
210 210 ... . .. 210 120 210 177 120 120 120 177 ... 726
210 ... ... . .. 210 120 ... 177 120 120 120 177 ... 727
... ... ... ... ... 230 .. . (Pl 203 203 .. . 209 209 728
... ... ... .. . . .. 230 ... 209 217 217 204 209 209 729
... ... ... ... ... 230 .. . 67 182 182 .. . 67 67 730

... ... ... .. . . .. 230 ... 177 182 182 204 177 177 731
... ... ... ... ... (Pl ... 110 180 (Pl .. . 209 209 732
... ... ... ... ... 161 ... 209 161 (Pl .. . 209 209 733
... ... ... ... ... (Pl ... 110 180 (Pl .. . 110 ... 734
... ... ... ... .. . 230 ... .. . 217 217 204 209 209 735
... ... ... ... ... 230 ... (Pl 204 204 .. . 209 209 736
... ... ... ... ... 230 ... 171 204 204 .. . 209 209 737
... ... ... ... .. . 161 ... 199 181 (Pl 76 199 199 738
(Pl Predicted or calculated by project staff'.
1987 1-165
1C5.2
Bolling Freezing Critical Constants Density Refractive Vapor

No. Compound Name Point Point at 60 F Index of Pressure
at l in air the Liquid at 100 r
atm at l atm at 77 r
Temp- Pressure Volume

erature
739 n-BUTYLAMINE 1B2 1B2 207 207 71 ... 1B2 . ..

740 ISOBUTYLAMINE 1B2 1B2 130 130 71 ... 1B2 . ..
741 sec-BUTYLAWINE 2 204 1B5 1B5 1B5 ... 1B2 . ..
742 tert-BUTYLAWI NE 1B2 76 207 207 207 ... 182 . ..
743 UREA 130 ,,1 78 130 71 ... ... . ..
744 AC ETON ITRI LE 182 16B 4 4 ... . .. 1B2 . ..
745 MORPHOLINE 199 171 130 130 71 ... 112 . ..
746 PYRIOINE 4 19 ,,9 ,,9 4 ... 171 . ..
747 ANILINE 4 (P) ,,9 ,,9 ,,9 ... 171 . ..
748 INOOLE 17 17 130 130 71 ... 17 . ..
749 QUI NOLI NE 20 20 20 20 71 ... 20 . ..
750 018ENZOPYRROLE 34 202 130 130 71 ... ... . ..
751 ACRIOINE 13 13 13 13 13 ... . .. . ..
752 METHYL FORMATE 182 182 182 182 182 210 182 210
753 METHYL ACETATE 182 182 1B2 182 182 210 182 210
754 ETHYL FORMATE 182 182 1B2 182 182 210 182 210
755 ETHYL ACETATE 182 182 ,,9 ,,9 ,,9 210 182 210
758 n-PROPYL FORMATE 182 1B2 182 1B2 182 210 1B2 210
757 VINYL ACETATE 171 171 130 130 71 ... 171 . ..
758 METHYL n-BUTYRATE 182 182 1B2 182 182 210 182 210
759 n·PROPYL ACETATE 182 1B2 1B2 182 182 210 182 210
760 ISOPROPYL ACETATE 182 182 130 130 71 210 182 210
761 n-8UTYL ACETATE 1B2 182 182 130 71 210 182 210
762 n-PENTYL ACETATE 182 1B2 130 130 71 210 182 210
763 OIMETHYL ETHER 182 182 1B2 182 182 ... 182 210
764 METHYL ETHYL ETHER 182 (P) 182 182 182 ... ,, 1 210
765 OIETHYL ETHER 1B2 182 182 182 1B2 ... 182 210
766 METHYL·te•t·BUTYL ETHER 182 182 5 5 71 ... 1B2 210
767 WETHYL-tert-AWYL ETHER ... ... ... ... . .. ... ... ...
768 TETRAHYOROFURAN 4 171 119 ,,9 ,,9 210 171 210
769 018ENZOFURAN 12 12 12 12 12 ... 12 . ..

770 AIR 82 99 82 B2 99 82 99 ...
771 AMMONIA 182 1B2 137 137 137 ... 197 210
772 ARGON 103 1B2 103 103 103 ... 1B2 . ..
773 BROMINE 182 203 137 137 107 ... 182 210
774 CARBON MONOX I OE 182 1B2 ,,9 ,,9 ,,9 ... 1B2 . ..
775 CARBON OIOXIOE 82 B2 82 82 137 82 1B2 ...
778 CARBONYL SULFIOE 136 206 175 175 175 ... 174 . ..
777 CHLORINE 1B2 85 137 137 137 210 1B2 210
(P) Pr"'ed1cted Or' calculated t>y project staff.
1-166 1987
1C5.2
Heat Capacity Viscosity of Keat of Net Heat or Surface Flash Keat or Gibbs Free Heat or Flammability
at 60 F the Liquid Vaporl:1atlon Combustion Tension Point Format ion Bner;y of Fusion Llmlts No.
at Normal of Liquid or the Temp- at 77 F Pormatlon at 77 F Volume Percent
Bolling Point at 77 F Llquid erature at 77 F ln Alr Mixture
1-~~~T""~~~--it--~~~.-~~~-1
at 77 F at 77 F
Ideal Liquid at lOO F at 200 F
Gas at l Lower Upper
atm
230 209 204 204 209 209 739

181 215 161 (P) 191 740
230 171 204 204 191 741
230 145 204 204 76 145 145 742
230 204 204 87 191 49 743
24 209 24 (P) 204 177 177 744

(P) 221 170 (P) 33 221 221 745
230 209 204 204 204 209 209 746
230 209 204 204 204 209 148 747
17 17 17 17 748
20 118 20 20 20 191 749

161 161 (P) 218 750
13 13 13 13 751
210 230 209 183 183 204 209 209 752
210 55 209 204 (P) 209 209 753
2io 210 171 209 183 183 Hi 209 209 754

2io 210 (P) 171 204 204 158 209 209 755
2io 210 53 209 180 (P) 191 756
(P) 171 123 123 209 209 757
210 210 (P) 210 209 183 183 191 758
180 209 183 183 209 209 759

210 (P) 171 184 184 65 65 760
210 210 (P) 209 183 183 209 209 761
210 (P) 171 182 184 191 762
2io 210 230 182 182 182 209 209 763
210 210 230 209 204 204 209 209 764

210 210 210 230 209 182 182 222 209 209 765
210 210 210 230 162 204 204 28 182 162 768
767
210 210 210 161 210 209 182 182 121 209 209 768
12 12 12 12 769
82 82 191 770
2io 210 (P) 106 106 52 209 771
208 772
(P) 217 203 203 773
210 2io 230 203 203 182 209 209 774

82 210 82 (P) 203 203 185 775
230 203 203 204 209 209 776
2io (P) 48 203 85 777
(P) = Predicted or cslculsted by project stsff.
1987 1-167
1C5.2
Bolling l'ree:zing Critical Constants Denaity Refractive Vapor

No. COftlPOund Name Point Point at 60 P Inde:z of Pr•••ure
at 1 in air the Liquid at 100 P
atm at l atm at 77 P

erature
77S FLUORINE 1S2 99 92 92 92 ... 136 ...

779 HELIUM-3 20S 1S2 20S 20S 1S2 ... 1S2 ...
7SO HELIUM-4 20S 20S 20S 20S 1S2 ... 1S2 . ..
7S1 HYOROGEN 1S2 1S2 137 137 137 ... 1S2 ...
7S2 HYOROGEN SROMIOE 1S2 1S2 137 137 99 210 1S2 210
7S3 HYOROGEN CHLORIOE 1S2 1S2 137 137 137 210 99 210
7S4 HYOROGEN CYAN I OE 1S2 1S2 137 137 137 ... 1S2 ...
7S5 HYOROGEN FLUOR I OE 1S2 100 1S2 1S2 1S2 210 1S2 210
7SS HYOROGEN SULFIOE S2 S2 S2 S2 137 S2 1S2 S2
7S7 KRYPTON 106 106 1S2 1S2 1S2 ... 1S2 . ..
7SS NEON 20S 20S 20S 20S 1S2 ... 1S2 ...
7S9 NITROGEN S2 S2 S2 S2 1S2 S2 99 ...
790 NITRIC OXIOE 1S2 202 137 137 137 ... 99 ...
791 NITROUS OXIOE 1S2 1S2 137 137 137 ... 136 ...
792 NITROGEN OIOXIOE 136 136 136 136 136 ... 136 ...
793 NITROGEN TETROXIOE 1S2 S4 137 137 136 ... 136 210
794 OXYGEN S2 S2 S2 S2 137 S2 99 ...
795 OZONE 1S2 35 137 137 137 ... ... . ..
796 SULFUR OIOXIOE 1S2 99 1S2 1S2 1S2 ... 99 210
797 SULFUR TRIOXIOE 1S2 1S2 137 137 137 ... 1S2 210
79S XENON 106 106 1S2 1S2 1S2 ... 1S2 . ..

799 CHLOROTR IF LUOROME THANE 1S2 64 117 117 117 210 134 ...
soo OICHLOROOI FLUOROME THANE 134 134 119 119 119 210 134 210
S01 TRI CHLOROF LUOROME THANE 134 134 119 119 119 210 110 210
S02 CARSON TETRACHLORIOE 1S2 1S2 119 119 119 210 1S2 210
S03 CARSON TETRAFLUORIOE 1S2 195 1S2 1S2 1S2 ... 134 ...
S04 CHLOROOI FLUOROME THANE 51 149 4 4 4 210 64 210
S05 OICH LOROFLUOROMETHANE 1S2 64 4 4 4 210 64 210
S06 CHLOROFORM 1S2 1S2 119 119 119 210 1S2 210
S07 TRI FLUOROMETHANE 1S2 213 1S2 1S2 1S2 210 64 ...
sos OICHLOROMETHANE 1S2 1S2 1S2 1S2 71 210 1S2 210
S09 METHYL CHLORIOE 1S2 1S5 119 119 119 210 1S2 210
S10 METHYL FLUORIOE 1S2 1S2 1S2 1S2 1S2 210 1S2 210
S11 VINYL CHLORIOE 1S2 1S2 193 193 193 ... 1S2 ...
S12 1. 1. 1-TRICHLOROETHANE 1S2 1S2 4 4 71 210 1S2 210
S13 1. 1. 2-TRICHLOROETHANE 1S2 204 130 130 71 210 1S2 210

S14 1. 1. 1-TRIFLUOROETHANE 1S2 1S2 1S2 1S2 1S2 210 1S2 210
S15 1. 1-0ICHLOROETHANE 1S2 1S2 119 119 119 210 1S2 210
S1S 1. 2-0ICHLOROETHANE 51 1S2 119 119 119 210 171 210
(P) Predicted or calculated by project •taff.
1-168 1987
1C5.2
Keat Capac 1 ty viscosity of Keat ot Net Keat ot Surtace Flash Keat of Gibbs Free Heat of Flammability
at 60 P' the Liquid Vaporization Combustion Tension Point P'ormation Energy ot P'usion Limits No.
at Normal ot Liquid ot the Tomp- at 77 P' Formation at 77 P' Volume Percent
Boil ln9 Point at 77 P' Liquid eraiture at 77 F in Air Mixture
at 77 P' at 77 P'
Ideal Liquid at lOO P' at 200 P'
Cao at l Lower Upper
atm
210 136 778

779
48 217 208 780
181 48 182 182 209 209 781
230 203 203 204 782
210 230 203 203 135 783

230 209 217 217 204 209 209 784
210 (Pl 203 203 99 785
82 82 (Pl 182 182 134 82 82 786
48 48 136 787
208 788
82 82 189 189 176 789
210 210 (Pl 182 182 204 790
210 210 (Pl 203 203 204 791
210 (Pl 203 203 792
210 (Pl 203 203 84 793

82 82 189 88 794
210 210 (Pl 182 182 200 795
210 210 203 203 204 796
210 210 (Pl 184 184 189 797
106 106 134 798

203 203 799
(Pl 203 203 800
(Pl 203 203 134 801
230 203 203 110 802
(Pl 203 203 195 803

{Pl 203 203 149 804
(Pl 203 203 805
210 210 230 203 203 171 806
(Pl 183 183 204 807
210 210 230 (Pl 203 203 204 209 209 808
210 210 230 183 183 134 209 209 809
210 (Pl 182 182 810
(Pl 177 184 184 111 177 177 811
210 210 (Pl 183 183 27 110 110 812
(Pl 183 183 204 191 813

(Pl 183 183 204 814
210 210 (Pl 110 183 183 204 110 110 815
230 209 217 217 176 209 209 816
(Pl = Pred 1 cted or ca I cu 1ated by project staff.
1987 1-169
1C5.2
Boiling Pree1in9 Critical Constants oenaity Rettactive Vapor

No. Compound Name Point Point at 60 P Index ot Preaaure
at l in air the Liquid at lOO P
atm at l atm at 77 p

erature
817 1, 1-0IFLUOROETHANE 182 182 119 119 119 210 182 210
818 ETHYL CH LORI OE 182 182 182 182 138 ... 182 210
819 ETHYL FLUOR! OE 182 182 182 182 71 210 182 210
820 1, 2-0ICHLOROPROPANE 182 182 130 130 71 ... 182 ...
821 ACETONE 182 182 119 119 119 ... 182 210
822 WETHYL ETHYL KETONE 182 (P) 182 182 182 ... 182 210
823 01 ETHYL KETONE (P) 182 182 182 182 ... 182 210
824 WE THYL-n-PROPYL KETONE 182 182 4 4 4 ... 182 210
825 WETHYL-n-BUTYL KETONE 182 182 4 4 71 ... 182 210
828 WE THYL I SOBUTYL KETONE 182 182 182 182 71 ... 182 . ..
827 CARBON 01 SULF I OE 171 171 137 137 137 ... 171 ...
828 WETHYL WERCAPTAN 189 189 119 119 4 ... ... ...
829 2. 3-0ITHIASUTANE 189 189 130 130 71 ... 189 . ..
830 01 WE TH~L SUL FI OE 51 51 51 51 51 ... 51 ...
831 ETHYL WERCAPTAN 189 189 4 4 4 ... 189 . ..
832 2-THIASUTANE ... ... ... ... ... ... ... . ..
833 1-PROPANETHIOL ... ... ... ... ... ... ... . ..
834 n-BUTANETHIOL 204 204 130 130 71 ... 171 ...
835 tert-BUTANE THIOL 189 189 130 130 71 ... 189 ...
836 2-SUTANETHIOL ... ... ... .. . ... .. . ... .. .
837 2-WE TH~L-1-PROPANE THIOL ... ... ... ... ... ... .. . . ..
838 3-THIAPENTANE 171 204 119 119 119 ... 171 . ..
839 2-THIAHEXANE ... ... ... ... ... ... ... . ..
840 3-THIAHEXANE ... ... ... ... ... .. . .. . . ..
841 1-PENTANETHIOL 189 189 130 130 71 ... 189 . ..
842 2-THIAHEPTANE ... ... ... ... ... . .. .. . . ..
843 1-HEXANE THIOL ... ... ... . .. ... ... ... . ..
844 1-HEPTANE THIOL ... ... ... ... ... ... .. . . ..
845 WATER 82 82 82 82 90 82 51 82
848 SULFURIC ACIO 106 106 130 130 201 ... 99 . ..
847 SOOIUW HYOROXIOE 105 105 (P) 130 153 ... 54 ...
848 PROPYLENE CARSO NATE ... ... ... ... ... .. . . .. ...
849 FURFURAL 81 171 130 171 71 ... 171 . ..
850 1,2-PROPYLENE GLYCOL 182 182 130 130 71 ... 182 . ..
851 01 ETHYLENE GLYCOL 47 173 130 130 71 ... 58 . ..
852 TETRAETHYLENE GLYCOL 202 57 13~ 130 71 ... 57 . ..
853 WONOE THANOLAWI NE 51 51 130 130 71 ... 171 . ..
854 OIETHANOLAWINE 51 51
, ...
59 59 71 ... 51 ...
855 OIGLYCOLAWINE ... ... ... ... ... .. . . ..
(P) Pred i ctad or ca 1cu1 ated by project staff.
1-170 1987
1C5.2
Heat Capacity Viscosity of Heat of Net Heat of Surface Plash Heat of Gibbs Pr•• Heat of Flammability
at 60 F th• Liquid Vaporization Combustion Tension Point Formation Energy ot Fusion Limits No.
at Normal ot Liquid ot the TeOIP- at 77 F Formation at 77 F Volume Percent
Boiling Pol"nt at 77 F Liquid erature at 77 F in Air Mixture
at 77 F at 77 F
Ideal Liquid at 100 F at 200 F
Gas at i Lower tipper
atm
210 210 (Pl 204 204 199 199 817

230 209 182 182 136 209 209 818
210 (Pl 183 183 819
(Pl 209 204 204 209 209 820
210 210 230 209 182 182 159 209 209 821
210 210 230 209 204 204 204 209 209 822
210 210 161 209 161 (Pl 171 97 97 823
210 210 161 178 182 182 152 178 178 824
210 210 161 221 182 182 199 199 825
(Pl 70 180 (Pl 209 209 826
(Pl 148 203 203 204 148 148 827

230 (Pl 1-89 189 204 209 209 828
230 178 189 189 189 191 829
230 171 189 189 189 51 51 830
230 163 189 181 204 209 209 831
832
833
210 210 230 178 204 204 204 834
230 189 186 189 835
836
837
(Pl 199 204 204 204 838
839
840
230 148 189 186 189 841
842
843
844
82 82 210 82 210 189 189 108 845
106 106 106 846
105 105 105 847

848
161 209 124 124 171 209 209 849
161 209 161 (Pl 209 209 850
46 209 46 (Pl 191 851
(Pl 57 180 (Pl 191 852

8 209 8 (P) 59 191 853
144 209 144 (Pl 171 191 854
855
(P) = Predicted or calculated by project staff.
1987 1-171
1C5.2
Bolling Freezing Critical Constants Density Refractive Vapor

No. Compound Name Point Point at 60 p Index of Pres1ure
at l in air th• Liquid at 100 p
atm at l atm at 77 p

erature
858 METHYL D!ETHANOLAM!NE 11D 11D 13D 130 71 ... 1 . ..

857 TRIETHANOLAM!NE (P) 51 59 59 71 ... 59 . ..
858 OI I SOPROPANOLAM! NE ... ... ... ... ... ... . .. . ..
859 N, N-D!METHYLFORMAMI DE 171 171 13D 13D 71 ... 63 . ..
860 N-METHYL-2-PYRROLI DONE 51 51 130 130 71 ... 51 ...
881 DIMETHYL SULFOX!DE 171 44 130 130 71 ... 171 . ..
882 SULFOLANE 51 51 13D 13D 71 ... 51 ...
883 SELEXOL 82A 82A ... ... . .. ... . .. . ..
(P) .:1: Predicted or calculated by project staff.
1-172 1987
1C5.2
Heat Capacity Viscosity ot Heat ot Net Heat ot Surface l"lash Heat ot Gibbs l"ree Heat ot Flammability
at 60 F the Liquid vaporization Combustion Tens ion Point Format ion Energy ot Fus ion Li mi ts No.
at Normal of Liquid ot the Temp- at 77 F Formation at 77 F Volume Percent
Bolling Po~nt at Liquid ar a tu re at 77 l" in A~r Mixture
77 "
at 77 r at 77 F
Ideal Liquid at 100 F • t 200 "
Gas at 1 Lower Upper
atm
(P) 1 170 (P) 856

144 51 144 (P) 59 191 857
858
161 209 161 (P) 171 171 171 859
(P) 111 180 (P) 89 89 860
(P) 221 131 131 171 209 209 861

(P) ,,, 170 (P) 37 862
82A 863
(P) = Predicted or calculated by project staff.
1987 1-173
DS4B-EB/May 1988
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DS4A - (1971) Physical Constants of Hydrocarbons C1 To C10

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ASTM Data Series DS 4B

~~l~ 1916 Race St., Philadelphia, PA 19103

Physical constants of hydrocarbon and non-hydrocarbon compounds I compiled by

Copyright © 1988 American Petroleum Institute

Printed in Ann Arbor, MI/May 1991

lA Fundamental Constants and Conversion Factors .................. . 1-2

1A2 Conversion Factors ........................................ . 1-4

1B Letter Symbols Used in Chemical Engineering ................... . 1-13

lC Property Definitions .......................................... . 1-19

1C2 Hydrocarbons-Secondary Properties ........................ . 1-86

1C3 Nonhydrocarbons-Primary Properties ....................... . 1-120

1C4 Nonhydrocarbons-Secondary Properties ..................... . 1-130

1C5 Key to References ......................................... . 1-136

Bibliography ..................................................... . 1-175

Revised Chapter 1 to First (1966), Second (1970),

Copyright © 1988 by ASTM International www.astm.org

Boltzmann constant 1.38066 x 10- 16 ergs per (molecule) (K)

Second radiation constant 1.43877 cm-deg C

Copyright © 1988 by ASTM International www.astm.org

TABLE 1A1.1 (Continued)

Conversion Factors-Engineering Units Vs. Metric Units

Units-+ Milli- Centi- Kilo-

3.9370 3.2808 1.0936 6.2137 103 10-6

6.2137 104 10-5

3.9370 3.2808 1.0936 109 106 105

Units-+ Square Square Square

Square Feet 144 1 0.11111 2.2957 x 10- 5 929.03 9.2903 x 10- 2

Square Yards 1,296 9 1 2.0661 x 10- 4 8,361.3 0.83613

Acres 6.2726 x 106 43,560 4,840 1 4.0469 x 10 7 4.0469 x 103

Square 1.0764 x 10- 3 1.1960 x 10- 4 2.4711 10-s_ 10-4

Square Meters 1,550 10.764 1.1960 2.4711 x 10- 4 104 1

Cubic Meters 61,023 35.315 1.3080 106 1

LIQUID VOLUME CONVERSIONS

Fluid Ounces 7.8125 6.5053 1.8601 1.0444 2.9574

Cubic 1.0567 2.6417 2.1997 6.2898 3.5315 1 x 10- 6

Note: According to ASME Guides SI-1 (22) and SI-4 (23),

Units-+ Ounces Pounds Ounces Pounds Tons Tons Metric

1.5432 1.1023 9.8421 10-3

Units-+ dynes Atmos- ~ mm Hg* in. Hg* lb [force] ft HiO

Bars 106 1 0.986923 1.01972 750.06 29.530 14.504 33.457 1x105

~ 980,670 0.98067 0.96784 1 735.56 28.959 14.223 32.809 98,066.5

in. Hg at 32 F 33,864 0.033864 0.033421 0.03453 25.400 1 0.49116 1.1330 3,386.4

10- 5 9.86923 1.01972 7.5006 2.9530 1.4504 3.3456

KINEMATIC VISCOSITY CONVERSIONS

ABSOLUTE VISCOSITY CONVERSIONS

lb [force]-sec __g_x 102

Btu Btu ft-lb ft-lb Metric cal

SPECIFIC ENERGY CONVERSIONS

joules (abs) joules (int) cal LT. cal Btu

SPECIFIC ENERGY PER DEGREE CONVERSIONS

joules (abs) joules (int) cal I.T. cal Btu

g-K g-K g-K g-K lb-deg F

HEAT FLUX CONVERSIONS

Btu cal kg-cal watts (abs) joules (abs)

HEAT TRANSFER COEFFICIENT CONVERSIONS

Btu cal kg-cal watts (abs) joules (abs)

THERMAL CONDUCTIVITY CONVERSIONS

LETTER SYMBOLS FOR THE PRINCIPAL CONCEPTS USED IN CHEMICAL ENGINEERING

AH}'q (Btu/lb)= fl.He (net, Btu/lb) - M~4(~b) (44) a - M:·~Hb) (18) ~