CELEX_02012R0231-20241027_EN_TXT

02012R0231 — EN — 27.10.2024 — 033.
001 — 1
This text is meant purely as a documentation tool and has no legal effect. The Union's institutions do not assume any liability
for its contents. The authentic versions of the relevant acts, including their preambles, are those published in the Official
Journal of the European Union and available in EUR-Lex. Those official texts are directly accessible through the links
embedded in this document
►B COMMISSION REGULATION (EU) No 231/2012

of 9 March 2012
laying down specifications for food additives listed in Annexes II and III to Regulation (EC)
No 1333/2008 of the European Parliament and of the Council
(Text with EEA relevance)
(OJ L 83, 22.3.2012, p. 1)
Amended by:
Official Journal
No page date
►M1 Commission Regulation (EU) No 1050/2012 of 8 November 2012 L 310 45 9.11.2012
►M2 Commission Regulation (EU) No 25/2013 of 16 January 2013 L 13 1 17.1.2013
►M3 Commission Regulation (EU) No 497/2013 of 29 May 2013 L 143 20 30.5.2013
►M4 Commission Regulation (EU) No 724/2013 of 26 July 2013 L 202 11 27.7.2013
►M5 Commission Regulation (EU) No 739/2013 of 30 July 2013 L 204 35 31.7.2013
►M6 Commission Regulation (EU) No 816/2013 of 28 August 2013 L 230 1 29.8.2013
►M8 Commission Regulation (EU) No 1274/2013 of 6 December 2013 L 328 79 7.12.2013
►M9 Commission Regulation (EU) No 264/2014 of 14 March 2014 L 76 22 15.3.2014
►M10 Commission Regulation (EU) No 298/2014 of 21 March 2014 L 89 36 25.3.2014
►M13 Commission Regulation (EU) No 685/2014 of 20 June 2014 L 182 23 21.6.2014
►M15 Commission Regulation (EU) No 957/2014 of 10 September 2014 L 270 1 11.9.2014
►M16 Commission Regulation (EU) No 966/2014 of 12 September 2014 L 272 1 13.9.2014
►M17 Commission Regulation (EU) 2015/463 of 19 March 2015 L 76 42 20.3.2015
►M18 Commission Regulation (EU) 2015/649 of 24 April 2015 L 107 17 25.4.2015
►M19 Commission Regulation (EU) 2015/1725 of 28 September 2015 L 252 12 29.9.2015
►M21 Commission Regulation (EU) 2016/1814 of 13 October 2016 L 278 37 14.10.2016
►M22 Commission Regulation (EU) 2017/324 of 24 February 2017 L 49 4 25.2.2017
►M23 Commission Regulation (EU) 2017/1399 of 28 July 2017 L 199 8 29.7.2017
►M24 Commission Regulation (EU) 2018/75 of 17 January 2018 L 13 24 18.1.2018
02012R0231 — EN — 27.10.2024 — 033.001 — 2

►M26 Commission Regulation (EU) 2018/681 of 4 May 2018 L 116 1 7.5.2018
►M31 Commission Regulation (EU) 2020/763 of 9 June 2020 L 182 8 10.6.2020
►M34 Commission Regulation (EU) 2022/650 of 20 April 2022 L 119 65 21.4.2022
►M37 Commission Regulation (EU) 2022/1396 of 11 August 2022 L 211 182 12.8.2022
►M39 Commission Regulation (EU) 2023/440 of 28 February 2023 L 64 4 1.3.2023
►M40 Commission Regulation (EU) 2023/447 of 1 March 2023 L 65 16 2.3.2023
02012R0231 — EN — 27.10.2024 — 033.001 — 3
▼B
COMMISSION REGULATION (EU) No 231/2012
of 9 March 2012
laying down specifications for food additives listed in Annexes II
and III to Regulation (EC) No 1333/2008 of the European
Parliament and of the Council
(Text with EEA relevance)
Article 1
Specifications for food additives
Specifications for food additives including colours and sweeteners listed

in Annex II and III to Regulation (EC) No 1333/2008 are laid down in
the Annex to this Regulation.
Article 2
Repeals
Directives 2008/60/EC, 2008/84/EC and 2008/128/EC are repealed with

effect from 1 December 2012.
Article 3
Transitional measures
Foodstuffs containing food additives that have been lawfully placed on

the market before 1 December 2012, but do not comply with this
Regulation, may continue to be marketed until stocks are exhausted.
Article 4
Entry into force
This Regulation shall enter into force on the 20th day following its
publication in the Official Journal of the European Union.
It shall apply from 1 December 2012.
However, the specifications laid down in the Annex for additives steviol
glycosides (E 960) and basic methacrylate copolymer (E 1205) shall
apply from the date of entry into force of this Regulation.
This Regulation shall be binding in its entirety and directly applicable in
the Member States.
02012R0231 — EN — 27.10.2024 — 033.001 — 4
▼B
ANNEX
▼M37
Ethylene oxide may not be used for sterilising purposes in food additives.
No residue above 0,1 mg/kg, irrespective of its origin, of ethylene oxide (sum of
ethylene oxide and 2-chloro-ethanol expressed as ethylene oxide (1)) shall be
present in food additives listed in Annexes II and III to Regulation (EC)
No 1333/2008, including mixtures of food additives.
▼B
Aluminium lakes for use in colours only where explicitly stated.
Definition: Aluminium lakes are prepared by reacting colours complying with

the purity criteria set out in the appropriate specification monograph
with alumina under aqueous conditions. The alumina is usually
freshly prepared undried material made by reacting aluminium
sulphate or chloride with sodium or calcium carbonate or bicar
bonate or ammonia. Following lake formation, the product is
filtered, washed with water and dried. Unreacted alumina may also
be present in the finished product.
HCl insoluble matter Not more than 0,5 %
ΝaΟΗ insoluble matter Νot more than 0,5 %, for Ε 127 erythrosine only
Ether extractable matter Not more than 0,2 % (under neutral conditions)
Specific purity criteria for the corresponding colours are applicable.
E 100 CURCUMIN
Synonyms CI Natural Yellow 3; Turmeric Yellow; Diferoyl Methane
Definition Curcumin is obtained by solvent extraction of turmeric i.e. the

ground rhizomes of strains of Curcuma longa L. In order to
obtain a concentrated curcumin powder, the extract is purified by
crystallization. The product consists essentially of curcumins; i.e.
the colouring principle (1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-
1,6-dien-3,5-dione) and its two desmethoxy derivatives in varying
proportions. Minor amounts of oils and resins naturally occurring in
turmeric may be present.
Curcumin is also used as the aluminium lake; the aluminium
content is less than 30 %.
Only the following solvents may be used in the extraction: ethy
lacetate, acetone, carbon dioxide, dichloromethane, n-butanol,
methanol, ethanol, hexane, propan-2-ol.
Colour Index No 75300
Einecs 207-280-5
Chemical name I 1,7-Bis(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione

II 1-(4-Hydroxyphenyl)-7-(4-hydroxy-3-methoxy-phenyl-)hepta-
1,6-diene-3,5-dione
III 1,7-Bis(4-hydroxyphenyl)hepta-1,6-diene-3,5-dione
Chemical formula I C21H20O6

II C20H18O5
III C19H16O4
Molecular weight I. 368,39 II. 338,39 III. 308,39
Assay Content not less than 90 % total colouring matters

E1%
1cm 1 607 at ca. 426 nm in ethanol
(1) i.e. ethylene oxide + 0,55* 2-chloroethanol.

02012R0231 — EN — 27.10.2024 — 033.001 — 5
▼B
Description Orange-yellow crystalline powder
Identification
Spectrometry Maximum in ethanol at ca. 426 nm
Melting range 179 °C-182 °C
Purity
9
Solvent residues Ethylacetate >
>
>
>
>
Acetone >
>
>
>
>
>
>
>
n-butanol >
>
>
>
=
Not more than 50 mg/kg, singly or in
Methanol
> combination
>
>
Ethanol >
>
>
>
>
>
>
>
Hexane >
>
>
>
>
>
;
Propan-2-ol
Dichloromethane: not more than 10 mg/kg
Arsenic Not more than 3 mg/kg
Lead Not more than 10 mg/kg
Mercury Not more than 1 mg/kg
Cadmium Not more than 1 mg/kg
Aluminium lakes of this colour may be used.

E 101 (i) RIBOFLAVIN
Synonyms Lactoflavin;
Definition
Colour Index No
Einecs 201-507-1
Chemical name 7,8-Dimethyl-10-(D-ribo-2,3,4,5-tetrahydroxy

pentyl)benzo(g)pteridine-2,4(3H,10H)-dione; 7,8-dimethyl-10-(1′-D-
ribityl)isoalloxazine
Chemical formula C17H20N4O6
Molecular weight 376,37
Assay Content not less than 98 % on the anhydrous basis

E1%
1cm 328 at ca. 444 nm in aqueous solution
Description Yellow to orange-yellow crystalline powder, with slight odour
Identification
9
Spectrometry The ratio A375/A267 is between 0,31 and >
>
0,33 >
=
in aqueous solution
The ratio A444/A267 is between 0,36 and >
>
>
;
0,39
Maximum in water at ca. 375 nm
Specific rotation [α]D20 between – 115° and – 140° in a 0,05 N sodium hydroxide
solution
Purity
Loss on drying Not more than 1,5 % (105 °C, 4 hours)

02012R0231 — EN — 27.10.2024 — 033.001 — 6
▼B
Sulphated ash Not more than 0,1 %
Primary aromatic amines Not more than 100 mg/kg (calculated as aniline)
▼M14
▼B
E 101 (ii) RIBOFLAVIN-5′-PHOSPHATE
Synonyms Riboflavin-5′-phosphate sodium
Definition These specifications apply to riboflavin 5′-phosphate together with

minor amounts of free riboflavin and riboflavin diphosphate.
Colour Index No
Einecs 204-988-6
Chemical name Monosodium(2R,3R,4S)-5-(3′)10′-dihydro-7′,8′-dimethyl-2′,4′-

dioxo-10′-benzo[γ]pteridinyl)-2,3,4-trihydroxypentyl phosphate;
monosodium salt of 5′-monophosphate ester of riboflavin
Chemical formula For the dihydrate form: C17H20N4NaO9P · 2H2O
For the anhydrous form: C17H20N4NaO9P
Assay Content not less than 95 % total colouring matters calculated as

C17H20N4NaO9P.2H2O
E1%
Description Yellow to orange crystalline hygroscopic powder, with slight odour
Identification
9
Spectrometry The ratio A375/A267 is between 0,30 and >
>
>
>
0,34 =
in aqueous solution
>
The ratio A444/A267 is between 0,35 and >
>
>
;
0,40
Maximum in water at ca. 375 nm
Specific rotation [α]D20 between + 38° and + 42° in a 5 molar HCl solution
Purity
Loss on drying Not more than 8 % (100 °C, 5 hours in vacuum over P2O5) for the
dihydrate form
Sulphated ash Not more than 25 %
Inorganic phosphate Not more than 1,0 % (calculated as PO4 on the anhydrous basis)
Subsidiary colouring matters Riboflavin (free): Not more than 6 %

Riboflavine diphosphate: Not more than 6 %
Primary aromatic amines Not more than 70 mg/kg (calculated as aniline)

02012R0231 — EN — 27.10.2024 — 033.001 — 7
▼B
▼M14
▼B
E 102 TARTRAZINE
Synonyms CI Food Yellow 4
Definition Tartrazine is prepared from 4-amino-benzenesulphonic acid, which is

diazotized using hydrochloric acid and sodium nitrite. The diazo
compound is then coupled with 4,5-dihydro-5-oxo-1-(4sulphophenyl)-
1H-pyrazole-3-carboxylic acid or with the methyl ester, the ethyl ester,
or a salt of this carboxylic acid. The resulting dye is purified and isolated
as the sodium salt. Tartrazine consists essentially of trisodium 5-
hydroxy-1-(4-sulfonatophenyl)-4-(4-sulfonatophenylazo)-H-pyrazole-
3-carboxylate and subsidiary colouring matters together with sodium
chloride and/or sodium sulphate as the principal uncoloured
components.
Tartrazine is described as the sodium salt. The calcium and the
potassium salt are also permitted.
Einecs 217-699-5
Chemical name Trisodium-5-hydroxy-1-(4-sulfonatophenyl)-4-(4-sulfonatop

henylazo)-H-pyrazole-3-carboxylate
Chemical formula C16H9N4Na3O9S2
Assay Content not less than 85 % total colouring matters calculated as the
sodium salt
E1%
Description Light orange powder or granules
Appearance of the aqueous solution Yellow
Identification
Spectrometry Maximum in water at ca. 426 nm
Purity
Water insoluble matter Not more than 0,2 %
Subsidiary colouring matters Not more than 1,0 %
Organic compounds other than colouring

matters:
9
4-hydrazinobenzene sulfonic acid >
>
>
>
>
>
>
4-aminobenzene-1-sulfonic acid >
>
>
>
>
>
5-oxo-1-(4-sulfophenyl)-2-pyra >
=
zoline-3-carboxylic acid Total not more than 0,5 %
>
>
>
>
4,4′-diazoaminodi(benzene sulfonic >
>
>
>
acid) >
>
>
>
>
>
;
Tetrahydroxysuccinic acid
02012R0231 — EN — 27.10.2024 — 033.001 — 8
▼B
Unsulfonated primary aromatic amines Not more than 0,01 % (calculated as aniline)
Ether extractable matter Not more than 0,2 % under neutral conditions
E 104 QUINOLINE YELLOW
Synonyms CI Food Yellow 13
Definition Quinoline Yellow is prepared by sulfonating 2-(2-quinolyl) indan-1,3-

dione or a mixture containing about two thirds 2-(2-quinolyl)indane-
1,3-dione and one third 2-(2-(6-methylquinolyl))indane-1,3-dione.
Quinoline Yellow consists essentially of sodium salts of a mixture of
disulfonates (principally), monosulfonates and trisulfonates of the
above compound and subsidiary colouring matters together with
sodium chloride and/or sodium sulphate as the principal uncoloured
components.
Quinoline Yellow is described as the sodium salt. The calcium and the
Einecs 305-897-5
Chemical name The disodium salts of the disulfonates of 2-(2-quinolyl) indan-1,3-

dione (principal component)
Chemical formula C18H9N Na2O8S2 (principal component)
Molecular weight 477,38 (principal component)
sodium salt
Quinoline Yellow shall have the following composition:
Of the total colouring matters present:
— not less than 80 % shall be disodium 2-(2-quinolyl) indan-1,3-
dione-disulfonates
— not more than 15 % shall be sodium 2-(2-quinolyl) indan-1,3-
dione-monosulfonates
— not more than 7,0 % shall be trisodium 2-(2-quinolyl) indan-1,3-
dione-trisulfonate
E1%
1cm 865 (principal component) at ca. 411 nm in aqueous acetic acid
solution
Description Yellow powder or granules
Appearance of the aqueous solution Yellow
Identification
Spectrometry Maximum in aqueous acetic acid solution of pH 5 at ca. 411 nm

02012R0231 — EN — 27.10.2024 — 033.001 — 9
▼B
Purity

matters:
9
2-methylquinoline >
>
>
>
>
>
>
>
2-methylquinoline-sulfonic acid >
>
>
>
>
=
Phthalic acid Total not more than 0,5 %
>
>
>
>
>
>
2,6-dimethyl quinoline >
>
>
>
>
>
>
;
2,6-dimethyl quinoline sulfonic acid
2-(2-quinolyl)indan-1,3-dione Not more than 4 mg/kg
E 110 SUNSET YELLOW FCF
Synonyms CI Food Yellow 3; Orange Yellow S
Definition Sunset Yellow FCF consists essentially of disodium 2-hydroxy-1-(4-

sulfonatophenylazo) naphthalene-6-sulfonate and subsidiary colouring
matters together with sodium chloride and/or sodium sulphate as the
principal uncoloured components. Sunset Yellow FCF is manufactured
by diazotizing 4-aminobenzenesulphonic acid using hydrochloric acid
and sodium nitrite or sulphuric acid and sodium nitrite. The diazo
compound is coupled with 6-hydroxy-2-naphthalene-sulphonic acid.
The dye is isolated as the sodium salt and dried.
Sunset Yellow FCF is described as the sodium salt. The calcium and the
Einecs 220-491-7
Chemical name Disodium 2-hydroxy-1-(4-sulfonatophenylazo)naphthalene-6-

sulfonate
sodium salt
E1%
1cm 555 at ca. 485 nm in aqueous solution at pH 7
02012R0231 — EN — 27.10.2024 — 033.001 — 10
▼B
Description Orange-red powder or granules
Appearance of the aqueous solution Orange

Identification
Spectrometry Maximum in water at ca. 485 nm at pH 7
Purity
1-(Phenylazo)-2-naphthalenol (Sudan I) Not more than 0,5 mg/kg
matters:
9
4-aminobenzene-1-sulfonic acid >
>
>
>
>
3-hydroxynaphthalene-2,7-disulfonic >
>
>
>
acid >
>
>
>
>
>
6-hydroxynaphthalene-2-sulfonic >
>
>
>
acid >
>
=
7-hydroxynaphthalene-1,3-disulfonic Total not more than 0,5 %
>
>
acid >
>
>
>
>
>
4,4′-diazoaminodi(benzene sulfonic >
>
>
>
acid) >
>
>
>
>
>
6,6′-oxydi(naphthalene-2-sulfonic >
>
>
;
acid)
▼M29
E 120 CARMINIC ACID, CARMINE
Synonyms CI Natural Red 4

Definition Carminic acid is obtained from aqueous, aqueous alcoholic or
alcoholic extracts from Cochineal, which consists of the dried
bodies of the female insect Dactylopius coccus Costa.
Carmines are aluminium lakes of carminic acid in which aluminium
and carminic acid are thought to be present in the molar ratio 1:2.
The colouring principle is carminic acid. Minor amounts of its
aminated form 4-aminocarminic acid may also be present.
In commercial products the colouring principle carminic acid may
be present in association with ammonium, calcium, potassium or
sodium cations, singly or in combination, and these cations may
also be present in excess. Commercial products may also contain
proteinaceous material derived from the source insect.
Einecs Carminic acid: 215-023-3; carmines: 215-724-4
Chemical name 7-β-D-glucopyranosyl-3,5,6,8-tetrahydroxy-1-methyl-9,10-dioxoan
thracene-2-carboxylic acid (carminic acid); carmine is the hydrated
aluminium chelate of this acid
Chemical formula C22H20O13 (carminic acid)
Molecular weight 492,39 (carminic acid)
02012R0231 — EN — 27.10.2024 — 033.001 — 11
▼M29
Assay Content not less than 90 % carminic acid; not less than 50 %
carminic acid in the chelates.
Description Red to dark red, friable, solid or powder
Identification
Spectrometry Carminic acid:
Maximum in aqueous ammonia solution at ca. 518 nm
Maximum in dilute hydrochloric solution at ca. 494 nm
E 1 %/1 cm 139 at peak around 494 nm in dilute hydrochloric acid
4-aminocarminic acid:
Maximum in aqueous ammonia solution at 535 nm
Maximum in dilute hydrochloric solution at 530 nm
E 1 %/1 cm 260 at peak around 535 nm in aqueous ammonia
solution, pH 9,5
In commercial products carminic acid may be differentiated from
its amine by HPLC
Purity
Solvent residues Ethanol: Not more than 150 mg/kg
Methanol: Not more than 50 mg/kg
Total ash Carminic acid: Not more than 5 %
Carmine: Not more than 12 %
Protein (N × 6,25) Carminic acid: Not more than 2,2 %
Carmine: Not more than 25 %
4-aminocarminic acid Not more than 3 % relative to carminic acid
Matter insoluble in dilute ammonia Carmine: Not more than 1 %
Lead Not more than 1,5 mg/kg
Mercury Not more than 0,5 mg/kg
Cadmium Not more than 0,1 mg/kg
Microbiological criteria
Salmonella spp. Absent in 10 g
▼B
E 122 AZORUBINE, CARMOISINE
Synonyms CI Food Red 3

Definition Azorubine consists essentially of disodium 4-hydroxy-3-(4-sulfonato-
1-naphthylazo) naphthalene-1-sulfonate and subsidiary colouring
matters together with sodium chloride and/or sodium sulphate as
the principal uncoloured components.
Azorubine is described as the sodium salt. The calcium and the
Einecs 222-657-4
Chemical name Disodium 4-hydroxy-3-(4-sulfonato-1-naphthylazo) naphthalene-1-
sulfonate
Assay Content not less than 85 % total colouring matters, calculated as the
sodium salt
E1%
02012R0231 — EN — 27.10.2024 — 033.001 — 12
▼B
Description Red to maroon powder or granules
Appearance of the aqueous solution Red
Identification
Purity
Subsidiary colouring matters Not more than 1 %

matters:
9
4-aminonaphthalene-1-sulfonic acid >
=
Total not more than 0,5 %
>
;
4-hydroxynaphthalene-1-sulfonic acid
E 123 AMARANTH
Definition Amaranth consists essentially of trisodium 2-hydroxy-1-(4-sulfonato-

1-naphthylazo) naphthalene-3,6-disulfonate and subsidiary colouring
matters together with sodium chloride and/or sodium sulphate as the
principal uncoloured components. Amaranth is manufactured by
coupling 4-amino-1-naphthalenesulphonic acid with 3-hydroxy-2,7-
naphthalenedisulphonic acid.
Amaranth is described as the sodium salt. The calcium and the
Einecs 213-022-2
Chemical name Trisodium 2-hydroxy-1-(4-sulfonato-1-naphthylazo) naphthalene-3,6-

disulfonate
sodium salt
E1%
02012R0231 — EN — 27.10.2024 — 033.001 — 13
▼B
Description Reddish-brown powder or granules
Identification
Purity

matters:
9
>
>
>
>
>
>
>
>
>
>
acid >
>
>
>
>
>
=
6-hydroxynaphthalene-2-sulfonic acid
>
>
>
>
>
>
>
acid >
>
>
>
>
>
>
>
7-hydroxynaphthalene-1,3-6- >
>
;
trisulfonic acid
E 124 PONCEAU 4R, COCHINEAL RED A
Synonyms CI Food Red 7; New Coccine
Definition Ponceau 4R consists essentially of trisodium 2-hydroxy-1-(4-

sulfonato-1-naphthylazo) naphthalene-6,8-disulfonate and subsidiary
colouring matters together with sodium chloride and/or sodium
sulphate as the principal uncoloured components. Ponceau 4R is
manufactured by coupling diazotized naphthionic acid to G acid
(2-naphthol-6,8- disulphonic acid) and converting the coupling
product to the trisodium salt.
Ponceau 4R is described as the sodium salt. The calcium and the
Einecs 220-036-2
Chemical name Trisodium 2-hydroxy-1-(4-sulfonato-1-naphthylazo) naphthalene-6,8-

disulfonate

02012R0231 — EN — 27.10.2024 — 033.001 — 14
▼B
sodium salt.
E1%
Description Reddish powder or granules
Identification
Purity

matters:
9
>
>
>
>
>
>
>
>
acid >
>
>
>
>
>
>
=
3-hydroxynaphthalene-2,7-disulfonic
acid >
>
>
>
>
>
6-hydroxynaphthalene-2-sulfonic acid >
>
>
>
>
>
>
>
7-hydroxynaphthalene-1,3-6- >
>
>
;
trisulfonic acid

E 127 ERYTHROSINE
Definition Erythrosine consists essentially of disodium 2-(2,4,5,7-tetraiodo-3-

oxido-6-oxoxanthen-9-yl) benzoate monohydrate and subsidiary
colouring matters together with water, sodium chloride and/or
sodium sulphate as the principal uncoloured components.
Erythrosine is manufactured by iodination of fluorescein, the
condensation product of resorcinol and phthalic anhydride
Erythrosine is described as the sodium salt. The calcium and the
Einecs 240-474-8
Chemical name Disodium 2-(2,4,5,7-tetraiodo-3-oxido-6-oxoxanthen-9-yl)benzoate

monohydrate
Chemical formula C20H6I4Na2O5 H2O

02012R0231 — EN — 27.10.2024 — 033.001 — 15
▼B
anhydrous sodium salt
E1%
1cm 1 100 at ca. 526 nm in aqueous solution at pH 7
Description Red powder or granules.
Identification
Spectrometry Maximum in water at ca. 526 nm at pH 7
Purity
Inorganic iodides Not more than 0,1 % (calculated as sodium iodide)
Subsidiary colouring matters (except Not more than 4,0 %

fluorescein)
Fluorescein Not more than 20 mg/kg

matters:
Tri-iodoresorcinol Not more than 0,2 %
2-(2,4-dihydroxy-3,5-diiodobenzoyl) Not more than 0,2 %

benzoic acid
Ether extractable matter From a solution of pH from 7 through 8, not more than 0,2 %
Aluminium Lakes of this colour may be used.

E 129 ALLURA RED AC
Definition Allura Red AC consists essentially of disodium 2-hydroxy-1-(2-

methoxy-5-methyl-4-sulfonato-phenylazo) naphthalene-6-sulfonate
and subsidiary colouring matters together with sodium chloride
and/or sodium sulphate as the principal uncoloured components.
Allura Red AC is manufactured by coupling diazotized 5-amino-4-
methoxy-2-toluenesulphonic acid with 6-hydroxy-2-naphthalene
sulphonic acid
Allura Red AC is described as the sodium salt. The calcium and the
Einecs 247-368-0
Chemical name Disodium 2-hydroxy-1-(2-methoxy-5-methyl-4-sulfonatophenylazo)

naphthalene-6-sulfonate

02012R0231 — EN — 27.10.2024 — 033.001 — 16
▼B
sodium salt
E1%
Description Dark red powder or granules
Identification
Purity

matters:
6-hydroxy-2-naphthalene sulfonic Not more than 0,3 %

acid, sodium salt
4-amino-5-methoxy-2-methyl Not more than 0,2 %

benezene sulfonic acid
6,6-oxybis (2-naphthalene sulfonic Not more than 1,0 %

acid) disodium salt
Ether extractable matter From a solution of pH 7, not more than 0,2 %
E 131 PATENT BLUE V
Synonyms CI Food Blue 5
Definition Patent Blue V consists essentially of the calcium or sodium compound of

[4-(α-(4-diethylaminophenyl)-5-hydroxy-2,4-disulfophenyl-methylidene)
2,5-cyclohexadien-1-ylidene] diethylammonium hydroxide inner salt and
subsidiary colouring matters together with sodium chloride and/or sodium
sulphate and/or calcium sulphate as the principal uncoloured components.
The potassium salt is also permitted.
Einecs 222-573-8
Chemical name The calcium or sodium compound of [4-(α-(4-diethylaminophenyl)-5-

hydroxy-2,4-disulfophenyl-methylidene) 2,5-cyclohexadien-1-ylidene]
diethyl-ammonium hydroxide inner salt
02012R0231 — EN — 27.10.2024 — 033.001 — 17
▼B
Chemical formula Calcium compound: C27H31N2O7S2Ca1/2

Sodium compound: C27H31N2O7S2Na
Molecular weight Calcium compound: 579,72

Sodium compound: 582,67
sodium salt
E1%
Description Dark blue powder or granules
Appearance of the aqueous solution Blue
Identification
Spectrometry Maximum in water at 638 nm at pH 5
Purity

matters:
9
3-hydroxy benzaldehyde >
>
>
>
>
>
>
>
3-hydroxy benzoic acid >
>
=
3-hydroxy-4-sulfobenzoic acid >
>
>
>
>
>
>
>
N,N-diethylamino benzene sulfonic >
>
;
acid
Leuco base Not more than 4,0 %
Ether extractable matter From a solution of pH 5 not more than 0,2 %
E 132 INDIGOTINE, INDIGO CARMINE
Definition Indigotine consists essentially of a mixture of disodium 3,3′dioxo-

2,2′-bi-indolylidene-5,5′-disulfonate, and disodium 3,3′-dioxo-2,2′-bi-
indolylidene-5,7′-disulfonate and subsidiary colouring matters
together with sodium chloride and/or sodium sulphate as the
principal uncoloured components.
Indigotine is described as the sodium salt. The calcium and the
Indigo carmine is obtained by sulphonation of indigo. This is accom
plished by heating indigo (or indigo paste) in the presence of
sulphuric acid. The dye is isolated and subjected to purification
procedures.
02012R0231 — EN — 27.10.2024 — 033.001 — 18
▼B
Einecs 212-728-8
Chemical name Disodium 3,3′-dioxo-2,2′-bi-indolylidene-5,5′-disulfonate
sodium salt;
disodium 3,3′-dioxo-2,2′-bi-indolylidene-5,7′-disulfonate: not more
than 18 %
E1%
Description Dark-blue powder or granules
Identification
Purity
Subsidiary colouring matters Excluding disodium 3,3′-dioxo-2,2′-bi-indolylidene-5,7′-disulfonate:

not more than 1,0 %

matters:
9
Isatin-5-sulfonic acid >
>
>
=
5-sulfoanthranilic acid Total not more than 0,5 %
>
>
>
;
Anthranilic acid

E 133 BRILLIANT BLUE FCF
Definition Brilliant Blue FCF consists essentially of disodium α-(4-(N-ethyl-3-

sulfonatobenzylamino) phenyl)-α-(4-N-ethyl-3-sulfonatobenzylamino)
cyclohexa-2,5-dienylidene) toluene-2-sulfonate and its isomers and
subsidiary colouring matters together with sodium chloride and/or
sodium sulphate as the principal uncoloured components.
Brilliant Blue FCF is described as the sodium salt. The calcium and the
Einecs 223-339-8
02012R0231 — EN — 27.10.2024 — 033.001 — 19
▼B
Chemical name Disodium α-(4-(N-ethyl-3-sulfonatobenzylamino) phenyl)-α-(4-N-

ethyl-3-sulfonatobenzylamino) cyclohexa-2,5-dienylidene) toluene-2-
sulfonate
sodium salt
E1%
1cm 1 630 at ca. 630 nm in aqueous solution
Description Reddish-blue powder or granules
Identification
Purity

matters:
Sum of 2-, 3- and 4-formyl benzene Not more than 1,5 %

sulfonic acids
3-((ethyl)(4-sulfophenyl) amino) Not more than 0,3 %

methyl benzene sulfonic acid
Ether extractable matter Not more than 0,2 % at pH 7
E 140 (i) CHLOROPHYLLS
Synonyms CI Natural Green 3; Magnesium Chlorophyll; Magnesium Phaeo

phytin
Definition Chlorophylls are obtained by solvent extraction of strains of edible

plant material, grass, lucerne and nettle. During the subsequent
removal of solvent, the naturally present coordinated magnesium
may be wholly or partly removed from the chlorophylls to give the
corresponding phaeophytins. The principal colouring matters are the
phaeophytins and magnesium chlorophylls. The extracted product,
from which the solvent has been removed, contains other pigments
such as carotenoids as well as oils, fats and waxes derived from the
source material. Only the following solvents may be used for the
extraction: acetone, methyl ethyl ketone, dichloromethane, carbon
dioxide, methanol, ethanol, propan-2-ol and hexane.
02012R0231 — EN — 27.10.2024 — 033.001 — 20
▼B
Einecs Chlorophylls: 215-800-7, chlorophyll a: 207-536-6, Chlorophyll b:

208-272-4
Chemical name The major colouring principles are:

Phytyl (132R,17S,18S)-3-(8-ethyl-132-methoxycarbonyl-2,7,12,18-
tetramethyl-13′-oxo-3-vinyl-131-132-17,18-tetrahydrocyclopenta
[at]-porphyrin-17-yl)propionate, (Phaeophytin a), or as the
magnesium complex (Chlorophyll a)
Phytyl (132R,17S,18S)-3-(8-ethyl-7-formyl-132-methoxycarbonyl-
2,12,18-trimethyl-13′-oxo-3-vinyl-131-132-17,18-tetrahydro
cyclopenta[at]-porphyrin-17-yl)propionate, (Pheophytin b), or as the
magnesium complex (Chlorophyll b)
Chemical formula Chlorophyll a (magnesium complex): C55H72MgN4O5

Chlorophyll a: C55H74N4O5
Chlorophyll b (magnesium complex): C55H70MgN4O6
Chlorophyll b: C55H72N4O6
Molecular weight Chlorophyll a (magnesium complex): 893,51

Chlorophyll a: 871,22
Chlorophyll b (magnesium complex): 907,49
Chlorophyll b: 885,20
Assay Content of total combined Chlorophylls and their magnesium

complexes is not less than 10 %
E1%
1cm 700 at ca. 409 nm in chloroform
Description Waxy solid ranging in colour from olive green to dark green
depending on the content of coordinated magnesium
Identification
Spectrometry Maximum in chloroform at ca. 409 nm
Purity
9
Solvent residues Acetone >
>
>
>
>
>
>
>
Methyl Ethyl ketone >
>
>
>
>
>
>
>
>
>
Methanol >
=
Not more than 50 mg/kg,
>
> singly or in combination
Ethanol >
>
>
>
>
>
>
>
>
>
Propan-2-ol >
>
>
>
>
>
>
;
Hexane
Dichloromethane: Not more than 10 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 21
▼B
E 140 (ii) CHLOROPHYLLINS
Synonyms CI Natural Green 5; Sodium Chlorophyllin; Potassium Chloro

phyllin
Definition The alkali salts of chlorophyllins are obtained by the saponification
of a solvent extract of strains of edible plant material, grass, lucerne
and nettle. The saponification removes the methyl and phytol ester
groups and may partially cleave the cyclopentenyl ring. The acid
groups are neutralised to form the salts of potassium and/or sodium.
Only the following solvents may be used for the extraction:
acetone, methyl ethyl ketone, dichloromethane, carbon dioxide,
methanol, ethanol, propan-2-ol and hexane.
Einecs 287-483-3
Chemical name The major colouring principles in their acid forms are:
— 3-(10-carboxylato-4-ethyl-1,3,5,8-tetramethyl-9-oxo-2-vinyl
phorbin-7-yl)propionate (chlorophyllin a)
and
— 3-(10-carboxylato-4-ethyl-3-formyl-1,5,8-trimethyl-9-oxo-2-
vinylphorbin-7-yl)propionate (chlorophyllin b)
Depending on the degree of hydrolysis the cyclopentenyl ring may
be cleaved with the resultant production of a third carboxyl
function.
Magnesium complexes may also be present.
Chemical formula Chlorophyllin a (acid form): C34H34N4O5
Chlorophyllin b (acid form): C34H32N4O6
Molecular weight Chlorophyllin a: 578,68
Chlorophyllin b: 592,66
Each may be increased by 18 daltons if the cyclopentenyl ring is
cleaved.
Assay Content of total chlorophyllins is not less than 95 % of the sample
dried at ca. 100 °C for 1 hour.
E1%
E1%
Description Dark green to blue/black powder

Identification
Spectrometry Maximum in aqueous phosphate buffer at pH 9 at ca. 405 nm and
at ca. 653 nm
Purity
9
>
>
>
>
Methyl ethyl ketone >
>
>
>
>
>
Methanol >
=
Not more than 50 mg/kg, singly or in
Ethanol > combination
>
>
>
>
>
>
Propan-2-ol >
>
>
>
>
;
Hexane
02012R0231 — EN — 27.10.2024 — 033.001 — 22
▼B
E 141 (i) COPPER COMPLEXES OF CHLOROPHYLLS
Synonyms CI Natural Green 3; Copper Chlorophyll; Copper Phaeophytin
Definition Copper chlorophylls are obtained by addition of a salt of copper to

the substance obtained by solvent extraction of strains of edible
plant material, grass, lucerne, and nettle. The product, from
which the solvent has been removed, contains other pigments
such as carotenoids as well as fats and waxes derived from the
source material. The principal colouring matters are the copper
phaeophytins. Only the following solvents may be used for the
extraction: acetone, methyl ethyl ketone, dichloromethane, carbon
dioxide, methanol, ethanol, propan-2-ol and hexane.
Einecs Copper chlorophyll a: 239-830-5; copper chlorophyll b: 246-020-5
Chemical name [Phytyl (132R,17S,18S)-3-(8-ethyl-132-methoxycarbonyl-2,7,12,18-

tetramethyl-13′-oxo-3-vinyl-131-132-17,18-tetrahydrocyclopenta[at]-
porphyrin-17-yl)propionate] copper (II) (Copper Chlorophyll a)
[Phytyl (132R,17S,18S)-3-(8-ethyl-7-formyl-132-methoxycarbonyl-
2,12,18-trimethyl-13′-oxo-3-vinyl-131-132-17,18-tetrahydro
cyclopenta[at]-porphyrin-17-yl)propionate] copper (II) (Copper
chlorophyll b)
Chemical formula Copper chlorophyll a: C55H72Cu N4O5

Copper chlorophyll b: C55H70Cu N4O6
Molecular weight Copper chlorophyll a: 932,75

Copper chlorophyll b: 946,73
Assay Content of total copper chlorophylls is not less than 10 %.

E1%
E1%
Description Waxy solid ranging in colour from blue green to dark green
depending on the source material
Identification
Spectrometry Maximum in chloroform at ca. 422 nm and at ca. 652 nm
Purity
9
>
>
>
>
>
>
>
>
>
>
>
>
>
>
Methanol >
=
>
Ethanol >
>
>
>
>
>
>
>
>
Propan-2-ol >
>
>
>
>
>
;
Hexane

02012R0231 — EN — 27.10.2024 — 033.001 — 23
▼B
Copper ions Not more than 200 mg/kg
Total copper Not more than 8,0 % of the total copper phaeophytins
E 141 (ii) COPPER COMPLEXES OF CHLOROPHYLLINS
Synonyms Sodium Copper Chlorophyllin; Potassium Copper Chlorophyllin; CI

Natural Green 5
Definition The alkali salts of copper chlorophyllins are obtained by the

addition of copper to the product obtained by the saponification
of a solvent extraction of strains of edible plant material, grass,
lucerne, and nettle; the saponification removes the methyl and
phytol ester groups and may partially cleave the cyclopentenyl
ring. After addition of copper to the purified chlorophyllins, the
acid groups are neutralised to form the salts of potassium and/or
sodium.
acetone, methyl ethyl ketone, dichloromethane, carbon dioxide
methanol, ethanol, propan-2-ol and hexane.
Einecs
Chemical name The major colouring principles in their acid forms are 3-(10-
Carboxylato-4-ethyl-1,3,5,8-tetramethyl-9-oxo-2-vinylphorbin-7-
yl)propionate, copper complex (Copper chlorophyllin a) and 3-(10-
Carboxylato-4-ethyl-3-formyl-1,5,8-trimethyl-9-oxo-2-vinylphorbin-
7-yl) propionate, copper complex (Copper chlorophyllin b)
Chemical formula Copper chlorophyllin a (acid form): C34H32Cu N4O5

Copper chlorophyllin b (acid form): C34H30Cu N4O6
Molecular weight Copper chlorophyllin a: 640,20

Copper chlorophyllin b: 654,18
Each may be increased by 18 daltons if the cyclopentenyl ring is
cleaved.
Assay Content of total copper chlorophyllins is not less than 95 % of the

sample dried at 100 °C for 1 h.
E1%
1cm 565 at ca. 405 nm in aqueous phosphate buffer at pH 7,5
E1%
1cm 145 at ca. 630 nm in aqueous phosphate buffer at pH 7,5
Description Dark green to blue/black powder
Identification
Spectrometry Maximum in aqueous phosphate buffer at pH 7,5 at ca. 405 nm and

at 630 nm
Purity
9
>
>
>
>
>
>
>
>
>
>
>
>
>
>
Methanol =
>
Ethanol >
>
>
>
>
>
>
>
Propan-2-ol >
>
>
>
>
>
;
Hexane
02012R0231 — EN — 27.10.2024 — 033.001 — 24
▼B
Copper ions Not more than 200 mg/kg
Total copper Not more than 8,0 % of the total copper chlorophyllins

E 142 GREEN S
Synonyms CI Food Green 4, Brilliant Green BS
Definition Green S consists essentially of sodium N-[4-[[4-(dimethylamino)phenyl]

2-hydroxy-3,6-disulfo-1-naphthalenyl)methylene]-2,5-cyclohexadien-1-
ylidene]-N-methylmethanaminium and subsidiary colouring matters
together with sodium chloride and/or sodium sulphate as the principal
uncoloured compounds.
Green S is described as the sodium salt. The calcium and the potassium
salt are also permitted.
Einecs 221-409-2
Chemical name Sodium N-[4-[[4-(dimethylamino)phenyl](2-hydroxy-3,6-disulfo-1-naph

thalenyl)-methylene]2,5-cyclohexadien-1-ylidene]-N-methylmethana
minium; Sodium 5-[4-dimethylamino-α-(4-dimethyliminocyclohexa-2,5-
dienylidene) benzyl]-6-hydroxy-7-sulfonato-naphthalene-2-sulfonate (alter
native chemical name).
Chemical formula C27H25N2NaO7S2
sodium salt
E1%
1cm 1 720 at ca. 632 nm in aqueous solution
Description Dark blue or dark green powder or granules
Appearance of the aqueous solution Blue or green
Identification
Purity

matters:
4,4′-bis(dimethylamino)-benzhydryl Not more than 0,1 %

alcohol
4,4′-bis(dimethylamino)-benzop Not more than 0,1 %

henone
3-hydroxynaphthalene-2,7-disulfonic Not more than 0,2 %

acid
02012R0231 — EN — 27.10.2024 — 033.001 — 25
▼B
E 150a PLAIN CARAMEL
Synonyms Caustic caramel
Definition Plain caramel is prepared by the controlled heat treatment of carbo

hydrates (commercially available food grade nutritive sweeteners
which are the monomers glucose and fructose and/or polymers
thereof, e.g. glucose syrups, sucrose, and/or invert syrups, and
dextrose). To promote caramelisation, acids, alkalis and salts may
be employed, with the exception of ammonium compounds and
sulphites.
Colour Index No
Einecs 232-435-9
Chemical name
Chemical formula
Molecular weight
Assay
Description Dark brown to black liquids or solids
Identification
Purity
Colour bound by DEAE cellulose Not more than 50 %
Colour bound by phosphoryl cellulose Not more than 50 %
Colour intensity (1) 0,01-0,12
Total nitrogen Not more than 0,1 %
Total sulphur Not more than 0,2 %
_____________
(1) Colour intensity is defined as the absorbance of a 0,1 % (w/v) solution of caramel colour solids in water in a 1 cm cell at 610 nm.
02012R0231 — EN — 27.10.2024 — 033.001 — 26
▼B
E 150b CAUSTIC SULPHITE CARAMEL
Synonyms
Definition Caustic sulphite caramel is prepared by the controlled heat treatment

of carbohydrates (commercially available food grade nutritive
sweeteners which are the monomers glucose and fructose and/or
polymers thereof, e.g. glucose syrups, sucrose, and/or invert
syrups, and dextrose) with or without acids or alkalis, in the
presence of sulphite compounds (sulphurous acid, potassium
sulphite, potassium bisulphite, sodium sulphite and sodium
bisulphite); no ammonium compounds are used.
Colour Index No
Einecs 232-435-9
Chemical name
Chemical formula
Molecular weight
Assay
Identification
Purity
Colour bound by DEAE cellulose More than 50 %
Total nitrogen Not more than 0,3 % (2)
Sulphur dioxide Not more than 0,2 % (2)
Total sulphur 0,3-3,5 % (2)
Sulphur bound by DEAE cellulose More than 40 %
Absorbance ratio of colour bound by 19-34

DEAE cellulose
Absorbance ratio (A280/560) Greater than 50
E 150c AMMONIA CARAMEL
Synonyms
Definition Ammonia caramel is prepared by the controlled heat treatment of

carbohydrates (commercially available food grade nutritive sweeteners
which are the monomers glucose and fructose and/or polymers thereof,
e.g. glucose syrups, sucrose, and/or invert syrups, and dextrose) with or
without acids or alkalis, in the presence of ammonium compounds
(ammonium hydroxide, ammonium carbonate, ammonium hydrogen
carbonate and ammonium phosphate); no sulphite compounds are
used.
_____________
(2) Expressed on equivalent colour basis i.e. is expressed in terms of a product having a colour intensity of 0,1 absorbance units.
02012R0231 — EN — 27.10.2024 — 033.001 — 27
▼B
Colour Index No
Einecs 232-435-9
Chemical name
Chemical formula
Molecular weight
Assay
Identification
Purity
Colour bound by DEAE cellulose Not more than 50 %
Colour bound by phosphoryl cellulose More than 50 %
Ammoniacal nitrogen Not more than 0,3 % (2)
4-methylimidazole Not more than 200 mg/kg (2)
2-acetyl-4-tetrahydroxy-butylimidazole Not more than 10 mg/kg (2)
Total sulphur Not more than 0,2 % (2)
Total nitrogen 0,7-3,3 % (2)
Absorbance ratio of colour bound by 13-35

phosphoryl cellulose
E 150d SULPHITE AMMONIA CARAMEL
Synonyms
Definition Sulphite ammonia caramel is prepared by the controlled heat

treatment of carbohydrates (commercially available food grade
nutritive sweeteners which are the monomers glucose and fructose
and/or polymers thereof (e.g. glucose syrups, sucrose, and/or invert
syrups, and dextrose) with or without acids or alkalis in the presence
of both sulphite and ammonium compounds (sulphurous acid,
potassium sulphite, potassium bisulphite, sodium sulphite, sodium
bisulphite, ammonium hydroxide, ammonium carbonate,
ammonium hydrogen carbonate, ammonium phosphate, ammonium
sulphate, ammonium sulphite and ammonium hydrogen sulphite).
Colour Index No
Einecs 232-435-9
Chemical name
Chemical formula
_____________
02012R0231 — EN — 27.10.2024 — 033.001 — 28
▼B
Molecular weight
Assay
Identification
Purity
Colour bound by DEAE cellulose More than 50 %
Ammoniacal nitrogen Not more than 0,6 % (2)
Sulphur dioxide Not more than 0,2 % (2)
4-methylimidazole Not more than 250 mg/kg (2)
Total nitrogen 0,3-1,7 % (2)
Total sulphur 0,8-2,5 % (2)
Nitrogen/sulphur ratio of alcohol 0,7-2,7

precipitate
Absorbance ratio of alcohol precipitate (3) 8-14
Absorbance ratio (A280/560) Not more than 50
▼M8
E 151 BRILLIANT BLACK PN
▼B
Synonyms CI Food Black 1
▼M8
Definition Brilliant Black PN consists essentially of tetrasodium-4-acetamido-5-
hydroxy-6-[7-sulfonato-4-(4-sulfonatophenylazo)-1-naphthylazo]
naphthalene-1,7-disulfonate and subsidiary colouring matters
together with sodium chloride and/or sodium sulphate as the
principal uncoloured components.
Brilliant Black PN is described as the sodium salt.
The calcium and the potassium salt are also permitted.
▼B
Einecs 219-746-5
Chemical name Tetrasodium 4-acetamido-5-hydroxy-6-[7-sulfonato-4-(4-sulfonatop

henylazo)-1-naphthylazo] naphthalene-1,7-disulfonate
_____________
(3) Absorbance ratio of alcohol precipitate is defined as the absorbance of the precipitate at 280 nm divided by the absorbance at
560 nm (1 cm cell).
02012R0231 — EN — 27.10.2024 — 033.001 — 29
▼B
sodium salt
E1%
1cm 530 at ca. 570 nm in solution
Description Black powder or granules
Appearance of the aqueous solution Black-bluish
Identification
Purity
Subsidiary colouring matters Not more than 4 % (expressed on the dye content)

matters:
9
4-acetamido-5-hydroxynaphthalene- >
>
>
>
1,7-disulfonic acid >
>
>
>
>
>
>
>
4-amino-5-hydroxynaphthalene-1,7- >
>
>
>
disulfonic acid >
=
>
>
8-aminonaphthalene-2-sulfonic acid- >
>
>
>
>
>
>
>
>
>
>
>
>
4,4′-diazoaminodi-(benzenesulfonic >
>
;
acid)
E 153 VEGETABLE CARBON
Synonyms Vegetable black
Definition Vegetable activated carbon is produced by the carbonisation of

vegetable material such as wood, cellulose residues, peat and
coconut and other shells. The activated carbon thus produced is
milled by a roller mill and the resulting highly activated powdered
carbon is treated by a cyclone. The fine fractio40800n from the
cyclone is purified by hydrochloric acid washing, neutralised and
then dried. The resulting product is what is known traditionally as
vegetable black. Products with a higher colouring power are
produced from the fine fraction by a further cyclone treatment or
by extra milling, followed by acid washing, neutralising and drying.
It consists essentially of finely divided carbon. It may contain minor
amounts of nitrogen, hydrogen and oxygen. Some moisture may be
absorbed on the product after manufacture.
02012R0231 — EN — 27.10.2024 — 033.001 — 30
▼B
Einecs 231-153-3
Chemical name Carbon
Chemical formula C
Atomic weight 12,01
Assay Content not less than 95 % of carbon calculated on an anhydrous

and ash-free basis
Loss on drying Not more than 12 % (120 °C 4 h)
Description Black, odourless powder
Identification
Solubility Insoluble in water and organic solvents
Burning When heated to redness it burns slowly without a flame
Purity
Ash (Total) Not more than 4,0 % (ignition temperature: 625 °C)
Polycyclic aromatic hydrocarbons Benzo(a)pyrene less than 50 μg/kg in the extract obtained by
extraction of 1 g of the product with 10 g pure cyclohexane in a
continuous extraction.
Alkali soluble matter The filtrate obtained by boiling 2 g of the sample with 20 ml N
sodium hydroxide and filtering shall be colourless
E 155 BROWN HT
Synonyms CI Food Brown 3
Definition Brown HT consists essentially of disodium 4,4′-(2,4-dihydroxy-5-

hydroxymethyl-1,3-phenylene bisazo) di (naphthalene-1-sulfonate)
and subsidiary colouring matters together with sodium chloride
and/or sulphate as the principal uncoloured components.
Brown HT is described as the sodium salt. The calcium and
Einecs 224-924-0
Chemical name Disodium 4,4′-(2,4-dihydroxy-5-hydroxymethyl-1,3-phenylene bisazo)di

(naphthalene-1-sulfonate)
sodium salt.
E1%
Description Reddish-brown powder or granules
Appearance of the aqueous solution Brown

02012R0231 — EN — 27.10.2024 — 033.001 — 31
▼B
Identification
Spectrometry Maximum in water of pH 7 at ca. 460 nm
Purity
Subsidiary colouring matters Not more than 10 % (TLC method)

matters:
4-aminonaphthalene- 1-sulfonic acid Not more than 0,7 %
Unsulfonated primary aromatic Not more than 0,01 % (calculated as aniline)

amines
Ether extractable matter Not more than 0,2 % in a solution of pH 7
E 160 a (i) BETA-CAROTENE
Synonyms CI Food Orange 5
Definition These specifications apply predominantly to all trans isomer of

beta-carotene together with minor amounts of other carotenoids.
Diluted and stabilised preparations may have different trans-cis
isomer ratios.
Einecs 230-636-6
Chemical name Beta-carotene; beta, beta-carotene
Chemical formula C40H56
Assay Not less than 96 % total colouring matters (expressed as beta-carotene)

E1%
1cm 2 500 at approximately by 440 nm to 457 nm in cyclohexane
Description Red to brownish-red crystals or crystalline powder
Identification
Spectrometry Maximum in cyclohexane at 453 nm to 456 nm
Purity
Subsidiary colouring matters Carotenoids other than beta-carotene: not more than 3,0 % of total
colouring matters

02012R0231 — EN — 27.10.2024 — 033.001 — 32
▼B
E 160 a (ii) PLANT CAROTENES
Definition Plant carotenes are obtained by solvent extraction of strains of

edible plants, carrots, vegetable oils, grass, alfalfa (lucerne) and
nettle.
The main colouring principle consists of carotenoids of which
beta-carotene accounts for the major part. Alpha, gamma-carotene
and other pigments may be present. Besides the colour pigments,
this substance may contain oils, fats and waxes naturally occurring
in the source material.
Only the following solvents may be used in the extraction: acetone,
methyl ethyl ketone, methanol, ethanol, propan-2-ol, hexane (1),
dichloromethane and carbon dioxide.
Einecs 230-636-6
Chemical name
Chemical formula Beta-carotene: C40H56
Molecular weight Beta-carotene: 536,88
Assay Content of carotenes (calculated as beta-carotene) is not less than

5 %. For products obtained by extraction of vegetables oils: not less
than 0,2 % in edible fats
E1%
1cm 2 500 at approximately 440 nm to 457 nm in cyclohexane
Description
Identification
Spectrometry Maximum in cyclohexane at 440 nm to 457 nm and 470 nm to

486 nm
Purity
9
>
>
>
>
>
>
>
>
>
>
>
>
Methanol =
Propan-2-ol >
>
>
>
>
>
Hexane >
>
>
>
>
>
>
;
Ethanol
Dichloromethane Not more than 10 mg/kg
E 160 a (iii) BETA-CAROTENE FROM Blakeslea trispora
Definition Obtained by a fermentation process using a mixed culture of the

two sexual mating types (+) and (–) of strains of the fungus
Blakeslea trispora. The beta-carotene is extracted from the
biomass with ethyl acetate or isobutyl acetate followed by
propan-2-ol and crystallised. The crystallised product consists
mainly of trans beta-carotene. Because of the natural process
approximately 3 % of the product consists of mixed carotenoids,
which is specific for the product.
_____________
(1) Benzene not more than 0,05 % v/v.
02012R0231 — EN — 27.10.2024 — 033.001 — 33
▼B
Einecs 230-636-6
Chemical name Beta-carotene; beta, beta-carotene
Assay Not less than 96 % total colouring matters (expressed as beta-carotene)

E1%
1cm 2 500 at approximately 440 nm to 457 nm in cyclohexane
Description Red, brownish-red or purple-violet crystals or crystalline powder

(colour varies according to extraction solvent used and conditions
of crystallisation)
Identification
Spectrometry Maximum in cyclohexane at 453 nm to 456 nm
Purity
9
Solvent residues Ethyl acetate =
Not more than 0,8 %, singly
Ethanol ; or in combination
Isobutyl acetate: Not more than 1,0 %
Propan-2-ol: Not more than 0,1 %
Subsidiary colouring matters Carotenoids other than beta-carotene: not more than 3,0 % of total
colouring matters
Moulds Not more than 100 colonies per gram
Yeasts Not more than 100 colonies per gram
Escherichia coli Absent in 5 g
E 160 a (iv) ALGAL CAROTENES
▼M8
Definition Mixed carotenes may also be produced from strains of the algae
Dunaliella salina. Beta-carotene is extracted using an essential oil.
The preparation is a 20 to 30 % suspension in edible oil. The ratio
of trans-cis isomers is in the range of 50/50 to 71/29.
The main colouring principle consists of carotenoids of which beta-
carotene accounts for the major part. Alpha-carotene, lutein, zeax
anthin and beta-cryptoxanthin may be present. Besides the colour
pigments, this substance may contain oils, fats and waxes naturally
occurring in the source material.
▼B
Einecs
Chemical name
Chemical formula Beta-Carotene: C40H56
Molecular weight Beta-Carotene: 536,88

02012R0231 — EN — 27.10.2024 — 033.001 — 34
▼B
Assay Content of carotenes (calculated as beta-carotene) is not less than
20 %
E1%
1cm 2 500 at approximately by 440 nm to 457 nm in cyclohexane
Description
Identification
Spectrometry Maximum in cyclohexane at 440 nm to 457 nm and 474 nm to

486 nm
Purity
Natural tocopherols in edible oil Not more than 0,3 %
▼M32
E 160 b (i) ANNATTO BIXIN
(I) SOLVENT-EXTRACTED BIXIN
Synonyms Annatto B, Orlean, Terre orellana, L. Orange, CI Natural Orange 4
Definition Solvent-extracted bixin is obtained by the extraction of the outer

coating of the seeds of the annatto tree (Bixa orellana L.) with one
or more of the following food grade solvents: acetone, methanol,
hexane, ethanol, isopropyl alcohol, ethyl acetate, alkaline alcohol or
supercritical carbon dioxide. The resulting preparation may be
acidified, followed by the removal of the solvent, drying and
milling.
Solvent-extracted bixin contains several coloured components; the
major colouring principle is cis-bixin, a minor colouring principle is
trans-bixin; thermal degradation products of bixin may also be
present as a result of processing.
Einecs 230-248-7
Chemical name cis-Bixin: Methyl (9-cis)-hydrogen-6,6'-diapo-Ψ,Ψ-carotenedioate
Chemical formula cis-Bixin: C25H30O4
Assay Not less than 85 % colouring matter (expressed as bixin)

E1 % 1cm 3090 at ca. 487 nm in tetrahydrofuran and acetone
Description Dark red-brown to red-purple powder
Identification
Solubility Insoluble in water, slightly soluble in ethanol
Spectrometry The sample in acetone shows absorbance maxima at about 425, 457
and 487 nm
Purity
Norbixin Not more than 5 % of total colouring matters
Residual Solvents Acetone: Not more than 30 mg/kg

Hexane: Not more than 25 mg/kg
Ethanol:
Isopropyl alcohol: not more than 50 mg/kg,
singly or in combination
Ethyl acetate:

02012R0231 — EN — 27.10.2024 — 033.001 — 35
▼M32
(II) AQUEOUS-PROCESSED BIXIN
Synonyms Annatto E, Orlean, Terre orellana, L. Orange, CI Natural Orange 4
Definition Aqueous-processed bixin is prepared by the extraction of the outer

coating of the seeds of the annatto tree (Bixa orellana L.) by
abrading the seeds in the presence of cold, mildly-alkaline water.
The resultant preparation is acidified to precipitate bixin which is
then filtered, dried and milled.
Aqueous-processed bixin contains several coloured components; the
major colouring principle is cis-bixin, a minor colouring principle is
trans-bixin; thermal degradation products of bixin may also be
present as a result of processing.
Einecs 230-248-7
Chemical name cis-Bixin: Methyl (9-cis)-hydrogen-6,6'-diapo-Ψ,Ψ-carotenedioate
Chemical formula cis-Bixin: C25H30O4
Assay Not less than 25 % colouring matter (expressed as bixin)

E1 % 1cm 3090 at ca. 487 nm in tetrahydrofuran and acetone
Identification
Solubility Insoluble in water, slightly soluble in ethanol
Spectrometry The sample in acetone shows absorbance maxima at about 425, 457
and 487 nm
Purity
Norbixin Not more than 7 % of total colouring matters
E 160 b (ii) ANNATTO NORBIXIN

(I) SOLVENT-EXTRACTED NORBIXIN
Synonyms Annatto C, Orlean, Terre orellana, L. Orange, CI Natural Orange 4
Definition Solvent-extracted norbixin is obtained from the outer coating of the

seeds of the annatto tree (Bixa orellana L.) by washing with one or
more of the following food grade solvents: acetone, methanol,
hexane, ethanol, isopropyl alcohol, ethyl acetate, alkaline alcohol
or supercritical carbon dioxide followed by solvent removal, crys
tallization and drying. Aqueous alkali is added to the resultant
powder, which is then heated to hydrolyse the colouring matter
and cooled. The aqueous solution is filtered, and acidified to
precipitate the norbixin. The precipitate is filtered, washed, dried
and milled, to give a granular powder.
02012R0231 — EN — 27.10.2024 — 033.001 — 36
▼M32
Solvent-extracted norbixin contains several coloured components;

the major colouring principle is cis-norbixin, a minor colouring
principle is trans-norbixin; thermal degradation products of
norbixin may also be present as a result of processing.
Einecs 208-810-8
Chemical name cis-Norbixin: 6,6'-Diapo-Ψ,Ψ-carotenedioic acid

cis-Norbixin dipotassium salt: Dipotassium 6,6'-diapo-Ψ,Ψ-caro
tenedioate
cis-Norbixin disodium salt: Disodium 6,6'-diapo-Ψ,Ψ-carotene
dioate
Chemical formula cis-Norbixin: C24H28O4

cis-Norbixin dipotassium salt: C24H26K2O4
cis-Norbixin disodium salt: C24H26Na2O4
Molecular weight 380,5 (acid), 456,7 (dipotassium salt), 424,5 (disodium salt)
Assay Not less than 85 % colouring matter (expressed as norbixin)

E1 % 1cm 2870 at ca. 482 nm in 0,5 % potassium hydroxide solution
Identification
Solubility Soluble in alkaline water, slightly soluble in ethanol
Spectrometry The sample in 0,5 % potassium hydroxide solution shows

absorbance maxima at about 453 nm and 482 nm
Purity
Residual Solvents Acetone: Not more than 30 mg/kg

Hexane: Not more than 25 mg/kg
Ethanol:
Isopropyl alcohol: not more than 50 mg/kg,
singly or in combination
Ethyl acetate:
(II) ALKALI-PROCESSED NORBIXIN, ACID-PRECIPITATED
Synonyms Annatto F, Orlean, Terre orellana, L. Orange, CI Natural Orange 4
Definition Alkali-processed norbixin (acid-precipitated) is prepared by the

extraction of the outer coating of the seeds of the annatto tree
(Bixa orellana L.) with aqueous alkali. The bixin is hydrolysed to
norbixin in hot alkaline solution and is acidified to precipitate the
norbixin. The precipitate is filtered, dried and milled to give a
granular powder.
Alkali-processed norbixin contains several coloured components; the
major colouring principle is cis-norbixin, a minor colouring principle
is trans-norbixin; thermal degradation products of norbixin may also
be present as a result of processing.

02012R0231 — EN — 27.10.2024 — 033.001 — 37
▼M32
Einecs 208-810-8

cis-Norbixin dipotassium salt: Dipotassium 6,6'-diapo-Ψ,Ψ-carotene
dioate
cis-Norbixin disodium salt: Disodium 6,6'-diapo-Ψ,Ψ-carotenedioate


Identification

Purity
(III) ALKALI-PROCESSED NORBIXIN, NOT ACID-PRECIPITATED
Synonyms Annatto G, Orlean, Terre orellana, L. Orange, CI Natural Orange 4
Definition Alkali-processed norbixin (not acid-precipitated) is prepared by the

extraction of the outer coating of the seeds of the annatto tree (Bixa
orellana L.) with aqueous alkali. The bixin is hydrolysed to norbixin
in hot alkaline solution. The precipitate is filtered, dried and milled
to give a granular powder. Extracts contain mainly the potassium or
sodium salt of norbixin as the major colouring matter.
Alkali-processed norbixin (not acid-precipitated) contains several
coloured components; the major colouring principle is cis-norbixin,
a minor colouring principle is trans-norbixin; thermal degradation
products of norbixin may also be present as a result of processing.
Einecs 208-810-8

cis-Norbixin dipotassium salt: Dipotassium 6,6'-diapo-Ψ,Ψ-carotene
dioate
cis-Norbixin disodium salt: Disodium 6,6'-diapo-Ψ,Ψ-carotenedioate

02012R0231 — EN — 27.10.2024 — 033.001 — 38
▼M32

Identification

Purity
▼B
E 160 c PAPRIKA EXTRACT, CAPSANTHIN, CAPSORUBIN
Synonyms Paprika Oleoresin
Definition Paprika extract is obtained by solvent extraction of the strains of

paprika, which consists of the ground fruits pods, with or without
seeds, of Capsicum annuum L., and contains the major colouring
principles of this spice. The major colouring principles are caps
anthin and capsorubin. A wide variety of other coloured
compounds is known to be present.
Only the following solvents may be used in the extraction:
methanol, ethanol, acetone, hexane, dichloromethane, ethyl
acetate, propan-2-ol and carbon dioxide.
Colour Index No
Einecs Capsanthin: 207-364-1, capsorubin: 207-425-2
Chemical name Capsanthin: (3R, 3′S, 5′R)-3,3′-dihydroxy-β,κ-carotene-6-one

Capsorubin: (3S, 3′S, 5R, 5R′)-3,3′-dihydroxy-κ,κ-carotene-6,6′-
dione
Chemical formula Capsanthin: C40H56O3
Capsorubin: C40H56O4
Molecular weight Capsanthin: 584,85
Capsorubin: 600,85
Assay Paprika extract: content not less than 7,0 % carotenoids

Capsanthin/capsorubin: not less than 30 % of total carotenoids
E1%
1cm 2 100 at ca. 462 nm in acetone
02012R0231 — EN — 27.10.2024 — 033.001 — 39
▼B
Description Dark-red viscous liquid
Identification
Spectrometry Maximum in acetone at ca. 462 nm
Colour reaction A deep blue colour is produced by adding one drop of sulphuric
acid to one drop of sample in 2-3 drops of chloroform
Purity
9
Solvent residues Ethyl acetate >
>
>
>
>
>
>
>
Methanol >
>
>
>
>
>
>
>
Ethanol =
>
Acetone >
>
>
>
>
>
>
>
Hexane >
>
>
>
>
>
;
Propan-2-ol
Capsaicin Not more than 250 mg/kg
E 160 d LYCOPENE
(i) SYNTHETIC LYCOPENE
Synonyms Lycopene from chemical synthesis
Definition Synthetic lycopene is a mixture of geometric isomeres of lycopenes

and is produced by the Wittig condensation of synthetic inter
mediates commonly used in the production of other carotenoids
used in food. Synthetic lycopene consists predominantly of
all-trans-lycopene together with 5-cis-lycopene and minor quantities
of other isomers. Commercial lycopene preparations intended for use
in food are formulated as suspensions in edible oils or
water-dispersible or water-soluble powder.
Einecs 207-949-1
Chemical name ψ,ψ-carotene, all-trans-lycopene, (all-E)-lycopene, (all-E)-

2,6,10,14,19,23,27,31-octamethyl-2,6,8,10,12,14 ,16,18,20,22,24,26,
30-dotriacontatridecaene
Assay Not less than 96 % total lycopenes (not less than 70 % all-trans-
lycopene)
E1%
1cm at 465-475 nm in hexane (for 100 % pure all-trans-lycopene)
is 3 450
Description Red crystalline powder

02012R0231 — EN — 27.10.2024 — 033.001 — 40
▼B
Identification
Spectrophotometry A solution in hexane shows an absorption maximum at approxi

mately 470 nm
Test for carotenoids The colour of the solution of the sample in acetone disappears after
successive additions of a 5 % solution of sodium nitrite and 1N
sulphuric acid
Solubility Insoluble in water, freely soluble in chloroform
Properties of 1 % solution in chloroform Is clear and has intensive red-orange colour
Purity
Loss on drying Not more than 0,5 % (40 °C, 4 h at 20 mm Hg)
Apo-12’-lycopenal Not more than 0,15 %
Triphenyl phosphine oxide Not more than 0,01 %
Solvent residues Methanol not more than 200 mg/kg,

Hexane, Propan-2-ol: Not more than 10 mg/kg each.
Dichloromethane: Not more than 10 mg/kg (in commercial prep
arations only)
(ii) LYCOPENE FROM RED TOMATOES
Synonyms Natural Yellow 27
Definition Lycopene is obtained by solvent extraction of red tomatoes (Lyco

persicon esculentum L.) with subsequent removal of the solvent.
Only the following solvent may be used: carbon dioxide, ethyl
acetate, acetone, propan-2-ol, methanol, ethanol and hexane. The
major colouring principle of tomatoes is lycopene; minor amounts
of other carotenoid pigments may be present. Besides the colour
pigments the product may contain oil, fats, waxes and flavour
components naturally occurring in tomatoes.
Einecs 207-949-1
Chemical name Ψ,Ψ-carotene, all-trans-lycopene, (all-E)-lycopene, (all-E)-

2,6,10,14,19,23,27,31-octamethyl-2,6,8,10,12,14,16,18,2 0,22,24,26,
Assay E1%
is 3 450.
Content not less than 5 % total colouring matters
Description Dark red viscous liquid
Identification
Spectrophotometry Maximum in hexane at ca. 472 nm

02012R0231 — EN — 27.10.2024 — 033.001 — 41
▼B
Purity
9
Solvent residues Propan-2-ol >
>
>
>
>
>
Hexane >
>
>
>
>
>
>
>
>
>
Acetone =
>
Ethanol >
>
>
>
>
>
>
>
Methanol >
>
>
>
>
>
;
Ethylacetate
Sulphated ash Not more than 1 %
(iii) LYCOPENE FROM BLAKESLEA TRISPORA
Synonyms Natural Yellow 27
Definition Lycopene from Blakeslea trispora is extracted from the fungal

biomass and purified by crystallisation and filtration. It consists
predominantly of all-trans-lycopene. It also contains minor quantities
of other carotenoids. Propan-2-ol and isobutyl acetate are the only
solvents used in the manufacture. Commercial lycopene preparations
intended for use in food are formulated as suspensions in edible oils
or water-dispersible or water-soluble powder.
Einecs 207-949-1
Chemical name Ψ,Ψ-carotene, all-trans-lycopene, (all-E)-lycopene, ((all-E)-

2,6,10,14,19,23,27,31-octamethyl-2,6,8,10,12,14 ,16,18,20,22,24,26,
Assay Not less than 95 % total lycopenes and not less than 90 % all-trans-
lycopene of all colouring matters
E1%
is 3 450
Description Red crystalline powder
Identification
Spectrophotometry A solution in hexane shows an absorption maximum at approxi

mately 470 nm
Test of carotenoids The colour of the solution of the sample in acetone disappears after
successive additions of a 5 % solution of sodium nitrite and 1N
sulphuric acid
Solubility Insoluble in water, freely soluble in chloroform
Properties of 1 % solution in chloroform Is clear and has intensive red-orange colour

02012R0231 — EN — 27.10.2024 — 033.001 — 42
▼B
Purity
Loss on drying Not more than 0,5 % (40 °C, 4 h at 20 mm Hg)
Other carotenoids Not more than 5 %
Solvent residues Propan-2-ol: not more than 0,1 %

Isobutyl acetate: not more than 1,0 %
Dichloromethane: not more than 10 mg/kg (in commercial prep
arations only)
E 160 e BETA-APO-8′-CAROTENAL (C30)
Definition These specifications apply predominantly to the all-trans isomer of

β-apo-8′-carotenal together with minor amounts of other carotenoids.
Diluted and stabilised forms are prepared from β-apo-8′-carotenal
meeting these specifications and include solutions or suspensions
of ß-apo-8′carotenal in edible fats or oils, emulsions and water
dispersible powders. These preparations may have different cis/
trans isomer ratios.
Einecs 214-171-6
Chemical name β-Apo-8′-carotenal; trans-β-Apo-8′carotene-aldehyde
Chemical formula C30H40O
Assay Not less than 96 % of total colouring matters

E1%
1cm 2 640 at 460-462 nm in cyclohexane
Description Dark violet crystals with metallic lustre or crystalline powder
Identification
Spectrometry Maximum in cyclohexane at 460-462 nm
Purity
Subsidiary colouring matters Carotenoids other than β-apo-8′-carotenal:

not more than 3,0 % of total colouring matters
E 161 b LUTEIN
Synonyms Mixed Carotenoids; Xanthophylls
Definition Lutein is obtained by solvent extraction of the strains of edible

fruits and plants, grass, lucerne (alfalfa) and Tagetes erecta. The
main colouring principle consists of carotenoids of which lutein
02012R0231 — EN — 27.10.2024 — 033.001 — 43
▼B
and its fatty acid esters account for the major part. Variable
amounts of carotenes will also be present. Lutein may contain
fats, oils and waxes naturally occurring in the plant material.
methanol, ethanol, propan-2-ol, hexane, acetone, methyl ethyl
ketone and carbon dioxide
Colour Index No
Einecs 204-840-0
Chemical name 3,3′-dihydroxy-d-carotene
Chemical formula C40H56O2
Assay Content of total colouring matter not less than 4 % calculated as

lutein
E1%
1cm 2 550 at ca. 445 nm in chloroform/ethanol (10 + 90) or in
hexane/ethanol/acetone (80 + 10 + 10)
Description Dark, yellowish brown liquid
Identification
Spectrometry Maximum in chloroform/ethanol (1:9) at ca. 445 nm
Purity
9
>
>
>
>
>
>
>
>
>
>
>
>
>
>
Methanol >
>
=
>
Ethanol >
>
>
>
>
>
>
>
>
Propan-2-ol >
>
>
>
>
>
>
;
Hexane
E 161g CANTHAXANTHIN
Definition These specifications apply to predominantly all-trans isomers of

canthaxanthin together with minor amounts of other carotenoids.
Diluted and stabilised forms are prepared from canthaxanthin
meeting these specifications and include solutions or suspensions
of canthaxanthin in edible fats or oils, emulsions and water
dispersible powders. These preparations may have different cis/
trans isomer ratios.

02012R0231 — EN — 27.10.2024 — 033.001 — 44
▼B
Einecs 208-187-2
Chemical name β-Carotene-4,4′-dione; canthaxanthin; 4,4′-dioxo-β-carotene
Assay Not less than 96 % of total colouring matters (expressed as

canthaxanthin)
8
>
> at ca. 485 nm in chloroform
>
>
>
>
>
>
< at 468-472 nm in cyclo
E1%
1cm 2 200 hexane
>
>
>
>
>
>
>
> at 464-467 nm in petroleum
:
ether
Description Deep violet crystals or crystalline powder
Identification
Spectrometry Maximum in chloroform at ca. 485 nm

Maximum in cyclohexane at 468-472 nm
Maximum in petroleum ether at 464-467 nm
Purity
Subsidiary colouring matters Carotenoids other than canthaxanthin: not more than 5,0 % of total
colouring matters
E 162 BEETROOT RED, BETANIN
Synonyms Beet Red
Definition Beet red is obtained from the roots of strains of red beets (Beta
vulgaris L. var. rubra) by pressing crushed beet as press juice or
by aqueous extraction of shredded beet roots and subsequent
enrichment in the active principle. The colour is composed of
different pigments all belonging to the class betalaine. The main
colouring principle consists of betacyanins (red) of which betanin
accounts for 75-95 %. Minor amounts of betaxanthin (yellow) and
degradation products of betalaines (light brown) may be present.
Besides the colour pigments the juice or extract consists of sugars,
salts, and/or proteins naturally occurring in red beets. The solution
may be concentrated and some products may be refined in order to
remove most of the sugars, salts and proteins.
Colour Index No
Einecs 231-628-5
Chemical name (S-(R′,R′)-4-(2-(2-Carboxy-5(β-D-glucopyranosyloxy)-2,3-dihydro-6-

hydroxy-1H-indol-1-yl)ethenyl)-2,3-dihydro-2,6-pyridine-dicarboxylic
acid; 1-(2-(2,6-dicarboxy-1,2,3,4-tetrahydro-4-pyridylidene)ethylidene)-
5-β-D-glucopyranosyloxy)-6-hydroxyindolium-2-carboxylate
02012R0231 — EN — 27.10.2024 — 033.001 — 45
▼B
Chemical formula Betanin: C24H26N2O13
Assay Content of red colour (expressed as betanine) is not less than 0,4 %
E1%
Description Red or dark red liquid, paste, powder or solid
Identification
Spectrometry Maximum in water of pH 5 at ca. 535 nm
Purity
Nitrate Not more than 2 g nitrate anion/g of red colour (as calculated from
assay).
E 163 ANTHOCYANINS
Synonyms
Definition Anthocyanins are obtained by maceration or extraction with

sulphited water, acidified water, carbon dioxide, methanol or
ethanol from the strains of vegetables and edible fruits, with
subsequent concentration and/or purification if necessary. The
resulting product can be transformed into powder by an industrial
drying process. Anthocyanins contain common components of the
source material, namely anthocyanine, organic acids, tannins,
sugars, minerals etc., but not necessarily in the same proportions
as found in the source material. Ethanol may naturally be present as
a result of the maceration process. The colouring principle is antho
cyanin. Products are marketed according to their colour strength as
determined by the assay. Colour content is not expressed using
quantitative units.
Colour Index No
Einecs 208-438-6 (cyanidin); 205-125-6 (peonidin); 208-437-0 (delphinidin);

211-403-8 (malvidin); 205-127-7 (pelargonidin); 215-849-4 (petunidin)
Chemical name 3,3′,4′,5,7-Pentahydroxy-flavylium chloride (cyanidin)

3,4′,5,7-Tetrahydroxy-3′-methoxyflavylium chloride (peonidin)
3,4′,5,7-Tetrahydroxy-3′,5′-dimethoxyflavylium chloride (malvidin)
3,5,7-Trihydroxy-2-(3,4,5,trihydroxyphenyl)-1-benzopyrylium
chloride (delphinidin)
3,3′4′,5,7-Pentahydroxy-5′-methoxyflavylium chloride (petunidin)
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-1-benzopyrilium chloride
(pelargonidin)
02012R0231 — EN — 27.10.2024 — 033.001 — 46
▼B
Chemical formula Cyanidin: C15H11O6Cl

Peonidin: C16H13O6Cl
Malvidin: C17H15O7Cl
Delphinidin: C15H11O7Cl
Petunidin: C16H13O7Cl
Pelargonidin: C15H11O5Cl
Molecular weight Cyanidin: 322,6

Peonidin: 336,7
Malvidin: 366,7
Delphinidin: 340,6
Petunidin: 352,7
Pelargonidin: 306,7
Assay E1%
1cm 300 for the pure pigment at 515-535 nm at pH 3,0
Description Purplish-red liquid, powder or paste, having a slight characteristic

odour
Identification
Spectrometry Maximum in methanol with 0,01 % conc. HCl

Cyanidin: 535 nm
Peonidin: 532 nm
Malvidin: 542 nm
Delphinidin: 546 nm
Petunidin: 543 nm
Pelargonidin: 530 nm
Purity
Solvent residues Methanol Not more than 50 mg/kg
Ethanol Not more than 200 mg/kg
Sulfur dioxide Not more than 1 000 mg/kg per percent pigment
E 170 CALCIUM CARBONATE
Synonyms CI Pigment White 18; Chalk
Definition Calcium carbonate is the product obtained from ground limestone or

by the precipitation of calcium ions with carbonate ions.
Einecs Calcium carbonate: 207-439-9

Limestone: 215-279-6
Chemical name Calcium carbonate
Chemical formula CaCO3

02012R0231 — EN — 27.10.2024 — 033.001 — 47
▼B
Description White crystalline or amorphous, odourless and tasteless powder
Identification
Solubility Practically insoluble in water and in alcohol. Dissolves with effer

vescence in diluted acetic acid, in diluted hydrochloric acid and in
diluted nitric acid, and the resulting solutions, after boiling, give
positive tests for calcium.
Purity
Acid-insoluble substances Not more than 0,2 %
Magnesium and alkali salts Not more than 1 %
Fluoride Not more than 50 mg/kg

9
Antimony (as Sb) >
>
>
>
>
>
>
>
Copper (as Cu) >
>
>
>
>
=
Chromium (as Cr) Not more than 100 mg/kg, singly or in combination
>
>
>
>
>
>
Zinc (as Zn) >
>
>
>
>
>
>
;
Barium (as Ba)
E 171 TITANIUM DIOXIDE
Synonyms CI Pigment White 6
Definition Titanium dioxide consists essentially of pure anatase and/or rutile

titanium dioxide which may be coated with small amounts of
alumina and/or silica to improve the technological properties of
the product.
The anatase grades of pigmentary titanium dioxide can only be made
by the sulphate process which creates a large amount of sulphuric
acid as a by-product. The rutile grades of titanium dioxide are
typically made by the chloride process.
Certain rutile grades of titanium dioxide are produced using mica
(also known as potassium aluminum silicate) as a template to form
the basic platelet structure. The surface of the mica is coated with
titanium dioxide using a specialised patented process.
Rutile titanium dioxide, platelet form is manufactured by subjecting
titanium dioxide (rutile) coated mica nacreous pigment to an
extractive dissolution in acid followed by an extractive dissolution
in alkali. All of the mica is removed during this process and the
resulting product is a platelet form of rutile titanium dioxide.
Einecs 236-675-5
02012R0231 — EN — 27.10.2024 — 033.001 — 48
▼B
Chemical name Titanium dioxide
Chemical formula TiO2
Assay Content not less than 99 % on an alumina and silica-free basis
Description White to slightly coloured powder
Identification
Solubility Insoluble in water and organic solvents. Dissolves slowly in hydro

fluoric acid and in hot concentrated sulphuric acid.
Purity
Loss on ignition Not more than 1,0 % on a volatile matter free basis (800 °C)
Aluminium oxide and/or silicon dioxide Total not more than 2,0 %
Matter soluble in 0,5 N HCl Not more than 0,5 % on an alumina and silica-free basis and, in
addition, for products containing alumina and/or silica, not more
than 1,5 % on the basis of the product as sold.
Water soluble matter Not more than 0,5 %
Cadmium Not more than 1 mg/kg after an extraction with 0,5 N HCl.
Antimony Not more than 2 mg/kg after an extraction with 0,5 N HCl.
Arsenic Not more than 1 mg/kg after an extraction with 0,5 N HCl.
Lead Not more than 10 mg/kg after an extraction with 0,5 N HCl.
Mercury Not more than 1 mg/kg after an extraction with 0,5 N HCl.
E 172 IRON OXIDES AND IRON HYDROXIDES
Synonyms Iron Oxide Yellow: CI Pigment Yellow 42 and 43
Iron Oxide Red: CI Pigment Red 101 and 102
Iron Oxide Black: CI Pigment Black 11
Definition Iron oxides and iron hydroxides are produced synthetically and
consist essentially of anhydrous and/or hydrated iron oxides. The
range of hues includes yellows, reds, browns and blacks. Food
quality iron oxides are primarily distinguished from technical
grades by the comparatively low levels of contamination by other
metals. This is achieved by the selection and control of the source
of the iron and/or by the extent of chemical purification during the
manufacturing process.
Colour Index No Iron Oxide Yellow: 77492
Iron Oxide Red: 77491
Iron Oxide Black: 77499

02012R0231 — EN — 27.10.2024 — 033.001 — 49
▼B
Einecs Iron Oxide Yellow: 257-098-5
Iron Oxide Red: 215-168-2
Iron Oxide Black: 235-442-5
Chemical name Iron Oxide Yellow: hydrated ferric oxide, hydrated iron (III) oxide
Iron Oxide Red: anhydrous ferric oxide, anhydrous iron (III) oxide
Iron Oxide Black: ferroso ferric oxide, iron (II, III) oxide
Chemical formula Iron Oxide Yellow: FeO(OH) · H2O
Iron Oxide Red: Fe2O3
Iron Oxide Black: FeO.Fe2O3
Molecular weight 88,85: FeO(OH)
159,70: Fe2O3
231,55: FeO.Fe2O3
Assay Yellow not less than 60 %, red and black not less than 68 % total
iron, expressed as iron
Description Powder; yellow, red, brown or black in hue
Identification
Solubility Insoluble in water and in organic solvents

Soluble in concentrated mineral acids
Purity
9
Water soluble matter Not more than 1,0 % >
>
>
>
>
>
>
>
Arsenic Not more than 3 mg/kg >
>
>
>
>
>
>
>
Cadmium Not more than 1 mg/kg >
>
>
>
>
>
>
>
>
>
Chromium Not more than 100 mg/kg >
>
>
>
>
=
Copper Not more than 50 mg/kg By total dissolution
>
>
>
>
>
>
Lead Not more than 10 mg/kg >
>
>
>
>
>
>
>
Mercury Not more than 1 mg/kg >
>
>
>
>
>
>
>
>
>
Nickel Not more than 200 mg/kg >
>
>
>
>
>
>
;
Zinc Not more than 100 mg/kg
E 173 ALUMINIUM
Synonyms CI Pigment Metal
Definition Aluminium powder is composed of finely divided particles of

aluminium. The grinding may or may not be carried out in the
presence of edible vegetable oils and/or food additive quality fatty
acids. It is free from admixture with substances other than edible
vegetable oils and/or food additive quality fatty acids.
02012R0231 — EN — 27.10.2024 — 033.001 — 50
▼B
Einecs 231-072-3
Chemical name Aluminium
Chemical formula Al
Atomic weight 26,98
Assay Not less than 99 % calculated as Al on an oil-free basis
Description A silvery-grey powder or tiny sheets
Identification
Solubility Insoluble in water and in organic solvents. Soluble in dilute hydro

chloric acid.
Test for aluminium A sample dissolved in dilute hydrochloric acid passes test
Purity
Loss on drying Not more than 0,5 % (105 °C, to constant weight)
E 174 SILVER
Synonyms Argentum
Definition
Einecs 231-131-3
Chemical name Silver
Chemical formula Ag
Atomic weight 107,87
Assay Content not less than 99,5 % Ag
Description Silver-coloured powder or tiny sheets
Identification
Purity
E 175 GOLD
Synonyms Pigment Metal 3; Aurum
Definition
Einecs 231-165-9
Chemical name Gold

02012R0231 — EN — 27.10.2024 — 033.001 — 51
▼B
Chemical formula Au
Atomic weight 197,0
Assay Content not less than 90 % Au
Description Gold-coloured powder or tiny sheets
Identification
Purity
9
Silver Not more than 7 % >
=
After complete
>
; dissolution
Copper Not more than 4 %
E 180 LITHOLRUBINE BK
Synonyms CI Pigment Red 57; Rubinpigment; Carmine 6B
Definition Lithol Rubine BK consists essentially of calcium 3-hydroxy-4-(4-

methyl-2-sulfonatophenylazo)-2-naphthalenecarboxylate and subsid-
iary colouring matters together with water, calcium chloride and/or
calcium sulphate as the principal uncoloured components.
Colour Index No 15850:1
Einecs 226-109-5
Chemical name Calcium 3-hydroxy-4-(4-methyl-2-sulfonatophenylazo)-2-naphthalene-

carboxylate
Chemical formula C18H12CaN2O6S
Assay Content not less than 90 % total colouring matters

E1%
1cm 200 at ca. 442 nm in dimethylformamide
Description Red powder
Identification
Spectrometry Maximum in dimethylformamide at ca. 442 nm
Purity

matters:
2-Amino-5-methylbenzenesulfonic Not more than 0,2 %

acid, calcium salt
3-hydroxy-2-naphthalenecarboxylic Not more than 0,4 %

acid, calcium salt
Unsulfonated primary aromatic amines Not more than 0,01 % (expressed as aniline)
02012R0231 — EN — 27.10.2024 — 033.001 — 52
▼B
Ether extractable matter From a solution of pH 7, not more than 0,2 %
E 200 SORBIC ACID
Synonyms
Definition
Einecs 203-768-7
Chemical name Sorbic acid; trans, trans-2,4-Hexadienoic acid
Chemical formula C 6 H 8O 2
▼M47
Description Colourless needles or white free flowing crystalline powder, having

a slight characteristic odour and showing no change in colour after
heating for 90 minutes at 105 °C
▼B
Identification
Melting range Between 133 °C and 135 °C, after vacuum drying for four hours in
a sulphuric acid desiccator
Spectrometry A propan-2-ol solution (1 in 4 000 000) shows absorbance maximum

at 254 ± 2 nm
Test for double bonds Passes test
Solubility Slightly soluble in water, soluble in ethanol.
Purity
Water content Not more than 0,5 % (Karl Fischer method)
Aldehydes Not more than 0,1 % (as formaldehyde)

02012R0231 — EN — 27.10.2024 — 033.001 — 53
▼B
E 202 POTASSIUM SORBATE
Synonyms
Definition
Einecs 246-376-1
Chemical name Potassium sorbate; Potassium (E,E)-2,4-hexadienoate; Potassium salt

of trans, trans 2,4-hexadienoic acid
Chemical formula C 6 H 7O 2 K
Assay Content not less than 99 % on the dried basis
▼M47
Description White crystalline powder or granules showing no change in colour

after heating for 90 minutes at 105 °C
▼B
Identification
Melting range for sorbic acid Melting range of sorbic acid isolated by acidification and not recryst
allised 133 °C to 135 °C after vacuum drying in a sulphuric acid
desiccator
Test for potassium Passes test
Purity
Acidity or alkalinity Not more than about 1,0 % (as sorbic acid or K2CO3)
Aldehydes Not more than 0,1 %, calculated as formaldehyde
▼M25
__________
▼B
E 210 BENZOIC ACID
Synonyms
Definition
Einecs 200-618-2
Chemical name Benzoic acid; Benzenecarboxylic acid; Phenylcarboxylic acid
Assay Content not less than 99,5 % on the anhydrous basis

02012R0231 — EN — 27.10.2024 — 033.001 — 54
▼B
Description White crystalline powder
Identification
Melting range 121,5 °C -123,5 °C
Sublimation test Passes test
Test for benzoate Passes test
pH About 4 (solution in water)
Purity
Loss on drying Not more than 0,5 % (3 hours, over sulphuric acid)
Chlorinated organic compounds Not more than 0,07 % expressed as chloride corresponding to 0,3 %
expressed as monochlorobenzoic acid
Readily oxidisable substances Add 1,5 ml of sulphuric acid to 100 ml of water, heat to boiling
point and add 0,1 N KMnO4 in drops, until the pink colour persists
for 30 seconds. Dissolve 1 g of the sample, weighed to the nearest
mg, in the heated solution, and titrate with 0,1 N KMnO4 to a pink
colour that persists for 15 seconds. Not more than 0,5 ml should be
required
Readily carbonisable substances A cold solution of 0,5 g of benzoic acid in 5 ml of 94,5 to 95,5 %
sulphuric acid must not show a stronger colouring than that of a
reference liquid containing 0,2 ml of cobalt chloride TSC (1), 0,3 ml
of ferric chloride TSC (2), 0,1 ml of copper sulphate TSC (3) and
4,4 ml of water
Polycyclic acids On fractional acidification of a neutralised solution of benzoic acid,

the first precipitate must not have a different melting point from that
of the benzoic acid
_____________
(1) Cobalt chloride TSC: dissolve approximately 65 g of cobalt chloride CoCl2·6H2O in a sufficient quantity of a mixture of 25 ml
hydrochloric acid and 975 ml of water to give a total volume of 1 litre. Place exactly 5 ml of this solution in a round-bottomed
flask containing 250 ml of iodine solution, add 5 ml of 3 % hydrogen peroxide, then 15 ml of a 20 % solution of sodium
hydroxide. Boil for 10 minutes, allow to cool, add 2 g of potassium iodide and 20 ml of 25 % sulphuric acid. After the precipitate
is completely dissolved, titrate the liberated iodine with sodium thiosulphate (0,1 N) in the presence of starch TS. 1 ml of sodium
thiosulphate (0,1 N) corresponds to 23,80 mg of CoCl2·6H2O. Adjust final volume of solution by the addition of a sufficient
quantity of the hydrochloric acid/water mixture to give a solution containing 59,5 mg of CoCl2·6H2O per ml.
(2) Ferric chloride TSC: dissolve approximately 55 g of ferric chloride in a sufficient quantity of a mixture of 25 ml of hydrochloric
acid and 975 ml of water to give a total volume of 1 litre. Place 10 ml of this solution in a round-bottomed flask containing 250 ml
of iodine solution, add 15 ml of water and 3 g of potassium iodide; leave the mixture to stand for 15 minutes. Dilute with 100 ml
of water then titrate the liberated iodine with sodium thiosulphate (0,1 N) in the presence of starch TS. 1 ml of sodium thiosulphate
(0,1 N) corresponds to 27,03 mg of FeCl3·6H2O. Adjust final volume of solution by the addition of a sufficient quantity of the
hydrochloric acid/water to give a solution containing 45,0 mg of FeCl3·6H2O per ml.
(3) Copper sulphate TSC: dissolve approximate by 65 g of copper sulphate CuSO4·5H2O in a sufficient quantity of a mixture of 25 ml
of hydrochloric acid and 975 ml of water to give a total volume of 1 litre. Place 10 ml of this solution in a round-bottomed flask
containing 250 ml of iodine solution, add 40 ml of water, 4 ml of acetic acid and 3 g of potassium iodide. Titrate the liberated
iodine with sodium thiosulphate (0,1 N) in the presence of starch TS (*). 1 ml of sodium thiosulphate (0,1 N) corresponds to
24,97 mg of CuSO4·5H2O. Adjust final volume of solution by the addition of a sufficient quantity of the hydrochloric acid/water
mixture to give a solution containing 62,4 mg of CuSO4·5H2O per ml.
(*) Starch TS: triturate 0,5 g starch (potato starch, maize starch or soluable starch) with 5 ml of water; to the resulting paste add a
sufficient quantity of water to give a total volume of 100 ml, stirring all the time. Boil for a few minutes, allow to cool, filter. The
starch must be freshly prepared.
02012R0231 — EN — 27.10.2024 — 033.001 — 55
▼B
E 211 SODIUM BENZOATE
Synonyms
Definition
Einecs 208-534-8
Chemical name Sodium benzoate; Sodium salt of benzenecarboxylic acid; Sodium

salt of phenylcarboxylic acid
Chemical formula C7H5O2Na
Assay Not less than 99 % of C7H5O2Na, after drying at 105 °C for four
hours
Description A white, almost odourless, crystalline powder or granules
Identification
Solubility Freely soluble in water, sparingly soluble in ethanol
Melting range for benzoic acid Melting range of benzoic acid isolated by acidification and not
recrystallised 121,5 °C to 123,5 °C, after drying in a sulphuric
acid desiccator
Test for sodium Passes test
Purity
required
Polycyclic acids On fractional acidification of a (neutralised) solution of sodium

benzoate, the first precipitate must not have a different melting
range from that of benzoic acid
Chlorinated organic compounds Not more than 0,06 % expressed as chloride, corresponding to
0,25 % expressed as monochlorobenzoic acid
Acidity or alkalinity Neutralisation of 1 g of sodium benzoate, in the presence of

phenolphthalein, must not require more than 0,25 ml of 0,1 N
NaOH or 0,1 N HCl
E 212 POTASSIUM BENZOATE
Synonyms
Definition
Einecs 209-481-3
Chemical name Potassium benzoate; Potassium salt of benzenecarboxylic acid;

Potassium salt of phenylcarboxylic acid
02012R0231 — EN — 27.10.2024 — 033.001 — 56
▼B
Chemical formula C7H5KO2·3H2O
Assay Content not less than 99 % C7H5KO2 after drying at 105 °C to

constant weight
Identification
recrystallised 121,5 °C to 123,5 °C, after vacuum drying in a
sulphuric acid desiccator
Purity
required
Readily carbonisable substances A cold solution of 0,5 g of benzoic acid in 5 ml 94,5 to 95,5 %
reference liquid containing 0,2 ml of cobalt chloride TSC, 0,3 ml of
ferric chloride TSC, 0,1 ml of copper sulphate TSC and 4,4 ml of
water
Polycyclic acids On fractional acidification of a (neutralised) solution of potassium

benzoate, the first precipitate must not have a different melting range
from that of benzoic acid
Acidity or alkalinity Neutralisation of 1 g of potassium benzoate, in the presence of

NaOH or 0,1 N HCl
E 213 CALCIUM BENZOATE
Synonyms Monocalcium benzoate
Definition
Einecs 218-235-4
Chemical name Calcium benzoate; Calcium dibenzoate
Chemical formula Anhydrous: C14H10O4Ca
Monohydrate: C14H10O4Ca·H2O
Trihydrate: C14H10O4Ca·3H2O
02012R0231 — EN — 27.10.2024 — 033.001 — 57
▼B
Molecular weight Anhydrous: 282,31
Monohydrate: 300,32
Trihydrate: 336,36
Assay Content not less than 99 % after drying at 105 °C
Description White or colourless crystals, or white powder
Identification
recrystallised 121,5 °C to 123,5 °C, after vacuum drying in a
Test for calcium Passes test
Purity
Loss on drying Not more than 17,5 % (105 °C, to constant weight)
required
Readily carbonisable substances Cold solution of 0,5 g of benzoic acid in 5 ml of 94,5 to 95,5 %
reference liquid containing 0,2 ml of cobalt chloride TSC, 0,3 ml of
ferric chloride TSC, 0,1 ml of copper sulphate TSC and 4,4 ml of
water
Polycyclic acids On fractional acidification of a (neutralised) solution of calcium

benzoate, the first precipitate must not be a different melting
range from that of benzoic acid
Acidity or alkalinity Neutralisation of 1 g of calcium benzoate, in the presence of

NaOH or 0,1 N HCl
E 214 ETHYL p-HYDROXYBENZOATE
Synonyms Ethylparaben; Ethyl p-oxybenzoate
Definition
Einecs 204-399-4
Chemical name Ethyl-p-hydroxybenzoate; Ethyl ester of p-hydroxybenzoic acid

02012R0231 — EN — 27.10.2024 — 033.001 — 58
▼B
Assay Content not less than 99,5 % after drying for two hours at 80 °C
Description Almost odourless, small, colourless crystals or a white, crystalline

powder
Identification
Melting range 115-118 °C
Test for p-hydroxybenzoate Melting range of p-hydroxybenzoic acid isolated by acidification and
not recrystallised: 213 °C to 217 °C, after vacuum drying in a
Test for alcohol Passes test
Purity
p-Hydroxybenzoic acid and salicylic acid Not more than 0,35 % expressed as p-hydroxybenzoic acid
E 215 SODIUM ETHYL p-HYDROXYBENZOATE
Synonyms
Definition
Einecs 252-487-6
Chemical name Sodium ethyl p-hydroxybenzoate; Sodium compound of the ethyl

ester of p-hydroxybenzoic acid
Assay Content of ethylester of p-hydroxybenzoic acid not less than 83 %

on the anhydrous basis
Description White, crystalline hygroscopic powder
Identification
Melting range 115 °C to 118 °C, after vacuum drying in a sulphuric acid desiccator
Test for p-hydroxybenzoate Melting range of p-hydroxybenzoic acid derived from the sample is
213 °C to 217 °C
pH 9,9-10,3 (0,1 % aqueous solution)
Purity
Loss on drying Not more than 5 %, (by vacuum drying in a sulphuric acid desic
cator)
Sulphated ash 37 to 39 %
02012R0231 — EN — 27.10.2024 — 033.001 — 59
▼B
E 218 METHYL p-HYDROXYBENZOATE
Synonyms Methylparaben; Methyl-p-oxybenzoate
Definition
Einecs 243-171-5
Chemical name Methyl p-hydroxybenzoate; Methyl ester of p-hydroxybenzoic acid
Assay Content not less than 99 % after drying for two hours at 80 °C
Description Almost odourless, small colourless crystals or white crystalline

powder
Identification
Melting range 125 °C - 128 °C
Test for p-hydroxybenzoate Melting range of p-hydroxybenzoic acid derived from the sample is
213 °C to 217 °C after drying for two hours at 80 °C
Purity
E 219 SODIUM METHYL p-HYDROXYBENZOATE
Synonyms
Definition
Einecs
Chemical name Sodium methyl p-hydroxybenzoate; Sodium compound of the

methylester of p-hydroxybenzoic acid
Description White, hygroscopic powder

02012R0231 — EN — 27.10.2024 — 033.001 — 60
▼B
Identification
Melting range The white precipitate formed by acidifying with hydrochloric acid a
10 % (w/v) aqueous solution of the sodium derivative of methyl p-
hydroxybenzoate (using litmus paper as indicator) shall, when
washed with water and dried at 80 °C for two hours, have a
melting range of 125 °C to 128 °C
pH 9,7-10,3 (0,1 % solution in carbon dioxide free water)
Purity
Water content Not more than 5 % (Karl Fischer method)
Sulphated ash 40 % to 44,5 % on the anhydrous basis
E 220 SULPHUR DIOXIDE
Synonyms
Definition
Einecs 231-195-2
Chemical name Sulphur dioxide; Sulphurous acid anhydride
Chemical formula SO2
Assay Content not less than 99 %
Description Colourless, non-flammable gas with strong pungent suffocating

odour
Identification
Test for sulphurous substances Passes test
Purity
Non-volatile residue Not more than 0,01 %
Sulphur trioxide Not more than 0,1 %
Selenium Not more than 10 mg/kg
Other gases not normally present in the No trace

air

02012R0231 — EN — 27.10.2024 — 033.001 — 61
▼B
E 221 SODIUM SULPHITE
Synonyms
Definition
Einecs 231-821-4
Chemical name Sodium sulphite (anhydrous or heptahydrate)
Chemical formula Anhydrous: Na2SO3
Heptahydrate: Na2SO37H2O
Heptahydrate: 252,16
Assay Anhydrous: Not less than 95 % of Na2SO3

and not less than 48 % of SO2
Heptahydrate: Not less than 48 % of Na2SO3

and not less than 24 % of SO2
Description White crystalline powder or colourless crystals
Identification
Test for sulphite Passes test
pH 8,5-11,5 (anhydrous: 10 % solution; heptahydrate: 20 % solution)
Purity
Thiosulphate Not more than 0,1 % based on the SO2 content
Iron Not more than 10 mg/kg based on the SO2 content
Selenium Not more than 5 mg/kg based on the SO2 content
▼M3
E 222 SODIUM HYDROGEN SULPHITE
▼B
Synonyms
Definition
Einecs 231-921-4
Chemical name Sodium bisulphite; Sodium hydrogen sulphite
Chemical formula NaHSO3 in aqueous solution
Assay Content not less than 32 % w/w NaHSO3
Description A clear, colourless to yellow solution
Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 62
▼B
pH 2,5-5,5 (10 % aqueous solution)
Purity
▼M3
▼B
E 223 SODIUM METABISULPHITE
Synonyms Pyrosulphite; Sodium pyrosulphite
Definition
Einecs 231-673-0
Chemical name Sodium disulphite; Disodium pentaoxodisulphate
Chemical formula Na2S2O5
Assay Content not less than 95 % Na2S2O5 and not less than 64 % of SO2
Description White crystals or crystalline powder
Identification
Purity
E 224 POTASSIUM METABISULPHITE
Synonyms Potassium pyrosulphite
Definition
Einecs 240-795-3
Chemical name Potassium disulphite; Potassium pentaoxo disulphate
Chemical formula K 2S 2 O 5

02012R0231 — EN — 27.10.2024 — 033.001 — 63
▼B
Assay Content not less than 90 % K2S2O5 and not less than 51,8 % of
SO2, the remainder being composed almost entirely of potassium
sulphate
Description Colourless crystals or white crystalline powder
Identification
Purity
E 226 CALCIUM SULPHITE
Synonyms
Definition
Einecs 218-235-4
Chemical name Calcium sulphite
Chemical formula CaSO3·2H2O
Assay Content not less than 95 % of CaSO3·2H2O and not less than 39 %
of SO2
Description White crystals or white crystalline powder
Identification
Purity
▼M8
E 227 CALCIUM HYDROGEN SULPHITE
▼B
Synonyms
Definition
Einecs 237-423-7
02012R0231 — EN — 27.10.2024 — 033.001 — 64
▼B
Chemical name Calcium bisulphite; Calcium hydrogen sulphite
Chemical formula Ca(HSO3)2
Assay 6 to 8 % (w/v) of sulphur dioxide and 2,5 to 3,5 % (w/v) of calcium

dioxide corresponding to 10 to 14 % (w/v) of calcium bisulphite
[Ca(HSO3)2]
Description Clear greenish-yellow aqueous solution having a distinct odour of

sulphur dioxide
Identification
Purity
▼M8
E 228 POTASSIUM HYDROGEN SULPHITE
▼B
Synonyms
Definition
Einecs 231-870-1
Chemical name Potassium bisulphite; Potassium hydrogen sulphite
Chemical formula KHSO3 in aqueous solution
Assay Content not less than 280 g KHSO3 per litre (or 150 g SO2 per litre)
Description Clear colourless aqueous solution
Identification
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 65
▼B
E 234 NISIN
Synonyms
Definition Nisin consists of several closely related polypeptides produced by

strains of Lactococcus lactis subsp. lactis
Einecs 215-807-5
Chemical name
Chemical formula C143H230N42O37S7
Molecular weight 3 354,12
Assay Nisin concentrate contains not less than 900 units per mg in a
mixture of non-fat milk solids and a minimum sodium chloride
content of 50 %
Description White powder
Identification
Purity
Loss on drying Not more than 3 % (102 °C to 103 °C, to constant weight)
E 235 NATAMYCIN
Synonyms Pimaricin
Definition Natamycin is a fungicide of the polyene macrolide group, and is

produced by strains of Streptomyces natalensis and other relevant
species
Einecs 231-683-5
Chemical name A stereoisomer of 22-(3-Amino-3,6-dideoxy-β-D- mannopyr

anosyloxy)-1,3,26-trihydroxy-12-methyl-10-oxo-6,11,28-triox
atricyclo[22.3.1.05,7]octacosa-8,14,16,18,20-pentaene-25-carboxylic
acid.
Chemical formula C33H47O13N
Description White to creamy-white crystalline powder
Identification
Colour reactions On adding a few crystals of natamycin on a spot plate, to a drop of:
concentrated hydrochloric acid, a blue colour develops,
concentrated phosphoric acid, a green colour develops,which
changes into pale red after a few minutes
Spectrometry A 0,0005 % w/v solution in 1 % methanolic acetic acid solution has

absorption maxima at about 290 nm, 303 nm and 318 nm, a
shoulder at about 280 nm and exhibits minima at about 250 nm,
295,5 nm and 311 nm
02012R0231 — EN — 27.10.2024 — 033.001 — 66
▼B
pH 5,5-7,5 (1 % w/v solution in previously neutralised mixture of 20

parts dimethylformamide and 80 parts of water)
Specific rotation [α]D20 + 250° to + 295° (a 1 % w/v solution in glacial acetic acid, at
20 °C and calculated with reference to the dried material)
Purity
Loss on drying Not more than 8 % (over P2O5, in vacuum at 60 °C to constant

weight)
Total plate count Not more than 100 colonies per gram
E 239 HEXAMETHYLENE TETRAMINE
Synonyms Hexamine; Methenamine
Definition
Einecs 202-905-8
Chemical name 1,3,5,7-Tetraazatricyclo [3.3.1.13,7]-decane, hexamethylenetetramine
Chemical formula C6H12N4
Description Colourless or white crystalline powder
Identification
Test for formaldehyde Passes test
Test for ammonia Passes test
Sublimation point: Approximately 260 °C
Purity
Loss on drying Not more than 0,5 % (at 105 °C in vacuum over P2O5 for 2 hours)
Sulphates Not more than 0,005 % expressed as SO4
Chlorides Not more than 0,005 % expressed as Cl
Ammonium salts Not detectable

02012R0231 — EN — 27.10.2024 — 033.001 — 67
▼B
E 242 DIMETHYL DICARBONATE
Synonyms DMDC; Dimethyl pyrocarbonate
Definition
Einecs 224-859-8
Chemical name Dimethyl dicarbonate; Pyrocarbonic acid dimethyl ester
Assay Content not less than 99,8 %
Description Colourless liquid, decomposes in aqueous solution. It is corrosive to

skin and eyes and toxic by inhalation and ingestion
Identification
Decomposition After dilution positive tests for CO2 and methanol
Melting point 17 °C
Boiling point 172 °C with decomposition
Density 20 °C Approximately 1,25 g/cm3
Infrared absorption spectrum Maxima at 1 156 and 1 832 cm-1
Purity
Dimethyl carbonate Not more than 0,2 %
Chlorine, total Not more than 3 mg/kg
▼M12
E 243 ETHYL LAUROYL ARGINATE
Synonyms Lauric arginate ethyl ester; lauramide arginine ethyl ester; ethyl-Να-
lauroyl-L-arginate·HCl; LAE;
▼M19
Definition Ethyl lauroyl arginate is synthesized by esterifying arginine with

ethanol, followed by reacting the ester with lauroyl chloride, in
aqueous media at a controlled temperature between 10 and 15 °C
and at a pH between 6,7 and 6,9. The resultant ethyl lauroyl arginate
is recovered as the hydrochloride salt, which is filtered and dried.
▼M12
ELINCS 434-630-6
Chemical name Ethyl-Να-dodecanoyl-L-arginate·HCl
Chemical formula C20H41N4O3Cl
Molecular Weight 421,02
Assay Not less than 85 % and not more than 95 %

02012R0231 — EN — 27.10.2024 — 033.001 — 68
▼M12
Identification
Solubility Freely soluble in water, ethanol, propylene glycol and glycerol
Purity
Να-Lauroyl-L-arginine Not more than 3 %
Lauric acid Not more than 5 %
Ethyl laurate Not more than 3 %
L-Arginine·HCl Not more than 1 %
Ethyl arginate·2HCl Not more than 1 %
▼M36
E 246 GLYCOLIPIDS
Synonyms
Definition The naturally occurring glycolipids are obtained by a fermentation

process using the wild type strain MUCL 53181 of the fungus
Dacryopinax spathularia (edible sweet osmanthus ear mushroom).
Glucose is used as a carbon source. The solvent-free downstream
process includes filtration and microfiltration to remove microbial
cells, precipitation and washing with buffered water to purify. The
product is pasteurized and spray-dried. The production process does
not chemically modify the glycolipids or change their innate
composition.
CAS number 2205009-17-0
Chemical name Glycolipids from Dacryopinax spathularia
Assay Not less than 93 % total glycolipid content on the dried basis.
Description Beige to light brown powder, weak characteristic odour
Identification
Solubility Complies (10 g/l in water)
pH Between 5,0 and 7,0 (10 g/l in water)
Turbidity Not more than 28 NTU (10 g/l in water)

02012R0231 — EN — 27.10.2024 — 033.001 — 69
▼M36
Purity
Water content Not more than 5 % (Karl Fischer Method)
Protein Not more than 3 % (factor N x 6,25)
Fat Not more than 2 % (gravimetric)
Sodium Not more than 3,3 %
Nickel Not more than 2 mg/kg
Total aerobic count Not more than 100 colonies per gram
Yeast and moulds Not more than 10 colonies per gram
Coliforms Not more than 3 MPN per gram
Salmonella spp. Absent in 25 g’
▼B
E 249 POTASSIUM NITRITE
Synonyms
Definition
Einecs 231-832-4
Chemical name Potassium nitrite
Chemical formula KNO2
Assay Content not less than 95 % on the anhydrous basis (1)
Description White or slightly yellow, deliquescent granules
Identification
Test for nitrite Passes test
pH 6,0-9,0 (5 % solution)
_____________
(1) May only be sold in a mixture with salt or a salt substitute.
02012R0231 — EN — 27.10.2024 — 033.001 — 70
▼M45
Purity
Loss on drying Not more than 3 % (4 hours, over silica gel)
Arsenic Not more than 0,1 mg/kg
▼B
E 250 SODIUM NITRITE
Synonyms
Definition
Einecs 231-555-9
Chemical name Sodium nitrite
Chemical formula NaNO2
Assay Content not less than 97 % on the anhydrous basis (1)
Description White crystalline powder or yellowish lumps
Identification
Test for nitrite Passes test
▼M45
Purity
Loss on drying Not more than 0,25 % (4 hours, over silica gel)
▼B
E 251 SODIUM NITRATE

(i) SOLID SODIUM NITRATE
Synonyms Chile saltpetre; Cubic or soda nitre
Definition
Einecs 231-554-3
Chemical name Sodium nitrate
Description White crystalline, slightly hygroscopic powder
_____________
(1) May only be sold in a mixture with salt or a salt substitute.
02012R0231 — EN — 27.10.2024 — 033.001 — 71
▼B
Identification
Test for nitrate Passes test
▼M45
Purity
Loss on drying Not more than 2 % (105 °C, 4 hours)
Nitrites Not more than 30 mg/kg expressed as NaNO2
▼B
(ii) LIQUID SODIUM NITRATE
Synonyms
Definition Liquid sodium nitrate is an aqueous solution of sodium nitrate as the
direct result of the chemical reaction between sodium hydroxide and
nitric acid in stoechiometric amounts, without subsequent crystalli
sation. Standardised forms prepared from liquid sodium nitrate
meeting these specifications may contain nitric acid in excessive
amounts, if clearly stated or labelled.
Einecs 231-554-3
Chemical name Sodium nitrate
Assay Content between 33,5 % and 40,0 % of NaNO3
Description Clear colourless liquid
Identification
pH 1,5-3,5
▼M45
Purity
Free nitric acid Not more than 0,01 %
Nitrites Not more than 10 mg/kg expressed as NaNO2
▼B
This specification refers to a 35 % aqueous solution.

E 252 POTASSIUM NITRATE
Synonyms Chile saltpetre; Cubic or soda nitre

Definition
Einecs 231-818-8
02012R0231 — EN — 27.10.2024 — 033.001 — 72
▼B
Chemical name Potassium nitrate
Chemical formula KNO3
Description White crystalline powder or transparent prisms having a cooling,

saline, pungent taste
Identification
▼M45
Purity
Nitrites Not more than 20 mg/kg expressed as KNO2
▼B
E 260 ACETIC ACID
Synonyms
Definition
Einecs 200-580-7
Chemical name Acetic acid; Ethanoic acid
Description Clear, colourless liquid having a pungent, characteristic odour
Identification
Boiling point 118 °C at 760 mm pressure (of mercury)
Specific gravity About 1,049
Test for acetate A one in three solution gives positive tests for acetate
Solidification point Not lower than 14,5 °C
Purity
Non-volatile residue Not more than 100 mg/kg
Formic acid, formates and other Not more than 1 000 mg/kg expressed as formic acid
oxidisable substances
Readily oxidisable substances Dilute 2 ml of the sample in a glass-stoppered container with 10 ml

of water and add 0,1 ml of 0,1 N potassium permanganate. The pink
colour does not change to brown within 30 minutes
02012R0231 — EN — 27.10.2024 — 033.001 — 73
▼B
▼M2
E 261 (i) POTASSIUM ACETATE
▼B
Synonyms
Definition
Einecs 204-822-2
Chemical name Potassium acetate
Description Colourless, deliquescent crystals or a white crystalline powder,

odourless or with a faint acetic odour
Identification
Test for acetate Passes test
Purity
▼M2
E 261 (ii) POTASSIUM DIACETATE
Synonyms
Definition Potassium diacetate is a molecular compound of potassium acetate

and acetic acid
Einecs 224-217-7
Chemical name Potassium hydrogen diacetate
Chemical formula C4H7KO4

02012R0231 — EN — 27.10.2024 — 033.001 — 74
▼M2
Assay Content 36 to 38 % of free acetic acid and 61 to 64 % of potassium

acetate
Description White crystals
Identification
pH 4,5-5 (10 % aqueous solution)
Purity
▼B
E 262 (i) SODIUM ACETATE
Synonyms
Definition
Einecs 204-823-8
Chemical name Sodium acetate
Chemical formula C2H3NaO2·nH2O (n = 0 or 3)
Trihydrate: 136,08
Assay Content (for both of anhydrous and trihydrate form) not less than
98,5 % on the anhydrous basis
Description Anhydrous: White, odourless, granular, hygro

scopic powder
Trihydrate: Colourless, transparent crystals or a

granular crystalline powder, odourless
or with a faint, acetic odour. Effloresces
in warm, dry air
02012R0231 — EN — 27.10.2024 — 033.001 — 75
▼B
Identification
Purity
Loss on drying Anhydrous: Not more than 2% (120 °C,

4 hours)
Trihydrate: Between 36 and 42 % (120 °C,

4 hours)
E 262 (ii) SODIUM DIACETATE
Synonyms
Definition Sodium diacetate is a molecular compound of sodium acetate and

acetic acid
Einecs 204-814-9
Chemical name Sodium hydrogen diacetate
Chemical formula C4H7NaO4·nH2O (n = 0 or 3)
Molecular weight 142,09 (anhydrous)
▼M34
Assay Content 39 to 43 % of free acetic acid and 57 to 60 % of sodium
acetate
▼B
Description White, hygroscopic crystalline solid with an acetic odour
Identification
Purity
E 263 CALCIUM ACETATE
Synonyms
Definition
Einecs 200-540-9
02012R0231 — EN — 27.10.2024 — 033.001 — 76
▼B
Chemical name Calcium acetate
Chemical formula Anhydrous: C4H6O4Ca
Monohydrate: C4H6O4Ca·H2O
Monohydrate: 176,18
Description Anhydrous calcium acetate is a white, hygroscopic, bulky,

crystalline solid with a slightly bitter taste. A slight odour of
acetic acid may be present. The monohydrate may be needles,
granules or powder
Identification
Purity
Loss on drying Not more than 11 % (155 °C to constant weight, for the monohy
drate)
▼M43
E 267 BUFFERED VINEGAR
Synonyms Buffered vinegar (liquid); buffered vinegar (powder)
Definition Buffered vinegar is a liquid or dried product prepared by adding

buffering agents to vinegar. The buffering agents used are sodium/
potassium hydroxides (E 524 to E 525) and sodium/potassium
carbonates (E 500 to E 501). The vinegar is compliant with the
European Standard EN 13188:2000 and is exclusively obtained
from an agricultural source origin (except wood/cellulose) by
double fermentation, alcoholic and acetous. The primary constituents
of buffered vinegar are acetic acid and its salts.
02012R0231 — EN — 27.10.2024 — 033.001 — 77
▼M43
Assay Liquid: 15–40 % (w/w) acetic acid equivalents
Powder: 55–75 % (w/w) acetic acid equivalents
2 to 20 % (w/w) free acetic acid
Description Liquid: colourless to brown viscous liquid
Powder: white to creamy-white crystalline powder
Identification Liquid: pH 4,75–7,5
Powder: pH 4,75–6,75 (10 % aqueous solution)
Purity
Cations Liquid: Not more than 10 % sodium and 30 % potassium
Powder: Not more than 30 % sodium and 40 % potassium
Water content Powder: Not more than 18 % (Karl Fischer Method)
Ethanol Not more than 0,5 % w/w
▼B
E 270 LACTIC ACID
Synonyms
Definition Consists of a mixture of lactic acid (C3H6O3) and lactic acid lactate
(C6H10O5). It is obtained by the lactic fermentation of sugars or is
prepared synthetically.
Lactic acid is hygroscopic and when concentrated by boiling, it
condenses to form lactic acid lactate, which on dilution and
heating hydrolyses to lactic acid.
Einecs 200-018-0
Chemical name Lactic acid; 2-Hydroxypropionic acid; 1-Hydroxyethane-1-carboxylic

acid
Description Colourless or yellowish, nearly odourless, syrupy liquid to solid
Identification
Test for lactate Passes test

02012R0231 — EN — 27.10.2024 — 033.001 — 78
▼B
Purity
Chloride Not more than 0,2 %
Sulphate Not more than 0,25 %
Iron Not more than 10 mg/kg
Note: This specification refers to a 80 % aqueous solution; for weaker aqueous

solutions, calculate values corresponding to their lactic acid content
E 280 PROPIONIC ACID
Synonyms
Definition
Einecs 201-176-3
Chemical name Propionic acid; Propanoic acid
Description Colourless or slightly yellowish, oily liquid with a slightly pungent

odour
Identification
Melting point – 22 °C
Distillation range 138,5 °C to 142,5 °C
Purity
Non-volatile residue Not more than 0,01 % when dried at 140 °C to constant weight
Aldehydes Not more than 0,1 % expressed as formaldehyde
E 281 SODIUM PROPIONATE
Synonyms
Definition
Einecs 205-290-4
Chemical name Sodium propionate; Sodium propanoate
02012R0231 — EN — 27.10.2024 — 033.001 — 79
▼B
Description White crystalline hygroscopic powder, or a fine white powder
Identification
Test for propionate Passes test
Purity
E 282 CALCIUM PROPIONATE
Synonyms
Definition
Einecs 223-795-8
Chemical name Calcium propionate
Chemical formula C6H10O4Ca
Assay Content not less than 99 %, after drying for two hours at 105 °C
Identification
Purity
▼M16
▼B
E 283 POTASSIUM PROPIONATE
Synonyms
Definition
Einecs 206-323-5
02012R0231 — EN — 27.10.2024 — 033.001 — 80
▼B
Chemical name Potassium propionate; Potassium propanoate
Chemical formula C3H5KO2
Identification
Purity
E 284 BORIC ACID
Synonyms Boracic acid; Orthoboric acid; Borofax
Definition
Einecs 233-139-2
Chemical name
Chemical formula H3BO3
Description Colourless, odourless, transparent crystals or white granules or

powder; slightly unctuous to the touch; occurs in nature as the
mineral sassolite
Identification
Melting point At approximately 171 °C
Burning test Burns with a nice green flame
Purity
Peroxides No colour develops with added KI-solution

02012R0231 — EN — 27.10.2024 — 033.001 — 81
▼B
E 285 SODIUM TETRABORATE (BORAX)
Synonyms Sodium borate
Definition
Einecs 215-540-4
Chemical name Sodium tetraborate; Sodium biborate; Sodium pyroborate;

Anhydrous tetraborate
Chemical formula Na2B4O7

Na2B4O7·10H2O
Assay
Description Powder or glass-like plates becoming opaque on exposure to air;

slowly soluble in water
Identification
Melting range Between 171 °C and 175 °C with decomposition
Purity
Peroxides No colour develops with added KI-solution
E 290 CARBON DIOXIDE
Synonyms Carbonic acid gas; Dry ice (solid form); Carbonic anhydride
Definition
Einecs 204-696-9
Chemical name Carbon dioxide
Chemical formula CO2
Assay Content not less than 99 % v/v on the gaseous basis
Description A colourless gas under normal environmental conditions with a

slight pungent odour. Commercial carbon dioxide is shipped and
handled as a liquid in pressurised cylinders or bulk storage
systems, or in compressed solid blocks of ‘dry ice’. Solid (dry
ice) forms usually contain added substances, such as propylene
glycol or mineral oil, as binders
Identification
Precipitate formation When a stream of the sample is passed through a solution of barium
hydroxide, a white precipitate is produced which dissolves with
effervescence in dilute acetic acid
Purity
Acidity 915 ml of gas bubbled through 50 ml of freshly boiled water must

not render the latter more acid to methylorange than is 50 ml freshly
boiled water to which has been added 1 ml of hydrochloric acid
(0,01 N)
02012R0231 — EN — 27.10.2024 — 033.001 — 82
▼B
Reducing substances, hydrogen 915 ml of gas bubbled through 25 ml of ammoniacal silver nitrate
phosphide and sulphide reagent to which has been added 3 ml of ammonia must not cause
clouding or blackening of this solution
Carbon monoxide Not more than 10 μl/l
Oil content Not more than 5 mg/kg
E 296 MALIC ACID
Synonyms Pomalous acid
Definition
Einecs 230-022-8, 210-514-9, 202-601-5
Chemical name hydroxybutanedioic acid; hydroxysuccinic acid
Description White or nearly white crystalline powder or granules
Identification
Test for malate Passes test
Purity
Fumaric acid Not more than 1,0 %
Maleic acid Not more than 0,05 %
E 297 FUMARIC ACID
Synonyms
Definition
Einecs 203-743-0
Chemical name trans-Butenedioic acid; trans-1,2-Ethylene-dicarboxylic acid
Description White crystalline powder or granules
Identification
Melting range 286-302 °C (closed capillary, rapid heating)
Test for 1,2-dicarboxylic acid Passes test
pH 3,0-3,2 (0,05 % solution at 25 °C)

02012R0231 — EN — 27.10.2024 — 033.001 — 83
▼B
Purity
E 300 ASCORBIC ACID, L-ASCORBIC ACID
Synonyms L-xylo-Ascorbic acid; L(+)- Ascorbic acid
Definition
Einecs 200-066-2
Chemical name L-ascorbic acid; Ascorbic acid; 2,3-Didehydro-L-threo-hexono-1,4-

lactone; 3-Keto-L-gulofuranolactone
Assay contains not less than 99 % of C6H8O6 after drying in a vacuum

desiccator over sulphuric acid for 24 hours,
Description White to pale yellow, odourless crystalline powder
Melting range Between 189 °C and 193 °C with decomposition
Identification
Test for ascorbic acid Passes test
pH Between 2,4 and 2,8 (2 % aqueous solution)
Specific rotation [α]D20 between + 20,5° and + 21,5° (10 % w/v aqueous solution)
Purity
Loss on drying Not more than 0,4 % (in vacuum over sulphuric acid, 24 hours)
E 301 SODIUM ASCORBATE
Synonyms Sodium L-ascorbate; L-Ascorbic acid monosodium salt
Definition
Einecs 205-126-1
Chemical name Sodium ascorbate; Sodium L-ascorbate; 2,3-Didehydro-L-threo-

hexono-1,4-lactone sodium enolate; 3-Keto-L-gulofurano-lactone
sodium enolate

02012R0231 — EN — 27.10.2024 — 033.001 — 84
▼B
Assay Sodium ascorbate, after drying in a vacuum desiccator over sulphuric

acid for 24 hours, contains not less than 99 % of C6H7O6Na
Description White or almost white, odourless crystalline powder which darkens

on exposure to light
Identification
Test for ascorbate Passes test
Specific rotation [α]D20 between + 103° and + 106° (10 % w/v aqueous solution)
Purity
Loss on drying Not more than 0,25 % (in vacuum over sulphuric acid, 24 hours)
E 302 CALCIUM ASCORBATE
Synonyms Calcium ascorbate dihydrate
Definition
Einecs 227-261-5
Chemical name Calcium ascorbate dihydrate; Calcium salt of 2,3-didehydro-L-threo-

hexono-1,4-lactone dihydrate
Chemical formula C12H14O12Ca·2H2O
Assay Content not less than 98 % on a volatile matter-free basis
Description White to slightly pale greyish-yellow odourless crystalline powder
Identification
Test for ascorbate Passes test
Specific rotation [α]D20 between + 95° and + 97° (5 % w/v aqueous solution)
Purity
Fluoride Not more than 10 mg/kg (expressed as fluorine)
Volatile matter Not more than 0,3 % determined by drying at room temperature for
24 hours in a desiccator containing sulphuric acid or phosphorus
pentoxide

02012R0231 — EN — 27.10.2024 — 033.001 — 85
▼B
E 304 (i) ASCORBYL PALMITATE
Synonyms L-ascorbyl palmitate
Definition
Einecs 205-305-4
Chemical name Ascorbyl palmitate; L-ascorbyl palmitate; 2,3-didehydro-L-threo-

hexono-1,4-lactone-6-palmitate; 6-palmitoyl-3-keto-L-gulofuranol
actone
Description White or yellowish-white powder with a citrus-like odour
Identification
Melting range Between 107 °C and 117 °C
Specific rotation [α]D20 between + 21° and + 24° (5 % w/v in methanol solution)
Purity
Loss on drying Not more than 2,0 % (vacuum oven, 56-60 °C, 1 hour)
E 304 (ii) ASCORBYL STEARATE
Synonyms
Definition
Einecs 246-944-9
Chemical name Ascorbyl stearate; L-ascorbyl stearate; 2,3-didehydro-L-threo-

hexono-1,4-lactone-6-stearate; 6-stearoyl-3-keto-L-gulofuranolactone
Description White or yellowish, white powder with a citrus-like odour
Identification
Melting point About 116 °C
Purity
Loss on drying Not more than 2,0 % (vacuum oven, 56-60 °C, 1 hour)

02012R0231 — EN — 27.10.2024 — 033.001 — 86
▼B
E 306 TOCOPHEROL-RICH EXTRACT
Synonyms
Definition Product obtained by the vacuum steam distillation of edible

vegetable oil products, comprising concentrated tocopherols and
tocotrienols
Contains tocopherols such as d-α-, d-β-, d-γ- and d-δ-tocopherols
Einecs
Chemical name
Chemical formula
Molecular weight 430,71 (d-α-tocopherol)
Assay Content not less than 34 % of total tocopherols
Description Brownish red to red, clear, viscous oil having a mild, characteristic
odour and taste. May show a slight separation of wax-like consti
tuents in microcrystalline form
Identification
By suitable gas liquid chromatographic

method
Specific rotation [α]D20 not less than + 20°
Solubility Insoluble in water. Soluble in ethanol. Miscible in ether
Purity
E 307 ALPHA-TOCOPHEROL
Synonyms dl-α-Tocopherol; (all rac)-α-Tocopherol
Definition
Einecs 233-466-0
Chemical name DL-5,7,8-Trimethyltocol; DL-2,5,7,8-tetramethyl-2-(4′,8′,12′-

trimethyltridecyl)-6-chromanol
Description Slightly yellow to amber, nearly odourless, clear, viscous oil which
oxidises and darkens on exposure to air or light
Identification
Solubility Insoluble in water, freely soluble in ethanol, miscible in ether

02012R0231 — EN — 27.10.2024 — 033.001 — 87
▼B
Spectrophotometry In absolute ethanol the maximum absorption is about 292 nm
Specific rotation [α]D25 0° ± 0,05° (1 in 10 solution in chloroform)
Purity
Refractive index [n]D20 1,503-1,507
Specific absorption in ethanol E1%

1cm (292 nm) 71-76
(0,01 g in 200 ml of absolute ethanol)
E 308 GAMMA-TOCOPHEROL
Synonyms dl-γ-Tocopherol
Definition
Einecs 231-523-4
Chemical name 2,7,8-trimethyl-2-(4′,8′,12′-trimethyltridecyl)-6-chromanol
Description Clear, viscous, pale yellow oil which oxidises and darkens on
exposure to air or light
Identification
Spectrometry Maximum absorptions in absolute ethanol at about 298 nm and

257 nm
Purity

1cm (298 nm) between 91 and 97
E1%
1cm (257 nm) between 5,0 and 8,0
E 309 DELTA-TOCOPHEROL
Synonyms
Definition
Einecs 204-299-0
Chemical name 2,8-dimethyl-2-(4′,8′,12′-trimethyltridecyl)-6-chromanol
Description Clear, viscous, pale yellowish or orange oil which oxidises and
darkens on exposure to air or light
02012R0231 — EN — 27.10.2024 — 033.001 — 88
▼B
Identification
Spectrometry Maximum absorptions in absolute ethanol at about 298 nm and

257 nm
Purity
Specific absorption E1%

1cm in ethanol E1%
1cm (298 nm) between 89 and 95
E1%
1cm (257 nm) between 3,0 and 6,0
E 310 PROPYL GALLATE
Synonyms
Definition
Einecs 204-498-2
Chemical name Propyl gallate; Propyl ester of gallic acid; n-propyl ester of 3,4,5-
trihydroxybenzoic acid
Description White to creamy-white, crystalline, odourless solid
Identification
Solubility Slightly soluble in water, freely soluble in ethanol, ether and

propane-1,2-diol
Melting range Between 146 °C and 150 °C after drying at 110 °C for four hours
Purity
Free acid Not more than 0,5 % (as gallic acid)
Chlorinated organic compound Not more than 100 mg/kg (as C1)

1cm (275 nm) not less than 485 and not more than 520
▼M30
__________
02012R0231 — EN — 27.10.2024 — 033.001 — 89
▼B
E 315 ERYTHORBIC ACID
Synonyms Isoascorbic acid; D-Araboascorbic acid
Definition
Einecs 201-928-0
Chemical name D-Erythro-hex-2-enoic acid γ-lactone; Isoascorbic acid; D-Isoas

corbic acid
Description White to slightly yellow crystalline solid which darkens gradually on

exposure to light
Identification
Melting range About 164 °C to 172 °C with decomposition
Test for ascorbic acid/colour reaction Passes test
Specific rotation [α]D25 10 % (w/v) aqueous solution between – 16,5° to – 18,0°
Purity
Loss on drying Not more than 0,4 % after drying under (reduced pressure on silica
gel, 3 hours)
Oxalate To a solution of 1 g in 10 ml of water add 2 drops of glacial acetic

acid and 5 ml of 10 % calcium acetate solution. The solution should
remain clear
E 316 SODIUM ERYTHORBATE
Synonyms Sodium isoascorbate
Definition
Einecs 228-973-9
Chemical name Sodium isoascorbate; Sodium D-isoascorbic acid; Sodium salt of

2,3-didehydro-D-erythro-hexono-1,4-lactone; 3-keto-D-gulofurano-
lactone sodium enolate monohydrate
Chemical formula C6H7O6Na·H2O
Assay Content not less than 98 % after drying in a vacuum desiccator over
sulphuric acid for 24 hours expressed on the monohydrate basis
02012R0231 — EN — 27.10.2024 — 033.001 — 90
▼B
Description White crystalline solid
Identification
Solubility Freely soluble in water, very slightly soluble in ethanol
Test for ascorbic acid/colour reaction Passes test
pH 5,5 to 8,0 (10 % aqueous solution)
Specific rotation [α]D25 10 % (w/v) aqueous solution between + 95° and + 98°
Purity
Loss on drying Not more than 0,25 % after drying (in vacuum over sulphuric acid,
24 hours)
Oxalate To a solution of 1 g in 10 ml of water add 2 drops of glacial acetic

acid and 5 ml of 10 % calcium acetate solution. The solution should
remain clear.
E 319 TERTIARY-BUTYLHYDROQUINONE (TBHQ)
Synonyms TBHQ
Definition
Einecs 217-752-2
Chemical name Tert-butyl-1,4-benzenediol; 2-(1,1-Dimethylethyl)-1,4-benzenediol
Assay Content not less than 99 % of C10H14O2
Description White crystalline solid having a characteristic odour
Identification
Solubility Practically insoluble in water; soluble in ethanol
Melting point Not less than 126,5 °C
Phenolics Dissolve about 5 mg of the sample in 10 ml of methanol and add

10,5 ml of dimethylamine solution (1 in 4). A red to pink colour is
produced
Purity
Tertiary-Butyl-p-benzoquinone Not more than 0,2 %
2,5-Di-tertiary-butyl hydroquinone Not more than 0,2 %
Hydroxyquinone Not more than 0,1 %
Toluene Not more than 25 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 91
▼B
E 320 BUTYLATED HYDROXYANISOLE (BHA)
Synonyms BHA
Definition
Einecs 246-563-8
Chemical name 3-Tertiary-butyl-4-hydroxyanisole; A mixture of 2-tertiary-butyl-4-

hydroxyanisole and 3-tertiary-butyl-4-hydroxyanisole
Assay Content not less than 98,5 % of C11H16O2 and not less than 85 % of
3-tertiary-butyl-4-hydroxyanisole isomer
Description White or slightly yellow flakes or waxy solid with a slight aromatic
smell
Identification
Solubility Insoluble in water, freely soluble in ethanol
Colour reaction Passes test for phenol groups
Purity
Sulphated ash Not more than 0,05 % after calcination at 800 ± 25 °C
Phenolic impurities Not more than 0,5 %
Specific absorption E1%

E1%
E 321 BUTYLATED HYDROXYTOLUENE (BHT)
Synonyms BHT
Definition
Einecs 204-881-4
Chemical name 2,6-Ditertiary-butyl-p-cresol; 4-Methyl-2,6-ditertiarybutylphenol
Chemical formula C15H24O
Description White, crystalline or flaked solid, odourless or having a characteristic

faint aromatic odour
Identification
Solubility Insoluble in water and propane- 1,2-diol

Freely soluble in ethanol
Melting point At 70 °C
02012R0231 — EN — 27.10.2024 — 033.001 — 92
▼B
Spectrometry The absorption in the range 230 to 320 nm of a 2 cm layer of a 1 in

100 000 solution in dehydrated ethanol exhibits a maximum only at
278 nm
Purity
Phenolic impurities Not more than 0,5 %

E 322 LECITHINS
Synonyms Phosphatides; Phospholipids
Definition Lecithins are mixtures or fractions of phosphatides obtained by

physical procedures from animal or vegetable foodstuffs; they also
include hydrolysed products obtained through the use of harmless
and appropriate enzymes. The final product must not show any signs
of residual enzyme activity
The lecithins may be slightly bleached in aqueous medium by means
of hydrogen peroxide. This oxidation must not chemically modify
the lecithin phosphatides
Einecs 232-307-2
Chemical name
Chemical formula
Molecular weight
Assay Lecithins: not less than 60,0 % of substances insoluble in acetone

Hydrolysed lecithins: not less than 56,0 % of substances insoluble in
acetone
Description Lecithins: brown liquid or viscous semi-liquid or powder

Hydrolysed lecithins: light brown to brown viscous liquid or paste
Identification
Test for choline Passes test
Test for phosphorus Passes test
Test for fatty acids Passes test
Test for hydrolysed lecithin To a 800 ml beaker add 500 ml of water (30-35 °C). Then slowly
add 50 ml of the sample with constant stirring. Hydrolysed lecithin
will form a homogeneous emulsion. Non-hydrolysed lecithin will
form a distinct mass of about 50 g
Purity
Loss on drying Not more than 2,0 % (105 °C, 1 hour)
Toluene-insoluble matter Not more than 0,3 %

02012R0231 — EN — 27.10.2024 — 033.001 — 93
▼B
Acid value Lecithins: not more than 35 mg of potassium hydroxide per gram
Hydrolysed lecithins: not more than 45 mg of potassium hydroxide
per gram
Peroxide value Equal to or less than 10
▼M35
E 322a OAT LECITHIN
Synonyms Fractionated oat oil
Definition Oat lecithin is a fractionated oat oil rich in polar lipids, mainly
galactolipids. Oat lecithin is produced from food grade oat kernels
that are sieved and extracted using ethanol at an elevated
temperature to produce a crude lipid extract. This crude extract
undergoes multistage evaporation and filtration, yielding crude oat
oil, which is separated, evaporated and filtered to produce oat
lecithin.
Only ethanol may be used in the extraction as extraction solvent.
Einecs 281-672-4
Assay Not less than 30 % of polar lipids insoluble in acetone
Description Yellowish-brown viscous liquid
Identification
Choline Not more than 2 g/100 g
Phosphorous Not less than 0,5 %
Polar lipids Not less than 35 % w/w
Neutral lipids 55–65 % w/w
Saturated 17–20 % w/w
Monounsaturated 38–42 % w/w
Polyunsaturated 38–42 % w/w
Purity
Loss of drying Not more than 2 %
Toluene-insoluble matter Not more than 1 % w/w
Acid value Not more than 30 mg KOH/g
Peroxide value less than 10 meq O2/kg fat
Solvent residues Ethanol: not more than 300 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 94
▼M35
Aerobic plate count Not more than 1 000 CFU/g
Yeast Not more than 100 CFU/g
Moulds Not more than 100 CFU/g
Enterobacteriaceae Not more than 10 CFU/g
Aerobic spores Not more than 1 CFU/g
Other
Gluten Not more than 20 mg/kg
▼B
E 325 SODIUM LACTATE
Synonyms
Definition
Einecs 200-772-0
Chemical name Sodium lactate; Sodium 2-hydroxypropanoate
Chemical formula C3H5NaO3
Assay Content not less than 57 % and not more than 66 %
Description Colourless, transparent, liquid. Odourless, or with a slight, char

acteristic odour
Identification
▼M3
▼B
pH 6,5 to 7,5 (20 % aqueous solution)
Purity
Acidity Not more than 0,5 % after drying expressed as lactic acid
Reducing substances No reduction of Fehling's solution
Note: This specification refers to a 60 % aqueous solution

E 326 POTASSIUM LACTATE
Synonyms
Definition
Einecs 213-631-3
Cheminal name Potassium lactate; Potassium 2-hydroxypropanoate
Assay Content not less than 57 % and not more than 66 %

02012R0231 — EN — 27.10.2024 — 033.001 — 95
▼B
Description Slightly viscous, almost odourless clear liquid. Odourless, or with a

slight, characteristic odour
Identification
Ignition Ignite potassium lactate solution to an ash. The ash is alkaline, and
an effervescence occurs when acid is added
Colour reaction Overlay 2 ml of potassium lactate solution on 5 ml of a 1 in 100

solution of catechol in sulphuric acid. A deep red colour is produced
at the zone of contact
Purity
Acidity Dissolve 1 g of potassium lactate solution in 20 ml of water, add 3

drops of phenolphthalein TS and titrate with 0,1 N sodium
hydroxide. Not more than 0,2 ml should be required

E 327 CALCIUM LACTATE
Synonyms
Definition
Einecs 212-406-7
Chemical name Calcium dilactate; Calcium dilactate hydrate; 2-Hydroxypropanoic

acid calcium salt
Chemical formula (C3H5O2)2 Ca·nH2O (n = 0 - 5)
Description Almost odourless, white crystalline powder or granules
Identification
Solubility Soluble in water and practically insoluble in ethanol
pH Between 6,0 and 8,0 (5 % solution)
Purity
Loss on drying anhydrous: not more than 3,0 % (120 °C, 4 hours)
with 1 molecule of water: not more than 8,0 % (120 °C, 4 hours)
with 3 molecules of water: not more than 20,0 % (120 °C, 4 hours)
with 4,5 molecules of water: not more than 27,0 % (120 °C,
4 hours)
Acidity Not more than 0,5 % of the dry matter expressed as lactic acid
02012R0231 — EN — 27.10.2024 — 033.001 — 96
▼B
E 330 CITRIC ACID
Synonyms
Definition Citric acid is produced from lemon or pineapple juice, by fermen

tation of carbohydrate solutions or other suitable media using
Candida spp. or non-toxicogenic strains of Aspergillus niger
Einecs 201-069-1
Chemical name Citric acid; 2-Hydroxy-1,2,3-propanetricarboxylic acid; β-Hydroxy

tricarballylic acid
Chemical formula (a) C6H8O7 (anhydrous)

(b) C6H8O7·H2O (monohydrate)
Molecular weight (a) 192,13 (anhydrous)

(b) 210,15 (monohydrate)
Assay Citric acid may be anhydrous or it may contain 1 molecule of water.

Citric acid contains not less than 99,5 % of C6H8O7, calculated on
the anhydrous basis
Description Citric acid is a white or colourless, odourless, crystalline solid,

having a strongly acid taste. The monohydrate effloresces in dry air
Identification
Solubility Very soluble in water; freely soluble in ethanol; soluble in ether
Purity
Water content Anhydrous citric acid contains not more than 0,5 % water; citric acid
monohydrate contains not more than 8,8 % water (Karl Fischer
method)
Sulphated ash Not more than 0,05 % after calcination at 800 ± 25 °C
Oxalates Not more than 100 mg/kg, expressed as oxalic acid, after drying
Readily carbonisable substances Heat 1 g of powdered sample with 10 ml of 98 % minimum

sulphuric acid in a water bath at 90 °C in the dark for one hour.
Not more than a pale brown colour should be produced (Matching
Fluid K)
02012R0231 — EN — 27.10.2024 — 033.001 — 97
▼B
E 331 (i) MONOSODIUM CITRATE
Synonyms Monobasic sodium citrate
Definition
Einecs 242-734-6
Chemical name Monosodium citrate; Monosodium salt of 2-hydroxy-1,2,3-propane

tricarboxylic acid
Chemical formula (a) C6H7O7Na (anhydrous)

(b) C6H7O7Na·H2O (monohydrate)
Molecular weight (a) 214,11 (anhydrous)

(b) 232,23 (monohydrate)
Description Crystalline white powder or colourless crystals
Identification
Test for citrate Passes test
Purity
Loss on drying anhydrous: not more than 1,0 % (140 °C, 0,5 hour)
monohydrate: not more than 8,8 % (180 °C, 4 hours)
Oxalates Not more than 100 mg/kg expressed as oxalic acid, after drying
E 331 (ii) DISODIUM CITRATE
Synonyms Dibasic sodium citrate
Definition
Einecs 205-623-3
Chemical name Disodium citrate; Disodium salt of 2-hydroxy-1,2,3-propanetricar

boxylic acid; Disodium salt of citric acid with 1,5 molecules of
water
Chemical formula C6H6O7Na2·1,5H2O
Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 98
▼B
Purity
E 331 (iii) TRISODIUM CITRATE
Synonyms Tribasic sodium citrate
Definition
Einecs 200-675-3
Chemical name Trisodium citrate; Trisodium salt of 2-hydroxy-1,2,3-propanetricar

boxylic acid; Trisodium salt of citric acid, in anhydrous, dihydrate or
pentahydrate form
Chemical formula Anhydrous: C6H5O7Na3

Hydrated: C6H5O7Na3·nH2O (n = 2 or 5)

294,10 (hydrated n = 2)
348,16 (hydrated n = 5)
Assay Not less than 99 % on the anhydrous basis
Identification
Purity
Loss of drying Anhydrous: not more than 1,0 % (180 °C, 18 hours)
Dihydrate: 10,0 to 13,0 % (180 °C, 18 hours)
Pentahydrate: not more than 30,3 % (180 °C, 4 hours)
E 332 (i) MONOPOTASSIUM CITRATE
Synonyms Monobasic potassium citrate
Definition
Einecs 212-753-4
Chemical name Monopotassium citrate; Monopotassium salt of 2-hydroxy-1,2,3-

propanetricarboxylic acid; Anhydrous monopotassium salt of citric
acid
02012R0231 — EN — 27.10.2024 — 033.001 — 99
▼B
Description White, hygroscopic, granular powder or transparent crystals
Identification
Purity
E 332 (ii) TRIPOTASSIUM CITRATE
Synonyms Tribasic potassium citrate
Definition
Einecs 212-755-5
Chemical name Tripotassium citrate; Tripotassium salt of 2-hydroxy-1,2,3-propane

tricarboxylic acid; Monohydrated tripotassium salt of citric acid
Chemical formula C6H5O7K3·H2O
Description White, hygroscopic, granular powder or transparent crystals
Identification
Purity
Oxalates Not more than 100 mg/kg (expressed as oxalic acid, after drying)

02012R0231 — EN — 27.10.2024 — 033.001 — 100
▼B
E 333 (i) MONOCALCIUM CITRATE
Synonyms Monobasic calcium citrate
Definition
Einecs
Chemical name Monocalcium citrate; Monocalcium salt of 2-hydroxy-1,2,3-propane

tricarboxylic acid; Monohydrate monocalcium salt of citric acid
Chemical formula (C6H7O7)2Ca·H2O
Description Fine white powder
Identification
Purity
Aluminium Not more than 30 mg/kg (only if added to food for infants and
young children)
Not more than 200 mg/kg (for all uses except food for infants and
young children)
Carbonates Dissolving 1 g of calcium citrate in 10 ml 2 N hydrochloric acid

must not liberate more than a few isolated bubbles
E 333 (ii) DICALCIUM CITRATE
Synonyms Dibasic calcium citrate
Definition
Einecs
Chemical name Dicalcium citrate; Dicalcium salt of 2-hydroxy-1,2,3-propanetricar

boxylic acid; Trihydrated dicalcium salt of citric acid
Chemical formula (C6H7O7)2Ca2·3H2O
Assay Not less than 97,5 % on the anhydrous basis

02012R0231 — EN — 27.10.2024 — 033.001 — 101
▼B
Identification
Purity
young children)
young children)

E 333 (iii) TRICALCIUM CITRATE
Synonyms Tribasic calcium citrate
Definition
Einecs 212-391-7
Chemical name Tricalcium citrate; Tricalcium salt of 2-hydroxy-1,2,3-propanetricar

boxylic acid; Tetrahydrated tricalcium salt of citric acid
Chemical formula (C6H6O7)2Ca3·4H2O
Assay Not less than 97,5 % on the anhydrous basis
Identification
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 102
▼B
young children)
young children)

E 334 L(+)-TARTARIC ACID, TARTARIC ACID
Synonyms
Definition
Einecs 201-766-0
Chemical name L-tartaric acid; L-2,3-dihydroxybutanedioic acid; d-α,β-dihydroxy

succinic acid
Description Colourless or translucent crystalline solid or white crystalline powder
Identification
Test for tartrate Passes test
Specific rotation [α]D20 between + 11,5° and + 13,5° (20 % w/v aqueous solution)
Purity
Loss on drying Not more than 0,5 % (over P2O5, 3 hours)
Sulphated ash Not more than 1 000 mg/kg (after calcination at 800 ± 25 °C)
E 335 (i) MONOSODIUM TARTRATE
Synonyms Monosodium salt of L-(+)-tartaric acid
Definition
Einecs
Chemical name Monosodium salt of L-2,3-dihydroxybutanedioic acid; Monohy

drated monosodium salt of L-(+)-tartaric acid
Chemical formula C4H5O6Na·H2O
Description Transparent colourless crystals

02012R0231 — EN — 27.10.2024 — 033.001 — 103
▼B
Identification
Purity
E 335 (ii) DISODIUM TARTRATE
Synonyms
Definition
Einecs 212-773-3
Chemical name Disodium L-tartrate; Disodium (+)-tartrate; Disodium salt of (+)-2,3-

dihydroxybutanedioic acid; Dihydrated disodium salt of L-(+)-tartaric
acid
Chemical formula C4H4O6Na2·2H2O
Description Transparent, colourless crystals
Identification
Solubility 1 gram is insoluble in 3 ml of water. Insoluble in ethanol
Purity
E 336 (i) MONOPOTASSIUM TARTRATE
Synonyms Monobasic potassium tartrate
Definition
Einecs
Chemical name Anhydrous monopotassium salt of L-(+)-tartaric acid; Monopot

assium salt of L-2,3-dihydroxybutanedioic acid
02012R0231 — EN — 27.10.2024 — 033.001 — 104
▼B
Description White crystalline or granulated powder
Identification
pH 3,4 (1 % aqueous solution)
Purity
E 336 (ii) DIPOTASSIUM TARTRATE
Synonyms Dibasic potassium tartrate
Definition
Einecs 213-067-8
Chemical name Dipotassium salt of L-2,3-dihydroxybutanedioic acid; Dipotassium

salt with half a molecule of water of L-(+)-tartaric acid
Chemical formula C4H4O6K2·½H2O
Description White crystalline or granulated powder
Identification
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 105
▼B
E 337 POTASSIUM SODIUM TARTRATE
Synonyms Potassium sodium L-(+)-tartrate; Rochelle salt; Seignette salt
Definition
Einecs 206-156-8
Chemical name Potassium sodium salt of L-2,3-dihydroxybutanedioic acid;

Potassium sodium L-(+)-tartrate
Chemical formula C4H4O6KNa·4H2O
Description Colourless crystals or white crystalline powder
Identification
Solubility 1 gram is soluble in 1 ml of water, insoluble in ethanol
Purity
Loss on drying Not more than 26,0 % and not less than 21,0 % (150 °C, 3 hours)
E 338 PHOSPHORIC ACID
Synonyms Orthophosphoric acid; Monophosphoric acid
Definition
Einecs 231-633-2
Chemical name Phosphoric acid
Chemical formula H3PO4
Assay Content not less than 67,0 % and not more than 85,7 %. Phosphoric
acid is commercially available as an aqueous solution at variable
concentrations.
Description Clear, colourless, viscous liquid
Identification
Test for acid Passes test
Test for phosphate Passes test

02012R0231 — EN — 27.10.2024 — 033.001 — 106
▼B
Purity
Volatile acids Not more than 10 mg/kg (as acetic acid)
Chlorides Not more than 200 mg/kg (expressed as chlorine)
Nitrates Not more than 5 mg/kg (as NaNO3)
Sulphates Not more than 1 500 mg/kg (as CaSO4)
E 339 (i) MONOSODIUM PHOSPHATE
Synonyms Monosodium monophosphate; Acid monosodium monophosphate;

Monosodium orthophosphate; Monobasic sodium phosphate;
Sodium dihydrogen monophosphate
Definition
Einecs 231-449-2
Chemical name Sodium dihydrogen monophosphate
Chemical formula Anhydrous: NaH2PO4

Monohydrate: NaH2PO4 · H2O
Dihydrate: NaH2PO4 · 2H2O

Monohydrate: 138,00
Dihydrate: 156,01
Assay After drying at 60 °C for one hour and then at 105 °C for four
hours, contains not less than 97 % of NaH2PO4
P2O5 content between 58,0 % and 60,0 % on the anhydrous basis
Description A white odourless, slightly deliquescent powder, crystals or granules
Identification
Solubility Freely soluble in water. Insoluble in ethanol or ether
Purity
Loss on drying The anhydrous salt loses not more than 2,0 %, the monohydrate not
more than 15,0 %, the dihydrate not more than 25 % (60 °C, 1 hour
then 105 °C, 4 hours)
Water insoluble matter Not more than 0,2 % on the anhydrous basis

02012R0231 — EN — 27.10.2024 — 033.001 — 107
▼B
E 339 (ii) DISODIUM PHOSPHATE
Synonyms Disodium monophosphate; Secondary sodium phosphate; Disodium

orthophosphate;
Definition
Einecs 231-448-7
Chemical name Disodium hydrogen monophosphate; Disodium hydrogen ortho

phosphate
Chemical formula Anhydrous:Na2HPO4

Hydrate: Na2HPO4 · nH2O (n = 2, 7 or 12)
Assay After drying at 40 °C for three hours and subsequently at 105 °C for
five hours, contains not less than 98 % of Na2HPO4
P2O5 content between 49 % and 51 % on the anhydrous basis
Description Anhydrous disodium hydrogen phosphate is a white, hygroscopic,

odourless powder. Hydrated forms available include the dihydrate: a
white crystalline, odourless solid; the heptahydrate: white, odourless,
efflorescent crystals or granular powder; and the dodecahydrate:
white, efflorescent, odourless powder or crystals
Identification
Solubility Freely soluble in water. Insoluble in ethanol
Purity
Loss on drying The anhydrous salt loses not more than 5,0 %, the dihydrate not
more than 22,0 %, the heptahydrate not more than 50,0 %, the
dodecahydrate not more than 61,0 % (40 °C, 3 hours then 105 °C,
5 hours)
E 339 (iii) TRISODIUM PHOSPHATE
Synonyms Sodium phosphate; Tribasic sodium phosphate; Trisodium ortho

phosphate
02012R0231 — EN — 27.10.2024 — 033.001 — 108
▼B
Definition Trisodium phosphate is obtained from aqueous solutions and cryst

allises in the anhydrous form and with 1/2, 1, 6, 8 or 12 H2O. The
dodecahydrate always crystallises from aqueous solutions with an
excess of sodium hydroxide. It contains ¼ molecule of NaOH
Einecs 231-509-8
Chemical name Trisodium monophosphate; Trisodium phosphate; Trisodium ortho

phosphate
Chemical formula Anhydrous: Na3PO4

Hydrated: Na3PO4 nH2O (n = 1/2, 1, 6, 8, or 12)
Assay Sodium phosphate anhydrous and the hydrated forms, with the
exception of the dodecahydrate, contain not less than 97,0 % of
Na3PO4 calculated on the dried basis. Sodium phosphate
dodecahydrate contains not less than 92,0 % of Na3PO4 calculated
on the ignited basis
Description White odourless crystals, granules or crystalline powder
Identification
Purity
Loss on ignition When dried at 120 °C for two hours and then ignited at about
800 °C for 30 minutes, the losses in weight are as follows:
anhydrous not more than 2,0 %, monohydrate not more than
11,0 %, dodecahydrate: between 45,0 % and 58,0 %
E 340 (i) MONOPOTASSIUM PHOSPHATE
Synonyms Monobasic potassium phosphate; Monopotassium monophosphate;

Mono potassium orthophosphate
Definition
Einecs 231-913-4
Chemical name Potassium dihydrogen phosphate; Monopotassium dihydrogen ortho

phosphate; Monopotassium dihydrogen monophosphate
Chemical formula KH2PO4

02012R0231 — EN — 27.10.2024 — 033.001 — 109
▼B
Assay Content not less than 98,0 % after drying at 105 °C for four hours
Description Odourless, colourless crystals or white granular or crystalline powder
Identification
Purity
E 340 (ii) DIPOTASSIUM PHOSPHATE
Synonyms Dipotassium monophosphate; Secondary potassium phosphate;

Dipotassium orthophosphate; Dibasic potassium phosphate
Definition
Einecs 231-834-5
Chemical name Dipotassium hydrogen monophosphate; Dipotassium hydrogen

phosphate; Dipotassium hydrogen orthophosphate
Chemical formula K2HPO4
Assay Content not less than 98 % after drying at 105 °C for four hours
Description Colourless or white granular powder, crystals or masses; deli

quescent substance, hygroscopic
Identification
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 110
▼B
Water insoluble matter Not more than 0,2 % (on the anhydrous basis)
E 340 (iii) TRIPOTASSIUM PHOSPHATE
Synonyms Tribasic potassium phosphate; Tripotassium orthophosphate
Definition
Einecs 231-907-1
Chemical name Tripotassium monophosphate; Tripotassium phosphate; Tripotassium

orthophosphate
Chemical formula Anhydrous: K3PO4

Hydrated: K3PO4 · nH2O (n = 1 or 3)
Assay Content not less than 97 % calculated on the ignited basis

P2O5 content between 30,5 % and 34,0 % on the ignited basis
Description Colourless or white, odourless hygroscopic crystals or granules.

Hydrated forms available include the monohydrate and trihydrate
Identification
Purity
Loss on ignition Anhydrous: not more than 3,0 %; hydrated: not more than 23,0 %
(determined by drying at 105 °C for one hour and then ignite at
about 800 °C ± 25 °C for 30 minutes)
Water insoluble matter Not more than 0,2 % (on the anhydrous basis)
E 341 (i) MONOCALCIUM PHOSPHATE
Synonyms Monobasic calcium phosphate; Monocalcium orthophosphate
Definition
Einecs 231-837-1
02012R0231 — EN — 27.10.2024 — 033.001 — 111
▼B
Chemical name Calcium dihydrogen phosphate
Chemical formula Anhydrous: Ca(H2PO4)2

Monohydrate: Ca(H2PO4)2 · H2O

252,08 (monohydrate)

Description Granular powder or white, deliquescent crystals or granules
Identification
CaO content Between 23,0 % and 27,5 % (anhydrous)

Between 19,0 % and 24,8 % (monohydrate)
Purity
Loss on drying Anhydrous: not more than 14 % (105 °C, 4 hours)

Monohydrate: not more than 17,5 % (105 °C, 4 hours)
Loss on ignition Anhydrous: not more than 17,5 % (after ignition at 800 °C ± 25 °C
for 30 minutes)
Monohydrate: not more than 25,0 % (determined by drying at
105 °C for one hour, then ignite at 800 °C ± 25 °C for 30 minutes)
young children)
young children)
E 341 (ii) DICALCIUM PHOSPHATE
Synonyms Dibasic calcium phosphate; Dicalcium orthophosphate
Definition
Einecs 231-826-1
Chemical name Calcium monohydrogen phosphate; Calcium hydrogen ortho

phosphate; Secondary calcium phosphate
Chemical formula Anhydrous: CaHPO4

Dihydrate: CaHPO4 · 2H2O

172,09 (dihydrate)
02012R0231 — EN — 27.10.2024 — 033.001 — 112
▼B
Assay Dicalcium phosphate, after drying at 200 °C for three hours,

contains not less than 98 % and not more than the equivalent of
102 % of CaHPO4
Description White crystals or granules, granular powder or powder
Identification
Solubility Sparingly soluble in water. Insoluble in ethanol
Purity
Loss on ignition Not more than 8,5 % (anhydrous), or 26,5 % (dihydrate) after
ignition at 800 °C ± 25 °C for 30 minutes
Aluminium Not more than 100 mg/kg for the anhydrous form and not more than
80 mg/kg for the dihydrated form (only if added to food for infants
and young children)
Not more than 600 mg/kg for the anhydrous form and not more than
500 mg/kg for the dihydrated form (for all uses except food for
infants and young children). This applies until 31 March 2015.
Not more than 200 mg/kg for the anhydrous form and the dihydrated
form (for all uses except food for infants and young children). This
applies from 1 April 2015.
E 341 (iii) TRICALCIUM PHOSPHATE
Synonyms Calcium phosphate, tribasic; Calcium orthophosphate; Pentacalcium

hydroxy monophosphate; Calcium hydroxyapatite
▼M31
Definition Tricalcium phosphate consists of a variable mixture of calcium phos

phates obtained from neutralisation of phosphoric acid with calcium
hydroxide or calcium carbonate and having the approximate
composition of 10CaΟ·3P2O5·Η2O
▼B
Einecs 235-330-6 (Pentacalcium hydroxy monophosphate)

231-840-8 (Calcium orthophosphate)
Chemical name Pentacalcium hydroxy monophosphate; Tricalcium monophosphate
Chemical formula Ca5(PO4)3 ·OH or Ca3(PO4)2
Molecular weight 502 or 310
Assay Content not less than 90 % calculated on the ignited basis

Description A white, odourless powder which is stable in air

02012R0231 — EN — 27.10.2024 — 033.001 — 113
▼B
Identification
Solubility Practically insoluble in water; insoluble in ethanol, soluble in dilute

hydrochloric and nitric acid
Purity
Loss on ignition Not more than 8 % after ignition at 800 °C ± 25 °C for 0,5 hour
young children)
young children). This applies until 31 March 2015
young children). This applies from 1 April 2015.
E 343 (i) MONOMAGNESIUM PHOSPHATE
Synonyms Magnesiumdihydrogenphosphate; Magnesiumphosphate, monobasic;

Monomagnesium orthophosphate
Definition
Einecs 236-004-6
Chemical name Monomagnesiumdihydrogenmonophosphate
Chemical formula Mg(H2PO4)2 nH2O (where n = 0 to 4)
Assay Not less than 51,0 % after ignition calculated as P2O5 at the ignited
basis (800 °C ± 25 °C for 30 minutes)
Description White, odourless, crystalline powder, slightly soluble in water
Identification
Test for magnesium Passes test
MgO content Not less than 21,5 % after ignition or at an anhydrous basis (105 °C,
4 hours)
Purity
Fluoride Not more than 10 mg/kg (as fluorine)

02012R0231 — EN — 27.10.2024 — 033.001 — 114
▼B
E 343 (ii) DIMAGNESIUM PHOSPHATE
Synonyms Magnesiumhydrogenphosphate; Magnesiumphosphate, dibasic; Dimag

nesium orthophosphate; Secondary magnesiumphosphate
Definition
Einecs 231-823-5
Chemical name Dimagnesiummonohydrogenmonophosph ate
Chemical formula MgHPO4 · nH2O (where n = 0-3)
Assay Not less than 96 % after ignition (800 °C ± 25 °C for 30 minutes)
Description White, odourless, crystalline powder, slightly soluble in water
Identification
MgO content Not less than 33,0 % calculated on the anhydrous basis (105 °C,
4 hours)
Purity
Fluoride Not more than 10 mg/kg (as fluorine)
▼M46
E 345 (i) TRIMAGNESIUM DICITRATE
Synonyms Magnesium citrate; trimagnesium citrate
Definition
Einecs 222-093-9
Chemical name Trimagnesium bis (2-hydroxypropane-1,2,3- tricarboxylate),

anhydrous
Chemical formula (C6H5O7)2 Mg3
Assay 15,0-16,5 % Mg on dry substance/matter equal to 92,8-102,1 %

trimagnesium dicitrate anhydrous
Description White or almost white, fine, slightly hygroscopic powder
Appearance of a solution Not more opalescent than ref. susp. III and not more intensely
coloured than ref. sol. Y7 or BY6
Identification
Test for citrate Positive
Test for magnesium Positive
pH (5 % solution) 6,0-8,5
Solubility Soluble in water, practically insoluble in ethanol (96 %), it dissolves

in diluted hydrochloric acid.
02012R0231 — EN — 27.10.2024 — 033.001 — 115
▼M46
Particle size by STEM method – Median (D50) particle size (number-based) not
below 130 nm
by laser diffraction method – Median (D50) particle size (mass-
based) not below 50 μm
Purity
Loss on drying Maximum 3,5 %, determined on 1 000 g by drying in an oven at

180 ± 10 °C for 5 h
Oxalic/oxalate ≤ 280 mg/kg (0,028 %) as oxalic acid
Sulfates ≤ 2 000 mg/kg (0,2 %)
Calcium ≤ 2 000 mg/kg (0,2 %)
Iron ≤ 100 mg/kg
Mercury ≤ 0,1 mg/kg
Lead ≤ 1 mg/kg
Cadmium ≤ 0,1 mg/kg
Arsenic ≤ 1 mg/kg
Not identified material No process or product related impurities. The unintended presence of
hydrated forms of trimagnesium dicitrate such as the nonahydrate
cannot be excluded.
▼B
E 350 (i) SODIUM MALATE
Synonyms Sodium salt of malic acid
Definition
Einecs
Chemical name Disodium DL-malate; disodium salt of hydroxybutanedioic acid
Chemical formula Hemihydrate: C4H4Na2O5 ½ H2O

Trihydrate: C4H4Na2O5 3H2O
Molecular weight Hemihydrate: 187,05

Trihydrate: 232,10
Description White crystalline powder or lumps
Identification
Azo dye formation Positive
Solubility Freely soluble in water

02012R0231 — EN — 27.10.2024 — 033.001 — 116
▼B
Purity
Loss on drying Hemihydrate: Not more than 7,0 % (130 °C, 4 hours)
Trihydrate: 20,5-23,5 % (130 °C, 4 hours)
Alkalinity Not more than 0,2 % as Na2CO3
E 350 (ii) SODIUM HYDROGEN MALATE
Synonyms Monosodium salt of DL-malic acid
Definition
Einecs
Chemical name Monosodium DL-malate; monosodium 2-DL-hydroxy succinate
Chemical formula C4H5NaO5
Identification
Purity
E 351 POTASSIUM MALATE
Synonyms Potassium salt of malic acid
Definition
Einecs
Chemical name Dipotassium DL-malate; dipotassium salt of hydroxybutanedioic acid
Chemical formula C 4 H 4K 2 O 5

02012R0231 — EN — 27.10.2024 — 033.001 — 117
▼B
Description Colourless or almost colourless aqueous solution
Identification
Purity
Alkalinity Not more than 0,2 % as K2CO3
E 352 (i) CALCIUM MALATE
Synonyms Calcium salt of malic acid
Definition
Einecs
Chemical name Calcium DL-malate; calcium-α-hydroxysuccinate; calcium salt of

hydroxybutanedioic acid
Chemical formula C4H5CaO5
Identification
Test for malate Passes test
Test 1,2-dicarboxylic acid Passes test
Solubility Slightly soluble in water
Purity
Alkalinity Not more than 0,2 % as CaCO3

02012R0231 — EN — 27.10.2024 — 033.001 — 118
▼B
E 352 (ii) CALCIUM HYDROGEN MALATE
Synonyms Monocalcium salt of DL-malic acid
Definition
Einecs
Chemical name Monocalcium DL-malate; monocalcium 2-DL-hydroxysuccinate
Chemical formula (C4H5O5)2Ca
Molecular weight
Identification
Purity
E 353 METATARTARIC ACID
Synonyms Ditartaric acid
Definition
Einecs
Chemical name Metatartaric acid
Molecular weight
Assay Not less than 99,5 %
Description Crystalline or powder form with a white or yellowish colour. Very

deliquescent with a faint odour of caramel
Identification
Solubility Very soluble in water and ethanol
Identification test Place a sample of 1 to 10 mg of this substance in a test tube with

2 ml of concentrated sulphuric acid and 2 drops of sulpho-resorcinol
reagent. When heated to 150 °C, an intense violet coloration appears
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 119
▼B
E 354 CALCIUM TARTRATE
Synonyms L-Calcium tartrate
Definition
Einecs
Chemical name Calcium L(+)-2,3-dihydroxybutanedioate di-hydrate
Chemical formula C4H4CaO6 · 2H2O
Description Fine crystalline powder with a white or off-white colour
Identification
Solubility Slightly soluble in water. Solubility approximately 0,01 g/100 ml

water (20 °C). Sparingly soluble in ethanol. Slightly soluble in
diethyl ether. Soluble in acids
Specific rotation [α]D20 + 7,0° to + 7,4° (0,1 % in a 1N HCl solution)
pH Between 6,0 and 9,0 (5 % slurry)
Purity
Sulphates Not more than 1 g/kg (as H2SO4)
E 355 ADIPIC ACID
Synonyms
Definition
Einecs 204-673-3
Chemical name Hexanedioic acid; 1,4-butanedicarboxylic acid
Description White odourless crystals or crystalline powder
Identification
Melting range 151,5-154,0 °C
Solubility Slightly soluble in water. Freely soluble in ethanol
Purity
Water Not more than 0,2 % (Karl Fischer method)
Sulphated ash Not more than 20 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 120
▼B
E 356 SODIUM ADIPATE
Synonyms
Definition
Einecs 231-293-5
Chemical name Sodium adipate
Chemical formula C6H8Na2O4
Assay Content not less than 99,0 % (on anhydrous basis)
Identification
Melting range 151-152 °C (for adipic acid)
Solubility Approximately 50 g/100 ml water (20 °C)
Purity
Water content Not more than 3 % (Karl Fischer)
E 357 POTASSIUM ADIPATE
Synonyms
Definition
Einecs 242-838-1
Chemical name Potassium adipate
Chemical formula C 6 H 8K 2 O 4
Assay Content not less than 99,0 % (on anhydrous basis)
Identification
Melting range 151-152 °C (for adipic acid)
Solubility Approximately 60 g/100 ml water (20 °C)
Purity
Water Not more than 3 % (Karl Fischer)

02012R0231 — EN — 27.10.2024 — 033.001 — 121
▼B
E 363 SUCCINIC ACID
Synonyms
Definition
Einecs 203-740-4
Chemical name Butanedioic acid
Assay Content no less than 99,0 %
Description Colourless or white, odourless crystals
Identification
Melting range 185,0-190,0 °C
Purity
Residue on ignition Not more than 0,025 % (800 °C, 15 min)
E 380 TRIAMMONIUM CITRATE
Synonyms Tribasic ammonium citrate
Definition
Einecs 222-394-5
Chemical name Triammonium salt of 2-hydroxypropan-1,2,3-tricarboxylic acid
Description White to off-white crystals or powder
Identification
Test for ammonium Passes test
Purity
Oxalate Not more than 0,04 % (as oxalic acid)

02012R0231 — EN — 27.10.2024 — 033.001 — 122
▼B
E 385 CALCIUM DISODIUM ETHYLENEDIAMINETETRAACETATE
Synonyms Calcium disodium EDTA; Calcium disodium edetate
Definition
Einecs 200-529-9
Chemical name N,N′-1,2-Ethanediylbis [N-(carboxymethyl)-glycinate] [(4-)-

O,O′,ON,ON]calciate(2)-disodium; Calcium disodium ethylenedia
minetetra acetate; Calcium disodium (ethylenedinitrilo)tetra acetate
Chemical formula C10H12O8CaN2Na2·2H2O
Description White, odourless crystalline granules or white to nearly white

powder, slightly hygroscopic
Identification
Chelating activity to metal ions Positive
Purity
Water content 5 to 13 % (Karl Fischer method)
E 392 EXTRACTS OF ROSEMARY
Synonyms Extract of rosemary leaf (antioxidant)
Definition Extracts of rosemary contain several components, which have been

proven to exert antioxidative functions. These components belong
mainly to the classes of phenolic acids, flavonoids, diterpenoids.
Besides the antioxidant compounds, the extracts can also contain
triterpenes and organic solvent extractable material specifically
defined in the following specification.
Einecs 283-291-9
Chemical name Rosemary extract (Rosmarinus officinalis)
Description Rosemary leaf extract antioxidant is prepared by extraction of the

leaves of Rosmarinus officinalis using a food approved solvent
system. Extracts may then be deodorised and decolourised.
Extracts may be standardised.
Identification
Reference antioxidative compounds: Carnosic acid (C20H28O4) and Carnosol (C20H26O4)

phenolic diterpenes
(which comprise not less than 90 % of the total phenolic diterpenes)
02012R0231 — EN — 27.10.2024 — 033.001 — 123
▼B
Reference key volatiles Borneol, Bornyl Acetate, Camphor, 1,8-Cineol, Verbenone
Density > 0,25 g/ml
Solubility Insoluble in water
Purity
Loss of drying < 5%
1 — Extracts of rosemary produced from dried rosemary leaves by acetone

extraction.
Description Extracts of rosemary are produced from dried rosemary leaves by

acetone extraction, filtration, purification and solvent evaporation,
followed by drying and sieving to obtain a fine powder or a liquid.
Identification
Content of reference antioxidative ≥ 10 % w/w, expressed as the total of carnosic acid and carnosol
compounds
Antioxidant/Volatiles — Ratio (Total % w/w of carnosic acid and carnosol) ≥ 15

(% w/w of reference key volatiles)*
(* as a percentage of total volatiles in the extract, measured by Gas
Chromatography — Mass Spectrometry Detection, ‘GC-MSD’)
Purity
Residual solvents Acetone: Not more than 500 mg/kg
2 — Extracts of rosemary prepared by extraction of dried rosemary leaves

by means of supercritical carbon dioxide.
Description Extracts of rosemary produced from dried rosemary leaves extracted

by means of supercritical carbon dioxide with a small amount of
ethanol as entrainer.
Identification
compounds
Antioxidant/Volatiles – Ratio (Total % w/w of carnosic acid and carnosol) ≥ 15

Chromatography — Mass Spectrometry Detection, ‘GC-MSD’)
Purity
Residual solvents Ethanol: not more than 2 %
3 — Extracts of rosemary prepared from a deodorised ethanolic extract of

rosemary.
Description Extracts of rosemary which are prepared from a deodorised ethanolic

extract of rosemary. The extracts may be further purified, for
example by treatment with active carbon and/or molecular distil
lation. The extracts may be suspended in suitable and approved
carriers or spray dried.
02012R0231 — EN — 27.10.2024 — 033.001 — 124
▼B
Identification
compounds

Chromatography – Mass Spectrometry Detection, ‘GC-MSD’)
Purity
Residual solvents Ethanol: not more than 500 mg/kg
4 — Extracts of rosemary decolourised and deodorised, obtained by a two-

step extraction using hexane and ethanol.
Description Extracts of rosemary which are prepared from a deodorised ethanolic

extract of rosemary, undergone a hexane extraction. The extract may
be further purified, for example by treatment with active carbon and/
or molecular distillation. They may be suspended in suitable and
approved carriers or spray dried.
Identification
compounds

Chromatography – Mass Spectrometry Detection, ‘GC-MSD’)
Purity
Residual solvents Hexane: not more than 25 mg/kg

Ethanol: not more than 500 mg/kg
E 400 ALGINIC ACID
Synonyms
Definition Linear glycuronoglycan consisting mainly of β-(1-4) linked D-man

nuronic and α-(1-4) linked L-guluronic acid units in pyranose ring
form. Hydrophilic colloidal carbohydrate extracted by the use of
dilute alkali from strains of various species of brown seaweeds
(Phaeophyceae)
Einecs 232-680-1
Chemical name
Chemical formula (C6H8O6)n
Molecular weight 10 000-600 000 (typical average)
Assay Alginic acid yields, on the anhydrous basis, not less than 20 % and
not more than 23 % of carbon dioxide (CO2), equivalent to not less
than 91 % and not more than 104,5 % of alginic acid (C6H8O6)n
(calculted on equivalent weight basis of 200)
Description Alginic acid occurs in filamentous, grainy, granular and powdered

forms. It is a white to yellowish brown and nearly odourless
02012R0231 — EN — 27.10.2024 — 033.001 — 125
▼B
Identification
Solubility Insoluble in water and organic solvents, slowly soluble in solutions

of sodium carbonate, sodium hydroxide and trisodium phosphate
Calcium chloride precipitation test To a 0,5 % solution of the sample in 1 M sodium hydroxide solution
add one fifth of its volume of a 2,5 % solution of calcium chloride.
A voluminous, gelatinous precipitate is formed. This test distin
guishes alginic acid from acacia gum, sodium carboxymethyl
cellulose, carboxymethyl starch, carrageenan, gelatin, gum ghatti,
karaya gum, locust bean gum, methyl cellulose and tragacanth gum.
Ammonium sulphate precipitation test To a 0,5 % solution of the sample in 1 M sodium hydroxide solution
add one half of its volume of a saturated solution of ammonium
sulphate. No precipitate is formed. This test distinguishes alginic
acid from agar, sodium carboxymethyl cellulose, carrageenan,
de-esterified pectin, gelatin, locust bean gum, methyl cellulose and
starch.
Colour reaction Dissolve as completely as possible 0,01 g of the sample by shaking

with 0,15 ml of 0,1 N sodium hydroxide and add 1 ml of acid ferric
sulphate solution. Within 5 minutes a cherry-red colour develops that
finally becomes deep purple.
pH Between 2,0 and 3,5 (3 % suspension)
Purity
Sulphated ash Not more than 8 % on the anhydrous basis
Sodium hydroxide (1 M solution) Not more than 2 % on the anhydrous basis

insoluble matter
Formaldehyde Not more than 50 mg/kg
Total plate count Not more than 5 000 colonies per gram
E 401 SODIUM ALGINATE
Synonyms
Definition
Einecs
Chemical name Sodium salt of alginic acid
Chemical formula (C6H7NaO6)n

02012R0231 — EN — 27.10.2024 — 033.001 — 126
▼B
Assay Yields, on the anhydrous basis, not less than 18 % and not more
than 21 % of carbon dioxide corresponding to not less than 90,8 %
and not more than 106,0 % of sodium alginate (calculated on
equivalent weight basis of 222)
Description Nearly odourless, white to yellowish fibrous or granular powder
Identification
Test for alginic acid Passes test
Purity
Water insoluble matter Not more than 2 % on the anhydrous basis
E 402 POTASSIUM ALGINATE
Synonyms
Definition
Einecs
Chemical name Potassium salt of alginic acid
Chemical formula (C6H7KO6)n
Assay Yields, on the anhydrous basis, not less than 16,5 % and not more
than 19,5 % of carbon dioxide corresponding to not less than 89,2 %
and not more than 105,5 % of potassium alginate (calculated on an
Identification
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 127
▼B
E 403 AMMONIUM ALGINATE
Synonyms
Definition
Einecs
Chemical name Ammonium salt of alginic acid
Chemical formula (C6H11NO6)n
than 21 % of carbon dioxide corresponding to not less than 88,7 %
and not more than 103,6 % ammonium alginate (calculated on an
Description White to yellowish fibrous or granular powder
Identification
Purity
Sulphated ash Not more than 7 % on the dried basis

02012R0231 — EN — 27.10.2024 — 033.001 — 128
▼B
E 404 CALCIUM ALGINATE
Synonyms Calcium salt of alginate
Definition
Einecs
Chemical name Calcium salt of alginic acid
Chemical formula (C6H7Ca1/2O6)n
than 21 % carbon dioxide corresponding to not less than 89,6 % and
not more than 104,5 % of calcium alginate (calculated on an
Identification
Purity
E 405 PROPANE-1,2-DIOL ALGINATE
Synonyms Hydroxypropyl alginate; 1,2-Propanediol ester of alginic acid;

Propylene glycol alginate
Definition
Einecs
Chemical name 1,2-Propanediol ester of alginic acid; varies in composition

according to its degree of esterification and the percentage of free
and neutralised carboxyl groups in the molecule
Chemical formula (C9H14O7)n (esterified)
than 20 % of carbon dioxide (CO2)
Description Nearly odourless, white to yellowish brown fibrous or granular

powder
02012R0231 — EN — 27.10.2024 — 033.001 — 129
▼B
Identification
Test for 1,2-propanediol Passes test (after hydrolysis)
Test for alginic acid Passes test (after hydrolysis)
Purity
Total propane-1,2-diol content Not less than 15 % and not more than 45 %
Free propane-1,2-diol content Not more than 15 %
E 406 AGAR
Synonyms Gelose; Kanten, Bengal, Ceylon, Chinese or Japanese isinglass;

Layor Carang
Definition Agar is a hydrophilic colloidal polysaccharide consisting mainly of

galactose units with a regular alternation of L and D isomeric forms.
These hexoses are alternately linked with alpha-1,3 and beta-1,4
bonds in the copolymer. On about every tenth D-galactopyranose
unit one of the hydroxyl groups is esterified with sulphuric acid
which is neutralised by calcium, magnesium, potassium or sodium.
It is extracted from certain strains of marine algae of the families
Gelidiaceae and Gracilariaceae and relevant red algae of the class
Rhodophyceae
Einecs 232-658-1
Chemical name
Chemical formula
Molecular weight
Assay The threshold gel concentration should not be higher than 0,25 %
Description Agar is odourless or has a slight characteristic odour. Unground agar

usually occurs in bundles consisting of thin, membranous, agglu
tinated strips, or in cut, flaked or granulated forms. It may be
light yellowish-orange, yellowish-grey to pale yellow, or colourless.
It is tough when damp, brittle when dry. Powdered agar is white to
yellowish-white or pale yellow. When examined in water under a
microscope, agar powder appears more transparent. In chloral
hydrate solution, the powdered agar appears more transparent than
in water, more or less granular, striated, angular and occasionally
contains frustules of diatoms. Gel strength may be standardised by
the addition of dextrose and maltodextrines or sucrose
02012R0231 — EN — 27.10.2024 — 033.001 — 130
▼B
Identification
Solubility Insoluble in cold water; soluble in boiling water
Purity
Ash Not more than 6,5 % on the anhydrous basis determined at 550 °C
Acid-insoluble ash (insoluble in approxi Not more than 0,5 % determined at 550 °C on the anhydrous basis
mately 3N Hydrochloric acid)
Insoluble matter (after stirring for 10 Not more than 1,0 %

minutes in hot water)
Starch Not detectable by the following method: to a 1 in 10 solution of the

sample add a few drops of iodine solution. No blue colour is
produced
Gelatin and other proteins Dissolve about 1 g of agar in 100 ml of boiling water and allow to
cool of about 50 °C. To 5 ml of the solution add 5 ml of trinitro
phenol solution (1 g of anhydrous trinitrophenol/100 ml of hot
water). No turbidity appears within 10 minutes
Water absorption Place 5 g to agar in a 100 ml graduated cylinder, fill to the mark
with water, mix and allow to stand at about 25 °C for 24 hours.
Pour the contents of the cylinder through moistened glass wool,
allowing the water to drain into a second 100 ml graduated
cylinder. Not more than 75 ml of water is obtained
E 407 CARRAGEENAN
Synonyms Products of commerce are sold under different names such as:
Irish moss gelose; Eucheuman (from Eucheuma spp.); Iridophycan
(from Iridaea spp.); Hypnean (from Hypnea spp.); Furcellaran or
Danish agar (from Furcellaria fastigiata); Carrageenan (from
Chondrus and Gigartina spp.)
Definition Carrageenan is obtained by extraction with water or dilute aqueous

alkali of strains of seaweeds of Gigartinaceae, Solieriaceae,
Hypneaceae and Furcellariaceae, families of the class Rhodo
phyceae (red seaweeds).
Carrageenan consists chiefly of the potassium, sodium, magnesium
and calcium sulphate esters of galactose and 3,6-anhydrogalactose
polysacharide. These hexoses are alternately linked α-1,3 and β-1,4
in the copolymer.
02012R0231 — EN — 27.10.2024 — 033.001 — 131
▼B
The prevalent polysaccharides in carrageenan are designated as

kappa, iota, lambda depending on the number of sulphate by
repeating unit (i.e. 1,2,3 sulphate). Between kappa and iota there
is a continuum of intermediate compositions differing in number
of sulphates per repeat units between 1 and 2.
During the process, no organic precipitant shall be used other than
methanol, ethanol and propan-2-ol.
The wording carrageenan is reserved for the non hydrolysed or
otherwise chemically degraded polymer.
Formaldehyde may be present as an adventitious impurity up to a
maximum of 5 mg/kg.
Einecs 232-524-2
Chemical name Sulphate esters of polygalactose
Chemical formula
Molecular weight
Assay
Description Yellowish to colourless, coarse to fine powder which is practically

odourless
Identification
Test for galactose Passes test
Test for anhydrogalactose Passes test
Test for sulphate Passes test
Solubility Soluble in hot water; insoluble in alcohol for a 1,5 % dilution
Purity
Solvent residues Not more than 0,1 % of methanol, ethanol, propan-2-ol, singly or in
combination
Viscosity Not less than 5 mPa.s (1,5 % solution at 75 °C)
Sulphates Not less than 15 % and not more than 40 % on the dried basis (as
SO4)
Ash Not less than 15 % and not more than 40 % determined on the dried
basis at 550 °C
Acid-insoluble ash Not more than 1 % on the dried basis (insoluble in 10 % hydro
chloric acid)
Acid-insoluble matter Not more than 2 % on the dried basis (insoluble in 1 % v/v
sulphuric acid)
Low molecular weight carrageenan Not more than 5 %

(Molecular weight fraction below 50 kDa)
02012R0231 — EN — 27.10.2024 — 033.001 — 132
▼B
E 407a PROCESSED EUCHEUMA SEAWEED
Synonyms PES (acronym for processed eucheuma seaweed). The PES obtained
from Euchema cottonii is generally called kappa PES and the PES
from Euchema spinosum iota PES.
Definition Processed eucheuma seaweed is obtained by aqueous alkaline

(KOH) treatment at high temperature of the strains of seaweeds
Eucheuma cottonii and Eucheuma spinosum, of the class Rhodo
phyceae (red seaweeds) followed by fresh water washing to
remove impurities and drying to obtain the product. Further purifi
cation may be achieved by washing with an alcohol. The alcohols
authorised are restricted to methanol, ethanol or propan-2-ol. The
product consists chiefly of the potassium, sodium, magnesium and
calcium sulphate esters of galactose and 3,6-anhydrogalactose poly
saccharide. Up to 15 % algal cellulose is also present in the product.
The wording processed eucheuma seaweed is reserved to the non
hydrolysed or otherwise chemically degraded polymer. Formal
dehyde may be present up to a maximum of 5 mg/kg.
Description Tan to yellowish, coarse to fine powder which is practically

odourless
Identification
Test for anhydrogalactose Passes test
Solubility Forms cloudy viscous suspensions in water. Insoluble in ethanol for

a 1,5 % solution.
Purity
Solvent residues Not more than 0,1 % of methanol, ethanol, propan-2-ol, singly or in
combination
Viscosity Not less than 5 mPa.s (1,5 % solution at 75 °C)
Sulphate Not less than 15 % and not more than 40 % on the dried basis (as
SO4)
Ash Not less than 15 % and not more than 40 % determined on the dried
basis at 550 °C
Acid-insoluble ash Not more than 1 % on the dried basis (insoluble in 10 % hydro
chloric acid)
Acid-insoluble matter Not less than 8 % and not more than 15 % on the dried basis
(insoluble in 1 % v/v sulphuric acid)
Low molecular weight carrageenan Not more than 5 %

(Molecular weight fraction below 50
kDa)

02012R0231 — EN — 27.10.2024 — 033.001 — 133
▼B
E 410 LOCUST BEAN GUM
Synonyms Carob bean gum; Algaroba gum
Definition Locust bean gum is the ground endosperm of the seeds of the strains
of carob tree, Cerationia siliqua (L.) Taub. (family Leguminosae).
Consists mainly of a high molecular weight hydrocolloidal polysac
charide, composed of galactopyranose and mannopyranose units
combined through glycosidic linkages, which may be described
chemically as galactomannan
Einecs 232-541-5
Chemical name
Chemical formula
Molecular weight 50 000-3 000 000
Assay Galactomannan content not less than 75 %
Description White to yellowish-white, nearly odourless powder
Identification
Test for mannose Passes test
Microscopic examination Place some ground sample in an aqueous solution containing 0,5 %
iodine and 1 % potassium iodide on a glass slide and examine under
microscope. Locust bean gum contains long stretched tubiform cells,
separated or slightly interspaced. Their brown contents are much less
regularly formed than in guar gum. Guar gum shows close groups of
round to pear shaped cells. Their contents are yellow to brown
Solubility Soluble in hot water, insoluble in ethanol
Purity
Ash Not more than 1,2 % determined at 800 °C
Protein (N × 6,25) Not more than 7 %
Acid-insoluble matter Not more than 4 %

sample add a few drops of iodine solution. No blue colour is
produced

02012R0231 — EN — 27.10.2024 — 033.001 — 134
▼B
Ethanol and propan-2-ol Not more than 1 %, single or in combination
E 412 GUAR GUM
Synonyms Gum cyamopsis; Guar flour

Definition Guar gum is the ground endosperm of the seeds of strains of the guar
plant, Cyamopsis tetragonolobus (L.) Taub. (family Leguminosae).
Consists mainly of a high molecular weight hydrocolloidal polysac
charide composed of galactopyranose and mannopyranose units
combined through glycosidic linkages, which may be described
chemically as galactomannan. The gum may be partially hydrolysed
by either heat treatment, mild acid or alcaline oxidative treatment for
viscosity adjustment.
Einecs 232-536-0
Chemical name
Chemical formula
Molecular weight 50 000-8 000 000
Assay Galactomannan content not less than 75 %
Description A white to yellowish-white, nearly odourless powder
Identification
Test for mannose Passes test
Solubility Soluble in cold water
Purity
Ash Not more than 5,5 % determined at 800 °C
Acid-insoluble matter Not more than 7 %
Protein Not more than 10 % (factor N x 6,25)
sample add a few drops of iodine solution. (No blue colour is
produced)
Organic peroxides Not more than 0,7 meq active oxygen/kg sample
Furfural Not more than 1 mg/kg
Pentachlorophenol Not more than 0,01 mg/kg
E 413 TRAGACANTH
Synonyms Tragacanth gum; Tragant

Definition Tragacanth is a dried exudation obtained from the stems and
branches of strains of Astragalus gummifer Labillardiere and other
Asiatic species of Astragalus (family Leguminosae). It consists
mainly of high molecular weight polysaccharides (galactoarabans
and acidic polysaccharides) which, on hydrolysis, yield galacturonic
acid, galactose, arabinose, xylose and fucose. Small amounts of
rhamnose and of glucose (derived from traces of starch and/or
cellulose) may also be present
02012R0231 — EN — 27.10.2024 — 033.001 — 135
▼B
Einecs 232-252-5
Chemical name
Chemical formula
Molecular weight Approximately 800 000
Assay
Description Unground Tragacanth gum occurs as flattened, lamellated, straight or

curved fragments or as spirally twisted pieces 0,5-2,5 mm thick and
up to 3 cm in length. It is white to pale yellow in colour but some
pieces may have a red tinge. The pieces are horny in texture, with a
short fracture. It is odourless and solutions have an insipid muci
laginous taste. Powdered tragacanth is white to pale yellow or
pinkish brown (pale tan) in colour
Identification
Solubility 1 g of the sample in 50 ml of water swells to form a smooth, stiff,

opalescent mucilage; insoluble in ethanol and does not swell in 60 %
(w/v) aqueous ethanol
Purity
Test for Karaya gum Negative. Boil 1 g with 20 ml of water until a mucilage is formed.
Add 5 ml of hydrochloric acid and again boil the mixture for five
minutes. No permanent pink or red colour develops
Total ash Not more than 4 %
Acid insoluble ash Not more than 0,5 %
Acid insoluble matter Not more than 2 %
E 414 ACACIA GUM
Synonyms Gum arabic
Definition Acacia gum is a dried exudation obtained from the stems and
branches of strains of Acacia senegal (L) Willdenow or closely
related species of Acacia (family Leguminosae). It consists mainly
of high molecular weight polysaccharides and their calcium,
magnesium and potassium salts, which on hydrolysis yield
arabinose, galactose, rhamnose and glucuronic acid
Einecs 232-519-5
Chemical name
Chemical formula
Assay
02012R0231 — EN — 27.10.2024 — 033.001 — 136
▼B
Description Unground acacia gum occurs as white or yellowish-white spheroidal

tears of varying sizes or as angular fragments and is sometimes
mixed with darker fragments. It is also available in the form of
white to yellowish-white flakes, granules, powder or spray-dried
material.
Identification
Solubility 1 g dissolves in 2 ml of cold water forming a solution which flows

readily and is acid to litmus, insoluble in ethanol
Purity
Loss on drying Not more than 17 % (105 °C, 5 hours) for granular and not more
than 10 % (105 °C, 4 hours) for spray-dried material
Starch or dextrin Boil a 1 in 50 solution of the gum and cool. To 5 ml add 1 drop of
iodine solution. No bluish or reddish colours are produced
Tannin To 10 ml of a 1 in 50 solution add about 0,1 ml of ferric chloride

solution (9 g FeCl3.6H2O made up to 100 ml with water).
No blackish colouration or blackish precipitate is formed
Hydrolysis products Mannose, xylose and galacturonic acid are absent (determined by
chromatography)
E 415 XANTHAN GUM
Synonyms
Definition Xanthan gum is a high molecular weight polysaccharide gum

produced by a pure-culture fermentation of a carbohydrate with
strains of Xanthomonas campestris, purified by recovery with
ethanol or propan-2-ol, dried and milled. It contains D-glucose and
D-mannose as the dominant hexose units, along with D-glucuronic
acid and pyruvic acid, and is prepared as the sodium, potassium or
calcium salt. Its solutions are neutral
Einecs 234-394-2
Chemical name
Chemical formula
Molecular weight Approximately 1 000 000
Assay Yields, on dried basis, not less than 4,2 % and not more than 5 % of
CO2 corresponding to between 91 % and 108 % of xanthan gum
02012R0231 — EN — 27.10.2024 — 033.001 — 137
▼B
Description Cream-coloured powder
Identification
Solubility Soluble in water. Insoluble in ethanol
Purity
Loss on drying Not more than 15 % (105 °C, 2,5 hours)
Total ash Not more than 16 % on the anhydrous basis determined at 650 °C
after drying at 105 °C for four hours
Pyruvic acid Not less than 1,5 %
Nitrogen Not more than 1,5 %
Ethanol and propan-2-ol Not more than 500 mg/kg singly or in combination
Xanthomonas campestris Viable cells absent in 1 g
E 416 KARAYA-GUM
Synonyms Katilo; Kadaya; Gum sterculia; Sterculia; Karaya, gum karaya;

Kullo; Kuterra
Definition Karaya gum is a dried exudation from the stems and branches of
strains of: Sterculia urens Roxburgh and other species of Sterculia
(family Sterculiaceae) or from Cochlospermum gossypium A.P. De
Candolle or other species of Cochlospermum (family Bixaceae). It
consists mainly of high molecular weight acetylated polysaccharides,
which on hydrolysis yield galactose, rhamnose, and galacturonic
acid, together with minor amounts of glucuronic acid
Einecs 232-539-4
Chemical name
Chemical formula
Molecular weight
Assay
Description Karaya gum occurs in tears of variable size and in broken irregular
pieces having a characteristic semi-crystalline appearance. It is pale
yellow to pinkish brown in colour, translucent and horny. Powdered
karaya gum is a pale grey to pinkish brown. The gum has a
distinctive odour of acetic acid
Identification
Solubility Insoluble in ethanol
Swelling in ethanol solution Karaya gum swells in 60 % ethanol distinguishing it from other
gums
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 138
▼B
Acid insoluble ash Not more than 1 %
Volatile acid Not less than 10 % (as acetic acid)
Starch Not detectable
E 417 TARA GUM
Definition Tara gum is obtained by grinding the endosperm of the seeds of

strains of Caesalpinia spinosa (family Leguminosae). It consists
chiefly of polysaccharides of high molecular weight composed
mainly of galactomannans. The principal component consists of a
linear chain of (1-4)-β-D-mannopyranose units with α-D-galactopy
ranose units attached by (1-6) linkages. The ratio of mannose to
galactose in tara gum is 3:1. (In locust bean gum this ratio is 4:1
and in guar gum 2:1)
Einecs 254-409-6
Chemical name
Chemical formula
Molecular weight
Assay
Description A white to white-yellow odourless powder
Identification
Solubility Soluble in water, insoluble in ethanol
Gel formation To an aqueous solution of the sample add small amounts of sodium
borate. A gel is formed
Purity
Loss on drying Not more than 15 %
Ash Not more than 1,5 %
Protein Not more than 3,5 % (factor N x 5,7)

02012R0231 — EN — 27.10.2024 — 033.001 — 139
▼B
E 418 GELLAN GUM
Synonyms
Definition Gellan gum is a high molecular weight polysaccharide gum

produced by a pure culture fermentation of a carbohydrate by
strains of Pseudomonas elodea, purified by recovery with
propan-2-ol or ethanol, dried, and milled. The high molecular
weight polysaccharide is principally composed of a tetrasaccharide
repeating unit of one rhamnose, one glucuronic acid, and two
glucoses, and substituted with acyl (glyceryl and acetyl) groups as
the O-glycosidically linked esters. The glucuronic acid is neutralised
to a mixed potassium, sodium, calcium, and magnesium salt
Einecs 275-117-5
Chemical name
Chemical formula
Assay Yields, on the dried basis, not less than 3,3 % and not more than
6,8 % of CO2
Description An off-white powder
Identification
Solubility Soluble in water, forming a viscous solution.

Insoluble in ethanol
Purity
Loss on drying Not more than 15 % after drying (105 °C, 2,5 hours)
Nitrogen Not more than 3 %
Propan-2-ol Not more than 750 mg/kg
Escherichia coli Negative in 5 g
Salmonella spp. Negative in 10 g
E 420 (i) SORBITOL
Synonyms D-glucitol; D-sorbitol
Definition Sorbitol is obtained by hydrogenation of D-glucose. It is mainly

composed of D-sorbitol. According to the level of D-glucose, the
part of the products which is not D-sorbitol is composed of related
substances such as mannitol, iditol, maltitol.
Einecs 200-061-5
Chemical name D-glucitol

02012R0231 — EN — 27.10.2024 — 033.001 — 140
▼B
Assay Content not less than 97 % of total glycitols and not less than 91 %
of D-sorbitol on dry weight basis (glycitols are compounds with the
structural formula CH2OH-(CHOH)n-CH2OH, where ‘n’ is an
integer).
Description White hygroscopic powder, crystalline powder, flakes or granules.
Appearance of the aqueous solution: The solution is clear.
Identification
Solubility Very soluble in water, slightly soluble in ethanol
Melting range 88 to 102 °C
Sorbitol monobenzylidene derivative To 5 g of the sample add 7 ml of methanol, 1 ml of benzaldehyde

and 1 ml of hydrochloric acid. Mix and shake in a mechanical
shaker until crystals appear. Filter with the aid of suction, dissolve
the crystals in 20 ml of boiling water containing 1 g of sodium
bicarbonate, filter while hot, cool the filtrate, filter with suction,
wash with 5 ml of methanol-water mixture (1 in 2) and dry in air.
The crystals so obtained melt between 173 and 179 °C
▼M4
Purity
Water content Not more than 1,5 % (Karl Fischer Method)
Conductivity Not more than 20 μS/cm (on 20 % dry solids solution) at

temperature 20 °C
Reducing sugars Not more than 0,3 % (expressed as glucose on dry weight basis)
Total sugars Not more than 1 % (expressed as glucose on dry weight basis)
Nickel Not more than 2 mg/kg (expressed on dry weight basis)
Arsenic Not more than 3 mg/kg (expressed on dry weight basis)
Lead Not more than 1 mg/kg (expressed on dry weight basis)
▼B
E 420 (ii) SORBITOL SYRUP
Synonyms D-glucitol syrup
Definition Sorbitol syrup formed by hydrogenation of glucose syrup is

composed of D-sorbitol, D-mannitol and hydrogenated saccharides.
The part of the product which is not D-sorbitol is composed mainly
of hydrogenated oligosaccharides formed by the hydrogenation of
glucose syrup used as raw material (in which case the syrup is
non-crystallising) or mannitol. Minor quantities of glycitols where
n ≤ 4 may be present (glycitols are compounds with the structural
formula CH2OH-(CHOH)n-CH2OH, where ‘n’ is an integer)
Einecs 270-337-8
Chemical name
Chemical formula
Molecular weight
Assay Content not less than 69 % total solids and not less than 50 % of
D-sorbitol on the anhydrous basis
02012R0231 — EN — 27.10.2024 — 033.001 — 141
▼B
Description Clear and colourless aqueous solution
Identification
Solubility Miscible with water, with glycerol, and with propane-1,2-diol
Sorbitol monobenzylidene derivative To 5 g of the sample add 7 ml of methanol, 1 ml of benzaldehyde

shaker until crystals appear. Filter with the aid of suction, dissolve
the crystals in 20 ml of boiling water containing 1 g of sodium
bicarbonate, filter while hot. Cool the filtrate filter with suction,
wash with 5 ml of methanol-water mixture (1 in 2) and dry in air.
The crystals so obtained melt between 173 and 179 °C
▼M4
Purity
Conductivity Not more than 10 μS/cm (on the product as such) at temperature
20 °C
E 421 (i) MANNITOL BY HYDROGENATION

▼B
(i) MANNITOL
Synonyms D-mannitol
▼M4
Definition Manufactured by catalytic hydrogenation of carbohydrate solutions
containing glucose and/or fructose.
The product contains min. 96 % mannitol. The part of the product
which is not mannitol is mainly composed of sorbitol (2 % max),
maltitol (2 % max) and isomalt (1,1 GPM (1-O-alpha-D-Glucopy
ranosyl-D-mannitol dehydrate): 2 % max and 1,6 GPS (6-O-alpha-
D- Glucopyranosyl-D-Sorbitol): 2 % max). Unspecified impurities
shall not represent more than 0,1 % of each.
▼B
Einecs 200-711-8
Chemical name D-mannitol
Assay Content not less than 96,0 % D-mannitol and not more than 102 %
on the dried basis
Description White, odourless, crystalline powder
Identification
Solubility Soluble in water, very slightly soluble in ethanol, practically

insoluble in ether
Melting range Between 164 and 169 °C
Infrared absorption spectrometry Comparison with a reference standard e.g. EP or USP
Specific rotation [α]D20 + 23° to + 25° (borate solution)

02012R0231 — EN — 27.10.2024 — 033.001 — 142
▼B
pH Between 5 and 8. Add 0,5 ml of a saturated solution of potassium
chloride to 10 ml of a 10 % w/v solution of the sample, then
measure the pH
▼M4
Purity

temperature 20 °C
Reducing sugars Not more than 0,3 % (expressed as glucose)
Total sugars Not more than 1 % (expressed as glucose)
▼B
(ii) MANNITOL MANUFACTURED BY FERMENTATION
Synonyms D-mannitol
Definition Manufactured by discontinuous fermentation under aerobic

conditions using a conventional strain of the yeast Zygosacchar
omyces rouxii. The part of the product which is not mannitol is
mainly composed of sorbitol, maltitol and isomalt.
Einecs 200-711-8
Chemical name D-mannitol
Assay Not less than 99 % on the dried basis
Description White, odourless crystalline powder
Identification
Solubility Soluble in water, very slightly soluble in ethanol, practically

insoluble in ether
Melting range Between 164 and 169 °C
Infrared absorption spectrometry Comparison with a reference standard e.g. EP or USP
Specific rotation [α]D20 + 23° to + 25° (borate solution)
pH Between 5 and 8
Add 0,5 ml of a saturated solution of potassium chloride to 10 ml of
a 10 % w/v solution of the sample, then measure the pH
▼M4
Purity
Arabitol Not more than 0,3 %

temperature 20 °C
Reducing sugars Not more than 0,3 % (expressed as glucose)
Total sugars Not more than 1 % (expressed as glucose)

02012R0231 — EN — 27.10.2024 — 033.001 — 143
▼B
Aerobic mesophilic bacteria Not more than 1 000 colonies per gram
Coliforms Absent in 10 g
Staphylococcus aureus Absent in 10 g
Pseudomonas aeruginosa Absent in 10 g
Moulds Not more than 100 colonies per gram
Yeasts Not more than 100 colonies per gram
▼M41
E 422 GLYCEROL
Synonyms Glycerin; Glycerine
Definition Glycerol is obtained only from vegetable oils and fats, either directly
or from the crude glycerol obtained as a by-product of biodiesel
production and undergoes purification processes that involve distil
lation, and other clean up steps to obtain refined glycerol.
Einecs 200-289-5
Chemical name 1,2,3-propanetriol; Glycerol; Trihydroxypropane
Assay Content not less than 98 % of glycerol on the anhydrous basis
Description Clear, colourless hygroscopic syrupy liquid with not more than a
slight characteristic odour, which is neither harsh nor disagreeable
Identification
Specific gravity (25 °C/25 °C) Not less than 1,257
Refractive index [n]D20 between 1,471 and 1,474
Purity
Sulphated ash Not more than 0,01 % determined at 800 ± 25 °C
Butanetriols Not more than 0,2 %
Acrolein Not more than 3 mg/kg
Fatty acids and esters Not more than 0,1 % calculated as butyric acid
Chlorinated compounds Not more than 30 mg/kg (as chlorine)
3-Monochloropropane-1,2-diol (3- MCPD) Not more than 0,1 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 144
▼M7
E 423 OCTENYL SUCCINIC ACID MODIFIED GUM ARABIC
Synonyms Gum arabic hydrogen octenylbutandioate; Gum arabic hydrogen

octenylsuccinate; OSA modified gum arabic; OSA modified gum
acacia
Definition Octenyl succinic acid modified gum arabic is produced by este

rifying gum arabic (Acacia seyal), or gum arabic (Acacia senegal)
in aqueous solution with not more than 3 % of octenyl succinic acid
anhydride. It is subsequently spray dried.
Einecs
Chemical name
Chemical formula
Weight Average Molecular Weight Fraction (i): 3,105 g/mol

Fraction (ii) 1,106 g/mol
Assay
Description Off-white to light tan, free flowing powder
Identification
Viscosity of a 5 % solution at 25 °C Not more than 30 mPa.s.
Precipitation reaction Forms flocculent precipitate in lead sub-acetate solution (TS)
Solubility Freely soluble in water; insoluble in ethanol
pH for a 5 % aqueous solution 3,5 to 6,5
Purity
Loss on drying Not more than 15 % (105 °C, 5 h)
Degree of esterification Not more than 0,6 %
Total ash Not more than 10 % (530 °C)
Acid-insoluble ash Not more than 0,5 %
Test for starch or dextrine Boil a 1 in 50 aqueous solution of the sample, add about 0,1 ml
iodine TS. No bluish or reddish colour should be produced.
Test for tannin-bearing gums To 10 ml of a 1 in 50 aqueous solution of the sample add about
0,1 ml ferric chloride TS. No blackish coloration or blackish
precipitate should be formed.
Residual octenyl succinic acid Not more than 0,3 %
Salmonella sp. Absent in 25 g

02012R0231 — EN — 27.10.2024 — 033.001 — 145
▼B
E 425 (i) KONJAC GUM
Synonyms
Definition Konjac gum is a water-soluble hydrocolloid obtained from the
Konjac flour by aqueous extraction. Konjac flour is the unpurified
raw product from the root of the perennial plant Amorphophallus
konjac. The main component of Konjac gum is the water-soluble
high-molecular-weight polysaccharide glucomannan, which consists
of D-mannose and D-glucose units at a molar ratio of 1,6:1,0,
connected by β(1-4)-glycosidic bonds. Shorter side chains are
attached through β(1-3)-glycosidic bonds, and acetyl groups occur
at random at a ratio of about 1 group per 9 to 19 sugar units
Einecs
Chemical name
Chemical formula
Molecular weight The main component, glucomannan, has an average molecular
weight of 200 000 to 2 000 000
Assay Not less than 75 % carbohydrate
Description A white to cream to light tan powder
Identification
Solubility Dispersible in hot or cold water forming a highly viscous solution
with a pH between 4,0 and 7,0
Gel formation Add 5 ml of a 4 % sodium borate solution to a 1 % solution of the
sample in a test tube, and shake vigorously. A gel forms
Formation of heat-stable gel Prepare a 2 % solution of the sample by heating it in a boiling water
bath for 30 min, with continuous agitation and then cooling the
solution to room temperature. For each g of the sample used to
prepare 30 g of the 2 % solution, add 1 ml of 10 % potassium
carbonate solution to the fully hydrated sample at ambient
temperature. Heat the mixture in a water bath to 85 °C, and
maintain for 2 h without agitation. Under these conditions a
thermally stable gel is formed
Purity
Starch Not more than 3 %
Protein Not more than 3 % (factor N × 5,7)
Viscosity (1 % solution) Not less than 3 kgm– 1s– 1
at 25 °C
Ether-soluble material Not more than 0,1 %
Total ash Not more than 5,0 % (800 °C, 3 to 4 hours)
Salmonella spp. Absent in 12,5 g
E 425 (ii) KONJAC GLUCOMANNAN
Synonyms
Definition Konjac glucomannan is a water-soluble hydrocolloid obtained from

Konjac flour by washing with water-containing ethanol. Konjac flour
is the unpurified raw product from the tuber of the perennial plant
Amorphophallus konjac. The main component is the water-soluble
high-molecular-weight polysaccharide glucomannan, which consists
of D-mannose and D-glucose units at a molar ratio of 1,6:1,0,
connected by β(1-4)-glycosidic bonds with a branch at about each
50th or 60th unit. About each 19th sugar residue is acetylated
02012R0231 — EN — 27.10.2024 — 033.001 — 146
▼B
Einecs
Chemical name
Chemical formula
Molecular weight 500 000 to 2 000 000
Assay Total dietary fibre: not less than 95 % on a dry weight basis
Description White to slightly brownish fine particle size, free flowing and
odourless powder
Identification
Solubility Dispersible in hot or cold water forming a highly viscous solution

with a pH between 5,0 and 7,0. Solubility is increased by heat and
mechanical agitation
Formation of heat-stable gel Prepare a 2 % solution of the sample by heating it in a boiling water
bath for 30 min, with continuous agitation and then cooling the
solution to room temperature. For each g of the sample used to
prepare 30 g of the 2 % solution, add 1 ml of 10 % potassium
carbonate solution to the fully hydrated sample at ambient
temperature. Heat the mixture in a water bath to 85 °C, and
maintain for 2 h without agitation. Under these conditions a
thermally stable gel is formed
Purity
Starch Not more than 1 %
Viscosity (1 % solution) Not less than 20 kgm– 1s– 1

at 25 °C
Protein Not more than 1,5 % (N × 5,7)

Determine nitrogen by Kjeldahl method. The percentage of nitrogen
in the sample multiplied by 5,7 gives the percent of protein in the
sample
Ether-soluble material Not more than 0,5 %
Sulphite (as SO2) Not more than 4 mg/kg
50 % Alcohol-soluble material Not more than 2,0 %
Total ash Not more than 2,0 % (800 °C, 3 to 4 hours)
Salmonella spp. Absent in 12,5 g
E 426 SOYBEAN HEMICELLULOSE
Synonyms
Definition Soybean Hemicellulose is a refined water-soluble polysaccharide

obtained from strain soybean fibre by hot water extraction.
No organic precipitant shall be used other than ethanol
Einecs
Chemical name Water soluble soybean polysaccharides; Water soluble soybean fibre
Chemical formula
Molecular weight
Assay Not less than 74 % carbohydrate

02012R0231 — EN — 27.10.2024 — 033.001 — 147
▼B
Description Free flowing white or yellowish white powder
Identification
Solubility Soluble in hot and cold water without gel formation
pH 5,5 ± 1,5 (1 % solution)
Purity
Protein Not more than 14 %
Viscosity Not more than 200 mPa.s (10 % solution)
Total ash Not more than 9,5 % (600 °C, 4 hours)
Ethanol Not more than 2 %
E 427 CASSIA GUM
Synonyms
Definition Cassia gum is the ground purified endosperm of the seeds of Cassia
tora and Cassia obtusifoli (Leguminosae) containing less than
0,05 % of Cassia occidentalis. It consists mainly of high
molecular weight polysaccharides composed primarily of a linear
chain of 1,4-β-D-mannopyranose units linked with 1,6-α-D-galac
topyranose units. The ratio of mannose to galactose is about 5:1.
In the manufacture the seeds are dehusked and degermed by thermal
mechanical treatment followed by milling and screening of the
endosperm. The ground endosperm is further purified by extraction
with propan-2-ol.
Assay Not less than 75 % of Galactomannan
Description Pale yellow to off-white, odourless powder
Identification
Solubility Insoluble in ethanol. Disperses well in cold water forming a colloidal

solution.
Gel formation with borate To an aqueous dispersion of the sample add sufficient sodium borate
test solution (TS) to raise the pH to above 9; a gel is formed.
Gel formation with xanthan gum Weigh 1,5 g of the sample and 1,5 g of xanthan gum and blend
them. Add this blend (with rapid stirring) into 300 ml water at 80 °C
in a 400 ml beaker. Stir until the mixture is dissolved and continue
stirring for an extra 30 min after dissolution (maintain the
temperature above 60 °C during the stirring process). Discontinue
stirring and allow the mixture to cool at room temperature for at
least 2 h.
02012R0231 — EN — 27.10.2024 — 033.001 — 148
▼B
A firm, viscoelastic gel forms after the temperature drops below

40 °C, but no such gel forms in a 1 % control solution of cassia
gum or xanthan gum alone prepared in a similar manner.
Viscosity Less than 500 mPa.s (25 °C, 2h, 1 % solution) corresponding to an
average molecular weight of 200 000-300 000 Da
Purity
Acid insoluble matter Not more than 2,0 %
pH 5,5-8 (1 % aqueous solution)
Crude fat Not more than 1 %
Protein Not more than 7 %
Total ash Not more than 1,2 %
Loss on drying Not more than 12 % (5h, 105 °C)
Total anthraquinones Not more than 0,5 mg/kg(detection limit)
Solvent residues Not more than 750 mg/kg Propan-2-ol
Total plate count Not more than 5 000 colony forming units per gram
Yeast and moulds Not more than 100 colony forming units per gram
E 431 POLYOXYETHYLENE (40) STEARATE
Synonyms Polyoxyl (40) stearate; Polyoxyethylene (40) monostearate

Definition A mixture of the mono- and diesters of edible commercial stearic
acid and mixed polyoxyethylene diols (having an average polymer
length of about 40 oxyethylene units) together with free polyol
Einecs
Chemical name
Chemical formula
Molecular weight
Description Cream-coloured flakes or waxy solid at 25 °C with a faint odour
Identification
Solubility Soluble in water, ethanol, methanol and ethyl acetate. Insoluble in
mineral oil
Congealing range 39-44 °C
Infrared absorption spectrum Characteristic of a partial fatty acid ester of a polyoxyethylated
polyol
Purity
Acid value Not more than 1
Saponification value Not less than 25 and not more than 35
Hydroxyl value Not less than 27 and not more than 40
1,4-Dioxane Not more than 5 mg/kg
02012R0231 — EN — 27.10.2024 — 033.001 — 149
▼M37
__________
▼B
Ethylene glycols (mono- and di-) Not more than 0,25 %
E 432 POLYOXYETHYLENE SORBITAN MONOLAURATE (POLY

SORBATE 20)
Synonyms Polysorbate 20; Polyoxyethylene (20) sorbitan monolaurate

Definition A mixture of the partial esters of sorbitol and its mono- and dian
hydrides with edible commercial lauric acid and condensed with
approximately 20 moles of ethylene oxide per mole of sorbitol
and its anhydrides
Einecs
Chemical name
Chemical formula
Molecular weight
Assay Content not less than 70 % of oxyethylene groups, equivalent to not
less than 97,3 % of polyoxyethylene (20) sorbitan monolaurate on
the anhydrous basis
Description A lemon to amber-coloured oily liquid at 25 °C with a faint char
acteristic odour
Identification
Solubility Soluble in water, ethanol, methanol, ethyl acetate and dioxane.
Insoluble in mineral oil and petroleum ether
polyol
Purity
1,4-dioxane Not more than 5 mg/kg
▼M37
__________
▼B
E 433 POLYOXYETHYLENE SORBITAN MONOOLEATE (POLY

SORBATE 80)
Synonyms Polysorbate 80; Polyoxyethylene (20) sorbitan monooleate

hydrides with edible commercial oleic acid and condensed with
and its anhydrides
02012R0231 — EN — 27.10.2024 — 033.001 — 150
▼B
Einecs
Chemical name
Chemical formula
Molecular weight
less than 96,5 % of polyoxyethylene (20) sorbitan monooleate on the
anhydrous basis
Description A lemon to amber-coloured oily liquid at 25 °C with a faint char
acteristic odour
Identification
Solubility Soluble in water, ethanol, methanol, ethyl acetate and toluene.
Insoluble in mineral oil and petroleum ether
polyol
Purity
▼M37
__________
▼B
E 434 POLYOXYETHYLENE SORBITAN MONOPALMITATE (POLY

SORBATE 40)
Synonyms Polysorbate 40; Polyoxyethylene (20) sorbitan monopalmitate
hydrides with edible commercial palmitic acid and condensed with
approximately 20 moles of ethylene oxide per mole of sorbitol and
its anhydrides
Einecs
Chemical name
Chemical formula
Molecular weight

less than 97 % of polyoxyethylene (20) sorbitan monopalmitate on
the anhydrous basis
Description A lemon to orange-coloured oily liquid or semi-gel at 25 °C with a

faint characteristic odour
Identification
Solubility Soluble in water, ethanol, methanol, ethyl acetate and acetone.

Insoluble in mineral oil
02012R0231 — EN — 27.10.2024 — 033.001 — 151
▼B
polyol
Purity
▼M37
__________
▼B
E 435 POLYOXYETHYLENE SORBITAN MONOSTEARATE (POLY

SORBATE 60)
Synonyms Polysorbate 60; Polyoxyethylene (20) sorbitan monostearate
hydrides with edible commercial stearic acid and condensed with
and its anhydrides
Einecs
Chemical name
Chemical formula
Molecular weight

less than 97 % of polyoxyethylene (20) sorbitan monostearate on the
anhydrous basis
Description A lemon to orange-coloured oily liquid or semi-gel at 25 °C with a

faint characteristic odour
Identification
Solubility Soluble in water, ethyl acetate and toluene. Insoluble in mineral oil
and vegetable oils

polyol
Purity
▼M37
__________
02012R0231 — EN — 27.10.2024 — 033.001 — 152
▼B
E 436 POLYOXYETHYLENE SORBITAN TRISTEARATE (POLY

SORBATE 65)
Synonyms Polysorbate 65; Polyoxyethylene (20) sorbitan tristearate
hydrides with edible commercial stearic acid and condensed with
and its anhydrides
Einecs
Chemical name
Chemical formula
Molecular weight

less than 96 % of polyoxyethylene (20) sorbitan tristearate on the
anhydrous basis
Description A tan-coloured, waxy solid at 25 °C with a faint characteristic odour
Identification
Solubility Dispersible in water. Soluble in mineral oil, vegetal oils, petroleum

ether, acetone, ether, dioxane, ethanol and methanol
Congealing range 29-33 °C

polyol
Purity
▼M37
__________
▼B

02012R0231 — EN — 27.10.2024 — 033.001 — 153
▼B
E 440 (i) PECTIN
Synonyms
Definition Pectin consists mainly of the partial methyl esters of polygal

acturonic acid and their ammonium, sodium, potassium and
calcium salts. It is obtained by extraction in an aqueous medium
of strains of appropriate edible plant material, usually citrus fruits
or apples. No organic precipitant shall be used other than methanol,
ethanol and propan-2-ol
Einecs 232-553-0
Chemical name
Chemical formula
Molecular weight
Assay Content not less than 65 % of galacturonic acid on the ash-free and
anhydrous basis after washing with acid and alcohol
Description White, light yellow, light grey or light brown powder
Identification
Solubility Soluble in water forming a colloidal, opalescent solution. Insoluble

in ethanol
Purity
Acid insoluble ash Not more than 1 % (insoluble in approximately 3N hydrochloric

acid)
Sulphur dioxide Not more than 50 mg/kg on the anhydrous basis
Nitrogen content Not more than 1,0 % after washing with acid and ethanol
Total insolubles Not more than 3 %
Solvent residues Not more than 1 % of free methanol, ethanol and propan-2-ol, singly
or in combination, on the volatile matter-free basis
E 440 (ii) AMIDATED PECTIN
Synonyms
Definition Amidated pectin consists mainly of the partial methyl esters and
amides of polygalacturonic acid and their ammonium, sodium,
potassium and calcium salts. It is obtained by extraction in an
aqueous medium of appropriate strains of edible plant material,
usually citrus fruits or apples and treatment with ammonia under
alkaline conditions. No organic precipitant shall be used other than
methanol, ethanol and propan-2-ol
Einecs
Chemical name
02012R0231 — EN — 27.10.2024 — 033.001 — 154
▼B
Chemical formula
Molecular weight
Assay Content not less than 65 % of galacturonic acid on the ash-free and
anhydrous basis after washing with acid and alcohol
Description White, light yellow, light greyish or light brownish powder
Identification
Solubility Soluble in water forming a colloidal, opalescent solution. Insoluble

in ethanol
Purity
Acid-insoluble ash Not more than 1 % (insoluble in approximately 3N hydrochloric

acid)
Degree of amidation Not more than 25 % of total carboxyl groups
Sulphur dioxide residue Not more than 50 mg/kg on the anhydrous basis
Nitrogen content Not more than 2,5 % after washing with acid and ethanol
Total insolubles: Not more than 3 %
Solvent residues Not more than 1 % of methanol, ethanol and propan-2-ol, singly or
in combination, on a volatile matter-free basis
E 442 AMMONIUM PHOSPHATIDES
Synonyms Ammonium salts of phosphatidic acid; Mixed ammonium salts of

phoshorylated glycerides
Definition A mixture of the ammonium compounds of phosphatidic acids

derived from edible fat and oil. One or two or three glyceride
moieties may be attached to phosphorus. Moreover, two phosphorus
esters may be linked together as phosphatidyl phosphatides
Einecs
Chemical name
Chemical formula
Molecular weight
Assay The phosphorus content is not less than 3 % and not more than
3,4 % by weight; the ammonium content is not less than 1,2 %
and not more than 1,5 % (calculated as N)
▼M3
Description Unctuous semi-solid to oily liquid
▼B
Identification
Solubility Soluble in fats. Insoluble in water. Partially soluble in ethanol and in

acetone
Test for glycerol Passes test
Test fatty acids Passes test

02012R0231 — EN — 27.10.2024 — 033.001 — 155
▼B
Purity
Petroleum ether insoluble matter Not more than 2,5 %
E 444 SUCROSE ACETATE ISOBUTYRATE
Synonyms SAIB
Definition Sucrose acetate isobutyrate is a mixture of the reaction products

formed by the esterification of food grade sucrose with acetic acid
anhydride and isobutyric anhydride, followed by distillation. The
mixture contains all possible combinations of esters in which the
molar ratio of acetate to butyrate is about 2:6
Einecs 204-771-6
Chemical name Sucrose diacetate hexaisobutyrate
Molecular weight 832-856 (approximate), C40H62O19: 846,9
Assay Content not less than 98,8 % and not more than 101,9 % of
C40H62O19
Description A pale straw-coloured liquid, clear and free of sediment and having
a bland odour
Identification
Solubility Insoluble in water. Soluble in most organic solvents
Refractive index [n]D40: 1,4492-1,4504
Specific gravity [d]25D: 1,141-1,151
Purity
Triacetin Not more than 0,1 %
Acid value Not more than 0,2
E 445 GLYCEROL ESTERS OF WOOD ROSIN
Synonyms Ester gum
Definition A complex mixture of tri- and diglycerol esters of resin acids from
wood rosin. The rosin is obtained by the solvent extraction of aged
pine stumps followed by a liquid-liquid solvent refining process.
Excluded from these specifications are substances derived from
gum rosin, and exudate of living pine trees, and substances
derived from tall oil rosin, a by-product of kraft (paper)
02012R0231 — EN — 27.10.2024 — 033.001 — 156
▼B
pulp processing. The final product is composed of approximately

90 % resin acids and 10 % neutrals (non-acidic compounds). The
resin acid fraction is a complex mixture of isomeric diterpenoid
monocarboxylic acids having the empirical molecular formula of
C20H30O2, chiefly abietic acid. The substance is purified by steam
stripping or by countercurrent steam distillation
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
Description Hard, yellow to pale amber-coloured solid
Identification
Solubility Insoluble in water, soluble in acetone
Infrared absorption spectrum Characteristic of the compound
Purity
Specific gravity of solution [d]2025 not less than 0,935 when determined in a 50 % solution in
d-limonene (97 %, boiling point 175,5-176 °C, d204: 0,84)
Ring and ball softening range Between 82 °C and 90 °C
Acid value Not less than 3 and not more than 9
Test for absence of tall oil rosin (sulphur When sulphur-containing organic compounds are heated in the
test) presence of sodium formate, the sulphur is converted to hydrogen
sulphide which can readily be detected by the use of lead acetate
paper. A positive test indicates the use of tall oil rosin instead of
wood rosin
E 450 (i) DISODIUM DIPHOSPHATE
Synonyms Disodium dihydrogen diphosphate; Disodium dihydrogen pyrop

hosphate; Sodium acid pyrophosphate; Disodium pyrophosphate
Definition
Einecs 231-835-0
Chemical name Disodium dihydrogen diphosphate
Chemical formula Na2H2P2O7
Assay Content not less than 95 % of disodium diphosphate

P2O5 content not less than 63,0 % and not more than 64,5 %
02012R0231 — EN — 27.10.2024 — 033.001 — 157
▼B
Description White powder or grains
Identification
Solubility Soluble in water
Purity
Water insoluble matter Not more than 1 %
Aluminium Not more than 200 mg/kg
E 450 (ii) TRISODIUM DIPHOSPHATE
Synonyms Trisodium pyrophosphate; Trisodium monohydrogen diphosphate;

Trisodium monohydrogen pyrophosphate; Trisodium diphosphate
Definition
Einecs 238-735-6
Chemical name
Chemical formula Monohydrate: Na3HP2O7 · H2O

Anhydrous: Na3HP2O7
Molecular weight Monohydrate: 261,95

Anhydrous: 243,93

P2O5 content not less than 57 % and not more than 59 %
Description White powder or grains, occurs anhydrous or as a monohydrate
Identification
Purity
Loss on ignition Not more than 4,5 % on the anhydrous compound (450-550 °C).
Not more than 11,5 % on the monohydrate basis
Loss on drying Not more than 0,5 % (105 °C, 4 hours) for anhydrous
Not more than 1,0 % (105 °C, 4 hours) for monohdyrate
02012R0231 — EN — 27.10.2024 — 033.001 — 158
▼B
E 450 (iii) TETRASODIUM DIPHOSPHATE
Synonyms Tetrasodium pyrophosphate; Tetrasodium disphosphate; Tetrasodium

phosphate
Definition
Einecs 231-767-1
Chemical name Tetrasodium diphosphate
Chemical formula Anhydrous: Na4P2O7

Decahydrate: Na4P2O7 · 10H2O

Decahydrate: 446,09
Assay Content not less than 95 % of Na4P2O7 on the ignited basis

P2O5 content not less than 52,5 % and not more than 54,0 %
Description Colourless or white crystals, or a white crystalline or granular

powder. The decahydrate effloresces slightly in dry air
Identification
Purity
Loss on ignition Not more than 0,5 % for the anhydrous salt, not less than 38 % and
not more than 42 % for the decahydrate (105 °C, 4 hours then
550 °C, 30 minutes)
Lead Not more than 1mg/kg
E 450 (v) TETRAPOTASSIUM DIPHOSPHATE
Synonyms Tetrapotassium pyrophosphate
Definition
Einecs 230-785-7
Chemical name Tetrapotassium diphosphate

02012R0231 — EN — 27.10.2024 — 033.001 — 159
▼B
Chemical formula K 4P 2 O 7
Assay Content not less than 95 % (800 °C for 0,5 hours)

P2O5 content not less than 42,0 % and not more than 43,7 % on the
anhydrous basis
Description Colourless crystals or white, very hygroscopic powder
Identification
Purity
Loss on ignition Not more than 2 % (105 °C, 4 hours then 550 °C, 30 minutes)
E 450 (vi) DICALCIUM DIPHOSPHATE
Synonyms Calcium pyrophosphate
Definition
Einecs 232-221-5
Chemical name Dicalcium diphosphate

Dicalcium pyrophosphate
Chemical formula Ca2P2O7

Description A fine, white, odourless powder
Identification
Solubility Insoluble in water. Soluble in dilute hydrochloric and nitric acids
pH Between 5,5 and 7,0 (10 % suspension in water)
Purity
Loss on ignition Not more than 1,5 % (800 °C ± 25 °C, 30 minutes

02012R0231 — EN — 27.10.2024 — 033.001 — 160
▼B
E 450 (vii) CALCIUM DIHYDROGEN DIPHOSPHATE
Synonyms Acid calcium pyrophosphate; Monocalcium dihydrogen pyrop

hosphate
Definition
Einecs 238-933-2
Chemical name Calcium dihydrogen diphosphate
Chemical formula CaH2P2O7

Description White crystals or powder
Identification
Purity
Acid-insoluble matter Not more than 0,4 %
Aluminium Not more than 800 mg/kg. This applies until 31 March 2015.
Not more than 200 mg/kg. This applies from 1 April 2015.
▼M10
E 450 (ix) MAGNESIUM DIHYDROGEN DIPHOSPHATE
Synonyms Acid magnesium pyrophosphate, monomagnesium dihydrogen

pyrophosphate; magnesium diphosphate, magnesium pyrophosphate
Definition Magnesium dihydrogen diphosphate is the acidic magnesium salt of

diphosphoric acid. It is manufactured by adding an aqueous
dispersion of magnesium hydroxide slowly to phosphoric acid,
until a molar ratio about 1:2 between Mg and P is reached. The
temperature is held under 60 °C during the reaction. About 0,1 %
hydrogen peroxide is added to the reaction mixture and the slurry is
then heated and milled.
02012R0231 — EN — 27.10.2024 — 033.001 — 161
▼M10
EINECS 244-016-8
Chemical name Mono magnesium dihydrogen diphosphate
Chemical formula MgH2P2O7
Assay P2O5 content not less than 68,0 % and not more than 70,5 %
expressed as P2O5
MgO content not less than 18,0 % and not more than 20,5 %
expressed as MgO
Description White crystals or powder
Identification
Solubility Slightly soluble in water, practically insoluble in ethanol
Particle size: The average particle size will deviate between 10 and 50 μm
Purity
Loss on ignition Not more than 12 % (800 °C, 0,5 hours)
Aluminium Not more than 50 mg/kg
Cadmium Not more than 1 mg/kg.
▼B
E 451 (i) PENTASODIUM TRIPHOSPHATE
Synonyms Pentasodium tripolyphosphate; Sodium tripolyphosphate
Definition
Einecs 231-838-7
Chemical name Pentasodium triphosphate
Chemical formula Na5O10P3 · nH2O (n = 0 or 6)
Assay Content not less than 85,0 % (anhydrous) or 65,0 % (hexahydrate)

(anhydrous) or not less than 43 % and not more than 45 %
(hexahydrate)
02012R0231 — EN — 27.10.2024 — 033.001 — 162
▼B
Description White, slightly hygroscopic granules or powder
Identification
Purity
Loss on drying Anhydrous: Not more than 0,7 % (105 °C, 1 hour)
Hexahydrate: Not more than 23,5 % (60 °C, 1 hour, then 105 °C,
4 hours)
Higher polyphosphates Not more than 1 %
E 451 (ii) PENTAPOTASSIUM TRIPHOSPHATE
Synonyms Pentapotassium tripolyphosphate; Potassium triphosphate; Potassium

tripolyphosphate
Definition
Einecs 237-574-9
Chemical name Pentapotassium triphosphate; Pentapotassium tripolyphosphate
Chemical formula K5O10P3

P2O5 content not less than 46,5 % and not more than 48 %
Description White, very hygroscopic powder or granules
Identification
Solubility Very soluble in water
Purity
Loss on ignition Not more than 0,4 % (105 °C, 4 hours, then 550 °C, 30 minutes)
Water insoluble matter Not more than 2 %

02012R0231 — EN — 27.10.2024 — 033.001 — 163
▼B
E 452 (i) SODIUM POLYPHOSPHATE

I. SOLUBLE POLYPHOSPHATE
Synonyms Sodium hexametaphosphate; Sodium tetrapolyphosphate; Graham's

salt; Sodium polyphosphates, glassy; Sodium polymetaphosphate;
Sodium metaphosphate
Definition Soluble sodium polyphosphates are obtained by fusion and

subsequent chilling of sodium orthophosphates. These compounds
are a class consisting of several amorphous, water-soluble polyphos
phates composed of linear chains of metaphosphate units, (NaPO3)x
where x ≥ 2, terminated by Na2PO4 groups. These substances are
usually identified by their Na2O/P2O5 ratio or their P2O5 content.
The Na2O/P2O5 ratios vary from about 1,3 for sodium tetrapoly
phosphate, where x = approximately 4; to about 1,1 for Graham's
salt, commonly called sodium hexametaphosphate, where x = 13 to
18; and to about 1,0 for the higher molecular weight sodium poly
phosphates, where x = 20 to 100 or more. The pH of their solutions
varies from 3,0 to 9,0
Einecs 272-808-3
Chemical name Sodium polyphosphate
Chemical formula Heterogenous mixtures of sodium salts of linear condensed poly

phosphoric acids of general formula H(n + 2)PnO(3n + 1) where ‘n’ is
not less than 2
Molecular weight (102)n
Assay P2O5 content not less than 60 % and not more than 71 % on the
ignited basis
Description Colourless or white, transparent platelets, granules, or powders
Identification
Purity
Loss on ignition Not more than 1 %
II. INSOLUBLE POLYPHOSPHATE
Synonyms Insoluble sodium metaphosphate; Maddrell's salt; Insoluble sodium

polyphosphate; IMP
Definition Insoluble sodium metaphosphate is a high molecular weight sodium

polyphosphate composed of two long metaphosphate chains
(NaPO3)x that spiral in opposite directions about a common axis.
The Na2O/P2O5 ratio is about 1,0. The pH of 1 in 3 suspension in
water is about 6,5
Einecs 272-808-3
02012R0231 — EN — 27.10.2024 — 033.001 — 164
▼B
Chemical name Sodium polyphosphate
Chemical formula Heterogenous mixtures of sodium salts of linear condensed poly

not less than 2
Assay P2O5 content not less than 68,7 % and not more than 70,0 %
Identification
Solubility Insoluble in water, soluble in mineral acids and in solutions of

potassium and ammonium (but not sodium) chlorides
pH About 6,5 (1 in 3 suspension in water)
Purity
E 452 (ii) POTASSIUM POLYPHOSPHATE
Synonyms Potassium metaphosphate; Potassium polymetaphosphate; Kurrol salt
Definition
Einecs 232-212-6
Chemical name Potassium polyphosphate
Chemical formula (KPO3)n

Heterogenous mixtures of potassium salts of linear condensed poly
not less than 2
Assay P2O5 content not less than 53,5 % and not more than 61,5 % on the
ignited basis
Description Fine white powder or crystals or colourless glassy platelets
Identification
Solubility 1 g dissolves in 100 ml of a 1 in 25 solution of sodium acetate
pH Not more than 7,8 (1 % suspension)
Purity
Cyclic phosphate Not more than 8 % on P2O5 content

02012R0231 — EN — 27.10.2024 — 033.001 — 165
▼B
E 452(iii) SODIUM CALCIUM POLYPHOSPHATE
Synonyms Sodium calcium polyphosphate, glassy
Definition
Einecs 233-782-9
Chemical name Sodium calcium polyphosphate
Chemical formula (NaPO3)n CaO where n is typically 5
Molecular weight
ignited basis
Description White glassy crystals, spheres
Identification
pH Approximately 5 to 7 (1 % m/m slurry)
CaO content 7 % - 15 % m/m
Purity
E 452 (iv) CALCIUM POLYPHOSPHATE
Synonyms Calcium metaphosphate; Calcium polymetaphosphate
Definition
Einecs 236-769-6
Chemical name Calcium polyphosphate
Chemical formula (CaP2O6)n

Heterogenous mixtures of calcium salts of condensed polyphos
phoric acids of general formula H(n + 2)PnO(n + 1) where ‘n’ is not
less than 2
ignited basis
Description Odourless, colourless crystals or white powder
Identification
Solubility Usually sparingly soluble in water. Soluble in acid medium

02012R0231 — EN — 27.10.2024 — 033.001 — 166
▼B
CaO content 27 to 29,5 %
Purity
Cyclic phosphate Not more than 8 % (on P2O5 content)
▼M23
E 456 POTASSIUM POLYASPARTATE
Synonyms
Definition Potassium polyaspartate is the potassium salt of polyaspartic acid,

produced from L-aspartic acid and potassium hydroxide. The
thermic process transforms the aspartic acid in polysuccinimide
that is insoluble. Polysuccinimide is treated with potassium
hydroxide allowing the opening of the ring and polymerisation of
the units. The last step is the spray drying phase, which results in a
light tan powder
CAS number 64723-18-8
Chemical name L-aspartic acid, homopolymer, potassium salt
Chemical formula [C4H4NO3K]n
Weight average molecular weight Approximately 5 300 g/mol
Assay Not less than 98 % on dry weight basis
Particle size Not less than 45 μm (not more than 1 % in weight of particles of
less than 45 μm)
Description A light brown odourless powder
Identification
Solubility Very soluble in water and slightly soluble in organic solvents
Purity
Degree of substitutions Not less than 91,5 % on dry weight basis
Loss on drying Not more than 11 % (105 °C,12 hours)
Potassium hydroxide Not more than 2 %
Aspartic acid Not more than 1 %
Other impurities Not more than 0,1 %

02012R0231 — EN — 27.10.2024 — 033.001 — 167
▼M23
▼B
E 459 BETA-CYCLODEXTRIN
Synonyms
Definition Beta-cyclodextrin is a non-reducing cyclic saccharide consisting of

seven α-1,4-linked D-glucopyranosyl units. The product is manufactured
by the action of the enzyme cycloglycosyltransferase (CGTase) obtained
from Bacillus circulans, Paenibacillus macerans or recombinant
Bacillus licheniformis strain SJ1608 on partially hydrolysed starch
Einecs 231-493-2
Chemical name Cycloheptaamylose
Chemical formula (C6H10O5)7
Molecular weight 1 135
Assay Content not less than 98,0 % of (C6H10O5)7 on an anhydrous basis
Description Virtually odourless white or almost white crystalline solid
Appearance of the aqueous solution Clear and colourless
Identification
Solubility Sparingly soluble in water; freely soluble in hot water; slightly

soluble in ethanol
Specific rotation [α]D25 + 160° to + 164° (1 % solution)
pH value: 5,0-8,0 (1 % solution)
Purity
Other cyclodextrins Not more than 2 % on an anhydrous basis
Solvent residues Not more than 1 mg/kg of each of toluene and trichloroethylene
▼M8
E 460 (i) MICROCRYSTALLINE CELLULOSE, CELLULOSE GEL
Synonyms
▼B
Definition Microcrystalline cellulose is purified, partially depolymerised

cellulose prepared by treating alpha-cellulose, obtained as a pulp
from strains of fibrous plant material, with mineral acids. The degree
of polymerisation is typically less than 400
Einecs 232-674-9
02012R0231 — EN — 27.10.2024 — 033.001 — 168
▼B
Chemical name Cellulose
Molecular weight About 36 000
Assay Not less than 97 % calculated as cellulose on the anhydrous basis
Particle size Not less than 5 μm (not more than 10 % of particles of less than
5 μm)
Description A fine white or almost white odourless powder
Identification
▼M24
Solubility Insoluble in water, ethanol, ether and dilute mineral acids. Practically
insoluble or insoluble in sodium hydroxide solution (concentration:
50 g NaOH/L)
▼B
Colour reaction To 1 mg of the sample, add 1 ml of phosphoric acid and heat on a
water bath for 30 minutes. Add 4 ml of a 1 in 4 solution of pyro
catechol in phosphoric acid and heat for 30 minutes. A red colour is
produced
Infrared absorption spectroscopy To be identified
Suspension test Mix 30 g of the sample with 270 ml of water in a high-speed
(12 000 rpm) power blender for 5 minutes. The resultant mixture
will be either a free-following suspension or a heavy, lumpy
suspension which flows poorly, if at all, settles only slightly and
contains many trapped air bubbles. If a free-flowing suspension is
obtained, transfer 100 ml into a 100-ml graduated cylinder and allow
to stand for 1 hour. The solids settles and a supernatant liquid
appears
pH The pH of the supernatant liquid is between 5,0 and 7,5 (10 %
suspension in water)
Purity
Sulphated ash Not more than 0,5 % (800 ± 25 °C)
To 20 ml of the dispersion obtained in Identification, suspension
test, add a few drops of iodine solution and mix. No purplish to
blue or blue colour should be produced
Carboxyl groups Not more than 1 %
E 460 (ii) POWDERED CELLULOSE
Definition Purified, mechanically disintegrated cellulose prepared by processing

alpha-cellulose obtained as a pulp from strains of fibrous plant
materials
Einecs 232-674-9
Chemical name Cellulose; Linear polymer of 1:4 linked glucose residues
Molecular weight (162)n (n is predominantly 1 000 and greater)
02012R0231 — EN — 27.10.2024 — 033.001 — 169
▼B
Particle size Not less than 5 μm (not more than 10 % of particles of less than
5 μm)
Description A white, odourless powder
Identification
Solubility Insoluble in water, ethanol, ether and dilute mineral acids. Slightly
soluble in sodium hydroxide solution
Suspension test Mix 30 g of the sample with 270 ml of water in a high-speed

(12 000 rpm) power blender for 5 minutes. The resultant mixture
will be either a free-flowing suspension or a heavy, lumpy
suspension which flows poorly, if at all, settles only slightly and
contains many trapped air bubbles. If a free-flowing suspension is
obtained, transfer 100 ml into a 100-ml graduated cylinder and allow
to stand for 1 hour. The solids settles and a supernatant liquid
appears
pH The pH of the supernatant liquid is between 5,0 and 7,5 (10 %

suspension in water)
Purity

To 20 ml of the dispersion obtained in Identification, suspension
test, add a few drops of iodine solution and mix. No purplish to
blue or blue colour should be produced
E 461 METHYL CELLULOSE
Synonyms Cellulose methyl ether
Definition Methyl cellulose is cellulose obtained directly from strains of fibrous

plant material and partially etherified with methyl groups
Einecs
Chemical name Methyl ether of cellulose
Chemical formula The polymers contain substituted anhydroglucose units with the
following general formula:
C6H7O2(OR1)(OR2)(OR3) where R1, R2, R3 each may be one of the
following:
— H
— CH3 or
— CH2CH3
Molecular weight From about 20 000 to 380 000
Assay Content not less than 25 % and not more than 33 % of methoxyl
groups (-OCH3) and not more than 5 % of hydroxyethoxyl groups
(-OCH2CH2OH)
02012R0231 — EN — 27.10.2024 — 033.001 — 170
▼B
Description Slightly hygroscopic white or slightly yellowish or greyish odourless

and tasteless, granular or fibrous powder
Identification
Solubility Swelling in water, producing a clear to opalescent, viscous, colloidal

solution.
Insoluble in ethanol, ether and chloroform.
Soluble in glacial acetic acid
pH Not less than 5,0 and not more than 8,0 (1 % colloidal solution)
Purity
E 462 ETHYL CELLULOSE
Synonyms Cellulose ethyl ether
Definition Ethyl cellulose is cellulose obtained directly from fibrous plant

material and partially etherified with ethyl groups
Einecs
Chemical name Ethyl ether of cellulose
C6H7O2(OR1)(OR2) where R1 and R2 may be any of the following:
— H
— CH2CH3
Molecular weight
Assay Content not less than 44 % and not more than 50 % of ethoxyl
groups (-OC2H5) on the dried basis (equivalent to not more than
2,6 ethoxyl groups per anhydroglucose unit)
Description Slightly hygroscopic white to off-white, odourless and tasteless

powder
Identification
Solubility Practically insoluble in water, in glycerol and in propane-1,2-diol but

soluble in varying proportions in certain organic solvents depending
upon the ethoxyl content. Ethyl cellulose containing less than 46 to
48 % of ethoxyl groups is freely soluble in tetrahydrofuran, in
methyl acetate, in chloroform and in aromatic hydrocarbon ethanol
mixtures. Ethyl cellulose containing 46 to 48 % or more of ethoxyl
groups is freely soluble in ethanol, in methanol, in toluene, in
chloroform and in ethyl acetate
Film forming test Dissolve 5 g of the sample in 95 g of an 80:20 (w/w) mixture of

toluene ethanol. A clear, stable, slightly yellow solution is formed.
Pour a few ml of the solution onto a glass plate and allow the
solvent to evaporate. A thick, tough, continuous, clear film remains.
The film is flammable
02012R0231 — EN — 27.10.2024 — 033.001 — 171
▼B
pH Neutral to litmus (1 % colloidal solution)
Purity
E 463 HYDROXYPROPYL CELLULOSE
Synonyms Cellulose hydroxypropyl ether
Definition Hydroxypropylcellulose is cellulose obtained directly from strains of

fibrous plant material and partially etherified with hydroxypropyl
groups
Einecs
Chemical name Hydroxypropyl ether of cellulose
C6H7O2(OR1)(OR2)(OR3), where R1, R2, R3 each may be one of the
following:
— H
— CH2CHOHCH3
— CH2CHO(CH2CHOHCH3)CH3
— CH2CHO[CH2CHO(CH2CHOHCH3)CH3]CH3
Molecular weight From about 30 000 to 1 000 000
Assay Content not more than 80,5 % of hydroxypropoxyl groups

(-OCH2CHOHCH3) equivalent to not more than 4,6 hydroxypropyl
groups per anhydroglucose unit on the anhydrous basis

Identification

solution. Soluble in ethanol. Insoluble in ether
Gas chromatography Determine the substituents by gas chromotography
Purity
Propylene chlorohydrins Not more than 0,1 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 172
▼M27
E 463a LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE (L-HPC)
Synonyms Cellulose hydroxypropyl ether, low substituted

Definition L-HPC is a low-substituted poly (hydroxypropyl) ether of cellulose.
L-HPC is manufactured by partial etherification of the anhydro
glucose units of pure cellulose (wood pulp) with propylene oxide/
hydroxypropyl groups. The resulting product is then purified, dried
and milled to yield low-substituted hydroxypropyl cellulose.
L-HPC contains not less than 5,0 % and not more than 16,0 % of
hydroxypropoxy groups, calculated on the dried basis.
L-HPC differs from hydroxypropyl cellulose (E 463) with respect to
the degree of molar substitution with hydroxypropoxy groups of the
glucose ring unit (0,2 for L-HPC vs 3,5 for E 463) of the cellulose
backbone.
IUPAC name Cellulose, 2-hydroxypropyl ether (low substituted)
Einecs number
Chemical name Hydroxypropyl ether of cellulose, low-substituted
C6H7O2(OR1)(OR2)(OR3)
where R1, R2, R3 each may be one of the following:
— H
— CH2CHOHCH3
— CH2CHO(CH2CHOHCH3)CH3
— CH2CHO[CH2CHO(CH2CHOHCH3)CH3]CH3
Molecular weight From about 30 000 to 150 000 g/mol
Assay The average number of hydroxypropoxy groups
(–OCH2CHOHCH3) corresponds to 0,2 hydroxypropyl groups per
anhydroglucose unit on the anhydrous basis
Particle size by laser diffraction method — Not less than 45 μm (not more than
1 % in weight of particles of less than 45 μm) and not more than
65 μm
by size-exclusion chromatography (SEC) — Average (D50) particle
size between 47,3 μm and 50,3 μm; D90 value (90 % below given
value) between 126,2 μm and 138 μm
Identification Passes test
Solubility Insoluble in water; swelling in water. It dissolves in a solution of
10 % sodium hydroxide producing a viscous solution.
Assay Determination of the degree of molar substitution by gas chroma
tography
pH Not less than 5,0 and not more than 7,5 (1 % colloidal suspension)
Purity
Residue on ignition Not more than 0,8 % determined at 800 °C ± 25 °C
Propylene chlorohydrins Not more than 0,1 mg/kg (on an anhydrous basis) (gas chroma
tography–mass spectrometry (GC–MS))
02012R0231 — EN — 27.10.2024 — 033.001 — 173
▼B
E 464 HYDROXYPROPYL METHYL CELLULOSE
Synonyms
Definition Hydroxypropyl methyl cellulose is cellulose obtained directly from

strains of fibrous plant material and partially etherified with methyl
groups and containing a small degree of hydroxypropyl substitution
Einecs
Chemical name 2-Hydroxypropyl ether of methylcellulose
following:
— H
— CH3
— CH2CHOHCH3
— CH2CHO (CH2CHOHCH3) CH3
— CH2CHO[CH2CHO (CH2CHOHCH3) CH3]CH3
Assay Content not less than 19 % and not more than 30 % methoxyl
groups (-OCH3) and not less than 3 % and not more than 12 %
hydroxypropoxyl groups (-OCH2CHOHCH3), on the anhydrous
basis

Identification

solution. Insoluble in ethanol
Gas chromatography Determine the substituents by gas chromatography
Purity
Sulphated ash Not more than 1,5 % for products with viscosities of 50 mPa.s or
above
Not more than 3 % for products with viscosities below 50 mPa.s
Propylene chlorohydrins Not more than 0,1 mg/kg
E 465 ETHYL METHYL CELLULOSE
Synonyms Methylethylcellulose
Definition Ethyl methyl cellulose is cellulose obtained directly from strains of

fibrous plant material and partially etherified with methyl and ethyl
groups
Einecs
Chemical name Ethyl methyl ether of cellulose

02012R0231 — EN — 27.10.2024 — 033.001 — 174
▼B
following:
— H
— CH3
— CH2CH3
Assay Content on the anhydrous basis not less than 3,5 % and not more
than 6,5 % of methoxyl groups (-OCH3) and not less than 14,5 %
and not more than 19 % of ethoxyl groups (-OCH2CH3), and not
less than 13,2 % and not more than 19,6 % of total alkoxyl groups,
calculated as methoxyl

Identification

solution. Soluble in ethanol. Insoluble in ether
Purity
Loss on drying Not more than 15 % for the fibrous form, and not more than 10 %
for the powdered form (105 °C to constant weight)
▼M8
E 466 SODIUM CARBOXY METHYL CELLULOSE, CELLULOSE GUM
Synonyms NaCMC; Sodium CMC
Definition Sodium carboxy methyl cellulose is the partial sodium salt of a

carboxymethyl ether of cellulose, the cellulose being obtained
directly from strains of fibrous plant material
▼B
Einecs
Chemical name Sodium salt of the carboxymethyl ether of cellulose
following:
— H
— CH2COONa
— CH2COOH
Molecular weight Higher than approximately 17 000 (degree of polymerisation

approximately 100)
Assay Content on the anhydrous basis not less than 99,5 %

02012R0231 — EN — 27.10.2024 — 033.001 — 175
▼B
Identification
Solubility Yields a viscous colloidal solution with water. Insoluble in ethanol
Foam test A 0,1 % solution of the sample is shaken vigorously. No layer of

foam appears. (This test permits the distinction of sodium carboxy
methyl cellulose from other cellulose ethers)
Precipitate formation To 5 ml of a 0,5 % solution of the sample, add 5 ml of 5 % solution

of copper sulphate or of aluminium sulphate. A precipitate appears.
(This test permits the distinction of sodium carboxymethyl cellulose
from other cellulose ethers and from gelatine, locust bean gum and
tragacanth)
Colour reaction Add 0,5 g powdered carboxy methyl cellulose sodium to 50 ml of

water, while stirring to produce an uniform dispersion. Continue the
stirring until a clear solution is produced, and use the solution for the
following test:
To 1 mg of the sample, diluted with an equal volume of water, in a
small test tube, add 5 drops of 1-naphthol solution. Incline the test
tube, and carefully introduce down the side of the tube 2 ml of
sulphuric acid so that it forms a lower layer. A red-purple colour
develops at the interface
Purity
Degree of substitution Not less than 0,2 and not more than 1,5 carboxymethyl groups
(-CH2COOH) per anhydroglucose unit
Loss on drying Not more than 12 % (105 °C to constant weight)
Total glycolate Not more than 0,4 %, calculated as sodium glycolate on the
anhydrous basis
Sodium Not more than 12,4 % on the anhydrous basis
E 468 CROSS-LINKED SODIUM CARBOXYMETHYLCELLULOSE,

CROSS-LINKED CELLULOSE GUM
Synonyms Cross-linked carboxymethyl cellulose; Cross-linked CMC; Cross-

linked sodium CMC;
Definition Cross-linked sodium carboxymethyl cellulose is the sodium salt of

thermally cross-linked partly O-carboxymethylated cellulose
Einecs
Chemical name Sodium salt of the cross-linked carboxymethyl ether cellulose
Chemical formula The polymers containing substituted anhydroglucose units with the
general formula:
C6H7O2(OR1)(OR2)(OR3) where R1, R2 and R3 may be any of the
following:
— H
— CH2COONa
— CH2COOH
Molecular weight
Assay
02012R0231 — EN — 27.10.2024 — 033.001 — 176
▼B
Description Slightly hygroscopic, white to off white, odourless powder
Identification
Precipitate formation Shake 1 g with 100 ml of a solution containing 4 mg/kg methylene

blue and allow to settle. The substance to be examined absorbs the
methylene blue and settles as a blue, fibrous mass
Colour reaction Shake 1 g with 50 ml of water. Transfer 1 ml of the mixture to a test

tube, add 1 ml water and 0,05 ml of freshly prepared 40 g/l solution
of alpha-naphthol in methanol. Incline the test tube and add carefully
2 ml of sulphuric acid down the side so that it forms a lower layer.
A reddish-violet colour develops at the interface
pH Not less than 5,0 and not more than 7,0 (1 % solution)
Purity
Water soluble matter Not more than 10 %
Degree of substitution Not less than 0,2 and not more than 1,5 carboxymethyl groups per
anhydroglucose unit
Sodium content Not more than 12,4 % on anhydrous basis
E 469 ENZYMATICALLY HYDROLYSED CARBOXYMETHYLCEL

LULOSE, ENZYMATICALLY HYDROLISED CELLULOSE GUM
Synonyms Sodium carboxymethyl cellulose, enzymatically hydrolysed
Definition Enzymatically hydrolysed carboxymethylcellulose is obtained from

carboxymethylcellulose by enzymatic digestion with a cellulase
produced by Trichoderma longibrachiatum (formerly T. reesei)
Einecs
Chemical name Carboxymethyl cellulose, sodium, partially enzymatically hydrolysed
Chemical formula Sodium salts of polymers containing substituted anhydroglucose

units with the general formula:
[C6H7O2(OH)x(OCH2COONa)y]n
where n is the degree of polymerisation
x = 1,50 to 2,80
y = 0,2 to 1,50
x + y = 3,0
(y = degree of substitution)
Molecular weight 178,14 where y = 0,20

282,18 where y = 1,50
Macromolecules: Not less than 800 (n about 4)
Assay Not less than 99,5 %, including mono- and disaccharides, on the
dried basis
02012R0231 — EN — 27.10.2024 — 033.001 — 177
▼B
Description White or slightly yellowish or greyish, odourless, slightly hygro

scopic granular or fibrous powder
Identification
Foam test Vigorously shake a 0,1 % solution of the sample. No layer of foam
appears. This test distinguishes sodium carboxymethyl cellulose,
whether hydrolysed or not, from other cellulose ethers and from
alginates and natural gums
Precipitate formation To 5 ml of a 0,5 % solution of the sample add 5 ml of a 5 %

solution of copper or aluminium sulphate. A precipitate appears.
This test distinguishes sodium carboxymethyl cellulose, whether
hydrolysed or not, from other cellulose ethers and from gelatine,
carob bean gum and tragacanth gum
Colour reaction Add 0,5 g of the powdered sample to 50 ml of water, while stirring
to produce a uniform dispersion. Continue the stirring until a clear
solution is produced. Dilute 1 ml of the solution with 1 ml of water
in a small test tube. Add 5 drops of 1-naphthol TS. Incline the tube,
and carefully introduce down the side of the tube 2 ml of sulphuric
acid so that it forms a lower layer. A red-purple colour develops at
the interface
Viscosity (60 % solids) Not less than 2 500 kgm– 1s– 1 at 25 °C corresponding to an average
molecule weight of 5 000 Da
Purity
Degree of substitution Not less than 0,2 and not more than 1,5 carboxymethyl groups per
anhydroglucose unit on the dried basis
Sodium chloride and sodium glycolate Not more than 0,5 % singly or in combination
Residual enzyme activity Passes test. No change in viscosity of test solution occurs, which
indicates hydrolysis of the sodium carboxymethyl cellulose
E 470a SODIUM, POTASSIUM AND CALCIUM SALTS OF FATTY

ACIDS
Synonyms
Definition Sodium, potassium and calcium salts of fatty acids occurring in food
oils and fats, these salts being obtained either from edible fats and
oils or from distilled food fatty acids.
Einecs
Chemical name
Chemical formula
Molecular weight
Assay Content on the anhydrous basis not less than 95 % (105 °C till a
constant weight)
Description White or creamy white light powders, flakes or semi-solids

02012R0231 — EN — 27.10.2024 — 033.001 — 178
▼B
Identification
Solubility Sodium and potassium salts: soluble in water and ethanol. Calcium
salts: insoluble in water, ethanol and ether
Test for cations Passes test
Purity
Sodium Not less than 9 % and not more than 14 % expressed as Na2O
Potassium Not less than 13 % and not more than 21,5 % expressed as K2O
Calcium Not less than 8,5 % and not more than 13 % expressed as CaO
Unsaponifiable matter Not more than 2 %
Free fatty acids Not more than 3 % estimated as oleic acid
Free alkali Not more than 0,1 % expressed as NaOH
Matter insoluble in alcohol Not more than 0,2 % (sodium and potassium salts only)
E 470b MAGNESIUM SALTS OF FATTY ACIDS
Synonyms
Definition Magnesium salts of fatty acids occurring in foods oils and fats, these
salts being obtained either from edible fats and oils or from distilled
food fatty acids
Einecs
Chemical name
Chemical formula
Molecular weight
Assay Content on the anhydrous basis not less than 95 % (105 °C till a
constant weight)
Description White or creamy-white light powders, flakes or semi-solids
Identification
Solubility Insoluble in water, partially soluble in ethanol and ether
Purity
Magnesium Not less than 6,5 % and not more than 11 % expressed as MgO
Free alkali Not more than 0,1 % expressed as MgO
Unsaponifiable matter Not more than 2 %

02012R0231 — EN — 27.10.2024 — 033.001 — 179
▼B
▼M42
E 471 MONO- AND DIGLYCERIDES OF FATTY ACIDS
Synonyms
Definition Mono- and diglycerides of fatty acids consist of mixtures of glycerol
mono-, di- and tri-esters of fatty acids occurring in food oils and
fats. They may contain small amounts of free fatty acids and
glycerol.
Glycerol used for the manufacture of mono- and diglycerides of fatty
acids should comply with the specifications for E 422.
E 471 shall be produced from fats and oils complying with Union
food safety requirements for edible fats and oils.
Einecs
Chemical name
Chemical formula
Molecular weight
Assay Content of mono- and di-esters: not less than 70 %
Content of erucic acid, including erucic acid bound in the mono/
diglyceride:
Not more than 0,2 % (only if added to food for infants and young
children)
Not more than 0,5 % (for all uses except for foods intended for
infants and young children)
Description The product varies from a pale yellow to pale brown oily liquid to a
white or slightly off-white hard waxy solid. The solids may be in the
form of flakes, powders or small beads.
Identification
Infrared absorption spectrum Characteristic of a partial fatty acid ester of a polyol
Solubility Insoluble in water, soluble in ethanol and toluene at 50 °C
Purity
Free glycerol Not more than 7 %
Polyglycerols Not more than 4 % diglycerol and not more than 1 % higher poly
glycerols both based on total glycerol content
Sum of 3-monochloropropanediol Not more than 0,75 mg/kg (only if added to food for infants and
(3-MCPD) and 3-MCPD fatty acid young children)
esters, expressed as 3-MCPD
Not more than 2,5 mg/kg (for all uses except for foods intended for
infants and young children)
Glycidyl esters of fatty acids, expressed From 30 July 2023 until 30 January 2024, not more than 5 mg/kg if
as glycidol added to food for infants and young children) and not more than
10 mg/kg for all other uses.
From 30 January 2024, not more than 5 mg/kg for all uses.
Total glycerol Not less than 16 % and not more than 33 %
Soap —
Purity criteria apply to the additive free of sodium, potassium and calcium salts
of fatty acids, however these substances may be present up to a maximum level
of 6 % (expressed as sodium oleate)
02012R0231 — EN — 27.10.2024 — 033.001 — 180
▼B
E 472 a ACETIC ACID ESTERS OF MONO- AND DIGLYCERIDES OF
FATTY ACIDS
Synonyms Acetic acid esters of mono- and diglycerides; Acetoglycerides;

Acetylated mono- and diglycerides; Acetic and fatty acid esters of
glycerol
Definition Esters of glycerol with acetic and fatty acids occurring in food fats
and oils. They may contain small amounts of free glycerol, free fatty
acids, free acetic acid and free glycerides
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
Description Clear, mobile liquids to solids, from white to pale yellow in colour
Identification
Test for acetic acid Passes test
Solubility Insoluble in water. Soluble in ethanol
Purity
Acids other than acetic and fatty acids Less than 1 %
Total acetic acid Not less than 9 % and not more than 32 %
Free fatty acids (and acetic acid) Not more than 3 % estimated as oleic acid
E 472 b LACTIC ACID ESTERS OF MONO- AND DIGLYCERIDES OF

FATTY ACIDS
Synonyms Lactic acid esters of mono- and diglycerides; Lactoglycerides;

Mono- and diglycerides of fatty acids esterified with lactic acid
Definition Esters of glycerol with lactic acid and fatty acids occurring in food
fats and oils. They may contain small amounts of free glycerol, free
fatty acids, free lactic acid and free glycerides
02012R0231 — EN — 27.10.2024 — 033.001 — 181
▼B
Description Clear, mobile liquids to waxy solids of variable consistency, from

white to pale yellow in colour
Identification
Test for glycerol, Passes test
Test for lactic acid Passes test
Solubility Insoluble in cold water but dispersible in hot water
Purity
Acids other than lactic and fatty acids Less than 1 %
Total lactic acid Not less than 13 % and not more than 45 %
Free fatty acids (and lactic acid) Not more than 3 % estimated as oleic acid
E 472 c CITRIC ACID ESTERS OF MONO- AND DIGLYCERIDES OF

FATTY ACIDS
Synonyms Citrem; Citric acid esters of mono- and diglycerides; Citroglycerides;

Mono- and diglycerides of fatty acids esterified with citric acid
Definition Esters of glycerol with citric acid and fatty acids occurring in food
oils and fats. They may contain small amounts of free glycerol, free
fatty acids, free citric acid and free glycerides. They may be partially
or wholly neutralised with sodium, potassium or calcium salts
suitable for the purpose and authorised as food additives according
to this Regulation.
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
Description Yellowish or light brown liquids to waxy solids or semi-solids
Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 182
▼B
Test for citric acid Passes test
Solubility Insoluble in cold water, dispersible in hot water, soluble in oils and
fats, insoluble in cold ethanol
Purity
Acids other than citric and fatty acids Less than 1 %
Total citric acid Not less than 13 % and not more than 50 %
Sulphated ash Non-neutralised products: not more than 0,5 % (800 ± 25 °C)
Partially or wholly neutralised products: not more than 10 %
(800 ± 25 °C)
of fatty acids, however, these substances may be present up to a maximum level
E 472 d TARTARIC ACID ESTERS OF MONO- AND DIGLYCERIDES

OF FATTY ACIDS
Synonyms Tartaric acid esters of mono- and diglycerides; Mono- and diglycerides
of fatty acids esterified with tartaric acid
Definition Esters of glycerol with tartaric acid and fatty acids occurring in food
fats and oils. They may contain small amounts of free glycerol, free
fatty acids, free tartaric acid and free glycerides
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
Description Sticky viscous yellowish liquids to hard yellow waxes
Identification
Test for tartaric acid Passes test
Purity
Acids other than tartaric and fatty acids Less than 1,0 %

02012R0231 — EN — 27.10.2024 — 033.001 — 183
▼B
Total tartaric acid Not less than 15 % and not more than 50 %
E 472 e MONO- AND DIACETYLTARTARIC ACID ESTERS OF MONO-
AND DIGLYCERIDES OF FATTY ACIDS
Synonyms Diacetyltartaric acid esters of mono- and diglycerides; Mono-and

diglycerides of fatty acids esterified with mono- and diacetyltartaric
acid; Diacetyltartaric and fatty acid esters of glycerol
Definition Mixed esters of glycerol with mono- and diacetyltartaric acids

(obtained from tartaric acid) and fatty acids occurring in food fats
and oils. They may contain small amounts of free glycerol, free fatty
acids, free tartaric and acetic acids and their combinations, and free
glycerides. Contains also tartaric and acetic esters of fatty acids
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
Description Sticky viscous liquids through a fat-like consistency to yellow waxes

which hydrolyse in moist air to liberate acetic acid
Identification
Purity
Acids other than acetic, tartaric and fatty Less than 1 %

acids

02012R0231 — EN — 27.10.2024 — 033.001 — 184
▼B
E 472 f MIXED ACETIC AND TARTARIC ACID ESTERS OF MONO-
AND DIGLYCERIDES OF FATTY ACIDS
Synonyms Mono- and diglycerides of fatty acids esterified with acetic acid and
tartaric acid
Definition Esters of glycerol with acetic and tartaric acids and fatty acids
occurring in food fats and oils. They may contain small amounts
of free glycerol, free fatty acids, free tartaric and acetic acids, and
free glycerides. May contain mono- and diacetyltartaric esters of
mono- and diglycerides of fatty acids
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
Description Sticky liquids to solids, from white to pale-yellow in colour
Identification
Purity
Acids other than acetic, tartaric and fatty Less than 1,0 %
acids

02012R0231 — EN — 27.10.2024 — 033.001 — 185
▼B
E 473 SUCROSE ESTERS OF FATTY ACIDS
Synonyms Sucroesters; Sugar esters
Definition Essentially the mono-, di- and triesters of sucrose with fatty acids
occurring in food fats and oils. They may be prepared from sucrose
and the methyl, ethyl and vinyl esters of food fatty acids (including
lauric acid) or by extraction from sucroglycerides. No organic
solvent other than dimethylsulphoxide, dimethylformamide, ethyl
acetate, propan-2-ol, 2-methyl-1-propanol, propylene glycol, methyl
ethyl ketone and supercritical carbondioxide may be used for their
preparation. p-methoxy phenol can be used as a stabiliser during the
manufacturing procedure.
Einecs
Chemical name
Chemical formula
Molecular weight
Description Stiff gels, soft solids or white to slightly greyish-white powders
Identification
Test for sugar Passes test
Solubility Sparingly soluble in water, soluble in ethanol
Purity
Sulphated ash Not more than 2 % (800 ± 25 °C)
Free sugar Not more than 5 %
p-methoxy-phenol Not more than 100 μg/kg
Acetaldehyde Not more than 50 mg/kg
Methanol Not more than 10 mg/kg
Dimethylsulphoxide Not more than 2 mg/kg
Dimethylformamide Not more than 1 mg/kg
2-methyl-1-propanol Not more than 10 mg/kg

9
Ethyl acetate >
>
>
=
Propan-2-ol Not more than 350 mg/kg, singly or in combination
>
>
>
;
Propylene glycol
Methyl ethyl ketone Not more than 10 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 186
▼B
E 474 SUCROGLYCERIDES
Synonyms Sugar glycerides
Definition Sucroglycerides are produced by reacting sucrose with an edible fat

or oil to produce a mixture of essentially mono-, di- and triesters of
sucrose and fatty acids (including lauric acid) together with residual
mono-, di- and triglycerides from fat or oil. No organic solvents
shall be used in their preparation other than cyclohexane, dimethyl
formamide, ethyl acetate, 2-methyl-1-propanol and propan-2-ol
Einecs
Chemical name
Chemical formula
Molecular weight
Assay Content not less than 40 % and not more than 60 % of sucrose fatty
acid esters
Description Soft solid masses, stiff gels or white to off-white powders
Identification
Solubility Insoluble in cold water, soluble in ethanol
Purity
Sulphated ash Not more than 2 % (800 ± 25 °C)
Free sugar Not more than 5 %
Free fatty acids Not more than 3 % (estimated as oleic acid)
Methanol Not more than 10 mg/kg
Dimethylformamide Not more than 1 mg/kg

9
2-Methyl-1-propanol >
=
Not more than 10 mg/kg, single or in combination
>
;
Cyclohexane
9
Ethyl acetate >
=
Not more than 350 mg/kg, single or in combination
>
;
Propan-2-ol
02012R0231 — EN — 27.10.2024 — 033.001 — 187
▼M41
E 475 POLYGLYCEROL ESTERS OF FATTY ACIDS
Synonyms Polyglycerol fatty acid esters; Polyglycerin esters of fatty acid esters
Definition Polyglycerol esters of fatty acids are produced by the esterification
of polyglycerol with food fats and oils or with fatty acids occurring
in foods fats and oils. The polyglycerol moiety is predominantly di-,
tri- and tetraglycerol and contains not more than 10 % of poly
glycerols equal to or higher than heptaglycerol.
The polyglycerol is produced from glycerol complying with the
specifications for E 422.
Einecs
Chemical name
Chemical formula
Molecular weight
Assay Content of total fatty acid ester not less than 90 %
Description Light yellow to amber, oily to very viscous liquids; light tan to
medium brown, plastic or soft solids; and light tan to brown, hard,
waxy solids
Identification
Test for polyglycerols Passes test
Solubility The esters range from very hydrophilic to very lipophilic, but as a
class tend to be dispersible in water and soluble in organic solvents
and oils
Purity
Acids other than fatty acids Less than 1 %
Total glycerol and polyglycerol Not less than 18 % and not more than 60 %
Free glycerol and polyglycerol Not more than 7 %
Sum of 3-monochloropropanediol Not more than 2,5 mg/kg
(3-MCPD) and 3-MCPD fatty acid
esters, expressed as 3-MCPD
Glycidyl fatty acid esters, expressed as Not more than 10 mg/kg. This applies from 20 July 2023 until
glycidol 20 January 2024.
Not more than 5 mg/kg. This applies from 20 January 2024.
Erucic acid Not more than 2 %
of 6 % (expressed as sodium oleate).
E 476 POLYGLYCEROL POLYRICINOLEATE
Synonyms Glycerol esters of condensed castor oil fatty acids; Polyglycerol

esters of polycondensed fatty acids from castor oil; Polyglycerol
esters of interesterified ricinoleic acid; PGPR
02012R0231 — EN — 27.10.2024 — 033.001 — 188
▼M41
Definition Polyglycerol polyricinoleate is prepared by the esterification of poly
glycerol with condensed castor oil fatty acids. Castor oil used for the
production of polyglycerol polyricinoleate is free of ricin.
The polyglycerol is produced from glycerol complying with the
specifications for E 422.
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
Description Clear, highly viscous liquid
Identification
Solubility Insoluble in water and in ethanol; soluble in ether, hydrocarbons and
halogenated hydrocarbons
Test for polyglycerols Passes test
Test for ricinoleic acid Passes test
Purity
Polyglycerols The polyglycerol moiety shall be composed of not less than 75 % of
di-, tri- and tetraglycerols and shall contain not more than 10 % of
polyglycerols equal to or higher than heptaglycerol
Sum of 3-monochloropropanediol Not more than 2,5 mg/kg
(3-MCPD) and 3-MCPD fatty acid
esters (expressed as 3-MCPD)
Glycidyl fatty acid esters (expressed as Not more than 1 mg/kg
glycidol)
▼B
E 477 PROPANE-1,2-DIOL ESTERS OF FATTY ACIDS
Synonyms Propylene glycol esters of fatty acids
Definition Consists of mixtures of propane-1,2-diol mono- and diesters of fatty

acids occurring in food fats and oils. The alcohol moiety is
exclusively propane-1,2-diol together with dimer and traces of
trimer. Organic acids other than food fatty acids are absent
Einecs
Chemical name
Chemical formula
Molecular weight
Assay Content of total fatty acid ester not less than 85 %
Description Clear liquids or waxy white flakes, beads or solids having a bland
odour
Identification
Test for propylene glycol Passes test

02012R0231 — EN — 27.10.2024 — 033.001 — 189
▼B
Purity
Acids other than fatty acids Less than 1 %
Total propane-1,2-diol Not less than 11 % and not more than 31 %
Free propane-1,2-diol Not more than 5 %
Dimer and trimer of propylene glycol Not more than 0,5 %
E 479 b THERMALLY OXIDISED SOYA BEAN OIL INTERACTED
WITH MONO- AND DIGLYCERIDES OF FATTY ACIDS
Synonyms TOSOM
Definition Thermally oxidised soya bean oil interacted with mono- and
diglycerides of fatty acids is a complex mixture of esters of
glycerol and fatty acids found in edible fat and fatty acids from
thermally oxidised soya bean oil. It is produced by interaction and
deodorisation under vacuum at 130 °C of 10 % of thermally
oxidised soya bean oil and 90 % mono- and diglycerides of food
fatty acids. Soya bean oil is exclusively made from strains of soya
beans
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
Description Pale yellow to light brown a waxy or solid consistency
Identification
Solubility Insoluble in water. Soluble in hot oil or fat
Purity
Free fatty acids Not more than 1,5 % estimated as oleic acid
Total fatty acids 83-90 %
Total glycerol 16-22 %
Fatty acid methyl esters, not forming Not more than 9 % of total fatty acid methyl esters
adduct with urea
02012R0231 — EN — 27.10.2024 — 033.001 — 190
▼B
Fatty acids, insoluble in petroleum ether Not more than 2 % of total fatty acids
Peroxide value Not more than 3
Epoxides Not more than 0,03 % oxirane oxygen
E 481 SODIUM STEAROYL-2-LACTYLATE
Synonyms Sodium stearoyl lactylate; Sodium stearoyl lactate
Definition A mixture of the sodium salts of stearoyl lactylic acids and its
polymers and minor amounts of sodium salts of other related
acids, manufactured by the reaction of stearic acid and lactic acid.
Other food fatty acids may also be present, free or esterified, due to
their presence in the stearic acid used
Einecs 246-929-7
Chemical name Sodium di-2-stearoyl lactate

Sodium di(2-stearoyloxy)propionate
Chemical formula C21H39O4Na; C19H35O4Na (major components)
Molecular weight
Assay
Description White or slightly yellowish powder or brittle solid with a char

acteristic odour
Identification
Test for lactic acid Passes test
Solubility Insoluble in water. Soluble in ethanol
Purity
Sodium Not less than 2,5 % and not more than 5 %
Ester value Not less than 90 and not more than 190
E 482 CALCIUM STEAROYL-2-LACTYLATE
Synonyms Calcium stearoyl lactate
Definition A mixture of the calcium salts of stearoyl lactylic acids and its
polymers and minor amounts of calcium salts of other related
acids, manufactured by the reaction of stearic acid and lactic acid.
Other food fatty acids may also be present, free or esterified, due to
their presence in the stearic acid used
02012R0231 — EN — 27.10.2024 — 033.001 — 191
▼B
Einecs 227-335-7
Chemical name Calcium di-2-stearoyl lactate
Calcium di(2-stearoyloxy)propionate
Chemical formula C42H78O8Ca; C38H70O8Ca, C40H74O8Ca (major components)
Molecular weight
Assay
Description White or slightly yellowish powder or brittle solid with a char
acteristic odour
Identification
Test for lactid acid Passes test
Solubility Slightly soluble in hot water
Purity
Calcium Not less than 1 % and not more than 5,2 %
▼M44
__________
▼B
E 491 SORBITAN MONOSTEARATE
Synonyms
Definition A mixture of the partial esters of sorbitol and its anhydrides with
edible, commercial stearic acid
Einecs 215-664-9
Chemical name
Chemical formula
Molecular weight
Assay Content not less than 95 % of a mixture of sorbitol, sorbitan, and
isosorbide esters
Description Light, cream- to tan-coloured beads or flakes or a hard, waxy solid
with a slight characteristic odour
Identification
Solubility Soluble at temperatures above its melting point in toluene, dioxane,
carbon tetrachloride, ether, methanol, ethanol and aniline; insoluble
in petroleum ether and acetone; insoluble in cold water but
dispersible in warm water; soluble with haze at temperatures
above 50 °C in mineral oil and ethyl acetate
▼M28
Identification test By acid value, iodine value (not more than 4), gas chromatography
▼B
Purity
02012R0231 — EN — 27.10.2024 — 033.001 — 192
▼B
E 492 SORBITAN TRISTEARATE
Synonyms
edible, commercial stearic acid
Einecs 247-891-4
Chemical name
Chemical formula
Molecular weight
isosorbide esters
Description Light, cream- to tan-coloured beads or flakes or hard, waxy solid
with a slight odour
Identification
Solubility Slightly soluble in toluene, ether, carbon tetrachloride and ethyl
acetate; dispersible in petroleum ether, mineral oil, vegetable oils,
acetone and dioxane; insoluble in water, methanol and ethanol
▼M28
▼B
Purity
E 493 SORBITAN MONOLAURATE
Synonyms
edible, commercial lauric acid
Einecs 215-663-3
Chemical name
Chemical formula
Molecular weight
02012R0231 — EN — 27.10.2024 — 033.001 — 193
▼B

isosorbide esters
Description Amber-coloured oily viscous liquid, light cream to tan-coloured

beads or flakes or a hard, waxy solid with a slight odour
Identification
Solubility Dispersible in hot and cold water
Purity
E 494 SORBITAN MONOOLEATE
Synonyms
edible, commercial oleic acid. Major constituent is 1,4-sorbitan
monooleate. Other constituents include isosorbide monooleate,
sorbitan dioleate and sorbitan trioleate
Einecs 215-665-4
Chemical name
Chemical formula
Molecular weight
Assay Content not less than 95 % of a mixture of sorbitol, sorbitan and

isosorbide esters
Description Amber-coloured viscous liquid, light cream to tan-coloured beads or

flakes or a hard, waxy solid with a slight characteristic odour
Identification
Solubility Soluble at temperatures above its melting point in ethanol, ether,

ethyl acetate, aniline, toluene, dioxane, petroleum ether and carbon
tetra-chloride. Insoluble in cold water, dispersible in warm water
Iodine value The residue of oleic acid, obtained from the saponification of the
sorbitan monooleate in assay, has a iodine value between 80 and 100
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 194
▼B
E 495 SORBITAN MONOPALMITATE
Synonyms Sorbitan palmitate

edible, commercial palmitic acid
Einecs 247-568-8
Chemical name
Chemical formula
Molecular weight
isosorbide esters
Description Light cream to tan-coloured beads or flakes or a hard, waxy solid
with a slight characteristic odour
Identification
Solubility Soluble at temperatures above its melting point in ethanol, methanol,
ether, ethyl acetate, aniline, toluene, dioxane, petroleum ether and
carbon tetrachloride. Insoluble in cold water but dispersible in warm
water
▼M28
▼B
Infrared absorption spectrum Characteristic of a partial fatty acid ester of polyol
Purity
Sulphate ash Not more than 0,5 %
▼M5
E 499 STIGMASTEROL-RICH PLANT STEROLS
Synonyms
Definition Stigmasterol-rich plant sterols are derived from soybeans and are a
chemically defined simple mixture that comprises not less than 95 %
of plant sterols (stigmasterol, β-sitosterol, campesterol and brassi
casterol), with stigmasterol representing not less than 85 % of the
stigmasterol-rich plant sterols.
02012R0231 — EN — 27.10.2024 — 033.001 — 195
▼M5
Einecs
Chemical name
Stigmasterol (3S,8S,9S,10R,13R,14S,17R)-17-(5-ethyl-6-methyl-hept-3-en-2-yl)-
10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17 -dodecahydro-1Hcyclo
penta[a]phenanthren-3-ol
β-Sitosterol (3S,8S,9S,10R,13R,14S,17R)-17-[(2S,5S)-5-ethyl-6-methylheptan-2-
yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,1 6,17-dodecahydro-1Hcy
clopenta[a]phenanthren-3-ol
Campesterol (3S,8S,9S,10R,13R,14S,17R)-17-(5,6-dimethylheptan-2-yl)-10,13-
dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dode cahydro-1Hcyclo
penta[a]phenanthren-3-ol
Brassicasterol (3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5R)-5,6- dimethylhept-3-en-

2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16 ,17-dodecahydro-
1Hcyclopenta[a]phenanthren-3-ol
Chemical formula
Stigmasterol C29H48O
β-Sitosterol C29H50O
Campesterol C28H48O
Brassicasterol C28H46O
Molecular weight
Stigmasterol 412,6 g/mol
β-Sitosterol 414,7 g/mol
Campesterol 400,6 g/mol
Brassicasterol 398,6 g/mol
Assay (products containing only free Content not less than 95 % on a total free sterol/stanol basis on the
sterols and stanols) anhydrous basis
Description Free-flowing, white to off-white powders, pills or pastilles;

colourless to pale yellow liquids
Identification
Solubility Practically insoluble in water. Phytosterols and phytostanols are

soluble in acetone and ethyl acetate.
Stigmasterol content Not less than 85 % (w/w)
Other plant sterols/stanols: either Not more than 15 % (w/w)

singularly or in combination including
Brassicasterol, campestanol, campesterol,
Δ-7-campesterol, cholesterol, chleros
terol, sitostanol and β-sitosterol.
Purity
Total Ash Not more than 0,1 %
Residual Solvents Ethanol: Not more than 5 000 mg/kg
Total plate count Not more than 1 000 CFU/g
Yeasts Not more than 100 CFU/g
Moulds Not more than 100 CFU/g

02012R0231 — EN — 27.10.2024 — 033.001 — 196
▼M5
Escherichia coli Not more than 10 CFU/g
▼B
E 500 (i) SODIUM CARBONATE
Synonyms Soda ash
Definition
Einecs 207-838-8
Chemical name Sodium carbonate
Chemical formula Na2CO3 · nH2O (n = 0, 1 or 10)
Assay Content not less than 99 % of Na2CO3 on the anhydrous basis
Description Colourless crystals or white, granular or crystalline powder

The anhydrous form is hygroscopic, the decahydrate efflorescent
Identification
Test for carbonate Passes test
Purity
Loss on drying Not more than 2 % (anhydrous), 15 % (monohydrate) or 55 %-65 %

(decahydrate) (70 °C raising gradually to 300 °C, to constant weight)
E 500 (ii) SODIUM HYDROGEN CARBONATE
Synonyms Sodium bicarbonate; sodium acid carbonate; Bicarbonate of soda;

Baking soda
Definition
Einecs 205-633-8
Chemical name Sodium hydrogen carbonate
Chemical formula NaHCO3
Description Colourless or white crystalline masses or crystalline powder
Identification
Purity
Loss on drying Not more than 0,25 % (over silica gel, 4 hours)
Ammonium salts No odour of ammonia detectable after heating

02012R0231 — EN — 27.10.2024 — 033.001 — 197
▼B
E 500 (iii) SODIUM SESQUICARBONATE
Synonyms
Definition
Einecs 208-580-9
Chemical name Sodium monohydrogen dicarbonate
Chemical formula Na2CO3 · NaHCO3 · 2H2O
Assay Content between 35,0 % and 38,6 % of NaHCO3 and between
46,4 % and 50,0 % of Na2CO3
Description White flakes, crystals or crystalline powder
Identification
Purity
Sodium chloride Not more than 0,5 %
E 501 (i) POTASSIUM CARBONATE
Synonyms
Definition
Einecs 209-529-3
Chemical name Potassium carbonate
Chemical formula K2CO3 · nH2O (n = 0 or 1,5)
Description White, very deliquescent powder.
The hydrate occurs as small, white, translucent crystals or granules
Identification
Solubility Very soluble in water. Insoluble in ethanol
Purity
Loss on drying Not more than 5 % (anhydrous) or 18 % (hydrate) (180 °C, 4 hours)
02012R0231 — EN — 27.10.2024 — 033.001 — 198
▼B
E 501 (ii) POTASSIUM HYDROGEN CARBONATE
Synonyms Potassium bicarbonate; Acid potassium carbonate
Definition
Einecs 206-059-0
Chemical name Potassium hydrogen carbonate
Chemical formula KHCO3
Assay Content not less than 99,0 % and not more than 101,0 % KHCO3 on
the anhydrous basis
Description Colourless crystals or white powder or granules
Identification
Purity
Loss on drying Not more than 0,25 % (over silica gel, 4 hours)
E 503 (i) AMMONIUM CARBONATE
Synonyms
Definition Ammonium carbonate consists of ammonium carbamate, ammonium

carbonate and ammonium hydrogen carbonate in varying proportions
Einecs 233-786-0
Chemical name Ammonium carbonate
Chemical formula CH6N2O2, CH8N2O3 and CH5NO3
Molecular weight Ammonium carbamate 78,06; ammonium carbonate 98,73;

ammonium hydrogen carbonate 79,06
Assay Content not less than 30,0 % and not more than 34,0 % of NH3
Description White powder or hard, white or translucent masses or crystals.

Becomes opaque on exposure to air and is finally converted into
white porous lumps or powder (of ammonium bicarbonate) due to
loss of ammonia and carbon dioxide
Identification
pH About 8,6 (5 % solution)

02012R0231 — EN — 27.10.2024 — 033.001 — 199
▼B
Purity
Non-volatile matter Not more than 500 mg/kg
Chlorides Not more than 30 mg/kg
Sulphate Not more than 30 mg/kg
E 503 (ii) AMMONIUM HYDROGEN CARBONATE
Synonyms Ammonium bicarbonate
Definition
Einecs 213-911-5
Chemical name Ammonium hydrogen carbonate
Chemical formula CH5NO3
Identification
pH About 8,0 (5 % solution)
Purity
Non-volatile matter Not more than 500 mg/kg
E 504 (i) MAGNESIUM CARBONATE
Synonyms Hydromagnesite
Definition Magnesium carbonate is a basic hydrated or a monohydrated

magnesium carbonate or a mixture of the two.
Einecs 208-915-9
Chemical name Magnesium carbonate
Chemical formula MgCO3 · nH2O
Assay Not less than 24 % and not more than 26,4 % of Mg
Description Odourless, light, white friable masses or as a bulky white powder

02012R0231 — EN — 27.10.2024 — 033.001 — 200
▼B
Identification
Solubility Practically insoluble both in water or ethanol
Purity
Calcium Not more than 0,4 %
E 504 (ii) MAGNESIUM HYDROXIDE CARBONATE
Synonyms Magnesium hydrogen carbonate; Magnesium subcarbonate (light or

heavy); Hydrated basic magnesium carbonate; Magnesium carbonate
hydroxide
Definition
Einecs 235-192-7
Chemical name Magnesium carbonate hydroxide hydrated
Chemical formula 4MgCO3Mg(OH)2 · 5H2O
Molecular weight 485
Assay Mg content not less than 40,0 % and not more than 45,0 %
calculated as MgO
Description Light, white friable mass or bulky white powder
Identification
Solubility Practically insoluble in water. Insoluble in ethanol
Purity
Calcium Not more than 1,0 %
E 507 HYDROCHLORIC ACID
Synonyms Hydrogen chloride; Muriatic acid
Definition
Einecs 231-595-7
Chemical name Hydrochloric acid

02012R0231 — EN — 27.10.2024 — 033.001 — 201
▼B
Chemical formula HCl
Assay Hydrochloric acid is commercially available in varying concen

trations. Concentrated hydrochloric acid contains not less than
35,0 % HCl
Description Clear, colourless or slightly yellowish, corrosive liquid having a

pungent odour
Identification
Test for chloride Passes test
Solubility Soluble in water and in ethanol
Purity
Total organic compounds Total organic compounds (non-fluorine containing): not more than
5 mg/kg
Benzene: not more than 0,05 mg/kg
Fluorinated compounds (total): not more than 25 mg/kg
Non-volatile matter Not more than 0,5 %
Reducing substances Not more than 70 mg/kg (as SO2)
Oxidising substances Not more than 30 mg/kg (as Cl2)
E 508 POTASSIUM CHLORIDE
Synonyms Sylvine; Sylvite
Definition
Einecs 231-211-8
Chemical name Potassium chloride
Chemical formula KCl
Description Colourless, elongated, prismatic or cubital crystals or white granular

powder. Odourless
Identification
Purity
Test for sodium Negative

02012R0231 — EN — 27.10.2024 — 033.001 — 202
▼B
E 509 CALCIUM CHLORIDE
Synonyms
Definition
Einecs 233-140-8
Chemical name Calcium chloride
Chemical formula CaCl2 · nH2O (n = 0,2 or 6)
Molecular weight 110,99 (anhydrous), 147,02 (dihydrate), 219,08 (hexahydrate)
Description White, odourless, hygroscopic powder or deliquescent crystals
Identification
Purity
Magnesium and alkali salts Not more than 5 % on the dried basis (calculated as sulphates)
E 511 MAGNESIUM CHLORIDE
Synonyms
Definition
Einecs 232-094-6
Chemical name Magnesium chloride
Chemical formula MgCl2 · 6H2O
Description Colourless, odourless, very deliquescent flakes or crystals
Identification
Solubility Very soluble in water, freely soluble in ethanol
Purity
Ammonium Not more than 50 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 203
▼B
E 512 STANNOUS CHLORIDE
Synonyms Tin chloride; Tin dichloride
Definition
Einecs 231-868-0
Chemical name Stannous chloride dihydrate
Chemical formula SnCl2 · 2H2O
Description Colourless or white crystals

May have a slight odour of hydrochloric acid
Identification
Test for tin (II) Passes test
Solubility Water: soluble in less than its own weight of water, but it forms an
insoluble basic salt with excess water
Ethanol: soluble
Purity
E 513 SULPHURIC ACID
Synonyms Oil of vitriol; Dihydrogen sulphate
Definition
Einecs 231-639-5
Chemical name Sulphuric acid
Chemical formula H2SO4
Assay Sulphuric acid is commercially available in varying concentrations.

The concentrated form contains not less than 96,0 %
Description Clear, colourless or slightly brown, very corrosive oily liquid
Identification
Solubility Miscible with water, with generation of much heat, also with ethanol
02012R0231 — EN — 27.10.2024 — 033.001 — 204
▼B
Purity
Ash Not more than 0,02 %
Reducing matter Not more than 40 mg/kg (as SO2)
Nitrate Not more than 10 mg/kg (on H2SO4 basis)
Chloride Not more than 50 mg/kg
E 514 (i) SODIUM SULPHATE
Synonyms
Definition
Einecs
Chemical name Sodium sulphate
Chemical formula Na2SO4 · nH2O (n = 0 or 10)

322,04 (decahydrate)
Description Colourless crystals or a fine, white, crystalline powder

The decahydrate is efflorescent
Identification
pH Neutral or slightly alkaline to litmus paper (5 % solution)
Purity
Loss on drying Not more than 1,0 % (anhydrous) or not more than 57 %
(decahydrate) at 130 °C
E 514 (ii) SODIUM HYDROGEN SULPHATE
Synonyms Acid sodium sulphate; Sodium bisulphate; Nitre cake
Definition
Chemical name Sodium hydrogen sulphate
Chemical formula NaHSO4

02012R0231 — EN — 27.10.2024 — 033.001 — 205
▼B
Description White, odourless crystals or granules
Identification
pH Solutions are strongly acidic
Purity
Loss on drying Not more than 0,8 %
E 515 (i) POTASSIUM SULPHATE
Synonyms
Definition
Einecs
Chemical name Potassium sulphate
Chemical formula K2SO4
Description Colourless or white crystals or crystalline powder
Identification
Solubility Freely soluble in water, insoluble in ethanol
Purity
E 515 (ii) POTASSIUM HYDROGEN SULPHATE
Synonyms Potassium bisulphate; Potassium acid sulphate
Definition
Einecs
Chemical name Potassium hydrogen sulphate
Chemical formula KHSO4

02012R0231 — EN — 27.10.2024 — 033.001 — 206
▼B
Description White deliquescent crystals, pieces or granules
Identification
Purity
E 516 CALCIUM SULPHATE
Synonyms Gypsum; Selenite; Anhydrite
Definition
Einecs 231-900-3
Chemical name Calcium sulphate
Chemical formula CaSO4 · nH2O (n = 0 or 2)
Molecular weight 136,14 (anhydrous), 172,18 (dihydrate)
Description Fine, white to slightly yellowish-white odourless powder
Identification
Solubility Slightly soluble in water, insoluble in ethanol
Purity
Loss on drying Anhydrous: not more than 1,5 % (250 °C, constant weight)
Dihydrate: not more than 23 % (250 °C, constant weight)
E 517 AMMONIUM SULPHATE
Synonyms
Definition
Einecs 231-984-1
Chemical name Ammonium sulphate

02012R0231 — EN — 27.10.2024 — 033.001 — 207
▼B
Chemical formula (NH4)2SO4
Assay Content not less than 99,0 % and not more than 100,5 %
Description White powder, shining plates or crystalline fragments
Identification
Purity
Loss on ignition Not more than 0,25 %
E 520 ALUMINIUM SULPHATE
Synonyms Alum
Definition
Einecs
Chemical name Aluminium sulphate
Chemical formula Al2(SO4)3
Assay Content not less than 99,5 % on the ignited basis
Description White powder, shining plates or crystalline fragments
Identification
Test for aluminium Passes test
pH 2,9 or above (5 % solution)
Purity
Loss on ignition Not more than 5 % (500 °C, 3 hours)
Alkalies and alkaline earths Not more than 0,4 %
E 521 ALUMINIUM SODIUM SULPHATE
Synonyms Soda alum; Sodium alum
Definition
Einecs 233-277-3
02012R0231 — EN — 27.10.2024 — 033.001 — 208
▼B
Chemical name Aluminium sodium sulphate
Chemical formula AlNa(SO4)2 · nH2O (n = 0 or 12)
Assay Content on the anhydrous basis not less than 96,5 % (anhydrous)
and 99,5 % (dodecahydrate)
Description Transparent crystals or white crystalline powder
Identification
Solubility Dodecahydrate is freely soluble in water. The anhydrous form is

slowly soluble in water. Both forms are insoluble in ethanol
Purity
Loss on drying Anhydrous form: not more than 10,0 % (220 °C, 16 hours)
Dodecahydrate: not more than 47,2 % (50-55 °C, 1 hour then
200 °C, 16 hours)
E 522 ALUMINIUM POTASSIUM SULPHATE
Synonyms Potassium alum; Potash alum
Definition
Einecs 233-141-3
Chemical name Aluminium potassium sulphate dodecahydrate
Chemical formula AlK(SO4)2 · 12 H2O
Description Large, transparent crystals or white crystalline powder
Identification
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 209
▼B
E 523 ALUMINIUM AMMONIUM SULPHATE
Synonyms Ammonium alum
Definition
Einecs 232-055-3
Chemical name Aluminium ammonium sulphate
Chemical formula AlNH4(SO4)2 · 12 H2O
Description Large, colourless crystals or white powder
Identification
Solubility Freely soluble in water, soluble in ethanol
Purity
Alkali metals and alkaline earths Not more than 0,5 %
E 524 SODIUM HYDROXIDE
Synonyms Caustic soda; Lye
Definition
Einecs 215-185-5
Chemical name Sodium hydroxide
Chemical formula NaOH
Assay Content of solid forms not less than 98,0 % of total alkali (as
NaOH). Content of solutions accordingly, based on the stated or
labelled percentage of NaOH
Description White or nearly white pellets, flakes, sticks, fused masses or other
forms. Solutions are clear or slightly turbid, colourless or slightly
coloured, strongly caustic and hygroscopic and when exposed to the
air they absorb carbon dioxide, forming sodium carbonate
02012R0231 — EN — 27.10.2024 — 033.001 — 210
▼B
Identification
pH Strongly alkaline (1 % solution)
Solubility Very soluble in water. Freely soluble in ethanol
Purity
Water insoluble and organic matter A 5 % solution is completely clear and colourless to slightly
coloured
Carbonate Not more than 0,5 % (as Na2CO3)
E 525 POTASSIUM HYDROXIDE
Synonyms Caustic potash
Definition
Einecs 215-181-3
Chemical name Potassium hydroxide
Chemical formula KOH
Assay Content not less than 85,0 % of alkali calculated as KOH
Description White or nearly white pellets, flakes, sticks, fused masses or other
forms
Identification
pH Strongly alkaline (1 % solution)
Solubility Very soluble in water. Freely soluble in ethanol
Purity
Water insoluble matter A 5 % solution is completely clear and colourless
Carbonate Not more than 3,5 % (as K2CO3)
E 526 CALCIUM HYDROXIDE
Synonyms Slaked lime; Hydrated lime
Definition
Einecs 215-137-3
Chemical name Calcium hydroxide
Chemical formula Ca(OH)2

02012R0231 — EN — 27.10.2024 — 033.001 — 211
▼B
Identification
Test for alkali Passes test
Solubility Slightly soluble in water. Insoluble in ethanol. Soluble in glycerol
Purity
Magnesium and alkali salts Not more than 2,7 %
Barium Not more than 300 mg/kg
E 527 AMMONIUM HYDROXIDE
Synonyms Aqua ammonia; Strong ammonia solution
Definition
Einecs
Chemical name Ammonium hydroxide
Chemical formula NH4OH
Assay Content not less than 27 % of NH3
Description Clear, colourless solution, having an exceedingly pungent, char

acteristic odour
Identification
Test for ammonia Passes test
Purity
Non-volatile matter Not more than 0,02 %
E 528 MAGNESIUM HYDROXIDE
Synonyms
Definition
Einecs
Chemical name Magnesium hydroxide
Chemical formula Mg(OH)2
Description Odourless, white bulky powder

02012R0231 — EN — 27.10.2024 — 033.001 — 212
▼B
Identification
Solubility Practically insoluble in water and in ethanol
Purity
Loss on ignition Not more than 33 % (800 °C to constant weight)
Calcium oxide Not more than 1,5 %
E 529 CALCIUM OXIDE
Synonyms Burnt lime
Definition
Einecs 215-138-9
Chemical name Calcium oxide
Chemical formula CaO
Description Odourless, hard, white or greyish white masses of granules, or white

to greyish powder
Identification
Reaction with water Heat is generated on moistening the sample with water
Solubility Slightly soluble in water. Insoluble in ethanol. Soluble in glycerol
Purity
Loss on ignition Not more than 10,0 % (ca. 800 °C to constant weight)
Magnesium and alkali salts Not more than 3,6 %
E 530 MAGNESIUM OXIDE
Synonyms
Definition
Einecs 215-171-9
Chemical name Magnesium oxide

02012R0231 — EN — 27.10.2024 — 033.001 — 213
▼B
Chemical formula MgO
Description A very bulky, white powder known as light magnesium oxide or a
relative dense, white powder known as heavy magnesium oxide. 5 g
of light magnesium oxide occupy a volume of at least 33 ml, while
5 g of heavy magnesium oxide occupy a volume of not more than
20 ml
Identification
Solubility Practically insoluble in water. Insoluble in ethanol
Purity
Loss on ignition Not more than 5,0 % (ca. 800 °C to constant weight)
Calcium oxide Not more than 1,5 %
▼M20
E 534 IRON TARTRATE
Synonyms Iron meso-tartrate; complexation product of sodium tartrate with

iron(III) chloride
Definition Iron tartrate is manufactured by the isomerisation of L-tartrate to an
equilibrium mixture of D-, L- and meso-tartrate followed by addition
of iron(III) chloride.
CAS number 1280193-05-9
Chemical name Iron(III) complexation product of D(+)-, L(-)- and meso-2,3 dihydro
xybutanedioic acids
Chemical formula Fe(OH)2 C4H4O6Na
Assay
meso-tartrate > 28 %, expressed as the anion on dry basis
D(-)- and L(+)-tartrate > 10 %, expressed as the anion on dry basis
Iron(III) > 8 %, expressed as the anion on dry basis
Description Dark green aqueous solution typically comprising ca 35 % by
weight complexation products
Identification Highly soluble in water
Positive tests for tartrate and iron
pH of a 35 % aqueous solution of complexation products between
3,5 and 3,9
Purity
Chloride Not more than 25 %
Sodium Not more than 23 %
Oxalate Not more than 1,5 % expressed as oxalate on dry basis
02012R0231 — EN — 27.10.2024 — 033.001 — 214
▼B
E 535 SODIUM FERROCYANIDE
Synonyms Yellow prussiate of soda; Sodium hexacyanoferrate
Definition
Einecs 237-081-9
Chemical name Sodium ferrocyanide
Chemical formula Na4Fe(CN)6 · 10 H2O
Description Yellow crystals or crystalline powder
Identification
Test for ferrocyanide Passes test
Purity
Free moisture Not more than 1,0 %
Free cyanide Not detectable
Ferricyanide Not detectable
E 536 POTASSIUM FERROCYANIDE
Synonyms Yellow prussiate of potash; Potassium hexacyanoferrate
Definition
Einecs 237-722-2
Chemical name Potassium ferrocyanide
Chemical formula K4Fe(CN)6 · 3 H2O
Description Lemon yellow crystals
Identification
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 215
▼B
E 538 CALCIUM FERROCYANIDE
Synonyms Yellow prussiate of lime; Calcium hexacyanoferrate
Definition
Einecs 215-476-7
Chemical name Calcium ferrocyanide
Chemical formula Ca2Fe(CN)6 · 12H2O
Description Yellow crystals or crystalline powder
Identification
Purity
E 541 SODIUM ALUMINIUM PHOSPHATE, ACIDIC
Synonyms SALP
Definition
Einecs 232-090-4
Chemical name Sodium trialuminium tetradecahydrogen octaphosphate tetrahydrate

(A); Trisodium dialuminium pentadecahydrogen octaphosphate (B)
Chemical formula NaAl3H14(PO4)8 · 4H2O (A)

Na3Al2H15(PO4)8 (B)
Molecular weight 949,88 (A)

897,82 (B)
Assay Content not less than 95,0 % (both forms)

02012R0231 — EN — 27.10.2024 — 033.001 — 216
▼B
Description White odourless powder
Identification
pH Acid to litmus
Solubility Insoluble in water. Soluble in hydrochloric acid
Purity
Loss on ignition 19,5-21,0 % (A) (750-800 °C, 2 hours)

15-16 % (B) (750-800 °C, 2 hours)
E 551 SILICON DIOXIDE
Synonyms Silica; Silicium dioxide
Definition Silicon dioxide is an amorphous substance, which is produced

synthetically by either a vapour-phase hydrolysis process, yielding
fumed silica, or by a wet process, yielding precipitated silica, silica
gel, or hydrous silica. Fumed silica is produced in essentially an
anhydrous state, whereas the wet-process products are obtained as
hydrates or contain surface absorbed water
Einecs 231-545-4
Chemical name Silicon dioxide
Chemical formula (SiO2)n
Molecular weight 60,08 (SiO2)
Assay Content after ignition not less than 99,0 % (fumed silica) or 94,0 %
(hydrated forms)
Description White, fluffy powder or granules. Hygroscopic
Identification
Test for silica Positive
Purity
Loss on drying Not more than 2,5 % (fumed silica, 105 °C, 2 hours)
Not more than 8,0 % (precipitated silica and silica gel, 105 °C,
2 hours)
02012R0231 — EN — 27.10.2024 — 033.001 — 217
▼B
Not more than 70 % (hydrous silica, 105 °C, 2 hours)
Loss on ignition Not more than 2,5 % after drying (1 000 °C, fumed silica)
Not more than 8,5 % after drying (1 000 °C, hydrated forms)
Soluble ionisable salts Not more than 5,0 % (as Na2SO4)
E 552 CALCIUM SILICATE
Synonyms
Definition Calcium silicate is a hydrous or anhydrous silicate with varying

proportions of CaO and SiO2. The product should be free of
asbestos.
Einecs 215-710-8
Chemical name Calcium silicate
Chemical formula
Molecular weight
Assay Content on the anhydrous basis:

— as SiO2 not less than 50 % and not more than 95 %
— as CaO not less than 3 % and not more than 35 %
Description White to off-white free-flowing powder that remains so after

absorbing relatively large amounts of water or other liquids
Identification
Test for silicate Passes test
Gel formation Forms a gel with mineral acids
Purity
Loss on ignition Not less than 5 % and not more than 14 % (1 000 °C, constant
weight)
Sodium Not more than 3 %
E 553a (i) MAGNESIUM SILICATE
Synonyms
Definition Magnesium silicate is a synthetic compound of which the molar ratio

of magnesium oxide to silicon dioxide is approximately 2:5
Einecs
Chemical name
02012R0231 — EN — 27.10.2024 — 033.001 — 218
▼B
Chemical formula
Molecular weight
Assay Content not less than 15 % of MgO and not less than 67 % of SiO2
on the ignited basis
Description Very fine, white, odourless powder, free from grittiness
Identification
Purity
Loss on ignition Not more than 15 % after drying (1 000 °C, 20 min)
Water soluble salts Not more than 3 %
Free alkali Not more than 1 % (as NaOH)
E 553a (ii) MAGNESIUM TRISILICATE
Synonyms
Definition
Einecs 239-076-7
Chemical name Magnesium trisilicate
Chemical formula Mg2Si3O8 · nH2O (approximate composition)
Molecular weight
Assay Content not less than 29,0 % of MgO and not less than 65,0 % of
SiO2 both on the ignited basis
Description Fine, white powder, free from grittiness
Identification
Purity
Loss on ignition Not less than 17 % and not more than 34 % (1 000 °C)
Water soluble salts Not more than 2 %
Free alkali Not more than 1 % (as NaOH)

02012R0231 — EN — 27.10.2024 — 033.001 — 219
▼B
E 553b TALC
Synonyms Talcum
Definition Naturally occurring form of hydrous magnesium silicate containing

varying proportions of such associated minerals as alpha-quartz,
calcite, chlorite, dolomite, magnesite, and phlogopite. The product
should be free of asbestos.
Einecs 238-877-9
Chemical name Magnesium hydrogen metasilicate
Chemical formula Mg3(Si4O10)(OH)2
Assay
Description Light, homogeneous, white or almost white powder, greasy to the

touch
Identification
Infrared absorption spectrum Characteristic peaks at 3 677, 1 018 and 669 cm-1
X-ray diffraction Peaks at 9,34/4,66/3,12 Å
Solubility Insoluble in water and ethanol
Purity
Acid soluble matter Not more than 6 %
Acid-soluble iron Not detectable
E 554 SODIUM ALUMINIUM SILICATE
Synonyms Sodium silicoaluminate; Sodium aluminosilicate; Aluminium sodium

silicate
Definition
Einecs
Chemical name Sodium aluminium silicate
Chemical formula
Molecular weight

— as SiO2 not less than 66,0 % and not more than 88,0 %
— as Al2O3 not less than 5,0 % and not more than 15,0 %
Description Fine white amorphous powder or beads
Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 220
▼B
Purity
Loss on ignition Not less than 5,0 % and not more than 11,0 % on the anhydrous
basis (1 000 °C to constant weight)
Sodium Not less than 5 % and not more than 8,5 % (as Na2O) on the
anhydrous basis
E 555 POTASSIUM ALUMINIUM SILICATE
Synonyms Mica
Definition Natural mica consists of mainly potassium aluminium silicate
(muscovite)
Einecs 310-127-6
Chemical name Potassium aluminium silicate
Chemical formula KAl2[AlSi3O10](OH)2
Description Light grey to white crystalline platelets or powder
Identification
Solubility Insoluble in water, diluted acids and alkali and organic solvents
Purity
Antimony Not more than 20 mg/kg
Zinc Not more than 25 mg/kg
Chromium Not more than 100 mg/kg
Copper Not more than 25 mg/kg
▼M3
E 556 CALCIUM ALUMINIUM SILICATE (1)
▼B
Synonyms Calcium aluminosilicate; Calcium silicoaluminate; Aluminium

calcium silicate
Definition
Einecs
Chemical name Calcium aluminium silicate
(1) Period of application: until 31 January 2014.

02012R0231 — EN — 27.10.2024 — 033.001 — 221
▼B
Chemical formula
Molecular weight
— as SiO2 not less than 44,0 % and not more than 50,0 %
— as Al2O3 not less than 3,0 % and not more than 5,0 %
— as CaO not less than 32,0 % and not more than 38,0 %
Description Fine white, free-flowing powder
Identification
Purity
Loss on ignition Not less than 14,0 % and not more than 18,0 on the anhydrous basis
(1 000 °C, constant weight)
▼M3
E 559 ALUMINIUM SILICATE (KAOLIN) (1)
▼B
Synonyms Kaolin, light or heavy

Definition Aluminium silicate hydrous (kaolin) is a purified white plastic clay
composed of kaolinite, potassium aluminium silicate, feldspar and
quartz. Processing should not include calcination. The raw
kaolinitic clay used in the production of aluminium silicate shall
have a level of dioxin which does not make it injurious to health or
unfit for human consumption. The product should be free of
asbestos
Einecs 215-286-4 (kaolinite)
Chemical name
Chemical formula Al2Si2O5(OH)4 (kaolinite)
Assay Content not less than 90 % (sum of silica and alumina, after
ignition)
Silica (SiO2) Between 45 % and 55 %
Alumina (Al2O3) Between 30 % and 39 %
Description Fine, white or greyish white, unctuous powder. Kaolin is made up
of loose aggregations of randomly oriented stacks of kaolinite
flakes or of individual hexagonal flakes
Identification
Test for alumina Passes test
X-ray diffraction Characteristic peaks at 7,18/3,58/2,38/1,78 Å
Infrared absorption spectrum Peaks at 3 700 and 3 620 cm-1
(1) Period of application: until 31 January 2014.

02012R0231 — EN — 27.10.2024 — 033.001 — 222
▼B
Purity
Loss on ignition Between 10 and 14 % (1 000 °C, constant weight)
Acid soluble matter Not more than 2 %
Iron Not more than 5 %
Potassium oxide (K2O) Not more than 5 %
Carbon Not more than 0,5 %
E 570 FATTY ACIDS
Synonyms
Definition Linear fatty acids, caprylic acid (C8), capric acid (C10), lauric acid
(C12), myristic acid (C14), palmitic acid (C16), stearic acid (C18),
oleic acid (C18:1)
Einecs
Chemical name Octanoic acid (C8); decanoic acid (C10); dodecanoic acid (C12);
tetradecanoic acid (C14); hexadecanoic acid (C16); octadecanoic
acid (C18); 9-octadecenoic acid (C18:1)
Chemical formula
Molecular weight
Assay Not less than 98 % by chromatography
Description A colourless liquid or white solid obtained from oils and fats
Identification
Identification test Individual fatty acids can be identified by acid value, iodine value,
gas chromatography
Purity
Residue on ignition Not more than 0,1 %
Unsaponifiable matter Not more than 1,5 %
E 574 GLUCONIC ACID
Synonyms D-gluconic acid; Dextronic acid
Definition Gluconic acid is an aqueous solution of gluconic acid and

glucono-delta-lactone
Einecs
Chemical name Gluconic acid
Chemical formula C6H12O7 (gluconic acid)

02012R0231 — EN — 27.10.2024 — 033.001 — 223
▼B
Assay Content not less than 49,0 % (as gluconic acid)
Description Colourless to light yellow, clear syrupy liquid
Identification
Formation of phenylhydrazine derivative Positive. Compound formed melts between 196 °C and 202 °C with
decomposition
Purity
Residue on ignition Not more than 1,0 % 550 °C +/– 20 °C till disappearance of organic
residues (black spots).
Reducing matter Not more than 2,0 % (as D-glucose)
Chloride Not more than 350 mg/kg
Sulphite Not more than 20 mg/kg
E 575 GLUCONO-DELTA-LACTONE
Synonyms Gluconolactone; GDL; D-Gluconic acid delta-lactone; Delta-gluco

nolactone
Definition Glucono-delta-lactone is the cyclic 1,5-intramolecular ester of

D-gluconic acid. In aqueous media it is hydrolysed to an equilibrium
mixture of D-gluconic acid (55 % - 66 %) and the delta- and
gamma-lactones
Einecs 202-016-5
Chemical name D-Glucono-1,5-lactone
Description Fine, white, nearly odourless, crystalline powder
Identification
Formation of phenylhydrazine derivative Positive. Compound formed melts between 196 °C and 202 °C with
of gluconic acid decomposition
Solubility Freely soluble in water. Sparingly soluble in ethanol
Purity
Reducing substances Not more than 0,5 % (as D-glucose)
E 576 SODIUM GLUCONATE
Synonyms Sodium salt of D-gluconic acid
Definition Manufactured by fermentation or chemical catalytic oxidation

02012R0231 — EN — 27.10.2024 — 033.001 — 224
▼B
Einecs 208-407-7
Chemical name Sodium D-gluconate
Chemical formula C6H11NaO7 (anhydrous)
Description White to tan, granular to fine, crystalline powder
Identification
Test for gluconate Passes test
Solubility Very soluble in water. Sparingly soluble in ethanol
Purity
Reducing matter Not more than 1,0 % (as D-glucose)
E 577 POTASSIUM GLUCONATE
Synonyms Potassium salt of D-gluconic acid

Definition
Einecs 206-074-2
Chemical name Potassium D-gluconate
Chemical formula C6H11KO7 (anhydrous)
C6H11KO7 · H2O (monohydrate)
Assay Content not less than 97,0 % and not more than 103,0 % on dried
basis
Description Odourless, free flowing white to yellowish white, crystalline powder
or granules
Identification
Purity
Loss on drying Anhydrous: not more than 3,0 % (105 °C, 4 hours, vacuum)
Monohydrate: not less than 6 % and not more than 7,5 % (105 °C,
4 hours, vacuum)
E 578 CALCIUM GLUCONATE
Synonyms Calcium salt of D-gluconic acid
Definition
Einecs 206-075-8
Chemical name Calcium di-D-gluconate

02012R0231 — EN — 27.10.2024 — 033.001 — 225
▼B
Chemical formula C12H22CaO14 (anhydrous)
C12H22CaO14 · H2O (monohydrate)
Molecular weight 430,38 (anhydrous form)

Assay anhydrous: Content not less than 98 % and not more than 102 % on
the dried basis
monohydrate: not less than 98 % and not more than 102 % on the
‘as is’ basis.
Description Odourless, white crystalline granules or powder, stable in air
Identification
Purity
Loss on drying Not more than 3,0 % (105 °C, 16 hours) (anhydrous)
Not more than 2,0 % (105 °C, 16 hours) (monohydrate)
E 579 FERROUS GLUCONATE
Synonyms
Definition
Einecs 206-076-3
Chemical name Ferrous di-D-gluconate dihydrate; Iron(II) di-gluconate dihydrate
Chemical formula C12H22FeO14·2H2O
Description Pale greenish-yellow to yellowish-grey powder or granules, which

may have a faint odour of burnt sugar
Identification
Solubility Soluble with slight heating in water. Practically insoluble in ethanol
Test for ferrous ion Passes test
Formation of phenylhy-drazine derivative Positive

of gluconic acid
pH Between 4 and 5,5 (10 % solution)
Purity
Oxalic acid Not detectable
Iron (Fe III) Not more than 2 %

02012R0231 — EN — 27.10.2024 — 033.001 — 226
▼B
Reducing substances Not more than 0,5 % expressed as glucose
E 585 FERROUS LACTATE
Synonyms Iron(II) lactate; Iron(II) 2-hydroxy propanoate;

Propanoic acid, 2-hydroxy-iron(2 +) salt (2:1)
Definition
Einecs 227-608-0
Chemical name Ferrous 2-hydroxy propanoate
Chemical formula C6H10FeO6· nH2O (n = 2 or 3)
Molecular weight 270,02 (dihydrate)

288,03 (trihydrate)
Description Greenish-white crystals or light green powder having a characteristic

smell
Identification
Solubility Soluble in water. Practically insoluble in ethanol
Test for ferrous ion Passes test
pH Between 4 and 6 (2 % solution)
Purity
Loss on drying Not more than 18 % (100 °C, under vacuum, approximately
700 mm Hg)
Iron (Fe III) Not more than 0,6 %
E 586 4-HEXYLRESORCINOL
Synonyms 4-Hexyl-1,3-benzenediol; Hexylresorcinol
Definition
Einecs 205-257-4
Chemical name 4-Hexylresorcinol
Assay Not less than 98 % on the dried basis (4 hours at room temperature)

02012R0231 — EN — 27.10.2024 — 033.001 — 227
▼B
Identification
Solubility Freely soluble in ether and acetone; very slightly soluble in water
Nitric acid test To 1 ml of a saturated solution of the sample, add 1 ml of nitric

acid. A light red colour appears
Bromine test To 1 ml of saturated solution of the sample, add 1 ml of bromine

TS. A yellow, flocculent precipitate dissolves producing a yellow
solution
Purity
Acidity Not more than 0,05 %
Resorcinol and other phenols Shake about 1 g of the sample with 50 ml of water for a few
minutes, filter, and to the filtrate add 3 drops of ferric chloride
TS. No red or blue colour is produced
E 620 GLUTAMIC ACID
Synonyms L-Glutamic acid; L-α-Aminoglutaric acid
Definition
Einecs 200-293-7
Chemical name L-Glutamic acid; L-2-amino-pentanedioic acid
Chemical formula C5H9NO4
Assay Content not less than 99,0 % and not more than 101,0 % on the
anhydrous basis
Solubility Sparingly soluble in water; practically insoluble in ethanol or ether
Identification
Test for glutamic acid (by thin layer Passes test

chromatography)
Specific rotation [α]D20 between + 31,5° and + 32,2°

(10 % solution (anhydrous basis) in 2N HCl, 200 mm tube)
pH Between 3,0 and 3,5 (saturated solution)
Purity
Pyrrolidone carboxylic acid Not more than 0,2 %

02012R0231 — EN — 27.10.2024 — 033.001 — 228
▼B
E 621 MONOSODIUM GLUTAMATE
Synonyms Sodium glutamate; MSG
Definition
Einecs 205-538-1
Chemical name Monosodium L-glutamate monohydrate
Chemical formula C5H8NaNO4 · H2O
anhydrous basis
Solubility Freely soluble in water; practically insoluble in ethanol or ether
Description White, practically odourless crystals or crystalline powder
Identification
Test for glutamic acid (by thin-layer Passes test

chromatography)

Purity
E 622 MONOPOTASSIUM GLUTAMATE
Synonyms Potassium glutamate; MPG
Definition
Einecs 243-094-0
Chemical name Monopotassium L-glutamate monohydrate
Chemical formula C5H8KNO4 · H2O
anhydrous basis
Identification

chromatography)
02012R0231 — EN — 27.10.2024 — 033.001 — 229
▼B
Purity
E 623 CALCIUM DIGLUTAMATE
Synonyms Calcium glutamate
Definition
Einecs 242-905-5
Chemical name Monocalcium di-L-glutamate
Chemical formula C10H16CaN2O8 · nH2O (n = 0, 1, 2 or 4)
anhydrous basis
Identification

chromatography)
Specific rotation [α]D20 between + 27,4° and + 29,2° (for calcium diglutamate with
n = 4) (10 % solution (anhydrous basis) in 2N HCl, 200 mm tube)
Purity
Water content Not more than 19,0 % (for calcium diglutamate with n = 4) (Karl
Fischer)
E 624 MONOAMMONIUM GLUTAMATE
Synonyms Ammonium glutamate
Definition
Einecs 231-447-1
Chemical name Monoammonium L-glutamate monohydrate
Chemical formula C5H12N2O4 · H2O
Assay Content not less than 99,0 % and not more 101,0 % on the
anhydrous basis
02012R0231 — EN — 27.10.2024 — 033.001 — 230
▼B
Identification

chromatography)

Purity
E 625 MAGNESIUM DIGLUTAMATE
Synonyms Magnesium glutamate
Definition
Einecs 242-413-0
Chemical name Monomagnesium di-L-glutamate tetrahydrate
Chemical formula C10H16MgN2O8 · 4H2O
anhydrous basis
Solubility Very soluble in water; practically insoluble in ethanol or ether
Description Odourless, white or off-white crystals or powder
Identification

chromatography)

Purity
E 626 GUANYLIC ACID
Synonyms 5'-Guanylic acid
Definition
Einecs 201-598-8
02012R0231 — EN — 27.10.2024 — 033.001 — 231
▼B
Chemical name Guanosine-5'-monophosphoric acid
Chemical formula C10H14N5O8P
Solubility Slightly soluble in water, practically insoluble in ethanol
Description Odourless, colourless or white crystals or white crystalline powder
Identification
Test for ribose Passes test
Test for organic phosphate Passes test
pH Between 1,5 and 2,5 (0,25 % solution)
Spectrometry Maximum absorption of a 20 mg/l solution in 0,01N HCl at 256 nm
Purity
Other nucleotides Not detectable by thin-layer chromatography
E 627 DISODIUM GUANYLATE
Synonyms Sodium guanylate; Sodium 5'-guanylate
Definition
▼M3
Einecs 226-914-1
▼B
Chemical name Disodium guanosine-5'-monophosphate
Chemical formula C10H12N5Na2O8P · nH2O (n = ca. 7)
Solubility Soluble in water, sparingly soluble in ethanol, practically insoluble

in ether
Identification
Spectrometry maximum absorption of a 20 mg/l solution in 0,01N HCl at 256 nm
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 232
▼B
E 628 DIPOTASSIUM GUANYLATE
Synonyms Potassium guanylate; Potassium 5'-guanylate
Definition
▼M3
Einecs 221-849-5
▼B
Chemical name Dipotassium guanosine-5'-monophosphate
Chemical formula C10H12K2N5O8P
Solubility Freely soluble in water, practically insoluble in ethanol
Identification
Purity
E 629 CALCIUM GUANYLATE
Synonyms Calcium 5'-guanylate
Definition
Einecs
Chemical name Calcium guanosine-5'-monophosphate
Chemical formula C10H12CaN5O8P · nH2O
Solubility Sparingly soluble in water
Description Odourless, white or off-white crystals or powder
Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 233
▼B
Purity
E 630 INOSINIC ACID
Synonyms 5'-Inosinic acid
Definition
Einecs 205-045-1
Chemical name Inosine-5'-monophosphoric acid
Chemical formula C10H13N4O8P
Solubility Freely soluble in water, slightly soluble in ethanol
Description Odourless, colourless or white crystals or powder
Identification
Purity
E 631 DISODIUM INOSINATE
Synonyms Sodium inosinate; Sodium 5'-inosinate
Definition
Einecs 225-146-4
Chemical name Disodium inosine-5'-monophosphate
Chemical formula C10H11N4Na2O8P · H2O
Solubility Soluble in water, sparingly soluble in ethanol, practically insoluble

in ether
Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 234
▼B
pH Between 7,0 and 8,5
Purity
Water content Not more than 28,5 % (Karl Fischer)
E 632 DIPOTASSIUM INOSINATE
Synonyms Potassium inosinate; Potassium 5'-inosinate
Definition
Einecs 243-652-3
Chemical name Dipotassium inosine-5'-monophosphate
Chemical formula C10H11K2N4O8P
Solubility Freely soluble in water; practically insoluble in ethanol
Identification
Purity
E 633 CALCIUM INOSINATE
Synonyms Calcium 5'-inosinate
Definition
Einecs
Chemical name Calcium inosine-5'-monophosphate
Chemical formula C10H11CaN4O8P · nH2O

02012R0231 — EN — 27.10.2024 — 033.001 — 235
▼B
Identification
Purity
E 634 CALCIUM 5'-RIBONUCLEOTIDE
Synonyms
Definition
Einecs
Chemical name Calcium 5′-ribonucleotide is essentially a mixture of calcium

inosine-5′-monophosphate and calcium guanosine-5′-monophosphate
Chemical formula C10H11N4CaO8P · nH2O

C10H12N5CaO8P · nH2O
Molecular weight
Assay Content of both major components not less than 97,0 %, and of each
component not less than 47,0 % and not more than 53 %, in every
case on the anhydrous basis
Description Odourless, white or nearly white crystals or powder
Identification
Purity
E 635 DISODIUM 5'-RIBONUCLEOTIDE
Synonyms Sodium 5'-ribonucleotide
Definition
Einecs
Chemical name Disodium 5'-ribonucleotide is essentially a mixture of disodium

inosine-5'-monophosphate and disodium guanosine-5'-mono
phosphate
02012R0231 — EN — 27.10.2024 — 033.001 — 236
▼B
Chemical formula C10H11N4O8P · nH2O
C10H12N5Na2O8P · nH2O
Molecular weight
Assay Content of both major components not less than 97,0 %, and of each
component not less than 47,0 % and not more than 53 %, in every
case on the anhydrous basis
Solubility Soluble in water, sparingly soluble in ethanol practically insoluble in

ether
Description Odourless, white or nearly white crystals or powder
Identification
Purity
E 640 GLYCINE AND ITS SODIUM SALT

(i) GLYCINE
Synonyms Aminoacetic acid; Glycocoll
Definition
Einecs 200-272-2
Chemical name Aminoacetic acid
Identification
Test for amino acid Passes test
Purity
(ii) SODIUM GLYCINATE
Synonyms
Definition
Einecs 227-842-3
02012R0231 — EN — 27.10.2024 — 033.001 — 237
▼B
Chemical name Sodium glycinate
Chemical formula C2H5NO2 Na
Molecular weight 98
Identification
Test for amino acid Passes test
Purity
▼M18
E 641 L-LEUCINE
Synonyms 2-Aminoisobutylacetic acid; L-2-Amino-4-methylvaleric acid; alpha-

Aminoisocaproic acid; (S)-2-Amino-4-methylpentanoic acid; L-Leu
Definition
Einecs 200-522-0
CAS number 61-90-5
Chemical name L-Leucine; L-2-Amino-4-methylpentanoic acid
anhydrous basis
Description White or almost white crystalline powder or shiny flakes
Identification
Solubility Soluble in water, acetic acid, dilute HCl and alkaline hydroxides and
carbonates; slightly soluble in ethanol

(4 % solution (anhydrous basis) in 6N HCl)
Purity
Loss on drying Not more than 0,5 % (100 °C – 105 °C)
Sulphated Ash Not more than 0,1 %
Sulphates Not more than 300 mg/kg
Ammonium Not more than 200 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 238
▼B
E 650 ZINC ACETATE
Synonyms Acetic acid, zinc salt, dihydrate
Definition
Einecs
Chemical name Zinc acetate dihydrate
Chemical formula C4H6O4 Zn · 2H2O
Assay Content not less than 98 % and not more than 102 % of C4H6O4 Zn
· 2H2O
Description Colourless crystals or fine, off-white powder
Identification
Test for zinc Passes test
Purity
Alkalines and alkaline earths Not more than 0,2 %
Organic volatile impurities Passes test
E 900 DIMETHYL POLYSILOXANE
Synonyms Polydimethyl siloxane; Silicone fluid; Silicone oil; Dimethyl silicone

02012R0231 — EN — 27.10.2024 — 033.001 — 239
▼B
Definition Dimethylpolysiloxane is a mixture of fully methylated linear

siloxane polymers containing repeating units of the formula (CH3)2
SiO and stabilised with trimethylsiloxy end-blocking units of the
formula (CH3)3 SiO
Einecs
Chemical name Siloxanes and silicones, di-methyl
Chemical formula (CH3)3-Si-[O-Si(CH3)2]n-O-Si(CH3)3
Molecular weight
Assay Content of total silicon not less than 37,3 % and not more than
38,5 %
Description Clear, colourless, viscous liquid
Identification
Specific gravity (25 °C/25 °C) Between 0,964 and 0,977
Infrared absorption spectrum The infrared absorption spectrum of a liquid film of the sample
between two sodium chloride plates exhibits relative maxima at
the same wavelengths as those of a similar preparation of Dimethyl
polysiloxane Reference Standard
Purity
Loss on drying Not more than 0,5 % (150 °C, 4h)
Viscosity Not less than 1,00 · 10– 4

m2s– 1
at 25 °C
E 901 BEESWAX, WHITE AND YELLOW
Synonyms White wax; Yellow wax
Definition Yellow bees wax is the wax obtained by melting the walls of the
honeycomb made by the honey bee, Apis mellifera L., with hot
water and removing foreign matter
White beeswax is obtained by bleaching yellow beeswax
Einecs 232-383-7
Chemical name
Chemical formula
Molecular weight
Assay
Description Yellowish white (white form) or yellowish to greyish brown (yellow

form) pieces or plates with a fine-grained and non-crystalline
fracture, having an agreeable, honey-like odour
Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 240
▼B
Solubility Insoluble in water, sparingly soluble in alcohol, very soluble in

chloroform and ether
Purity
Saponification value 87-104
Peroxide value Not more than 5
Glycerol and other polyols Not more than 0,5 % (as glycerol)
Ceresin, paraffins and certain other Transfer 3,0 g of the sample to a 100 ml round-bottomed flask, add
waxes 30 ml of a 4 % w/v solution of potassium hydroxide in
aldehyde-free ethanol and boil gently under a reflux condenser for
2 h. Remove the condenser and immediately insert a thermometer.
Place the flask in water at 80 °C and allow to cool, swirling the
solution continuously. No precipitate is formed before the
temperature reaches 65 °C, although the solution may be opalescent.
Fats, Japan wax, rosin and soaps Boil 1 g of the sample for 30 min with 35 ml of a 1 in 7 solution of
sodium hydroxide, maintaining the volume by the occasional
addition of water, and cool the mixture. The wax separates and
the liquid remains clear. Filter the cold mixture and acidify the
filtrate with hydrochloric acid. No precipitate is formed.
E 902 CANDELILLA WAX
Synonyms
Definition Candelilla wax is a purified wax obtained from the leaves of the
candelilla plant, Euphorbia antisyphilitica
Einecs 232-347-0
Chemical name
Chemical formula
Molecular weight
Assay
Description Hard, yellowish brown, opaque to translucent wax
Identification
Melting range Between 68,5 °C and 72,5 °C
Solubility Insoluble in water, soluble in chloroform and toluene
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 241
▼B
E 903 CARNAUBA WAX
Synonyms
Definition Carnauba wax is a purified wax obtained from the leaf buds and
leaves of the Brazilian Mart wax palm, Copernicia cerifera
Einecs 232-399-4
Chemical name
Chemical formula
Molecular weight
Assay
Description Light brown to pale yellow powder or flakes or hard and brittle solid
with a resinous fracture
Identification
Solubility Insoluble in water, partly soluble in boiling ethanol, soluble in

chloroform and diethyl ether
Purity
Unsaponifiable matter Not less than 50 % and not more than 55 %
E 904 SHELLAC
Synonyms Bleached shellac; White shellac
Definition Shellac is the purified and bleached lac, the resinous secretion of the
insect Laccifer (Tachardia) lacca Kerr (Fam. Coccidae)
Einecs 232-549-9
Chemical name
Chemical formula
Molecular weight
Assay
Description Bleached shellac — off-white, amorphous, granular resin

Wax-free bleached shellac — light yellow, amorphous, granular
resin
Identification
Solubility Insoluble in water; freely (though very slowly) soluble in alcohol;

slightly soluble in acetone
Acid value Between 60 and 89

02012R0231 — EN — 27.10.2024 — 033.001 — 242
▼B
Purity
Loss on drying Not more than 6,0 % (40 °C, over silica gel, 15 hours)
Rosin Absent
Wax Bleached shellac: not more than 5,5 %

Wax-free bleached shellac: not more than 0,2 %
E 905 MICROCRYSTALLINE WAX
Synonyms Petroleum wax; Hydrocarbon wax; Fischer-Tropsch wax; Synthetic

wax; Synthetic paraffin
Definition Refined mixtures of solid, saturated hydrocarbons, obtained from

petroleum or synthetic feedstocks
Description White to amber, odourless wax
Identification
Solubility Insoluble in water, very slightly soluble in ethanol

Alternative [n]D1201,426-1,440
Purity
Molecular weight Average not less than 500
Viscosity Not less than 1,1 × 10– 5

m2s– 1at 100 °C
Alternative: Not less than 0,8 × 10– 5
m2s– 1at 120 °C, if solid at
100 °C
Carbon number at 5 % distillation point Not more than 5 % of molecules with carbon number less than 25
Colour Passes test
Sulphur Not more than 0,4 wt %
Polycyclic aromatic compounds Benzo(a)pyrene no more than 50 μg/kg
E 907 HYDROGENATED POLY-1-DECENE
Synonyms Hydrogenated polydec-1-ene; Hydrogenated poly-alpha-olefin
Definition
Einecs
Chemical name
Chemical formula C10nH20n+2 where n = 3-6
Molecular weight 560 (average)
Assay Not less than 98,5 % of hydrogenated poly-1-decene, having the

following oligomer distribution:
C30: 13-37 %
C40: 35-70 %
C50: 9-25 %
C60: 1-7 %
02012R0231 — EN — 27.10.2024 — 033.001 — 243
▼B
Description
Identification
Solubility Insoluble in water; slightly soluble in ethanol; soluble in toluene
Burning Burns with a bright flame and a paraffin-like characteristic smell
Viscosity Between 5,7 × 10– 6

and 6,1 × 10– 6
m2s– 1
at 100 °C
Purity
Compounds with carbon number less Not more than 1,5 %

than 30
Readily carbonisable substances After 10 minutes shaking in a boiling water bath, a tube of sulphuric
acid with a 5 g sample of hydrogenated poly-1-decene is not darker
than a very slight straw colour
▼M15
__________
▼B
E 914 OXIDISED POLYETHYLENE WAX
Synonyms
Definition Polar reaction products from mild oxidation of polyethylene
Einecs
Chemical name Oxidised polyethylene
Chemical formula
Molecular weight
Assay
Description Almost white flakes, powder, granules or pellets
Identification
Density Between 0,92 and 1,05 (20 °C)
Drop point Greater than 95 °C
Purity
Viscosity Not less than 8,1 · 10– 5

m2s– 1
at 120 °C
Other wax types Not detectable (by differential scanning calorimetry and/or infrared
spectroscopy)
Oxygen Not more than 9,5 %
Chromium Not more than 5 mg/kg

02012R0231 — EN — 27.10.2024 — 033.001 — 244
▼B
E 920 L-CYSTEINE
Synonyms
Definition L-cysteine hydrochloride or hydrochloride monohydrate. Human hair

may not be used as a source for this substance
Einecs 200-157-7 (anhydrous)
Chemical name
Chemical formula C3H7NO2S · HCl · nH2O (where n = 0 or 1)
anhydrous basis
Description White powder or colourless crystals
Identification
Solubility Freely soluble in water and in ethanol
Melting range Anhydrous form melts at about 175 °C
Specific rotation [α]D20: between + 5,0° and + 8,0° or

[α]D25: between + 4,9° and 7,9°
Purity
Loss on drying Between 8,0 % and 12,0 %

Not more than 2,0 % (anhydrous form)
Ammonium-ion Not more than 200 mg/kg
E 927b CARBAMIDE
Synonyms Urea
Definition
Einecs 200-315-5
Chemical name
Chemical formula CH4N2O

02012R0231 — EN — 27.10.2024 — 033.001 — 245
▼B
Description Colourless to white, prismatic, crystalline powder or small, white
pellets
Identification

Soluble in ethanol
Precipitation with nitric acid To pass the test a white, crystalline precipitate is formed
Colour reaction To pass the test a reddish-violet colour is produced
Melting range 132 °C to 135 °C
Purity
Ethanol-insoluble matter Not more than 0,04 %
Alkalinity Passes test
Ammonium-ion Not more than 500 mg/kg
Biuret Not more than 0,1 %
E 938 ARGON
Synonyms
Definition
Einecs 231-147-0
Chemical name Argon
Chemical formula Ar
Atomic weight 40
Assay Not less than 99 %
Description Colourless, odourless, non-flammable gas
Identification
Purity
Water content Not more than 0,05 %
Methane and other hydrocarbons Not more than 100 μl/l (calculated as methane)
E 939 HELIUM
Synonyms
Definition
Einecs 231-168-5
Chemical name Helium
Chemical formula He
Atomic weight 4

02012R0231 — EN — 27.10.2024 — 033.001 — 246
▼B
Identification
Purity
E 941 NITROGEN
Synonyms
Definition
Einecs 231-783-9
Chemical name Nitrogen
Chemical formula N2
Molecular weight 28
Identification
Purity
Nitrogen dioxide and nitrogen oxide Not more than 10 μl/l
Oxygen Not more than 1 %
E 942 NITROUS OXIDE
Synonyms
Definition
Einecs 233-032-0
Chemical name Nitrous oxide
Chemical formula N 2O
Molecular weight 44
Description Colourless, non-flammable gas, sweetish odour
Identification
Purity
Nitrogen dioxide and nitrogen oxide Not more than 10 μl/l

02012R0231 — EN — 27.10.2024 — 033.001 — 247
▼B
E 943a BUTANE
Synonyms n-Butane
Definition
Einecs
Chemical name Butane
Chemical formula CH3CH2CH2CH3
Description Colourless gas or liquid with mild, characteristic odour
Identification
Vapour pressure 108,935 kPa at 20 °C
Purity
Methane Not more than 0,15 % v/v
Ethane Not more than 0,5 % v/v
Propane Not more than 1,5 % v/v
Isobutane Not more than 3,0 % v/v
1,3-butadiene Not more than 0,1 % v/v
Moisture Not more than 0,005 %
E 943b ISOBUTANE
Synonyms 2-Methyl propane
Definition
Einecs
Chemical name 2-methyl propane
Chemical formula (CH3)2CH CH3
Identification
Purity
Propane Not more than 2,0 % v/v
n-Butane Not more than 4,0 % v/v

02012R0231 — EN — 27.10.2024 — 033.001 — 248
▼B
E 944 PROPANE
Synonyms
Definition
Einecs
Chemical name Propane
Chemical formula CH3CH2CH3
Identification
Purity
Isobutane Not more than 2,0 % v/v
n-Butane Not more than 1,0 % v/v
E 948 OXYGEN
Synonyms
Definition
Einecs 231-956-9
Chemical name Oxygen
Chemical formula O2
Molecular weight 32
Identification
Purity
E 949 HYDROGEN
Synonyms
Definition
Einecs 215-605-7
Chemical name Hydrogen
Chemical formula H2
Molecular weight 2
02012R0231 — EN — 27.10.2024 — 033.001 — 249
▼B
Description Colourless, odourless, highly flammable gas
Identification
Purity
Water content Not more than 0,005 % v/v
Oxygen Not more than 0,001 % v/v
Nitrogen Not more than 0,07 % v/v
E 950 ACESULFAME K
Synonyms Acesulfame potassium; Potassium salt of 3,4-dihydro-6-methyl-

1,2,3-oxathiazin-4-one-2,2-dioxide
Definition
Einecs 259-715-3
Chemical name 6-methyl-1,2,3-oxathiazin-4(3H)-one-2,2-dioxide potassium salt
Chemical formula C4H4KNO4S
Assay Content not less than 99 % of C4H4KNO4S on the anhydrous basis
Description Odourless, white, crystalline powder. Approximately 200 times as

sweet as sucrose
Identification
Solubility Very soluble in water, very slightly soluble in ethanol
Ultraviolet absorption Maximum 227 ± 2 nm for a solution of 10 mg in 1 000 ml of water
Test for potassium Passes test (test the residue obtained by igniting 2 g of the sample)
Precipitation test Add a few drops of a 10 % solution of sodium cobaltnitrite to a

solution of 0,2 g of the sample in 2 ml of acetic acid and 2 ml of
water. A yellow precipitate is produced
Purity
Organic impurities Passes test for 20 mg/kg of UV active components
E 951 ASPARTAME
Synonyms Aspartyl phenylalanine methyl ester
Definition
Einecs 245-261-3
Chemical name N-L-α-Aspartyl-L-phenylalanine-1-methyl ester, 3-amino-N-(α-

carbomethoxy-phenethyl)-succinamic acid-N-methyl ester

02012R0231 — EN — 27.10.2024 — 033.001 — 250
▼B
Assay Not less than 98 % and not more than 102 % of C14H18N2O5 on the
anhydrous basis
Description White, odourless, crystalline powder having a sweet taste.

Approximately 200 times as sweet as sucrose
Identification
Solubility Slightly soluble in water and in ethanol
pH Between 4,5 and 6,0 (1 in 125 solution)
Specific rotation [α]D20: + 14,5° to + 16,5°

Determine in a 4 in 100/15 N formic acid solution within 30 minutes
after preparation of the sample solution
Purity
Sulphated ash Not more than 0,2 % (expressed on dry weight basis)
Transmittance The transmittance of a 1 % solution in 2N hydrochloric acid,

determined in a 1-cm cell at 430 nm with a suitable spectropho
tometer, using 2N hydrochloric acid as a reference, is not less
than 0,95, equivalent to an absorbance of not more than
approximately 0,022
5-Benzyl-3,6-dioxo-2-piperazineacetic Not more than 1,5 % (expressed on dry weight basis)

acid
E 952 CYCLAMIC ACID AND ITS Na AND Ca SALTS

(i) CYCLAMIC ACID
Synonyms Cyclohexylsulphamic acid; Cyclamate
Definition
Einecs 202-898-1
Chemical name Cyclohexanesulphamic acid; cyclohexylaminosulphonic acid
Chemical formula C6H13NO3S
Assay Cyclohexylsulphamic acid contains not less than 98 % and not more
than the equivalent of 102 % of C6H13NO3S, calculated on the
anhydrous basis
Description A practically colourless, white crystalline powder. Approximately 40

times as sweet as sucrose
Identification
Precipitation test Acidify a 2 % solution with hydrochloric acid, add 1 ml of an

approximately molar solution of barium chloride in water and
filter if any haze or precipitate forms. To the clear solution add
1 ml of a 10 % solution of sodium nitrite. A white precipitate forms.
Purity
Loss on drying Not more than 1 % (105 °C, 1 hour)
Selenium Not more than 30 mg/kg (expressed as selenium on dry weight

basis)
02012R0231 — EN — 27.10.2024 — 033.001 — 251
▼B
Cyclohexylamine Not more than 10 mg/kg (expressed on dry weight basis)
Dicyclohexylamine Not more than 1 mg/kg (expressed on dry weight basis)
Aniline Not more than 1 mg/kg (expressed on dry weight basis)
(ii) SODIUM CYCLAMATE
Synonyms Cyclamate; Sodium salt of cyclamic acid

Definition
Einecs 205-348-9
Chemical name Sodium cyclohexanesulphamate, sodium cyclohexylsulphamate
Chemical formula C6H12NNaO3S and the dihydrate form C6H12NNaO3S·2H2O
Molecular weight 201,22 calculated on the anhydrous form
237,22 calculated on the hydrated form
Assay Not less than 98 % and not more than 102 % on the dried basis
Dihydrate form: not less than 84 % on the dried basis
Description White, odourless crystals or crystalline powder. Approximately 30
Identification
Solubility Soluble in water, practically insoluble in ethanol
Purity
Not more than 15,2 % (105 °C, 2 hours) for the dihydrate form
basis)
(iii) CALCIUM CYCLAMATE
Synonyms Cyclamate; Calcium salt of cyclamic acid
Definition
Einecs 205-349-4
Chemical name Calcium cyclohexanesulphamate, calcium cyclohexylsulphamate
Chemical formula C12H24CaN2O6S2· 2H2O
Assay Not less than 98 % and not more than 101 % on the dried basis
Description White, colourless crystals or crystalline powder. Approximately 30

Identification
Solubility Soluble in water, sparingly soluble in ethanol

02012R0231 — EN — 27.10.2024 — 033.001 — 252
▼B
Purity

Not more than 8,5 % (140 °C, 4 hours) for the dihydrate form

basis)
E 953 ISOMALT
Synonyms Hydrogenated isomaltulose.
Definition Manufactured by enzymatic conversion of sucrose with nonviable

cells of Protaminobacter rubrum followed by catalytic hydroge
nation
Einecs
Chemical name Isomalt is a mixture of hydrogenated mono- and disaccharides whose

principal components are the disaccharides:
6-O-α-D-Glucopyranosyl-D-sorbitol (1,6-GPS) and
1-O-α-D-Glucopyranosyl-D-mannitol dihydrate (1,1-GPM)
Chemical formula 6-O-α-D-Glucopyranosyl-D-sorbitol: C12H24O11

1-O-α-D-Glucopyranosyl-D-mannitol dihydrate: C12H24O11.2H2O
Molecular weight 6-O-α-D-Glucopyranosyl-D-sorbitol: 344,3

1-O-α-D-Glucopyranosyl-D-mannitol dihydrate: 380,3
Assay Content not less than 98 % of hydrogenated mono- and disaccharides

and not less than 86 % of the mixture of 6-O-α-D-Glucopyranosyl-D-
sorbitol and 1-O-α-D-Glucopyranosyl-D-mannitol dihydrate determined
on the anhydrous basis.
▼M4
Description Odourless, white, slightly hygroscopic, crystalline mass or aqueous
solution with a minimum concentration of 60 %
▼B
Identification
Solubility Soluble in water, very slightly soluble in ethanol.
HPLC test Comparison with an appropriate reference standard of Isomalt shows

that the 2 principal peaks in the chromatogram of the test solution
are similar in retention time to the 2 principal peaks in the chroma
togram obtained with the reference solution.
▼M4
Purity
Water content Not more than 7 % for solid product (Karl Fischer Method)

temperature 20 °C
D-Mannitol Not more than 3 %
D-Sorbitol Not more than 6 %

02012R0231 — EN — 27.10.2024 — 033.001 — 253
▼M4
▼B
E 954 SACCHARIN AND ITS Na. K AND Ca SALTS

(i) SACCHARIN
Synonyms
Definition
Einecs 201-321-0
Chemical name 3-Oxo-2,3dihydrobenzo(d)isothiazol-1,1-dioxide
Chemical formula C7H5NO3S
Assay Not less than 99 % and not more than 101 % of C7H5NO3S on the
anhydrous basis
Description White crystals or a white crystalline powder, odourless or with a

faint, aromatic odour. Approximately between 300 and 500 times as
sweet as sucrose
Identification
Solubility Slightly soluble in water, soluble in basic solutions, sparingly soluble

in ethanol
Purity
Benzoic and salicylic acid To 10 ml of a 1 in 20 solution, previously acidified with five drops
of acetic acid, add three drops of an approximately molar solution of
ferric chloride in water. No precipitate or violet colour appears
o-Toluenesulphonamide Not more than 10 mg/kg (expressed on dry weight basis)
p-Toluenesulphonamide Not more than 10 mg/kg (expressed on dry weight basis)
Benzoic acid p-sulphonamide Not more than 25 mg/kg (expressed on dry weight basis)
Readily carbonisable substances Absent
Selenium Not more than 30 mg/kg (expressed on dry weight basis)
(ii) SODIUM SACCHARIN
Synonyms Saccharin; Sodium salt of saccharin
Definition
Einecs 204-886-1
Chemical name Sodium o-benzosulphimide; sodium salt of 2,3-dihydro-3-oxobenzi

sosulphonazole; oxobenzisosulphonazole; 1,2-benzisothiazolin-3-
one-1, 1-dioxide sodium salt dihydrate
02012R0231 — EN — 27.10.2024 — 033.001 — 254
▼B
Chemical formula C7H4NNaO3S·2H2O
Assay Not less than 99 % and not more than 101 % of C7H4NNaO3S on
the anhydrous basis
Description White crystals or a white crystalline efflorescent powder, odourless

or with a faint odour. Approximately between 300 and 500 times as
sweet as sucrose in dilute solutions
Identification
Purity
(iii) CALCIUM SACCHARIN
Synonyms Saccharin; Calcium salt of saccharin
Definition
Chemical name Calcium o-benzosulphimide; calcium salt of 2,3-dihydro-3-oxoben

zisosulphonazole; 1,2-benzisothiazolin-3-one-1,1-dioxide calcium
salt hydrate (2:7)
Einecs 229-349-9
Chemical formula C14H8CaN2O6S2·3½H2O
Assay Not less than 95 % of C14H8CaN2O6S2 on the anhydrous basis

faint odour. Approximately between 300 and 500 times as sweet as
sucrose in dilute solutions
Identification
Solubility Freely soluble in water, soluble in ethanol
Purity
02012R0231 — EN — 27.10.2024 — 033.001 — 255
▼B
o-Toluenesulphonamide Not more than 10 mg/kg expressed (on dry weight basis)
p-Toluenesulphonamide Not more than 10 mg/kg expressed (on dry weight basis)
Benzoic acid p-sulphonamide Not more than 25 mg/kg expressed (on dry weight basis)
(iv) POTASSIUM SACCHARIN
Synonyms Saccharin; Potassium salt of saccharin

Definition
Einecs
Chemical name Potassium o-benzosulphimide; potassium salt of 2,3-dihydro-3-
oxobenzisosulphonazole; potassium salt of 1,2-benzisothiazolin-3-
one-1,1-dioxide monohydrate
Chemical formula C7H4KNO3S·H2O
Assay Not less than 99 % and not more than 101 % of C7H4KNO3S on the
anhydrous basis
faint odour, having an intensely sweet taste, even in very dilute
solutions. Approximately between 300 and 500 times as sweet as
sucrose
Identification
Purity
E 955 SUCRALOSE
Synonyms 4,1’,6’-Trichlorogalactosucrose
Definition
Einecs 259-952-2
Chemical name 1,6-Dichloro-1,6-dideoxy-β-D-fructofuranosyl-4-chloro-4-deoxy-α-D-
galactopyranoside
Chemical formula C12H19Cl3O8
02012R0231 — EN — 27.10.2024 — 033.001 — 256
▼B
Assay Content not less than 98 % and not more than 102 % C12H19Cl3O8
calculated on an anhydrous basis.
Description White to off-white, practically odourless, crystalline powder.
Identification
Solubility Freely soluble in water, methanol and ethanol

Slightly soluble in ethyl acetate
Infrared absorption spectrum The infrared spectrum of a potassium bromide dispersion of the
sample exhibits relative maxima at similar wave numbers as those
shown in the reference spectrum obtained using a sucralose reference
standard.
Thin layer chromatography The main spot in the test solution has the same Rf value as that of
the main spot of standard solution A referred to in the test for other
chlorinated disaccharides. This standard solution is obtained by
dissolving 1,0g of sucralose reference standard in 10 ml of methanol.
Specific rotation [α]D20 + 84,0° to + 87,5° calculated on the anhydrous basis (10 %
w/v solution)
Purity
Other chlorinated disaccharides Not more than 0,5 %
Chlorinated monosaccharides Not more than 0,1 %
Triphenylphosphine oxide Not more than 150 mg/kg
Methanol Not more than 0,1 %
E 957 THAUMATIN
Synonyms
Definition
Einecs 258-822-2
Chemical name Thaumatin is obtained by aqueous extraction (pH 2,5 to 4) of the

arils of the fruit of strains of Thaumatococcus daniellii (Benth) and
consists essentially of the proteins thaumatin I and thaumatin II
together with minor amounts of plant constituents derived from the
source material
Chemical formula Polypeptide of 207 amino acids
Molecular weight Thaumatin I 22209

Thaumatin II 22293
Assay Not less than 15,1 % nitrogen on the dried basis equivalent to not
less than 93 % proteins (N × 6,2)
Description Odourless, cream-coloured powder. Approximately 2 000 to 3 000

Identification
Solubility Very soluble in water, insoluble in acetone
Purity
Carbohydrates Not more than 3 % (expressed on dry weight basis)
Sulphated ash Not more than 2 % (expressed on dry weight basis)
Aluminium Not more than 100 mg/kg (expressed on dry weight basis)
02012R0231 — EN — 27.10.2024 — 033.001 — 257
▼B
Total aerobic microbial count Not more than 1 000 colonies per gram
E 959 NEOHESPERIDINE DIHYDROCHALCONE
Synonyms Neohesperidin dihydrochalcone; NHDC; Hesperetin dihydro

chalcone-4′-β-neohesperidoside; Neohesperidin DC
Definition It is obtained by catalytic hydrogenation of neohesperidin
Einecs 243-978-6
Chemical name 2-O-α-L-rhamnopyranosyl-4′-β-D-glucopyranosyl hesperetin dihy

drochalcone.
Description Off-white, odourless, crystalline powder. Approximately between

1 000 and 1 800 times as sweet as sucrose
Identification
Solubility Freely soluble in hot water, very slightly soluble in cold water,
practically insoluble in ether and benzene
Ultraviolet absorption maximum 282 to 283 nm for a solution of 2 mg in 100 ml methanol
Neu's test Dissolve about 10 mg of neohesperidine DC in 1 ml methanol, add

1 ml of a 1 % 2-aminoethyl diphenyl borate methanolic solution. A
bright yellow colour is produced
Purity
Arsenic Not more than 3 mg/kg expressed on dry weight basis
▼M33
E 960a STEVIOL GLYCOSIDES FROM STEVIA
▼M21
Synonyms
Definition The manufacturing process comprises two main phases: the first
involving water extraction of the leaves of the Stevia rebaudiana
Bertoni plant and preliminary purification of the extract by
employing ion exchange chromatography to yield a steviol
glycoside primary extract, and the second involving recrystallisation
of the steviol glycosides from methanol or aqueous ethanol
resulting in a final product containing not less than 95 % of the
below identified 11 related steviol glycosides, in any combination
and ratio.
The additive may contain residues of ion-exchange resins used in
the manufacturing process. Several other related steviol glycosides
that may be generated as a result of the production process, but do
not occur naturally in the Stevia rebaudiana plant have been
identified in small amounts (0,10 to 0,37 % w/w).
02012R0231 — EN — 27.10.2024 — 033.001 — 258
▼M21
Chemical name Steviolbioside: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)

oxy]kaur-16-en-18-oic acid
Rubusoside: 13-β-D-glucopyranosyloxykaur-16-en-18-oic acid, β-
D-glucopyranosyl ester
Dulcoside A: 13-[(2-O-α–L-rhamnopyranosyl-β–D-glucopyranosyl)
oxy]kaur-16-en-18-oic acid, β-D-glucopyranosyl ester
Stevioside: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyrano
syl)oxy]kaur-16-en-18-oic acid, β-D-glucopyranosyl ester
Rebaudioside A: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopy
ranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid, β-D-
glucopyranosyl ester
Rebaudioside B: 13-[(2-O-β–D-glucopyranosyl-3-O-β–D-glucopy
ranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid
Rebaudioside C: 13-[(2-O-α–L-rhamnopyranosyl-3-O-β–D-glucopy
Rebaudioside D: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopy
ranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid, 2-O-β-D-
glucopyranosyl-β-D-glucopyranosyl ester
Rebaudioside E: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyrano
syl)oxy]kaur-16-en-18-oic acid, 2-O-β-D-glucopyranosyl-β-D-
Rebaudioside F: 13[(2-O-β-D-xylofurananosyl-3-O-β-D-glucopy
Rebaudioside M: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopy
glucopyranosyl-3-O-β-D-glucopyranosyl-β-D-glucopyranosyl ester
Molecular formula Trivial name Formula Conversion factor
Steviol C20 H30 O3 1,00
Steviolbioside C32 H50 O13 0,50
Rubusoside C32 H50 O13 0,50
Dulcoside A C38 H60 O17 0,40
Stevioside C38 H60 O18 0,40
Rebaudioside A C44 H70 O23 0,33
Rebaudioside B C38 H60 O18 0,40
Rebaudioside C C44 H70 O22 0,34
Rebaudioside D C50 H80 O28 0,29
Rebaudioside E C44 H70 O23 0,33
Rebaudioside F C43 H68 O22 0,34
Rebaudioside M C56 H90 O33 0,25

02012R0231 — EN — 27.10.2024 — 033.001 — 259
▼M21
Molecular weight and CAS No Trivial name CAS Number Molecular weight
(g/mol)
Steviol 318,46
Steviolbioside 41093-60-1 642,73
Rubusoside 64849-39-4 642,73
Dulcoside A 64432-06-0 788,87
Stevioside 57817-89-7 804,88
Rebaudioside A 58543-16-1 967,01
Rebaudioside B 58543-17-2 804,88
Rebaudioside C 63550-99-2 951,02
Rebaudioside D 63279-13-0 1 129,15
Rebaudioside E 63279-14-1 967,01
Rebaudioside F 438045-89-7 936,99
Rebaudioside M 1220616-44-3 1 291,30
Assay Not less than 95 % steviolbioside, rubusoside, dulcoside A,

stevioside, rebaudiosides A, B, C, D, E, F and M on the dried
basis, in any combination and ratio.
Description White to light yellow powder, approximately between 200 and 350
times sweeter than sucrose (at 5 % sucrose equivalency).
Identification
Solubility Freely soluble to slightly soluble in water
Purity
Loss on drying Not more than 6 % (105 °C, 2h)
Residual solvents Not more than 200 mg/kg methanol

Not more than 5 000 mg/kg ethanol
▼M33
E 960c(i) REBAUDIOSIDE M PRODUCED VIA ENZYME MODIFICATION OF STEVIOL GLYCOSIDES
FROM STEVIA
Synonyms
Definition Rebaudioside M is a steviol glycoside composed predominantly of

rebaudioside M with minor amounts of other steviol glycosides
such as rebaudioside A, rebaudioside B, rebaudioside D, rebau
dioside I, and stevioside.
Rebaudioside M is obtained via enzymatic bioconversion of
puriﬁed steviol glycoside leaf extracts (95% steviol glycosides) of
the Stevia rebaudiana Bertoni plant using UDP-glucosyltransferase
and sucrose synthase enzymes produced by the genetically
modified yeasts K. phaffi (formerly known as Pichia pastoris)
UGT-a and K. phaffi UGT-b that facilitate the transfer of glucose
from sucrose and UDP-glucose to steviol glycosides via glycosidic
bonds.
02012R0231 — EN — 27.10.2024 — 033.001 — 260
▼M33
After removal of the enzymes by solid-liquid separation and heat

treatment, the purification involves concentration of the rebau
dioside M by resin adsorption, followed by recrystallisation of
rebaudioside M resulting in a final product containing not less
than 95 % of rebaudioside M. ►M38 Viable cells of the yeasts
K. phaffii UGT-a and K. phaffii UGT-b and their DNA shall not be
detected in the food additive. ◄
Chemical name Rebaudioside M: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopy

Rebaudioside M C56 H90 O33 0,25
(g/mol)
Rebaudioside M 1220616-44-3 1,291.29
Assay Not less than 95 % rebaudioside M on the dried basis.
Identification
Purity
Residual solvent Not more than 5 000 mg/kg ethanol
Residual protein Not more than 5 mg/kg
Particle size Not less than 74 μm [using a mesh #200 sieve with a particle size
limit of 74 μm]
02012R0231 — EN — 27.10.2024 — 033.001 — 261
▼M38
E 960c(ii) REBAUDIOSIDE M PRODUCED VIA ENZYMATIC CONVERSION OF HIGHLY PURIFIED
REBAUDIOSIDE A STEVIA LEAF EXTRACTS
Synonyms
Definition Rebaudioside M produced via enzymatic conversion of highly

purified rebaudioside A stevia leaf extracts is a steviol glycoside
composed predominantly of rebaudioside M with minor amounts of
other steviol glycosides such as rebaudioside A and rebaudioside D.
Rebaudioside M is produced via enzymatic conversion of highly
purified steviol glycoside rebaudioside A extracts (95 % steviol
glycosides) obtained from Stevia rebaudiana Bertoni plant using
UDP-glucosyltransferase and sucrose synthase enzymes produced
by the genetically modified strains of E. coli (pPM294, pFAF170
and pSK401) that facilitate the transfer of glucose from sucrose and
UDP-glucose to steviol glycosides via glycosidic bonds. After
removal of the enzymes by solid-liquid separation and heat
dioside M by resin adsorption, followed by recrystallisation of
the steviol glycosides resulting in a final product containing not
less than 95 % of rebaudioside M. Viable cells of E. coli (pPM294,
pFAF170 and pSK401) and their DNA shall not be detected in the
food additive.
Chemical name Rebaudioside M: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopy

Rebaudioside M C56H90O33 0,25
(g/mol)
Rebaudioside M 1220616-44-3 1 291,29
Assay Not less than 95 % rebaudioside M on the dried basis.
Identification
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 262
▼M38
limit of 74 μm]
E 960c(iii) REBAUDIOSIDE D PRODUCED VIA ENZYMATIC CONVERSION OF HIGHLY PURIFIED

REBAUDIOSIDE A STEVIA LEAF EXTRACTS
Synonyms
Definition Rebaudioside D produced via enzymatic conversion of highly

purified rebaudioside A stevia leaf extracts is a steviol glycoside
composed predominantly of rebaudioside D with minor amounts of
other steviol glycosides such as rebaudioside A and rebaudioside M.
Rebaudioside D is produced via enzymatic conversion of highly
purified steviol glycoside rebaudioside A extracts (95 % steviol
removal of the enzymes by solid-liquid separation and heat treatment,
the purification involves concentration of the rebaudioside D by resin
adsorption, followed by recrystallisation of the steviol glycosides
resulting in a final product containing not less than 95 % of rebau
dioside D and rebaudioside A. Viable cells of E. coli (pPM294,
pFAF170 and pSK401) and their DNA shall not be detected in the
food additive.
Chemical name Rebaudioside D: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopy

glucopyranosyl-β-D-glucopyranosyl ester.
Rebaudioside A: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopy
Rebaudioside D C50H80O28 0,29
Rebaudioside A C44H70O23 0,33
(g/mol)
Rebaudioside D 63279-13-0 1 291,15
Assay Not less than 95 % rebaudiosides D and A on the dried basis.
Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 263
▼M38
Purity
limit of 74 μm]
E 960c(iv) REBAUDIOSIDE AM PRODUCED VIA ENZYMATIC CONVERSION OF HIGHLY PURIFIED

STEVIOSIDE STEVIA LEAF EXTRACTS
Synonyms
Definition Rebaudioside AM produced via enzymatic convertion of highly

purified stevioside stevia leaf extracts is a steviol glycoside
composed predominantly of rebaudioside AM with minor
amounts of other steviol glycosides such as stevioside and rebau
dioside E.
Rebaudioside AM is produced via enzymatic conversion of highly
purified steviol glycoside stevioside extracts (95 % steviol
removal of the enzymes by solid-liquid separation and heat
dioside AM by resin adsorption, followed by recrystallisation of
the steviol glycosides resulting in a final product containing not
less than 95 % of rebaudioside AM. Viable cells of E. coli
(pPM294, pFAF170 and pSK401) and their DNA shall not be
detected in the food additive.
Chemical name Rebaudioside AM: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopy

ranosyl)oxy]kaur-16-en-18-oic acid, 2- O-β-D-glucopyranosyl-3-O-
β-D-glucopyranosyl-β-D-glucopyranosyl ester.
Rebaudioside AM C50 H80 O28 0,29
(g/mol)
Rebaudioside AM 2222580-26-7 1 291,15

02012R0231 — EN — 27.10.2024 — 033.001 — 264
▼M38
Assay Not less than 95 % rebaudioside AM on the dried basis.
Identification
Purity
limit of 74 μm]
▼M40
E 960d GLUCOSYLATED STEVIOL GLYCOSIDES
Synonyms
Definition Mixture of larger glycosides of steviol derived by glucosylation of

steviol glycosides extracted from leaves of Stevia rebaudiana
Bertoni plant. The mixture is composed of glucosylated steviol
glycosides and residual parent steviol glycosides from Stevia leaf.
Glucosylated steviol glycosides are produced by treating the steviol
glycosides, extracted from Stevia leaf, and starch suitable for
human consumption with Cyclomaltodextrin glucanotransferase
(EC 2.4.1.19) derived from a non-GMO strain of Anoxybacillus
caldiproteolyticus St-88. The enzyme transfers glucose units from
the starch to the steviol glycosides. The resulting material is heated
and treated with activated carbon to remove the enzyme, then
passed through adsorption/desorption resin to remove residual
hydrolysed starch (dextrin), followed by purification and prep
aration of the final product using processes that may include decol
ourisation, concentration and spray drying.
Chemical name Steviolbioside: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)

oxy]kaur-16-en-18-oic acid
Rubusoside: 13-β-D-glucopyranosyloxykaur-16-en-18-oic acid, β-
D-glucopyranosyl ester
Dulcoside A: 13-[(2-O-α–L-rhamnopyranosyl-β–D-glucopyranosyl)-
oxy]kaur-16-en-18-oic acid, β-D-glucopyranosyl ester
Stevioside: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-
kaur-16-en-18-oic acid, β-D-glucopyranosyl ester
Rebaudioside A: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopyrano-
syl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid, β-D- glucopy
ranosyl ester
02012R0231 — EN — 27.10.2024 — 033.001 — 265
▼M40
Rebaudioside B: 13-[(2-O-β–D-glucopyranosyl-3-O-β–D-glucopy
ranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid
Rebaudioside C: 13-[(2-O-α–L-rhamnopyranosyl-3-O-β–D-glucopy
ranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid, β-D-glucopy
ranosyl ester
Rebaudioside D: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopy
glucopyranosyl-β-D-glucopyranosyl ester
Rebaudioside E: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopy
ranosyl)oxy]kaur-16-en-18-oic acid, 2-O-β-D-glucopyranosyl-β-D-
Rebaudioside F: 13-[(2-O-β-D-xylofurananosyl-3-O-β-D-glucopy
ranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid, β-D-glucopy
ranosyl ester
Rebaudioside M: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopy
And their glucosylated derivatives (1-20 added glucose units)
n-Glucosylated C(32+n*6)H(50+n*10)O
Steviolbioside (13+n*5)
Rubusoside (13+n*5)
Dulcoside A (17+n*5)
Stevioside (18+n*5)
Rebaudioside A (23+n*5)
Rebaudioside B (18+n*5)
Rebaudioside C (22+n*5)
Rebaudioside D (28+n*5)
Rebaudioside E (23+n*5)
Rebaudioside F (22+n*5)
Rebaudioside M (33+n*5)
n: number of glucose units enzymatically added to the parent

steviol glycoside (n = 1-20)
Typical conversion factor for glucosylated steviol glycosides
mixtures = 0,20 (on the dried, dextrin-free, basis)
Steviol C20H30O3 1,00

02012R0231 — EN — 27.10.2024 — 033.001 — 266
▼M40
Steviolbioside C32H50O13 0,50
Rubusoside C32H50O13 0,50
Dulcoside A C38H60O17 0,40
Stevioside C38H60O18 0,40
Rebaudioside A C44H70O23 0,33
Rebaudioside B C38H60O18 0,40
Rebaudioside C C44H70O22 0,34
Rebaudioside D C50H80O28 0,29
Rebaudioside E C44H70O23 0,33
Rebaudioside F C43H68O22 0,34
Rebaudioside M C56H90O33 0,25
(g/mol)
n-Glucosylated Not available 642,73+n*162,15

Steviolbioside

Rubusoside

Dulcoside A

Stevioside

Rebaudioside A

Rebaudioside B

Rebaudioside C

Rebaudioside D

Rebaudioside E

Rebaudioside F

Rebaudioside M
Steviol 318,46
Steviolbioside 41093-60-1 642,73
Rubusoside 64849-39-4 642,73
Dulcoside A 64432-06-0 788,87
Stevioside 57817-89-7 804,88
Rebaudioside B 58543-17-2 804,88
Rebaudioside C 63550-99-2 951,02
Rebaudioside D 63279-13-0 1 129,15
Rebaudioside E 63279-14-1 967,01
Rebaudioside F 438045-89-7 936,99
Rebaudioside M 1220616-44-3 1 291,30

02012R0231 — EN — 27.10.2024 — 033.001 — 267
▼M40
Assay Not less than 95 % of total steviol glycosides, comprised of above

mentioned steviol glycosides along with their glucosylated
derivatives (1-20 added glucose units), on the dried, dextrin-free,
basis.
Identification
Purity
Loss on drying Not more than 6 % (105 °C, 2 h)
Residual solvent Not more than 200 mg/kg methanol

Not more than 3 000 mg/kg ethanol
Total (aerobic) plate count Not more than 1 000 CFU/g
Yeast and moulds Not more than 200 CFU/g
E. coli Negative in 1 g
Salmonella Negative in 25 g
▼B
E 961 NEOTAME
Synonyms N-[N-(3,3-dimethylbutyl)-L-α-aspartyl]-L-phenylalanine 1-methyl ester;

N(3,3-dimethylbutyl)-L-aspartyl-L-phenylalanine methyl ester.
Definition Neotame is manufactured by reaction under hydrogen pressure of

aspartame with 3,3,-dimethylbutyraldehyde in methanol in presence
of a palladium/carbon catalyst. It is isolated and purified by
filtration, where diatomaceous earth may be used. After solvent
removal via distillation, neotame is washed with water, isolated by
centrifugation and finally vacuum dried.
CAS Nr. 165450-17-9
Chemical name N-[N-(3,3-dimethylbutyl)-L-α-aspartyl]-L-phenylalanine 1-methyl

ester
Description white to off-white powder
Assay Not less than 97,0 % on the dried basis
Identification
Solubility 4,75 % (w/w) at 60 °C in water, soluble in ethanol and ethyl acetate

02012R0231 — EN — 27.10.2024 — 033.001 — 268
▼B
Purity
Water content Not more than 5 % (Karl Fischer, sample size 25 ± 5mg)
Melting range 81 °C to 84 °C
N-[(3,3-dimethylbutyl)-L-α-aspartyl]-L- Not more than 1,5 %

phenylalanine
E 962 SALT OF ASPARTAME-ACESULFAME
Synonyms Aspartame-acesulfame; Aspartame-acesulfame salt
Definition The salt is prepared by heating an approximately 2:1 ratio (w/w) of

aspartame and acesulfame K in solution at acidic pH and allowing
crystallisation to occur. The potassium and moisture are eliminated.
The product is more stable than aspartame alone.
Einecs
Chemical name 6-Methyl-1,2,3-oxathiazine-4(3H)-one-2,2-dioxide salt of

L-phenylalanyl-2-methyl-L-α-aspartic acid
Chemical formula C18H23O9N3S
Assay 63,0 % to 66,0 % aspartame (dry basis) and 34,0 % to 37,0 %

acesulfame (acid form on a dry basis)
Description A white, odourless, crystalline powder
Identification
Solubility Sparingly soluble water; slightly soluble in ethanol
Transmittance The transmittance of a 1 % solution in water determined in a 1 cm

cell at 430 nm with a suitable spectrophotometer using water as a
reference, is not less than 0,95, equivalent to an absorbance of not
more than approximately 0,022.
Specific rotation [α]D20 + 14,5° to + 16,5°

Determine at a concentration of 6,2 g in 100 ml formic acid (15N)
within 30 min of preparation of the solution. Divide the calculated
specific rotation by 0,646 to correct for the aspartame content of the
salt of aspartame-acesulfame
02012R0231 — EN — 27.10.2024 — 033.001 — 269
▼B
Purity
5-Benzyl-3,6-dioxo-2-piperazineacetic Not more than 0,5 %

acid
▼M1
E 964 POLYGLYCITOL SYRUP
Synonyms Hydrogenated starch hydrolysate, hydrogenated glucose syrup and

polyglucitol
Definition A mixture consisting mainly of maltitol and sorbitol and lesser

amounts of hydrogenated oligo- and polysaccharides and maltro
triitol. It is manufactured by the catalytic hydrogenation of a
mixture of starch hydrolysates consisting of glucose, maltose and
higher glucose polymers, similar to the catalytic hydrogenation
process used for the manufacture of maltitol syrup. The resulting
syrup is desalted by ion exchange and concentrated to the desired
level.
Einecs
Chemical name Sorbitol: D-glucitol
Maltitol: (α)-D-Glucopyranosyl-1,4-D-glucitol
Chemical formula Sorbitol: C6H14O6
Maltitol: C12H24O11
Molecular weight Sorbitol: 182,2
Maltitol: 344,3
Assay Content not less than 99 % of total hydrogenated saccharides on the

anhydrous basis, not less than 50 % higher molecular weight
polyols, not more than 50 % of maltitol and not more than 20 %
of sorbitol on the anhydrous basis.
Description Colourless and odourless clear viscous liquid
Identification
Solubility Very soluble in water and slightly soluble in ethanol
Test for maltitol Passes test
Test for sorbitol To 5 g of the sample add 7 ml of methanol, 1 ml of benzaldehyde

shaker until crystals appear. Filter the crystals and dissolve in
20 ml of boiling water containing 1 g of sodium bicarbonate.
Filter the crystals, wash with 5 ml of a water-methanol mixture (1
in 2) and dry in the air. The crystals of the monobenzylidine
derivative of sorbitol so obtained melt between 173 and 179 °C.
Purity
Reducing sugars Not more than 0,3 %

02012R0231 — EN — 27.10.2024 — 033.001 — 270
▼B
E 965 (i) MALTITOL
Synonyms D-Maltitol; Hydrogenated maltose
Definition Maltitol is obtained by hydrogenation of D-maltose. It is mainly

composed of D-maltitol. It may contain small amounts of sorbitol
and related polyhydric alcohols.
Einecs 209-567-0
Chemical name (α)-D-Glucopyranosyl-1,4-D-glucitol
Assay Content not less than 98 % D-maltitol C12H24O11 on the anhydrous

basis
Identification
Specific rotation [α]D20 + 105,5° to + 108,5° (5 % w/v solution)
▼M4
Purity
Appearance of the aqueous solution The solution is clear and colourless

temperature 20 °C
Reducing sugars Not more than 0,1 % (expressed as glucose on an anhydrous basis)
Nickel Not more than 2 mg/kg (expressed on anhydrous basis)
Arsenic Not more than 3 mg/kg (expressed on anhydrous basis)
Lead Not more than 1 mg/kg (expressed on anhydrous basis)
▼B
E 965 (ii) MALTITOL SYRUP
Synonyms Hydrogenated high-maltose-glucose syrup; Hydrogenated glucose

syrup; Maltitol liquid
Definition A mixture consisting of mainly maltitol with sorbitol and hydro

genated oligo- and polysaccharides. It is manufactured by the
catalytic hydrogenation of high maltose-content glucose syrup or
by the hydrogenation of its individual components followed by
blending. The article of commerce is supplied both as a syrup and
as a solid product.
Einecs
Chemical name
Chemical formula
Molecular weight
Assay Content not less than 99 % of total hydrogenated saccharides on the

anhydrous basis and not less than 50 % of maltitol on the anhydrous
basis
Description Colourless and odourless, clear viscous liquids or white crystalline

masses
02012R0231 — EN — 27.10.2024 — 033.001 — 271
▼B
Identification
HPLC test Comparison with an appropriate reference standard of Maltitol shows

that the principle peak in the chromatogram of the test solution is
similar in retention time to the principal peak in the chromatogram
obtained with the reference solution (ISO 10504:1998).
▼M4
Purity
Appearance of the aqueous solution The solution is clear and colourless
Conductivity Not more than 10 μS/cm (on the product as such) at temperature
20 °C
Reducing sugars Not more than 0,3 % (expressed as glucose on an anhydrous basis)
▼B
E 966 LACTITOL
Synonyms Lactit; Lactositol; Lactobiosit
Definition Lactitol is manufactured via catalytic hydrogenation of lactose
Einecs 209-566-5
Chemical name 4-O-β-D-Galactopyranosyl-D-glucitol
Assay Not less than 95 % on the dry weight basis
Description Crystalline powder or colourless solution. Crystalline products occur

in anhydrous, monohydrate and dihydrate forms. Nickel is used as a
catalyst.
Identification
Specific rotation [α]D20 = + 13° to + 16° calculated on the anhydrous basis (10 % w/v
aqueous solution)
Purity
Water content Crystalline products; not more than 10,5 % (Karl Fischer method)
Other polyols Not more than 2,5 % (on the anhydrous basis)
Chlorides Not more than 100 mg/kg (expressed on dry weight basis)
Sulphates Not more than 200 mg/kg (expressed on dry weight basis)
Arsenic Not more than 3 mg/kg (expressed on dry weight basis

02012R0231 — EN — 27.10.2024 — 033.001 — 272
▼B
E 967 XYLITOL
Synonyms Xylitol
Definition Xylitol is mainly composed of D-xylitol. The part which is not

D-xylitol is composed of related substances such as L-arabinitol,
galactitol, mannitol, sorbitol
Einecs 201-788-0
Chemical name D-xylitol
Assay Not less than 98,5 % as xylitol on the anhydrous basis
Description White, crystalline powder, practically odourless.
Identification
Solubility Very soluble in water, sparingly soluble in ethanol
pH 5 to 7 (10 % w/v aqueous solution)
Infrared absorption spectroscopy Comparison with a reference standard e.g. EP or USP.
▼M4
Purity

temperature 20 °C
Other polyhydric alcohols Not more than 1 % (expressed on dry weight basis)
▼B
E 968 ERYTHRITOL
Synonyms Meso-erythritol; Tetrahydroxybutane; Erythrite
Definition Obtained by fermentation of carbohydrate source by safe and

suitable food grade osmophilic yeasts such as Moniliella pollinis
or Moniliella megachilensis, followed by purification and drying
Einecs 205-737-3
Chemical name 1,2,3,4-Butanetetrol
Assay Not less than 99 % after drying
Description White, odourless, non-hygroscopic, heat-stable crystals with a

sweetness of approximately 60-80 % that of sucrose.
02012R0231 — EN — 27.10.2024 — 033.001 — 273
▼B
Identification
Solubility Freely soluble in water, slightly soluble in ethanol, insoluble in

diethyl ether.
▼M4
Purity
Loss on drying Not more than 0,2 % (70 °C, 6 hours, in a vacuum desiccator)

temperature 20 °C
Reducing substances Not more than 0,3 % expressed as D-glucose
Ribitol and glycerol Not more than 0,1 %
▼M11
E 969 ADVANTAME
Synonyms
Definition Advantame (ANS9801) is produced by chemical synthesis in a three-

step process; production of the principal manufacturing intermediate, 3-
hydroxy-4-methoxycinnamaldehyde (HMCA), followed by hydroge
nation to form 3-(3-hydroxy-4-methoxyphenyl) propionaldehyde
(HMPA). In the final step, the HMPA methanol solution (filtrate) is
combined with aspartame to give the imine that under selective hydroge
nation forms advantame. The solution is allowed to crystallise and crude
crystals are washed. The product is re-crystallised and crystals are
separated, washed and dried.
CAS No. 714229-20-6
Chemical name N-[N-[3-(3-hydroxy-4-methoxyphenyl) propyl]-α-aspartyl]-L-pheny

lalanine 1-methyl ester, monohydrate (IUPAC);
L-phenylalanine, N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-
alpha-aspartyl-, 2-methyl ester, monohydrate (CA)
Molecular formula C24H30N2O7·H2O
Molecular weight 476,52 g/mol (monohydrate)
Assay Not less than 97,0 % and not more than 102,0 % on an anhydrous
basis
Description White to yellow powder
Identification
Melting Point 101,5 °C
Purity
N-[N-[3-(3-hydroxy-4-metho Not more than 1,0 %

xyphenyl)propyl-α-aspartyl]-L-pheny
lalanine (ANS9801-acid)
Total other related substances Not more than 1,5 %
Residual Solvents Isopropyl acetate: Not more than 2 000 mg/kg

Methyl acetate: Not more than 500 mg/kg
2-Propanol: Not more than 500 mg/kg
02012R0231 — EN — 27.10.2024 — 033.001 — 274
▼M11
Palladium Not more than 5,3 mg/kg
Platinum Not more than 1,7 mg/kg
▼B
E 999 QUILLAIA EXTRACT
Synonyms Soapbark extract; Quillay bark extract; Panama bark extract; Quillai
extract; Murillo bark extract; China bark extract
Definition Quillaia extract is obtained by aqueous extraction of Quillaia

saponaria Molina, or other Quillaia species, trees of the family
Rosaceae. It contains a number of triterpenoid saponins consisting
of glycosides of quillaic acid. Some sugars including glucose,
galactose, arabinose, xylose, and rhamnose are also present, along
with tannin, calcium oxalate and other minor components
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
Description Quillaia extract in the powder form is light brown with a pink tinge.
It is also available as an aqueous solution
Identification
Purity
Water content Not more than 6,0 % (Karl Fischer method) (powder form only)
E 1103 INVERTASE
Synonyms
Definition Invertase is produced from Saccharomyces cerevisiae
Einecs 232-615-7
Enzyme Commission No EC 3.2.1.26
Systematic name β-D-Fructofuranoside fructohydrolase

02012R0231 — EN — 27.10.2024 — 033.001 — 275
▼B
Chemical name
Chemical formula
Molecular weight
Assay
Description
Identification
Purity
Total bacterial count Not more than 50 000 colonies per gram
Coliforms Not more than 30 colonies per gram
E 1105 LYSOZYME
Synonyms Lysozyme hydrochloride; Muramidase
Definition Lysozyme is a linear polypeptide obtained from hens' egg whites

consisting of 129 amino acids. It possesses enzymatic activity in its
ability to hydrolyse the β(1-4) linkages between N-acetylmuramic
acid and N-acetylglucosamine in the outer membranes of bacterial
species, in particular gram-positive organisms. Is usually obtained as
the hydrochloride
Einecs 232-620-4
Enzyme Commission No EC 3.2.1.17
Chemical name
Chemical formula
Molecular weight About 14 000
Assay Content not less than 950 mg/g on the anhydrous basis
Description White, odourless powder having a slightly sweet taste
Identification
Isoelectric point 10,7
Spectrophotometry Absorption maximum of an aqueous solution (25 mg/100 ml) at

281 nm, a minimum at 252 nm
Purity
Water content Not more than 6,0 % (Karl Fischer method) (powder form only)
Nitrogen Not less than 16,8 % and not more than 17,8 %

02012R0231 — EN — 27.10.2024 — 033.001 — 276
▼B
Total bacterial count Not more than 5 × 104 colonies per gram
Staphylococcus aureus Absent in 1 g
E 1200 POLYDEXTROSE
Synonyms Modified polydextroses
Definition Randomly bonded glucose polymers with some sorbitol end-groups,

and with citric acid or phosphoric acid residues attached to the
polymers by mono or diester bonds. They are obtained by melting
and condensation of the ingredients and consist of approximately 90
parts D-glucose, 10 parts sorbitol and 1 part citric acid and/or 0,1
part phosphoric acid. The 1,6-glucosidic linkage predominates in the
polymers but other linkages are present. The products contain small
quantities of free glucose, sorbitol, levoglucosan (1,6-anhydro-D-
glucose) and citric acid and may be neutralised with any food
grade base and/or decolourised and deionised for further purification.
The products may also be partially hydrogenated with Raney nickel
catalyst to reduce residual glucose. Polydextrose-N is neutralised
polydextrose
Einecs
Chemical name
Chemical formula
Molecular weight
Assay Content not less than 90 % of polymer on the ash free and
anhydrous basis
Description White to light tan-coloured solid. Polydextroses dissolve in water to

give a clear, colourless to straw coloured solution
Identification
Test for reducing sugar Passes test
pH Between 2,5 and 7,0 for polydextrose (10 % solution)

Between 5,0 and 6,0 for polydextrose-N (10 % solution)
Purity
Sulphated ash Not more than 0,3 % (polydextrose)

Not more than 2,0 % (polydextrose N)
Nickel Not more than 2 mg/kg for hydrogenated polydextroses
1,6-Anhydro-D-glucose Not more than 4,0 % on the ash-free and the dried basis
Glucose and sorbitol Not more than 6,0 % combined on the ash-free and the dried basis;
glucose and sorbitol are determined separately
Molecular weight limit Negative test for polymers of molecular weight greater than 22 000
02012R0231 — EN — 27.10.2024 — 033.001 — 277
▼B
5-Hydroxy-methylfurfural Not more than 0,1 % (polydextrose)
Not more than 0,05 % (polydextrose-N)
E 1201 POLYVINYLPYRROLIDONE
Synonyms Povidone; PVP; Soluble polyvinylpyrrolidone
Definition
Einecs
Chemical name Polyvinylpyrrolidone, poly-[1-(2-oxo-1-pyrrolidinyl)-ethylene]
Chemical formula (C6H9NO)n
Average molecular weight Not less than 25 000
Assay Content not less than 11,5 % and not more than 12,8 % of
nitrogen (N) on the anhydrous basis
Description White or nearly white powder
Identification
Solubility Soluble in water and in ethanol. Insoluble in ether
Purity
Aldehyde Not more than 500 mg/kg (as acetaldehyde)
Free-N-vinylpyrrolidone Not more than 10 mg/kg
Hydrazine Not more than 1 mg/kg
E 1202 POLYVINYLPOLYPYRROLIDONE
Synonyms Crospovidone; Cross-linked polyvidone; Insoluble polyvinylpyr

rolidone
Definition Polyvinylpolypyrrolidone is a poly-[1-(2-oxo-1-pyrrolidinyl)-ethylene],

cross linked in a random fashion. It is produced by the polymerisation
of N-vinyl-2-pyrrolidone in the presence of either caustic catalyst or
N, N'-divinyl-imidazolidone. Due to its insolubility in all common
solvents the molecular weight range is not amenable to analytical
determination
Einecs
Chemical name Polyvinylpyrrolidone; poly-[1-(2-oxo-1-pyrrolidinyl)-ethylene]
Chemical formula (C6H9NO)n
Molecular weight
Assay Content not less than 11 % and not more than 12,8 % nitrogen (N)
on the anhydrous basis
Description A white hygroscopic powder with a faint, non-objectionable odour
Identification
Solubility Insoluble in water, ethanol and ether

02012R0231 — EN — 27.10.2024 — 033.001 — 278
▼B
pH Between 5,0 and 8,0 (1 % suspension in water)
Purity
Water-soluble matter Not more than 1 %
Free-N,N'-divinyl-imidazolidone Not more than 2 mg/kg
E 1203 POLYVINYL ALCOHOL
Synonyms Vinyl alcohol polymer, PVOH

Definition Polyvinyl alcohol is a synthetic resin prepared by the polymerisation
of vinyl acetate, followed by partial hydrolysis of the ester in the
presence of an alkaline catalyst. The physical characteristics of the
product depend on the degree of polymerisation and the degree of
hydrolysis.
Chemical name Ethenol homopolymer
Chemical formula (C2H3OR)n where R = H or COCH3
Description Odourless, tasteless, translucent, white or cream-coloured granular
powder
Identification
▼M17
Solubility Soluble in water; Practically insoluble or insoluble in ethanol
(≥ 99,8 %)
▼B
Precipitation reaction Dissolve 0,25 g of the sample in 5 ml of water with warming and let
the solution cool to room temperature. The addition of 10 ml of
ethanol to this solution leads to a white, turbid or flocculent
precipitate.
Colour reaction Dissolve 0,01 g of the sample in 100 ml of water with warming and
let the solution cool to room temperature. A blue colour is produced
when adding (to 5 ml solution) one drop of iodine test solution (TS)
and a few drops of boric acid solution
Dissolve 0,5 g of the sample in 10 ml of water with warming and let
the solution cool to room temperature. A dark red to blue colour is
produced after adding one drop of iodine TS to 5 ml of solution.
Viscosity 4,8 to 5,8 mPa.s (4 % solution at 20 °C) corresponding to an
average molecular weight of 26 000-30 000 Da
Purity
Ester value Between 125 and 153 mg KOH/g
Degree of hydrolysis 86,5 to 89,0 %
Solvent residues Not more than 1,0 % Methanol, 1,0 % Methyl acetate
pH 5,0 to 6,5 (4 % solution)
Residue in ignition Not more than 1,0 %
02012R0231 — EN — 27.10.2024 — 033.001 — 279
▼B
E 1204 PULLULAN
Synonyms
Definition Linear, neutral glucan consisting mainly of maltotriose units

connected by -1,6 glycosidic bonds. It is produced by fermentation
from a food-grade hydrolysed starch using a non-toxin-producing
strain of Aureobasidium pullulans. After completion of the fermen
tation, the fungal cells are removed by microfiltration, the filtrate is
heat-sterilised and pigments and other impurities are removed by
adsorption and ion exchange chromatography
Einecs 232-945-1
Chemical name
Molecular weight
Assay Not less than 90 % of glucan on the dried basis
Description White to off-white odourless powder
Identification
Solubility Soluble in water, practically insoluble in ethanol
pH 5,0 to 7,0 (10 % solution)
Precipitation with polyethylene glycol Add 2 ml of polyethylene glycol 600 to 10 ml of a 2 % aqueous

600 solution of pullulan. A white precipitate is formed
Depolymerisation with pullulanase Prepare two test tubes each with 10 ml of a 10 % pullulan solution.
Add 0,1 ml pullulanase solution having activity 10 units/g to one
test tube, and 0,1 ml water to the other. After incubation at about
25 °C for 20 minutes, the viscosity of the pullulanase-treated
solution is visibly lower than that of the untreated solution
Viscosity 100 to 180 mm2/s (10 % w/w aqueous solution at 30 °C)
Purity
Loss on drying Not more than 6 % (90 °C, pressure not more than 50 mm Hg,
6 hours)
Mono-, di- and oligosaccharides Not more than 10 % expressed as glucose
Coliforms Absent in 25 g
E 1205 BASIC METHACRYLATE COPOLYMER
Synonyms Basic butylated methacrylate copolymer; amino methacrylate

copolymer; aminoalkyl methacrylate copolymer E; butyl metha
crylate, dimethylaminoethyl methacrylate, methyl methacrylate
polymer; butyl methacrylate, methyl methacrylate, dimethylami
noethyl methacrylate polymer
▼M22
Definition Basic methacrylate copolymer is manufactured by thermic controlled
polymerisation of the monomers methyl methacrylate, butyl metha
crylate and dimethylaminoethyl methacrylate (dissolved in propan-2-
ol), by using a free radical donor initiator system. An alkyl
mercaptane is used as chain modifying agent. The polymer
solution is extruded and granulated under vacuum to remove
residual volatile components. The granules resulting are commer
cialized as such or undergo a milling step (micronisation).
02012R0231 — EN — 27.10.2024 — 033.001 — 280
▼B
Chemical name Poly(butyl methacrylate-co-(2-dimethylaminoethyl)methacrylate-co-
methyl methacrylate) 1:2:1
Chemical formula Poly[(CH2:C(CH3)CO2(CH2)2N(CH3)2)-co-(CH2:C(CH3)CO2CH3)-

co-(CH2:C(CH3)CO2(CH2)3CH3)]

estimated by gel permeation chroma
tography
▼M22
Particle size of the powder (when used < 50 μm at least 95 %
forms a film)
< 20 μm at least 50 %
< 3 μm not more than 10 %
▼B
Assay 20,8-25,5 % dimethylaminoethyl (DMAE) groups on dry substance
(according to Ph. Eur. 2.2.20 ‘potentio
metric titration’)
Description Granules are colourless to yellow tinged, the powder is white
Identification
Viscosity of a 12,5 % solution in 60:40 3-6 mPa.s

(w/w/) propan-2-ol to acetone
Solubility 1 g dissolves in 7 g Methanol, Ethanol, propan-2-ol, dich

loromethane, aqueous Hydrochloric acid 1N.
Not soluble in petroleum ether.
▼M6
Purity
Loss of drying Not more than 2,0 % (105 °C, 3 h)
Alkali value 162-198 mg KOH/g of dried substance
Residual monomers Butylmethacrylate < 1 000 mg/kg

Methyl methacrylate < 1 000 mg/kg
Dimethylaminoethyl methacrylate < 1 000 mg/kg
Solvent residues propan-2-ol < 0,5 %

Butanol < 0,5 %
Methanol < 0,1 %
E 1206 NEUTRAL METHACRYLATE COPOLYMER
Synonyms Ethyl acrylate methyl methacrylate polymer; Ethyl acrylate, methyl

methacrylate polymer; Ethyl acrylate, polymer with methyl metha
crylate; Methyl methacrylate, ethyl acrylate polymer; Methyl metha
crylate, polymer with ethyl acrylate
02012R0231 — EN — 27.10.2024 — 033.001 — 281
▼M6
Definition Neutral methacrylate copolymer is a fully polymerised copolymer of

methyl methacrylate and ethyl acrylate. It is produced using a
process of emulsion polymerisation. It is manufactured by redox
initiated polymerisation of the monomers ethyl acrylate, methyl
methacrylate by using a free radical donor redox initiator system
stabilised with polyethylene glycol monostearyl ether and vinylic
acid/sodium hydroxide. Residual monomers are removed by means
of water vapour distillation.
CAS No 9010-88-2
Chemical name Poly(ethylacrylate-co-methyl methacrylate) 2:1
Chemical formula Poly[(CH2:CHCO2CH2CH3)-co-(CH2:C(CH3)CO2CH3)]
Assay/Residue on evaporation 28,5–31,5 %

1 g dispersion is dried in an oven for 3 hours at 110 °C.
Description Milky-white dispersion (the commercial form is a 30 % dispersion

of the dry substance in water) of low viscosity with a faint char
acteristic odour.
Identification
Infrared absorption spectroscopy Characteristic of the compound
Viscosity Max. 50 mPa.s, 30 rpm/20 °C (Brookfield viscosimetry)
pH-value 5,5–8,6
Relative density (at 20 °C) 1,037–1,047
Solubility The dispersion is miscible with water in any proportion. The

polymer and the dispersion are freely soluble in acetone, ethanol
and isopropyl alcohol. Not soluble when mixed with 1 N sodium
hydroxide in a ratio of 1:2.
Purity
Sulphated ash Not more than 0,4 % in the dispersion
Residual monomers Total of monomers (sum of methyl methacrylate and ethyl acrylate):
not more than 100 mg/kg in the dispersion
Residual emulsifier Polyethylene glycol monostearyl ether (macrogol stearyl ether 20)
not more than 0,7 % in the dispersion
Solvent residues Ethanol not more than 0,5 % in the dispersion

Methanol not more than 0,1 % in the dispersion
Arsenic Not more than 0,3 mg/kg in the dispersion
Lead Not more than 0,9 mg/kg in the dispersion
Mercury Not more than 0,03 mg/kg in the dispersion
Cadmium Not more than 0,3 mg/kg in the dispersion
E 1207 ANIONIC METHACRYLATE COPOLYMER
Synonyms Methyl acrylate, methyl methacrylate, methacrylic acid polymer;

Methacrylic acid, polymer with methyl acrylate and methyl metha
crylate
02012R0231 — EN — 27.10.2024 — 033.001 — 282
▼M6
Definition Anionic methacrylate copolymer is a fully polymerised copolymer of

methacrylic acid, methyl methacrylate and methyl acrylate. It is
manufactured in aqueous medium by emulsion polymerisation of
methyl methacrylate, methyl acrylate and methacrylic acid using a
free radical initiator stabilised with sodium lauryl sulphate and poly
oxyethylene sorbitan monooleate (polysorbate 80). Residual
monomers are removed by means of water vapour distillation.
CAS No 26936-24-3
Chemical name Poly (methyl acrylate-co-methylmethacrylate-co-methacrylic acid)

7:3:1
Chemical formula Poly[(CH2:CHCO2CH3)-co-(CH2:C(CH3)CO2CH3)-co-

(CH2:C(CH3)COOH)]
Assay/Residue on evaporation 28,5–31,5 %

1 g of the dispersion is dried in an oven for 5 hours at 110 °C.
9,2–12,3 % methacrylic acid units on dry substance.
Description Milky-white dispersion (the commercial form is a 30 % dispersion

of the dry substance in water) of low viscosity with a faint char
acteristic odour.
Identification
Infrared absorption spectroscopy Characteristic of the compound
Viscosity Max. 20 mPa.s, 30 rpm/20 °C (Brookfield viscosimetry)
pH-value 2,0–3,5
Relative density (at 20 °C) 1,058–1,068
Solubility The dispersion is miscible with water in any proportion. The

polymer and the dispersion are freely soluble in acetone, ethanol
and isopropyl alcohol. Soluble when mixed with 1 N sodium
hydroxide in a ratio of 1:2. Soluble above pH 7,0.
Purity
Acid value 60–80 mg KOH/g of dried substance
Sulphated ash Not more than 0,2 % in the dispersion
Residual monomers Total of monomers (sum of methacrylic acid, methyl methacrylate

and methyl acrylate): not more than 100 mg/kg in the dispersion
Residual emulsifiers Sodium lauryl sulphate not more than 0,3 % on the dry substance
Polysorbate 80 not more than 1,2 % on the dry substance
Solvent residues Methanol not more than 0,1 % in the dispersion
Arsenic Not more than 0,3 mg/kg in the dispersion
Lead Not more than 0,9 mg/kg in the dispersion
Mercury Not more than 0,03 mg/kg in the dispersion
Cadmium Not more than 0,3 mg/kg in the dispersion

02012R0231 — EN — 27.10.2024 — 033.001 — 283
▼M9
E 1208 POLYVINYLPYRROLIDONE-VINYL ACETATE COPOLYMER
Synonyms Copolyvidon; copovidone; 1-vinyl-2-pyrrolidone-vinyl acetate

copolymer; 2-pyrrolidinone, 1-ethenyl-, polymer with ethenyl acetate
Definition It is produced by free radical copolymerisation of N-vinyl-2-

pyrrolidone and vinyl acetate in solution in propan-2-ol, in the
presence of initiators.
Einecs
Chemical name Acetic acid, ethenyl ester, polymer with 1-ethenyl-2-pyrrolidinone
Chemical formula (C6H9NO)n.(C4H6O2)m
Average Viscosity Molecular Weight Between 26 000 and 46 000 g/mol.
Assay Nitrogen content 7,0-8,0 %
Description The physical state is described as a white to yellowish-white powder

or flakes with an average particle size of 50-130 μm.
Identification
Solubility Freely soluble in water, ethanol, ethylene chloride and ether.
European Colour Test (BY Colour) Minimum BY5
K-value (1) (1 % solids in aqueous 25,2-30,8

solution)
pH value 3,0-7,0 (10 % aqueous solution)
Purity
Vinylacetate component in copolymer Not more than 42,0 %
Free vinyl acetate Not more than 5 mg/kg
Aldehyde Not more than 2 000 mg/kg (as acetaldehyde)
Hydrazine Not more than 0,8 mg/kg
Peroxide content Not more than 400 mg/kg
Propan-2-ol Not more than 150 mg/kg
_____________
(1) K-value: dimensionless index, calculated from kinematic viscosity measurements of dilute solutions, used to indicate the likely
degree of polymerisation or molecular size of a polymer.
02012R0231 — EN — 27.10.2024 — 033.001 — 284
▼M13
E 1209 POLYVINYL ALCOHOL-POLYETHYLENE GLYCOL-GRAFT-COPOLYMER
Synonyms Macrogol poly(vinyl alcohol) grafted co-polymer; poly(ethan-1,2-

diol-graft-ethanol); ethenol, polymer with oxirane, graft; oxirane,
polymer with ethanol, graft; ethylene oxide-vinyl alcohol graft
co-polymer
Definition Polyvinyl alcohol-polyethylene glycol-graft-co-polymer is a synthetic
co-polymer that consists of approximately 75 % PVA units and
25 % PEG units.
Chemical name Polyvinyl alcohol-polyethylene glycol-graft-co-polymer

Chemical formula
Weight Average Molecular Weight 40 000 to 50 000 g/mol

Description White to faintly yellow powder
Identification
Solubility Freely soluble in water and dilute acids and dilute solutions of alkali
hydroxides; practically insoluble in ethanol, acetic acid, acetone, and
chloroform
IR Spectrum Must comply

pH value 5,0-8,0
Purity
Ester Value 10 to 75 mg/g KOH
Dynamic viscosity 50 to 250 mPa·s

Sulphated Ash Not more than 2 %
Vinyl Acetate Not more than 20 mg/kg

Acetic acid/Total Acetate Not more than 1,5 %
▼M26
Ethylene glycols (mono- and di-) Not more than 400 mg/kg (singly or in combination)
▼M13
▼M37
__________
▼M13
▼M39
E 1210 CARBOMER
Synonyms carbomer, carboxypolymethylene; carbomer homopolymer
Definition High-molecular mass polymers obtained by polymerisation of

acrylic acid and crosslinking with allyl pentaerythritol. The
polymers are synthesised in ethyl acetate using a peroxide to
initiate free-radical polymerisation.
CAS No 9007-20-9 (primary CAS), 9003-01-4 (secondary CAS)

02012R0231 — EN — 27.10.2024 — 033.001 — 285
▼M39
Chemical name Carbomer homopolymer, allyl pentaerythritol cross-linked
Chemical formula -(CH2-CH)m-(XM)p
COOH
m: number of monomer units; XM: crosslinker, p: number of

crosslinker units, with m>>p
Weight average molecular weight
Assay Carboxylic acid content not less than 56 % and not more than
68 % (on dried substance)
Description White or almost white, fluffy, hygroscopic powder or granules
Identification
Attenuated total reflective infra-red spec Characteristic of the compound

troscopy
Proton nuclear magnetic resonance spec
troscopy
Viscosity (Brookfield viscosimetry, 20 Type B Type A Type A

rpm) 25 °C
29 400-39 400 4 000-11 000 mPa.s
mPa.s
Physical form powder powder granules
Pass through 40 mesh, % 425 μm - - 95 min
Pass through 100 mesh, % 150 μm - - 10 max
Solubility Insoluble in water. Water-swellable and forms hydrogels in aqueous

dispersions.
Purity
Residual monomers Acrylic acid not more than 100 mg/kg
Residual crosslinker tri and tetra-allyl pentaerythritol not more than 1 000 mg/kg
Residual solvant Ethyl acetate not more than 0,5 % w/w
2-ethylhexanol not more than 100 mg/kg
2-ethylhexylacetate not more than 100 mg/kg
Lower molecular weight fraction < 1 000 Not more than 0,75 % w/w
Da
Sulphated ashes Not more than 2,5 %
▼B
E 1404 OXIDISED STARCH
Synonyms
Definition Oxidised starch is starch treated with sodium hypochlorite
Einecs
Chemical name
Chemical formula
Molecular weight
Assay
02012R0231 — EN — 27.10.2024 — 033.001 — 286
▼B
Description White or nearly white powder or granules or (if pregelatinised)

flakes, amorphous powder or coarse particles
Identification
Microscopic observation Passes test (if not pregelatinised)
Iodine staining Passes test (dark blue to light red colour)
Purity
Loss on drying Not more than 15,0 % for cereal starch

Not more than 21,0 % for potato starch
Not more than 18,0 % for other starches
Carboxyl groups Not more than 1,1 % (on an anhydrous basis)
Sulphur dioxide Not more than 50 mg/kg for modified cereal starches (on an
anhydrous basis)
Not more than 10 mg/kg for other modified starches, unless
otherwise specified (on an anhydrous basis)
Lead Not more than 2 mg/kg (on an anhydrous basis)
E 1410 MONOSTARCH PHOSPHATE
Synonyms
Definition Monostarch phosphate is starch esterified with ortho-phosphoric

acid, or sodium or potassium ortho-phosphate or sodium tripoly
phosphate
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification
Purity

02012R0231 — EN — 27.10.2024 — 033.001 — 287
▼B
Residual phosphate Not more than 0,5 % (as P) for wheat or potato starch (on an
anhydrous basis)
Not more than 0,4 % (as P) for other starches (on an anhydrous
basis)
anhydrous basis)
E 1412 DISTARCH PHOSPHATE
Synonyms
Definition Distarch phosphate is starch cross-linked with sodium trimeta

phosphate or phosphorus oxychloride
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification
Purity

anhydrous basis)
basis)
anhydrous basis)

02012R0231 — EN — 27.10.2024 — 033.001 — 288
▼B
E 1413 PHOSPHATED DISTARCH PHOSPHATE
Synonyms
Definition Phosphated distarch phosphate is starch having undergone a combi

nation of treatments as described for monostarch phosphate and for
distarch phosphate
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification
Purity

anhydrous basis)
basis)
anhydrous basis)
E 1414 ACETYLATED DISTARCH PHOSPHATE
Synonyms
Definition Acetylated distarch phosphate is starch cross-linked with sodium

trimetaphosphate or phosphorus oxychloride and esterified by
acetic anhydride or vinyl acetate
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 289
▼B
Purity

Acetyl groups Not more than 2,5 % (on an anhydrous basis)
anhydrous basis)
basis)
Vinyl acetate Not more than 0,1 mg/kg (on an anhydrous basis)
anhydrous basis)
E 1420 ACETYLATED STARCH
Synonyms Starch acetate
Definition Acetylated starch is starch esterified with acetic anhydride or vinyl

acetate
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification
Purity

Vinyl acetate Not more than 0,1 mg/kg (on an anhydrous basis)
anhydrous basis)

02012R0231 — EN — 27.10.2024 — 033.001 — 290
▼B
E 1422 ACETYLATED DISTARCH ADIPATE
Synonyms
Definition Acetylated distarch adipate is starch cross-linked with adipic

anhydride and esterified with acetic anhydride
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification
Purity

Adipate groups Not more than 0,135 % (on an anhydrous basis)
anhydrous basis)
E 1440 HYDROXYPROPYL STARCH
Synonyms
Definition Hydroxypropyl starch is starch etherified with propylene oxide
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification

02012R0231 — EN — 27.10.2024 — 033.001 — 291
▼B
Purity

Hydroxypropyl groups Not more than 7,0 % (on an anhydrous basis)
Propylene chlorohydrin Not more than 1 mg/kg (on an anhydrous basis)
anhydrous basis)
E 1442 HYDROXYPROPYL DISTARCH PHOSPHATE
Synonyms
Definition Hydroxypropyl distarch phosphate is starch cross-linked with sodium

trimetaphosphate or phosphorus oxychloride and etherified with
propylene oxide
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification
Purity

Hydroxypropyl groups Not more than 7,0 % (on an anhydrous basis)
anhydrous basis)
basis)
Propylene chlorohydrin Not more than 1 mg/kg (on an anhydrous basis)
anhydrous basis)
02012R0231 — EN — 27.10.2024 — 033.001 — 292
▼B
E 1450 STARCH SODIUM OCTENYL SUCCINATE
Synonyms SSOS
Definition Starch sodium octenyl succinate is starch esterified with octe

nylsuccinic anhydride
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification
Purity

Octenylsuccinyl groups Not more than 3 % (on an anhydrous basis)
Octenylsuccinic acid residue Not more than 0,3 % (on an anhydrous basis)
anhydrous basis)
E 1451 ACETYLATED OXIDISED STARCH
Synonyms
Definition Acetylated oxidised starch is starch treated with sodium hypochlorite

followed by esterification with acetic anhydride
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

02012R0231 — EN — 27.10.2024 — 033.001 — 293
▼B
Identification
Purity

Carboxyl groups Not more than 1,3 % (on an anhydrous basis)
anhydrous basis)
E 1452 STARCH ALUMINIUM OCTENYL SUCCINATE
Synonyms
Definition Starch aluminium octenyl succinate is starch esterified with octe

nylsuccinic anhydride and treated with aluminium sulphate
Einecs
Chemical name
Chemical formula
Molecular weight
Assay

Identification
Purity
Loss on drying Not more than 21,0 %
Octenylsuccinyl groups Not more than 3 % (on an anhydrous basis)
Octenylsuccinic acid residue Not more than 0,3 % (on an anhydrous basis)
anhydrous basis)
Not more than 10 mg/kg for the other modified starches, unless
Aluminium Not more than 0,3 % (on an anhydrous basis)

02012R0231 — EN — 27.10.2024 — 033.001 — 294
▼B
E 1505 TRIETHYL CITRATE
Synonyms Ethyl citrate
Definition
Einecs 201-070-7
Chemical name Triethyl-2-hydroxypropan-1,2,3-tricarboxylate
Description Odourless, practically colourless, oily liquid
Identification
Specific gravity (25 °C/25 °C) 1,135-1,139
Purity
Acidity Not more than 0,02 % (as citric acid)
E 1517 GLYCERYL DIACETATE
Synonyms Diacetin
Definition Glyceryl diacetate consist predominantly of a mixture of the 1, 2-

and 1,3-diacetates of glycerol, with minor amounts of the mono- and
tri-esters
Einecs
Chemical name Glyceryl diacetate; 1, 2, 3-propanetriol diacetate
Description Clear, colourless, hygroscopic, somewhat oily liquid with a slight,

fatty odour
Identification
Solubility Soluble in water. Miscible with ethanol
Boiling range Between 259 and 261 °C
Purity
Acidity Not more than 0,4 % (as acetic acid)

02012R0231 — EN — 27.10.2024 — 033.001 — 295
▼B
E 1518 GLYCERYL TRIACETATE
Synonyms Triacetin
Definition
Einecs 203-051-9
Chemical name Glyceryl triacetate


Description Colourless, somewhat oily liquid having a slightly fatty odour
Identification

Specific gravity (25 °C/25 °C) Between 1,154 and 1,158

Boiling range Between 258 and 270 °C
Purity
Sulphated ash Not more than 0,02 % (as citric acid)

E 1519 BENZYL ALCOHOL
Synonyms Phenylcarbinol; Phenylmethyl alcohol; Benzenemethanol;

Alpha-hydroxytoluene
Definition
Einecs
Chemical name Benzyl alcohol; Phenylmethanol
Chemical formula C 7 H 8O

Description Colourless, clear liquid with a faint, aromatic odour
Identification
Solubility Soluble in water, ethanol and ether

Test for peroxides Passes test
Distillation range Not less than 95 % v/v distils between 202 and 208 °C
Purity

Aldehydes Not more than 0,2 % v/v (as benzaldehyde)

02012R0231 — EN — 27.10.2024 — 033.001 — 296
▼B
E 1520 PROPANE-1,2-DIOL
Synonyms Propylene glycol
Definition
Einecs 200-338-0
Chemical name 1,2-dihydroxypropane
Description Clear, colourless, hygroscopic, viscous liquid
Identification
Solubility Soluble in water, ethanol and acetone
Purity
Distillation test 99,5 % of the product distils between 185-189 °C. The remaining
0,5 % consists mainly of dimers and traces of trimers from
propylene glycol.
E 1521 POLYETHYLENE GLYCOL
Synonyms PEG; Macrogol; Polyethylene oxide
Definition Addition polymers of ethylene oxide and water usually designated

by a number roughly corresponding to the molecular weight.
Chemical name alpha-Hydro-omega-hydroxypoly (oxy-1,2-ethanediol)
Chemical formula (C2H4O)n H2O (n = number of ethylene oxide units corresponding to

a molecular weight of 6 000, about 140)
Average molecular weight 380 to 9 000 Da
Assay PEG 400: Not less than 95 % and not more than 105 %
PEG 3000: Not less than 90 % and not more than 110 %
PEG 6000:Not less than 90 % and not more than 110 %
PEG 8000: Not less than 87,5 % and not more than 112,5 %
Description PEG 400 is a clear, viscous, colourless or almost colourless hygro

scopic liquid
PEG 3000, PEG 3350, PEG 4000, PEG 6000 and PEG 8000 are
white or almost white solids with a waxy or paraffin-like appearance
02012R0231 — EN — 27.10.2024 — 033.001 — 297
▼B
Identification
Melting range PEG 400: 4-8 °C
PEG 3000: 50-56 °C
PEG 3350: 53-57 °C
PEG 4000: 53-59 °C
PEG 6000:55-61 °C
PEG 8000: 55-62 °C
Viscosity PEG 400: 105 to 130 mPa.s at 20 °C
PEG 3000: 75 to 100 mPa.s at 20 °C
PEG 3350: 83 to 120 mPa.s at 20 °C
PEG 4000: 110 to 170 mPa.s at 20 °C
PEG 6000: 200 to 270 mPa.s at 20 °C
PEG 8000: 260 to 510 mPa.s at 20 °C
For polyethylene glycols having a average molecular weight greater
than 400, the viscosity is determined on a 50 per cent m/m solution
of the candidate substance in water
Solubility PEG 400 is miscible with water, very soluble in acetone, in alcohol
and in methylene chloride, practically insoluble in fatty oils and in
mineral oils
PEG 3000 and PEG 3350: very soluble in water and in methylene
chloride, very slightly soluble in alcohol, practically insoluble in
fatty oils and in mineral oils
PEG 4000, PEG 6000 and PEG 8000: very soluble in water and in
methylene chloride, practically insoluble in alcohol and in fatty oils
and in mineral oils.
Purity
Hydroxyl value PEG 400: 264-300
PEG 3000: 34-42
PEG 3350: 30-38
PEG 4000: 25-32
PEG 6000: 16-22
PEG 8000: 12-16
▼M37
__________
▼B
Ethylene glycol and diethylene glycol Total not more than 0,25 % °w/w individually or in combination

CELEX_02012R0231-20241027_EN_TXT

Uploaded by

Copyright:

Available Formats

CELEX_02012R0231-20241027_EN_TXT

Uploaded by

Document Information

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

CELEX_02012R0231-20241027_EN_TXT

Uploaded by

Copyright:

Available Formats

02012R0231 — EN — 27.10.2024 — 033.

►B COMMISSION REGULATION (EU) No 231/2012

►M25 Commission Regulation (EU) 2018/98 of 22 January 2018 L 17 14 23.1.2018

Specifications for food additives including colours and sweeteners listed

Directives 2008/60/EC, 2008/84/EC and 2008/128/EC are repealed with

Foodstuffs containing food additives that have been lawfully placed on

Definition: Aluminium lakes are prepared by reacting colours complying with

Synonyms CI Natural Yellow 3; Turmeric Yellow; Diferoyl Methane

Definition Curcumin is obtained by solvent extraction of turmeric i.e. the

Colour Index No 75300

Chemical name I 1,7-Bis(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione

Chemical formula I C21H20O6

Molecular weight I. 368,39 II. 338,39 III. 308,39

Assay Content not less than 90 % total colouring matters

(1) i.e. ethylene oxide + 0,55* 2-chloroethanol.

Spectrometry Maximum in ethanol at ca. 426 nm

Melting range 179 °C-182 °C

Dichloromethane: not more than 10 mg/kg

Arsenic Not more than 3 mg/kg

Lead Not more than 10 mg/kg

Mercury Not more than 1 mg/kg

Cadmium Not more than 1 mg/kg

Aluminium lakes of this colour may be used.

Chemical name 7,8-Dimethyl-10-(D-ribo-2,3,4,5-tetrahydroxy­

Chemical formula C17H20N4O6

Molecular weight 376,37

Assay Content not less than 98 % on the anhydrous basis

Description Yellow to orange-yellow crystalline powder, with slight odour

Maximum in water at ca. 375 nm

Loss on drying Not more than 1,5 % (105 °C, 4 hours)

Sulphated ash Not more than 0,1 %

Arsenic Not more than 3 mg/kg

Lead Not more than 2 mg/kg

Mercury Not more than 1 mg/kg

Cadmium Not more than 1 mg/kg

Synonyms Riboflavin-5′-phosphate sodium

Definition These specifications apply to riboflavin 5′-phosphate together with

Chemical name Monosodium(2R,3R,4S)-5-(3′)10′-dihydro-7′,8′-dimethyl-2′,4′-

Chemical formula For the dihydrate form: C17H20N4NaO9P · 2H2O

For the anhydrous form: C17H20N4NaO9P

Molecular weight 514,36

Assay Content not less than 95 % total colouring matters calculated as

Description Yellow to orange crystalline hygroscopic powder, with slight odour

Maximum in water at ca. 375 nm

Sulphated ash Not more than 25 %

Subsidiary colouring matters Riboflavin (free): Not more than 6 %

Primary aromatic amines Not more than 70 mg/kg (calculated as aniline)

Lead Not more than 2 mg/kg

Mercury Not more than 1 mg/kg

Cadmium Not more than 1 mg/kg

Synonyms CI Food Yellow 4

Definition Tartrazine is prepared from 4-amino-benzenesulphonic acid, which is

Colour Index No 19140

Chemical name Trisodium-5-hydroxy-1-(4-sulfonatophenyl)-4-(4-sulfonatop­

Chemical formula C16H9N4Na3O9S2

Molecular weight 534,37

Description Light orange powder or granules

Appearance of the aqueous solution Yellow

Spectrometry Maximum in water at ca. 426 nm

Water insoluble matter Not more than 0,2 %

Chemical name 7,8-Dimethyl-10-(D-ribo-2,3,4,5-tetrahydroxy

Chemical name Trisodium-5-hydroxy-1-(4-sulfonatophenyl)-4-(4-sulfonatop