Tefluthrin

Tefluthrin
Names
	IUPAC name (1S,3S)-rel-2,3,5,6-Tetrafluoro-4-methylbenzyl 3-((Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropanecarboxylate
Identifiers
CAS Number	79538-32-2
ChEBI	CHEBI:9430
ChemSpider	9709620
Jmol 3D model	Interactive image
PubChem	11534837
	InChI InChI=1S/C17H14ClF7O2/c1-6-11(19)13(21)7(14(22)12(6)20)5-27-15(26)10-8(16(10,2)3)4-9(18)17(23,24)25/h4,8,10H,5H2,1-3H3/b9-4-/t8-,10-/m1/s1 Key: ZFHGXWPMULPQSE-SZGBIDFHSA-N ; InChI=1/C17H14ClF7O2/c1-6-11(19)13(21)7(14(22)12(6)20)5-27-15(26)10-8(16(10,2)3)4-9(18)17(23,24)25/h4,8,10H,5H2,1-3H3/b9-4-/t8-,10-/m1/s1 Key: ZFHGXWPMULPQSE-SZGBIDFHBO ;
	SMILES Cl\C(=C/[C@@H]2[C@H](C(=O)OCc1c(F)c(F)c(c(F)c1F)C)C2(C)C)C(F)(F)F ;
Properties
Chemical formula	C17H14ClF7O2
Molar mass	418.74 g·mol−1
Vapor pressure	{{{value}}}
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Tefluthrin is an organic compound. It is classified as a pyrethroid, meaning that in terms of chemical structure, it resembles the naturally occurring insecticide pyrethrin. It was designed to be effective against soil pests.^[1] With an LD50 for rats of at 29 mg/kg, Tefluthrin is one of the most toxic pyrethroids.^[2]

References

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↑ D. M. Soderlund, et al., "Mechanisms of pyrethroid neurotoxicity: implications for cumulative risk assessment", Toxicology 2002, volume 171, pp. 3-59. doi:10.1016/s0300-483x(01)00569-8

External Links

Tefluthrin in the Pesticide Properties DataBase (PPDB)

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[1] Lua error in package.lua at line 80: module 'strict' not found.

[2] D. M. Soderlund, et al., "Mechanisms of pyrethroid neurotoxicity: implications for cumulative risk assessment", Toxicology 2002, volume 171, pp. 3-59. doi:10.1016/s0300-483x(01)00569-8

[1]

[2]

v t e Pest control: insecticides
Carbamates	Aldicarb Bendiocarb Carbaryl Carbofuran Ethienocarb Fenobucarb Oxamyl Methomyl Propoxur
Inorganic compounds	Aluminium phosphide Boric acid Chromated copper arsenate Copper(II) arsenate Copper(I) cyanide Diatomaceous earth Lead hydrogen arsenate Paris Green Scheele's Green
Insect growth regulators	Benzoylureas Diflubenzuron Flufenoxuron Hydroprene Lufenuron Methoprene Pyriproxyfen
Neonicotinoids	Acetamiprid Clothianidin Dinotefuran Imidacloprid Nitenpyram Nithiazine Thiacloprid Thiamethoxam
Organochlorides	Aldrin Beta-HCH Carbon tetrachloride Chlordane Cyclodiene 1,2-DCB 1,4-DCB 1,1-DCE 1,2-DCE DDD DDE DDT Dicofol Dieldrin Endosulfan Endrin Heptachlor Kepone Lindane Methoxychlor Mirex Tetradifon Toxaphene
Organophosphorus	Acephate Azamethiphos Azinphos-methyl Bensulide Chlorethoxyfos Chlorfenvinphos Chlorpyrifos Chlorpyrifos-methyl Coumaphos Demeton-S-methyl Diazinon Dicrotophos Diisopropyl fluorophosphate Dimethoate Dioxathion Disulfoton Ethion Ethoprop Fenamiphos Fenitrothion Fenthion Fosthiazate Isoxathion Malathion Methamidophos Methidathion Mevinphos Monocrotophos Naled Omethoate Oxydemeton-methyl Parathion Parathion-methyl Phenthoate Phorate Phosalone Phosmet Phoxim Pirimiphos-methyl Quinalphos Temefos Tebupirimfos Terbufos Tetrachlorvinphos Tribufos Trichlorfon
Pyrethroids	Acrinathrin Allethrins Bifenthrin Bioallethrin Cyfluthrin Cyhalothrin Cypermethrin Cyphenothrin Deltamethrin Empenthrin Esfenvalerate Etofenprox Fenvalerate Flumethrin Imiprothrin Metofluthrin Permethrin Phenothrin Prallethrin Pyrethrin (I, II; chrysanthemic acid) Pyrethrum Resmethrin Silafluofen Tefluthrin Tetramethrin Tralomethrin Transfluthrin
Ryanoids	Chlorantraniliprole Cyantraniliprole Flubendiamide Ryanodine Ryanodol
Other chemicals	Amitraz Azadirachtin Chlordimeform Chlorfenapyr Cyromazine Fenazaquin Fenoxycarb Fipronil Hydramethylnon Indoxacarb Limonene Pyridaben Pyriprole Ryanodine Sesamex Spinosad Sulfluramid Tebufenozide Tebufenpyrad Veracevine Xanthone
Metabolites	Oxon Malaoxon Paraoxon TCPy
Biopesticides	Bacillus thuringiensis Baculovirus Beauveria bassiana Beauveria brongniartii Metarhizium acridum Metarhizium anisopliae Nomuraea rileyi Lecanicillium lecanii Paecilomyces fumosoroseus Paenibacillus popilliae Purpureocillium lilacinum

Tefluthrin

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Names

IUPAC name (1S,3S)-rel-2,3,5,6-Tetrafluoro-4-methylbenzyl 3-((Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropanecarboxylate
Identifiers
CAS Number	79538-32-2^Y
ChEBI	CHEBI:9430^N
ChemSpider	9709620^Y
Jmol 3D model	Interactive image
PubChem	11534837
InChI InChI=1S/C17H14ClF7O2/c1-6-11(19)13(21)7(14(22)12(6)20)5-27-15(26)10-8(16(10,2)3)4-9(18)17(23,24)25/h4,8,10H,5H2,1-3H3/b9-4-/t8-,10-/m1/s1^Y Key: ZFHGXWPMULPQSE-SZGBIDFHSA-N^Y InChI=1/C17H14ClF7O2/c1-6-11(19)13(21)7(14(22)12(6)20)5-27-15(26)10-8(16(10,2)3)4-9(18)17(23,24)25/h4,8,10H,5H2,1-3H3/b9-4-/t8-,10-/m1/s1 Key: ZFHGXWPMULPQSE-SZGBIDFHBO
SMILES Cl\C(=C/[C@@H]2[C@H](C(=O)OCc1c(F)c(F)c(c(F)c1F)C)C2(C)C)C(F)(F)F
Properties
Chemical formula	C₁₇H₁₄ClF₇O₂
Molar mass	418.74 g·mol⁻¹
Vapor pressure	{{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references