permethrin (CHEBI:34911)

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ChEBI Name	permethrin

ChEBI ID	CHEBI:34911

Definition	A cyclopropanecarboxylate ester in which the esterifying alcohol is 3-phenoxybenzyl alcohol and the cyclopropane ring is substituted with a 2,2-dichlorovinyl group and with gem-dimethyl groups.

Stars	This entity has been manually annotated by the ChEBI Team.

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Formula

C21H20Cl2O3

Net Charge

Average Mass

391.28710

Monoisotopic Mass

390.07895

InChI

InChI=1S/C21H20Cl2O3/c1-21(2)17(12-18(22)23)19(21)20(24)25-13-14-7-6-10-16(11-14)26-15-8-4-3-5-9-15/h3-12,17,19H,13H2,1-2H3

InChIKey

RLLPVAHGXHCWKJ-UHFFFAOYSA-N

SMILES

CC1(C)C(C=C(Cl)Cl)C1C(=O)OCc1cccc(Oc2ccccc2)c1

Roles Classification
Biological Role(s):	pyrethroid ester insecticide

Application(s):	scabicide An acaricide that kills mites of the genus Sarcoptes. pyrethroid ester insecticide pyrethroid ester acaricide agrochemical An agrochemical is a substance that is used in agriculture or horticulture. ectoparasiticide

ChEBI Ontology
Outgoing	permethrin (CHEBI:34911) has functional parent 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid (CHEBI:39308) permethrin (CHEBI:34911) has role agrochemical (CHEBI:33286) permethrin (CHEBI:34911) has role ectoparasiticide (CHEBI:38956) permethrin (CHEBI:34911) has role pyrethroid ester acaricide (CHEBI:39259) permethrin (CHEBI:34911) has role pyrethroid ester insecticide (CHEBI:39116) permethrin (CHEBI:34911) has role scabicide (CHEBI:73333) permethrin (CHEBI:34911) is a cyclopropanecarboxylate ester (CHEBI:50351) permethrin (CHEBI:34911) is a cyclopropanes (CHEBI:51454)

Incoming	trans-permethrin (CHEBI:62521) is a permethrin (CHEBI:34911)

IUPAC Name

3-phenoxybenzyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate

INN	Source
permethrin	ChemIDplus

Synonyms	Sources
(3-Phenoxyphenyl)methyl (±)-cis,trans-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate	ChemIDplus
3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropane carboxylic acid, (3-phenoxyphenyl) methyl ester	ChemIDplus
Permethrin	KEGG COMPOUND

Last Modified

22 February 2017