Structure via PubChem · Public domain (PubChem)
Phenothrin
Sign in to saveAlso known as Sumithrin, 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid (3-phenoxyphenyl)methyl ester
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In the Vinony graph
Within Vinony's link graph, Phenothrin is referenced by 744 other articles, and connects out to head louse, carbamate and acaricide.
Vinony files it under (3-phenoxyphenyl)methyl 2,2,3-trimethylcyclopropane-1-carboxylates, Chembox having GHS data and Chrysanthemate esters.
Its subject is documented across 15 Wikipedia language editions.
Chemical data
- Formula
- C23H26O3
- Molecular weight
- 350.4 g/mol
- IUPAC name
- (3-phenoxyphenyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate
- SMILES
- CC(=CC1C(C1(C)C)C(=O)OCC2=CC(=CC=C2)OC3=CC=CC=C3)C
- InChIKey
- SBNFWQZLDJGRLK-UHFFFAOYSA-N
- XLogP
- 6.2
- Polar surface area
- 35.5 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
Withdrawn- Max clinical phase
- Approved
- Molecule type
- Small molecule
- Indications
- parasitic infection
via ChEMBL · EBI
Research
198 papers- Evaluation of the genotoxicity of the pyrethroid insecticide phenothrin.Mutation research. Genetic toxicology and environmental mutagenesis · 2014
- Phenothrin lotions in the treatment of head louse infestation.Journal of the Royal Society of Health · 1988
- Head lice.BMJ clinical evidence · 2009
- Head lice.BMJ clinical evidence · 2011
- d-Phenothrin-induced oxidative DNA damage in rat liver and kidney determined by HPLC-ECD/DAD.Environmental toxicology · 2015
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 350.188
- Has use
- insecticide
Show 3 more facts
- chemical formula
- C₂₃H₂₆O₃
- Commons category
- Phenothrin
- canonical SMILES
- CC(=CC1C(C1(C)C)C(=O)OCC2=CC(=CC=C2)OC3=CC=CC=C3)C
via Wikidata · CC0
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