Structure via PubChem · Public domain (PubChem)
etofenprox
Sign in to saveAlso known as Ethofenprox, Ethophenprox
Etofenprox is a pyrethroid derivative which is used as an insecticide. Mitsui Chemicals Agro Inc. is the main manufacturer of the chemical. It is also used as an ingredient in flea medication for cats and dogs.
Chemical data
- Formula
- C25H28O3
- Molecular weight
- 376.5 g/mol
- IUPAC name
- 1-ethoxy-4-[2-methyl-1-[(3-phenoxyphenyl)methoxy]propan-2-yl]benzene
- SMILES
- CCOC1=CC=C(C=C1)C(C)(C)COCC2=CC(=CC=C2)OC3=CC=CC=C3
- InChIKey
- YREQHYQNNWYQCJ-UHFFFAOYSA-N
- XLogP
- 7
- Polar surface area
- 27.7 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 376.204
- Has use
- insecticide
Show 4 more facts
- chemical formula
- C₂₅H₂₈O₃
- canonical SMILES
- CCOC1=CC=C(C=C1)C(C)(C)COCC2=CC(=CC=C2)OC3=CC=CC=C3
- World Health Organisation international non-proprietary name
- etofenprox
- Commons category
- Ethofenprox
via Wikidata · CC0
~3 min read
Encyclopedic overview
6 sectionsContents
- General uses
- Hazards to humans and domestic animals
- Environmental hazards
- Environmental persistence
- Physical and chemical hazards
- References
{{chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 447039021 | ImageFile = Etofenprox.svg | ImageClass = skin-invert-image | ImageSize = 200px | ImageAlt = Skeletal formula | ImageFile1 = Etofenprox-3D-balls.png | ImageClass1 = bg-transparent | ImageSize1 = 200px | ImageAlt1 = Ball-and-stick model | PIN = 1-{[2-(4-Ethoxyphenyl)-2-methylpropoxy]methyl}-3-phenoxybenzene | OtherNames = Ethofenprox, MTI-500, Trebon, Zenivex |Section1= |Section2= |Section3= }}
Etofenprox is a pyrethroid derivative which is used as an insecticide. Mitsui Chemicals Agro Inc. is the main manufacturer of the chemical. It is also used as an ingredient in flea medication for cats and dogs.
Excerpted from Wikipedia’s “etofenprox” article, available under the CC BY-SA 4.0 licence.