| Weight | 419.908 g/mol |
|---|---|
| Formula | C25H22ClNO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 7 |
fenvalerate
esfenvalerate · Pydrin · pydrin, (R-(R*,R*))-isomer
51630-58-1, 66267-77-4, 67614-33-9, 67614-32-8
Score:
#53 in Biology
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#55 in Chemistry
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- Acute toxicity, bioconcentration, and persistence of AC 222,705, benthiocarb, chlorpyrifos, fenvalerate, methyl parathion, and permethrin in the estuarine environment. (Journal of Agricultural and Food Chemistry, 1983)
- Metabolic effects of dinoseb, diazinon and esfenvalerate in eyed eggs and alevins of Chinook salmon (Oncorhynchus tshawytscha) determined by 1H NMR metabolomics (Aquatic Toxicology, 2006)
- Effects of dissolved organic carbon on accumulation and acute toxicity of fenvalerate, deltamethrin and cyhalothrin to Daphnia magna (straus) (Environmental Toxicology and Chemistry, 1991)
- Esterases and Esfenvalerate Resistance in AustralianHelicoverpa armigera(Hbner) Lepidoptera:Noctuidae (Pesticide Biochemistry and Physiology, 1996)
- Study on the relation between occupational fenvalerate exposure and spermatozoa DNA damage of pesticide factory workers. (Occupational and Environmental Medicine, 2004)
- Individual variability in esterase activity and CYP1A levels in Chinook salmon (Oncorhynchus tshawytscha) exposed to esfenvalerate and chlorpyrifos (Aquatic Toxicology, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H332: Harmful if inhaled
Warning Acute toxicity, inhalation - Category 4 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 - esfenvalerate
- Pydrin
- pydrin, (R-(R*,R*))-isomer
- WL 43775
- fenvalarate
- Sumi-alpha
- S-5602
- alpha-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3- methylbutyrate
- Sumicidin
- alpha-cyano-3-phenoxybenzyl alpha-isopropyl-4-chlorophenyl acetate
- Belmark
- pydrin, (R-(R*,S*))-isomer
- pydrin, (S-(R*,S*))-isomer
- pydrin, (S-(R*,R*))-isomer
-
SMILESCC(C)C(C1=CC=C(C=C1)Cl)C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3
-
InChIKeyNYPJDWWKZLNGGM-UHFFFAOYSA-N
- Pubchem - fenvalerate
- Wikipedia - fenvalerate
Fenvalerate is an insecticide. It is a mixture of four optical isomers which have different insecticidal activities. The 2-S alpha (or SS) configuration, known as esfenvalerate, is the most insecticidally active isomer.
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Synthesis
Diphenyl oxide
+
Reactant
(Friedel-Crafts alkylation)
Reactant
+
phenoxyalcohol
(Dakin oxidation)
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fenvalerate
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