Weight | 376.496 g/mol |
---|---|
Formula | C25H28O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 3 |
Rotatable Bonds | 9 |
Etofenprox (80844-07-1)
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- Sigma-Aldrich - Etofenprox134.00 USD
- Fisher Scientific - Search for Etofenprox
- TCI - Search for Etofenprox
- Organosilane insecticides. Part I: Biological and physical effects of isosteric replacement of silicon for carbon in etofenprox and MTI800 (Pesticide Science, 1990)
- Insecticidal Effect of Controlled Release Formulations of Etofenprox Based on Nano-bio Technique (Journal of The Faculty of Agriculture Kyushu University, 2011)
- Determination of Etofenprox in environmental samples by HPLC after anionic surfactant micelle-mediated extraction (coacervation extraction) (Analytical and Bioanalytical Chemistry, 2006)
- Risk assessment of etofenprox (vectron) on non-target aquatic fauna compared with other pesticides used as Simulium larvicide in a tropical environment (Chemosphere, 2001)
- Residual Characteristics of Etofenprox and Methoxyfenozide in Chinese Cabbage (2009)
- Contamination of rice by etofenprox, diethylphthalate and alkylphenols: effects on first delivery and sperm count in mice (Journal of Toxicological Sciences, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H336: May cause drowsiness or dizziness
Warning Specific target organ toxicity, single exposure; Narcotic effects - Category 3 - H362: May cause harm to breast-fed children
- 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 -
SMILESCCOC1=CC=C(C=C1)C(C)(C)COCC2=CC(=CC=C2)OC3=CC=CC=C3
-
InChIKeyYREQHYQNNWYQCJ-UHFFFAOYSA-N
- Pubchem - Etofenprox
- Wikipedia - etofenprox
Etofenprox is a pyrethroid derivative which is used as an insecticide. Mitsui Chemicals Agro Inc. is the main manufacturer of the Chemical.
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Synthesis
Reactant
+
phenoxyalcohol
(Dakin oxidation)
PHENETOLE
+
Reactant
(Friedel-Crafts alkylation)
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