| Weight | 422.874 g/mol |
|---|---|
| Formula | C23H22ClF3O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
BIFENTHRIN (82657-04-3)
Score:
#389 in Biology
,
#407 in Chemistry
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- Enantioselectivity in Estrogenic Potential and Uptake of Bifenthrin (Environmental Science & Technology, 2007)
- Stabilized polymeric nanoparticles for controlled and efficient release of bifenthrin. (Pest Management Science, 2008)
- Dissipation behavior of bifenthrin residues in tea and its brew (Food Control, 2005)
- Degradation of bifenthrin, chlorpyrifos and imidacloprid in soil and bedding materials at termiticidal application rates (Pesticide Science, 1999)
- Freshwater community responses to mixtures of agricultural pesticides: Effects of atrazine and bifenthrin (Environmental Toxicology and Chemistry, 1993)
- Enantioselective cytotoxicity of the insecticide bifenthrin on a human amnion epithelial (FL) cell line (Toxicology, 2008)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H300: Fatal if swallowed
Danger Acute toxicity, oral - Category 1, 2 - H331: Toxic if inhaled
Danger Acute toxicity, inhalation - Category 3 - H372: Causes damage to organs through prolonged or repeated exposure
Danger Specific target organ toxicity, repeated exposure - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESCC1=C(C=CC=C1COC(=O)C2C(C2(C)C)C=C(C(F)(F)F)Cl)C3=CC=CC=C3
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InChIKeyOMFRMAHOUUJSGP-UHFFFAOYSA-N
- Pubchem - BIFENTHRIN
- Wikipedia - Bifenthrin
Bifenthrin is a pyrethroid insecticide used primarily against the red imported fire ant by influencing its nervous system. It has a high toxicity to aquatic organisms. Although it is listed as a restricted use chemical in the United States, it is allowed to be sold for daily use, provided the product sold has a low concentration of bifenthrin.
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BIFENTHRIN
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