| Weight | 349.43 g/mol |
|---|---|
| Formula | C22H23NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
Fenpropathrin (39515-41-8)
fenpropathrin, (R)-isomer · fenpropathrin, (+-)-isomer · fenpropathrin, (S)-isomer
Score:
#126 in Environmental science
,
#1386 in Biology
,
#1621 in Chemistry
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- Development of an Enzyme-Linked Immunosorbent Assay for the Detection of the Pyrethroid Insecticide Fenpropathrin (Journal of Agricultural and Food Chemistry, 1998)
- Cloning of a sodium channel gene and identification of mutations putatively associated with fenpropathrin resistance in Tetranychus urticae (Pesticide Biochemistry and Physiology, 2010)
- Heat Capacities and Thermodynamic Properties of Fenpropathrin (C22H23O3N) (Journal of Thermal Analysis and Calorimetry, 2001)
- Fenpropathrin Biodegradation Pathway in Bacillus sp. DG-02 and Its Potential for Bioremediation of Pyrethroid-Contaminated Soils (Journal of Agricultural and Food Chemistry, 2014)
- Isomer- and enantioselective degradation and chiral stability of fenpropathrin and fenvalerate in soils. (Chemosphere, 2009)
- Photodegradation of the pyrethroid insecticide fenpropathrin in water, on soil and on plant foliage (Pesticide Science, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H330: Fatal if inhaled
Danger Acute toxicity, inhalation - Category 1, 2 - H361: Suspected of damaging fertility or the unborn child
Warning Reproductive toxicity - Category 2 - 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 - fenpropathrin, (R)-isomer
- fenpropathrin, (+-)-isomer
- fenpropathrin, (S)-isomer
-
SMILESCC1(C(C1(C)C)C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3)C
-
InChIKeyXQUXKZZNEFRCAW-UHFFFAOYSA-N
- Pubchem - Fenpropathrin
- Wikipedia - fenpropathrin
Fenpropathrin (brand names Danitol, Meothrin), or fenopropathrin, is a widely used pyrethroid insecticide in agriculture and household. A person developed Parkinson's disease after six months of daily exposure to fenpropathrin, and animal tests subsequently revealed that the compound is a dopaminergic neurotoxin. It has thus been implicated as an environmental risk factor for Parkinson's disease.
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Synthesis
Diphenyl oxide
+
Reactant
(Friedel-Crafts alkylation)
Reactant
+
phenoxyalcohol
(Dakin oxidation)
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