Fenpyroximate Chemical Properties

Melting point:

101.1-102.4°

Boiling point:

546.2±60.0 °C(Predicted)

Density 

1.25g/cm3

storage temp. 

Store at -20°C

Water Solubility 

Insoluble in water

solubility 

Chloroform: Slightly soluble,Methanol: Slightly soluble

form 

powder to crystal

pka

1.58±0.10(Predicted)

color 

White to Light yellow to Light orange

Stability:

Light Sensitive

LogP

6.443 (est)

CAS DataBase Reference

134098-61-6(CAS DataBase Reference)

EPA Substance Registry System

Fenpyroximate (134098-61-6)

Safety Information

RIDADR 

UN3082 (liquid)

HS Code 

29331990

Hazardous Substances Data

134098-61-6(Hazardous Substances Data)

Toxicity

LD50 in male, female rats (mg/kg): 480, 245 orally; >2000, >2000 dermally; LC50 (48hr) in carp: 6.1 mg/l; LC50 (3hr) in daphnia pulex: 85 mg/l (Konno)

Fenpyroximate Usage And Synthesis

Uses

Acaricide.

Definition

ChEBI: Fenpyroximate is a pyrazole acaricide and a tert-butyl ester. It has a role as a mitochondrial NADH:ubiquinone reductase inhibitor. It derives from a hydride of a 1H-pyrazole.

Agricultural Uses

Acaricide, Miticide, Insecticide: Used to control spider mites in greenhouses.

Trade name

AKARI®; HOE® 555-02A; NNI®-850; SEQUEL®

Metabolic pathway

When fenpyroximate is administered orally to rats, radiocarbons from 14C-fenpyroximate are rapidly and almost completely excreted in the urine and feces within 72 h, and fenyproximate seems to be metabolized via oxidation of the tert-butyl group and methyl group at the 3-position in the pyrazole ring, p- hydroxylation in the phenoxy moiety, N-demethylation, hydrolysis of the tert-butyl ester, cleavage of the oxime ether bond, and/or E/Z isomerization. In soils, 12 degradation products are identified, and in sterilized soils the degradation of fenpyroximate and CO2, evolution are negligible. Fenpyroximate degrades through hydrolysis of tert-butyl ester, isomerization or cleavage of the oxime ether, N-demethylation, oxidation of the methyl group at the 3-position on the pyrazole ring, and hydroxylation of the phenoxy ring, and is finally mineralized to CO2 and/or bound to soil organic matter.

Fenpyroximate(134098-61-6)Related Product Information

• Butyl benzoate
• tert-Butanol
• ETHANE
• Dimethyl ether
• 3,5-Dimethylbenzoic acid
• Dimethyl sulfate
• 4,4'-Diphenylmethane diisocyanate
• tert-Butyl peroxybenzoate
• 4-Methoxybenzoic acid
• Dimethyl sulfoxide
• Diethoxydimethylsilane
• Dimethyl carbonate
• Methylene Blue
• Dacthal
• Dimethyl disulfide
• Isobutyl chloroformate
• phenoxybenzamine
• Diisobutyl phthalate