134098-61-6 Usage
Description
Fenpyroximate is a synthetic acaricide, miticide, and insecticide that belongs to the class of amidinohydrazones. It is characterized by its ability to disrupt the molting process of arthropods, leading to their death. Fenpyroximate is effective against a wide range of pests, including spider mites, whiteflies, and thrips, making it a valuable tool in agricultural and horticultural settings.
Uses
Used in Agricultural Industry:
Fenpyroximate is used as an acaricide for controlling spider mites in greenhouses. It is particularly effective in managing populations of two-spotted spider mites, red spider mites, and other economically important mite species.
Fenpyroximate is also used as a miticide to protect crops from damage caused by various mite species. Its ability to target the molting process makes it a potent tool in preventing mite infestations and reducing the need for chemical treatments.
Furthermore, Fenpyroximate serves as an insecticide, targeting pests such as whiteflies and thrips. Its broad-spectrum activity allows it to be used in integrated pest management programs, helping to maintain crop health and yield while minimizing the environmental impact of pesticide use.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 134098-61-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,9 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 134098-61:
(8*1)+(7*3)+(6*4)+(5*0)+(4*9)+(3*8)+(2*6)+(1*1)=126
126 % 10 = 6
So 134098-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C25H28N2O4/c1-18-22(23(27(5)26-18)30-21-9-7-6-8-10-21)15-16-29-17-19-11-13-20(14-12-19)24(28)31-25(2,3)4/h6-16H,17H2,1-5H3/b16-15-
134098-61-6Relevant articles and documents
ACTIVE COMPOUND COMBINATIONS HAVING INSECTICIDAL AND ACARICIDAL PROPERTIES
-
, (2010/08/18)
The novel active compound combinations comprising a compound of the formula (I-1) or (I-2) and the active compounds (1) to (26) listed in the description have very good insecticidal and acaricidal properties.
Pyrazole oxime derivatives and compositions
-
, (2008/06/13)
A pyrazole oxime derivative represented by the general formula (I) which is useful as an insecticide and fungicide, STR1 wherein the structural elements are defined in the specification, and the method of controlling said pests. The compounds represented by the general formula (I) can be synthesized by the methods disclosed in the specification.