???????
|
|
??????? ??
- ???
- 101.1-102.4°
- ?? ?
- 546.2±60.0 °C(Predicted)
- ??
- 1.25g/cm3
- ?? ??
- Store at -20°C
- ???
- ?? ???
- ???
- Chloroform: Slightly soluble,Methanol: Slightly soluble
- ??? ??
- powder to crystal
- ?? ?? (pKa)
- 1.58±0.10(Predicted)
- ??
- White to Light yellow to Light orange
- Henry's Law Constant
- 4.6×100 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
- ???
- ???
- ?? ??
- agriculture
environmental
- InChI
- 1S/C24H27N3O4/c1-17-21(22(27(5)26-17)30-20-9-7-6-8-10-20)15-25-29-16-18-11-13-19(14-12-18)23(28)31-24(2,3)4/h6-15H,16H2,1-5H3/b25-15+
- InChIKey
- YYJNOYZRYGDPNH-MFKUBSTISA-N
- SMILES
- Cc1nn(C)c(Oc2ccccc2)c1\C=N\OCc3ccc(cc3)C(=O)OC(C)(C)C
- LogP
- 6.443 (est)
- CAS ??????
- 134098-61-6(CAS DataBase Reference)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ????(UN No.) | UN3082 (liquid) | ||
|---|---|---|---|
| WGK ?? | WGK 3 | ||
| HS ?? | 29331990 | ||
| ???? ??? | 6.1A - Combustible acute toxic Cat. 1 and 2 very toxic hazardous materials |
||
| Hazard Classifications | Acute Tox. 2 Inhalation Acute Tox. 3 Oral Aquatic Acute 1 Aquatic Chronic 1 Skin Sens. 1B |
||
| ?? ?? ??? | 134098-61-6(Hazardous Substances Data) | ||
| ?? | 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) | ||
| ???? ?? | KE-05-0263 | ||
| ?????? ??? | 97-1-342;06-4-50 | ||
| ?? ? ???? | ????: ????; ???(??)????: ??????? ? ?? 25% ?? ??? ??? |
??????? C??? ??, ??, ??
??
Acaricide.???
Acaricide, Miticide, Insecticide: Used to control spider mites in greenhouses.???
AKARI®; HOE® 555-02A; NNI®-850; SEQUEL®?? ?? ??
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.??????? ?? ?? ? ???
???
???????
??
Potassium hydroxide solution
4-????????
1,3-???-5-????
???
Methanol solution of sodium methoxide
??????
?? ??????
Butyl benzoate
?????
?? ??
??????? ?? ??
???( 196)?? ??
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