2,3,5-TRIMETHACARB
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2,3,5-TRIMETHACARB 속성
- 녹는점
- 118-123°C
- 끓는 점
- 329.46°C (rough estimate)
- 밀도
- 1.0945 (rough estimate)
- 증기압
- 6.8 x 10-3 Pa (25 °C)
- 굴절률
- 1.5080 (estimate)
- 저장 조건
- Refrigerator
- 용해도
- 클로로포름(약간 용해됨), 메탄올(약간 용해됨)
- 물리적 상태
- 고체
- 물리적 상태
- 단단한 모양
- 수용성
- >58 mg l-1 (23 °C)
- 색상
- 흰색에서 황백색까지
안전
| 유엔번호(UN No.) | 2757 | ||
|---|---|---|---|
| 위험 등급 | 6.1(b) | ||
| 포장분류 | III | ||
| 독성 | rabbit,LD50,skin,> 2500mg/kg (2500mg/kg),Shell Chemical Company. Vol. CODE, |
2,3,5-TRIMETHACARB C화학적 특성, 용도, 생산
용도
Trimethacarb is an insecticide with primarily stomach action. It is mainly used to control corn root worm larvae in maize but it also controls a wide range of insect and mollusc pests. Trimethacarb acts as a bird and mammal repellent.신진 대사 경로
The metabolic pathways of trimethacarb in plants, mammals and insects involve mainly oxidation of N-methyl or ring-methyl substituents and conjugation. Some hydroxylation of the phenyl ring and ester hydrolysis occurs. The metabolism of trimethacarb was reviewed by Fukuto (1972), Kuhr and Dorough (1976) and by Schlagbauer and Schlagbauer (1972).Degradation
Trimethacarb is hydrolysed by strong acids and alkalis but aqueous solutions are stable to light (PM). Trimethacarb was applied to bean leaves and exposed to natural sunlight for 4 days. Both isomers were decomposed more rapidly when exposed to sunlight compared with normal light in the laboratory. The compounds were almost completely decomposed. Major photoproducts resulted from hydroxylation of methyl substituents of the phenyl ring (2 and 3) and of the N-methyl group (5 and 6) (see Schemes 1 and 2). There were few products of hydrolysis (Slade and Casida, 1970; Kuhr and Dorough, 1976).2,3,5-TRIMETHACARB 준비 용품 및 원자재
원자재
준비 용품
2,3,5-TRIMETHACARB 공급 업체
글로벌( 17)공급 업체
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