Triasulfuron

Triasulfuron 구조식 이미지
카스 번호:
82097-50-5
상품명:
Triasulfuron
동의어(영문):
LOGRAN;AMBER(R);LOGRAN(R);cga-131036;TRISULFURON;TRIASULFURON;TRIASULPHURON;Triasulfuron 0;Biotin Impurity 46;yl)amino)carbonyl)-
CBNumber:
CB3324532
분자식:
C14H16ClN5O5S
포뮬러 무게:
401.83
MOL 파일:
82097-50-5.mol
MSDS 파일:
SDS

Triasulfuron 속성

녹는점
178°C
끓는 점
150-260 °C
밀도
1.5218 (rough estimate)
증기압
0Pa at 25℃
굴절률
1.5630 (estimate)
저장 조건
0-6°C
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨, 가열)
산도 계수 (pKa)
4.34±0.10(Predicted)
BRN
7151883
LogP
1.6-2.6 at 25℃ and pH5-9
해리상수
4.64 at 20℃
CAS 데이터베이스
82097-50-5(CAS DataBase Reference)
EPA
Triasulfuron (82097-50-5)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 N
위험 카페고리 넘버 50/53
안전지침서 60-61
유엔번호(UN No.) UN3077 9/PG 3
WGK 독일 2
RTECS 번호 DB1554000
HS 번호 29350090
유해 물질 데이터 82097-50-5(Hazardous Substances Data)
독성 LD50 in rats (mg/kg): >5000 orally; >2000 dermally; LC50 (4 hr) in rats: >5185 mg/m3 by inhalation (Amrein, Gerber)
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H332 흡입하면 유해함 급성 독성 물질 흡입 구분 4 경고 GHS hazard pictograms P261, P271, P304+P340, P312
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P271 옥외 또는 환기가 잘 되는 곳에서만 취급하시오.
P273 환경으로 배출하지 마시오.
P391 누출물을 모으시오.
P501 ...에 내용물 / 용기를 폐기 하시오.

Triasulfuron MSDS


2-(2-Chloroethoxy)-N-(((4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino)carbonyl)benzenesulfonamide

Triasulfuron C화학적 특성, 용도, 생산

용도

Herbicide.

정의

ChEBI: An N-sulfonylurea that is N-[o-(2-chloroethoxy)phenyl]sulfonylurea in which one of the hydrogens attached to the non-sulfonylated nitrogen has been replaced by a 4-methoxy-6-methyl-1,3,5-triazin-2-yl group A herbicide used to control broad-leaved weeds in cereals, its use within the EU has been banned after September 2017 on the grounds of potential groundwater contamination and risks to aquatic life.

농업용

Herbicide: Used for the control of annual ryegrass, paradoxa grass and a wide range of broadleaf weeds in wheat and the post-emergence control of wild radishes in wheat, oats and barley. Registered for use in EU countries . Registered for use in the U.S

상품명

AMBER®; CGA 131036®; LOGRAN®; RAVE®

신진 대사 경로

Triasulfuron undergoes hydrolytic degradation, especially under acidic conditions, giving rise to cleavage of the sulfonylurea linkage, producing the major products 2-(2-chloroethoxy)benzenesulfonamide and 4-methyl-6-methoxy-2-amino-1,3,5-triazine and the minor product acetyltriuret. In plants, hydroxylation occurs at the 5-position of the phenyl ring to yield 5- hydroxytriasulfuron as a primary metabolite which is a major metabolite from the plant microsomal system.
By mammals, orally administered triasulfuron is mainly excreted in the urine, and O-dealkylation of 2- chloroethoxy and 6-methoxy groups, and hydroxylation at the 5-position of the phenyl ring and at the 4-methyl group of the triazine ring are observed. By UV irradiation, 2-chloroethoxybenzene is interestingly identified with (4-methoxyl-6-methyl-1,3,5-triazine)urea, and, in sunlight, with these two products, 2-amino-4- methoxyl-6-methyltriazine and 2-(2- chloroethoxy)benzenesulfonamide are identified.

Triasulfuron 준비 용품 및 원자재

원자재

준비 용품


Triasulfuron 공급 업체

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