신메틸린

신메틸린
신메틸린 구조식 이미지
카스 번호:
87818-31-3
한글명:
신메틸린
동의어(한글):
신메틸린
상품명:
Cinmethylin
동의어(영문):
cinch;argold;SKH 301;sd95481;WL 95481;CINMETHYLIN;exo-(+-)-xy);(2.2.1)heptane;Caswell No. 731G;Cinmethylin [iso]
CBNumber:
CB2407074
분자식:
C18H26O2
포뮬러 무게:
274.4
MOL 파일:
87818-31-3.mol
MSDS 파일:
SDS

신메틸린 속성

녹는점
25°C
끓는 점
313°C
밀도
d20 1015 kg/m3
굴절률
1.4800 (estimate)
인화점
147 °C
저장 조건
0-6°C
CAS 데이터베이스
87818-31-3(CAS DataBase Reference)
EPA
Cinmethylin (87818-31-3)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,N
위험 카페고리 넘버 20-51/53
안전지침서 23-61-22
유엔번호(UN No.) UN3082 9/PG 3
WGK 독일 3
RTECS 번호 RN8762000
HS 번호 29321900
독성 LD50 orally in rats: 4.5 g/kg; LD50 dermally in rabbits: >2 g/kg (Lee)
기존화학 물질 97-3-378
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
H411 장기적 영향에 의해 수생생물에 유독함 수생 환경유해성 물질 - 만성 구분 2
예방조치문구:
P273 환경으로 배출하지 마시오.

신메틸린 C화학적 특성, 용도, 생산

개요

Cinmethylinwas developed by Shell Chemical Company in the early 1980s as a weed control agent for monocotyledonous species. This herbicide controls important grasses such as green foxtail (Setaria viridis) and barnyardgrass (Echinochloa crus-galli) and suppresses the growth of several broadleaf weeds such as prickly sida (Sida spinosa) and velvetleaf (Abutilon theophrasti).

용도

Cinmethylin is used as pre-emergence grass herbicide. Cinmethylin is member of the cineole eucalyptol family.

Pharmacology

Cinmethylin is active on several important grasses in rice (Echinochloa spp., Cyperus spp., and Monochoria vaginalis) at rates from 25 to 100 g ai/ha (5). Its chemical and toxicological features (low persistence in environment and low mammalian toxicity) generated a significant level of interest in its use as a rice herbicide.

신진 대사 경로

When rats are administered 14C-cinmethylin orally, the major route of its elimination is via urinary excretion. A complex degradation pattern of cinmethylin is observed and the metabolic pathways involve hydroxylation, oxidation at the benzyl and cineol portions, conjugation with glucuronic acid and glycine, and cleavage of the ether linkage. When rats are administered 14C-cinmethylin by stomach incubation, two minor metabolites are identified as o- (acetoxymethyl)benzoic acid and 9-(acetoxymethyl)-a- carboxycinmethylin.

신메틸린 준비 용품 및 원자재

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