클로퀸토세트-멕실

한글명:클로퀸토세트-멕실

카스 번호99607-70-2

상품명:Cloquintocet-mexyl

CBNumberCB3243431

분자식C18H22ClNO3

포뮬러 무게335.83

MOL 파일99607-70-2.mol

동의어(한글)

클로퀸토세트-멕실

화학적 성질

녹는점	69°
끓는 점	448.4±30.0 °C(Predicted)
밀도	1.163±0.06 g/cm3(Predicted)
증기압	0-54.4Pa at 25-185.9℃
저장 조건	Sealed in dry,2-8°C
용해도	클로로포름(약간 용해됨), DMSO(약간 용해됨), 에틸아세테이트(약간 용해됨)
물리적 상태	Solid
산도 계수 (pKa)	1.94±0.29(Predicted)
색상	흰색에서 황백색까지
Merck	14,2401
안정성	안정적인. 강한 산화제와 호환되지 않습니다.
LogP	5.2-5.24 at 25℃ and pH5-9.1
표면장력	56.8-57.2mN/m at 590μg/L and 20℃
해리상수	3.55 at 20℃
CAS 데이터베이스	99607-70-2(CAS DataBase Reference)
EPA	Cloquintocet-mexyl (99607-70-2)

위험 및 안전 성명

위험품 표기	Xi
위험 카페고리 넘버	43
안전지침서	36/37
유엔번호(UN No.)	UN 3077
WGK 독일	2
RTECS 번호	AG1265000
HS 번호	2933.49.3000
독성	LD50 in rats (mg/kg): >2000 orally; >2000 dermally; LC50 (4 hr) in rats: >935 mg/m3 by inhalation (Amrein)

그림문자(GHS)

클로퀸토세트-멕실 화학적 특성, 용도, 생산

개요
Cloquintocet-mexyl is a colourless crystalline herbicide safener. It is categorized as Class III toxin.
화학적 성질
beige solid
용도
Cloquintocet-mexyl is a herbicide. It is used to control coarse annual grass of the family poaceae (gramineae). lt was developed by the swiss ciba geigy in the 1980s and the patent has expired.
농업용
Cloquintocet-mexyl is a safener that can be used in conjunction with various herbicides to reduce phytotoxicity to crops. Though effective as a safener, the manufacture, storage, and use of cloquintocet-mexyl containing products can present challenges owing to its sensitivity to water and its low melting temperature (i.e., 61-69° C. for technical material). When products containing cloquintocet-mexyl are prepared, stored, or used in the presence of water, cloquin tocet-mexyl can undergo hydrolysis to form cloquintocet acid, and/or form a needle-shaped, crystalline hydrate that can, lead to clogged spray nozzles during spray applications and/or possibly increased levels of crop phytotoxicity.
Carcinogenicity
In accordance with the EPA Proposed EPA Weight-of-the-Evidence Categories, August 1999, the HIARC classified cloquintocet-mexyl as "not likely to be a human carcinogen." Carcinogenicity studies in rats and mice did not show increased incidence of spontaneous tumor formation. With negative mutagenic test battery, it is suggested that cloquintocet-mexyl (CGA 185072) is not likely to be a human carcinogen.
신진 대사
Metabolism studies in rats indicated that approximately 40% of the administered dose of cloquintocet-mexyl was absorbed through the gastrointestinal tract and subsequently excreted via the urine. Fecal excretion accounted for approximately 60% of the administered dose. The chemical was rapidly eliminated (more than 80% of the administered dose) via feces and urine within 48 hours post-dosing. Sex, dosing regime, and dose levels had little effect on the excretion pattern. Excretion patterns were similar between the biliary cannulated and non-cannulated animals indicating that there was no enterohepatic circulation of the chemical. Three days after administration, tissue radioactivity accounted for less than 0.3% of the administered dose (or was non-detectable) and was not detectable in the expired air. At day three post-dosing, most tissue residues of radioactivity were below the limit of detection. The major metabolic pathway of cloquintocet-mexyl was ester hydrolysis to yield 5-chloro-8-quinolinoxy acetic acid, the major metabolite in the fecal and urinary pools.

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