클로르메포스

한글명:클로르메포스

카스 번호24934-91-6

상품명:CHLORMEPHOS

CBNumberCB4364182

분자식C5H12ClO2PS2

포뮬러 무게234.7

MOL 파일24934-91-6.mol

동의어(한글)

클로르메포스

O,O-다이에틸 S-(클로로메틸) 다이싸이오포스페이트

S-(클로로메틸) O,O-다이에틸 포스포로다이싸이오에이트

화학적 성질

녹는점	25°C
끓는 점	bp1mm 93-95°; bp0.1 Torr 81-85°
밀도	d20 1.260
증기압	7.6 Pa (30 °C)
굴절률	nD220 1.5244
인화점	100 °C
저장 조건	0-6°C
수용성	60mgl^-1(20°C)
물리적 상태	액체
EPA	Chlormephos (24934-91-6)

위험 및 안전 성명

위험품 표기	T+,N
위험 카페고리 넘버	27/28-50/53
안전지침서	28-36/37-45-60-61-27
유엔번호(UN No.)	3018
RTECS 번호	TD5170000
위험 등급	6.1(a)
포장분류	II
유해 물질 데이터	24934-91-6(Hazardous Substances Data)
독성	LD50 in rats (mg/kg): 7 orally; 27 dermally; LC50 in fish: 1.5 mg/l (Lynch)

그림문자(GHS)

클로르메포스 화학적 특성, 용도, 생산

용도
Chlormephos is used to control soil insects such as wireworms in a number of crops.
일반 설명
Colorless liquid. Used as a soil insecticide. Not registered as a pesticide in the U.S.
공기와 물의 반응
Slightly soluble in water [Farm Chemicals Handbook].
반응 프로필
Organophosphates, such as CHLORMEPHOS, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.
건강위험
(Non-Specific -- Organophosphorus Pesticide, Liquid, n.o.s.) CHLORMEPHOS is poisonous; it may be fatal if inhaled, swallowed, or absorbed through the skin.
화재위험
(Non-Specific -- Organophosphorus Pesticide, Liquid, n.o.s.) Container may explode in heat of fire. Fire and runoff from control water may produce irritating or poisonous gases.
신진 대사 경로
Chlormephos is a soil insecticide with considerable vapour phase activity. The main soil metabolite is ethion. The mechanism of hydrolysis of chlormephos is mainly by the nucleophilic attack of OH- on the Smethylene carbon to yield O,O-diethyl phosphorodithioate and in this respect it is similar to mecarbam. This mechanism may afford ethion when the nucleophile is O,O-diethyl phosphorodithioate. The other mechanism of hydrolysis is by attack on phosphorus to yield O,O-diethyl phosphorothioate and these two routes of hydrolytic degradation apparently dominate the metabolism of the insecticide.
신진 대사
In soils, chlormephos is converted to ethion by reaction with the hydrolytic product, O,O-diethyl hydrogen phosphorothioate.

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