바미도티온

한글명:바미도티온

카스 번호2275-23-2

상품명:Vamidothion

CBNumberCB2771555

분자식C8H18NO4PS2

포뮬러 무게287.34

MOL 파일2275-23-2.mol

동의어(한글)

바미도티온

O,O-디메틸S-(2-(1-메틸카르바모일에틸티오)에틸포스포로티오산염

바미도산염

화학적 성질

녹는점	35.5°C
끓는 점	72.8°C
밀도	1.240±0.06 g/cm3(Predicted)
증기압	9×10^-6 Pa (est.)
인화점	2 °C
저장 조건	0-6°C
수용성	4,000,000mg l^-1
산도 계수 (pKa)	15.22±0.46(Predicted)
CAS 데이터베이스	2275-23-2(CAS DataBase Reference)
NIST	Phosphorothioic acid, o,o-dimethyl s-[2-[[1-methyl-2-(methylamino)-2-oxoethyl]thio]ethyl] ester(2275-23-2)
EPA	Vamidothion (2275-23-2)

위험 및 안전 성명

위험품 표기	T;N,N,T,Xn,F
위험 카페고리 넘버	21-25-50-36-20/21/22-11
안전지침서	36/37-45-61-16
유엔번호(UN No.)	UN 2811
WGK 독일	2
RTECS 번호	TF7900000
위험 등급	6.1(b)
포장분류	III
유해 물질 데이터	2275-23-2(Hazardous Substances Data)
독성	LD50 oral in rabbit: 160mg/kg

그림문자(GHS)

바미도티온 MSDS

바미도티온 화학적 특성, 용도, 생산

개요
Vamidothion is a colorless crystalline substance,. It is readily soluble in water (4 kg/L) and most organic solvents except aliphatic hydrocarbons. Log Kow = 0.12. It decomposes in strong alkaline and acidic media.
용도
Vamidothion is a phosphorothioic insecticide for apples and potatoes.
정의
ChEBI: An organic thiophosphate that is N-methyl-2-[(2-sulfanylethyl)sulfanyl]propanamide in which the thiol group has been converted to the corresponding O,O-dimethyl thiophoshate. Formerly used as an inse ticide and acaricide, it is no longer approved for use within the European Union.
Pharmacology
Pyriproxyfen formulations demonstrate persistent efficacy. For example, a water-based 5.3% pyriproxyfen spot-on formulation applied to cats was reported to completely prevent the hatching of flea eggs for at least 46 days after treatment and continued to provide greater than 96% control until day 60 (57). Because pyriproxyfen is efficacious at very low concentrations, trace amounts of the chemical, when transferred from treated pets to their environments, are sufficient to inhibit the development of larvae.
신진 대사 경로
Vamidothion is mainly metabolised via oxidation to its sulfoxide; further oxidation to the corresponding sulfone has been observed in houseflies but occurs much less readily than with other thioether-containing organophosphates (e.g. phorate). The sulfoxide is then hydrolysed via P-S and C-S bond cleavage to give the thiol or hydroxyl derivatives and dimethyl phosphate and O,O-dimethyl phosphorothioate respectively. O-Demethylation apparently occurs as a major degradation process in plants but has not been observed in soil or in animals. N-Demethylation and hydrolysis to the corresponding carboxylic acid, such as occurs with dimethoate, does not apparently happen in the case of vamidothion.

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