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바미도티온

바미도티온
바미도티온 구조식 이미지
카스 번호:
2275-23-2
한글명:
바미도티온
동의어(한글):
바미도티온
상품명:
Vamidothion
동의어(영문):
nph83;nph-83;KILVAL;10465rp;rp-9895;trucidor;ent26,613;vamidoate;Kilval[R];r.p.10,465
CBNumber:
CB2771555
분자식:
C8H18NO4PS2
포뮬러 무게:
287.34
MOL 파일:
2275-23-2.mol

바미도티온 속성

녹는점
35.5°C
끓는 점
72.8°C
증기압
9×10-6 Pa (est.)
인화점
2 °C
저장 조건
0-6°C
수용성
4,000,000 mg l-1
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
Phosphorothioic acid, O,O-dimethyl S-[2-[[1-methyl-2-(methylamino)- 2-oxoethyl]thio]ethyl] ester(2275-23-2)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
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)
그림문자(GHS):
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H225 고인화성 액체 및 증기 인화성 액체 구분 2 위험 P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 P264, P280, P305+P351+P338,P337+P313P
예방조치문구:
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.

바미도티온 MSDS


Dimethyl phosphorothioate 2-((2-mercaptoethyl)thio)-N-methylpropionamide S-ester

바미도티온 C화학적 특성, 용도, 생산

용도

Vamidothion is a phosphorothioic insecticide for apples and potatoes.

용도

Vamidothion is a systemic insecticide used to control Homoptera in cotton, fruit and rice.

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.

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.

Degradation

Vamidothion is decomposed in strongly acidic or alkaline media (PM). Barceld et al. (1993) examined the photolysis of vamidothion in water containing 2-4% methanol and 5% acetone as a photosensitiser irradiated by a xenon arc (suntest) lamp. Metabolites were analysed and characterised by HPLC, thermospray MS and UV (diode array) spectra. The main degradation product identified was vamidothion sulfoxide (2). This product of vamidothion photolysis is shown in Scheme 1.

바미도티온 준비 용품 및 원자재

원자재

준비 용품


바미도티온 공급 업체

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