메티다티온

메티다티온
메티다티온 구조식 이미지
카스 번호:
950-37-8
한글명:
메티다티온
동의어(한글):
메티다티온;S-2,3-디하이드로-5-메톡시-2-옥소-1,3,4-티아디아졸-3-일메틸 O,O디메틸포스포로디티오에이트;포스포로디티오익산,S-((5-메톡시-2-옥소-1,3,4-티아디아졸-3(2H)-일)메틸)O,O-디메틸에스테르
상품명:
Methidathion
동의어(영문):
DMTP;faat;sphat;oms844;NC2964;gs13005;hionate;OMS 844;Somonil;gs-13005
CBNumber:
CB4160797
분자식:
C6H11N2O4PS3
포뮬러 무게:
302.33
MOL 파일:
950-37-8.mol
MSDS 파일:
SDS

메티다티온 속성

녹는점
39-40°C
끓는 점
347.7±52.0 °C(Predicted)
밀도
1.51 g/cm3
증기압
2.5×10-4 Pa (20 °C)
인화점
100 °C
저장 조건
0-6°C
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨)
산도 계수 (pKa)
-4.17±0.40(Predicted)
물리적 상태
고체
물리적 상태
단단한 모양
색상
무색
수용성
0.024g/100mL
BRN
619915
안정성
공기 민감성, 수분 민감성
CAS 데이터베이스
950-37-8(CAS DataBase Reference)
NIST
Methidathion(950-37-8)
EPA
Methidathion (950-37-8)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T+;N,N,T+
위험 카페고리 넘버 21-28-50/53-41-26-24
안전지침서 22-28-36/37-45-60-61-39-26
유엔번호(UN No.) UN 2811
WGK 독일 3
RTECS 번호 TE2100000
위험 등급 6.1(a)
포장분류 II
유해 물질 데이터 950-37-8(Hazardous Substances Data)
독성 LD50 in adult male, female rats (mg/kg): 31, 32 orally (Gaines, Linder)
기존화학 물질 KE-12739
유해화학물질 필터링 97-1-76
함량 및 규제정보 물질구분: 유독물질; 혼합물(제품)함량정보: 메티다티온 및 이를 1% 이상 함유한 혼합물
그림문자(GHS): GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H318 눈에 심한 손상을 일으킴 심한 눈 손상 또는 자극성 물질 구분 1 위험 GHS hazard pictograms P280, P305+P351+P338, P310
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P262 눈, 피부, 의복에 묻지 않도록 하시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
1
3 0

메티다티온 MSDS


Methidathion

메티다티온 C화학적 특성, 용도, 생산

개요

Methidation is used as an insecticide. Cross-sensitivity was described to dichlorvos.

화학적 성질

Methidathion is a colorless crystalline pesticide at room temperature. It is sparingly soluble in water, but very soluble in octanol, ethanol, xylene, acetone, and cyclohexane. Methidathion is a non-systemic organophosphorous insecticide and acaricide with stomach and contact action. It is used to control a variety of insects and mites on crops and fruit plants. Methidathion is highly toxic to animals and humans. The US EPA grouped methidathion as a class I toxic substance and as an RUP.

용도

Methidathion is an organophosphate insecticide and was examined for human health and toxicological concerns.

일반 설명

Methidathion is a colourless crystalline pesticide at room temperature. It is sparingly soluble in water but very soluble in octanol, ethanol, xylene, acetone, and cyclohexane.

공기와 물의 반응

Stable in neutral or weak acid solution. Hydrolyzed by alkali. [EPA, 1998].

반응 프로필

Organophosphates, such as Methidathion, 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.

위험도

Toxic by ingestion, a cholinesterase inhibitor.

건강위험

Methidathion is poisonous to humans. Its toxic effects are by action on the nervous system. Human volunteers ingesting 0.11 mg/kg/day for 6 weeks had no clinical effects.

화재위험

(Non-Specific -- Organophosphorus Pesticide, n.o.s.) Container may explode in heat of fire. Fire and runoff from fire control water may produce irritating or poisonous gases. Stable in neutral or weak acid solution. Hydrolyzed by alkali.

농업용

Insecticide: A U.S. EPA restricted Use Pesticide (RUP). Not approved for use in EU countries . There are no residential uses for methidathion. Methidathion is a non-systemic organophosphate insecticide and acaricide with stomach and contact action. The compound is used to control a variety of insects and mites in many crops such as nuts, artichokes, olives, cotton, fruits, vegetables, tobacco, alfalfa, and sunflowers, and also in greenhouses and on rose cultures. It is especially useful against scale insects.

상품명

CIBA-GEIGY® GS 13005®; COBRACIDE®; FISONS NC® 2964; GEIGY® 13005; GS-13005®; SOMONIC®; SOMONIL®; SURPRACIDE®; SUPRATHION®; ULTRACID®; ULTRACIDE®

색상 색인 번호

Methidation is an organophosphorus compound used as an insecticide. Cross-sensitivity was described to Dichlorvos.

Safety Profile

Poison by ingestion and skin contact. Moderately toxic by inhalation. Human mutation data reported. Human systemic effects: coma, lachrymation, miosis. A severe eye irritant. An insecticide. When heated to decomposition it emits very toxic fumes of NOx, POx, and SOx

Carcinogenicity

In a chronic toxicity/carcinogenicity study, rats were fed diets with 0, 4, 40, or 100 ppm methidathion (equivalent to 0, 0.16, 1.72, or 4.91 mg/kg/day (males) and 0, 0.22, 2.20, or 6.93 mg/kg/day (females)) for 2 years, and there was no evidence of carcinogenicity in either males or females . Body weight decreases occurred in both sexes at the highest dose throughout the study.

환경귀착

Photolytic. When methidathion in an aqueous buffer solution (25°C and pH 7.0) was exposed to filtered UV light (l >290 nm) for 24 hours, 17% decomposed to 5-methoxy- 3H-1,3,4-thiadiazol-2-one. At 50°C, 56% was degraded after 24 hours. Degradation occurred via hydrolysis of the thiol bond of the phosphorodithioic ester. Under acidic and alkaline conditions, hydrolytic cleavage occurred at the C-S and P-S bonds, respectively (Burkhard and Guth, 1979). Smith et al. (1978) demonstrated that methidathion degraded to methidathion oxon at a faster rate in six air-dried soils than in moist soils. Half-lives for methidathion in the air-dried soils ranged from 19 to 110 days. In addition, methidathion degraded faster in an air-dried soil exposed to ozone (half-lives 2.5 to 7.0 days).
Chemical/Physical. Emits toxic fumes of phosphorus, nitrogen and sulfur oxides when heated to decomposition (Sax and Lewis, 1987). Methidathion oxon was also found in fogwater collected near Parlier, CA (Glotfelty et al., 1990). It was suggested

신진 대사 경로

The main route of methidathion metabolism in animals and plants is via hydrolysis or oxidation (or hydrolysis of the oxon) to yield the 3- thiomethyl-5-methoxy-1,3,4-thiadiazoldee rivative. This may either lose methanethiol to yield the methoxy-1,3,4thiadiazolinone or be conjugated as the cysteine derivative via a route involving desmethylmethidathion (in plants). In plants and mammals an additional route involves the methylation of the thiomethyl methoxy-1,3,4-thiadiazolinone derivative by S-adenosylmethionine followed by oxidation to the corresponding sulfoxide and sulfone which are excreted in the urine in mammals. Another route of detoxification in insects, plants and mammals is via demethylation of the 5-methoxy group of the 1,3,4-thiadiazolinone ring to form a metabolite which may be conjugated in plants. As is common with many phosphorothioates, the active acetylcholinesterase inhibitor, methidaoxon, is usually detected in metabolism studies but at very low concentration due to its rapid rate of hydrolysis.

신진 대사

The principal degradation route is similar both in animals and plants, that is, cleavage of the P?S bond via oxidative desulfuration (activation) to the oxon followed by hydrolysis to O,O-dimethyl hydrogen phosphorothioate and the 3-thiomethyl-5-methoxythiadiazole derivative, which is further degraded or conjugated. Methidathion is rapidly degraded in soil; DT50 in soil is 3–18 d.

운송 방법

Color code—Blue: Health Hazard/Poison: Store in a secure poison location. Prior to working with this chemical, personnel should be trained on its proper handling and storage. Store in tightly closed containers in a cool, wellventilated area

폐기물 처리

Treat with strong alkali, mix with soil and bury in the case of small quantities. For large quantities, use incineration with effluent gas scrubbing

주의 사항

Occupational workers should be very careful during use and chemical management of methidathion. As this chemical substance is a highly toxic pesticide, it has been grouped by the US EPA as toxicity class I. The containers and labels of the products should bear the signal word DANGER. Methidathion is an RUP, except for use in nurseries, and on saffl ower and sunfl owers.

메티다티온 준비 용품 및 원자재

원자재

준비 용품


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