티오파녹스

티오파녹스
티오파녹스 구조식 이미지
카스 번호:
39196-18-4
한글명:
티오파녹스
동의어(한글):
티오파녹스;싸이오파녹스;1-(2,2-다이메틸-1-메틸싸이오메틸프로필리덴아미노옥시)-N-메틸폼아마이드;1-(2,2-디메틸-1-메틸티오메틸프로필리덴아미노-옥시)-N-메틸포름아미드;3,3-다이메틸-1-(메틸싸이오)2-뷰탄온 O-((메틸아미노)카보닐)옥심;3,3-다이메틸-1-(메틸싸이오)-2-뷰탄온 O-(메틸카밤오일)옥심;3,3-다이메틸-1-(메틸싸이오)-2-뷰탄온 O-[(메틸아미노)카보닐]옥심;3,3-다이메틸-1-메틸싸이오뷰탄온 O-메틸카밤오일옥심;3,3-디메틸-1-(메틸티오)-2-부타논 O-((메틸아미노)카르보닐)옥심;다카목스;베넬룩스
상품명:
THIOFANOX
동의어(영문):
benelux;DACAMOX;DS 15647;ds-15647;ent27851;ENT 27851;THIOFANOX;Thiolanox;thiofanox0;Thiofanocarb
CBNumber:
CB6699581
분자식:
C9H18N2O2S
포뮬러 무게:
218.32
MOL 파일:
39196-18-4.mol

티오파녹스 속성

녹는점
57℃
밀도
1.1664 (rough estimate)
증기압
2.3×10-2 Pa (25 °C)
굴절률
1.6800 (estimate)
인화점
>100 °C
저장 조건
0-6°C
수용성
5.2g 1l-1(22°C)
산도 계수 (pKa)
13.82±0.46(Predicted)
EPA
Thiofanox (39196-18-4)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T+,N
위험 카페고리 넘버 27/28-50/53
안전지침서 27-36/37-45-60-61
유엔번호(UN No.) 2757
WGK 독일 3
RTECS 번호 EL8200000
위험 등급 6.1(a)
포장분류 II
HS 번호 29309090
유해 물질 데이터 39196-18-4(Hazardous Substances Data)
기존화학 물질 KE-05-0510
유해화학물질 필터링 97-1-322
함량 및 규제정보 물질구분: 유독물질; 혼합물(제품)함량정보: 티오파녹스 및 이를 1.0% 이상 함유한 혼합물
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
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.
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P310 삼켰다면 즉시 의료기관(의사)의 진찰을 받으시오.

티오파녹스 C화학적 특성, 용도, 생산

화학적 성질

Thiofanox is a colorless solid with a pungent odor.

용도

Thiofanox is a systemic soil insecticide used for the control of aphids, mites, thrips, plant bugs, leafhoppers and beetles in/on sugar beet and potatoes.

일반 설명

THIOFANOX is a colorless solid with a pungent odor. Used as a systemic insecticide and acaricide.

공기와 물의 반응

Thio and dithiocarbamates slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids.

반응 프로필

THIOFANOX is a thiocarbamate. Flammable gases are generated by the combination of thiocarbamates and dithiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates and dithiocarbamates are incompatible with acids, peroxides, and acid halides.

건강위험

THIOFANOX is a carbamate pesticide. Carbamate pesticides are moderately to highly toxic. It is a cholinesterase inhibitor.

화재위험

(Non-Specific -- Carbamate Pesticide, Solid, n.o.s.) Container may explode in heat of fire. When heated to decomposition, THIOFANOX emits very toxic fumes of nitrogen and sulfur oxides. Stable at normal storage temperature; reasonably stable to hydrolysis at less than 86F at pH 5-9.

Pharmacology

The insecticidal carbamates are cholinergic. Poisoned insects and animals exhibit violent convulsions and other neuromuscular disturbances. These insecticides carbamylate acetylcholinesterase and may have a direct action on acetylcholine receptors. The mechanism of interaction with acetylcholinesterase is analogous to the normal three-step hydrolysis of acetylcholine. However, the third reaction step is much slower for the carbamylated enzyme than for the acetylated one. The importance of structural complementarity of the insecticidal carbamates to the active site of acetylcholinesterase is demonstrated by the pronounced difference in activities of D-2-(sec-butylphenyl) methylcarbamate and L-2-(sec-butylphenyl) methylcarbamate (the L isomer is five times more toxic) and of the 2-, 3-, and 4-substituted phenylmethylcarbamates, where the 4-isomers are virtually inactive.
Detoxification of carbamate insecticides occurs in vivo through microsomal hydroxylation, N-demethylation of carbamyl nitrogen, side chain oxidation, and ring hydroxylation. Methylenedioxyphenyl synergists prevent oxidation

잠재적 노출

A potential danger to those involved in the manufacture, formulation and application of this thiocarbamate systemic insecticide and acaricide.

신진 대사 경로

The hydrolytic degradation and metabolism of thiofanox in soils, plants and animals follow a common pathway. Oxidation of the S-methyl moiety is the primary reaction to yield the thiofanox sulfoxide and sulfone. Hydrolysis of the carbamate linkage to yield the oximes is only a minor pathway for thiofanox and its oxidation products (Scheme 1).

운송 방법

UN2757 Carbamate pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

비 호환성

Thiocarbamate esters are combustible. They react violently with powerful oxidizers such as calcium hypochlorite. Poisonous gases are generated by the thermal decomposition of thiocarbamate compounds, including carbon disulfide, oxides of sulfur, oxides of nitrogen, hydrogen sulfide, ammonia, and methylamine. Many materials in this group slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids. Flammable gases are generated by the combination of

폐기물 처리

In accordance with 40CFR 165 recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.

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