캡타폴

캡타폴
캡타폴 구조식 이미지
카스 번호:
2425-06-1
한글명:
캡타폴
동의어(한글):
캡타폴;켑타폴;2-(1,1,2,2-테트라클로로에틸설판일)-3a,4,7,7a-테트라하이드로아이소인돌-1,3-다이온;3a,4,7,7a-테트라하이드로-2-((1,1,2,2-사염화에틸)티오)-1H-이소인돌-1,3(2H)-디온;3a,4,7,7a-테트라하이드로-2-[(1,1,2,2-테트라클로로에틸)싸이오]-1H-아이소인돌-1,3(2H)-다이온;3a,4,7,7a-테트라하이드로-N-(1,1,2,2-테트라클로로에테인설펜일)프탈이미드;N-(1,1,2,2-테트라클로로에틸싸이오)-4-사이클로헥센-1,2-다이카복스이미드;N-(1,1,2,2-테트라클로로에틸싸이오)-4-사이클로헥센-1,2-다이카복시이미드;N-(1,1,2,2-테트라클로로에틸싸이오)-4-테트라하이드로프탈이미드;N-(1,1,2,2-테트라클로로에틸싸이오)사이클로헥스-4-엔-1,2-다이카복스이미드;N-[(1,1,2,2-테트라클로로에틸)싸이오]-4-사이클로헥센-1,2-다이카복스이미드;N-[(1,1,2,2-테트라클로로에틸)싸이오]사이클로헥스-4-엔-1,2-다이카복스이미드;디폴라탄;아르보실;폴시드
상품명:
CAPTAFOL
동의어(영문):
Sulfonimide;cs5623;Folcid;haipen;FOLTAF;Cs 5623;Difosan;kenofol;Sanspor;Captatol
CBNumber:
CB9773422
분자식:
C10H9Cl4NO2S
포뮬러 무게:
349.06
MOL 파일:
2425-06-1.mol
MSDS 파일:
SDS

캡타폴 속성

녹는점
160-161°
끓는 점
365.7±52.0 °C(Predicted)
밀도
1.4682 (rough estimate)
증기압
1.1 x 10-6 Pa (20 °C)
굴절률
1.6000 (estimate)
인화점
>100 °C
저장 조건
0-6°C
용해도
Chloroform (Sparingly), Dichloromethane (Very Slightly), Methanol (Slightly)
물리적 상태
고체
물리적 상태
단단한 모양
산도 계수 (pKa)
-2.67±0.20(Predicted)
수용성
1.4mg l-1(20°C)
색상
흰색에서 황백색까지
Merck
13,1777
IARC
2A (Vol. 53) 1991
EPA
Captafol (2425-06-1)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T,N
위험 카페고리 넘버 45-43-50/53
안전지침서 53-45-60-61
유엔번호(UN No.) UN3077 9/PG 3
RTECS 번호 GW4900000
HS 번호 29305000
유해 물질 데이터 2425-06-1(Hazardous Substances Data)
독성 LD50 in rats, rabbits (mg/kg): 2500-6200 orally; 15400 dermally (Ben-Dyke)
기존화학 물질 KE-33295
유해화학물질 필터링 97-1-260;06-4-33
함량 및 규제정보 물질구분: 금지물질; 혼합물(제품)함량정보: 켑타폴 및 이를 0.1% 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
H317 알레르기성 피부 반응을 일으킬 수 있음 피부 과민성 물질 구분 1 경고 GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H350 암을 일으킬 수 있음 (노출되어도 암을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 발암성 물질 구분 1A, 1B 위험 GHS hazard pictograms
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P272 작업장 밖으로 오염된 의복을 반출하지 마시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P321 (…) 처치를 하시오.
P333+P313 피부자극성 또는 홍반이 나타나면 의학적인 조치·조언를 구하시오.
P363 다시 사용전 오염된 의류는 세척하시오.
P391 누출물을 모으시오.
P501 ...에 내용물 / 용기를 폐기 하시오.

캡타폴 C화학적 특성, 용도, 생산

화학적 성질

Captafol is a white crystalline solid.

용도

Captafol is used to control a wide range of fungal diseases on many crops.

정의

ChEBI: A dicarboximide that captan in which the trichloromethyl group is replaced by a 1,1,2,2-tetrachloroethyl group. A broad-spectrum fungicide used to control diseases in fruit and potatoes, it is no longer approved for use in the European Community.

일반 설명

White crystalline solid with a slight, but pungent odor. Mp: 162°C. Practically insoluble in water. Only slightly soluble in organic solvents. Technical CAPTAFOL is a wettable light tan powder that is used as a fungicide. Inhaled dust irritates the respiratory tract. Irritates skin and damages eyes. Acute oral toxicity in humans is low. Not persistent in the environment (decomposes with a half-life of 11 days in the soil). Highly toxic to fish and other aquatic organisms.

반응 프로필

CAPTAFOL is non-flammable but, on heating, may decompose to generate toxic fumes, such as sulfur oxides, hydrogen sulfide, hydrochloric acid, and phosgene. Stable at room temperature when dry but readily hydrolysed, especially in an alkaline environment. CAPTAFOL and mixtures containing high concentrations of CAPTAFOL may react violently with alkali. Incompatible with acids, acid chlorides, acid anhydrides, and strong oxidizing agents. Sulfhydryl compounds such as glutathione and cysteine cause a rapid chemical decomposition.

위험도

Absorbed by skin. Probable carcinogen.

농업용

Fungicide: Captafol is a General Use Pesticide and used for the control of practically all forms of fungal diseases except powdery mildew. It is also used as a seed protectorant on cotton, rice and peanut crops. Not registered for use in the U.S. or in EU countries. There are 20 global suppliers.

상품명

CAPTATOL®; CAPTOFOL®; CRISFOLATAN®; DIFOLATAN®[C]; DIFOCAP®[C]; DIFOSAN®; FOLCID®; HAIPEN®; KENOFOL®; MERPAFOL®; ORTHO® 5865[C]; PILLARTAN®; SANSEAL®; SANSPOR®; SANTAR-SM®; SULFONIMIDE®; SULPHEIMIDE®

색상 색인 번호

Captafol is a pesticide, belonging to thiophthalimide group. Occupational contact dermatitis was reported in an agricultural worker who had multiple sensitizations

Safety Profile

Confirmed carcinogen with experimental carcinogenic data. Poison by intraperitoneal route. Moderately toxic by ingestion. An experimental teratogen. Other experimental reproductive effects. Mutation data reported. A fungicide. When heated to decomposition it emits very toxic fumes of Cl-, NO,, and SOx

잠재적 노출

Captafol is a thiophthalimide fungicide. Those engaged in the manufacture, formulation, and application of this fungicide. Captafol is not currently registered for use on field crops or stored produce in the United States.

Carcinogenicity

Captafol is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals and supporting data on mechanisms of carcinogenesis.

환경귀착

The primary toxicity following captafol exposure probably occurs through a hypersensitivity mechanism. Most experiments suggest captafol to be DNA active.

신진 대사 경로

Captafol contains an unstable tetrachloroethylthio (sulfenyl) moiety that has been shown to undergo rapid hydrolytic and metabolic degradation to tetrahydrophthalimide (2). By analogy with captan, presumably the tetrachloroethylthio moiety can be transferred to the sulfur atoms of thiols such as cysteine and glutathone. Thus in the presence of thiols such as glutathione, captafol is probably cleaved at the N-S bond to form thiophosgene (3) and other gaseous products such as hydrogen sulfide, hydrogen chloride and carbonyl sulfide. Thiophosgene is rapidly hydrolysed by water. The tetrachloroethylthio group and thiophosgene are believed to be intermediates in the formation of thiazolidine-2- thione-6carboxylic acid (4) which is an addition product with cysteine. A thiazolidine derivative of glutathione is also formed (5). Biotransformation of captafol in mammals generates primarily thiophosgene (3) and tetrahydrophthalimide (2). Tetrahydrophthalimide (2) and various of its derivatives are excreted in the urine. There were no reports of 2-thiazolidinethione-4-carboxylic acid (4) in the urine.

운송 방법

UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN 2773 Phthalimide derivative pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

비 호환성

Reacts violently with bases, causing fire and explosion hazard. Not compatible with strong acids or acid vapor, oxidizers. Strong alkaline conditions contribute to instability. Attacks some metals.

폐기물 처리

Hydrolysis.

캡타폴 준비 용품 및 원자재

원자재

준비 용품


캡타폴 공급 업체

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