벤젠술포닐클로라이드

벤젠술포닐클로라이드
벤젠술포닐클로라이드 구조식 이미지
카스 번호:
98-09-9
한글명:
벤젠술포닐클로라이드
동의어(한글):
벤젠설폰일클로라이드;벤젠설포닐염화물;벤젠술포닐염화물;벤젠술포닐클로라이드;벤젠설포닐염화물;벤젠설폰일 클로라이드
상품명:
Benzenesulfonyl chloride
동의어(영문):
benzenesulfonyl;Benzenesulphochloride;Phenylsulfonyl chloride;BENZENESULPHONYL CHLORIDE;BENZENE SULFOCHLORIDE;Benzolsulfonylchlorid;bsc-refined;AKOS BBS-00004356;benzolsulfochloride;rcrawastenumberu020
CBNumber:
CB6854744
분자식:
C6H5ClO2S
포뮬러 무게:
176.62
MOL 파일:
98-09-9.mol
MSDS 파일:
SDS

벤젠술포닐클로라이드 속성

녹는점
13-15 °C (lit.)
끓는 점
251-252 °C (lit.)
밀도
1.384 g/mL at 25 °C (lit.)
증기압
0.04 mm Hg ( 20 °C)
굴절률
n20/D 1.551(lit.)
인화점
>230 °F
저장 조건
Store below +30°C.
용해도
알코올: 용해 가능
물리적 상태
액체
색상
투명한
수용성
분해될 수 있음
감도
Moisture Sensitive
Merck
14,1072
BRN
606926
안정성
안정적인. 물, 강산화제, 강염기, 메틸 포름아미드, 디메틸 설폭사이드와 혼합되지 않습니다.
LogP
3.39 at 23℃
CAS 데이터베이스
98-09-9(CAS DataBase Reference)
NIST
Benzenesulfonyl chloride(98-09-9)
EPA
Benzenesulfonyl chloride (98-09-9)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 C
위험 카페고리 넘버 20/22-34-42/43-29-22
안전지침서 23-26-36/37/39-45
유엔번호(UN No.) UN 2225 8/PG 3
WGK 독일 1
RTECS 번호 DB8750000
F 고인화성물질 21
TSCA Yes
위험 등급 8
포장분류 III
HS 번호 29049090
유해 물질 데이터 98-09-9(Hazardous Substances Data)
독성 LD50 orl-rat: 1960 mg/kg MEPAAX 20,513,69
기존화학 물질 KE-02638
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
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H314 피부에 심한 화상과 눈에 손상을 일으킴 피부부식성 또는 자극성물질 구분 1A, B, C 위험 GHS hazard pictograms P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
예방조치문구:
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P303+P361+P353 피부(또는 머리카락)에 묻으면 오염된 모든 의복은 벗거나 제거하시오 피부를 물로 씻으시오/샤워하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
0
3 0
W

벤젠술포닐클로라이드 C화학적 특성, 용도, 생산

화학적 성질

Benzenesulfonyl chloride is a colorless oily liquid with a pungent odor. Insoluble in water, soluble in ethanol and ether. Can react with ammonia, amine and alcohol to produce benzenesulfonamide and benzene sulfonate respectively. It is toxic, irritates skin, eyes and mucous membranes, corrosive, and can cause burns. Oral LD50 1960mg/kg in rats.

용도

Benzenesulfonyl chloride reacts with Grignard reagents to form oxindoles from N-unsubstituted indoles. It is widely used to check the assay of thiamine in different food products. It is involved in the synthesis of alpha-disulfones, sulfonamides and sulfoante esters as precursor. It is a derivatization reagent for the determination of various amines in waste water and surface water at the sub-ppb level by gas chromatography-mass spectrometry. It is common reagent used in Hinsberg test for detection and distinguishing the type of amines as primary, secondary and tertiary amines.

생산 방법

The most convenient method for the production of benzenesulfonyl chlorides is the chlorosulfonation reaction of benzene or substituted benzene with chlorosulfuric acid. Sulfonation and formation of the sulfonyl chlo- ride take place in one reaction sequence:
Ar-H+Cl-SO3H→ArSO3H+HCl
ArSO3H+Cl-SO3H=ArSO2Cl+H2SO4
Sulfone is formed in a side reaction of the chlorosulfonation. The amount of sulfone formation can be reduced by diluting with a solvent, by using a large excess of chlorosulfuric acid, or by adding sulfone-inhibiting substances, e.g., alkali metal and ammonium salts, acetic acid, phosphoric acid, dimethylformamide, or amidosulfuric acid.
For industrial chlorosulfonation the chlorosulfuric acid is introduced into a cast-steel or enameled steel vessel and 10 – 25 mol% of the aromatic compound is stirred in at 25 – 30 ℃, whereupon sulfonation of the aromatic compound and HCl formation occur. The formation of sulfonyl chloride is initiated by heating the reactants to 50 – 80 ℃. The reaction is exothermic. The sulfonyl chloride is isolated by draining the reaction mass onto water and simultaneous cooling. Excess chlorosulfuric acid is decomposed, and the sulfonyl chloride either precipitates or separates as an organic liquid phase. The quality of the chlorosulfuric acid affects the yield.
Other chlorinating agents, such as phosgene, thionyl chloride, sulfuryl chloride, or phosphorus pentachloride, can be used instead of chlorosulfu- ricacid. When thionyl chloride is used the sulfonyl chloride is obtained from the sulfonic acid in high yield and without formation of sulfuric acid.

일반 설명

A colorless to slightly yellow solid that melts at approximately 40°F. Very irritating to skin, eyes and mucous membranes. May emit toxic fumes when heated to high temperatures. Used to make dyes and other chemicals.

공기와 물의 반응

Insoluble and stable in cold water [Merck]. Decomposes in hot water to produce corrosive and toxic hydrochloric acid and benzenesulfonic acid. Rate of reaction decreases as temperature decreases.

반응 프로필

Benzenesulfonyl chloride is incompatible with strong oxidizing agents and bases, including amines. Corrodes metals in the presence of water due to slow formation of hydrochloric acid and benzenesulfonic acid [USCG, 1999]. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291].

건강위험

May be fatal if inhaled, swallowed or absorbed through skin. Contact may cause skin and eye burns. Irritating to eyes, skin and mucous membranes. INGESTION: May cause abdominal spasm and vomiting.

Safety Profile

Poison by intraperitoneal route. Adangerous storage hazard. It may explode in a sealedbottle. Explosive reaction with dimethyl sulfoxide. Reactsvigorously with methyl formamide. When heated todecomposition it emits toxic fumes of Cl- and SO

잠재적 노출

It is used as a chemical intermediate for benzenesulfonamides, thiophenol, glybuzole (hypoglycemic agent), N-2-chloroehtylamides, benzonitrile; for its esters-useful as insecticides, and miticides.

운송 방법

UN2225 Benzene sulfonyl chloride, Hazard class: 8; Labels: 8—Corrosive material.

Purification Methods

Distil the sulfonyl chloride, then treat it with 3mole % each of toluene and AlCl3, and allow it to stand overnight. The sulfonyl chloride is distilled off at 1mm pressure and then carefully fractionally distilled at 10mm in an all-glass column. [Adams & Marvel Org Synth Coll Vol I 84 1941, Jensen & Brown J Am Chem Soc 80 4042 1958, Beilstein 11 IV 49.] It is TOXIC.

비 호환성

Violent reaction with strong oxidizers, dimethyl sulfoxide, and methyl formamide. It is very reactive with bases and many organic compounds. Incompatible with ammonia, aliphatic amines. Water contact forms hydrochloric and chlorosulfonic acids. Aqueous solutions of this chemical are strong acids that react violently with bases. Attacks metals in presence of moisture.

벤젠술포닐클로라이드 준비 용품 및 원자재

원자재

준비 용품


벤젠술포닐클로라이드 공급 업체

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