염화 티오닐

염화 티오닐
염화 티오닐 구조식 이미지
카스 번호:
7719-09-7
한글명:
염화 티오닐
동의어(한글):
염화티오닐;염화술피닐;염화싸이오닐(염화티오닐);티오닐클로라이드;염화티오닐;염화 티오닐;설퍼 클로라이드 옥사이드;설포러스 다이클로라이드;설포러스 옥시클로라이드;설피닐클로라이드;티오닐 다이클로라이드
상품명:
Thionyl chloride
동의어(영문):
SOCl2;Sulfurous dichloride;ThionyL;THIONYL DICHLORIDE;Thionylchlorid;Sulfinyl chloride;SULFUROUS OXYCHLORIDE;Sulfinyl dichloride;THIONYL CHLORIDEGC STANDARD;Thionyl chloride, 1M soln. in dichloroMethane
CBNumber:
CB9190771
분자식:
Cl2OS
포뮬러 무게:
118.97
MOL 파일:
7719-09-7.mol
MSDS 파일:
SDS

염화 티오닐 속성

녹는점
-105 °C
끓는 점
79 °C(lit.)
밀도
1.64 g/mL at 20 °C
증기 밀도
4.1 (vs air)
증기압
97 mm Hg ( 20 °C)
굴절률
n20/D 1.518(lit.)
인화점
105°C
저장 조건
Store at RT.
용해도
톨루엔, 클로로포름, 벤젠, 사염화탄소 및 디에틸 에테르와 혼합 가능합니다.
물리적 상태
액체
색상
≤50(APHA)
냄새
특유의 자극적인 냄새
수용성
물과 반응
감도
Moisture Sensitive
Merck
14,9348
노출 한도
ACGIH: TWA 50 ppm
OSHA: TWA 25 ppm; STEL 125 ppm
NIOSH: IDLH 2300 ppm
Dielectric constant
9.1(22℃)
안정성
물과 격렬하게 반응함. 대부분의 일반적인 금속, 강한 환원제, 강한 염기, 알코올, 아민과 호환되지 않습니다.
CAS 데이터베이스
7719-09-7(CAS DataBase Reference)
NIST
Thionyl chloride(7719-09-7)
EPA
Thionyl chloride (7719-09-7)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 C
위험 카페고리 넘버 14-20/22-29-35-40-34-20/21/22
안전지침서 26-36/37/39-45-28-27
유엔번호(UN No.) UN 1836 8/PG 1
WGK 독일 1
RTECS 번호 XM5150000
F 고인화성물질 19
TSCA Yes
위험 등급 8
포장분류 I
HS 번호 28121095
유해 물질 데이터 7719-09-7(Hazardous Substances Data)
기존화학 물질 KE-33794
유해화학물질 필터링 97-1-208
사고대비 물질 필터링 83
함량 및 규제정보 물질구분: 유독물질; 혼합물(제품)함량정보: 염화 티오닐 및 이를 25% 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
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
H331 흡입하면 유독함 급성 독성 물질 흡입 구분 3 위험 GHS hazard pictograms P261, P271, P304+P340, P311, P321,P403+P233, P405, P501
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
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
4 2
W

염화 티오닐 MSDS


Thionyl chloride

염화 티오닐 C화학적 특성, 용도, 생산

물성

분자량(MW) 118.9654, 녹는점(°C) - 104 ,비중 1.631, 끓는점(°C) 76 ,인화점(°C) 105.무색에서 희미한 노랑 또는 희미한 붉은색 연기를 내며, 굴절력을 갖는 액체.

용도

황(S)을 포함하는 화학무기(Sulfur mustard, Amiton)의 원료- 살충제, 제초제, 계면활성제, 약품, 비타민, 염료 등의 제조용 중간체로 이용하기 위한 유기산의 산 염화물로의 변환에 이용. 리튬-염화티오닐 고성능 배터리에 이용. 고혈압 치료제, 의약품의 원료, 류마티스 치료제, 섬유 계면활성제, 구충제, 항생제의 원료, 방부제, 전자기기, 플라스틱 첨가제 등.

안전성

다른 연소물(목재, 종이, 오일 등)에 불이 붙을 수 있음. 물과 격렬히 반응함. 가연성의 독가스는 좁은 지역에 모임. 하수구 불량은 화재나 폭발위험이 있음.

화학적 성질

Thionyl chloride is a pale yellow to reddish liquid. Suffocating odor like sulfur dioxide. Fumes form when exposed to moist air.

물리적 성질

Pale yellow to red fuming liquid; suffocating odor; refractive index 1.517 at 20°C; density 1.631 g/mL at 20°C; freezes at -101°C; boils at 75.6°C; decomposes at 140°C; decomposes in water; soluble in benzene, chloroform, and carbon tetrachloride.

용도

Thionyl chloride (SOCl2) is used as a chlorinating agent in manufacturing organic compounds. It is also used as a solvent in high-energy lithium batteries.

제조 방법

Sulfurous oxychloride can be prepared by oxidation of sulfur dichloride with sulfur trioxide: SCl2 + SO3 → SOCl2 + SO2
Also, the compound can be prepared by reacting sulfur dioxide with phosphorus pentachloride: SO2 + PCl5 → SOCl2 + POCl3.

정의

ChEBI: Thionyl chloride is a sulfinyl halide in which both of the halide atoms are chorines. It is a sulfinyl halide and a chlorine molecular entity.

일반 설명

Thionyl chloride appears as a colorless to yellow fuming liquid with a suffocating pungent odor. Boiling point 79 °C. A lachrymator. Highly corrosive and toxic. Long-term inhalation of low concentrations or short-term inhalation of high concentrations has adverse health effects.

반응 프로필

Thionyl chloride reacts, potentially explosively, with dimethyl sulfoxide or dimethylformamide containing traces of iron or zinc [Spitulnik, M. J., Chem. Eng. News, 1977, 55(31), p. 31]. Undergoes violent reactions with bases (ammonia, sodium hydroxide, potassium hydroxide, amines), alkali metals (sodium, potassium), esters (ethyl acetate), toluene mixed with ethanol / water [Bretherick, 5th ed., 1995, p. 1325]. Has an expansion ratio from gas to liquid of nearly 1000:1. Hence may cause an explosion if heated while contained [MCA Case History No. 1808]. 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]. Perchloric acid ignites on contact with sulfinyl chloride. (Bailar, 1973, Vol. 2, 1442). SOCl2 reacts with esters, such as ethyl acetate, forming toxic SO2 gas and water soluble/toxic acyl chlorides, catalyzed by Fe or Zn (Spagnuolo, C.J. et al. 1992. Chemical and Engineering News 70(22):2.).

위험도

Strong irritant to skin, tissue, and upper respiratory tract.

건강위험

CORROSIVE and/or TOXIC; inhalation, ingestion or contact (skin, eyes) with vapors, dusts or substance may cause severe injury, burns or death. Fire will produce irritating, corrosive and/or toxic gases. Reaction with water may generate much heat that will increase the concentration of fumes in the air. Contact with molten substance may cause severe burns to skin and eyes. Runoff from fire control or dilution water may cause pollution.

화재위험

EXCEPT FOR ACETIC ANHYDRIDE (UN1715), THAT IS FLAMMABLE, some of these materials may burn, but none ignite readily. May ignite combustibles (wood, paper, oil, clothing, etc.). Substance will react with water (some violently), releasing corrosive and/or toxic gases and runoff. Flammable/toxic gases may accumulate in confined areas (basement, tanks, hopper/tank cars, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated or if contaminated with water. Substance may be transported in a molten form.

Safety Profile

Moderately toxic by inhalation. The material itself is more toxic than sulfur dioxide. Has a pungent odor similar to that of sulfur dioxide; it fumes upon exposure to air. Violent reaction with water releases hydrogen chloride and sulfur dioxide. Both these decomposition products constitute serious toxicity hazards. A corrosive irritant that causes burns to the skin and eyes. A powerful chlorinating agent. Potentially explosive reaction with ammonia, bis(dimethy1amino)sulfoxide - (above 80℃), chloryl perchlorate, 1,2,3- cyclohexanetrione trioxime + sulfur dioxide, dimethyl sulfoxide, hexafluoroisopropylideneaminolithium. Violent reaction or ignition with 2,4-hexadiyn-1-6-di01, onitrobenzoyl acetic acid, o-nitrophenylacetic acid, sodum (ignites at 300℃). Incompatible with ammonia, dimethyl formamide + trace iron or zinc, linseed oil + quinoline, toluene + ethanol + water. When heated to decomposition it emits toxic fumes of SOx and Cl-. See also HYDROGEN CHLORIDE and SULFUR DIOXIDE.

잠재적 노출

Thionyl chloride is used as specialty chlorinating agent, particularly in preparation of organic acid chlorides; in organic synthesis; as a catalyst.

운송 방법

UN1836 Thionyl chloride, Hazard class: 8; Labels: 8-Corrosive material.

Purification Methods

Crude SOCl2 can be freed from sulfuryl chloride, sulfur monochloride and sulfur dichloride by refluxing it with sulfur and then fractionally distilling twice. [The SOCl2 is converted to SO2 and sulfur chlorides. The S2Cl2 (b 135.6o) is left in the residue, whereas SCl2 (b 59o) passes over in the forerun.] The usual purification is to distil it from quinoline (50g SOCl2 to 10g quinoline) to remove acid impurities, followed by distillation from boiled linseed oil (50g SOCl2 to 20g of oil). Precautions must be taken to exclude moisture. Thionyl chloride is used extensively in organic syntheses and can be prepared by distillation of technical SOCl2 in the presence of diterpene (12g/250mL SOCl2), and avoiding overheating. Further purification is achieved by redistillation from linseed oil (1-2%) [Rigby Chem Ind (London) 1508 1969]. Gas chromatographically pure material is obtained by distillation from 10% (w/w) triphenyl phosphite [Friedman & Wetter J Chem Soc (A) 36 1967, Larsen et al. J Am Chem Soc 108 6950 1986]. HARMFUL VAPOURS.

비 호환성

Reacts violently with water releasing sulfur dioxide and hydrogen chloride. Keep away from water, acids, alcohols, alkalis, ammonia, chloryl perchlorate.

폐기물 처리

Spray on a thick layer of a (1:1) mixture of dry soda ash and slaked lime behind a shield. After mixing, spray water from an atomizer with great precaution. Transfer slowly into a large amount of water. Neutralize and drain into the sewer with sufficient water.

염화 티오닐 준비 용품 및 원자재

원자재

준비 용품

ALPHA-ACETYL-2-HYDROXY-BETA-OXO-BENZENEPROPANOIC ACID MONO SODIUM SALT Cyclopentanecarbonyl chloride QUINOLINE-2-CARBONYL CHLORIDE 2,6-Pyridinedicarboxylic acid chloride 1-PHENOXY-2-CHLOROPROPANE 2,3-DICHLOROPYRIDINE-5-CARBONYL CHLORIDE Cinnamamide 염화 N-(클로로메틸렌)-N-메틸메탄아미늄 (1:1) Reactive Turquoise Blue Kn-G 1-(1-2-HYDROXYPHENYL)ETHENYL)-1H-IMIDAZOLE M-TOLYL-METHANESULFONYL CHLORIDE (2-HYDROXY-PHENYL)-ACETIC ACID METHYL ESTER NICLOFOLAN 4-Ethylbenzoyl chloride H-DL-PRO-OME HCL O-TOLYL-METHANESULFONYL CHLORIDE 3,4,5-TRICHLOROTHIOPHENE-2-CARBONYL CHLORIDE ETHYL 2-ACETYLOXY-A-(1-HYDROXYETHYLIDENE)-B-OXOBENZENE PROPANOATE METHYL 3-AMINOBENZOATE 6,8-다이클로로 에틸 옥타노에이트 2-Naphthoyl chloride ETHYL 6-(HYDROXYMETHYL)PYRIDINE-2-CARBOXYLATE 3-Thiophenecarbonyl chloride Z-cis-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropane carbonyl chloride 클로로(2-)에틸메틸슐파이드 N,N-BIS(2-CHLOROETHYL)-P-TOLUENESULFONAMIDE 2-(Chloromethyl)-5-propoxypyridine 클로르다이메폼(클로르디메포름) 6,8-dichlorooctanoic acid 3-Chloropropanesulfonyl chloride (2-FLUORO-PHENYL)-METHANESULFONYL CHLORIDE 5-Amino-2,4,6-triiodoisophthaloyl dichloride (2,5-DIMETHOXYPHENYL)ACETYL CHLORIDE 2-NITRO-ALPHA-TOLUENESULFONYL CHLORIDE 1-Naphthoyl chloride 4-Fluorophenylacetyl chloride 3-(2-METHOXY-PHENYL)-PROPIONYL CHLORIDE M-TOLYL-ACETYL CHLORIDE 4,6-DIMETHOXYPYRIMIDINE-2-CARBONYL CHLORIDE ethyl 2-[2-(diethylamino)ethyl]acetoacetate CARBETAPENTANE CITRATE

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