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Thionyl chloride

CAS No.7719-09-7
Chemical Name:Thionyl chloride
Synonyms:SOCl2;Thionylchlorid;sulfinylchloride;THIONYL CHLORIDE;Sulfoxidechloride;Sulfinyl chloride;SULPHINYLCHLORIDE;chloruredethionyle;THIONYL DICHLORIDE;Sulfinyl dichloride
CBNumber:CB9190771
Molecular Formula:Cl2OS
Formula Weight:118.97
MOL File:7719-09-7.mol
Thionyl chloride Property
mp : -105 °C
bp : 79 °C(lit.)
density : 1.64 g/mL at 20 °C
vapor pressure : 97 mm Hg ( 20 °C)
refractive index : n20/D 1.518(lit.)
Fp : 105°C
storage temp. : Store at RT.
color : ≤50(APHA)
Water Solubility : REACTS
Sensitive : Moisture Sensitive
Merck : 14,9348
Stability:: Reacts violently with water. Incompatible with most common metals, strong reducing agents, strong bases, alcohols, amines.
CAS DataBase Reference: 7719-09-7(CAS DataBase Reference)
NIST Chemistry Reference: Thionyl chloride(7719-09-7)
Safety
Hazard Codes : C
Risk Statements : 14-20/22-29-35-40-34-20/21/22
Safety Statements : 26-36/37/39-45-28-27
RIDADR : UN 1836 8/PG 1
WGK Germany : 1
RTECS : XM5150000
F : 19
HazardClass : 8
PackingGroup : I
HS Code : 28121095
Hazardous Substances Data: 7719-09-7(Hazardous Substances Data)

Thionyl chloride Chemical Properties,Usage,Production

Chemical Properties
Colorless to slightly yellow liquid
General Description
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.
Reactivity Profile
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.).
Health Hazard
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.
Fire Hazard
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.
Thionyl chloride Preparation Products And Raw materials
Raw materials
Sulfur Disulfur dichloride Chlorine Sulfur trioxide Chlorosulfonic acid Sulfur dichloride
Preparation Products
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 (Chloromethylene)dimethyliminium chloride 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 Ethyl 6,8-dichlorooctanoate 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 2-CHLOROETHYL METHYL SULFIDE N,N-BIS(2-CHLOROETHYL)-P-TOLUENESULFONAMIDE 2-(Chloromethyl)-5-propoxypyridine CHLORDIMEFORM Ethyl 6,8-dichloro caprylate 3-Chloropropanesulfonyl chloride (2-FLUORO-PHENYL)-METHANESULFONYL CHLORIDE 5-Amino-2,4,6- triiodisophthaloyl acid 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
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7719-09-7(Thionyl chloride)Related Search:
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Halogenation Chlorination chloruredethionyle SOCl2 Sulfinyl chloride Sulfinyl dichloride sulfinylchloride Sulfoxidechloride Sulfur chloride oxide Sulfur chloride oxide (Cl2SO) Sulfur chloride oxide (scl2o) Sulfur oxychloride (socl2) sulfurchlorideoxide sulfurchlorideoxide(cl2so) Sulfurous dichloride sulfurousdichloride Thionyl chloride (socl2) Thionylchlorid 7719-09-7 SULFUR DICHLORIDE OXIDE SULFUROUS OXYCHLORIDE THIONYL CHLORIDE THIONYL DICHLORIDE C-X Bond Formation (Halogen) Synthetic Reagents Sulforous oxychloride Thionylchloridecolorlesspaleyellowliq Sulphoxide chloride THIONYL CHLORIDE, REAGENTPLUS, >=99% THIONYL CHLORIDE REAGENT GRADE 97% THIONYL CHLORIDE REAGENTPLUS(TM) 99.& THIONYL CHLORIDE REAGENTPLUS(TM) >=9& THIONYL CHLORIDE, TECH. THIONYL CHLORIDE 2.0M SOLUTION IN & THIONYL CHLORIDEGC STANDARD Thionyl chloride, 99.5+% Cl2OS ClHOS 719-09-7 SULPHINYLCHLORIDE SULPHUROUSOXYCHLORIDE 7719-09-07 Inorganics Thionyl chloride, 99+% Chlorination Halogenation Synthetic Organic Chemistry Thionyl Chloride (ca. 1mol/L in Dichloromethane) thionyl dichloride thionyl chloride Reagent Grade Thionyl chloride solution Electrolytes C-X Bond Formation (Halogen) Synthetic Reagents ChlorinationMaterials Science ElectrolytesEssential Chemicals Alternative Energy Reagent Plus
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