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Trichloroacetonitrile

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Trichloroacetonitrile Basic information
Product Name:Trichloroacetonitrile
Synonyms:trichloromethylcarbonitrile;Trichlroacetonitrile;TRICHLOROACETONITRILE, 1000MG, NEAT;Trichloroacetonitrile,97%;TRICHLORACETONITRILE;Trichlorocyanomethane;Trichloroacetonitrile ,98%;Trichloromethylnitrile
CAS:545-06-2
MF:C2Cl3N
MW:144.39
EINECS:208-885-7
Product Categories:Building Blocks;C1 to C5;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Pyridines ,Halogenated Heterocycles;C1 to C5Specialty Synthesis;Glycosylating Reagents;Carbohydrate Synthesis;C1 to C5;Cyanides/Nitriles;Nitrogen Compounds;NitrilesVolatiles/ Semivolatiles;Alpha Sort;Chemical Class;ChloroAnalytical Standards;Halogenated;TP - TZ;T-ZAlphabetic;Organics;Aliphatics;Halides;YP00036
Mol File:545-06-2.mol
Trichloroacetonitrile Structure
Trichloroacetonitrile Chemical Properties
Melting point -42 °C
Boiling point 83-84 °C(lit.)
density 1.44 g/mL at 25 °C(lit.)
vapor pressure 58 mm Hg ( 20 °C)
refractive index n20/D 1.441(lit.)
Fp None
storage temp. Store below +30°C.
solubility <0.1 g/100 mL at 21.5°C
form Liquid
color Clear colorless to very slightly yellow
Odorodor of chloral and hydrogen cyanide
Water Solubility <0.1 g/100 mL at 21.5 ºC
Sensitive Lachrymatory
Merck 14,9628
BRN 605572
Dielectric constant4.6(60℃)
Exposure limitsNIOSH: IDLH 25 mg/m3
Stability:Stable, but water sensitive. Incompatible with acids, water, steam. May hydrolyze in alkali or acid conditions. Flammable.
CAS DataBase Reference545-06-2(CAS DataBase Reference)
IARC3 (Vol. 52, 71) 1999
NIST Chemistry ReferenceAcetonitrile, trichloro-(545-06-2)
EPA Substance Registry SystemTrichloroacetonitrile (545-06-2)
Safety Information
Hazard Codes T,N
Risk Statements 23/24/25-51/53
Safety Statements 45-61
RIDADR UN 3276 6.1/PG 3
WGK Germany 3
RTECS AM2450000
Hazard Note Toxic/Lachrymatory
TSCA Yes
HazardClass 8
PackingGroup II
HS Code 29269095
Hazardous Substances Data545-06-2(Hazardous Substances Data)
ToxicityLD50 orally in rats: 0.25 g/kg (Smyth)
MSDS Information
ProviderLanguage
Cyanotrichloromethane English
SigmaAldrich English
ACROS English
ALFA English
Trichloroacetonitrile Usage And Synthesis
Chemical Propertiescolourless to slightly yellow liquid
UsesTrichloroacetonitrile is involved as a reagent in Overman rearrangement, which is used to prepare alylic amines from allylic alcohols. It is also used to prepare bistrichloroacetimidates from diols leading to dihyrooxazines through acid catalyzed cyclization. Further, it is utilized in the synthesis of trichloroacetimidates by 1,8-Diazobicyclo[5.4.0]undec-7-ene (DBU) catalyzed addition of allylic alcohols. It finds application in the study of the methoxy methyl (MOM) catalyzed aza-Claisen rearrangement.
UsesInsecticide.
DefinitionChEBI: Trichloroacetonitrile is an aliphatic nitrile and an organochlorine compound.
Production MethodsTrichloroacetonitrile can be obtained by dehydration of trichloroacetamide with phosphorous pentoxide or by chlorination of acetonitrile with chlorine. Vapor phase chlorination in the presence of water and photochemical chlorination in the presence of catalysts such as HgCl2 or AlCl3 have been reported. Trichloroacetonitrile is an organic intermediate used, for example, in the synthesis of the fungicide etridiazole.
Air & Water ReactionsHighly flammable. Insoluble in water.
Reactivity ProfileMay be sensitive to light and heat. Trichloroacetonitrile may react with water, steam, acid or acid fumes. Trichloroacetonitrile may hydrolyze under acidic or alkaline conditions. . The reaction of benzene and Trichloroacetonitrile evolves toxic chloroform and HCl gasses. (Hagedorn, F., H.-P. Gelbke, and Federal Republic of Germany. 2002. Nitriles. In Ullman Encyclopedia of Industrial Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA.).
HazardStrong irritant to tissue. Questionable carcinogen.
Fire HazardTrichloroacetonitrile is combustible.
Safety ProfilePoison by ingestion and intravenous routes. Moderately toxic by inhalation and skin contact. Human mutation data reported. A skin and severe eye irritant. An experimental teratogen. Other experimental reproductive effects. When heated to decomposition or in reaction with water, steam, acid, or acid fumes it produces toxic fumes of CN-, Cl-, and NOx. Used as an insecticide. See also NITRILES and CYANIDE.
Tag:Trichloroacetonitrile(545-06-2) Related Product Information
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