1,1,2-Trichloroethane

1,1,2-Trichloroethane
1,1,2-Trichloroethane
1,1,2-Trichloroethane
Names
Preferred IUPAC name
1,1,2-Trichloroethane
Other names
1,1,2-TCA
vinyl trichloride

symmetrical Trichloroethane
monochlorethylen chloride (archaic)
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.061 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C2H3Cl3/c3-1-2(4)5/h2H,1H2 checkY
    Key: UBOXGVDOUJQMTN-UHFFFAOYSA-N checkY
  • InChI=1/C2H3Cl3/c3-1-2(4)5/h2H,1H2
    Key: UBOXGVDOUJQMTN-UHFFFAOYAA
  • ClCC(Cl)Cl
  • C(C(Cl)Cl)Cl
Properties
C2H3Cl3
Molar mass 133.40 g/mol
Appearance colorless liquid[1]
Odor sweet, chloroform-like[1] (in high concentrations)
Density 1.435 g/cm3
Melting point −37 °C (−35 °F; 236 K)
Boiling point 110 to 115 °C (230 to 239 °F; 383 to 388 K)
0.4% (20°C)[1]
Vapor pressure 19 mmHg (20°C)[1]
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability (yellow): no hazard codeSpecial hazards (white): no code
3
1
Explosive limits 6–15.5%[1]
Lethal dose or concentration (LD, LC):
1200 mg/kg (rat, orally)[2]
13,100 mg/m3 (cat, 4.5 hr)
2000 ppm (rat, 4 hr)[3]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 10 ppm (45 mg/m3) [skin][1]
REL (Recommended)
 Ca TWA 10 ppm (45 mg/m3) [skin][1]
IDLH (Immediate danger)
 Ca [100 ppm][1]
Related compounds
Related compounds
 1,1,1-Trichloroethane; Trichloroethylene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

1,1,2-Trichloroethane, vinyl trichloride or 1,1,2-TCA, is an organochloride solvent with the molecular formula C2H3Cl3 and the structural formula CH2Cl—CHCl2. It is a colourless, sweet-smelling liquid that does not dissolve in water, but is soluble in most organic solvents. It is an isomer of 1,1,1-trichloroethane, and a byproduct of its manufacture.

It is used as a solvent and as an intermediate in the synthesis of 1,1-dichloroethylene.[4]

  1. ^ a b c d e f g h NIOSH Pocket Guide to Chemical Hazards. "#0628". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ 1,1,2-Trichloroethane toxicity
  3. ^ "1,1,2-Trichloroethane". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  4. ^ Toxicological profile for 1,1,2-trichloroethane (PDF) (Report). Agency for Toxic Substances and Disease Registry (ATSDR). March 2021. Archived (PDF) from the original on 2022-03-05. Retrieved 2023-08-23.