Chemistry:1,1,1,2-Tetrachloroethane

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Short description: Chemical compound
1,1,1,2-Tetrachloroethane[1]
Skeletal formula of 1,1,1,2-tetrachloroethane
Ball-and-stick model of 1,1,1,2-tetrachloroethane
Names
Preferred IUPAC name
1,1,1,2-Tetrachloroethane
Other names
R-130a; acetylidene tetrachloride, asymmetrical tetrachloroethane
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
UNII
Properties
C2H2Cl4
Molar mass 167.848 g/mol
Appearance Clear liquid
Density 1.5532 g/cm3
Melting point −70.2 °C (−94.4 °F; 203.0 K)
Boiling point 130.5 °C (266.9 °F; 403.6 K)
0.1% (20°C)[2]
Vapor pressure 14 mmHg (25°C)[2]
Hazards
NIOSH (US health exposure limits):
PEL (Permissible)
none[2]
REL (Recommended)
Handle with caution in the workplace.[2]
IDLH (Immediate danger)
N.D.[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Tracking categories (test):

1,1,1,2-Tetrachloroethane is a chlorinated hydrocarbon. It is a colorless liquid with a sweet chloroform-like odor. It is used as a solvent and in the production of wood stains and varnishes. It is an isomer of 1,1,2,2-Tetrachloroethane

Production

1,1,1,2-Tetrachloroethane can be obtained by a two-step addition reaction of acetylene with chlorine (via dichloroethene), but this mainly produces 1,1,2,2-tetrachloroethane.

[math]\ce{ C2H2 + Cl2 -> C2H2Cl2 }[/math] [math]\ce{ C2H2Cl2 + Cl2 -> C2H2Cl4 }[/math]

It can be obtained directly by chlorination of 1,1,2-trichloroethane:[3]

[math]\ce{ CHCl2-CH2Cl + Cl2 -> CHCl2-CCl3 + HCl }[/math]

Safety

IARC has classified 1,1,1,2-tetrachloroethane as a possible carcinogen for humans in 2014.[4]

See also

References