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Names | |||
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Preferred IUPAC name
Chloroethene | |||
Other names
Vinyl chloride monomer
VCM Chloroethylene Refrigerant-1140 | |||
Identifiers | |||
3D model (JSmol)
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1731576 | |||
ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.000.756 | ||
EC Number |
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100541 | |||
KEGG | |||
PubChem CID
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RTECS number |
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UNII | |||
UN number | 1086 | ||
CompTox Dashboard (EPA)
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Properties | |||
C2H3Cl | |||
Molar mass | 62.50 g·mol−1 | ||
Appearance | Colorless gas | ||
Odor | pleasant[1] | ||
Density | 0.911 g/cc | ||
Melting point | −153.8 °C (−244.8 °F; 119.3 K) | ||
Boiling point | −13.4 °C (7.9 °F; 259.8 K) | ||
2.7 g/L (0.0432 mol/L) | |||
Vapor pressure | 2580 mmHg at 20 °C (68 °F) | ||
-35.9·10−6 cm3/mol | |||
Thermochemistry | |||
Heat capacity (C)
|
0.8592 J/K/g (gas) 0.9504 J/K/g (solid) | ||
Std enthalpy of
formation (ΔfH⦵298) |
−94.12 kJ/mol (solid) | ||
Hazards | |||
GHS labelling: | |||
Danger | |||
H220, H350 | |||
P201, P202, P210, P281, P308+P313, P377, P381, P403, P405, P501 | |||
NFPA 704 (fire diamond) | |||
Flash point | −61 °C (−78 °F; 212 K) | ||
Explosive limits | 3.6–33%[1] | ||
NIOSH (US health exposure limits): | |||
PEL (Permissible)
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TWA 1 ppm C 5 ppm [15-minute][1] | ||
REL (Recommended)
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Ca[1] | ||
IDLH (Immediate danger)
|
Ca [N.D.][1] | ||
Related compounds | |||
Related chloroethenes
|
dichloroethylenes, trichloroethylene, tetrachloroethylene, allyl chloride | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Vinyl chloride is an organochloride with the formula H2C=CHCl. It is also called vinyl chloride monomer (VCM) or chloroethene. This colorless compound is an important industrial chemical chiefly used to produce the polymer polyvinyl chloride (PVC). Vinyl chloride monomer is among the top twenty largest petrochemicals (petroleum-derived chemicals) in world production.[2] The United States remains the largest vinyl chloride manufacturing region because of its low-production-cost position in chlorine and ethylene raw materials. China is also a large manufacturer and one of the largest consumers of vinyl chloride.[3] Vinyl chloride is a flammable gas that has a sweet odor and is carcinogenic. It can be formed in the environment when soil organisms break down chlorinated solvents. Vinyl chloride that is released by industries or formed by the breakdown of other chlorinated chemicals can enter the air and drinking water supplies. Vinyl chloride is a common contaminant found near landfills.[4] Before the 1970s, vinyl chloride was used as an aerosol propellant and refrigerant.[5][6]
Ullmann
was invoked but never defined (see the help page).