1,2-Dichloroethene

1,2-Dichloroethene
cis-1,2-Dichloroethene (Z)
trans-1,2-Dichloroethene (E)
Names
IUPAC name
1,2-Dichloroethene
Other names
1,2-Dichloroethylene
1,2-DCE
sym-Dichloroethylene
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.007.956
KEGG
Properties
C2H2Cl2
Molar mass 96.95 g/mol
Appearance clear liquid[1]
Odor acrid, chloroform-like[1]
Density Z: 1.28 g/cm³
E: 1.26 g/cm³
Melting point Z: -81.47 °C
E: -49.44 °C
Boiling point Z: 60.2 °C
E: 48.5 °C
  • -51.0·10−6 cm3/mol (cis)
  • -48.9·10−6 cm3/mol (trans)
Z: 1.9 D
E: 0 D
Hazards
Flash point 2–4 °C; 36–39 °F; 275–277 K
Explosive limits 5.6%-12.8%[1]
Lethal dose or concentration (LD, LC):
770 mg/kg (oral, rat)
1275 mg/kg (oral, rat, trans-isomer)[2]
21,273 ppm (mouse, 6 hr, trans-isomer)[2]
16,000 ppm (rat, 6 hr, cis-isomer)[2]
US health exposure limits (NIOSH):
PEL (Permissible)
 TWA 200 ppm (790 mg/m3)[1]
REL (Recommended)
 TWA 200 ppm (790 mg/m3)[1]
IDLH (Immediate danger)
 1000 ppm[1]
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

1,2-Dichloroethene, commonly called 1,2-dichloroethylene or 1,2-DCE, is an organochloride with the molecular formula C2H2Cl2. It is a highly flammable, colorless liquid with a sharp, harsh odor. It can exist as either of two geometric isomers, cis-1,2-dichloroethene or trans-1,2-dichloroethene, but is often used as a mixture of the two. They have modest solubility in water. These compounds have few industrial applications,[3] although they are fundamental given their simple stoichiometries.

Production

cis-DCE, the Z isomer, is obtainable by the controlled chlorination of acetylene:

C2H2 + Cl2 → C2H2Cl2

Industrially both isomers arise as byproduct of the production of vinyl chloride, which is produced on a vast scale. Unlike vinyl chloride, the 1,2-dichloroethylene isomers do not polymerize.[3]

trans-DCE has applications including electronics cleaning, precision cleaning, and certain metal cleaning applications.[4]

E-Z relative stability

In contrast to most cis-trans compounds, the Z isomer (cis) is more stable than the E isomer (trans) by 0.4 kcal/mol.[5]

Safety

These compounds have "moderate oral toxicity to rats".[3]

See also

References

  1. 1 2 3 4 5 6 "NIOSH Pocket Guide to Chemical Hazards #0195". National Institute for Occupational Safety and Health (NIOSH).
  2. 1 2 3 "1,2-Dichloroethylene". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).
  3. 1 2 3 E.-L. Dreher; T. R. Torkelson; K. K. Beutel (2011). "Chlorethanes and Chloroethylenes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.o06_o01.
  4. ↑ http://www.axiall.com/Products/Chlorovinyls/Chlorinated-Solvents-and-Feedstock/
  5. ↑ Pitzer, Kenneth S.; Hollenberg, J. L. (1954). "cis- and trans-Dichloroethylenes. The Infrared Spectra from 130–400 Cm.–1 and the Thermodynamic Properties". J. Am. Chem. Soc. 76 (6): 1493–1496. doi:10.1021/ja01635a010.
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