1,1-Dichloroethane

From Infogalactic: the planetary knowledge core
(Redirected from 1,1-dichloroethane)
Jump to: navigation, search
1,1-Dichloroethane
1,1-Dichloroethane
1,1-dichloroethane-3D-vdW.png
Names
IUPAC name
1,1-Dichloroethane
Other names
ethylidene dichloride
ethylidene chloride
CFC-150a
1,1-DCA
Asymmetrical dichloroethane
1,1-Ethylidene dichloride
Identifiers
75-34-3 YesY
ChEMBL ChEMBL45079 YesY
ChemSpider 6125 YesY
Jmol 3D model Interactive image
KEGG C18247 YesY
PubChem 6365
  • InChI=1S/C2H4Cl2/c1-2(3)4/h2H,1H3 YesY
    Key: SCYULBFZEHDVBN-UHFFFAOYSA-N YesY
  • InChI=1/C2H4Cl2/c1-2(3)4/h2H,1H3
    Key: SCYULBFZEHDVBN-UHFFFAOYAY
  • ClC(Cl)C
Properties
C2H4Cl2
Molar mass 98.96 g/mol
Appearance colorless, oily liquid[1]
Odor chloroform-like[1]
Density 1.2 g/cm3
Melting point −97 °C (−143 °F; 176 K)
Boiling point 57.2 °C (135.0 °F; 330.3 K)
0.6%[1]
Vapor pressure 182 mmHg (20°C)[1]
Vapor pressure {{{value}}}
Related compounds
Related compounds
1,2-Dichloroethane (ethylene dichloride); *1,1-Dichloroethene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

1,1-Dichloroethane is a chlorinated hydrocarbon. It is a colorless oily liquid with a chloroform-like odor. It is not easily soluble in water, but miscible with most organic solvents.

Large volumes of 1,1-dichloroethane are manufactured, with annual production exceeding 1 million pounds in the United States. It is mainly used as a feedstock in chemical synthesis, chiefly of 1,1,1-trichloroethane. It is also used as a solvent for plastics, oils and fats, as a degreaser, as a fumigant in insecticide sprays, in halon fire extinguishers, and in cementing of rubber. It is used in manufacturing of high-vacuum resistant rubber and for extraction of temperature-sensitive substances. Thermal cracking at 400–500 °C and 10 MPa yields vinyl chloride. In the past, 1,1-dichloroethane was used as a surgical inhalational anesthetic.

In the atmosphere, 1,1-dichloroethane decomposes with half-life of 62 days, chiefly by reaction of photolytically produced hydroxyl radicals.

References

  1. 1.0 1.1 1.2 1.3 Cite error: Invalid <ref> tag; no text was provided for refs named PGCH

External links