1,1-Dichloroethane
1,1-Dichloroethane | |
---|---|
1,1-Dichloroethane | |
Other names ethylidene dichloride ethylidene chloride CFC-150a 1,1-DCA | |
style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
CAS number | 75-34-3 |
UNII | ADIASHOIDHA |
SMILES | Script error: No such module "collapsible list". |
style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
Molecular formula | C2H4Cl2 |
Molar mass | 98.96 g/mol |
Density | 1.2 g/cm³ |
Melting point |
-97 °C |
Boiling point |
57.2 °C |
style="background: #F8EABA; text-align: center;" colspan="2" | Related compounds | |
Related compounds | 1,2-Dichloroethane (ethylene dichloride); *1,1-Dichloroethene |
(what is this?) (verify) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
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
External links
it:1,1-dicloroetano ku:1,1-Dîklorêtan nl:1,1-dichloorethaan ja:1,1-ジクロロエタン pt:1,1-Dicloroetano ru:1,1-дихлорэтан fi:1,1-dikloorietaani sv:1,1-Dikloretan