1,1-Dichloroethane | | Names Preferred IUPAC name 1,1-Dichloroethane Other names Ethylidene dichloride Ethylidene chloride CFC-150a 1,1-DCA Asymmetrical dichloroethane 1,1-Ethylidene dichloride Asymmetric dichloroethane Identifiers CAS Number * 75-34-3 Y 3D model (JSmol) * Interactive image ChEMBL | * ChEMBL45079 Y ChemSpider | * 6125 Y KEGG | * C18247 Y PubChem CID * 6365 UNII | * 0S989LNA44 Y InChI * InChI=1S/C2H4Cl2/c1-2(3)4/h2H,1H3 Y Key: SCYULBFZEHDVBN-UHFFFAOYSA-N Y * InChI=1/C2H4Cl2/c1-2(3)4/h2H,1H3 Key: SCYULBFZEHDVBN-UHFFFAOYAY SMILES * ClC(Cl)C Properties Chemical formula | 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) Solubility in water | 0.6%[1] Vapor pressure | 182 mmHg (20°C)[1] Magnetic susceptibility (χ) | −57.4·10−6 cm3/mol Hazards Flash point | −17 °C; 2 °F; 256 K[1] Explosive limits | 5.4–11.4%[1] NIOSH (US health exposure limits): PEL (Permissible) | TWA 100 ppm (400 mg/m3)[1] REL (Recommended) | TWA 100 ppm (400 mg/m3)[1] IDLH (Immediate danger) | 3000 ppm[1] 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 YN ?) 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. ## Contents * 1 Safety * 2 See also * 3 References * 4 External links ## Safety 1,1-dichloroethane has been on the California Proposition 65 list of known carcinogens since 1990.[2] In the atmosphere, 1,1-dichloroethane decomposes with half-life of 62 days, chiefly by reaction of photolytically produced hydroxyl radicals. ## See also * Dichloroethene * Dichloroethane ## References 1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 NIOSH Pocket Guide to Chemical Hazards. "#0194". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0194.html. 2. ↑ "1,1-Dichloroethane". California Office of Environmental Health Hazard Assessment. https://oehha.ca.gov/proposition-65/chemicals/11-dichloroethane. ## External links * Dichloroethane and Dichloroethene on members.optushome.com.au * ATSDR - Toxic Substances Portal * CDC - NIOSH Pocket Guide to Chemical Hazards 0.00 (0 votes) Original source: https://en.wikipedia.org/wiki/1,1-Dichloroethane. Read more | Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:1,1-Dichloroethane&oldid=2494089" *[CID]: Compound ID