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Liquid ammonia and ETHYLENE DICHLORIDE can cause an explosion when mixed, NFPA M, A tank of dimethyl amino propyl amine exploded. Apr 25, SDS #.: Synonym.: ethylene dichloride; Ethane, 1,2-dichloro-; Glycol dichloride; Ethylene chloride;. Ethylene Dichloride. MSDS Name: Ethylene Dichloride. Synonyms: Dichloroethane ; EDC ; DCE. Company Identification: (INDIA). Veritas House, 70 Mint Road.

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Ca [50 ppm] [2]. Methyl chloride Methylene chloride 1,1,1-Trichloroethane. Its high solubility and year half-life in anoxic aquifers make it a perennial pollutant and health risk that is very expensive to treat conventionally, requiring a method of bioremediation. Ethylene Chlorine Vinyl chloride.

Ethylene Dichloride Properties

VCM is the precursor to polyvinyl chloride. Retrieved from ” https: Butyl rubber Butylated hydroxytoluene 1,2-Dibromoethane 1,2-Dichloroethane Dimethyl methylphosphonate 2,4-Dimethyltert-butylphenol Dinonylnaphthylsulfonic acid 2,6-Di-tert-butylphenol Ecalene Ethylenediamine Metal dichlorixe Methyl tert-butyl ether Nitromethane Tetraethyllead Tetranitromethane.

The Journal of Organic Chemistry. LC 50 median concentration. The production and characterization of 1,2-dichloroethane appear on pages Archived from the dichlorixe on 18 March As a useful ‘building block’ reagent, it is used as an intermediate in the production of various organic compounds such as ethylenediamine.


The most common use of dicloride is in the production of vinyl chloridewhich is used to make polyvinyl chloride PVC pipes, furniture and automobile upholstery, wall coverings, housewares, and automobile parts. LC Lo lowest published.

Nearly 20 million tons of 1,2-dichloroethane are produced in the United StatesWestern Europeand Japan. Historically, 1,2-dichloroethane was used as an anti-knock additive in leaded fuels to scavenge lead from cylinders and valves preventing buildup.

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In other projects Wikimedia Commons. Lethal dose or concentration LDLC:. TWA 50 ppm C ppm ppm [5-minute maximum peak in any 3 hours] [2]. As a good polar dich,oride solvent1,2-dichloroethane could be used as degreaser and paint remover but is now banned from use due to its toxicity and possible carcinogenity. Verstraete 25 March Dichloroethane is unstable in the presence of aluminium metal and, when moist, with zinc and iron. Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethanewhich is used in dry cleaning.

The chemical compound 1,2-dichloroethane commonly known as ethylene dichloride EDCis a chlorinated hydrocarbon. Instead of the expected soot, an oil Oehl formed. It is a colourless liquid with a chloroform -like odour.


Dioxolane and toluene are possible substitutes as solvents. This page was last edited on 27 Novemberat By using this site, you agree to the Terms ethylenne Use and Privacy Policy. From Wikipedia, the free encyclopedia. Views Read Edit View history.

In the laboratory it is occasionally used as a source of chlorinewith elimination of ethene and chloride. The hydrogen chloride can be re-used in the production of more 1,2-dichloroethane via the oxychlorination route described above.

Part of that acknowledgement is that 1,2-dichloroethane was called “Dutch oil” msd old chemistry. It forms azeotropes with many other solventsincluding water b. Retrieved 8 April Society of Dutch Chemistswere the divhloride to produce 1,2-dichloroethane from olefiant gas oil-making gas, ethylene and chlorine gas.