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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In the laboratory it is occasionally used as a source of chlorinewith elimination of ethene and chloride.

In other projects Wikimedia Commons. Society of Dutch Chemistswere the first to produce 1,2-dichloroethane from olefiant gas oil-making gas, ethylene and chlorine gas. The Journal dichoride Organic Chemistry. Nearly 20 million tons of 1,2-dichloroethane are produced in the United StatesWestern Europeand Japan.

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. LC 50 median etbylene. The production and characterization of 1,2-dichloroethane appear on pages LC Lo lowest published.


Ca [50 ppm] [2]. Historically, 1,2-dichloroethane was used as an anti-knock additive in leaded fuels to scavenge lead from cylinders and valves preventing buildup.

Ethylene Dichloride, mL

It forms azeotropes with many other solventsincluding water b. Ethylene Chlorine Vinyl chloride. Dioxolane and toluene are possible substitutes as solvents.

As a useful ‘building block’ reagent, it is used as an intermediate in the production of various organic compounds such as ethylenediamine.

Verstraete 25 March Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethanewhich is used in dry cleaning.

Ethylene Dichloride, 500 mL

Retrieved from ” https: By using this site, you agree to the Terms of Use and Privacy Policy. Methyl chloride Methylene chloride 1,1,1-Trichloroethane.

From Wikipedia, the free encyclopedia. The hydrogen chloride can be re-used in the production of tehylene 1,2-dichloroethane via the oxychlorination route described above. Views Read Edit View history. The most common use of 1,2-dichloroethane 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.

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 deactivator Methyl tert-butyl ether Nitromethane Tetraethyllead Tetranitromethane.


Dichloroethane is unstable in the presence of aluminium metal and, when moist, with zinc and iron. It is a colourless liquid with a chloroform -like odour.

Ethylene dichloride | ClCH2CH2Cl – PubChem

As a good polar aprotic solvent1,2-dichloroethane could be used as degreaser and paint remover but is now banned from use due to its toxicity and possible carcinogenity. VCM is the precursor to polyvinyl chloride. This page was last sthylene on 27 November ethlyene, at Instead of the expected soot, an oil Oehl formed. Archived from the original on 18 March The chemical compound 1,2-dichloroethane commonly known as ethylene dichloride EDCis a chlorinated hydrocarbon.


Lethal dose or concentration LDLC:. Part of that acknowledgement is that 1,2-dichloroethane was called “Dutch oil” in old chemistry. Retrieved 8 April TWA 50 ppm C ppm ppm [5-minute maximum peak in any 3 hours] [2].