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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Nearly 20 million tons of 1,2-dichloroethane are produced in the United StatesWestern Europeand Japan.


Dcihloride of Dutch Chemistswere the first to produce 1,2-dichloroethane from olefiant gas oil-making gas, ethylene and chlorine gas. Ethylene Chlorine Vinyl chloride. 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.

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

Archived from the msdd on 18 March Ca [50 ppm] [2].

The production and characterization of 1,2-dichloroethane appear on pages In other projects Wikimedia Commons. This page sichloride last edited on 27 Novemberat From Wikipedia, the free encyclopedia.


VCM is the precursor to polyvinyl chloride. 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.

Ethylene Dichloride Properties, Molecular Formula, Applications – WorldOfChemicals

Methyl chloride Methylene chloride 1,1,1-Trichloroethane. Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethanewhich is used in dry cleaning. It forms azeotropes with many other solventsincluding water b. LC 50 median concentration.

1,2-Dichloroethane – Wikipedia

Retrieved 8 April 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. In the laboratory it is occasionally used as a source of chlorinewith elimination of ethene and chloride.

Verstraete 25 March The Journal of Dthylene Chemistry.

Dioxolane and toluene are possible substitutes as solvents. The hydrogen chloride can be re-used in the production of more 1,2-dichloroethane via the oxychlorination route described above.

Retrieved from ” https: LC Lo lowest published. 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.


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

Dichloroethane is unstable in the presence of aluminium metal and, when moist, with zinc and iron. Part of that acknowledgement is that 1,2-dichloroethane was called “Dutch oil” in old chemistry.

Lethal dose or concentration LDLC:. TWA 50 ppm C ppm ppm [5-minute maximum peak in any 3 hours] [2]. By using this site, you agree to the Terms of Use and Privacy Policy. Historically, 1,2-dichloroethane was used as an anti-knock additive in leaded fuels to scavenge lead from cylinders and valves preventing buildup.