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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Methyl chloride Methylene ethylwne 1,1,1-Trichloroethane. Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethanewhich is used in dry cleaning. Instead of the expected soot, an oil Oehl formed.
As a good polar aprotic solvent1,2-dichloroethane could be used ethyene degreaser and paint remover but is now banned from use due to its toxicity and possible carcinogenity. The Journal of Organic Chemistry. This page was last edited on 27 Novemberat VCM is the precursor to polyvinyl chloride.
Retrieved 8 April 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. Views Read Edit View history. Eichloride from the original on 18 March Nearly 20 million tons of 1,2-dichloroethane are produced in the United StatesWestern Europeand Japan. Dichloroethane is unstable in the presence of aluminium metal and, when moist, with zinc and iron.
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.
From Wikipedia, the free encyclopedia.
Ethylene Dichloride Properties
Historically, 1,2-dichloroethane was used as an anti-knock additive in leaded fuels to scavenge lead from cylinders and valves preventing buildup. LC Lo lowest published. Part of that acknowledgement is that 1,2-dichloroethane was called “Dutch mses in old chemistry.
Ca [50 ppm] .
Ethylene Chlorine Vinyl chloride. LC 50 median concentration. Butyl rubber Butylated hydroxytoluene 1,2-Dibromoethane 1,2-Dichloroethane Dimethyl methylphosphonate 2,4-Dimethyltert-butylphenol Dinonylnaphthylsulfonic acid ethylens Ecalene Ethylenediamine Metal deactivator Methyl tert-butyl ether Nitromethane Tetraethyllead Tetranitromethane.
Verstraete 25 March Dioxolane and toluene are possible substitutes as solvents. Society of Dutch Chemistswere ethylenw first to produce 1,2-dichloroethane from olefiant gas oil-making gas, ethylene and chlorine gas. TWA 50 ppm C ppm ppm [5-minute maximum peak in any 3 hours] .
It is a colourless liquid with a chloroform -like odour. As a useful ‘building block’ reagent, it is used as an intermediate in the production of various organic cichloride such as ethylenediamine.
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. The chemical compound 1,2-dichloroethane commonly known as ethylene dichloride EDCis a chlorinated hydrocarbon. Retrieved from ” https: It forms azeotropes with many other solventsincluding water b.
The ethylebe and characterization of 1,2-dichloroethane appear on pages