ETHYLENE DICHLORIDE MSDS PDF

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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Instead of the expected soot, an oil Oehl formed. 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.

Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethanewhich is used in dry diichloride. 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 dichlorire. VCM is the precursor to polyvinyl chloride.

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Archived from the original on 18 March 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. The chemical compound 1,2-dichloroethane commonly known as ethylene dichloride EDCis a chlorinated hydrocarbon.

Ethylene Dichloride Properties, Molecular Formula, Applications – WorldOfChemicals

ethylsne Retrieved from ” https: The production and characterization of 1,2-dichloroethane appear on pages Methyl chloride Methylene chloride 1,1,1-Trichloroethane. The hydrogen chloride can be re-used in the production of more 1,2-dichloroethane via the oxychlorination route described above.

TWA 50 ppm C ppm ppm [5-minute maximum peak in any 3 hours] [2]. Ethylene Chlorine Vinyl chloride.

1,2-Dichloroethane

It forms azeotropes with many other solventsincluding water b. 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.

This page was last edited on 27 Novemberat The Journal of Organic Chemistry. Views Read Edit View history. Nearly 20 million tons of 1,2-dichloroethane are produced in the United StatesWestern Europe dichlkride, and Japan.

Lethal dose or concentration LD ehylene, LC:.

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

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LC Lo lowest published. Society of Dutch Chemistswere the first to produce 1,2-dichloroethane from olefiant gas oil-making gas, ethylene and chlorine gas.

LC 50 median concentration.

In the laboratory it is occasionally used as a source of chlorinewith elimination of ethene and 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. Dioxolane and toluene are possible substitutes as solvents. By using this site, you agree to the Terms of Use and Privacy Policy. Verstraete 25 March Part of that acknowledgement is that 1,2-dichloroethane was called “Dutch oil” in old chemistry.

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