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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1,2-Dichloroethane – Wikipedia

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

The Journal of Organic Chemistry. Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethanewhich is used in dry cleaning. Historically, 1,2-dichloroethane was used as an anti-knock additive in leaded fuels to scavenge lead from cylinders and valves preventing buildup. It forms azeotropes with many other solventsincluding water b. The chemical compound 1,2-dichloroethane commonly known as ethylene dichloride EDCis a chlorinated hydrocarbon.


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. It is a colourless liquid with a chloroform -like odour. Verstraete 25 March Retrieved 8 April The production and characterization of 1,2-dichloroethane appear on pages In the laboratory it is occasionally used as a source of chlorinewith elimination of ethene and chloride.


VCM is the precursor to polyvinyl chloride. Ethylene Chlorine Vinyl chloride.

Nearly 20 million tons of 1,2-dichloroethane are produced in the United StatesWestern Europeand Japan. LC Lo lowest published. Methyl chloride Methylene chloride 1,1,1-Trichloroethane. TWA 50 ppm C ppm ppm [5-minute maximum peak in any 3 hours] [2].

Ethylene dichloride | ClCH2CH2Cl – PubChem

Ca [50 ppm] [2]. Views Read Edit View history. The hydrogen chloride can be re-used in the production of more 1,2-dichloroethane via the oxychlorination route described above.

Dioxolane and toluene are possible substitutes as solvents. LC 50 median concentration. Lethal dose or concentration LDLC:. By using this site, you agree ddichloride the Terms of Use and Privacy Policy. Retrieved from ” https: Dichloroethane is unstable in the presence of aluminium metal and, when moist, with zinc and iron.


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

Archived from the original on 18 March Part of that acknowledgement is that 1,2-dichloroethane was called “Dutch oil” in old chemistry. Its high solubility and year half-life in anoxic aquifers make it ,sds perennial pollutant and health risk that is very expensive to treat conventionally, requiring a method of bioremediation.

Society of Dutch Chemistswere the first to produce 1,2-dichloroethane from olefiant gas oil-making gas, ethylene and chlorine gas. Ethjlene Wikipedia, the free encyclopedia.