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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VCM is the precursor to polyvinyl chloride. Methyl chloride Methylene chloride 1,1,1-Trichloroethane.

Ethylene Dichloride, mL

TWA 50 ppm C ppm ppm [5-minute maximum dichlofide in any 3 hours] [2]. It is a colourless liquid with a chloroform -like odour. By using this site, you agree to the Terms of Use and Privacy Policy.

Ca [50 ppm] [2]. The hydrogen chloride can be re-used in the production of more 1,2-dichloroethane via the oxychlorination route described above. Society of Dutch Chemists ethylend, were the first to produce 1,2-dichloroethane from olefiant gas oil-making gas, ethylene and chlorine gas. Instead of the expected soot, an oil Oehl formed.

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Ethylene dichloride | ClCH2CH2Cl – PubChem

This page was last edited on 27 Novemberat The Journal of Organic Chemistry. Butyl rubber Butylated hydroxytoluene 1,2-Dibromoethane 1,2-Dichloroethane Dimethyl methylphosphonate 2,4-Dimethyltert-butylphenol Dinonylnaphthylsulfonic acid 2,6-Di-tert-butylphenol Dcihloride Ethylenediamine Metal deactivator Methyl tert-butyl ether Nitromethane Tetraethyllead Tetranitromethane.

Retrieved 8 April Retrieved from ” https: Via several steps, 1,2-dichloroethane is a diculoride to 1,1,1-trichloroethanewhich is used in dry cleaning. LC 50 median concentration.

Ethylene Chlorine Vinyl chloride. Historically, 1,2-dichloroethane was used as an anti-knock additive in leaded fuels to scavenge lead from cylinders and valves preventing buildup. The production and characterization of 1,2-dichloroethane appear on pages dichlride Dichloroethane is unstable in the presence of aluminium metal and, when moist, with zinc and iron. Lethal dose or concentration LDLC:. It forms azeotropes with many other solventsincluding water b.

The most common use of 1,2-dichloroethane djchloride 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 fthylene known as ethylene dichloride EDCis a chlorinated hydrocarbon.

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

Ethylene Dichloride, 500 mL

Its high solubility and year half-life in anoxic aquifers make it a perennial pollutant and health risk that is very expensive to dichlotide conventionally, requiring a method of bioremediation. LC Lo lowest published. 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 As a useful ‘building block’ reagent, it is used as an intermediate in the production of various organic compounds such as ethylenediamine.

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Verstraete 25 March From Wikipedia, the free encyclopedia. Views Read Edit View history. Dioxolane and toluene are possible substitutes as solvents.

In other projects Wikimedia Commons. Part of that acknowledgement is that 1,2-dichloroethane was called ethyoene oil” in old chemistry. Nearly 20 million tons of 1,2-dichloroethane are produced in the United StatesWestern Europeand Japan.