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  2. 1,2-Dichloroethylene - Wikipedia

    en.wikipedia.org/wiki/1,2-dichloroethylene

    1,2-Dichloroethylene or 1,2-DCE is the name for a pair of organochlorine compounds with the molecular formula C 2 H 2 Cl 2. The two compounds are isomers, each being colorless liquids with a sweet odor. It can exist as either of two geometric isomers, cis-1,2-dichloroethene or trans-1,2-dichloroethene, but is often used as a mixture of the two ...

  3. 1,2-Dichloroethane - Wikipedia

    en.wikipedia.org/wiki/1,2-Dichloroethane

    The most common use of 1,2-dichloroethane is in the production of vinyl chloride, which is used to make polyvinyl chloride (PVC) pipes, furniture and automobile upholstery, wall coverings, housewares, and automobile parts. [4] 1,2-Dichloroethane is also used generally as an intermediate for other organic chemical compounds, and as a solvent.

  4. Dichloroethene - Wikipedia

    en.wikipedia.org/wiki/Dichloroethene

    Dichloroethene or dichloroethylene, often abbreviated as DCE, can refer to any one of several isomeric forms of the organochloride with the molecular formula C 2 H 2 Cl 2: There are three isomers: 1,1-Dichloroethylene; 1,2-Dichloroethylene (E and Z)

  5. Dichloroethane - Wikipedia

    en.wikipedia.org/wiki/Dichloroethane

    Dichloroethane can refer to either of two isomeric organochlorides with the molecular formula C 2 H 4 Cl 2: 1,1-Dichloroethane (ethylidene chloride) 1,2-Dichloroethane (ethylene dichloride)

  6. 1,1,2,2-Tetrachloroethane - Wikipedia

    en.wikipedia.org/wiki/1,1,2,2-Tetrachloroethane

    1,1,2,2-tetrachloroethane was used in large amounts to produce other chemicals like trichloroethylene, tetrachloroethylene, and 1,2-dichloroethylene. [6] Because of its possible carcinogen effects on humans, the production of 1,1,2,2-tetrachloroethane has decreased significantly and is no longer widely used as an end-product. [7]

  7. Tetrachloroethylene - Wikipedia

    en.wikipedia.org/wiki/Tetrachloroethylene

    Bioremediation usually entails reductive dechlorination under anaerobic conditions by Dehalococcoides spp. [39] Under aerobic conditions, degradation may occur via co-metabolism by Pseudomonas sp. [40] Products of biological reductive dechlorination include trichloroethylene, cis-1,2-dichloroethylene, vinyl chloride, ethylene and chloride.