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  2. 1,3-Dichloropropane - Wikipedia

    en.wikipedia.org/wiki/1,3-Dichloropropane

    1,3-Dichloropropane is a compound of chlorine, hydrogen, and carbon. It may be found as a contaminant in soil fumigants containing 1,3-dichloropropene. [2]

  3. 1,3-Dichloropropene - Wikipedia

    en.wikipedia.org/wiki/1,3-Dichloropropene

    1,3-Dichloropropene, sold under diverse trade names, is an organochlorine compound with the formula C 3 H 4 Cl 2. It is a colorless liquid with a sweet smell. It is a colorless liquid with a sweet smell.

  4. C3H6Cl2 - Wikipedia

    en.wikipedia.org/wiki/C3H6Cl2

    1,3-Dichloropropane Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  5. Dichloropropane - Wikipedia

    en.wikipedia.org/wiki/Dichloropropane

    Dichloropropane can refer to any of several chemical compounds: 1,1-Dichloropropane; 1,2-Dichloropropane; 1,3-Dichloropropane; 2,2-Dichloropropane; See also

  6. 1,3-Dichloropropan-2-ol - Wikipedia

    en.wikipedia.org/wiki/1,3-Dichloropropan-2-ol

    1,3-DCP is a believed to be a carcinogen and mutagen. [4] The International Agency for Research on Cancer classifies it as a Group 2B carcinogen ("possibly carcinogenic to humans"). [5] Along with 3-monochloropropane-1,2-diol (3-MCPD), 1,3-DCP is found in some Asian style sauces such as soy sauce and oyster sauce. [6] [7] [8]

  7. List of chlorinated propanes - Wikipedia

    en.wikipedia.org/wiki/List_of_chlorinated_propanes

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  8. 1,2-Dichloropropane - Wikipedia

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

    1,2-Dichloropropane is an intermediate in the production of perchloroethylene and other chlorinated chemicals. [4] It was once used as a soil fumigant, chemical intermediate, as well as an industrial solvent and was found in paint strippers, varnishes, and furniture finish removers but some of these uses have been discontinued.

  9. Allyl chloride - Wikipedia

    en.wikipedia.org/wiki/Allyl_chloride

    At lower temperatures, the main product is 1,2-dichloropropane, but at 500 °C, allyl chloride predominates, being formed via a free radical reaction: CH 3 CH=CH 2 + Cl 2 → ClCH 2 CH=CH 2 + HCl. An estimated 800,000 tonnes were produced this way in 1997. [4]