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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.
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 ] It has low acute toxicity.
In other projects Wikidata item; Appearance. move to sidebar hide. The chemical abbreviation 1,3 ... 1,3-Dichloropropene This page was last edited on 13 March 2018 ...
In other projects Wikidata item; Appearance. move to sidebar hide. Dichloropropane can refer to any of several chemical compounds: 1,1-Dichloropropane; 1,2 ...
[2] [3] 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]
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.
Pre-1980s, agricultural use of chloropropane-containing soil fumigants for use as pesticides and nematicides was prevalent in the United States. Some soil fumigants, which contained a mixture of primarily 1,3-dichloropropene and 1,2-dichloropropane, and in which 1,2,3-TCP was a minor component, e.g., trade name of D-D, were marketed for the cultivation of various crops including citrus fruits ...
R-dichlorprop (dichlorprop-p). Dichlorprop possesses a single asymmetric carbon and is therefore a chiral molecule, however only the R-isomer is active as an herbicide.When dichlorprop was first marketed in the 1960s, it was sold as racemic mixture of stereoisomers, but since then advances in asymmetric synthesis have made possible the production of the enantiopure compound.