![]() J Agric Food Chem 20:649–656Īstrand I (1975) Uptake of solvents in the blood and tissues of man. November (unpublished)Īnderson KJ, Leighty EG, Takahaski MT (1972) Evaluation of herbicides for possible mutagenic properties. November (unpublished)Īnderson D, Richardson CR a (1976) Para-dichlorobenzene: cytogenic study in the rat. November (unpublished)Īnderson D, Hodge MCE a (1976) Para-dichlorobenzene: dominant lethal study in the mouse. This process is experimental and the keywords may be updated as the learning algorithm improves.Īnderson D a (1976) Para-dichlorobenzene: Estimation of its mutagenic potential in the Salmonella typhimurium plate incorporation mutagenicity assay. These keywords were added by machine and not by the authors. Production levels for the meta-isomer were not reported but are believed to be small. Production of the DCB isomers in 1981 was 11 million lb (4.99 million kg) for the ortho-isomer and 15 million (6.8 million kg) for the para-isomer. There are no natural sources for the three isomers of dichlorobenzene (DCB). For the structures and properties of ortho-, meta-, and para-dichlorobenzene, see Tables 1, 2, and 3, respectively. The first is used as a solvent, chemical intermediate, and deodorizer the second has no documented use and the third is used as a deodorizer and insecticide. Historically, p-DCB is also known as PDB. Ortho-, meta-, and para-dichlorobenzene (1,2-dichlorobenzene, 1,3-dichloro-benzene, 1,4-dichlorobenzene, respectively) are also called o-DCB, m-DCB, and p-DCB.
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