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・ 1-Hexene (data page)
・ 1-hydroxy-2-naphthoate 1,2-dioxygenase
・ 1-hydroxy-2-naphthoate hydroxylase
・ 1-Hydroxy-7-azabenzotriazole
・ 1-Hydroxycarotenoid 3,4-desaturase
・ 1-Hydroxyphenanthrene
・ 1-Hydroxypyrene
・ 1-Ichi
・ 1,4-Cycloheptadiene
・ 1,4-Cyclohexadiene
・ 1,4-Cyclohexanedione
・ 1,4-Diamino-2,3-dihydroanthraquinone
・ 1,4-Diazepine
・ 1,4-Dibromobenzene
・ 1,4-Dichloro-2-nitrobenzene
1,4-Dichlorobenzene
・ 1,4-Dichlorobut-2-ene
・ 1,4-dihydroxy-2-naphthoate polyprenyltransferase
・ 1,4-dihydroxy-2-naphthoyl-CoA hydrolase
・ 1,4-Dihydroxyanthraquinone
・ 1,4-Dimethoxybenzene
・ 1,4-Dioxane
・ 1,4-Dioxene
・ 1,4-Dioxin
・ 1,4-lactonase
・ 1,4-Naphthoquinone
・ 1,4-Thiazepine
・ 1,5-anhydro-D-fructose dehydratase
・ 1,5-anhydro-D-fructose reductase
・ 1,5-anhydro-D-fructose reductase (1,5-anhydro-D-mannitol-forming)


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1,4-Dichlorobenzene : ウィキペディア英語版
1,4-Dichlorobenzene

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1,4-Dichlorobenzene (''p''-DCB or ''para''-dichlorobenzene, sometimes abbreviated as PDB or para) is an organic compound with the formula C6H4Cl2. This colorless solid has a strong odor. In terms of its structure, the molecule consists of two chlorine atoms substituted for hydrogen at opposing sites on a benzene ring. ''p''-DCB is used as a pesticide and a deodorant, most familiarly in mothballs in which it is a replacement for the more traditional naphthalene due to its flammability. ''p''-DCB is also used as a precursor in the production of the polymer poly(p-phenylene sulfide).
== Production ==
''p''-DCB is produced by chlorination of benzene using ferric chloride as a catalyst:
:C6H6 + 2 Cl2 → C6H4Cl2 + 2 HCl
The chief impurity is the 1,2 isomer. The compound can be purified by fractional crystallisation, taking advantage of its relatively high melting point of 53.5 °C; the isomeric dichlorobenzenes and chlorobenzene melt well below room temperature.〔

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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