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| Section2 = | Section4 = | Section7 = }} 1,4-Dioxane, often simply called dioxane because the 1,2 and 1,3 isomers of dioxane are rare, is a heterocyclic organic compound. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether. It is classified as an ether. Dioxane is used mainly as a stabilizer for the solvent trichloroethane. It is an occasionally used solvent for a variety of practical applications as well as in the laboratory. ==Synthesis and structure== Dioxane is produced by the acid-catalysed dehydration of diethylene glycol, which in turn arises from the hydrolysis of ethylene oxide. The molecule is centrosymmetric, meaning that it adopts a chair conformation, typical of relatives of cyclohexane. The molecule is conformationally flexible, and the boat conformation is easily adopted, as required for chelation to metal cations. In 1985, the global production capacity for dioxane was between 11,000 and 14,000 tons.〔 In 1990, the total U.S. production volume of dioxane was between 10,500,000 and 18,300,000 pounds. Dioxane has three isomers: in addition to 1,4-dioxane, 1,2-dioxane and 1,3-dioxane are also known. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「1,4-Dioxane」の詳細全文を読む スポンサード リンク
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