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・ 1-alpha-O-Galloylpunicalagin
・ 1-Amino-2-propanol
・ 1-Amino-2-propanone
・ 1-Amino-3-phenylindole
・ 1-aminocyclopropane-1-carboxylate deaminase
・ 1,3-Benzodioxolyl-N-methylbutanamine
・ 1,3-Benzodioxolyl-N-methylpentanamine
・ 1,3-Benzodioxolylbutanamine
・ 1,3-beta-D-glucan phosphorylase
・ 1,3-beta-galactosyl-N-acetylhexosamine phosphorylase
・ 1,3-Beta-glucan synthase
・ 1,3-beta-oligoglucan phosphorylase
・ 1,3-Bis(dicyanomethylene)squarate
・ 1,3-Bis(diphenylphosphino)propane
・ 1,3-Bisphosphoglyceric acid
1,3-Butadiene
・ 1,3-Butadiene (data page)
・ 1,3-Butanediol
・ 1,3-Cycloheptadiene
・ 1,3-Cyclohexadiene
・ 1,3-DCP
・ 1,3-Dehydroadamantane
・ 1,3-Diaminopropane
・ 1,3-Diazepine
・ 1,3-Dibromopropane
・ 1,3-Dichlorobenzene
・ 1,3-Dichloropropane
・ 1,3-Dichloropropene
・ 1,3-Difluoro-2-propanol
・ 1,3-Dihydroxyanthraquinone


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1,3-Butadiene : ウィキペディア英語版
1,3-Butadiene

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1,3-Butadiene is a simple conjugated diene with the formula C4H6 . It is an important industrial chemical used as a monomer in the production of synthetic rubber. The word butadiene usually refers to 1,3–butadiene which has the structure H2C=CH—CH=CH2.
Although butadiene breaks down quickly in the atmosphere, it is nevertheless found in ambient air in urban and suburban areas as a consequence of its constant emission from motor vehicles. The EPA lists it as the "mobile source air toxic" with the highest normalized risk factor, exceeding that of formaldehyde, the second riskiest air toxic emitted by motor vehicles, by a factor of more than 20.
The name butadiene can also refer to the isomer, 1,2–butadiene, which is a cumulated diene with structure H2C=C=CH—CH3. However, this allene is difficult to prepare and has no industrial significance. This diene is also not expected to act as a diene in a Diels–Alder reaction due to its structure. To effect a Diels-Alder reaction only a conjugated diene will suffice. The rest of this article concerns only 1,3–butadiene.
==History==
In 1863, the French chemist E. Caventou isolated a previously unknown hydrocarbon from the pyrolysis of amyl alcohol. This hydrocarbon was identified as butadiene in 1886, after Henry Edward Armstrong isolated it from among the pyrolysis products of petroleum. In 1910, the Russian chemist Sergei Lebedev polymerized butadiene, and obtained a material with rubber-like properties. This polymer was, however, found to be too soft to replace natural rubber in many applications, notably automobile tires.
The butadiene industry originated in the years leading up to World War II. Many of the belligerent nations realized that in the event of war, they could be cut off from rubber plantations controlled by the British Empire, and sought to reduce their dependence on natural rubber. In 1929, Eduard Tschunker and Walter Bock, working for IG Farben in Germany, made a copolymer of styrene and butadiene that could be used in automobile tires. Worldwide production quickly ensued, with butadiene being produced from grain alcohol in the Soviet Union and the United States and from coal-derived acetylene in Germany.

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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