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・ 2,5-Dimethoxy-4-trifluoromethylamphetamine
・ 2'-phosphotransferase
・ 2(x)ist
・ 2+1
・ 2+1 road
・ 2+2
・ 2+2 (2012 film)
・ 2+2 (car body style)
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・ 2,000 Feet Away
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2,2'-Azobis(2-amidinopropane) dihydrochloride
・ 2,2'-Bipyridine
・ 2,2'-Bis(2-indenyl) biphenyl
・ 2,2'-Dipyridyldisulfide
・ 2,2,2-Trichlorethoxycarbonyl chloride
・ 2,2,2-Trichloroethanol
・ 2,2,2-Trifluoroethanol
・ 2,2,3,3-Tetramethylsuccinic acid
・ 2,2,4,4-Tetramethyl-1,3-cyclobutanediol
・ 2,2,4,4-Tetramethyl-3-t-butyl-pentane-3-ol
・ 2,2,4-Trimethylpentane
・ 2,2,5,5-Tetramethyltetrahydrofuran
・ 2,2,6,6-Tetramethylpiperidine
・ 2,2-Di-2-furylpropane
・ 2,2-dialkylglycine decarboxylase (pyruvate)


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2,2'-Azobis(2-amidinopropane) dihydrochloride : ウィキペディア英語版
2,2'-Azobis(2-amidinopropane) dihydrochloride

2,2'-Azobis(2-amidinopropane) dihydrochloride (AAPH) is a chemical compound used to study the chemistry of the oxidation of drugs.
It is a free radical-generating azo compound. It is gaining prominence as a model oxidant in small molecule and protein therapeutics for its ability to initiate oxidation reactions via both nucleophilic and free radical mechanisms.
2,2′-azobis (2-amidinopropane) dihydrochloride has been used in experiments on linoleic acid subjected to induced oxidation with different combinations of binary mixtures of natural phenolics. The experiments show that some binary mixtures can lead to a synergetic antioxidant effect while other mixtures lead to an antagonistic effect.〔Antioxidant activity of phenolic compounds in 2,2′-azobis (2-amidinopropane) dihydrochloride (AAPH)-induced oxidation: Synergistic and antagonistic effects. M. N. Peyrat-Maillard, M. E. Cuvelier and C. Berset, Journal Of The American Oil Chemists' Society, 2003, Volume 80, Number 10, pages 1007-1012, 〕
== References ==


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