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・ 4-HO-MPT
・ 4-HO-pyr-T
・ 4-HO-αMT
・ 4-HTMPIPO
・ 4-Hydroxy-2-alkylquinoline
・ 4-hydroxy-2-oxoglutarate aldolase
・ 4-Hydroxy-2-oxopentanoic acid
・ 4-hydroxy-2-oxovalerate aldolase
・ 4-Hydroxy-3-methoxymethamphetamine
・ 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase
・ 4-Hydroxy-3-methylbut-2-enyl diphosphate reductase
・ 4-hydroxy-4-methyl-2-oxoglutarate aldolase
・ 4-Hydroxy-4-methylpentanoic acid
・ 4-Hydroxy-5-methoxydimethyltryptamine
・ 4-Hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl glucoside beta-D-glucosidase
4-Hydroxy-TEMPO
・ 4-hydroxy-tetrahydrodipicolinate reductase
・ 4-hydroxy-tetrahydrodipicolinate synthase
・ 4-hydroxyacetophenone monooxygenase
・ 4-Hydroxyamphetamine
・ 4-Hydroxybenzaldehyde
・ 4-hydroxybenzaldehyde dehydrogenase
・ 4-hydroxybenzoate 1-hydroxylase
・ 4-Hydroxybenzoate 3-hydroxylase
・ 4-hydroxybenzoate 3-monooxygenase
・ 4-hydroxybenzoate 3-monooxygenase (NAD(P)H)
・ 4-hydroxybenzoate 4-O-beta-D-glucosyltransferase
・ 4-hydroxybenzoate decarboxylase
・ 4-Hydroxybenzoate geranyltransferase
・ 4-hydroxybenzoate nonaprenyltransferase


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4-Hydroxy-TEMPO : ウィキペディア英語版
4-Hydroxy-TEMPO

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4-Hydroxy-TEMPO or TEMPOL, formally 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl, is a heterocyclic compound. Like the related TEMPO, it is used as a catalyst and chemical oxidant by virtue of being a stable radical. It's major appeal over TEMPO is that is significantly cheaper, being produced from triacetone amine, which it itself made via the condensation of acetone and ammonia. This makes it economically viable on an industrial scale.
In medicine, it is recognized as an agent for detoxifying reactive oxygen species. It catalyses the disproportionation of superoxide.
==References==


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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