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・ Dimethylargininase
・ Dimethylbenzimidazole
・ Dimethylbenzylamine
・ Dimethylbutadiene
・ Dimethylbutane
・ Dimethyldiborane
・ Dimethyldichlorosilane
・ Dimethyldiethoxysilane
・ Dimethyldioxirane
・ Dimethylethanolamine
・ Dimethylformamide
・ Dimethylglycine
・ Dimethylglycine dehydrogenase
・ Dimethylglycine N-methyltransferase
・ Dimethylglycine oxidase
Dimethylglyoxime
・ Dimethylheptylpyran
・ Dimethylhexane
・ Dimethylhistidine N-methyltransferase
・ Dimethylhydrazine
・ Dimethyllysergamide
・ Dimethylmagnesium
・ Dimethylmalate dehydrogenase
・ Dimethylmaleate hydratase
・ Dimethylmercury
・ Dimethylol ethylene urea
・ Dimethylphenethylamine
・ Dimethylphenylphosphine
・ Dimethylphenylpiperazinium
・ Dimethylpiperidine


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Dimethylglyoxime : ウィキペディア英語版
Dimethylglyoxime

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Dimethylglyoxime is a chemical compound described by the formula CH3C(NOH)C(NOH)CH3. Its abbreviation is dmgH2 for neutral form, and dmgH for anionic form, where H stands for hydrogen. This colourless solid is the dioxime derivative of the diketone butane-2,3-dione (also known as diacetyl). DmgH2 is used in the analysis of palladium or nickel. Its coordination complexes are of theoretical interest as models for enzymes and as catalysts. Many related ligands can be prepared from other diketones, e.g. benzil.
==Preparation==
Dimethylglyoxime can be prepared from butanone first by reaction with ethyl nitrite followed by sodium hydroxylamine monosulfonate:
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