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・ 1,4,6-Androstatriene-3,17-dione
・ 1,4,7-Triazacyclononane
・ 1,4,7-Trithiacyclononane
・ 1,4-a-glucan 6-a-glucosyltransferase
・ 1,4-Benzodioxine
・ 1,4-Benzoquinone
・ 1,4-beta-D-xylan synthase
・ 1,4-Butanediol
・ 1,4-Butynediol
・ 1,1,1-Trifluoroethane
・ 1,1,1-Tris(aminomethyl)ethane
・ 1,1,2,2,3,3-Hexachloropropane
・ 1,1,2,2-Tetrachloroethane
・ 1,1,2-Trichloro-1,2,2-trifluoroethane
・ 1,1,2-Trichloroethane
1,1,3,3-Tetramethylguanidine
・ 1,1,3-Trichloropropene
・ 1,1-Bis(diphenylphosphino)methane
・ 1,1-Dibromoethane
・ 1,1-Dichloro-1-fluoroethane
・ 1,1-Dichloroethane
・ 1,1-Dichloroethene
・ 1,1-Diethoxyethane
・ 1,1-Difluoroethane
・ 1,1-Difluoroethylene
・ 1,1-Ethanedithiol
・ 1,2,3 Soleils
・ 1,2,3,4,6-Pentagalloyl glucose
・ 1,2,3,4-Tetraphenylnaphthalene
・ 1,2,3,5-Tetrahydroxybenzene


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

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Tetramethylguanidine is an organic compound with the formula HNC(N(CH3)2)2. This colourless liquid is a strong base with a higher pKa than typical amines.
It was originally prepared from tetramethylthiourea via ''S''-methylation and amination, but alternative methods start from cyanogen iodide.
==Uses==
TMG is mainly used as a strong, non-nucleophilic base for alkylations, often as a substitute for the more expensive bases DBU and DBN.〔 Since it is highly water-soluble, it is easily removed from mixtures in organic solvents. It is also used as a base-catalyst in the production of polyurethane.

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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