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The bond length for C=N is 1.279 Å, and for the N-C bond it is 1.458 Å. The ∠ C=N-C is 116.6°. [4] The electric dipole moment is 1.53 Debye. [6] When heated to 535°, N-methylmethanimine decomposes to hydrogen cyanide (HCN) and methane (CH 4). [4] Between 400 and 550°C, the cyclic amine, aziridine decomposes to a mixture of N ...
The molecular formula C 2 H 5 N (molar mass: 43.07 g/mol, exact mass: 43.0422 u) can refer to: Aziridine; Ethanimine or its tautomer, vinylamine; N-Methylmethanimine
Methylamine has been produced industrially since the 1920s (originally by Commercial Solvents Corporation for dehairing of animal skins). [4] This was made possible by Kazimierz Smoleński [] and his wife Eugenia who discovered amination of alcohols, including methanol, on alumina or kaolin catalyst after WWI, filed two patent applications in 1919 [5] and published an article in 1921.
N-Methylethanolamine is a clear, colorless, hygroscopic, amine-like smelling liquid which is miscible with water and ethanol in any ratio. Aqueous solutions react strongly basic and are therefore corrosive. The substance is easily biodegradable and has no potential of bioaccumulation due to its water miscibility.
The bitartrate salt of DMAE, i.e. N,N-dimethylethanolamine bitartrate, is sold as a dietary supplement. [5] It is a white powder providing 37% DMAE. [6] Animal tests show possible benefit for improving spatial memory [7] and working memory. [8]
Ethylmethylamine, or N-methylethanamine, is a compound with the chemical formula C 3 H 9 N. It is corrosive and highly flammable. [1] References This page was last ...
N,N-Diethylmethylamine (diethylmethylamine, DEMA) is a tertiary amine with the formula C 5 H 13 N. N,N-Diethylmethylamine is a clear, colorless to pale yellow liquid at room temperature, and is used in various industrial and scientific applications including water desalination as well as analytical and organic chemistry. [1] [2] [3] [4]
Structural parameters determined by microwave spectroscopy include a C=N bond length of 1.27 Å, an N–H bond length of 1.02 Å and an H−N=C bond angle of 110.5°. [2] Because unhindered imines polymerize or oligomerize when concentrated, methylene imine has not been isolated as a liquid or bulk solid.