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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 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]
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.
Dr. Cox's Barbed Wire Liniment and Antiseptic, made by Myers Laboratory. Marketed as treatment for minor wounds (contains iodine) for livestock and humans, such as barbed wire scratches. [10] IcyHot is a line of liniments produced and marketed by Chattem, now a subsidiary of Sanofi. [11]
Esoterica is an over-the-counter topical ointment applied to the skin for the purpose of lightening freckles, age spots, chloasma, melasma, and other skin discolorations due to a benign localized increase in the production of melanin.
Methenamine, also known as 1,3,5,7-tetraazaadamantane, is a simple cyclic hydrocarbon with a cage-like structure and is similar in structure to adamantane (tricyclo[3.3.1.1 3,7]decane). [ 2 ] [ 13 ] [ 7 ] [ 8 ] [ 37 ] It is specifically the analogue of adamantane in which the carbon atoms at the 1, 3, 4, and 7 positions have been replaced with ...
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.