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  2. Ethylmethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylmethylamine

    Ethyl(methyl)amine. Identifiers CAS Number. 624-78-2 ... This page was last edited on 2 September 2024, at 12:46 (UTC).

  3. Ethanolamine - Wikipedia

    en.wikipedia.org/wiki/Ethanolamine

    Ethanolamine (2-aminoethanol, monoethanolamine, ETA, or MEA) is a naturally occurring organic chemical compound with the formula HOCH 2 CH 2 NH 2 or C 2 H 7 NO. [8] The molecule is bifunctional, containing both a primary amine and a primary alcohol. Ethanolamine is a colorless, viscous liquid with an odor reminiscent of ammonia. [9]

  4. N-Methylethanolamine - Wikipedia

    en.wikipedia.org/wiki/N-Methylethanolamine

    N-Methylethanolamine is an alkanolamine with the formula CH 3 NHCH 2 CH 2 OH. It is flammable, corrosive, colorless, viscous liquid. [2] It is an intermediate in the biosynthesis of choline. With both an amine and a hydroxyl functional groups, it is a useful intermediate in the chemical synthesis of various

  5. Dimethylethanolamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylethanolamine

    Dimethylethanolamine (DMAE or DMEA) is an organic compound with the formula (CH 3) 2 NCH 2 CH 2 OH. It is bifunctional, containing both a tertiary amine and primary alcohol functional groups. It is a colorless viscous liquid. It is used in skin care products for improving skin tone and also taken orally as a nootropic.

  6. Methyldiethanolamine - Wikipedia

    en.wikipedia.org/wiki/Methyldiethanolamine

    MDEA is less reactive towards CO 2, but has an equilibrium loading capacity approaching 1 mole CO 2 per mole amine. [2] It also requires less energy to regenerate. [2] To combine the advantages of MDEA and the smaller amines, MDEA is usually mixed with a catalytic promoter such as piperazine, PZ, or a fast reacting amine such as MEA to retain reactivity, but lower regeneration costs.

  7. Methylamine - Wikipedia

    en.wikipedia.org/wiki/Methylamine

    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.

  8. Aminoethylethanolamine - Wikipedia

    en.wikipedia.org/wiki/Aminoethylethanolamine

    This article about an amine is a stub. You can help Wikipedia by expanding it.

  9. N-Methylphenethylamine - Wikipedia

    en.wikipedia.org/wiki/N-Methylphenethylamine

    N-Methylphenethylamine (NMPEA) is a naturally occurring trace amine neuromodulator in humans that is derived from the trace amine, phenethylamine (PEA). [2] [3] It has been detected in human urine (<1 μg over 24 hours) [4] and is produced by phenylethanolamine N-methyltransferase with phenethylamine as a substrate, which significantly increases PEA's effects.