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  2. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    Ethylamine, also known as ethanamine, is an organic compound with the formula CH 3 CH 2 NH 2. This colourless gas has a strong ammonia -like odor. It condenses just below room temperature to a liquid miscible with virtually all solvents.

  3. 4-Methylphenethylamine - Wikipedia

    en.wikipedia.org/wiki/4-Methylphenethylamine

    4-Methylphenethylamine (4MPEA), also known as para-methylphenethylamine, is an organic compound with the chemical formula of C 9 H 13 N.4MPEA is a human trace amine associated receptor 1 (TAAR1) agonist, [2] a property which it shares with its monomethylated phenethylamine isomers, such as amphetamine (α-methylphenethylamine), β-methylphenethylamine, and N-methylphenethylamine (a trace amine).

  4. 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.

  5. N,N-Diethylmethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-diethylmethylamine

    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.

  6. Petasis reaction - Wikipedia

    en.wikipedia.org/wiki/Petasis_reaction

    Vinylboronic acid is first coupled with L-arabinose 1 and Bis(4-methoxyphenyl)methanamine 2 to form an stereochemically defined allyl amine 3. Afterwards, the sequence of dipolar cycloaddition, base-mediated N–O bond breakage and hydrolysis then complete the synthesis of N-acetylneuraminic acid.

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  8. Route of administration - Wikipedia

    en.wikipedia.org/wiki/Route_of_administration

    Intradermal, (into the skin itself) is used for skin testing some allergens, and also for mantoux test for tuberculosis. Intralesional (into a skin lesion), is used for local skin lesions, e.g. acne medication. Intramuscular (into a muscle), e.g. many vaccines, antibiotics, and long-term psychoactive agents. Recreationally the colloquial term ...

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