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  2. 1-Aminopentane - Wikipedia

    en.wikipedia.org/wiki/1-aminopentane

    1-Aminopentane is an organic compound with the formula CH 3 (CH 2) 4 NH 2. It is used as a solvent , as a raw material in the manufacture of a variety of other compounds, including dyes, emulsifiers , and pharmaceutical products, [ 1 ] and as a flavoring agent .

  3. C5H13N - Wikipedia

    en.wikipedia.org/wiki/C5H13N

    The molecular formula C 5 H 13 N (molar mass: 87.166 g/mol, exact mass: 87.10480 u) may refer to: 1-Aminopentane; 3-Aminopentane; N,N-Diethylmethylamine;

  4. Aminopentane - Wikipedia

    en.wikipedia.org/wiki/Aminopentane

    Aminopentane may refer to: 1-Aminopentane; 2-Aminopentane; 3-Aminopentane This page was last edited on 4 August 2019, at 16:05 (UTC). Text is available under the ...

  5. Enthalpy of neutralization - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_of_neutralization

    In chemistry and thermodynamics, the enthalpy of neutralization (ΔH n) is the change in enthalpy that occurs when one equivalent of an acid and a base undergo a neutralization reaction to form water and a salt. It is a special case of the enthalpy of reaction. It is defined as the energy released with the formation of 1 mole of water.

  6. Indolylpropylaminopentane - Wikipedia

    en.wikipedia.org/wiki/Indolylpropylaminopentane

    The effects of MAEs appear to be mediated by intracellular TAAR1 agonism coupled with uptake by monoamine transporters into monoaminergic neurons. [3] [4] In contrast to amphetamines, IPAP has no classical monoamine releasing agent actions. [1] [3] It is a weak MAO-A inhibitor similarly to BPAP. [1] [2] [5]

  7. Adiponitrile - Wikipedia

    en.wikipedia.org/wiki/Adiponitrile

    Because of the industrial value of adiponitrile, many methods have been developed for its synthesis. Early industrial methods started from furfural and later by the chlorination of butadiene to give 1,4-dichloro-2-butene, which with sodium cyanide, converts to 3-hexenedinitrile, which in turn can be hydrogenated to adiponitrile: [4]

  8. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    CH 3 CHO + NH 3 + H 2 → CH 3 CH 2 NH 2 + H 2 O. Ethylamine can be prepared by several other routes, but these are not economical. Ethylene and ammonia combine to give ethylamine in the presence of a sodium amide or related basic catalysts. [5] H 2 C=CH 2 + NH 3 → CH 3 CH 2 NH 2. Hydrogenation of acetonitrile, acetamide, and nitroethane ...

  9. Phosphoric acids and phosphates - Wikipedia

    en.wikipedia.org/wiki/Phosphoric_acids_and...

    Since the ends are condensed, its formula has one less H 2 O (water) than tripolyphosphoric acid. The general formula of a phosphoric acid is H n−2x+2 P n O 3n−x+1, where n is the number of phosphorus atoms and x is the number of fundamental cycles in the molecule's structure; that is, the minimum number of bonds that would have to be ...

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