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  2. Aliphatic amine - Wikipedia

    en.wikipedia.org/?title=Aliphatic_amine&redirect=no

    From a subtopic: This is a redirect from a subtopic of the target article or section.. If the redirected subtopic could potentially have its own article in the future, then also tag the redirect with {{R with possibilities}} and {{R printworthy}}.

  3. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...

  4. Béchamp reduction - Wikipedia

    en.wikipedia.org/wiki/Béchamp_reduction

    Tertiary aliphatic nitro compounds, however, are converted in good yield to the amine using the Béchamp reduction. [6] The reduction proceeds in a multistep manner. First, the nitro group is reduced to nitroso, which undergoes hydrogenation to a hydroxylamino group prior to further reduction to the amine. [7] Proposed mechanism of the Bechamp ...

  5. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Aliphatic compounds can be saturated, joined by single bonds (), or unsaturated, with double bonds or triple bonds ().If other elements (heteroatoms) are bound to the carbon chain, the most common being oxygen, nitrogen, sulfur, and chlorine, it is no longer a hydrocarbon, and therefore no longer an aliphatic compound.

  6. Zincke reaction - Wikipedia

    en.wikipedia.org/wiki/Zincke_reaction

    With secondary amines and not primary amines the Zincke reaction takes on a different shape forming so-called Zincke aldehydes in which the pyridine ring is ring-opened with the terminal iminium group hydrolyzed to an aldehyde: [4] Zincke aldehydes. This variation has been applied in the synthesis of novel indoles: [11] Zincke aldehydes Kearney ...

  7. Epoxy - Wikipedia

    en.wikipedia.org/wiki/Epoxy

    Aliphatic, cycloaliphatic and aromatic amines are all employed as epoxy hardeners. Amine type hardeners will alter both the processing properties (viscosity, reactivity) and the final properties (mechanical, temperature and heat resistance) of the cured copolymer network. Thus amine structure is normally selected according to the application.

  8. Polyethylenimine - Wikipedia

    en.wikipedia.org/wiki/Polyethylenimine

    Polyethylenimine (PEI) or polyaziridine is a polymer with repeating units composed of the amine group and two carbon aliphatic CH 2 CH 2 spacers. Linear polyethyleneimines contain all secondary amines , in contrast to branched PEIs which contain primary, secondary and tertiary amino groups.

  9. 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.