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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. Transamination - Wikipedia

    en.wikipedia.org/wiki/Transamination

    A second type of transamination reaction can be described as a nucleophilic substitution of one amine or amide anion on an amine or ammonium salt. [1] For example, the attack of a primary amine by a primary amide anion can be used to prepare secondary amines: RNH 2 + R'NH − → RR'NH + NH 2

  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. Chemosynthesis - Wikipedia

    en.wikipedia.org/wiki/Chemosynthesis

    Venenivibrio stagnispumantis gains energy by oxidizing hydrogen gas.. In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules (usually carbon dioxide or methane) and nutrients into organic matter using the oxidation of inorganic compounds (e.g., hydrogen gas, hydrogen sulfide) or ferrous ions as a source of energy, rather than sunlight, as in ...

  6. 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atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...

  7. Hydroxy group - Wikipedia

    en.wikipedia.org/wiki/Hydroxy_group

    Sulfuric acid contains two hydroxy groups.. Water, alcohols, carboxylic acids, and many other hydroxy-containing compounds can be readily deprotonated due to a large difference between the electronegativity of oxygen (3.5) and that of hydrogen (2.1).

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  9. Phenylpropylaminopentane - Wikipedia

    en.wikipedia.org/wiki/Phenylpropylaminopentane

    1-Phenyl-2-propylaminopentane (PPAP; developmental code name MK-306) is an experimental drug related to selegiline which acts as a catecholaminergic activity enhancer (CAE). [1] [2] [3] [4]

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