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  2. 2-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/2-Methylpyridine

    2-Methylpyridine, or 2-picoline, is the compound described with formula C 6 H 7 N. 2-Picoline is a colorless liquid that has an unpleasant odor similar to pyridine. It is mainly used to make vinylpyridine and the agrichemical nitrapyrin .

  3. Picoline - Wikipedia

    en.wikipedia.org/wiki/Picoline

    By 1879, the Austrian chemist Hugo Weidel had succeeded in isolating and characterizing three isomers of picoline, which he denoted α–, β–, and γ–picoline: [10] α–picoline was the main component of impure picoline; it was accompanied by small quantities of β–picoline; and γ–picoline was produced by Baeyer's dry distillation of ...

  4. 3-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/3-Methylpyridine

    3-Methylpyridine or 3-picoline, is an organic compound with formula 3-CH 3 C 5 H 4 N. It is one of three positional isomers of methylpyridine, whose structures vary according to where the methyl group is attached around the pyridine ring. This colorless liquid is a precursor to pyridine derivatives that have applications in the pharmaceutical ...

  5. Picolinic acid - Wikipedia

    en.wikipedia.org/wiki/Picolinic_acid

    Picolinic acid is an organic compound with the formula NC 5 H 4 CO 2 H.It is a derivative of pyridine with a carboxylic acid (COOH) substituent at the 2-position. It is an isomer of nicotinic acid and isonicotinic acid, which have the carboxyl side chain at the 3- and 4-positions, respectively.

  6. 4-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/4-Methylpyridine

    It forms via the reaction of acetaldehyde and ammonia in the presence of an oxide catalyst. The method also affords some 2-methylpyridine . 4-Methylpyridine is of little intrinsic value but is a precursor to other commercially significant species, often of medicinal interest.

  7. Thermal decomposition - Wikipedia

    en.wikipedia.org/wiki/Thermal_decomposition

    The reaction is usually endothermic as heat is required to break chemical bonds in the compound undergoing decomposition. If decomposition is sufficiently exothermic, a positive feedback loop is created producing thermal runaway and possibly an explosion or other chemical reaction. Thermal decomposition is a chemical reaction where heat is a ...

  8. Category:Degradation reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Degradation_reactions

    Degradation reactions reduce the number of atoms in a molecule through a specific type of chemical transformation. Pages in category "Degradation reactions" The following 15 pages are in this category, out of 15 total.

  9. Cometabolism - Wikipedia

    en.wikipedia.org/wiki/Cometabolism

    Cometabolism is defined as the simultaneous degradation of two compounds, in which the degradation of the second compound (the secondary substrate) depends on the presence of the first compound (the primary substrate). [1] This is in contrast to simultaneous catabolism, where each substrate is catabolized concomitantly by different enzymes.