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  2. Hydrophobicity scales - Wikipedia

    en.wikipedia.org/wiki/Hydrophobicity_scales

    [26] 1-butanol and pyridine were used as the mobile phase in this particular scale and glycine was used as the reference value. Pliska and his coworkers [ 27 ] used thin layer chromatography to relate mobility values of free amino acids to their hydrophobicities.

  3. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Pyridine is a basic heterocyclic organic compound with the chemical formula C 5 H 5 N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom (=N−). It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish

  4. Sweetness - Wikipedia

    en.wikipedia.org/wiki/Sweetness

    Some of the amino acids are mildly sweet: alanine, glycine, and serine are the sweetest. Some other amino acids are perceived as both sweet and bitter. The sweetness of 5% solution of glycine in water compares to a solution of 5.6% glucose or 2.6% fructose. [14]

  5. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  6. Glycine - Wikipedia

    en.wikipedia.org/wiki/Glycine

    Although glycine can be isolated from hydrolyzed proteins, this route is not used for industrial production, as it can be manufactured more conveniently by chemical synthesis. [23] The two main processes are amination of chloroacetic acid with ammonia , giving glycine and hydrochloric acid , [ 24 ] and the Strecker amino acid synthesis , [ 25 ...

  7. Purine metabolism - Wikipedia

    en.wikipedia.org/wiki/Purine_metabolism

    The amino acid glycine contributes all its carbon (2) and nitrogen (1) atoms, with additional nitrogen atoms from glutamine (2) and aspartic acid (1), and additional carbon atoms from formyl groups (2), which are transferred from the coenzyme tetrahydrofolate as 10-formyltetrahydrofolate, and a carbon atom from bicarbonate (1). Formyl groups ...

  8. Chichibabin reaction - Wikipedia

    en.wikipedia.org/wiki/Chichibabin_reaction

    The reaction occurs faster under more basic conditions but only up to a point because when electron density builds up on the α-carbon, it makes it less electrophilic. The strongest base known to aminate is 4-dimethylaminopyridine (pKa 9.37). [3]

  9. Glycin - Wikipedia

    en.wikipedia.org/wiki/Glycin

    Glycin, or N-(4-hydroxyphenyl)glycine, is N-substituted p-aminophenol. It is a photographic developing agent used in classic black-and-white developer solutions. [2] It is not identical to, but derived from glycine, the proteinogenic amino acid. It is typically characterized as thin plates of white or silvery powder, although aged samples ...