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  2. Pyridine (data page) - Wikipedia

    en.wikipedia.org/wiki/Pyridine_(data_page)

    Phase behavior Triple point: 231.48 K (–41.67 °C), ? Pa Critical point: 619 K (346 °C), 5660 Pa Std enthalpy change of fusion, Δ fus H o: 8.28 kJ/mol Std entropy change

  3. Pyridinium chloride - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chloride

    Containing a pyridinium ion, pyridinium chloride has a pK a of approximately 5, slightly more acidic than that of typical amines.This is due to the hybridization of the nitrogen: the nitrogen is sp 2 hybridized and more electronegative than those nitrogens in ammonium cations, which are sp 3 hybridized.

  4. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Pyridine and poly(4-vinyl) pyridine have been shown to form conducting molecular wires with remarkable polyenimine structure on UV irradiation, a process which accounts for at least some of the visible light absorption by aged pyridine samples. These wires have been theoretically predicted to be both highly efficient electron donors and ...

  5. 3-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/3-Methylpyridine

    3-methyl pyridine is biodegradable, although it degrades more slowly and volatilize more readily from water samples than either 2-methyl- or 4-methyl-pyridine., [7] [8] 3-Methylpyridine is the main precursor to niacin , one of the B vitamins .

  6. Pyridinium chlorochromate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chlorochromate

    Pyridinium chlorochromate in a vial. Pyridinium chlorochromate (PCC) is a yellow-orange salt with the formula [C 5 H 5 NH] + [CrO 3 Cl] −.It is a reagent in organic synthesis used primarily for oxidation of alcohols to form carbonyls.

  7. 2-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloropyridine

    Although pyridine is an excellent source of carbon, nitrogen, and energy for certain microorganisms, introduction of a halogen moiety significantly retards degradation of the pyridine ring. With the exception of 4-chloropyridine, each of the mono- and di-substituted chloropyridines were found to be relatively resistant to microbiological ...

  8. 2,4,6-Trimethylpyridine - Wikipedia

    en.wikipedia.org/wiki/2,4,6-trimethylpyridine

    2,4,6-Trimethylpyridine (2,4,6-collidine) is an organic compound which belongs to the heterocycles (more precisely, heteroaromatics).It consists of a pyridine ring substituted with three methyl groups.

  9. Cetylpyridinium chloride - Wikipedia

    en.wikipedia.org/wiki/Cetylpyridinium_chloride

    Cetylpyridinium chloride is known to cause tooth staining in approximately 3 percent of users. [14] The Crest brand has noted that this staining is actually an indication that the product is working as intended, as the stains are a result of bacteria dying on the teeth. [15]