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  2. 4-tert-Butylphenol - Wikipedia

    en.wikipedia.org/wiki/4-tert-Butylphenol

    It has also found use as a plasticizer. Bisphenol A is difunctional and used to produce epoxy resin and polycarbonate. 4-tert-Butylphenol is monofunctional and so in polymer science terms, bisphenol A is a polymer chain extender but 4-tert-butylphenol is a chain stopper or sometimes called endcapper. It is thus use to control molecular weight ...

  3. Bis(2,4-di-tert-butylphenyl) pentaerythritol diphosphite ...

    en.wikipedia.org/wiki/Bis(2,4-di-tert-butyl...

    Bis(2,4-di-tert-butylphenyl) pentaerythritol diphosphite is an organophosphite used as a polymer stabilizer in plastics. Like other phosphite antioxidants it primarily acts to remove hydroperoxides and is typically used in combination with hindered phenolic antioxidants such as pentaerythritol tetrakis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate) .

  4. 2,4-Di-tert-butylphenol - Wikipedia

    en.wikipedia.org/wiki/2,4-di-tert-butylphenol

    2,4-Di-tert-butylphenol (2,4-DTBP) is a white solid with a phenolic odour. It is primarily used as a raw material for the production of several commercially important antioxidants and phenolic benzotriazole-type UV absorbers. It also finds use as a starting material in the synthesis of agrochemicals, fragrances and catalysts (i.e. Jacobsen's ...

  5. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    In reaction depicted below 3,4,5-trimethylphenol reacts with singlet oxygen generated from oxone/sodium carbonate in an acetonitrile/water mixture to a para-peroxyquinole. This hydroperoxide is reduced to the quinole with sodium thiosulfate. Phenols are oxidized to hydroquinones in the Elbs persulfate oxidation.

  6. Alkylphenol - Wikipedia

    en.wikipedia.org/wiki/Alkylphenol

    The term is usually reserved for commercially important propylphenol, butylphenol, amylphenol, heptylphenol, octylphenol, nonylphenol, dodecylphenol and related "long chain alkylphenols" (LCAPs). Methylphenols and ethylphenols are also alkylphenols, but they are more commonly referred to by their specific names, cresols and xylenols. [ 1 ]

  7. 2,4,6-Tri-tert-butylphenol - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Tri-tert-butylphenol

    [5] 2,4,6-tri-tert-butylphenol is also found as a by-product in the synthesis of the disubstitution products 2,4-DTBP and 2,6-DTBP, which are more widely used antioxidants. [2] Synthese von 2,4,6-Tri-tert-butylphenol mit Isobuten. A synthesis of 2,4,6-tri-tert-butylphenol has been described that is also suitable as a teaching experiment.

  8. You Just Got a Slow Cooker—Here Are 16 Heart-Healthy ... - AOL

    www.aol.com/just-got-slow-cooker-16-140000338.html

    This simple vegetarian pasta bake is rich in protein and comes together effortlessly in the slow cooker, for a convenient one-pot meal. The combination of sun-dried tomatoes, sun-dried tomato ...

  9. 2-tert-Butylphenol - Wikipedia

    en.wikipedia.org/wiki/2-Tert-butylphenol

    2-tert-Butyl phenol is an organic compound with the formula (CH 3) 3 CC 6 H 4 OH. It is one of three isomeric tert-butyl phenols. It is a colorless oil that dissolves in basic water. It can be prepared by acid-catalyzed alkylation of phenol with isobutene. [2]