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  2. 4-tert-Butylphenol - Wikipedia

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

    4-tert-Butylphenol 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 white solid with a distinct phenolic odor.

  3. Tris(2,4-di-tert-butylphenyl)phosphite - Wikipedia

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

    Melting point: 181–184 °C (358–363 °F; 454–457 K) ... The compound is a phosphite ester formed by the reaction of 2,4-di-tert-butylphenol with phosphorus ...

  4. Bisphenol A - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A

    Melting point: 155 °C (311 °F ... temperature. 510 °C (950 °F ... 4-tert-Butylphenol - used as a chain-length regulator in the production of polycarbonates and ...

  5. 2,4-Dimethyl-6-tert-butylphenol - Wikipedia

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

    2,4-Dimethyl-6-tert-butylphenol is the organic compound with the formula Me 2 (tert-Bu)C 6 H 2 OH (Me = methyl, tert-Bu = tertiary butyl). It is a colorless oil that is classified as an alkylated phenol .

  6. 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 .

  7. Butylated hydroxytoluene - Wikipedia

    en.wikipedia.org/wiki/Butylated_hydroxytoluene

    The chemical synthesis of BHT in industry has involved the reaction of p-cresol (4-methylphenol) with isobutylene (2-methylpropene), catalyzed by sulfuric acid: [11] CH 3 (C 6 H 4)OH + 2 CH 2 =C(CH 3) 2 → ((CH 3) 3 C) 2 CH 3 C 6 H 2 OH. Alternatively, BHT has been prepared from 2,6-di-tert-butylphenol by hydroxymethylation or aminomethylation ...

  8. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    The effect of the tert-butyl group on the progress of a chemical reaction is called the Thorpe–Ingold effect illustrated in the Diels-Alder reaction below. Compared to a hydrogen substituent, the tert-butyl substituent accelerates the reaction rate by a factor of 240. [2] tert-Butyl effect. The tert-butyl effect is an example of steric hindrance.

  9. 4-tert-Butylcatechol - Wikipedia

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

    4-tert-Butylcatechol (TBC) is an organic chemical compound which is a derivative of catechol. [1] TBC is available in the form of a solid crystal flake [ 2 ] and 85% solution in methanol [ 3 ] or water.