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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. Bisphenol A - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A

    Density: 1.217 g/cm 3 [1] ... BPA is produced on an industrial scale by the condensation reaction ... 4-tert-Butylphenol - used as a chain-length regulator in the ...

  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 .

  5. Category:Tert-butyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Tert-butyl_compounds

    Pages in category "Tert-butyl compounds" The following 200 pages are in this category, out of approximately 203 total. This list may not reflect recent changes .

  6. File:4-tert-butylphenol.svg - Wikipedia

    en.wikipedia.org/wiki/File:4-tert-butylphenol.svg

    English: Chemical structure of 4-tert-butylphenol, also known as p-tert-butylphenol or para-tert-butylphenol. Date: 23 July 2018: Source: Own work: Author: Hbf878:

  7. 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.

  8. 2,6-Di-tert-butylphenol - Wikipedia

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

    2,6-Di-tert-butylphenol is an organic compound with the structural formula 2,6-((CH 3) 3 C) 2 C 6 H 3 OH. This colorless solid alkylated phenol and its derivatives are used industrially as UV stabilizers and antioxidants for hydrocarbon -based products ranging from petrochemicals to plastics. [ 1 ]

  9. 2,4,6-Tri-tert-butylphenol - Wikipedia

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

    The oxidation of 2,4,6-tri-tert-butylphenol in the alkaline to the intensely blue-colored phenoxy radical can also occur with potassium ferricyanide. [1] [9] [6] The 2,4,6-tri-tert-butylphenoxy radical forms blue crystals on cooling to -70 °C which are stable at room temperature for several weeks and only gradually turn yellow. [9]