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  2. tert-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylbenzene

    tert-Butylbenzene is an organic compound classified as an aromatic hydrocarbon. Its structure consists of a benzene ring substituted with a tert -butyl group . It is a flammable colorless liquid which is nearly insoluble in water but miscible with organic solvents.

  3. 1,3,5-Tris(4-(tert-butyl)-3-hydroxy-2,6-dimethylbenzyl)-1,3,5 ...

    en.wikipedia.org/wiki/1,3,5-Tris(4-(tert-butyl...

    Firstly, 2,4-dimethyl-6-tert-butylphenol is reacted with formaldehyde and HCl (Blanc reaction) to generate a chloromethyl group in the less hindered meta position. This intermediate then reacts with cyanuric acid to give the desired product.

  4. tert-Butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_alcohol

    tert-Butyl alcohol is the simplest tertiary alcohol, with a formula of (CH 3) 3 COH (sometimes represented as t-BuOH). Its isomers are 1-butanol, isobutanol, and butan-2-ol. tert-Butyl alcohol is a colorless solid, which melts near room temperature and has a camphor-like odor. It is miscible with water, ethanol and diethyl ether.

  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. 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.

  7. Tris(3,5-di-tert-butyl-4-hydroxybenzyl) isocyanurate - Wikipedia

    en.wikipedia.org/wiki/Tris(3,5-di-tert-butyl-4...

    Tris(3,5-di-tert-butyl-4-hydroxybenzyl) isocyanurate is a high molecular weight additive, with low volatility. It is well suited to stabilising polyolefins against degradation caused by long term heat aging. [1] It is an approved food contact material in the US. [2]

  8. P4-t-Bu - Wikipedia

    en.wikipedia.org/wiki/P4-t-Bu

    P 4-t-Bu can also be regarded as tetrameric triaminoiminophosphorane of the basic structure H−N=P(−NH 2) 3. The homologous series of P 1 to P 7 polyaminophosphazenes [1] [2] of the general formula [() =] = with preferably methyl groups as R 1, a methyl group or tert-butyl group as and even-numbered x between 0 and 6 (P 4-t-Bu: R 1 = Me, R 2 ...

  9. sec-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/Sec-Butylbenzene

    iso-Butylbenzene, n-Butylbenzene, tert-Butylbenzene Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references