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  2. 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.

  3. List of Amazon brands - Wikipedia

    en.wikipedia.org/wiki/List_of_Amazon_brands

    These are available on Amazon.com, Amazon Fresh, Prime Pantry, Prime Now, Amazon Go, and Whole Foods Market. Amazon houses its in-house brand offerings under the “Our Brands” label, which is separate from exclusive brands. Exclusive brand items are third party offerings sold exclusively through Amazon. [1]

  4. Mattress pad - Wikipedia

    en.wikipedia.org/wiki/Mattress_pad

    A mattress topper on a boxspring mattress. A mattress pad, mattress topper, or underpad is designed to lie atop a mattress.Made from a variety of materials including wool, cotton, memory foam, feather and latex, [1] its function is to provide an extra layer of comfort, especially when the existing mattress is worn or uncomfortable.

  5. tert-Butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_alcohol

    tert-Butyl alcohol is used as a solvent, ethanol denaturant, paint remover ingredient, and gasoline octane booster and oxygenate.It is a chemical intermediate used to produce methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE) by reaction with methanol and ethanol, respectively, and tert-butyl hydroperoxide (TBHP) by reaction with hydrogen peroxide.

  6. Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate ...

    en.wikipedia.org/wiki/Octadecyl_3-(3,5-di-tert...

    Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate is significantly less volatile than simpler phenolic antioxidants such as butylhydroxytoluene (BHT). This makes it more suitable to stabilising plastics, as it is not driven out by the high temperatures experienced during plastic extrusion and moulding, [2] when they are heated to 150-320 °C (300–600 °F). [3]

  7. tert-Butyl peroxybenzoate - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_peroxybenzoate

    A standard procedure for the preparation of peresters is the acylation of tert-butyl hydroperoxide with benzoyl chloride. [6] In the reaction a large excess of tert-butyl hydroperoxide is used and the hydrogen chloride formed is removed in vacuo whereby a virtually quantitative yield is obtained. Synthesis of tert-butylperoxybenzoate

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