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  2. 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.

  3. Butanol - Wikipedia

    en.wikipedia.org/wiki/Butanol

    Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).

  4. Comparison of psychoactive alcohols in alcoholic drinks

    en.wikipedia.org/wiki/Comparison_of_psychoactive...

    None (tertiary alcohol) 0.07% in beer: 70 mg/100 mL (see tert-Pentyl alcohol in ref) Found in cassava fermented drinks: 1000 mg/kg 2-Methylpropan-2-ol None (tertiary alcohol) Identified, not quantified, in beer [5] 2743 mg/kg 2-Phenylethan-1-ol ? 0.1% in non-yeasted cider (Kieser 1964): 100 mg/100 mL 1790 mg/kg 3-Methylbutan-1-ol ?

  5. 1-Butanol - Wikipedia

    en.wikipedia.org/wiki/1-Butanol

    1-Butanol, also known as butan-1-ol or n-butanol, is a primary alcohol with the chemical formula C 4 H 9 OH and a linear structure. Isomers of 1-butanol are isobutanol, butan-2-ol and tert-butanol. The unmodified term butanol usually refers to the straight chain isomer.

  6. List of alkanols - Wikipedia

    en.wikipedia.org/wiki/List_of_alkanols

    In other projects Wikimedia Commons ... This list is ordered by the number of carbon atoms in an alcohol. C1. Methanol; C2 ... tert-Butyl alcohol; C5 1-Pentanol ...

  7. 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.

  8. Jane C. Garvey - Pay Pals - The Huffington Post

    data.huffingtonpost.com/paypals/jane-c-garvey

    From September 2009 to December 2012, if you bought shares in companies when Jane C. Garvey joined the board, and sold them when she left, you would have a 168.1 percent return on your investment, compared to a 34.4 percent return from the S&P 500.

  9. 2-Butanol - Wikipedia

    en.wikipedia.org/wiki/2-Butanol

    Like other butanols, butan-2-ol has low acute toxicity. The LD 50 is 4400 mg/kg (rat, oral). [6]Several explosions have been reported [7] [8] [9] during the conventional distillation of 2-butanol, apparently due to the buildup of peroxides with the boiling point higher than that of pure alcohol (and therefore concentrating in the still pot during distillation).