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  2. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    Butan-2-yl (sec-butyl) group is chiral. The carbon atom at position 2 is a stereocenter. It has four different groups attached: −H, −CH 3, −CH 2 −CH 3, and −R (the R group is not equal to those three groups). The names of the two chiral groups are: (2S)-butan-2-yl and (2R)-butan-2-yl.

  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. Isobutanol - Wikipedia

    en.wikipedia.org/wiki/Isobutanol

    Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH 3) 2 CHCH 2 OH (sometimes represented as i-BuOH).This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters.

  5. 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).

  6. 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.

  7. sec-Butyl acetate - Wikipedia

    en.wikipedia.org/wiki/Sec-Butyl_acetate

    sec-Butyl acetate, or s-butyl acetate, is an ester commonly used as a solvent in lacquers and enamels, where it is used in the production of acyclic polymers, vinyl resins, and nitrocellulose. [3] It is a clear flammable liquid with a sweet smell.

  8. Descriptor (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Descriptor_(Chemistry)

    The terms sec and tert are considered obsolete and should only be used for unsubstituted sec-butoxy, sec-butyl [26] [27] or tert-butyl groups. [ 28 ] [ 27 ] There are various spellings such as "sec-butyl", "s-butyl", "sBu" or "bus" which are also considered obsolete.

  9. Butyl acetate - Wikipedia

    en.wikipedia.org/wiki/Butyl_acetate

    n-Butyl acetate is an organic compound with the formula CH 3 CO 2 (CH 2) 3 CH 3.A colorless, flammable liquid, it is the ester derived from n-butanol and acetic acid.It is found in many types of fruit, where it imparts characteristic flavors and has a sweet smell of banana or apple.