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  2. 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.

  3. 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. It is used as an industrial solvent. [7]

  4. C6H12O2 - Wikipedia

    en.wikipedia.org/wiki/C6H12O2

    The molecular formula C 6 H 12 O 2 (Molar mass: 116.15 g/mol) may refer to: Carboxylic acids with formula C 6 H 12 O 2: Hexanoic acid; 4-Methylpentanoic acid; Esters with formula C 6 H 12 O 2: Butyl acetate; sec-Butyl acetate; tert-Butyl acetate; Ethyl butyrate; Isobutyl acetate; Isoamyl formate; Methyl pentanoate; Methyl pivalate; Propyl ...

  5. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  6. File:Sec-butyl acetate.svg - Wikipedia

    en.wikipedia.org/wiki/File:Sec-butyl_acetate.svg

    This image of a simple structural formula is ineligible for copyright and therefore in the public domain, because it consists entirely of information that is common property and contains no original authorship.

  7. Isocyanate - Wikipedia

    en.wikipedia.org/wiki/Isocyanate

    Isocyanates react with water to form carbon dioxide: RNCO + H 2 O → RNH 2 + CO 2. This reaction is exploited in tandem with the production of polyurethane to give polyurethane foams. The carbon dioxide functions as a blowing agent. [12] Isocyanates also react with amines to give ureas: R 2 NH + R'NCO → R 2 NC(O)N(H)R'

  8. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    Skeletal formula of butyl (here connected to an R group) Common name Preferred IUPAC name Alternate notation Fully systematic name Symbol; n-butyl butyl butyl butan-1-yl Bu, n-Bu, nBu, n Bu sec-butyl butan-2-yl 1-methylpropyl butan-2-yl s-Bu, sBu, s Bu isobutyl, iso-butyl 2-methylpropyl 2-methylpropyl 2-methylpropan-1-yl i-Bu, iBu, i Bu tert ...

  9. 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).