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  2. 2-Pentanol - Wikipedia

    en.wikipedia.org/wiki/2-Pentanol

    2-Pentanol (IUPAC name: pentan-2-ol; also called sec-amyl alcohol) is an organic chemical compound.It is used as a solvent and an intermediate in the manufacturing of other chemicals. 2-Pentanol is a component of many mixtures of amyl alcohols sold industrially. 2-Pentanol is chiral and thus can be obtained as either of two stereoisomers designated as (R)-(−)-2-pentanol and (S)-(+)-2-pentanol.

  3. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    2-Methylbutan-1-ol: 128.7 3-methyl-1-butanol or isoamyl alcohol or isopentyl alcohol primary 3-Methylbutan-1-ol: 131.2 2,2-dimethyl-1-propanol or neopentyl alcohol primary 2,2-Dimethylpropan-1-ol: 113.1 2-pentanol or sec-amyl alcohol or methyl (n) propyl carbinol secondary Pentan-2-ol: 118.8 3-methyl-2-butanol or sec-isoamyl alcohol or methyl ...

  4. List of alkanols - Wikipedia

    en.wikipedia.org/wiki/List_of_alkanols

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  6. tert-Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Amyl_alcohol

    tert-Amyl alcohol (TAA) or 2-methylbutan-2-ol (2M2B), is a branched pentanol. Historically, TAA has been used as an anesthetic [3] and more recently as a recreational drug. [4] TAA is mostly a positive allosteric modulator for GABA A receptors in the same way as ethanol. [5] The psychotropic effects of TAA and ethanol are similar, though distinct.

  7. Vinyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Vinyl_alcohol

    At room temperature, acetaldehyde (H 3 CC(O)H) is more stable than vinyl alcohol (H 2 C=CHOH) by 42.7 kJ/mol. [3] Vinyl alcohol gas isomerizes to the aldehyde with a half-life of 30 min at room temperature. [1] H 2 C=CHOH → H 3 CC(O)H The industrial synthesis of acetaldehyde (Wacker process) proceeds via the intermediacy of a vinyl alcohol ...

  8. Oleyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Oleyl_alcohol

    Oleyl alcohol / ˈ oʊ l i ˌ ɪ l, ˈ oʊ l i əl /, [1] or cis-9-octadecen-1-ol, is an unsaturated fatty alcohol with the molecular formula C 18 H 36 O or the condensed structural formula CH 3 (CH 2) 7 −CH=CH−(CH 2) 8 OH. It is a colorless oil, mainly used in cosmetics.

  9. Ribitol - Wikipedia

    en.wikipedia.org/wiki/Ribitol

    Ribitol, or adonitol, is a crystalline pentose alcohol (C 5 H 12 O 5) formed by the reduction of ribose.It occurs naturally in the plant Adonis vernalis [2] as well as in the cell walls of some Gram-positive bacteria, in the form of ribitol phosphate, in teichoic acids. [3]

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