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  2. 2-Hexanol - Wikipedia

    en.wikipedia.org/wiki/2-Hexanol

    2-Hexanol (hexan-2-ol) is a six-carbon alcohol in which the hydroxy group (OH) is located on the second carbon atom. Its chemical formula is C 6 H 14 O or C 6 H 13 OH. It is an isomer of the other hexanols. 2-Hexanol has a chiral center and can be resolved into two different enantiomers. Its toxicity is based on metabolism to hexane-2,5-dione. [3]

  3. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is the organic compound with the formula HOCH(CH 2) 5. The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl group. [4] This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature.

  4. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    In chemistry, an alcohol (from Arabic al-kuḥl 'the kohl'), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom. [ 3 ] [ 4 ] Alcohols range from the simple, like methanol and ethanol , to complex, like sugars and cholesterol .

  5. Hexanol - Wikipedia

    en.wikipedia.org/wiki/Hexanol

    Hexanol may refer to any of the following isomeric organic compounds with the formula C 6 H 13 OH: Structure Type IUPAC name Boiling point (°C) Primary Hexan-1-ol ...

  6. 2-Ethylhexanol - Wikipedia

    en.wikipedia.org/wiki/2-Ethylhexanol

    2-Ethylhexanol exhibits low toxicity in animal models, with LD50 ranging from 2-3 g/kg (rat). [3] 2-Ethylhexanol has been identified as a cause of indoor air quality related health problems, such as respiratory system irritation, as a volatile organic compound. 2-Ethylhexanol is emitted to air from a PVC flooring installed on concrete that had not been dried properly.

  7. List of alkanols - Wikipedia

    en.wikipedia.org/wiki/List_of_alkanols

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  8. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    It can also be named by replacing the "-oic acid" of their corresponding carboxylic acids with "-carbonitrile." The prefix form is "cyano-." Functional class IUPAC nomenclature may also be used in the form of alkyl cyanides. For example, CH 3 CH 2 CH 2 CH 2 C≡N is called pentanenitrile or butyl cyanide.

  9. File:2-hexanol-Line-Structure.svg - Wikipedia

    en.wikipedia.org/wiki/File:2-hexanol-Line...

    The following other wikis use this file: Usage on azb.wikipedia.org ۲-هقزانول; Usage on fa.wikipedia.org ۲-هگزانول; Usage on fi.wikipedia.org