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  2. 1-Octanol - Wikipedia

    en.wikipedia.org/wiki/1-Octanol

    Boiling point: 195 °C (383 °F; 468 K) [1] Solubility in water. ... 1-Octanol, also known as octan-1-ol, is the organic compound with the molecular formula CH 3 (CH ...

  3. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44 ...

  4. Octanol - Wikipedia

    en.wikipedia.org/wiki/Octanol

    Octanols are alcohols with the formula C 8 H 17 OH. A simple and important member is 1-octanol , with an unbranched chain of carbons. Other commercially important octanols are 2-octanol and 2-ethylhexanol .

  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. Alcohol (chemistry) - Wikipedia

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

    The boiling point of the alcohol ethanol is 78.29 °C, compared to 69 °C for the hydrocarbon hexane, ... An idealized synthesis of 1-octanol is shown: ...

  7. Octanal - Wikipedia

    en.wikipedia.org/wiki/Octanal

    A colorless fragrant liquid with a fruit-like odor, it occurs naturally in citrus oils. It is used commercially as a component in perfumes and in flavor production for the food industry. It is usually produced by hydroformylation of heptene and the dehydrogenation of 1-octanol. [1] Octanal can also be referred to as caprylic aldehyde or C8 ...

  8. Octyl acetate - Wikipedia

    en.wikipedia.org/wiki/Octyl_acetate

    It is classified as an ester that is formed from 1-octanol (octyl alcohol) and acetic acid. It is found in oranges, grapefruits, and other citrus products. [10] Octyl acetate can be synthesized by the Fischer esterification of 1-octanol and acetic acid: CH 3 (CH 2) 7 OH + CH 3 CO 2 H → CH 3 (CH 2) 7 O 2 CCH 3 + H 2 O

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