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  2. Oleylamine - Wikipedia

    en.wikipedia.org/wiki/Oleylamine

    Oleylamine is an organic compound with a molecular formula C 18 H 35 NH 2. [1] It is an unsaturated fatty amine related to the fatty acid oleic acid.The pure compound is a clear and colorless liquid.

  3. Ethoxylation - Wikipedia

    en.wikipedia.org/wiki/Ethoxylation

    As alcohol ethoxylate based surfactants are non-ionic they typically require longer ethoxylate chains than their sulfonated analogues in order to be water-soluble. [14] Examples synthesized on an industrial scale include octyl phenol ethoxylate, polysorbate 80 and poloxamers. Ethoxylation is commonly practiced, albeit on a much smaller scale ...

  4. Fatty alcohol - Wikipedia

    en.wikipedia.org/wiki/Fatty_alcohol

    Fatty alcohol are converted to their ethoxylates by treatment with ethylene oxide: [6] RCH 2 OH + n C 2 H 4 O → RCH 2 (OCH 2 CH 2) n OH. The resulting fatty alcohol ethoxylates are important surfactants. Another large class of surfactants are the sodium alkylsulfates such as sodium dodecylsulfate (SDS).

  5. Fatty amine - Wikipedia

    en.wikipedia.org/wiki/Fatty_amine

    Fatty amines are commonly prepared from fatty acids; which are themselves obtained from natural sources, typically seed-oils.The overall reaction is sometimes referred to as the Nitrile Process [3] and begins with a reaction between the fatty acid and ammonia at high temperature (>250 °C) and in the presence of a metal oxide catalyst (e.g., alumina or zinc oxide) to give the fatty nitrile.

  6. 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.

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  8. Oleic acid - Wikipedia

    en.wikipedia.org/wiki/Oleic_acid

    Reduction of the carboxylic acid group yields oleyl alcohol. Ozonolysis of oleic acid is an important route to azelaic acid. The coproduct is nonanoic acid: [15] H 17 C 8 CH=CHC 7 H 14 CO 2 H + 4"O" → HO 2 CC 7 H 14 CO 2 H + H 17 C 8 CO 2 H. Esters of azelaic acid find applications in lubrication and plasticizers.

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