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  2. 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.

  3. Oleic acid - Wikipedia

    en.wikipedia.org/wiki/Oleic_acid

    In chemical terms, oleic acid is classified as a monounsaturated omega-9 fatty acid, abbreviated with a lipid number of 18:1 cis-9, and a main product of Δ9-desaturase. [2] It has the formula CH 3 −(CH 2) 7 −CH=CH−(CH 2) 7 −COOH. [3] [page needed] The name derives from the Latin word oleum, which means oil. [4]

  4. 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.

  5. Butyl oleate - Wikipedia

    en.wikipedia.org/wiki/Butyl_oleate

    Butyl oleate is a fatty acid ester and an organic chemical found in liquid form. It has the formula C 22 H 42 O 2 and the CAS Registry Number 142-77-8. [ 2 ] It is REACH registered and produced or imported into the European Union with the EC number of 205-559-6.

  6. Oleoylethanolamide - Wikipedia

    en.wikipedia.org/wiki/Oleoylethanolamide

    Oleoylethanolamide (OEA) is an endogenous peroxisome proliferator-activated receptor alpha (PPAR-α) agonist.It is a naturally occurring ethanolamide lipid that regulates feeding and body weight in vertebrates ranging from mice to pythons.

  7. Oleamide - Wikipedia

    en.wikipedia.org/wiki/Oleamide

    Oleamide is an organic compound with the formula CH 3 (CH 2) 7 CH=CH(CH 2) 7 CONH 2. [3] It is the amide derived from the fatty acid oleic acid. It is a colorless waxy solid and occurs in nature. Sometimes labeled as a fatty acid primary amide (FAPA), it is biosynthesized from N-oleoylglycine. [4]

  8. N-Oleoylsarcosine - Wikipedia

    en.wikipedia.org/wiki/N-Oleoylsarcosine

    A standard method for the preparation of N-acylamino acids is the Schotten-Baumann reaction, in which oleoyl chloride (from oleic acid and, e.g. phosphorus trichloride) is added to an aqueous solution of N-methylglycine at pH 10 (kept constant by the addition of sodium hydroxide solution).

  9. List of saturated fatty acids - Wikipedia

    en.wikipedia.org/wiki/List_of_saturated_fatty_acids

    Common Name Systematic Name Structural Formula Lipid Numbers Propionic acid: Propanoic acid CH 3 CH 2 COOH C3:0 Butyric acid: Butanoic acid CH 3 (CH 2) 2 COOH C4:0 Valeric acid: Pentanoic acid CH 3 (CH 2) 3 COOH C5:0 Caproic acid: Hexanoic acid CH 3 (CH 2) 4 COOH C6:0 Enanthic acid: Heptanoic acid CH 3 (CH 2) 5 COOH C7:0 Caprylic acid: Octanoic ...