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  2. Oleamide - Wikipedia

    en.wikipedia.org/wiki/Oleamide

    Oleamide has been found in Ziziphus jujuba, also known as Jujube fruit. [14]Synthetic oleamide has a variety of industrial uses, including as a lubricant. [15]Oleamide was found to be leaching out of polypropylene plastics in laboratory experiments, affecting experimental results. [16]

  3. 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.

  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. 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. Is It Safe to Use Expired Vitamins? The Truth About Vitamin ...

    www.aol.com/vitamins-expire-nutritionists-weigh...

    What are the possible side effects of taking expired vitamins? “There isn’t a promise that the vitamin will pack a full punch if you take it after the expiration date, but there aren’t any ...

  7. Hydroxylamine - Wikipedia

    en.wikipedia.org/wiki/Hydroxylamine

    Ammonium sulfate, [NH 4] 2 SO 4, a side-product insoluble in liquid ammonia, is removed by filtration; the liquid ammonia is evaporated to give the desired product. [4] The net reaction is: 2 NO − 2 + 4 SO 2 + 6 H 2 O + 6 NH 3 → 4 SO 2− 4 + 6 [NH 4] + + 2 NH 2 OH. A base then frees the hydroxylamine from the salt:

  8. Palmitoylethanolamide - Wikipedia

    en.wikipedia.org/wiki/Palmitoylethanolamide

    The analgesic and antihyperalgesic effects of PEA in two models of acute and persistent pain seemed to be explained at least partly via the de novo neurosteroid synthesis. [ 24 ] [ 25 ] In chronic granulomatous pain and inflammation model, PEA could prevent nerve formation and sprouting, mechanical allodynia, and PEA inhibited dorsal root ...

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