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  2. Oleylamine - Wikipedia

    en.wikipedia.org/wiki/Oleylamine

    Oleylamine reacts with carboxylic acid to form its carboxylate salt through an exothermic reaction. [8] [9] Its carboxylate salt can further condensate into amides through the loss of one water molecule. In the presence of acetic acid, oleylamin forms with DNA insoluble complexes with the radii of the particles equal 60–65 nm. [10]

  3. File:Lake Erie food web.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Lake_Erie_food_web.pdf

    Original file (1,650 × 1,275 pixels, file size: 748 KB, MIME type: application/pdf, 2 pages) This is a file from the Wikimedia Commons . Information from its description page there is shown below.

  4. Harpic - Wikipedia

    en.wikipedia.org/wiki/Harpic

    The original toilet cleaner was invented by Harry Pickup (hence the origin of the name Harpic [2]), who was based in Roscoe Street, Scarborough, in North Yorkshire.He also invented Oxypic, which was a sealant used in cast iron heating systems, and patented the Lock & Lift circular manhole covers, which were used initially by the British Military.

  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. Oleamide - Wikipedia

    en.wikipedia.org/wiki/Oleamide

    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] Since polypropylene is used in a wide number of food containers such as those for yogurt, the problem is being studied. [17]

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  8. Hydroxylamine - Wikipedia

    en.wikipedia.org/wiki/Hydroxylamine

    Hydroxylamine can also be used to highly selectively cleave asparaginyl-glycine peptide bonds in peptides and proteins. [32] It also bonds to and permanently disables (poisons) heme-containing enzymes. It is used as an irreversible inhibitor of the oxygen-evolving complex of photosynthesis on account of its similar structure to water.

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