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  2. 1,6-Hexanediol - Wikipedia

    en.wikipedia.org/wiki/1,6-hexanediol

    1,6-Hexanediol is an organic compound ... 2,5-Hexanediol and 1,4-butanediol have been observed to have minimal effect on behavior of disorderd proteins as ...

  3. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    Examples include ethane-1,2-diol or ethylene glycol HO−(CH 2) 2 −OH, a common ingredient of antifreeze products. Another example is propane-1,2-diol , or alpha propylene glycol, HO−CH 2 −CH(OH)−CH 3 , used in the food and medicine industry, as well as a relatively non-poisonous antifreeze product.

  4. 1,6-Hexanediol diacrylate - Wikipedia

    en.wikipedia.org/wiki/1,6-Hexanediol_diacrylate

    1,6-Hexanediol diacrylate (HDDA or HDODA) is a difunctional acrylate ester monomer used in the manufacture of polymers. [ 1 ] [ 2 ] It is particularly useful for use in ultraviolet light cure applications. [ 3 ]

  5. What Happens To Your Body When You Eat Oatmeal Every Day - AOL

    www.aol.com/15-side-effects-eating-oatmeal...

    To lessen the side effects, start with a small quantity and increase gradually to the chosen amount. When you start eating oat bran, the harmful outcomes from your body will probably disappear." 3.

  6. 1,6-Hexanediol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/1,6-Hexanediol_diglycidyl...

    1,6-Hexanediol diglycidyl ether is an organic chemical in the glycidyl ether family. It is an aliphatic compound that is a colorless liquid. It has two epoxide (oxirane) groups per molecule. Its main use is in modifying epoxy resins especially viscosity reduction whilst flexibilizing. [2] It is REACH registered. [3]

  7. 2,5-Hexanediol - Wikipedia

    en.wikipedia.org/wiki/2,5-Hexanediol

    2,5-Hexanediol is an organic compound with the formula CH 3 CH(OH)CH 2 CH 2 CH(OH)CH 3. It is both a glycol and a secondary alcohol. [1] It is a colorless water-soluble viscous liquid. [2] [3] [4] The chemical properties are well understood and have been extensively reported and studied. [5]

  8. Dihydrolevoglucosenone - Wikipedia

    en.wikipedia.org/wiki/Dihydrolevoglucosenone

    At elevated temperature and in the presence of a palladium catalyst, hydrogenolysis of dihydrolevoglucosenone via levoglucosanol selectively yields tetrahydrofuran-2,5-dimethanol (THF-dimethanol), [8] which is a biodegradable solvent and a bio-based precursor to 1,6-hexanediol (and 1,6-diaminohexane). [16]

  9. Side effect - Wikipedia

    en.wikipedia.org/wiki/Side_effect

    Possible side effects of nicotine [2] [3] The World Health Organization and other health organisations characterise the probability of experiencing side effects as: [4] [5] Very common, ≥ 1 ⁄ 10; Common (frequent), 1 ⁄ 10 to 1 ⁄ 100; Uncommon (infrequent), 1 ⁄ 100 to 1 ⁄ 1000; Rare, 1 ⁄ 1000 to 1 ⁄ 10000; Very rare, < 1 ⁄ 10000