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  2. Hexane-2,5-dione - Wikipedia

    en.wikipedia.org/wiki/Hexane-2,5-dione

    2,5-Hexanedione reacts with lysine residues in axonal proteins by Schiff base formation followed by cyclization to give pyrroles. Oxidation of the pyrrole residues then causes cross-linking and denaturation of proteins, which perturbs axonal transport and function and causes damage to nerve cells.

  3. 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]

  4. Petroleum benzine - Wikipedia

    en.wikipedia.org/wiki/Petroleum_benzine

    These results suggest that other components found in petroleum benzine may have additive, synergistic or potentiative effects on the biological effects of n-hexane. [7] Namely, 1000 ppm n-hexane, 3000 ppm n-heptane, and 1000 ppm toluene were reported to have depressing effects on the body weight gain of rats.

  5. 2-Hexanone - Wikipedia

    en.wikipedia.org/wiki/2-hexanone

    2-Hexanone (methyl butyl ketone, MBK) is a ketone used as a general solvent and in paints. It dissolves cellulose nitrate, vinyl polymers and copolymers, and natural and synthetic resins. It dissolves cellulose nitrate, vinyl polymers and copolymers, and natural and synthetic resins.

  6. 5-Nonanone - Wikipedia

    en.wikipedia.org/wiki/5-Nonanone

    5-Nonanone was expected to be metabolized to a γ-diketone (a diketone with the second oxygen three carbons away from the first, e.g. 2,5- or 3,6-diketones). Metabolic studies confirmed the in vivo ω-oxidation of 5-nonanone to 2,5-nonanedione and 2-hexanone. Subsequent oxidative and decarboxylative steps also produce 2,5-hexanedione.

  7. Dimedone - Wikipedia

    en.wikipedia.org/wiki/Dimedone

    Dimedone is an organic compound with the formula (CH 3) 2 C(CH 2) 2 (CO) 2 (CH 2). Classified as a cyclic diketone, it is a derivative of 1,3-cyclohexanedione. It is a white solid that is soluble in water, as well as ethanol and methanol. It once was used as a reagent to test for the aldehyde functional group.

  8. Acetylpropionyl - Wikipedia

    en.wikipedia.org/wiki/Acetylpropionyl

    Acetylpropionyl, also known as acetyl propionyl or 2,3-pentanedione, [1] is an organic compound, specifically a diketone. [2] Uses for acetylpropionyl include as a: Solvent for cellulose acetate, paints, inks, and lacquers; Starting material for dyes, pesticides, and drugs

  9. 1,5-Hexadiene - Wikipedia

    en.wikipedia.org/wiki/1,5-Hexadiene

    1,5-Hexadiene is the organic compound with the formula (CH 2) 2 (CH=CH 2) 2. It is a colorless, volatile liquid. It is a colorless, volatile liquid. It is used as a crosslinking agent and precursor to a variety of other compounds.