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  2. Neopentyl glycol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol

    Neopentyl glycol (IUPAC name: 2,2-dimethylpropane-1,3-diol) is an organic chemical compound. It is used in the synthesis of polyesters , paints , lubricants , and plasticizers . When used in the manufacture of polyesters, it enhances the stability of the product towards heat, light, and water.

  3. Dibromo neopentyl glycol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Dibromo_neopentyl_glycol...

    Dibromo neopentyl glycol diglycidyl ether is a brominated version of neopentyl glycol diglycidyl ether. It is an aliphatic organic chemical in the glycidyl ether family that is used in epoxy resin formulations. It has the molecular formula C 11 H 18 Br 2 O 4

  4. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    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. On commercial scales, the main route to vicinal diols is the hydrolysis of epoxides .

  5. Neopentyl glycol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol...

    Neopentyl glycol diglycidyl ether (NPGDGE) is an organic chemical in the glycidyl ether family. It is aliphatic and a colorless liquid. It has the formula C 11 H 20 O 4 and the CAS registry number of 17557-23-2. [2] It has two oxirane groups per molecule. [3] Its principle use is in modifying epoxy resins.

  6. Neopentyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_alcohol

    Neopentyl alcohol can be prepared from the hydroperoxide of diisobutylene. [3] It can also be prepared by the reduction of trimethylacetic acid with lithium aluminium hydride . Neopentyl alcohol was the first described in 1891 by L. Tissier, who prepared it by reduction of a mixture of trimethyl acetic acid and trimethylacetyl chloride with ...

  7. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    or neopentyl alcohol primary 2,2-Dimethylpropan-1-ol: 113.1 2-pentanol or sec-amyl alcohol or methyl (n) propyl carbinol secondary Pentan-2-ol: 118.8 3-methyl-2-butanol or sec-isoamyl alcohol or methyl isopropyl carbinol secondary 3-Methylbutan-2-ol: 113.6 3-Pentanol secondary Pentan-3-ol: 115.3 2-methyl-2-butanol or tert-amyl alcohol tertiary

  8. Pentaerythritol - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol

    Pentaerythritol was first reported in 1891 by German chemist Bernhard Tollens and his student P. Wigand. [5] It may be prepared via a base-catalyzed multiple-addition reaction between acetaldehyde and 3 equivalents of formaldehyde to give pentaerythrose (CAS: 3818-32-4), followed by a Cannizzaro reaction with a fourth equivalent of formaldehyde to give the final product plus formate ion.

  9. Glossary of chemical formulae - Wikipedia

    en.wikipedia.org/wiki/Glossary_of_chemical_formulae

    neopentyl glycol: 101-38-2 C 5 H 12 O 4: pentaerythritol: 115-77-5 C 5 H 12 O 5: xylitol: 87-99-0 C 5 H 13 N N,N-diethylmethylamine: 616-39-7 C 6 F 5 COOH: pentafluorobenzoic acid: 602-94-8 C 6 H 2 Cl 3 NO 2,6-Dichloroquinone-4-chloroimideGibbs reagent C 6 H 3 Br 3 O: 2,4,6-Tribromophenol: C 6 H 3 Cl 3 O: 2,4,6-Trichlorophenol: C 6 H 4 BrNO 2: ...