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  2. 1,3-Propanediol - Wikipedia

    en.wikipedia.org/wiki/1,3-Propanediol

    1,3-Propanediol is the organic compound with the formula CH 2 (CH 2 OH) 2. This 3-carbon diol is a colorless viscous liquid that is miscible with water. Products

  3. 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.

  4. 1,3-Propane sultone - Wikipedia

    en.wikipedia.org/wiki/1,3-Propane_sultone

    1,3-Propane sultone is the organosulfur compound with the formula (CH 2) 3 SO 3. It is a cyclic sulfonate ester, a class of compounds called sultones . [ 2 ] [ 3 ] It is a readily melting colorless solid.

  5. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    2,2-Disubstituted propane-1,3-diols are prepared in this way. Examples include 2-methyl-2-propyl-1,3-propanediol and neopentyl glycol. 1,3-Diols can be prepared by hydration of α,β-unsaturated ketones and aldehydes. The resulting keto-alcohol is hydrogenated. Another route involves the hydroformylation of epoxides followed by hydrogenation of ...

  6. C3H8O2 - Wikipedia

    en.wikipedia.org/wiki/C3H8O2

    The molecular formula C 3 H 8 O 2 may refer to: Dimethoxymethane; 2-Methoxyethanol; Propanediol. 1,2-Propanediol (propylene glycol), a vicinal diol; 1,3-Propanediol (trimethylene glycol) 1,1-Propanediol (geminal diol) 2,2-Propanediol (geminal diol)

  7. Glycerol-1,2-carbonate - Wikipedia

    en.wikipedia.org/wiki/Glycerol-1,2-carbonate

    Glycerol-1,2-carbonate is formally the cyclic ester of carbonic acid with ... or 3-chloro-1,2-propanediol or ... with anhydrous zinc sulfate as a heterogeneous ...

  8. C7H16O2 - Wikipedia

    en.wikipedia.org/wiki/C7H16O2

    The molecular formula C 7 H 16 O 2 (molar mass: 132.203 g/mol) may refer to: ... 2-Methyl-2-propyl-1,3-propanediol This page was last edited on 31 March 2023, at 01: ...

  9. Expanding monomer - Wikipedia

    en.wikipedia.org/wiki/Expanding_monomer

    The third possibility is using dibutyltin oxide and carbon disulfide: [1]: 38 1,3-propanediol is reacting with dibutyltin oxide to 2,2-dibutyl-1,3,2-dioxastannane and carbon disulfide to the cyclic sulfite of 1,3-propanediol. Both are forming together 1,5,7,11-tetraoxa-spiro[5.5]undecane