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  2. Butyric acid - Wikipedia

    en.wikipedia.org/wiki/Butyric_acid

    The butyrate or butanoate ion, C 3 H 7 COO −, is the conjugate base of butyric acid. It is the form found in biological systems at physiological pH . A butyric (or butanoic) compound is a carboxylate salt or ester of butyric acid.

  3. Butyl propionate - Wikipedia

    en.wikipedia.org/wiki/Butyl_propionate

    Butyl propionate is used to make fragrances, perfumes and as a flavoring.It is also used in paints and primers for auto body or engine, appliance coatings (paints designed specifically for painting household items and vehicles like microwave ovens, refrigerators and automobiles), enamels, lacquers, and printing inks, as a solvent for adhesives and nitrocellulose, and in polymerization ...

  4. Propyl propanoate - Wikipedia

    en.wikipedia.org/wiki/Propyl_propanoate

    Propyl propanoate (also known as propyl propionate and n-propyl propionate) is the organic compound with the molecular formula C 6 H 12 O 2. It is the ester of propanol and propionic acid. Like most esters, propyl propanoate is a colorless liquid with a fruity odor. The scent of propyl propionate is described as a chemically tinged pineapple or ...

  5. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    The effect of the tert-butyl group on the progress of a chemical reaction is called the Thorpe–Ingold effect illustrated in the Diels-Alder reaction below. Compared to a hydrogen substituent, the tert-butyl substituent accelerates the reaction rate by a factor of 240. [2] tert-Butyl effect. The tert-butyl effect is an example of steric hindrance.

  6. Propyl group - Wikipedia

    en.wikipedia.org/wiki/Propyl_group

    From left to right: the two isomeric groups propyl and 1-methylethyl (iPr or isopropyl), and the non-isomeric cyclopropyl group. In organic chemistry, a propyl group is a three-carbon alkyl substituent with chemical formula −CH 2 CH 2 CH 3 for the linear form.

  7. Pentyl propanoate - Wikipedia

    en.wikipedia.org/wiki/Pentyl_propanoate

    Chemical formula. C 8 H 16 O 2 Molar mass: ... Propyl propanoate Butyl propanoate Hexyl propanoate Pentyl acetate Pentyl butanoate: Except where otherwise noted, ...

  8. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    Polymer nomenclature usually applies to idealized representations meaning minor structural irregularities are ignored. A polymer can be named in one of two ways. Source-based nomenclature can be used when the monomer can be identified. Alternatively, more explicit structure-based nomenclature can be used when the polymer structure is proven.

  9. C4H8O2 - Wikipedia

    en.wikipedia.org/wiki/C4H8O2

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