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  2. Methyl propionate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propionate

    Methyl propionate, also known as methyl propanoate, is an organic compound with the molecular formula CH 3 CH 2 CO 2 CH 3. It is a colorless liquid with a fruity, rum -like odor. [ 2 ]

  3. Propionic acid - Wikipedia

    en.wikipedia.org/wiki/Propionic_acid

    The propionate / ˈ p r oʊ p i ə n eɪ t /, or propanoate, ion is C 2 H 5 COO −, the conjugate base of propionic acid. It is the form found in biological systems at physiological pH. A propionic, or propanoic, compound is a carboxylate salt or ester of propionic acid. In these compounds, propionate is often written in shorthand, as CH 3 CH ...

  4. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).

  5. Phenylacetone - Wikipedia

    en.wikipedia.org/wiki/Phenylacetone

    Phenylacetone, also known as phenyl-2-propanone, is an organic compound with the chemical formula C 6 H 5 CH 2 COCH 3.It is a colorless oil that is soluble in organic solvents.It is a mono-substituted benzene derivative, consisting of an acetone attached to a phenyl group.

  6. Testosterone propionate - Wikipedia

    en.wikipedia.org/wiki/Testosterone_propionate

    Testosterone esters were synthesized for the first time in 1936, and were found to have greatly improved potency relative to testosterone. [12] Among the esters synthesized, testosterone propionate was the most potent, and for this reason, was selected for further development, subsequently being marketed. [ 12 ]

  7. Methylmalonic acid - Wikipedia

    en.wikipedia.org/wiki/Methylmalonic_acid

    Propionate metabolism pathway with methylmalonic acid as a by-product. Methylmalonic acid is a by-product of the propionate metabolism pathway. [2] The starting sources for this are the following with the respective approximate contributions to whole body propionate metabolism in brackets: [3]

  8. Isobutane - Wikipedia

    en.wikipedia.org/wiki/Isobutane

    Since the longest continuous chain in isobutane contains only three carbon atoms, the preferred IUPAC name is 2-methylpropane but the locant (2-) is typically omitted in general nomenclature as redundant; C2 is the only position on a propane chain where a methyl substituent can be located without altering the main chain and forming the ...

  9. Sodium propionate - Wikipedia

    en.wikipedia.org/wiki/Sodium_propionate

    Structure of sodium propionate, with methyl groups and H atoms omitted. [5] Color code: red = O, blue = Na. Anhydrous sodium propionate is a polymeric structure, featuring trigonal prismatic Na + centers bonded to six oxygen ligands provided by the carboxylates. A layered structure is observed, with the hydrophobic ethyl groups projecting into ...