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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. Methyl propiolate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propiolate

    Methyl propiolate is an organic compound with the formula HC 2 CO 2 CH 3. It is the methyl ester of propiolic acid , the simplest acetylenic carboxylic acid . It is a colorless liquid that is miscible with organic solvents.

  5. 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]

  6. 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 ...

  7. Isobutyric acid - Wikipedia

    en.wikipedia.org/wiki/Isobutyric_acid

    In humans, isobutyric acid is a minor product of the gut microbiome and can also be produced by metabolism of its esters found in food. [13] It has a characteristic odor like rancid butter [ 14 ] (4-carbon organic compounds take the root, butyl, which is in turn from butyric which is in turn from the Latin word for butter and the Greek ...

  8. 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 ]

  9. 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 ...