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2. 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 ...

3. Propanol - Wikipedia

   en.wikipedia.org/wiki/Propanol

   Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... There are two isomers of propanol. 1-Propanol, n-propanol, or propan-1-ol: ...

4. 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 ...

5. List of viscosities - Wikipedia

   en.wikipedia.org/wiki/List_of_viscosities

   Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... 1-Propanol (propyl alcohol) C 3 H 8 O 1.945 [37] 2-Propanol (isopropyl alcohol) C ...

6. Propyl hexanoate - Wikipedia

   en.wikipedia.org/wiki/Propyl_hexanoate

   Propyl hexanoate (C 9 H 18 O 2), also known as propyl caproate, is an ester formed by the reaction of propanol with hexanoic acid.Although it is a completely different ester, propyl hexanoate shares the same chemical formula with methyl octanoate, ethyl heptanoate, butyl pentanoate, etc. because they all have the same total carbon chain length.

7. Propionyl-CoA - Wikipedia

   en.wikipedia.org/wiki/Propionyl-CoA

   Propionyl-CoA is a coenzyme A derivative of propionic acid.It is composed of a 24 total carbon chain (without the coenzyme, it is a 3 carbon structure) and its production and metabolic fate depend on which organism it is present in. [1] Several different pathways can lead to its production, such as through the catabolism of specific amino acids or the oxidation of odd-chain fatty acids. [2]