enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. 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. Ammonium propionate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_propionate

    Ammonium propionate or ammonium propanoate is the ammonium salt of propionic acid. It has the chemical formula NH 4 (C 2 H 5 COO). Reaction.

  6. Propionic anhydride - Wikipedia

    en.wikipedia.org/wiki/Propionic_anhydride

    Propanoyl propanoate. Identifiers ... 1.015 g/cm 3, liquid Melting point: −42 °C (−44 °F; 231 K) Boiling point: 167 to 170 °C (333 to 338 °F; 440 to 443 K)

  7. 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 ]

  8. Propionyl chloride - Wikipedia

    en.wikipedia.org/wiki/Propionyl_chloride

    It is a colorless, corrosive, volatile liquid. It is used as a reagent for organic synthesis. In derived chiral amides and esters, the methylene protons are diastereotopic. [2] There have been efforts [3] to schedule Propionyl chloride as a DEA List 1 Chemical as it can be used to synthesize fentanyl.

  9. 1-Propanol (data page) - Wikipedia

    en.wikipedia.org/wiki/1-Propanol_(data_page)

    Solid properties Std enthalpy change of formation, Δ f H o solid-763 kJ/mol Standard molar entropy, S o solid: 112.7 J/(mol K) Heat capacity, c p: 106.3 J/(mol K) at –124 °C Liquid properties Std enthalpy change of formation, Δ f H o liquid –303.0 kJ/mol Standard molar entropy, S o liquid: 192.8 J/(mol K) Enthalpy of combustion, Δ c H o ...