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  2. Propionate fermentation - Wikipedia

    en.wikipedia.org/wiki/Propionate_fermentation

    Propionate fermentation is a form of fermentation with propionic acid as one of the products. This process is done through the fermentation pathway of bacteria. It is used in a variety of industrial, food-making, and medical applications.

  3. Oxaprozin - Wikipedia

    en.wikipedia.org/wiki/Oxaprozin

    Oxaprozin, also known as oxaprozinum, is a nonsteroidal anti-inflammatory drug (NSAID), [2] used to relieve the inflammation, swelling, stiffness, and joint pain associated with osteoarthritis and rheumatoid arthritis. Chemically, it is a propionic acid derivative. Safety and efficacy has been established in children over 6 years with juvenile ...

  4. Category:Propionic acids - Wikipedia

    en.wikipedia.org/wiki/Category:Propionic_acids

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... Propionic acid; A. Allenolic acid; Alminoprofen;

  5. Loxoprofen - Wikipedia

    en.wikipedia.org/wiki/Loxoprofen

    Download as PDF; Printable version; ... in the propionic acid derivatives group, ... It was patented in 1977 and approved for medical use in 1986. [2]

  6. Propionic acid - Wikipedia

    en.wikipedia.org/wiki/Propionic_acid

    Propionic acid inhibits the growth of mold and some bacteria at levels between 0.1 and 1% by weight. As a result, some propionic acid produced is consumed as a preservative for both animal feed and food for human consumption. For animal feed, it is used either directly or as its ammonium salt. This application accounts for about half of the ...

  7. Profen (drug class) - Wikipedia

    en.wikipedia.org/wiki/Profen_(drug_class)

    The profens are a class of nonsteroidal anti-inflammatory drugs. [1] Profens are also known as 2-arylpropionic acids to reflect their chemical structure. [2] The most common example of a profen is ibuprofen, which has been sold under the brand name Profen among others.

  8. Propionic acidemia - Wikipedia

    en.wikipedia.org/wiki/Propionic_acidemia

    In many cases, propionic acidemia can damage the brain, heart, kidney, liver, cause seizures and delays to normal development such as walking or talking. The accumulation of propionic acid is known to induce differential responses in different organs. The heart and liver are specific targets of the complication.

  9. Propiophenone - Wikipedia

    en.wikipedia.org/wiki/Propiophenone

    It is also prepared commercially by ketonization of benzoic acid and propionic acid over calcium acetate and alumina at 450–550 °C: [1] C 6 H 5 CO 2 H + CH 3 CH 2 CO 2 H → C 6 H 5 C(O)CH 2 CH 3 + CO 2 + H 2 O. Ludwig Claisen discovered that α-methoxystyrene forms this compound when heated for an hour at 300 °C (65% yield). [2] [3]

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