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  2. Succinic acid - Wikipedia

    en.wikipedia.org/wiki/Succinic_acid

    Succinic acid (/ s ə k ˈ s ɪ n ɪ k /) is a dicarboxylic acid with the chemical formula (CH 2) 2 (CO 2 H) 2. [5] In living organisms, succinic acid takes the form of an anion, succinate, which has multiple biological roles as a metabolic intermediate being converted into fumarate by the enzyme succinate dehydrogenase in complex 2 of the electron transport chain which is involved in making ...

  3. Ustilaginaceae - Wikipedia

    en.wikipedia.org/wiki/Ustilaginaceae

    Succinic acid is utilized as a precursor to pharmaceutical ingredients, such as additives, solvents, and polymers, but also as a food additive and dietary supplement. [8] Another category of metabolites produced by smut fungi contains extracellular glycolipids, such as mannosylerythritol lipids and ustilagic acid.

  4. List of food additives - Wikipedia

    en.wikipedia.org/wiki/List_of_food_additives

    Additives are used for many purposes but the main uses are: Acids Food acids are added to make flavors "sharper", and also act as preservatives and antioxidants. Common food acids include vinegar, citric acid, tartaric acid, malic acid, folic acid, fumaric acid, and lactic acid.

  5. Tartaric acid - Wikipedia

    en.wikipedia.org/wiki/Tartaric_acid

    The acid itself is added to foods as an antioxidant E334 and to impart its distinctive sour taste. Naturally occurring tartaric acid is a useful raw material in organic synthesis. Tartaric acid, an alpha-hydroxy-carboxylic acid, is diprotic and aldaric in acid characteristics and is a dihydroxyl derivative of succinic acid.

  6. Octenylsuccinic acid - Wikipedia

    en.wikipedia.org/wiki/Octenylsuccinic_acid

    Octenylsuccinic acid is a manufactured ingredient in foods. [1] It is used to treat gum arabic , [ 1 ] and also in waxy maize production [ 2 ] and for rice starch production. [ 3 ]

  7. Stobbe condensation - Wikipedia

    en.wikipedia.org/wiki/Stobbe_condensation

    The Stobbe condensation entails the reaction of an aldehyde or ketone with an ester of succinic acid to generate alkylidene succinic acid or related derivatives. [1] The reaction consumes one equivalent of metal alkoxide. Commonly, diethylsuccinate is a component of the reaction. The usual product is salt of the half-ester.

  8. Breaking Out? Succinic Acid Should Be On Your Radar ASAP - AOL

    www.aol.com/breaking-succinic-acid-radar-asap...

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  9. Daminozide - Wikipedia

    en.wikipedia.org/wiki/Daminozide

    While described by the FDA as an amino acid derivative, [2] daminozide is more formally and correctly described as a dicarboxylic acid monohydrazide. [8] [citation needed] It is the product of the condensation of succinic acid with 2,2-dimethylhydrazine, [citation needed] and in its pure form is a high-melting temperature water-soluble white crystalline solid.

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