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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. Alkenylsuccinic anhydrides - Wikipedia

    en.wikipedia.org/wiki/Alkenylsuccinic_anhydrides

    The patent describes the reaction of the alkenes with excess maleic anhydride at 200 °C in an autoclave. The excess alkene is removed by distillation in vacuo, the resulting alkenyl succinic anhydride hydrolyzed with dilute sodium hydroxide solution and the disodium salt reacted with an acid to achieve an alkenebutanedioic acid.

  4. Nickel succinate - Wikipedia

    en.wikipedia.org/wiki/Nickel_succinate

    The neutral nickel succinate NiC 4 H 2 O 4 ·4H 2 O, can be made from succinic acid and nickel carbonate. [3] It dehydrates between 114 and 200°, Andydrous nickel succinate breaks down at 380° and over 450°C only nickel oxide is left. [3] The gaseous decomposition products mainly consist of water, methane, ethylene, propane and carbon dioxide.

  5. 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.

  6. Dibasic ester - Wikipedia

    en.wikipedia.org/wiki/Dibasic_ester

    Dibasic ester or DBE is an ester of a dicarboxylic acid.Depending on the application, the alcohol may be methanol or higher molecular weight monoalcohols. Mixtures of different methyl dibasic esters are commercially produced from short-chain acids such as adipic acid, glutaric acid, and succinic acid. [1]

  7. Category:Succinates - Wikipedia

    en.wikipedia.org/wiki/Category:Succinates

    Succinic acid This page was last edited on 25 January 2021, at 18:37 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...

  8. Succimer - Wikipedia

    en.wikipedia.org/wiki/Succimer

    Succimer is an isomer of 2,3-dimercaptosuccinic acid. 2,3-dimercaptosuccinic acid is the organosulfur compound with the formula HO 2 CCH(SH)CH(SH)CO 2 H. This colorless solid contains two carboxylic acid and two thiol groups, the latter being responsible for its mildly unpleasant odour.

  9. Succinyl chloride - Wikipedia

    en.wikipedia.org/wiki/Succinyl_chloride

    It is the acyl chloride derivative of succinic acid and a simple diacid chloride. It is a colorless liquid. It is a colorless liquid. It used as a reagent in organic synthesis .