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  2. Mixed acid fermentation - Wikipedia

    en.wikipedia.org/wiki/Mixed_acid_fermentation

    The methyl red (MR) test can detect whether the mixed acid fermentation pathway occurs in microbes when given glucose. A pH indicator is used that turns the test solution red if the pH drops below 4.4. [12] If the fermentation pathway has taken place, the mixture of acids it has produced will make the solution very acidic and cause a red colour ...

  3. 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]

  4. N-Hydroxysuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Hydroxysuccinimide

    A common way to synthesize an NHS-activated acid is to mix NHS with the desired carboxylic acid and a small amount of an organic base in an anhydrous solvent. A coupling reagent such as dicyclohexylcarbodiimide (DCC) or 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) is then added to form a highly reactive activated acid intermediate.

  5. Diethyl succinate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_succinate

    Being a diester, diethyl succinate is a particularly versatile building block. It participates in acyloin condensation to give 2-hydroxycyclobutanone. [1] Via condensation with oxalate esters, it serves as a precursor to ketoglutaric acid. [2]

  6. Succinic acid fermentation - Wikipedia

    en.wikipedia.org/wiki/Succinic_acid_fermentation

    For both these scenarios the mass based succinic acid yield is 1.12 g/g. This implies that the theoretical maximum yield is such that more succinic acid is formed than glucose consumed due to the fixation of carbon dioxide. Figure 3: Metabolic pathway for producing succinic acid without byproducts. NADH balance is achieved by oxidative TCA branch.

  7. 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.

  8. 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 ...

  9. Acid–base extraction - Wikipedia

    en.wikipedia.org/wiki/Acid–base_extraction

    Acid–base extraction is a subclass of liquid–liquid extractions and involves the separation of chemical species from other acidic or basic compounds. [1] It is typically performed during the work-up step following a chemical synthesis to purify crude compounds [2] and results in the product being largely free of acidic or basic impurities.