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  2. 2,6-Naphthalenedicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/2,6-Naphthalenedi...

    2,6-Naphthalenedicarboxylic acid is an organic compound with the formula C 10 H 6 (CO 2 H) 2. This colorless solid is one of several isomers of naphthalenedicarboxylic acid. This colorless solid is one of several isomers of naphthalenedicarboxylic acid.

  3. 2,5-Furandicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/2,5-Furandicarboxylic_acid

    2,5-Furandicarboxylic acid (FDCA) is an organic chemical compound consisting of two carboxylic acid groups attached to a central furan ring. It was first reported as dehydromucic acid by Rudolph Fittig and Heinzelmann in 1876, who produced it via the action of concentrated hydrobromic acid upon mucic acid . [ 2 ]

  4. Dicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Dicarboxylic_acid

    Dicarboxylic acids are used in the preparation of copolymers such as polyamides and polyesters. The most widely used dicarboxylic acid in the industry is adipic acid, which is a precursor in the production of nylon. Other examples of dicarboxylic acids include aspartic acid and glutamic acid, two amino acids in the human body.

  5. 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]

  6. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    The oxidation of primary alcohols to carboxylic acids can be carried out using a variety of reagents, but O 2 /air and nitric acid dominate as the oxidants on a commercial scale. Large scale oxidations of this type are used for the conversion of cyclohexanol alone or as a mixture with cyclohexanone to adipic acid. Similarly cyclododecanol is ...

  7. Polyethylene naphthalate - Wikipedia

    en.wikipedia.org/wiki/Polyethylene_naphthalate

    Two major manufacturing routes exist for polyethylene naphthalate (PEN), i.e. an ester or an acid process, named according to whether the starting monomer is a diester or a diacid derivative, respectively. In both cases for PEN, the glycol monomer is ethylene glycol.

  8. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    pentanedioic acid: glutaric acid propane-1,3-dicarboxylic acid n-pyrotartaric acid: HOOC(CH 2) 3 COOH 2-oxopentanedioic acid: α-ketoglutaric acid 2-ketoglutaric acid 2-oxoglutaric acid oxoglutaric acid: HOOC(CH 2) 2 COCOOH 3-oxopentanedioic acid: acetonedicarboxylic acid 3-oxoglutaric acid β-ketoglutaric acid 3-ketoglutaric acid: HOOCCH 2 ...

  9. Polyethylene furan-2,5-dicarboxylate - Wikipedia

    en.wikipedia.org/wiki/Polyethylene_furan-2,5-di...

    [2] [3] As an aromatic polyester from ethylene glycol it is a chemical analogue of polyethylene terephthalate (PET) and polyethylene naphthalate (PEN). PEF has been described in (patent) literature since 1951, [ 4 ] but has gained renewed attention since the US department of energy proclaimed its building block, FDCA, as a potential bio-based ...