Date published: 2025-10-19

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2,5-Furandicarboxylic Acid (CAS 3238-40-2)

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Alternate Names:
Dehydromucic Acid
Application:
2,5-Furandicarboxylic Acid is a mutagenesis research chemicals
CAS Number:
3238-40-2
Molecular Weight:
156.09
Molecular Formula:
C6H4O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2,5-Furandicarboxylic acid (FDCA) is a renewable organic compound with applications in materials science research due to its potential as a substitute for terephthalic acid in the production of polyesters and plastics. Researchers are particularly interested in 2,5-Furandicarboxylic acid for its role in synthesizing polyethylene furanoate (PEF), a biobased polymer that exhibits superior barrier properties and could offer a more sustainable alternative to traditional petroleum-based plastics. In the realm of green chemistry, 2,5-Furandicarboxylic acid is a key subject of study because it can be produced from biomass, presenting a more environmentally friendly approach to polymer production. Investigations into catalysis also feature 2,5-Furandicarboxylic acid, where scientists are exploring efficient catalytic systems to optimize its synthesis from renewable resources like fructose or other sugars.


2,5-Furandicarboxylic Acid (CAS 3238-40-2) References

  1. Advances in catalytic production of bio-based polyester monomer 2,5-furandicarboxylic acid derived from lignocellulosic biomass.  |  Zhang, J., et al. 2015. Carbohydr Polym. 130: 420-8. PMID: 26076643
  2. Self-sustained enzymatic cascade for the production of 2,5-furandicarboxylic acid from 5-methoxymethylfurfural.  |  Carro, J., et al. 2018. Biotechnol Biofuels. 11: 86. PMID: 29619082
  3. Biocatalytic production of 2,5-furandicarboxylic acid: recent advances and future perspectives.  |  Yuan, H., et al. 2020. Appl Microbiol Biotechnol. 104: 527-543. PMID: 31820067
  4. Recent Advances in Carboxylation of Furoic Acid into 2,5-Furandicarboxylic Acid: Pathways towards Bio-Based Polymers.  |  Drault, F., et al. 2020. ChemSusChem. 13: 5164-5172. PMID: 32725856
  5. Heterogeneous Catalytic Conversion of Sugars Into 2,5-Furandicarboxylic Acid.  |  Deshan, ADK., et al. 2020. Front Chem. 8: 659. PMID: 32850671
  6. 2,5-Furandicarboxylic acid production from furfural by sequential biocatalytic reactions.  |  Kawanabe, K., et al. 2021. J Biosci Bioeng. 132: 18-24. PMID: 33846091
  7. Facile Production of 2,5-Furandicarboxylic Acid via Oxidation of Industrially Sourced Crude 5-Hydroxymethylfurfural.  |  Zuo, X., et al. 2022. ChemSusChem. 15: e202102050. PMID: 34913609
  8. Production of the 2,5-Furandicarboxylic Acid Bio-Monomer From 5-Hydroxymethylfurfural Over a Molybdenum-Vanadium Oxide Catalyst.  |  Liu, J., et al. 2022. Front Chem. 10: 853112. PMID: 35372283
  9. Current Advances in the Sustainable Conversion of 5-Hydroxymethylfurfural into 2,5-Furandicarboxylic Acid.  |  Totaro, G., et al. 2022. ChemSusChem. 15: e202200501. PMID: 35438242
  10. Efficient Catalytic Conversion of 5-Hydroxymethylfurfural to 2,5-Furandicarboxylic Acid over Ruthenium Cluster-Embedded Ni(OH)2 Catalyst.  |  Chai, X., et al. 2022. ChemSusChem. 15: e202200863. PMID: 35716074
  11. Alloy-Driven Efficient Electrocatalytic Oxidation of Biomass-Derived 5-Hydroxymethylfurfural towards 2,5-Furandicarboxylic Acid: A Review.  |  Guo, M., et al. 2022. ChemSusChem. 15: e202201074. PMID: 35790081
  12. Production of 2,5-furandicarboxylic acid via oxidation of 5-hydroxymethylfurfural over Pt/C in a continuous packed bed reactor.  |  Wadaugsorn, K., et al. 2022. RSC Adv. 12: 18084-18092. PMID: 35800325
  13. 2,5-Furandicarboxylic Acid: An Intriguing Precursor for Monomer and Polymer Synthesis.  |  Marshall, A., et al. 2022. Molecules. 27: PMID: 35807313

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,5-Furandicarboxylic Acid, 1 g

sc-220810
1 g
$92.00