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MilliporeSigma

722081

Sigma-Aldrich

2,5-Furandicarboxylic acid

97%

Sinónimos:

Dehydromucic acid, FDCA

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About This Item

Fórmula empírica (notación de Hill):
C6H4O5
Número de CAS:
Peso molecular:
156.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

powder

mp

>300 °C

SMILES string

OC(=O)c1ccc(o1)C(O)=O

InChI

1S/C6H4O5/c7-5(8)3-1-2-4(11-3)6(9)10/h1-2H,(H,7,8)(H,9,10)

InChI key

CHTHALBTIRVDBM-UHFFFAOYSA-N

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Application

2,5-Furandicarboxylic acid (FDCA) is a renewable, greener substitute for terephthalate in the production of polyesters. It is widely used as a precursor for the synthesis of bio-based polyesters and various other polymers.

Applications of FDCA in the synthesis of several metal-organic frameworks (MOFs) have also been reported.

Other Notes

2,5-Furandicarboxylic acid has been included among Top 10 biorefinery carbohydrate derivatives for the production of biobased industrial products.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

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Niki Poulopoulou et al.
Polymers, 12(1) (2020-01-23)
Intending to expand the thermo-physical properties of bio-based polymers, furan-based thermoplastic polyesters were synthesized following the melt polycondensation method. The resulting polymers, namely, poly(ethylene 2,5-furandicarboxylate) (PEF), poly(propylene 2,5-furandicarboxylate) (PPF), poly(butylene 2,5-furandicarboxylate) (PBF) and poly(1,4-cyclohexanedimethylene 2,5-furandicarboxylate) (PCHDMF) are used in blends
Giulia Guidotti et al.
International journal of molecular sciences, 20(9) (2019-05-06)
Biopolymers are gaining increasing importance as substitutes for plastics derived from fossil fuels, especially for packaging applications. In particular, furanoate-based polyesters appear as the most credible alternative due to their intriguing physic/mechanical and gas barrier properties. In this study, block
The furan counterpart of poly (ethylene terephthalate): An alternative material based on renewable resources.
Gandini A, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 47(1), 295-298 (2009)
Synthesis and properties of a bio-based epoxy resin from 2, 5-furandicarboxylic acid (FDCA).
Deng J, et al.
Royal Society of Chemistry Advances, 5(21), 15930-15939 (2015)
Three luminescent metal?organic frameworks constructed from trinuclear zinc (ii) clusters and furan-2, 5-dicarboxylate.
Li H H, et al.
CrystEngComm, 17(27), 5101-5109 (2015)

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