722081
2,5-Furandicarboxylic acid
97%
Synonym(s):
Dehydromucic acid, FDCA
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About This Item
Empirical Formula (Hill Notation):
C6H4O5
CAS Number:
Molecular Weight:
156.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
221-800-8
MDL number:
Product Name
2,5-Furandicarboxylic acid, 97%
InChI key
CHTHALBTIRVDBM-UHFFFAOYSA-N
InChI
1S/C6H4O5/c7-5(8)3-1-2-4(11-3)6(9)10/h1-2H,(H,7,8)(H,9,10)
SMILES string
OC(=O)c1ccc(o1)C(O)=O
assay
97%
form
powder
mp
>300 °C
functional group
carboxylic acid
Quality Level
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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.
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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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)
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
Lucia Maini et al.
Polymers, 10(3) (2019-04-11)
α and β crystalline phases of poly(ethylene furanoate) (PEF) were determined using X-ray powder diffraction by structure resolution in direct space and Rietveld refinement. Moreover, the α' structure of a PEF sample was refined from data previously reported for PEF
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)
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