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
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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.
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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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)
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)
Technology development for the production of biobased products from biorefinery carbohydrates?the US Department of Energy?s ?Top 10? revisited.
Bozell J J and Petersen G R,
Green Chemistry, 12(4), 539-554 (2010)
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
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