Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

722081

Sigma-Aldrich

2,5-Furandicarboxylic acid

97%

Synonym(s):

Dehydromucic acid, FDCA

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C6H4O5
CAS Number:
3238-40-2
Molecular Weight:
156.09
EC Number:
221-800-8
MDL number:
MFCD00016582
UNSPSC Code:
12352100
PubChem Substance ID:
329763895
NACRES:
NA.22
form:
powder
Assay:
97%
Pricing and availability is not currently available.

Assay

97%

form

powder

mp

>300 °C

functional group

carboxylic acid

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

2,5-Furandicarboxylic acid (FDCA) is a renewable, greener substitute for terephthalate in the production of polyesters.[1] It is widely used as a precursor for the synthesis of bio-based polyesters and various other polymers.[2][3][4][5]

Applications of FDCA in the synthesis of several metal-organic frameworks (MOFs) have also been reported.[6][7]

Other Notes

2,5-Furandicarboxylic acid has been included among Top 10 biorefinery carbohydrate derivatives for the production of biobased industrial products.[1]

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000394470
0000370106
0000370106
0000394470
0000288691

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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)
Crystalline Capsules: Metal?Organic Frameworks Locked by Size?Matching Ligand Bolts.
Wang H, et al.
Angewandte Chemie (International Edition in English), 54(20), 5966-5970 (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)
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
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service