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728373

Sigma-Aldrich

2,5-Furandicarboxaldehyde

97%

Synonym(s):

2,5-Diformylfuran, 2,5-Furandicarbaldehyde, 5-Formylfurfural

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About This Item

Empirical Formula (Hill Notation):
C6H4O3
CAS Number:
823-82-5
Molecular Weight:
124.09
Beilstein:
109424
EC Number:
212-520-7
MDL number:
MFCD00671517
UNSPSC Code:
12352100
PubChem Substance ID:
329764395
NACRES:
NA.22

Quality Level

100

Assay

≥96.5% (HPLC)
97%

form

powder

storage temp.

−20°C

SMILES string

O=Cc1ccc(C=O)o1

InChI

1S/C6H4O3/c7-3-5-1-2-6(4-8)9-5/h1-4H

InChI key

PXJJKVNIMAZHCB-UHFFFAOYSA-N

General description

2,5-Furandicarboxaldehyde is an oxidation product of 5-hydroxymethyl furfural. It is used as an organic building block in chemical synthesis. It is also used as a precursor for the production of valuable biopolymers.

Application

2,5- Furandicarboxaldehyde can be used in the synthesis of sustainable thin–film composite (TFC) membranes by interfacial polymerization reaction with chitosan and it also acts as a fluorescent chemo sensor for Hg2+ ions.
2,5-Furandicarboxaldehyde can be used as a building block in the fabrication of sustainable thin-film composite (TFC) membranes by the interfacial polymerization reaction with chitosan.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

728373-VAR:
728373-1G:
728373-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF6725
BCBV9853
BCBM6360V
BCBN0651V
BCBL7496V

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Maria Ventura et al.
ChemSusChem, 11(8), 1305-1315 (2018-03-08)
Mixed oxides based on MgO⋅CeO2 were used as efficient catalysts in the aerobic oxidation of 5-hydroxymethylfurfural (5-HMF) to afford, with very high selectivity, either 2,5-diformylfuran (DFF, 99 %) or 2-formyl-5-furancarboxylic acid (FFCA, 90 %), depending on the reaction conditions. 5-Hydroxymethyl-2-furancarboxylic acid (HMFCA
Kasanneni Tirumala Venkateswara Rao et al.
ChemSusChem, 11(18), 3323-3334 (2018-07-15)
A highly active and inexpensive Co-Mn mixed-oxide catalyst was prepared and used for selective oxidation of 5-hydroxymethylfurfural (HMF) into 2, 5-furandicarboxylic acid (FDCA). Co-Mn mixed-oxide catalysts with different Co/Mn molar ratios were prepared through a simple solid-state grinding method-a low-cost
Zi-Wei Wang et al.
Bioresource technology, 303, 122930-122930 (2020-02-11)
The main aim of this work was to firstly develop a selective oxidation approach for biologically converting 5-hydroxymethylfurfural and furfural into the corresponding furan-based carboxylic acids with recombinant Escherichia coli HMFOMUT. Whole-cells of this recombinant strain harbored good biocatalytic activity
Hiram F Ramírez-Cahero et al.
Food chemistry, 245, 1131-1140 (2017-12-31)
The radiolytic decomposition of glucose, fructose, sucrose, ascorbic acid (H

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