![]() | |
Names | |
---|---|
Other names
Furan-2,5-dicarboxaldehyde,
2,5-Diformylfuran
| |
Identifiers | |
3D model (
JSmol)
|
|
Abbreviations | FDC |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.011.382 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C6H4O3 | |
Molar mass | 124.095 g·mol−1 |
Hazards | |
GHS labelling: | |
![]() | |
Warning | |
H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P305+P351+P338 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
2,5-Furandicarboxaldehyde (FDC) is an organic compound with the molecular formula C4H2O(CHO)2. It consists of a furan ring with aldehyde groups on the 2 and 5 position. It is therefore classified as a dialdehyde.
2,5-Furandicarboxaldehyde is an oxidation product of 5-hydroxymethyl furfural (HMF), which in turn can be prepared from fructose. Alternatively, methods have been developed to convert fructose in one step to 2,5-furandicarboxaldehyde. [1] The conversion from fructose to HMF and FDC can be performed relatively efficiently and following the principles of green chemistry. As such, these materials are often considered as "greener" bio-based alternatives.[ citation needed]
2,5-Furandicarboxaldehyde can be used in the preparation of polyimine vitrimers. [2] It can also be applied as an alternative to glutaraldehyde as crosslinking agent for covalent enzyme immobilisation. [3]
![]() | |
Names | |
---|---|
Other names
Furan-2,5-dicarboxaldehyde,
2,5-Diformylfuran
| |
Identifiers | |
3D model (
JSmol)
|
|
Abbreviations | FDC |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.011.382 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C6H4O3 | |
Molar mass | 124.095 g·mol−1 |
Hazards | |
GHS labelling: | |
![]() | |
Warning | |
H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P305+P351+P338 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
2,5-Furandicarboxaldehyde (FDC) is an organic compound with the molecular formula C4H2O(CHO)2. It consists of a furan ring with aldehyde groups on the 2 and 5 position. It is therefore classified as a dialdehyde.
2,5-Furandicarboxaldehyde is an oxidation product of 5-hydroxymethyl furfural (HMF), which in turn can be prepared from fructose. Alternatively, methods have been developed to convert fructose in one step to 2,5-furandicarboxaldehyde. [1] The conversion from fructose to HMF and FDC can be performed relatively efficiently and following the principles of green chemistry. As such, these materials are often considered as "greener" bio-based alternatives.[ citation needed]
2,5-Furandicarboxaldehyde can be used in the preparation of polyimine vitrimers. [2] It can also be applied as an alternative to glutaraldehyde as crosslinking agent for covalent enzyme immobilisation. [3]