Page last updated: 2024-12-07

2,5-furandicarboxylic acid

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

2,5-furandicarboxylic acid (FDCA) is a promising bio-based building block for the production of polymers, bioplastics, and other materials. It is derived from biomass sources, specifically from the furan compound 5-hydroxymethylfurfural (HMF), which is a versatile platform chemical.

FDCA's synthesis can be achieved through various methods, including oxidation of HMF using different catalysts and oxidizing agents.

The properties of FDCA, such as its rigidity and its ability to form strong intermolecular interactions, make it a suitable replacement for terephthalic acid in the production of polyethylene terephthalate (PET) and other polyesters.

FDCA-based polymers offer several advantages over traditional petroleum-based polymers, including their biodegradability, renewable origin, and potential for reduced greenhouse gas emissions.

The research focus on FDCA is driven by the need to develop sustainable and environmentally friendly alternatives to petroleum-based materials, reduce our dependence on fossil fuels, and contribute to a circular economy. The ongoing research explores efficient and cost-effective synthesis routes, the development of new FDCA-based polymers with improved properties, and the scale-up of production processes for industrial applications.'

furan-2,5-dicarboxylic acid : A member of the class of furans carrying two carboxy substituents at positions 2 and 5. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID76720
CHEBI ID84212
SCHEMBL ID38726
MeSH IDM0548979

Synonyms (56)

Synonym
73c4jj695c ,
einecs 221-800-8
furane-alpha,alpha'-dicarboxylic acid
unii-73c4jj695c
nsc 40740
ec 221-800-8
2,5-furandicarboxylic acid ,
furane-.alpha.,.alpha.'-dicarboxylic acid
dehydromucic acid
nsc-40740
nsc40740
furan-2,5-dicarboxylic acid
3238-40-2
EC-000.1599
furan-2,5-dicarbonsaeure
A5809
2,5-furandicarboxylicacid
C20450
2,5-furandicarboxylate
F0710
AKOS005169851
FT-0600520
AM20090470
AR-360/40225989
S6320
furan-2,5-dicarboxylicacid
CHEBI:84212
SCHEMBL38726
2,5-furan dicarboxylic acid
furan 2,5-dicarboxylic acid
DTXSID0062927
mfcd00016582
SY016939
Q-102496
PS-8853
AC-22967
2,5-furandicarboxylic acid, 97%
CS-W002105
GEO-01437
furane-a,a'-dicarboxylate
furan 2,5-dicarboxylate
dehydroschleimsaeure
dehydromucate
HY-W002105
STL508281
7fn ,
2,5 furan dicarboxylic acid
BCP16192
Q4596798
furane-2,5-dicarboxylic acid
furane-a,a'-dicarboxylic acid
fdca
1-boc-3-([(4-trifluoromethyl-phenyl)-amino]-methyl)-azetidine
EN300-110895
BBL037231
Z1255427253

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" These limitations can be efficiently overcome with the addition of catalase to the reaction medium, which removes the hydrogen peroxide formed during the oxidations, and the controlled dosage of the substrate to limit the amount of FFCA accumulated in the reaction."( Optimizing operational parameters for the enzymatic production of furandicarboxylic acid building block.
Martínez, AT; Sánchez-Ruiz, MI; Serrano, A, 2021
)
0.62
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
human urinary metaboliteAny metabolite (endogenous or exogenous) found in human urine samples.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
furansCompounds containing at least one furan ring.
dicarboxylic acidAny carboxylic acid containing two carboxy groups.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (62)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (1.61)29.6817
2010's34 (54.84)24.3611
2020's27 (43.55)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 39.77

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index39.77 (24.57)
Research Supply Index4.14 (2.92)
Research Growth Index6.26 (4.65)
Search Engine Demand Index53.29 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (39.77)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews9 (14.52%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other53 (85.48%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]