2,5-Furandicarboxylic acid

Modify Date: 2024-01-01 19:09:00

2,5-Furandicarboxylic acid Structure
2,5-Furandicarboxylic acid structure
Common Name 2,5-Furandicarboxylic acid
CAS Number 3238-40-2 Molecular Weight 156.093
Density 1.6±0.1 g/cm3 Boiling Point 419.2±30.0 °C at 760 mmHg
Molecular Formula C6H4O5 Melting Point >310°C (dec.)
MSDS Chinese USA Flash Point 207.3±24.6 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 2,5-Furandicarboxylic acid


2,5-Furandicarboxylic acid is a biomass-derived diacid that can be used to make polymers including polyethylene furandicarboxylate (PEF).

 Names

Name furan-2,5-dicarboxylic acid
Synonym More Synonyms

 2,5-Furandicarboxylic acid Biological Activity

Description 2,5-Furandicarboxylic acid is a biomass-derived diacid that can be used to make polymers including polyethylene furandicarboxylate (PEF).
Related Catalog
Target

Human Endogenous Metabolite

References

[1]. Graham R. Dick, et al. A scalable carboxylation route to furan-2,5-dicarboxylic acid. Green Chemistry. 10 May 2017.

 Chemical & Physical Properties

Density 1.6±0.1 g/cm3
Boiling Point 419.2±30.0 °C at 760 mmHg
Melting Point >310°C (dec.)
Molecular Formula C6H4O5
Molecular Weight 156.093
Flash Point 207.3±24.6 °C
Exact Mass 156.005875
PSA 87.74000
LogP -0.02
Vapour Pressure 0.0±1.0 mmHg at 25°C
Index of Refraction 1.581
Storage condition Hygroscopic, -20°C Freezer, Under Inert Atmosphere
Stability Light Sensitive, Very Hygroscopic

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H319
Precautionary Statements P280-P305 + P351 + P338-P337 + P313
Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases S26-S36/37/39
RIDADR NONH for all modes of transport
HS Code 2932190090

 Synthetic Route

 Customs

HS Code 2932190090
Summary 2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

 Articles3

More Articles
Age-related reference values for urinary organic acids in a healthy Turkish pediatric population.

Clin. Chem. 40(6) , 862-6, (1994)

Organic acid concentrations were quantified by gas chromatography and the individual acids identified by mass spectrometry in urine specimens from a healthy Turkish pediatric population of ages 2 days...

Carbon dioxide utilization via carbonate-promoted C-H carboxylation.

Nature 531 , 215-9, (2016)

Using carbon dioxide (CO2) as a feedstock for commodity synthesis is an attractive means of reducing greenhouse gas emissions and a possible stepping-stone towards renewable synthetic fuels. A major i...

The identification and metabolic origin of 2-furoylglycine and 2,5-furandicarboxylic acid in human urine.

Clin. Chim. Acta 41 , 199-207, (1972)

 Synonyms

Furan 2,5-dicarboxylic acid
Dehydroschleimsaeure
Dehydromucate
MFCD00016582
Dehydromucic acid
2,5-furandicarboxylate
2,5-dicarboxyfuran
furan-2,5-dicarbonsaeure
Furan-2,5-dicarboxylic acid
EINECS 221-800-8
2,5-Furandicarboxylic acid
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