2,5-Furandicarboxylic acid

Names

[ Name ]:
2,5-Furandicarboxylic acid

[Synonym ]:
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

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]:

Natural Products >> Acids and Aldehydes

Research Areas >> Others

[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.

[Related Small Molecules]

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

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

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

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

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%

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)

Related Compounds

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