2,5-Furandicarboxylic acid structure
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Common Name | 2,5-Furandicarboxylic acid | ||
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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 |
Signal Word | Warning |
Use of 2,5-Furandicarboxylic acid2,5-Furandicarboxylic acid is a biomass-derived diacid that can be used to make polymers including polyethylene furandicarboxylate (PEF). |
Name | furan-2,5-dicarboxylic acid |
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Synonym | More Synonyms |
Description | 2,5-Furandicarboxylic acid is a biomass-derived diacid that can be used to make polymers including polyethylene furandicarboxylate (PEF). |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
References |
Density | 1.6±0.1 g/cm3 |
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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 |
Symbol |
GHS07 |
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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 |
Precursor 10 | |
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DownStream 9 | |
HS Code | 2932190090 |
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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% |
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... |
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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... |
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The identification and metabolic origin of 2-furoylglycine and 2,5-furandicarboxylic acid in human urine.
Clin. Chim. Acta 41 , 199-207, (1972)
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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 |