Record Information |
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Version | 1.0 |
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Creation date | 2015-10-09 22:28:18 UTC |
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Update date | 2017-01-19 02:36:12 UTC |
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FoodComEx ID | PC000098 |
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FoodDB Record | FDB000951 |
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Chemical Information |
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Name | 2-Furancarboxylic acid |
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Description | Isolated from roots of Phaseolus vulgaris (kidney bean)
Furoic acid is a metabolite that appears in the urine of workers occupationally exposed to furfural and is marker of exposure to this compound. Furfural is a heterocyclic aldehyde that is commonly used as a solvent in industry. It is readily absorbed into the body via the lungs and has significant skin absorption. Furfural is an irritant of the eyes, mucous membranes, and skin and is a central nervous system depressant. Furfural as a confirmed animal carcinogen with unknown relevance to humans (It has been suggested that is a substance that produces hepatic cirrhosis). Once in the body, furfural is metabolized rapidly via oxidation to the metabolite furoic acid, which is then conjugated with glycine and excreted in the urine in both free and conjugated forms. (PMID: 3751566, 4630229, 12587683). Furoic acid is a biomarker for the consumption of beer. |
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CAS Number | 88-14-2 |
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Structure | |
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Synonyms | Synonym | Source |
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α-furancarboxylic acid | biospider | α-furoic acid | biospider | 2-Carboxyfuran | biospider | 2-furancarboxilic acid | biospider | 2-Furancarboxylate | Generator | 2-Furanoate | biospider | 2-Furanoic acid | biospider | 2-Furoate | biospider | 2-Furoic acid | biospider | 2-Furoic acid [per EINECS] | biospider | 2-Furoic acid, 8CI | db_source | 2-FUROIC ACID, PRACT | biospider | A-furancarboxylate | biospider | A-furancarboxylic acid | biospider | A-furoate | biospider | a-Furoic acid | db_source | Acide 2-furoique | ChEBI | Acido 2-furoico | ChEBI | Alpha-furancarboxylate | biospider | Alpha-furancarboxylic acid | biospider | Alpha-furoate | biospider | Alpha-furoic acid | biospider | B-furancarboxylate | biospider | B-furancarboxylic acid | biospider | B-furoate | biospider | B-furoic acid | biospider | Beta-furancarboxylate | biospider | Beta-furancarboxylic acid | biospider | Beta-furoate | biospider | Beta-furoic acid | biospider | FOA | biospider | Furan-2-carbonsaeure | ChEBI | Furan-2-carboxylic acid | biospider | Furancarboxylate | biospider | Furancarboxylic acid | biospider | Furancarboxylic acid-(2) | biospider | Furoate | biospider | Furoic acid | biospider | Furoica | biospider | Pyromucate | biospider | Pyromucic acid | db_source | α-furancarboxylate | Generator | α-furancarboxylic acid | Generator | α-furoate | Generator | α-furoic acid | Generator |
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Chemical Formula | C5H4O3 |
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IUPAC name | furan-2-carboxylic acid |
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InChI Identifier | InChI=1S/C5H4O3/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7) |
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InChI Key | SMNDYUVBFMFKNZ-UHFFFAOYSA-N |
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Isomeric SMILES | OC(=O)C1=CC=CO1 |
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Average Molecular Weight | 112.0835 |
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Monoisotopic Molecular Weight | 112.016043994 |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as furoic acids. These are organic compounds containing a furoic acid moiety, with a structure characterized by a furan ring bearing a carboxylic acid group at the C2 or C3 carbon atom. |
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Kingdom | Organic compounds |
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Super Class | Organoheterocyclic compounds |
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Class | Furans |
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Sub Class | Furoic acid and derivatives |
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Direct Parent | Furoic acids |
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Alternative Parents | |
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Substituents | - Furoic acid
- Heteroaromatic compound
- Oxacycle
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Carboxylic acid derivative
- Organic oxygen compound
- Organic oxide
- Hydrocarbon derivative
- Organooxygen compound
- Aromatic heteromonocyclic compound
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Molecular Framework | Aromatic heteromonocyclic compounds |
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External Descriptors | |
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Physico-Chemical Properties - Experimental |
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Property | Value | Reference |
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Experimental logP | 0.64 | POMONA (1987) |
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Experimental Water Solubility | 37.1 mg/mL at 15 oC | YALKOWSKY,SH & DANNENFELSER,RM (1992) |
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Melting Point | Mp 133-134° | DFC |
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Foods of Origin |
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Food | Content Range | Average | Reference |
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Food | | | Reference |
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Production Data |
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Production Method | commercial |
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Production Method Reference | Not Available |
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Production Method Reference File | Not Available |
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Quantity Available | Production upon request, up to 1 g |
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Delivery Time | Not Available |
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Storage Form | solid |
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Storage Conditions | -80°C |
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Stability | Not Available |
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Purity | Not Available |
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Spectra |
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Spectral Data Upon Request | Not Available |
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Provider Information |
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Commercial Vendors |
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AKSci | A024 |
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AKSci | J10740 |
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MetaSci | HMDB0000617 |
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Sigma-Aldrich | HMDB0000617 |
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Toronto Research Chemicals | F863775 |
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