| Record Information |
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| Version | 1.0 |
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| Creation date | 2015-10-09 22:33:01 UTC |
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| Update date | 2017-01-19 02:36:38 UTC |
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| FoodComEx ID | PC000837 |
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| FoodDB Record | FDB023903 |
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| Chemical Information |
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| Name | D-Glucurono-6,3-lactone |
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| Description | D-glucurono-6,3-lactone participates in ascorbate and aldarate metabolism. D-glucurono-6,3-lactone is produced by the reaction between D-glucaric acid and the enzyme, aldehyde dehydrogenase (NAD+) [EC: 1.2.1.3]. [HMDB] |
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| CAS Number | 32449-92-6 |
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| Structure | |
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| Synonyms | | Synonym | Source |
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| D-glucurone | hmdb | | D-Glucuronic acid lactone | HMDB | | D-Glucurono-3,6-lactone | hmdb | | D-glucuronolactone | hmdb | | Dicurone | hmdb | | Glucofuranurono-6,3-lactone | hmdb | | Glucoxy | HMDB | | Glucurolactone | hmdb | | Glucuron | HMDB | | Glucurone | HMDB | | Glucuronic acid lactone | hmdb | | Glucuronolactone | HMDB | | Glucuronosan | hmdb | | Gluronsan | hmdb | | Glycurone | HMDB | | Guronsan | HMDB | | Reulatt s.s. | hmdb |
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| Chemical Formula | C6H8O6 |
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| IUPAC name | (3R,3aR,5R,6R,6aR)-3,5,6-trihydroxy-hexahydrofuro[3,2-b]furan-2-one |
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| InChI Identifier | InChI=1S/C6H8O6/c7-1-3-4(12-5(1)9)2(8)6(10)11-3/h1-5,7-9H/t1-,2-,3-,4-,5-/m1/s1 |
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| InChI Key | OGLCQHRZUSEXNB-WHDMSYDLSA-N |
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| Isomeric SMILES | O[C@@H]1O[C@@H]2[C@@H](O)C(=O)O[C@@H]2[C@H]1O |
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| Average Molecular Weight | 176.1241 |
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| Monoisotopic Molecular Weight | 176.032087988 |
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| Chemical Taxonomy |
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| Description | Belongs to the class of organic compounds known as isosorbides. These are organic polycyclic compounds containing an isosorbide(1,4-Dianhydrosorbitol) moiety, which consists of two -oxolan-3-ol rings. |
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| Kingdom | Organic compounds |
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| Super Class | Organoheterocyclic compounds |
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| Class | Furofurans |
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| Sub Class | Isosorbides |
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| Direct Parent | Isosorbides |
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| Alternative Parents | |
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| Substituents | - Isosorbide
- Gamma butyrolactone
- Monosaccharide
- Tetrahydrofuran
- Carboxylic acid ester
- Hemiacetal
- Lactone
- Secondary alcohol
- Monocarboxylic acid or derivatives
- Polyol
- Carboxylic acid derivative
- Oxacycle
- Hydrocarbon derivative
- Carbonyl group
- Organic oxide
- Organic oxygen compound
- Alcohol
- Organooxygen compound
- Aliphatic heteropolycyclic compound
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| Molecular Framework | Aliphatic heteropolycyclic compounds |
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| External Descriptors | Not Available |
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| Physico-Chemical Properties - Experimental |
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| Property | Value | Reference |
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| Experimental logP | Not Available | |
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| Experimental Water Solubility | Not Available | |
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| Melting Point | Not Available | |
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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 3 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 | H861 |
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| AKSci | J93459 |
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| MetaSci | HMDB0006355 |
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| Sigma-Aldrich | HMDB0006355 |
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| Toronto Research Chemicals | G596900 |
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