L-xylo-hex-2-ulosonic acid manufacturers
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| | L-xylo-hex-2-ulosonic acid Basic information |
| Product Name: | L-xylo-hex-2-ulosonic acid | | Synonyms: | L-Xylohexulosonic acid;2-Keto-L-gulonsure;2-Oxo-2-deoxy-L-gulonic acid;2-Oxo-L-gulonic acid;L-xylo-2-Hexulosonic acid;3-Keto-L-gulonic acid;Einecs 208-403-5;Idonic acid, 2-keto-, L- | | CAS: | 526-98-7 | | MF: | C6H10O7 | | MW: | 194.14 | | EINECS: | 208-403-5 | | Product Categories: | | | Mol File: | 526-98-7.mol |  |
| | L-xylo-hex-2-ulosonic acid Chemical Properties |
| Melting point | 171 °C | | Boiling point | 550.6±50.0 °C(Predicted) | | density | 1.757±0.06 g/cm3(Predicted) | | vapor pressure | 0Pa at 25℃ | | solubility | DMSO (Slightly), Water (Slightly) | | pka | 2.10±0.54(Predicted) | | form | Solid | | color | Off-White to Pale Beige | | Water Solubility | 335.3g/L at 20℃ | | Stability: | Hygroscopic | | LogP | -3.08 at 22℃ |
| | L-xylo-hex-2-ulosonic acid Usage And Synthesis |
| Uses | 2-Keto-L-gulonic Acid is used in biological studies for the formation of sorbitol metabolism by Acetobacter melanogenus. | | Definition | ChEBI: 2-dehydro-L-idonic acid is a ketoaldonic acid. It is functionally related to a L-idonic acid and a L-gulonic acid. It is a conjugate acid of a 2-dehydro-L-idonate. | | Purification Methods | Crystallise 2-keto-L-gulonic acid from half its weight of water, wash it with Me2CO and dry it in vacuo. [Reichstein et al. Helv Chim Acta 17 311 1934, NMR: Crawford et al. J Am Chem Soc 102 2220 1980. Beilstein 3 IV 1985.] |
| | L-xylo-hex-2-ulosonic acid Preparation Products And Raw materials |
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