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Chemodex
Glucuronolactone
Product Details | |
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Synonyms | D-(+)-Glucuronic acid γ-lactone; D-(+)-Glucurono-6,3-lactone; D-Glucurono-6,3-lactone; D-Glucurone |
Product Type | Chemical |
Properties | |
Formula | C6H8O6 |
MW | 176.12 |
CAS | 32449-92-6 |
Purity Chemicals | ≥98% (HPLC) |
Appearance | White powder. |
Solubility | Soluble in water. |
Identity | Determined by NMR. |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | OGLCQHRZUSEXNB-VGASXLIASA-N |
Smiles | O[C@@H]1[C@@H](OC2=O)[C@@H]([C@@H]2O)OC1O |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +20°C |
Long Term Storage | +20°C |
Handling Advice | Protect from light and moisture. |
Use/Stability | Stable for at least 2 years after receipt when stored at +20°C. |
Documents | |
MSDS | Inquire |
Product Specification Sheet | |
Datasheet | Download PDF |
Naturally occurring carbohydrate derivative that is an important structural component of nearly all connective tissues and is also found in many plant gums. Metabolized to glucaric acid, xylitol, and L-xylulose, and humans may also be able to use glucuronolactone as a precursor for ascorbic acid synthesis. Used as a detoxicant. The liver uses glucose to create glucuronolactone, which inhibits the enzyme B-glucuronidase (metabolizes glucuronides), which should cause blood-glucuronide levels to rise. Glucuronides combine with toxic substances, such as morphine and depot medroxyprogesterone acetate, by converting them to water-soluble glucuronide-conjugates which are excreted in the urine. Used as building block and starting reagent for synthesis of drugs, optically active glucopyranoses and long-chain alkyl glucofuranosides.
(1) C.A. Marsh; Biochem. J. 99, 22 (1966) | (2) S.H. Kim, et al.; Acta Crystallogr. 22, 733 (1967) | (3) L. Trahan, et al.; Rev. Can. Biol. 29, 7 (1970) | (4) T. Kuzuya, et al.; Endocrinol. Jpn. 20, 369 (1973) | (5) A. Kirschning, et al.; Bioorg. Med. Chem. Lett. 7, 903 (1997) | (6) S. Suzuki, et al.; J. Chromatogr. Sci. 36, 357 (1998) | (7) A.F. Glawar, et al.; Chemistry 18, 9341 (2012)