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Chemical Structure
Chemical Structure
Chemical Structure

Glucuronolactone [32449-92-6]

Research Use Only
CDX-G0044
Chemodex
CAS Number32449-92-6
Product group Chemicals
Estimated Purity>98%
Molecular Weight176.12
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Glucuronolactone [32449-92-6]
  • Delivery Days Customer
    10
  • CAS Number
    32449-92-6
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Molecular Formula
    C6H8O6
  • Molecular Weight
    176.12
  • Scientific Description
    Chemical. CAS: 32449-92-6. Formula: C6H8O6. MW: 176.12. Synthetic. 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. - 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.
  • SMILES
    O[C@@H]1[C@@H](OC2=O)[C@@H]([C@@H]2O)OC1O
  • Storage Instruction
    RT
  • UNSPSC
    12352200