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    Glucuronolactone

    Available from stock

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      Glucuronolactone

      SKU
      G0044

      Category: Carbohydrates

      Synonyms
      D-(+)-Glucuronic acid γ , -lactone , D-(+)-Glucurono-6,3-lactone , D-Glucurono-6,3-lactone , D-Glucurone
      32449-92-6
      CAS-Number
      C6H8O6_x000D_
      Molecular Formula
      176.12
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (HPLC)
      Appearance
      White powder
      Identity
      1H-NMR

      Properties

      Solvents
      water
      Melting Point
      171-175°C
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      RT
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at RT.
      Transportation
      Not dangerous goods
      Description
      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
      InChi Key
      OGLCQHRZUSEXNB-VGASXLIASA-N
      References
      C.A. Marsh, Biochem. J. 99, 22 (1966) , S.H. Kim, et al., Acta Crystallogr. 22, 733 (1967) , L. Trahan, et al., Rev. Can. Biol. 29, 7 (1970) , T. Kuzuya, et al., Endocrinol. Jpn. 20, 369 (1973) , A. Kirschning, et al., Bioorg. Med. Chem. Lett. 7, 903 (1997) , S. Suzuki, et al., J. Chromatogr. Sci. 36, 357 (1998) , A.F. Glawar, et al., Chemistry 18, 9341 (2012)
      InChi
      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

      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.

      SKU: G0044 Category: Carbohydrates
      • Additional information

      Additional information

      Synonyms

      D-(+)-Glucuronic acid γ, -lactone, D-(+)-Glucurono-6,3-lactone, D-Glucurono-6,3-lactone, D-Glucurone

      Purity

      ≥98% (HPLC)

      Appearance

      White powder

      CAS-Number

      32449-92-6

      Molecular Formula

      C6H8O6_x000D_

      Molecular Weight

      176.12

      Identity

      1H-NMR

      Solvents

      water

      Melting Point

      171-175°C

      Smiles

      O[C@@H]1[C@@H](OC2=O)[C@@H]([C@@H]2O)OC1O

      InChi Key

      OGLCQHRZUSEXNB-VGASXLIASA-N

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      RT

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at RT.

      Transportation

      Not dangerous goods

      References

      C.A. Marsh, Biochem. J. 99, 22 (1966), S.H. Kim, et al., Acta Crystallogr. 22, 733 (1967), L. Trahan, et al., Rev. Can. Biol. 29, 7 (1970), T. Kuzuya, et al., Endocrinol. Jpn. 20, 369 (1973), A. Kirschning, et al., Bioorg. Med. Chem. Lett. 7, 903 (1997), S. Suzuki, et al., J. Chromatogr. Sci. 36, 357 (1998), A.F. Glawar, et al., Chemistry 18, 9341 (2012)

      InChi

      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

      Quantity

      25 g, 250 g, 500 g, Bulk

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