Cas no 21675-47-8 (D-Xylo-2-Hexulosonic Acid)

D-Xylo-2-Hexulosonic Acid is a keto sugar acid derivative with notable applications in biochemical and pharmaceutical research. Its unique structure, featuring a ketone group at the C-2 position, makes it a valuable intermediate in the synthesis of specialized carbohydrates and glycoconjugates. This compound is particularly useful in studies involving metabolic pathways, enzymatic reactions, and the development of bioactive molecules. Its high purity and stability under controlled conditions ensure reliable performance in experimental settings. Researchers value D-Xylo-2-Hexulosonic Acid for its role in advancing understanding of sugar metabolism and its potential in designing novel therapeutic agents.
D-Xylo-2-Hexulosonic Acid structure
D-Xylo-2-Hexulosonic Acid structure
Product Name:D-Xylo-2-Hexulosonic Acid
CAS No:21675-47-8
MF:C6H10O7
MW:194.139402866364
CID:1058503
PubChem ID:159793
Update Time:2025-05-19

D-Xylo-2-Hexulosonic Acid Chemical and Physical Properties

Names and Identifiers

    • 2-Keto-D-gulonic Acid
    • 2-Keto-D-gulonic Acid Discontinued: see X750300
    • 2-Keto-D-gulonic Acid Discontinued: see X750300
    • D-Sorbosonic acid
    • D-Xylo-2-Hexulosonic Acid
    • D-xylo-Hex-2-ulosonic acid
    • Q63395365
    • (3R,4S,5R)-3,4,5,6-tetrahydroxy-2-oxohexanoic acid
    • J-010199
    • D-Xylo-hexulosonic Acid
    • Gulonic acid, 2-oxo-
    • 2-Keto-L-idonic acid
    • rel-(3R,4S,5R)-3,4,5,6-Tetrahydroxy-2-oxohexanoic acid
    • Provitamin C
    • SCHEMBL5803285
    • AD9F87F8-6B21-4645-830E-44DED44E8741
    • VBUYCZFBVCCYFD-FLRLBIABSA-N
    • xylo-2-Hexulosonic acid
    • 21675-47-8
    • Carboxy-xylose
    • DTXSID901313625
    • 16533-48-5
    • Inchi: 1S/C6H10O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h2-4,7-10H,1H2,(H,12,13)/t2-,3+,4-/m1/s1
    • InChI Key: VBUYCZFBVCCYFD-FLRLBIABSA-N
    • SMILES: O[C@H]([C@H](C(C(=O)O)=O)O)[C@@H](CO)O

Computed Properties

  • Exact Mass: 194.04265265g/mol
  • Monoisotopic Mass: 194.04265265g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 5
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 5
  • Complexity: 201
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 3
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -2.9
  • Topological Polar Surface Area: 135?2

Experimental Properties

  • Melting Point: >158°C (dec.)
  • Solubility: DMSO, Methanol, Water

D-Xylo-2-Hexulosonic Acid Security Information

  • Hazardous Material transportation number:NONH for all modes of transport
  • Storage Condition:Room Temperature

D-Xylo-2-Hexulosonic Acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd.
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D-Xylo-2-Hexulosonic Acid Related Literature

Additional information on D-Xylo-2-Hexulosonic Acid

D-Xylo-2-Hexulosonic Acid (CAS No. 21675-47-8): An Overview and Recent Advances

D-Xylo-2-Hexulosonic Acid (CAS No. 21675-47-8) is a unique and versatile compound that has garnered significant attention in the fields of chemistry, biochemistry, and pharmaceutical research. This compound, also known as Xylo-2-hexulosonic acid or Xylonic acid, is a six-carbon sugar acid derived from the oxidation of D-xylose. Its structural and chemical properties make it an important molecule in various biological processes and industrial applications.

The chemical structure of D-Xylo-2-Hexulosonic Acid is characterized by a hexose backbone with a carboxylic acid group at the C-2 position. This unique configuration imparts specific reactivity and solubility properties, making it suitable for a wide range of applications. The compound is highly soluble in water, which enhances its utility in aqueous environments, such as biological systems and industrial processes.

Recent studies have highlighted the potential of D-Xylo-2-Hexulosonic Acid in various biological contexts. One notable area of research is its role in carbohydrate metabolism. As a derivative of D-xylose, D-Xylo-2-Hexulosonic Acid can be metabolized by certain microorganisms, contributing to the breakdown of complex carbohydrates. This property has implications for understanding microbial metabolism and developing new biotechnological processes for producing valuable chemicals from renewable resources.

In the pharmaceutical industry, D-Xylo-2-Hexulosonic Acid has shown promise as a potential therapeutic agent. Research has indicated that it may have anti-inflammatory and antioxidant properties, which could be beneficial in treating various diseases. For instance, studies have explored its effects on reducing oxidative stress and inflammation in cellular models, suggesting potential applications in conditions such as arthritis and neurodegenerative disorders.

The synthesis of D-Xylo-2-Hexulosonic Acid has been optimized through various methods, including enzymatic and chemical routes. Enzymatic methods involve the use of specific enzymes to catalyze the oxidation of D-xylose to D-Xylo-2-Hexulosonic Acid. These methods are generally more environmentally friendly and can produce high yields with fewer by-products. Chemical synthesis methods, on the other hand, often involve multi-step processes that can be more challenging but offer greater control over the final product's purity and yield.

One recent advancement in the synthesis of D-Xylo-2-Hexulosonic Acid involves the use of biocatalytic approaches. Researchers have developed novel biocatalysts that can efficiently convert D-xylose to D-Xylo-2-Hexulosonic Acid under mild conditions. These biocatalysts not only improve the yield but also reduce the environmental impact of the synthesis process, making it more sustainable.

In addition to its biological and pharmaceutical applications, D-Xylo-2-Hexulosonic Acid has found use in analytical chemistry. Its unique chemical properties make it a valuable reagent for various analytical techniques, such as high-performance liquid chromatography (HPLC) and mass spectrometry (MS). These techniques are essential for characterizing complex mixtures and identifying trace amounts of compounds in biological samples.

The safety profile of D-Xylo-2-Hexulosonic Acid is another important aspect to consider. Extensive toxicological studies have shown that it is generally safe for use in both laboratory settings and industrial applications. However, as with any chemical compound, proper handling and storage procedures should be followed to ensure safety.

In conclusion, D-Xylo-2-Hexulosonic Acid (CAS No. 21675-47-8) is a multifaceted compound with significant potential in various fields. Its unique chemical structure and properties make it a valuable molecule for research and development in areas such as carbohydrate metabolism, pharmaceuticals, biotechnology, and analytical chemistry. Ongoing research continues to uncover new applications and optimize existing methods for its production and use, further solidifying its importance in the scientific community.

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