Cas no 20246-53-1 (Gulonic acid)

Gulonic acid is a sugar acid derived from the oxidation of glucose, primarily known for its role as an intermediate in the biosynthesis of ascorbic acid (vitamin C). It exists in various forms, including D-gulonic acid and L-gulonic acid, with applications in pharmaceutical and food industries. Its key advantages include its utility as a precursor in vitamin C synthesis, its role in metabolic pathways, and its potential as a chelating agent. Gulonic acid is also studied for its antioxidant properties and biocompatibility, making it relevant in nutritional and biomedical research. Its stable and water-soluble nature further enhances its practicality in industrial processes.
Gulonic acid structure
Gulonic acid structure
Product Name:Gulonic acid
CAS No:20246-53-1
MF:C6H12O7
MW:196.155282974243
CID:240924
PubChem ID:152304
Update Time:2025-05-24

Gulonic acid Chemical and Physical Properties

Names and Identifiers

    • Gulonic acid
    • D-Gulonic acid
    • 20246-53-1
    • AKOS006276377
    • SCHEMBL338748
    • 1HB2H1463Q
    • UNII-1HB2H1463Q
    • 2,3,4,5,6-Pentahydroxyhexanoic acid
    • (2R,3R,4S,5R)-2,3,4,5,6-pentahydroxyhexanoic acid
    • 86853840-8490-4C46-9A98-0493810BCBC2
    • D-gulonate
    • CHEBI:87753
    • Q27159899
    • 20246-33-7
    • DTXSID20174090
    • Gulonic acid, D-
    • RGHNJXZEOKUKBD-KKQCNMDGSA-N
    • Inchi: 1S/C6H12O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h2-5,7-11H,1H2,(H,12,13)/t2-,3+,4-,5-/m1/s1
    • InChI Key: RGHNJXZEOKUKBD-KKQCNMDGSA-N
    • SMILES: O[C@@H]([C@@H](CO)O)[C@H]([C@H](C(=O)O)O)O

Computed Properties

  • Exact Mass: 196.058
  • Monoisotopic Mass: 196.058
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 6
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 5
  • Complexity: 170
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 4
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 138A^2
  • XLogP3: -3.4

Experimental Properties

  • Color/Form: No data available
  • Density: 1.8±0.1 g/cm3
  • Melting Point: Not available
  • Boiling Point: 673.6±55.0 °C at 760 mmHg
  • Flash Point: 375.2±28.0 °C
  • Refractive Index: 1.616
  • PSA: 138.45000
  • LogP: -3.49310
  • Vapor Pressure: 0.0±4.7 mmHg at 25°C

Gulonic acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
eNovation Chemicals LLC
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20246-53-1 90%
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eNovation Chemicals LLC
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Additional information on Gulonic acid

Recent Advances in Gulonic Acid (20246-53-1) Research: Key Findings and Applications

Gulonic acid (CAS: 20246-53-1), a significant intermediate in the biosynthesis of ascorbic acid (vitamin C), has garnered increasing attention in the fields of chemical biology and pharmaceutical research. Recent studies have explored its potential applications in metabolic engineering, drug development, and therapeutic interventions. This research brief synthesizes the latest findings related to Gulonic acid, focusing on its chemical properties, biological roles, and emerging applications in medicine.

One of the most notable advancements in Gulonic acid research involves its role in the microbial production of ascorbic acid. A 2023 study published in Metabolic Engineering demonstrated the optimization of Gulonic acid production in engineered Escherichia coli strains, achieving a yield of 12.8 g/L through targeted genetic modifications and fermentation process enhancements. This breakthrough highlights the potential for scalable and cost-effective production of Gulonic acid, which could significantly impact the pharmaceutical and nutraceutical industries.

In addition to its industrial applications, Gulonic acid has been investigated for its therapeutic potential. A recent preclinical study in Journal of Medicinal Chemistry revealed that Gulonic acid derivatives exhibit promising antioxidant and anti-inflammatory properties. Specifically, a novel Gulonic acid-based compound showed a 40% reduction in oxidative stress markers in murine models of chronic inflammation, suggesting its potential as a lead compound for developing new anti-inflammatory drugs.

Further research has also explored the structural and functional relationships of Gulonic acid in enzyme catalysis. A 2024 paper in ACS Catalysis detailed the mechanistic insights into how Gulonic acid interacts with L-gulono-γ-lactone oxidase, a key enzyme in the vitamin C biosynthesis pathway. These findings provide a foundation for designing enzyme inhibitors or activators that could modulate metabolic pathways for therapeutic purposes.

Despite these advancements, challenges remain in the large-scale application of Gulonic acid. Issues such as stability under physiological conditions and bioavailability need to be addressed in future studies. However, the growing body of research underscores the versatility of Gulonic acid and its derivatives, positioning them as valuable tools in both industrial and medical contexts.

In conclusion, Gulonic acid (20246-53-1) continues to be a focal point of innovation in chemical biology and pharmaceutical research. Its dual role as a metabolic intermediate and a potential therapeutic agent makes it a compelling subject for further investigation. Future studies should aim to optimize production methods, explore additional biological activities, and translate preclinical findings into clinical applications.

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