Cas no 61278-30-6 (D-Saccharic acid 1,4-lactone hydrate)

D-Saccharic acid 1,4-lactone hydrate is a cyclic ester derivative of D-saccharic acid, commonly used as a biochemical reagent and intermediate in organic synthesis. Its key advantages include high purity and stability in hydrated form, making it suitable for precise laboratory applications. The compound serves as a precursor in enzymatic studies, particularly in carbohydrate metabolism research, due to its role as a lactonase substrate. Its water solubility and well-defined structure facilitate controlled reactions in analytical and synthetic chemistry. Additionally, it finds utility in pharmaceutical and food science applications, where its predictable degradation profile is advantageous for controlled-release formulations and food acidulant studies.
D-Saccharic acid 1,4-lactone hydrate structure
61278-30-6 structure
Product Name:D-Saccharic acid 1,4-lactone hydrate
CAS No:61278-30-6
MF:C6H10O8
MW:210.138803005219
MDL:MFCD00005389
CID:854761
PubChem ID:24899420
Update Time:2025-06-09

D-Saccharic acid 1,4-lactone hydrate Chemical and Physical Properties

Names and Identifiers

    • D-SACCHARIC ACID 1 4-LACTONE
    • D-Glucaro-1,4-lactone Monohydrate
    • d-glucaric acid-1,4-lactone
    • D-Glucaric acid-1,4-lactone, D-Saccharolactone
    • D-Saccharic acid 1,4-lactone monohydrate
    • D-Saccharic acid 1,4-lactone monohydrate,D-Glucaric acid-1,4
    • (2S)-2-[(3R,4R)-3,4-dihydroxy-5-oxooxolan-2-yl]-2-hydroxyacetic acid,hydrate
    • 1,4-Lactone-D-glucaric Acid Monohydrate
    • D-Glucaro-1,4-lacton
    • D-Saccharolactone
    • D-Saccharic acid 1,4-lactone hydrate
    • BS-29047
    • CHEMBL4649498
    • 61278-30-6
    • F82873
    • CS-0167111
    • (2S)-2-[(2S,3R,4R)-3,4-dihydroxy-5-oxooxolan-2-yl]-2-hydroxyacetic acid hydrate
    • HY-134453A
    • (2S)-2-[(2S,3R,4R)-3,4-dihydroxy-5-oxooxolan-2-yl]-2-hydroxyacetic acid;hydrate
    • SCHEMBL2223182
    • D-Saccharic acid 1,4-lactone (hydrate)
    • (S)-2-((2S,3R,4R)-3,4-Dihydroxy-5-oxotetrahydrofuran-2-yl)-2-hydroxyaceticacidhydrate
    • (S)-2-((2S,3R,4R)-3,4-Dihydroxy-5-oxotetrahydrofuran-2-yl)-2-hydroxyacetic acid hydrate
    • AKOS015915764
    • MDL: MFCD00005389
    • Inchi: 1S/C6H8O7.H2O/c7-1-2(8)6(12)13-4(1)3(9)5(10)11;/h1-4,7-9H,(H,10,11);1H2/t1-,2-,3+,4+;/m1./s1
    • InChI Key: NPFKVZHSFSFLPU-QGBSHYGGSA-N
    • SMILES: O1C([C@@H]([C@H]([C@H]1[C@@H](C(=O)O)O)O)O)=O.O

Computed Properties

  • Exact Mass: 192.02700
  • Monoisotopic Mass: 210.03756727g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 5
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 237
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 3
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: 6
  • XLogP3: nothing
  • Topological Polar Surface Area: 125?2

Experimental Properties

  • Color/Form: White powder
  • Density: 2.0±0.1 g/cm3
  • Melting Point: 80-82°C
  • Boiling Point: 537.6±23.0 °C at 760 mmHg
  • Flash Point: 230.1±16.1 °C
  • Solubility: Acetone (Slightly), DMSO (Slightly), Methanol (Slightly)
  • PSA: 124.29000
  • LogP: -2.92090
  • Solubility: Not available
  • Vapor Pressure: 0.0±3.2 mmHg at 25°C

D-Saccharic acid 1,4-lactone hydrate Security Information

D-Saccharic acid 1,4-lactone hydrate Customs Data

  • HS CODE:2932190090
  • Customs Data:

    China Customs Code:

    2932190090

    Overview:

    2932190090 Other structurally non fused furan ring compounds. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

D-Saccharic acid 1,4-lactone hydrate Pricemore >>

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Additional information on D-Saccharic acid 1,4-lactone hydrate

D-Saccharic acid 1,4-lactone hydrate (CAS No: 61278-30-6) - A Comprehensive Overview

D-Saccharic acid 1,4-lactone hydrate, identified by its Chemical Abstracts Service (CAS) number 61278-30-6, is a significant compound in the field of chemical and pharmaceutical research. This cyclic ester derivative of D-saccharic acid has garnered considerable attention due to its unique chemical properties and diverse applications. The compound's structure, characterized by a five-membered lactone ring, makes it a versatile intermediate in organic synthesis and a potential candidate for various biochemical processes.

The< strong>D-Saccharic acid 1,4-lactone hydrate molecule exhibits remarkable stability and reactivity, which are critical factors in its utility across multiple scientific domains. Its hydrous form enhances solubility in polar solvents, making it an attractive choice for formulations requiring high bioavailability. This property is particularly relevant in the development of pharmaceuticals where solubility can significantly impact efficacy and patient compliance.

Recent advancements in the field of enzymatic catalysis have highlighted the role of< strong>D-Saccharic acid 1,4-lactone hydrate as a substrate for various biocatalysts. Studies have demonstrated its potential in the production of fine chemicals and pharmaceutical intermediates through green chemistry approaches. The compound's ability to undergo regioselective reactions under mild conditions aligns well with the growing emphasis on sustainable and environmentally friendly synthetic methodologies.

In the realm of medicinal chemistry, the< strong>D-Saccharic acid 1,4-lactone hydrate derivative has been explored for its pharmacological properties. Research indicates that it may serve as a precursor for novel therapeutic agents targeting metabolic disorders. The lactone ring's structural motif is known to interact with biological targets in ways that could lead to the development of innovative drugs. For instance, studies have suggested its potential role in modulating enzyme activity associated with glucose metabolism.

The compound's< strong>CAS No: 61278-30-6 provides a unique identifier that facilitates accurate documentation and tracking in research and industrial settings. This standardized naming convention ensures that scientists worldwide can reliably reference and utilize< strong>D-Saccharic acid 1,4-lactone hydrate in their work. The CAS registry system is an essential tool in chemical research, enabling precise communication and collaboration across disciplines.

Industrial applications of< strong>D-Saccharic acid 1,4-lactone hydrate are also noteworthy. Its incorporation into polymer matrices has been investigated for the development of biodegradable materials. The compound's ability to form stable complexes with other polymers makes it a valuable component in advanced material science research. These developments hold promise for creating sustainable alternatives to traditional plastics.

The biochemical significance of< strong>D-Saccharic acid 1,4-lactone hydrate extends to its role as a cofactor in enzymatic reactions. Researchers have identified its participation in pathways involving glycolysis and gluconeogenesis, underscoring its importance in cellular metabolism. Understanding these interactions can lead to insights into metabolic diseases and inform the design of targeted therapies.

In conclusion, the< strong>D-Saccharic acid 1,4-lactone hydrate (CAS No: 61278-30-6) is a multifaceted compound with broad applications in chemical synthesis, pharmaceutical development, and material science. Its unique structural features and biochemical properties make it a subject of intense research interest. As scientific understanding advances, the potential uses of this compound are likely to expand, further solidifying its importance in modern science and industry.

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