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  • 41670-99-9, 八乙酰壳二糖, Chitobiose octaacetate, CAS:41670-99-9
41670-99-9, 八乙酰壳二糖, Chitobiose octaacetate, CAS:41670-99-9

41670-99-9, 八乙酰壳二糖, Chitobiose octaacetate, CAS:41670-99-9

41670-99-9 , 八乙酰壳二糖,
Chitobiose octaacetate,
CAS:41670-99-9
C28H40N2O17 / 676.62
MFCD00083612

Chitobiose octaacetate

八乙酰壳二糖,

Chitobiose octaacetate (CBA) is a disaccharide derivative that is commonly used in scientific research as a precursor for synthesizing chitin and chitosan, two biopolymers that have various practical applications in industry and biomedicine. CBA is a derivative of chitin, which is a natural polysaccharide found in the exoskeletons of crustaceans, insects, and fungi.

Synthesis and Characterization

CBA can be synthesized from chitobiose by acetylation using acetic anhydride and pyridine as catalysts. The resulting product can be purified using column chromatography techniques and analyzed using analytical methods, like nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, and infrared (IR) spectroscopy.

Analytical Methods

NMR is a powerful method for determining the purity and identity of CBA. Proton (^1H) and carbon-13 (^13C) NMR spectra can be used to confirm the structure and acetylation pattern of the molecule. IR and mass spectroscopy techniques are also commonly used to identify the functional groups and molecular weight of CBA.

Biological Properties

CBA has been shown to have antibacterial and antifungal properties, making it a potentially useful compound for controlling microbial growth in various settings. It has also been studied for its immunostimulatory properties, as it can activate complement pathways and macrophage phagocytosis.

Toxicity and Safety in Scientific Experiments

While CBA has been shown to be relatively non-toxic to cells in vitro, more studies are needed to determine its potential toxicity in vivo. It is important to use appropriate safety measures and follow guidelines for handling and disposing of CBA in scientific experiments.

Applications in Scientific Experiments

CBA is commonly used as a precursor for synthesizing chitin and chitosan, two biopolymers that have various practical applications in industry and biomedicine. Chitosan, for example, has been shown to have antimicrobial, wound healing, and drug delivery properties.

Current State of Research

Research on CBA has focused on its synthesis, chemical and physical properties, and potential applications in medical and industrial settings. Recent studies have explored its potential as a scaffold material for tissue engineering and as a drug delivery vehicle for targeted therapies.

Potential Implications in Various Fields of Research and Industry

CBA could have implications in various fields, including agriculture, biomedicine, and environmental remediation. For example, it could be used as a natural pesticide for controlling insect pests, as well as a wound healing agent for improving skin regeneration. It could also be used for removing heavy metals from contaminated soils and waters.

Limitations and Future Directions

One limitation of CBA is its relatively high production cost and labor-intensive synthesis. Future research could focus on developing more efficient synthesis methods and on exploring its potential as a sustainable and eco-friendly alternative to synthetic polymers. Other potential research directions include investigating its mechanisms of action in biological systems and exploring its potential as a diagnostic tool for detecting microbial infections.

In conclusion, chitobiose octaacetate is a versatile molecule that has the potential to be a valuable tool in scientific research and various fields of industry. Its unique properties and potential applications make it a fascinating subject for further investigation and development.

CAS Number41670-99-9
Product NameChitobiose octaacetate
IUPAC Name[(2R,3S,4R,5R)-5-acetamido-3-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-diacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4,6-diacetyloxyoxan-2-yl]methyl acetate
Molecular FormulaC28H40N2O17
Molecular Weight676.62 g/mol
InChIInChI=1S/C28H40N2O17/c1-11(31)29-21-26(43-17(7)37)24(20(10-40-14(4)34)45-27(21)44-18(8)38)47-28-22(30-12(2)32)25(42-16(6)36)23(41-15(5)35)19(46-28)9-39-13(3)33/h19-28H,9-10H2,1-8H3,(H,29,31)(H,30,32)/t19-,20-,21-,22-,23-,24-,25-,26-,27?,28+/m1/s1
InChI KeyJUYKRZRMNHWQCD-NCBZWLQXSA-N
SMILESCC(=O)NC1C(C(C(OC1OC2C(OC(C(C2OC(=O)C)NC(=O)C)OC(=O)C)COC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C
Synonyms2-(Acetylamino)-2-deoxy-4-O-[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-D-glucopyranose 1,3,6-Triacetate; Peracetylchitobiose;
Canonical SMILESCC(=O)NC1C(C(C(OC1OC2C(OC(C(C2OC(=O)C)NC(=O)C)OC(=O)C)COC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C
Isomeric SMILESCC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1O[C@@H]2[C@H](OC([C@@H]([C@H]2OC(=O)C)NC(=O)C)OC(=O)C)COC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C


CAS No: 7284-18-6,41670-99-9 Synonyms: N,N'-Diacetylchitobiose hexaacetatePeracetylchitobiose MDL No: MFCD00083612 Chemical Formula: C28H40N2O17 Molecular Weight: 676.62

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