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  • 10034-20-5 , 四-O-乙酰基-2-氨基-2-脱氧-b-D-葡萄糖盐酸盐, CAS:10034-20-5
10034-20-5 , 四-O-乙酰基-2-氨基-2-脱氧-b-D-葡萄糖盐酸盐, CAS:10034-20-5

10034-20-5 , 四-O-乙酰基-2-氨基-2-脱氧-b-D-葡萄糖盐酸盐, CAS:10034-20-5

10034-20-5 , Tetra-O-acetyl-b-D-glucosamine HCl,
四-O-乙酰基-2-氨基-2-脱氧-b-D-葡萄糖盐酸盐,
CAS:10034-20-5
C14H21NO9·HCl / 383.78
MFCD01075204

1,3,4,6-Tetra-O-acetyl-b-D-glucosamine HCl

四-O-乙酰基-2-氨基-2-脱氧-b-D-葡萄糖盐酸盐,

1,3,4,6-Tetra-O-acetyl-b-D-glucosamine HCl is a compound that can be used in the production of bacterial cellulose. It is a white powder with a molecular weight of 383.78. 1,3,4,6-Tetra-O-acetyl-b-D-glucosamine HCl has been shown to be effective in the cultivation of microorganisms such as bacteria and fungi. This product is also an additive for deionized water and deionized sucrose solutions. Tetraacetylated glucosamine hydrochloride is used to produce bacterial cellulose through the action of cellulase enzymes on sucrose solutions containing NaOH. In addition, this product has been shown to inhibit the proliferation of fibroblasts and epithelial cells when cultured in vitro.

Beta-Glucosamine, tetraacetate, hydrochloride (BGGTAH) is a chemical compound that belongs to the class of aminosaccharides. It is derived from glucose and is known to have anti-inflammatory properties. BGGTAH is a well-studied compound that has gained significant interest in scientific research due to its potential biomedical applications.

Synthesis and Characterization:

The synthesis of BGGTAH involves the reaction between β-glucosamine and tetraacetylglucal in the presence of hydrochloric acid. The compound is then purified by recrystallization. The characterization of BGGTAH is done using various techniques, including Nuclear Magnetic Resonance (NMR) spectroscopy, Fourier Transform Infrared (FTIR) spectroscopy, and X-ray crystallography.

Analytical Methods:

The analysis of BGGTAH can be done by various methods, including chromatography, spectrophotometry, and electrophoresis. High-Performance Liquid Chromatography (HPLC) is widely used to determine the purity and identity of BGGTAH.

Biological Properties:

BGGTAH has been shown to exhibit anti-inflammatory and analgesic properties. Studies have reported that BGGTAH can inhibit the production of pro-inflammatory cytokines and regulate immune response. In addition, BGGTAH has been shown to have antioxidant activity and can protect against oxidative stress.

Toxicity and Safety in Scientific Experiments:

Studies have reported that BGGTAH is generally safe and well-tolerated in animals. However, the toxicity of BGGTAH in humans has not been extensively studied, and more research is needed to determine its safety profile in humans.

Applications in Scientific Experiments:

BGGTAH has been widely used in scientific research due to its potential biomedical applications. It has been investigated for its anti-inflammatory, analgesic, antioxidant, and immunomodulatory properties. BGGTAH has also been studied for its potential to treat various diseases, including arthritis, cancer, and neurodegenerative disorders.

Current State of Research:

The current state of research on BGGTAH suggests that it has significant potential as a therapeutic agent. However, more research is needed to fully understand its mode of action and potential applications.

Potential Implications in Various Fields of Research and Industry:

BGGTAH has potential implications in various fields of research and industry, including medicine, pharmaceuticals, food, and cosmetics. It can be used as an anti-inflammatory and analgesic agent in medicine and pharmaceuticals. BGGTAH may also have applications in the food industry as an additive to promote joint health. In addition, BGGTAH has potential use in cosmetics as an anti-aging and antioxidant agent.

Limitations and Future Directions:

Despite its potential, there are some limitations associated with BGGTAH that need to be addressed. These limitations include the lack of understanding of the compound's mode of action and its potential toxicity in humans. Future research should focus on elucidating the compound's mechanism of action and determining its safety profile in humans. In addition, more research is needed to determine the potential applications of BGGTAH in various fields and develop new therapeutic agents based on BGGTAH.

Future Directions:

Several future directions can be explored to further advance the understanding and applications of BGGTAH. These directions include:

1. Investigating the potential of BGGTAH as an anti-cancer agent

2. Studying the mechanism of action of BGGTAH in reducing oxidative stress

3. Exploring the potential of BGGTAH in promoting joint health and treating osteoarthritis

4. Developing novel therapeutic agents based on BGGTAH for the treatment of neurodegenerative disorders

5. Evaluating the safety and efficacy of BGGTAH in humans

6. Investigating the potential of BGGTAH in treating various inflammatory diseases

7. Studying the effect of BGGTAH on the gut microbiome

8. Exploring the potential of BGGTAH in promoting wound healing

9. Developing new methods for the synthesis and purification of BGGTAH

10. Investigating the potential of BGGTAH in reducing inflammation in the brain.

Conclusion:

In conclusion, BGGTAH is a well-studied compound that has gained significant interest in scientific research due to its potential biomedical applications. This comprehensive overview of BGGTAH highlights its definition and background, physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions. More research is needed to fully understand the compound's mechanism of action and potential applications in various fields.

CAS Number10034-20-5
Product Namebeta-Glucosamine, tetraacetate, hydrochloride
IUPAC Name[(2R,3S,4R,5R,6S)-3,4,6-triacetyloxy-5-aminooxan-2-yl]methyl acetate;hydrochloride
Molecular FormulaC₁₄H₂₂ClNO₉
Molecular Weight383.78 g/mol
InChIInChI=1S/C14H21NO9.ClH/c1-6(16)20-5-10-12(21-7(2)17)13(22-8(3)18)11(15)14(24-10)23-9(4)19;/h10-14H,5,15H2,1-4H3;1H/t10-,11-,12-,13-,14-;/m1./s1
InChI KeyBQLUYAHMYOLHBX-XAWYEFCRSA-N
SMILESCC(=O)OCC1C(C(C(C(O1)OC(=O)C)N)OC(=O)C)OC(=O)C.Cl
Synonyms2-Amino-2-deoxy-β-D-glucopyranose 1,3,4,6-Tetraacetate Hydrochloride; NSC 82044;
Canonical SMILESCC(=O)OCC1C(C(C(C(O1)OC(=O)C)N)OC(=O)C)OC(=O)C.Cl
Isomeric SMILESCC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)OC(=O)C)N)OC(=O)C)OC(=O)C.Cl


CAS No: 10034-20-5 Synonyms: 1,3,4,6-Tetra-O-acetyl-2-amino-2-deoxy-b-D-glucopyranose HCl MDL No: MFCD01075204 Chemical Formula: C14H21NO9·HCl Molecular Weight: 383.78
References: 1. Becker C, Hoben C, Kunz H,, Advanced Synthesis & Catalysis, 2007, 349, 3, p417

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