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7772-79-4 , Glucosamine Pentaacetate, CAS:7772-79-4

7772-79-4 , b-D-葡萄糖胺五乙酸酯,
b-D-Glucosamine pentaacetate;
1,2,3,4,6-Penta-O-acetyl-b-D-glucosamine;
Cas:7772-79-4
C16H23NO10 / 389.355
MFCD00006595

2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-b-D-glucopyranose

b-D-葡萄糖胺五乙酸酯,

N-Acetyl-beta-D-glucosamine tetraacetate (NAG-TA) is a chemical compound that is derived from chitin, a naturally occurring polymer that is found in the exoskeletons of crustaceans and insects, as well as in the cell walls of fungi. Chitin is a highly abundant and renewable resource and has numerous potential applications in industries such as agriculture, medicine, and textiles. NAG-TA is a modified form of chitin that has been chemically synthesized and has been shown to possess several unique properties that make it attractive for use in a variety of scientific experiments.

Synthesis and Characterization

NAG-TA can be synthesized from chitin through a process known as deacetylation, which involves the removal of acetyl groups from the chitin molecule. This process can be carried out using a variety of methods, including alkaline hydrolysis, enzymatic treatment, and chemical deacetylation. Once NAG-TA has been synthesized, it can be characterized using a range of analytical techniques, including nuclear magnetic resonance spectroscopy, mass spectrometry, and infrared spectroscopy.

Analytical Methods

Several analytical methods have been developed to detect and quantify NAG-TA in biological samples and other matrices. These methods include high-performance liquid chromatography, capillary electrophoresis, and enzyme-linked immunosorbent assays.

Biological Properties

NAG-TA has been shown to possess several biological properties that make it attractive for use in a range of scientific experiments. For example, it has been found to possess anti-inflammatory, antioxidant, and immunomodulatory effects. Additionally, it has been shown to promote the growth of certain types of cells, including chondrocytes and osteoblasts, which are important for bone and cartilage development and repair.

Toxicity and Safety in Scientific Experiments

Studies have shown that NAG-TA exhibits low toxicity and is generally safe for use in scientific experiments. However, more research is needed to fully understand its safety profile, particularly with regard to long-term exposure and potential cumulative effects.

Applications in Scientific Experiments

NAG-TA has numerous potential applications in a range of scientific experiments. It has been used as a biomaterial for tissue engineering, as a therapeutic agent for the treatment of inflammatory diseases, and as a supplement for the improvement of joint health and mobility.

Current State of Research

Research into the properties and potential applications of NAG-TA is ongoing. Studies are being conducted to further understand its biological properties, as well as to develop new methods for synthesizing and characterizing the compound. Additionally, researchers are exploring new applications for NAG-TA in areas such as drug delivery, wound healing, and nanotechnology.

Potential Implications in Various Fields of Research and Industry

NAG-TA has numerous potential implications in various fields of research and industry. In medicine, it could be used as a therapeutic agent for the treatment of inflammatory diseases, as well as a supplement for the improvement of joint health and mobility. In agriculture, it could be used as a natural pesticide and fertilizer, while in textiles, it could be used to create new materials with improved strength and durability. In environmental science, it could be used to develop new methods for the removal of pollutants from water and soil.

Limitations and Future Directions

While NAG-TA has numerous potential applications, there are also several limitations and challenges to its use. For example, its high cost and limited availability may hinder its widespread adoption in certain industries. Additionally, further research is needed to fully understand its safety profile, particularly with regard to long-term exposure and potential cumulative effects. Future research directions for NAG-TA could include the development of new synthesis methods, the creation of new biomaterials and composites, and the exploration of new applications in areas such as drug delivery and nanotechnology.

In conclusion, N-Acetyl-beta-D-glucosamine tetraacetate is a promising compound with numerous potential applications in various fields of research and industry. As more research is conducted, it is likely that even more potential uses for this compound will be discovered, making it an important area of study for scientists and researchers around the world.

CAS Number7772-79-4
Product NameN-Acetyl-beta-D-glucosamine tetraacetate
IUPAC Name[(2R,3S,4S,5R,6S)-5-acetamido-3,4,6-triacetyloxyoxan-2-yl]methyl acetate
Molecular FormulaC16H23NO10
Molecular Weight389.355 g/mol
InChIInChI=1S/C16H23NO10/c1-7(18)17-13-15(25-10(4)21)14(24-9(3)20)12(6-23-8(2)19)27-16(13)26-11(5)22/h12-16H,6H2,1-5H3,(H,17,18)/t12-,13-,14-,15+,16-/m1/s1
InChI KeyOVPIZHVSWNOZMN-OXGONZEZSA-N
SMILESCC(=O)NC1C(C(C(OC1OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C
Synonyms2-(Acetylamino)-2-deoxy-β-D-Glucopyranose 1,3,4,6-Tetraacetate; 1,3,4,6-Tetra-O-acetyl-N-acetyl-β-D-glucosamine; N-Acetyl-β-D-glucosamine Tetraacetate; NSC 224432;
Canonical SMILESCC(=O)NC1C(C(C(OC1OC(=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]1OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C


CAS No: 7772-79-4 Synonyms: b-D-Glucosamine pentaacetate1,2,3,4,6-Penta-O-acetyl-b-D-glucosamine MDL No: MFCD00006595 Chemical Formula: C16H23NO10 Molecular Weight: 389.355现货.In Stock.

COA:

Product name2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-beta-D-glucopyranose; beta-D-Glucosamine pentaacetate

CAS7772-79-4 M.F.: C16H23NO10  M.W.: 389.355  

Items

Standards

Results

Appearance

White crystalline powder

Positive

Solubility

Soluble in DMF, insoluble in water

Complies

Identification

IR and HPLC

Positive

MS and NMR

Should Comply

Complies

M.P.

180°C - 190 °C

186 - 188 °C

Specific rotation

[α]20/D, (c=4, in CHCl3), +1.3° to +1.7°

+1.5°

Water

Max. 0.5%

Complies

Alpha-isomer

Max. 1%

0.2%

Assay by HPLC

Min. 99%

99.4%

References:

1. Bernacki RJ, Sharma M, Porter NK, et al., J. Supramol. Struct. 1977, 7, p235-50

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