alpha-D-Galactopyranosepentaacetate
98%
- Product Code: 103862
Alias:
1,2,3,4,6-Penta-O-acetylated-α-D-galactose
CAS:
4163-59-1
Molecular Weight: | 390.34 g./mol | Molecular Formula: | C₁₆H₂₂O₁₁ |
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EC Number: | MDL Number: | MFCD00064081 | |
Melting Point: | Boiling Point: | 434.77°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C |
Product Description:
Alpha-D-Galactopyranosepentaacetate is widely used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the production of galactose derivatives, which are essential in biochemical research and pharmaceutical development. This compound is particularly valuable in glycosylation reactions, where it acts as a protected galactosyl donor, enabling the construction of oligosaccharides and glycoproteins. Its acetyl groups provide stability during chemical reactions, making it a preferred choice in carbohydrate chemistry. Additionally, it is utilized in the study of enzyme mechanisms and the development of glycosidase inhibitors, which have potential applications in treating metabolic disorders and viral infections.
Product Specification:
Test | Specification |
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Appearance | White To Off-white Powder |
Purity (%) | 97.5-100 |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | $96.01 |
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25.000 | 10-20 days | $216.02 |
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100.000 | 10-20 days | $594.06 |
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500.000 | 10-20 days | $1,494.15 |
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alpha-D-Galactopyranosepentaacetate
Alpha-D-Galactopyranosepentaacetate is widely used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the production of galactose derivatives, which are essential in biochemical research and pharmaceutical development. This compound is particularly valuable in glycosylation reactions, where it acts as a protected galactosyl donor, enabling the construction of oligosaccharides and glycoproteins. Its acetyl groups provide stability during chemical reactions, making it a preferred choice in carbohydrate chemistry. Additionally, it is utilized in the study of enzyme mechanisms and the development of glycosidase inhibitors, which have potential applications in treating metabolic disorders and viral infections.
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