6-Azido-6-deoxy-D-galactopyranose
95%
- Product Code: 103763
CAS:
66927-03-5
| Molecular Weight: | 205.17 g./mol | Molecular Formula: | C₆H₁₁N₃O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03265529 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
6-Azido-6-deoxy-D-galactopyranose is primarily utilized in the field of chemical biology and glycochemistry for the synthesis of glycoconjugates and glycoproteins. Its azido functional group allows for efficient click chemistry reactions, particularly the copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling the selective labeling and modification of biomolecules. This compound is instrumental in studying carbohydrate-protein interactions, facilitating the development of glycoconjugate vaccines and probes for imaging cellular processes. Additionally, it serves as a precursor in the preparation of structurally diverse galactose derivatives, which are valuable in drug discovery and the investigation of metabolic pathways. Its applications extend to material science, where it is used to functionalize surfaces and polymers for biocompatible materials.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Faint Brown Powder |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,560.00 |
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| 0.250 | 10-20 days | ฿17,880.00 |
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6-Azido-6-deoxy-D-galactopyranose
6-Azido-6-deoxy-D-galactopyranose is primarily utilized in the field of chemical biology and glycochemistry for the synthesis of glycoconjugates and glycoproteins. Its azido functional group allows for efficient click chemistry reactions, particularly the copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling the selective labeling and modification of biomolecules. This compound is instrumental in studying carbohydrate-protein interactions, facilitating the development of glycoconjugate vaccines and probes for imaging cellular processes. Additionally, it serves as a precursor in the preparation of structurally diverse galactose derivatives, which are valuable in drug discovery and the investigation of metabolic pathways. Its applications extend to material science, where it is used to functionalize surfaces and polymers for biocompatible materials.
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