1,3,4,6-Tetra-O-acetyl-2-[(azidoacetyl)amino]-2-deoxy-β-D-galactopyranose
≥98%
- Product Code: 103628
CAS:
1404472-50-9
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|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily used in the synthesis of complex carbohydrates and glycoconjugates, which are essential in biochemical and pharmaceutical research. It serves as a key intermediate in the preparation of glycosylated molecules, particularly in the development of glycoproteins and glycolipids. These molecules play a critical role in studying cell-cell interactions, immune responses, and pathogen recognition. Additionally, it is utilized in click chemistry reactions, where the azido group enables efficient and selective conjugation with alkynes, facilitating the creation of labeled biomolecules for imaging, diagnostics, and drug delivery systems. Its acetylated form also aids in protecting reactive hydroxyl groups during synthetic processes, ensuring precise and controlled glycosylation reactions.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White Powder |
| Purity (%) | 98-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿3,570.00 |
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| 0.025 | 10-20 days | ฿12,830.00 |
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| 0.100 | 10-20 days | ฿35,980.00 |
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1,3,4,6-Tetra-O-acetyl-2-[(azidoacetyl)amino]-2-deoxy-β-D-galactopyranose
This compound is primarily used in the synthesis of complex carbohydrates and glycoconjugates, which are essential in biochemical and pharmaceutical research. It serves as a key intermediate in the preparation of glycosylated molecules, particularly in the development of glycoproteins and glycolipids. These molecules play a critical role in studying cell-cell interactions, immune responses, and pathogen recognition. Additionally, it is utilized in click chemistry reactions, where the azido group enables efficient and selective conjugation with alkynes, facilitating the creation of labeled biomolecules for imaging, diagnostics, and drug delivery systems. Its acetylated form also aids in protecting reactive hydroxyl groups during synthetic processes, ensuring precise and controlled glycosylation reactions.
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| Stable in pH range | - |
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