Propargyl-PEG4-tetra-Ac-beta-D-galactose
≥95%
- Product Code: 109413
CAS:
1397682-61-9
| Molecular Weight: | 562.5599999999999 g./mol | Molecular Formula: | C₂₅H₃₈O₁₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Propargyl-PEG4-tetra-Ac-beta-D-galactose is widely used in bioconjugation and chemical biology research. Its application primarily revolves around its role as a versatile linker in the synthesis of glycoconjugates, which are essential for studying cell-surface interactions and glycosylation processes. The propargyl group enables efficient click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), allowing for the attachment of biomolecules or probes to study biological systems. This compound is also valuable in the development of targeted drug delivery systems, where its PEG4 spacer enhances solubility and stability, while the galactose moiety facilitates specific targeting to receptors like asialoglycoprotein receptors on liver cells. Additionally, it serves as a key intermediate in the synthesis of complex glycans for glycan array platforms, enabling high-throughput screening of carbohydrate-protein interactions. Its application extends to the design of diagnostic tools and imaging agents, where its functional groups allow for precise labeling and detection in cellular and molecular studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $432.04 |
+
-
|
Propargyl-PEG4-tetra-Ac-beta-D-galactose
Propargyl-PEG4-tetra-Ac-beta-D-galactose is widely used in bioconjugation and chemical biology research. Its application primarily revolves around its role as a versatile linker in the synthesis of glycoconjugates, which are essential for studying cell-surface interactions and glycosylation processes. The propargyl group enables efficient click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), allowing for the attachment of biomolecules or probes to study biological systems. This compound is also valuable in the development of targeted drug delivery systems, where its PEG4 spacer enhances solubility and stability, while the galactose moiety facilitates specific targeting to receptors like asialoglycoprotein receptors on liver cells. Additionally, it serves as a key intermediate in the synthesis of complex glycans for glycan array platforms, enabling high-throughput screening of carbohydrate-protein interactions. Its application extends to the design of diagnostic tools and imaging agents, where its functional groups allow for precise labeling and detection in cellular and molecular studies.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :