Propargyl-PEG9-bromide
98%
- Product Code: 55536
CAS:
2055042-83-4
| Molecular Weight: | 515.43 g./mol | Molecular Formula: | C₂₁H₃₉BrO₉ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29079385 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Propargyl-PEG9-bromide is widely used in the field of bioconjugation and polymer chemistry. Its primary application is as a linker or spacer molecule in the synthesis of complex macromolecules. The propargyl group allows for click chemistry reactions, particularly the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is highly efficient and selective. This property makes it valuable for attaching various functional groups, such as drugs, fluorescent dyes, or targeting moieties, to biomolecules like proteins, peptides, or nucleic acids. Additionally, the PEG (polyethylene glycol) chain provides solubility, stability, and reduced immunogenicity, making it suitable for use in drug delivery systems and therapeutic applications. Its bromide group further enables alkylation reactions, expanding its utility in organic synthesis and material science. Overall, it is a versatile reagent for designing advanced biomaterials and therapeutics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿72,000.00 |
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Propargyl-PEG9-bromide
Propargyl-PEG9-bromide is widely used in the field of bioconjugation and polymer chemistry. Its primary application is as a linker or spacer molecule in the synthesis of complex macromolecules. The propargyl group allows for click chemistry reactions, particularly the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is highly efficient and selective. This property makes it valuable for attaching various functional groups, such as drugs, fluorescent dyes, or targeting moieties, to biomolecules like proteins, peptides, or nucleic acids. Additionally, the PEG (polyethylene glycol) chain provides solubility, stability, and reduced immunogenicity, making it suitable for use in drug delivery systems and therapeutic applications. Its bromide group further enables alkylation reactions, expanding its utility in organic synthesis and material science. Overall, it is a versatile reagent for designing advanced biomaterials and therapeutics.
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