DBCO-PEG4-NH-Boc
≥95%
- Product Code: 56128
CAS:
2353410-17-8
Molecular Weight: | 623.74 g./mol | Molecular Formula: | C₃₄H₄₅N₃O₈ |
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Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is widely used in bioconjugation and click chemistry applications. It serves as a linker molecule, enabling the attachment of biomolecules such as peptides, proteins, or antibodies to other functional groups or surfaces. The DBCO (dibenzocyclooctyne) group allows for strain-promoted azide-alkyne cycloaddition (SPAAC), a type of click reaction that is highly efficient and does not require a catalyst. The PEG4 spacer provides flexibility and solubility, enhancing the stability and functionality of the conjugated molecules. The NH-Boc (amine-protected with tert-butyloxycarbonyl) group allows for further chemical modifications after deprotection, making it versatile for multi-step synthesis. It is particularly valuable in drug delivery systems, diagnostic probes, and the development of bioconjugated materials for research and therapeutic purposes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | Ft155,147.16 |
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DBCO-PEG4-NH-Boc
This chemical is widely used in bioconjugation and click chemistry applications. It serves as a linker molecule, enabling the attachment of biomolecules such as peptides, proteins, or antibodies to other functional groups or surfaces. The DBCO (dibenzocyclooctyne) group allows for strain-promoted azide-alkyne cycloaddition (SPAAC), a type of click reaction that is highly efficient and does not require a catalyst. The PEG4 spacer provides flexibility and solubility, enhancing the stability and functionality of the conjugated molecules. The NH-Boc (amine-protected with tert-butyloxycarbonyl) group allows for further chemical modifications after deprotection, making it versatile for multi-step synthesis. It is particularly valuable in drug delivery systems, diagnostic probes, and the development of bioconjugated materials for research and therapeutic purposes.
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