DBCO-PEG4-amine

95%

  • Product Code: 76670
  CAS:    1840886-10-3
Molecular Weight: 523.6 g./mol Molecular Formula: C₂₉H₃₇N₃O₆
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: -20°C
Product Description: DBCO-PEG4-amine is widely used in bioconjugation and click chemistry applications due to its unique properties. The DBCO (dibenzocyclooctyne) group enables strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, which are highly efficient and do not require a catalyst. This makes it ideal for labeling biomolecules such as proteins, antibodies, and nucleic acids without disrupting their functionality. The PEG4 spacer provides flexibility and solubility, enhancing the stability and biocompatibility of the conjugated products. It is commonly employed in drug delivery systems, diagnostic assays, and the development of bioconjugate therapeutics. Additionally, its amine group allows for further functionalization, enabling the attachment of various targeting moieties or imaging agents. This versatility makes it a valuable tool in biomedical research and therapeutic development.
Product Specification:
Test Specification
APPEARANCE Solid
PURITY 94.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.010 10-20 days $646.91
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0.050 10-20 days $2,058.26
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DBCO-PEG4-amine
DBCO-PEG4-amine is widely used in bioconjugation and click chemistry applications due to its unique properties. The DBCO (dibenzocyclooctyne) group enables strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, which are highly efficient and do not require a catalyst. This makes it ideal for labeling biomolecules such as proteins, antibodies, and nucleic acids without disrupting their functionality. The PEG4 spacer provides flexibility and solubility, enhancing the stability and biocompatibility of the conjugated products. It is commonly employed in drug delivery systems, diagnostic assays, and the development of bioconjugate therapeutics. Additionally, its amine group allows for further functionalization, enabling the attachment of various targeting moieties or imaging agents. This versatility makes it a valuable tool in biomedical research and therapeutic development.
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