Propargyl-peg4-sulfone-peg4-t-butyl ester

95%

Reagent Code: #109411
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CAS Number 2055024-43-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 584.72 g/mol
Formula C₂₆H₄₈O₁₂S
badge Registry Numbers
MDL Number MFCD30182061
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Propargyl-peg4-sulfone-peg4-t-butyl ester is primarily utilized in bioconjugation and click chemistry applications. Its propargyl group enables efficient and selective reactions with azides via copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable for labeling biomolecules such as proteins, peptides, and nucleic acids. The PEG4 spacers enhance solubility and reduce steric hindrance, improving reaction efficiency in aqueous environments. This compound is also employed in the development of drug delivery systems, where its sulfone group can act as a linker for controlled release mechanisms. Additionally, it finds use in material science for surface functionalization and the creation of biofunctionalized polymers. The t-butyl ester group provides stability during synthesis and can be selectively deprotected for further modifications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days €2,703.69
Propargyl-peg4-sulfone-peg4-t-butyl ester
Propargyl-peg4-sulfone-peg4-t-butyl ester is primarily utilized in bioconjugation and click chemistry applications. Its propargyl group enables efficient and selective reactions with azides via copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable for labeling biomolecules such as proteins, peptides, and nucleic acids. The PEG4 spacers enhance solubility and reduce steric hindrance, improving reaction efficiency in aqueous environments. This compound is also employed in the development of drug delivery systems, where its sulfone group can act as a linker for controlled release mechanisms. Additionally, it finds use in material science for surface functionalization and the creation of biofunctionalized polymers. The t-butyl ester group provides stability during synthesis and can be selectively deprotected for further modifications.
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