
Acid-PEG1-tris-PEG3-azide
| Catalog Number | R14-0334 |
| Category | Azides |
| Molecular Formula | C41H75N13O19 |
| Molecular Weight | 1054.11 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Acid-PEG1-tris-PEG3-azide is a multifunctional reagent that combines a carboxylic acid group with an azide moiety through a polyethylene glycol (PEG) spacer. This molecular architecture facilitates its integration into copper-catalyzed azide–alkyne cycloaddition reactions, enabling efficient bioconjugation and surface modification applications. The PEG linker enhances solubility and flexibility, making it suitable for use in diverse labeling and polymer functionalization strategies.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >90% by HPLC |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Oil |
Product Specification
| Storage | -20 °C |
Application
Acid-PEG1-tris-PEG3-azide is a multi-azide, acid-functionalized polyethylene glycol (PEG) click chemistry reagent designed for copper-free or copper-mediated azide–alkyne cycloaddition workflows. Its architecture combines a terminal acid handle with a tris-PEG3 azide presentation, providing multiple reactive azide sites while maintaining high aqueous compatibility and reduced nonspecific interactions. This reagent is commonly used to install multivalent azide functionality on PEGylated scaffolds, surfaces, and biomolecular conjugates for downstream labeling, crosslinking, and imaging reagent assembly.
1. Multivalent Biomolecule Labeling
Acid-PEG1-tris-PEG3-azide is widely used to introduce multivalent azide groups onto proteins, peptides, and nucleic-acid conjugates where increased labeling density can improve probe brightness and signal stability in analytical workflows. Researchers often pair this reagent with complementary alkyne-bearing partners to generate uniformly PEGylated conjugates for platform development in chemical biology and molecular imaging. The PEG spacer system helps maintain colloidal stability and reduces aggregation during conjugation and subsequent handling, which is particularly valuable when preparing libraries of labeled biomolecules for screening and assay optimization.
2. PEG-Based Hydrogel Crosslinking
Acid-PEG1-tris-PEG3-azide supports the fabrication of PEG-rich biomaterials by enabling multivalent crosslinking with difunctional or multifunctional alkyne components. Materials scientists use it to tune network formation by varying the azide loading and the alkyne crosslinker architecture, producing hydrogels suited for controlled presentation of bioactive motifs and for creating stable, water-swollen matrices for research use. The acid functionality and extended PEG chains contribute to reproducible gel formation behavior and facilitate downstream functionalization steps, such as adding additional clickable handles for sequential assembly of complex material constructs.
3. Surface Functionalization for Assays
Acid-PEG1-tris-PEG3-azide is used to decorate solid supports and microarray surfaces with azide-rich PEG layers, enabling consistent attachment of alkyne-functional capture reagents and reporter probes. Diagnostic reagent developers and platform engineers rely on PEG-mediated surface passivation to lower background binding while maintaining reactive accessibility for click-based immobilization. The tris-azide design helps increase the effective surface density of reactive sites, supporting robust conjugation of fluorescent, affinity, or mass-tagging components used in workflow development for biosensing and analytical assays.
4. Multisite Imaging Probe Assembly
Acid-PEG1-tris-PEG3-azide is a practical building block for constructing multicomponent imaging probes, where multiple clickable handles are needed to integrate fluorophores, affinity tags, or imaging reporters onto a single PEG-based scaffold. Molecular imaging and chemical biology groups commonly use it to assemble probes that require controlled spacing between functional groups, improving reagent homogeneity and simplifying batch-to-batch preparation. The PEG3 azide arms provide a straightforward route to generate probe architectures with defined multivalency, which is advantageous when preparing imaging reagent sets for method development and comparative studies.
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