
Azido-PEG5-azide
| Catalog Number | R14-0340 |
| Category | Azides |
| Molecular Formula | C12H24N6O5 |
| Molecular Weight | 332.36 |
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Product Introduction
Azido-PEG5-azide features two azide groups linked by a polyethylene glycol (PEG) spacer consisting of five ethylene glycol units. This bifunctional reagent participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, enabling efficient bioconjugation and surface modification processes. The PEG spacer enhances solubility and flexibility, making Azido-PEG5-azide suitable for applications in macromolecular assembly and polymer functionalization where increased hydrophilicity is desired.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >95% |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Colorless oil |
Product Specification
| Storage | 0-10 °C |
Application
Azido-PEG5-azide is a PEG-based bifunctional azide reagent designed for copper-free and copper-mediated azide–alkyne click chemistry workflows. Its flexible poly(ethylene glycol) spacer and terminal azide groups enable efficient installation of bioorthogonal handles onto surfaces, polymers, and biomolecules while maintaining aqueous compatibility. This reagent is commonly used in chemical biology and biomaterials research where multivalent labeling, crosslinking, and modular probe construction benefit from PEG-mediated solubility and spacing control.
1. Multivalent Probe Labeling
Azido-PEG5-azide is widely used to build multivalent labeling reagents for chemical biology applications, where two azide termini provide convenient orthogonal attachment points to alkyne-functional targets. Researchers employ it to generate higher-avidity binding architectures for imaging probes, enrichment tags, and affinity reagents, especially when PEG spacing helps reduce steric constraints during conjugation. The PEG5 linker often improves handling in aqueous buffers and supports consistent performance across labeling workflows that require repeated click steps or downstream assembly of complex probe formats.
2. Biomaterials Surface Functionalization
Azido-PEG5-azide is suitable for introducing clickable azide functionality onto biomaterial surfaces and polymeric scaffolds, enabling subsequent conjugation to alkyne-bearing coatings, ligands, or crosslinkers. In materials science and interface engineering, the PEG spacer helps mitigate nonspecific interactions and supports stable presentation of reactive groups at the material boundary. This makes the reagent useful for preparing clickable hydrogel components, functional coatings, and modular surface platforms used in biosensing, materials characterization, and advanced scaffold construction.
3. Two-Point Crosslinking and Gels
Azido-PEG5-azide is commonly applied as a bifunctional crosslinking linker in click-based gelation and network formation strategies, where its two azide groups can react with complementary alkyne handles on polymers or crosslinkable components. The PEG5 segment provides a flexible distance between attachment points, which can influence network spacing, swelling behavior, and mechanical tunability in click-assembled materials. Such workflows are frequently adopted in biomaterials laboratories to generate reproducible, modular hydrogel systems and to incorporate clickable sites for post-fabrication functionalization.
4. Modular Conjugation Platforms
Azido-PEG5-azide supports modular conjugation schemes for assembling complex constructs from smaller building blocks, including PEGylated linkers, labeled macromolecules, and multicomponent reagent libraries. Because the reagent carries terminal azides, it can be used to standardize the introduction of click handles into diverse substrates, from polymer conjugates to biomolecule derivatives, facilitating consistent downstream coupling to alkyne-functional partners. This approach is particularly valuable for iterative probe or material development, where maintaining a reliable reactive group for repeated click steps streamlines manufacturing of research-grade conjugates.
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