
Azido-PEG1-azide
| Catalog Number | R14-0343 |
| Category | Azides |
| Molecular Formula | C4H8N6O |
| Molecular Weight | 156.15 |
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Product Introduction
Azido-PEG1-azide features dual azide functional groups separated by a short polyethylene glycol (PEG) spacer, facilitating its use in bioorthogonal chemistry and surface modification applications. This compound participates in copper-catalyzed azide–alkyne cycloaddition (CuAAC) reactions, enabling the formation of stable triazole linkages for bioconjugation and polymer functionalization. Its symmetrical architecture supports the installation of azide groups on various substrates, allowing for subsequent click chemistry transformations in complex molecular assemblies.
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-PEG1-azide is a PEG-based bifunctional azide reagent designed for click chemistry workflows that require orthogonal or multivalent azide presentation. As a poly(ethylene glycol) linker bearing two terminal azide groups, it enables efficient incorporation of azide handles into biomolecules, surfaces, and polymeric materials for subsequent copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) or related azide-based conjugation strategies. Its flexible, hydrophilic PEG spacer is widely used to improve solubility, reduce nonspecific interactions, and provide controlled spacing between reactive partners in chemical biology and materials research.
1. Multivalent Surface Functionalization
Azido-PEG1-azide is commonly used to introduce two azide termini onto material surfaces, allowing subsequent attachment of multiple ligands, probes, or capture elements via CuAAC. Researchers in biomaterials and surface chemistry apply this reagent to create dense yet well-spaced functional coatings on glass, polymer films, and nanoparticle platforms where PEG-mediated hydration helps limit aggregation and improves reagent accessibility. The bifunctional azide design supports multivalent binding architectures in assay development and enables modular replacement of surface components without changing the underlying PEG scaffold.
2. Bioconjugation Linker for Probes
Azido-PEG1-azide serves as a practical PEG linker for preparing azide-bearing bioconjugation intermediates used in chemical biology toolkits. Protein engineering and conjugation workflows often incorporate PEG spacers to tune hydrophilicity and reduce steric hindrance during downstream labeling, and the dual-azide functionality supports sequential or multiplexed CuAAC labeling strategies. This reagent is frequently selected when researchers want to install multiple reactive handles on a single construct, facilitating the attachment of fluorescent tags, affinity moieties, or other imaging reagents while maintaining colloidal stability in complex experimental buffers.
3. Polymer and Hydrogel Crosslinking Handles
Azido-PEG1-azide is used in polymer chemistry and soft-matter research to install azide groups that can be converted into crosslinking or functionalization sites through click reactions. In hydrogel and polymer network design, the PEG spacer provides flexibility and improved mass transport, while the two azide groups enable incorporation into multicomponent architectures where crosslink density and spacing can be tuned by controlling azide availability. This approach is widely adopted for creating clickable polymer materials, responsive coatings, and modular biomaterials platforms that can be functionalized with different alkyne-bearing components.
4. Molecular Imaging Probe Assembly
Azido-PEG1-azide is frequently employed in the assembly of molecular imaging and detection probes that rely on click-based modular conjugation. The reagent’s PEG backbone helps manage hydrophilicity and reduces nonspecific surface interactions, which is valuable when constructing probe conjugates that must remain stable during labeling and purification. Dual azide termini support efficient incorporation of multiple probe elements or reporter groups onto a single scaffold, enabling streamlined synthesis of imaging reagents and diagnostic reagent components that are compatible with azide–alkyne conjugation workflows.
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