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Product Introduction
Alkyne-PEG9-N3 is a bifunctional reagent featuring an alkyne group and an azide moiety, making it suitable for copper-catalyzed azide–alkyne cycloaddition (CuAAC) reactions. The polyethylene glycol (PEG) spacer with nine ethylene glycol units enhances solubility and flexibility, facilitating efficient conjugation in aqueous environments. This reagent is commonly used in bioconjugation and surface modification applications, enabling the assembly of complex macromolecular structures and the functionalization of biomolecules.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | ≥95% |
Product Specification
| Storage | Store at -5 °C,keep in dry and avoid sunlight. |
Application
Alkyne-PEG9-N3 is a polyethylene glycol (PEG)-spaced bifunctional click chemistry reagent that combines a terminal alkyne handle with an azide (N3) group for orthogonal bioorthogonal conjugation workflows. As a PEGylated platform, it is commonly used to introduce flexible, hydrophilic linkers that improve solubility and reduce nonspecific interactions in labeling, surface functionalization, and probe assembly. The reagent’s dual reactive motifs make it relevant for constructing modular molecular imaging agents, affinity reagents, and biomaterial surfaces using azide–alkyne click strategies.
1. Molecular Imaging Probe Assembly
Alkyne-PEG9-N3 is used in molecular imaging and diagnostic reagent development to build modular probe architectures where a PEG spacer helps tune hydrodynamic behavior and conjugate stability. Researchers incorporate the PEG-linked alkyne/azide functionality to connect targeting ligands, reporter scaffolds, and signal-generating moieties through click-compatible handles, enabling consistent multicomponent assembly for imaging workflows. The flexible PEG segment is particularly valuable when assembling conjugates that must remain dispersible in aqueous labeling buffers and imaging-relevant media.
2. Surface Functionalization For Biomaterials
Alkyne-PEG9-N3 supports click-based functionalization of biomaterial surfaces and interfaces, where PEG-mediated spacing can improve accessibility of reactive groups and mitigate steric crowding. In materials science and chemical biology labs, the reagent is employed to introduce clickable alkyne/azide sites onto polymer films, hydrogels, and nanoparticle coatings, facilitating subsequent attachment of affinity tags, capture ligands, or fluorescent reporters. This approach is widely used for creating reproducible, chemically defined material platforms for assay development and surface-based molecular recognition studies.
3. Targeted Affinity Reagent Construction
Alkyne-PEG9-N3 is applied to the construction of affinity reagents and binding probes that require controlled linker length between recognition elements and downstream detection handles. By leveraging the reagent’s PEG spacer and click-compatible functional groups, developers can assemble conjugates for pull-down workflows, biosensor reagent panels, and multiplexed binding assays where consistent conjugation geometry improves reagent handling and labeling uniformity. The dual functionality enables flexible pairing with complementary click partners to generate a library of conjugates for research tool development.
4. PEG-Linker For Multicomponent Labeling
Alkyne-PEG9-N3 is commonly used as a PEG-based linker component in multicomponent labeling schemes, including reagent kits for assembling fluorescent, biotin-like, or capture-tagged constructs. Chemical biology teams use the alkyne and azide handles to stage stepwise conjugation with separate partners, allowing modular design of complex probes while maintaining aqueous compatibility and reducing aggregation tendencies. This PEG-linker strategy is especially useful when downstream applications demand conjugates with improved solubility, reduced nonspecific adsorption, and robust performance in routine labeling and wash conditions.
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