
Azido-PEG5-aldehyde
| Catalog Number | R14-0350 |
| Category | Azides |
| Molecular Formula | C20H30N4O7 |
| Molecular Weight | 438.47 |
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Product Introduction
Azido-PEG5-aldehyde is a bifunctional reagent featuring an azide group and an aldehyde moiety, connected by a polyethylene glycol (PEG) spacer consisting of five ethylene glycol units. The azide functionality participates in copper-catalyzed azide–alkyne cycloaddition (CuAAC) and strain-promoted azide–alkyne cycloaddition (SPAAC), facilitating orthogonal conjugation with alkyne-bearing molecules in click chemistry applications. Meanwhile, the aldehyde group allows for further derivatization through reactions such as reductive amination, making this reagent suitable for applications in bioconjugation, surface modification, and polymer functionalization.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >95% |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Colorless oil |
Product Specification
| Storage | -20 °C |
Application
Azido-PEG5-aldehyde is a bifunctional click chemistry reagent combining an azide handle with a PEG5 spacer and a reactive aldehyde group. It is commonly used in bioorthogonal conjugation workflows where the azide enables strain-promoted or copper-catalyzed azide–alkyne cycloaddition to install tags, probes, or biomolecules onto PEGylated scaffolds. The aldehyde functionality supports parallel coupling to amines or hydrazide/oxyamine-type partners, making this reagent valuable for building modular conjugates, surface coatings, and imaging-ready materials with controlled spacing and improved solubility.
1. Bioconjugation Linker Design
Azido-PEG5-aldehyde is widely used as a modular linker for preparing conjugates that require both a clickable azide and an aldehyde-reactive handle. Researchers employ it to introduce an aldehyde for subsequent attachment to amine-bearing targets such as peptides, proteins, or polymeric carriers, while retaining the azide for later installation of fluorophores, affinity tags, or other functional moieties via click chemistry. The PEG5 spacer helps reduce steric crowding and supports more reproducible labeling densities in multistep reagent assembly, which is particularly useful when downstream applications demand consistent probe spacing.
2. Fluorophore And Probe Assembly
Azido-PEG5-aldehyde supports the construction of imaging and detection reagents by enabling sequential functionalization routes. The aldehyde group can be used to couple to amine-functional dyes, recognition elements, or scaffold proteins, generating an intermediate conjugate that still contains the azide for click-based diversification. This approach is commonly adopted in chemical biology laboratories that need to rapidly exchange reporters (e.g., different fluorophores or enrichment handles) while keeping the core conjugation chemistry consistent across probe batches.
3. Surface Coating And Materials Functionalization
Azido-PEG5-aldehyde is used to functionalize polymeric and biomaterials surfaces where a stable aldehyde-bearing intermediate is needed before click installation of reactive or binding components. In biomaterials science workflows, the aldehyde functionality facilitates attachment to amine-containing coatings or surface-presented nucleophiles, while the azide enables subsequent grafting of ligands, capture reagents, or imaging tags through click chemistry. The PEG5 spacer improves accessibility of the azide on the material surface, which can be important for maintaining efficient labeling and uniform functional coverage in diagnostic reagent development and surface-based assays.
4. Molecular Imaging Reagent Building
Azido-PEG5-aldehyde is frequently selected for assembling molecular imaging reagents that benefit from orthogonal, stepwise functionalization. The azide handle allows late-stage installation of imaging reporters or targeting motifs using click chemistry, while the aldehyde group provides a convenient entry point for coupling to amine-functional carriers or scaffold components used to tune probe architecture. This design strategy is commonly used to generate libraries of structurally related imaging probes with controlled linker length and improved solubility, supporting efficient optimization of labeling workflows in research settings.
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