
Azide-PEG2-aldehyde | CAS 184006-13-1
| Catalog Number | R14-0374 |
| Category | Azides |
| Molecular Formula | C6H11N3O3 |
| Molecular Weight | 173.17 |
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Product Introduction
Azide-PEG2-Aldehyde is a versatile and highly reactive linker containing an aliphatic aldehyde group and azide group.
Chemical Information
Application
Chemical Information
| Synonyms | Ald-CH2-PEG2-Azide |
| IUPAC Name | 2-[2-(2-azidoethoxy)ethoxy]acetaldehyde |
| SMILES | C(COCCOCC=O)N=[N+]=[N-] |
| InChI | InChI=1S/C6H11N3O3/c7-9-8-1-3-11-5-6-12-4-2-10/h2H,1,3-6H2 |
| InChIKey | OJEKEINAGFAPKG-UHFFFAOYSA-N |
| Appearance | Colorless Liquid |
Application
Azide-PEG2-aldehyde is a bifunctional click chemistry reagent combining an azide handle with a short PEG spacer terminating in an aldehyde group. As an azide-bearing building block, it is compatible with azide-selective bioorthogonal conjugation workflows, while the aldehyde enables rapid coupling to amine-containing biomolecules and polymer backbones used in probe and material assembly. The PEG2 linker improves solubility and helps preserve accessibility of both reactive termini, making this reagent useful for constructing modular conjugates, surface-functionalized materials, and imaging or diagnostic reagent platforms that require orthogonal handle management.
1. Bioorthogonal Probe Conjugation
Azide-PEG2-aldehyde is used to introduce an azide functionality into biomolecule- and polymer-based probe platforms while simultaneously providing an aldehyde for downstream attachment to amine-bearing targets. Researchers commonly incorporate the azide handle to enable subsequent click-based ligation to complementary alkyne partners, facilitating modular assembly of fluorescent probes, affinity reagents, and multi-component sensor constructs. The PEG2 spacer supports conjugate handling in aqueous buffers and helps maintain reactivity of the aldehyde during labeling steps that precede or follow click coupling.
2. Surface Functionalization For Materials
Azide-PEG2-aldehyde supports preparation of functional surfaces and coatings where an aldehyde-reactive group is used to anchor the reagent to amine-containing substrates, followed by azide-directed click immobilization. This workflow is attractive for building reusable assay surfaces, chromatography media, and biomaterial interfaces that require controlled density and spacing of reactive sites for later attachment of ligands, capture molecules, or reporter tags. The PEG2 segment contributes to improved surface wettability and reduces steric constraints, which is particularly valuable when immobilizing bulky biomolecular components.
3. Multivalent Ligand And Polymer Assembly
Azide-PEG2-aldehyde is frequently employed as a linker for assembling multivalent ligand architectures and polymer conjugates that benefit from orthogonal reactivity. The aldehyde group enables coupling to amines on peptides, proteins, or polymer scaffolds, while the azide handle allows subsequent installation of imaging reporters, affinity groups, or crosslinking elements via click chemistry. This design is well suited to generating well-defined conjugate libraries where modular substitution at the azide position supports rapid variation of binding or readout components without re-engineering the primary scaffold.
4. Diagnostic Reagent And Assay Platforms
Azide-PEG2-aldehyde is used in the development of diagnostic reagent components and assay platforms that require stable, modular conjugation strategies. By installing an azide handle onto amine-bearing reagents or carriers through aldehyde coupling, teams can later append reporter moieties, recognition elements, or signal-amplifying constructs using complementary click partners. The PEG2 spacer helps maintain aqueous compatibility and supports consistent conjugate performance during reagent formulation and handling in typical laboratory assay workflows.
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