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Product Introduction
Silane-PEG-Azide, MW 2,000 is a PEGylation reagent with azido and triethoxysilane moieties. The azide can be used for copper-catalyzed Click Chemistry reactions with alkynes, DBCO and BCN. The triethoxysilane moiety is used for surface modification. The hydrophilic PEG linkers increase the water solubility properties of compounds in aqueous media.
Product Specification
Application
Product Specification
| Storage | -20 °C |
Application
Silane-PEG-Azide (MW 2K) is a PEGylated azide-functional silane designed to enable robust surface and material functionalization via azide handle chemistry. As a click chemistry reagent, it is commonly used as the azide partner for strain-promoted or copper-catalyzed azide–alkyne cycloaddition workflows, allowing researchers to install bioorthogonal labels, ligands, or reactive biomolecular conjugates onto inorganic and hybrid substrates. The silane architecture supports attachment to oxide-rich surfaces, while the PEG spacer improves accessibility and reduces nonspecific interactions in downstream labeling and assembly applications.
1. Surface PEGylation Platforms
Silane-PEG-Azide (MW 2K) is widely used to create PEG-rich, azide-functional coatings on glass, silica, and other oxide-containing materials, providing a convenient immobilized click handle for subsequent conjugation steps. This format is particularly valuable for building modular interfaces where biomolecules, targeting moieties, or imaging tags are attached after surface preparation, enabling consistent functional density and improved probe accessibility. Researchers often select this reagent when they need stable surface anchoring from the silane end combined with a flexible PEG spacer that helps maintain the activity of attached ligands and reduces steric hindrance during labeling.
2. Biomolecule Conjugation Chemistry
Silane-PEG-Azide (MW 2K) supports click-based coupling of azide-bearing surfaces or PEG layers to alkyne-functional biomolecules, including peptides, proteins, and nucleic-acid reagents used in chemical biology workflows. In practical downstream development, the reagent is used to generate azide-presenting platforms that can be decorated with fluorophores, affinity tags, or engineered binding domains using standard click reagents, streamlining the preparation of functional bioconjugates. The PEG spacer is also leveraged to improve colloidal stability and presentation of conjugated components, which is useful when assembling multicomponent labeling schemes for assays and probe libraries.
3. Molecular Imaging Probe Assembly
Silane-PEG-Azide (MW 2K) is used to prepare azide-functional imaging materials and probe surfaces that can be rapidly decorated with alkyne-containing reporters for fluorescence-based and other optical readouts. By introducing an azide handle onto a stable silane-anchored PEG layer, researchers can standardize probe attachment across different substrate formats, such as patterned slides, sensor chips, and imaging-compatible surfaces. This approach is commonly adopted in molecular imaging reagent development to enable reproducible labeling densities and to facilitate swapping of reporter chemistries without re-optimizing the surface functionalization step.
4. Diagnostic and Assay Surfaces
Silane-PEG-Azide (MW 2K) is frequently incorporated into diagnostic reagent development and assay platform engineering where azide-functional surfaces are needed for controlled immobilization of detection elements. The silane-mediated attachment supports durable coupling to oxide-based substrates, while the PEG layer provides a hydrated interface that can help mitigate nonspecific adsorption during assay workflows. Teams building multiplexed or modular assay surfaces often rely on the azide handle to attach detection probes, capture ligands, or reporter conjugates through click-compatible alkyne partners, supporting scalable manufacturing of consistent functional interfaces for research diagnostics and analytical tools.
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