
Azide-PEG8-Tos
| Catalog Number | R14-0188 |
| Category | Azides |
| Molecular Formula | C23H39N3O10S |
| Molecular Weight | 549.6 |
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Product Introduction
Azide-PEG8-Tos is a heterobifunctional crosslinker that features an azide group and a tosylate moiety separated by an eight-unit polyethylene glycol (PEG) spacer. This reagent is commonly used in click chemistry applications, where the azide group can participate in copper-catalyzed azide-alkyne cycloaddition reactions, enabling the conjugation of biomolecules or the functionalization of surfaces. The tosylate group serves as a leaving group for nucleophilic substitution reactions, allowing for further chemical modifications or the installation of additional functional groups.
Product Specification
Application
Product Specification
| Storage | -20 °C |
Application
Azide-PEG8-Tos is a PEG-based azide building block bearing a tosylate leaving group, designed for click chemistry-enabled conjugation workflows where an azide handle is required on a flexible, water-compatible linker. As an azide-functional reagent, it is commonly used in strain-promoted or copper-catalyzed azide–alkyne cycloaddition strategies to install biomolecular or material tags with improved solubility and reduced nonspecific interactions. The PEG8 spacer and tosylate functionality make it particularly relevant for downstream coupling to amine- or thiol-containing targets, enabling modular assembly of labeled probes, surfaces, and bioconjugates.
1. Bioconjugation Linker Use
Azide-PEG8-Tos is used as a versatile PEG linker in bioconjugation pipelines to introduce an azide functional group while maintaining aqueous compatibility and conformational flexibility. Researchers employ Azide-PEG8-Tos to prepare azide-bearing intermediates that can be carried forward into azide–alkyne click labeling of proteins, peptides, carbohydrates, and nucleic-acid related constructs. The PEG8 segment helps maintain accessibility of the reactive handle for subsequent click steps, which is valuable when building multicomponent labeling schemes such as dual-tag probes or orthogonally functionalized conjugates.
2. Surface Immobilization For Assays
Azide-PEG8-Tos is applied in immobilization workflows where azide-functional PEG linkers are needed to present reactive sites on solid supports for assay development and research instrumentation. Materials scientists and assay developers use Azide-PEG8-Tos to create azide-terminated surfaces that can be patterned or uniformly functionalized prior to click-based attachment of capture ligands, affinity reagents, or reporter molecules. The combination of a PEG spacer with a tosylate leaving group supports practical coupling to appropriately functionalized substrates, improving linker hydration and reducing steric hindrance during downstream click immobilization.
3. Molecular Imaging Probe Assembly
Azide-PEG8-Tos is commonly incorporated into molecular imaging and labeling reagent development to generate azide-bearing components that can be rapidly assembled with complementary alkyne partners. Probe developers use Azide-PEG8-Tos to prepare clickable intermediates for attaching fluorophores, affinity tags, or imaging scaffolds via azide–alkyne cycloaddition, supporting modular synthesis of libraries of structurally related probes. The PEG8 linker is particularly useful in probe design where solubility and reduced aggregation are important for consistent labeling and handling during imaging reagent preparation.
4. Diagnostic Reagent Development
Azide-PEG8-Tos is used in the development of research diagnostic reagents that rely on robust, modular conjugation chemistry to generate labeled detection components. Reagent designers employ Azide-PEG8-Tos to introduce azide handles into antibody fragments, binding proteins, or polymeric detection elements, enabling subsequent click-based attachment of reporters and secondary recognition moieties. The PEG8 spacer supports reliable presentation of the clickable group and helps maintain reagent behavior in aqueous assay buffers, which is advantageous for constructing multivalent detection formats and standardized reagent sets.
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