
mPEG8-azide | CAS 869718-80-9
| Catalog Number | R14-0170 |
| Category | Azides |
| Molecular Formula | C₁₇H₃₅N₃O₈ |
| Molecular Weight | 409.48 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
m-PEG8-azide is a polyethylene glycol (PEG)-based PROTAC linker. m-PEG8-azide can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | m-PEG8-azide;mPEG8-N3; 25-Azido-2,5,8,11,14,17,20,23-octaoxapentacosane |
| Purity | >97% |
| IUPAC Name | 1-azido-2-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethane |
| SMILES | COCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C17H35N3O8/c1-21-4-5-23-8-9-25-12-13-27-16-17-28-15-14-26-11-10-24-7-6-22-3-2-19-20-18/h2-17H2,1H3 |
| InChIKey | ANQOCZRUHGJYCX-UHFFFAOYSA-N |
| Appearance | Colorless Liquid |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
mPEG8-azide is a methoxy-terminated polyethylene glycol (mPEG) bearing a terminal azide, designed for bioorthogonal click chemistry workflows. As an azide-functionalized PEG reagent, it is commonly used in strain-promoted azide–alkyne cycloaddition (SPAAC) and related azide click formats to install PEG handles onto biomolecules, surfaces, and materials under mild conditions. Its PEG chain provides water solubility and steric shielding, making mPEG8-azide a widely adopted building block for creating PEGylated conjugates, antifouling coatings, and imaging or assay-ready platforms.
1. Biomolecule PEGylation
mPEG8-azide is frequently used to introduce a defined PEG spacer onto proteins, peptides, and other biomolecular scaffolds via azide click coupling to complementary cyclooctyne or strained-alkyne partners. Researchers employ this approach to generate PEGylated conjugates that improve colloidal stability, reduce non-specific interactions in complex media, and tune hydrodynamic properties for downstream labeling and analytical workflows. In molecular biology and chemical biology laboratories, mPEG8-azide is also used to create modular conjugation sites for subsequent multistep assembly of probes, affinity reagents, or polymer-supported biomaterials.
2. Surface Antifouling Coatings
mPEG8-azide is well suited for preparing antifouling and biointerface materials where PEG presentation at a surface is critical. By incorporating azide functionality into coating chemistries and then performing click coupling with appropriate strained-alkyne linkers, materials scientists can install PEG layers that help suppress protein adsorption and reduce background in assays. This use case is common in microfluidics, biosensor sample handling, and diagnostic reagent development, where stable surface passivation supports reproducible binding and signal readouts over repeated experimental cycles.
3. Imaging Probe Conjugation
mPEG8-azide is used as a PEG handle for constructing imaging-ready conjugates that require improved solubility and controlled probe architecture. In research settings, the azide group enables orthogonal attachment to imaging tags, affinity ligands, or scaffold components bearing complementary strained-alkyne functionalities, allowing probe assembly under conditions compatible with sensitive labeling reagents. The mPEG spacer can also help modulate probe distribution in assay formats and enhance handling characteristics for fluorescence, luminescence, or other molecular detection modalities used in chemical biology tool development.
4. Polymer and Hydrogel Functionalization
mPEG8-azide is commonly incorporated into polymer networks, hydrogels, and PEG-based materials to introduce clickable PEG segments for post-fabrication functionalization. By using azide click chemistry to attach additional functional moieties, researchers can create materials with tunable surface chemistry, controlled ligand density, or modular incorporation of reactive handles for further conjugation. This approach is widely used in biomaterials science to build assay-compatible scaffolds, cell-interaction platforms, and customizable reagent carriers where stepwise material modification is preferred over one-pot synthesis.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry