
m-PEG16-azide
| Catalog Number | R14-0166 |
| Category | Azides |
| Molecular Formula | C₃₃H₆₇N₃O₁₆ |
| Molecular Weight | 761.90 |
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Product Introduction
m-PEG16-azide is a polyethylene glycol (PEG)-based PROTAC linker. m-PEG16-azide can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | (3,6,9,12,15,18,21,24,27,30,33,36,39,42,45,48-Hexadecaoxanonatetracontane-1-yl) azide |
| Purity | 98% |
| IUPAC Name | 1-azido-2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethane |
| SMILES | COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C33H67N3O16/c1-37-4-5-39-8-9-41-12-13-43-16-17-45-20-21-47-24-25-49-28-29-51-32-33-52-31-30-50-27-26-48-23-22-46-19-18-44-15-14-42-11-10-40-7-6-38-3-2-35-36-34/h2-33H2,1H3 |
| InChIKey | QWARPFMDFWZEFQ-UHFFFAOYSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
m-PEG16-azide is a methoxy-terminated polyethylene glycol (PEG) azide reagent designed for copper-free and copper-mediated azide–alkyne click chemistry workflows. As a linear, water-compatible PEG handle bearing a terminal azide, it provides a flexible hydrophilic spacer that improves solubility and reduces nonspecific interactions in labeling, surface modification, and conjugation strategies. The reagent is commonly used to install PEG chains onto biomolecules, polymers, and material surfaces, enabling formation of PEGylated constructs for analytical probes, bioconjugation reagents, and functionalized biomaterials.
1. Protein PEGylation
m-PEG16-azide is widely used in bioconjugation pipelines where PEG chains are introduced onto proteins or protein-derived reagents to tune hydrodynamic size, colloidal stability, and surface behavior. Researchers typically pair m-PEG16-azide with complementary alkyne-bearing partners to generate PEGylated protein conjugates for downstream assays, affinity workflows, and long-term storage of labeled reagents. The terminal azide functionality makes it compatible with established click chemistry labeling strategies, while the PEG16 spacer supports reduced aggregation and improved handling in aqueous buffers.
2. Surface And Material Functionalization
m-PEG16-azide supports click-enabled modification of polymer films, hydrogels, and other material surfaces that require hydrophilic PEG interfaces. In materials science and chemical biology, the reagent is used to introduce PEG layers or PEG linkers that can modulate protein adsorption, cell-interaction profiles, and nonspecific binding in experimental platforms. By reacting with alkyne-functional surfaces or alkyne-bearing capture chemistries, m-PEG16-azide enables fabrication of anti-fouling coatings and PEG-mediated attachment points for subsequent immobilization of biomolecules or imaging reagents.
3. Molecular Imaging Probe Building
m-PEG16-azide is commonly incorporated into probe development workflows where PEG spacing is needed between a targeting or recognition element and a detectable reporter. Chemical biology groups use the azide handle to conjugate alkyne-functional imaging components, improving aqueous solubility and helping maintain probe accessibility by providing a flexible linker. The PEG16 length is particularly useful when constructing multi-component labeling schemes, such as attaching contrast or tracking moieties while minimizing steric hindrance and aggregation during probe formulation.
4. Polymer And Nanoparticle Conjugates
m-PEG16-azide is applied in the synthesis of PEG-functional polymers and nanoparticle conjugates used as research tools for controlled surface chemistry and modular assembly. In industrial and academic settings, the azide group serves as a reactive handle for attaching alkyne-bearing ligands, stabilizers, or analytical tags, while the PEG16 chain contributes to colloidal stability and reduced nonspecific interactions. This makes m-PEG16-azide a practical reagent for building clickable, well-defined conjugate architectures in formulation-oriented R&D and materials characterization studies.
5. Diagnostic Reagent Linkers
m-PEG16-azide is used to prepare clickable linker systems for assembling reagent components in diagnostic-relevant assay development and analytical chemistry workflows. By enabling PEG installation through azide–alkyne conjugation, the reagent helps create consistent spacing between assay surfaces, capture chemistries, and labeling moieties, which can be important for reproducible binding behavior in complex assay matrices. Researchers leverage the terminal azide to integrate PEG linkers into modular reagent designs, supporting robust conjugate construction for multiplexed labeling and surface-based analytical formats.
Computed Properties
| XLogP3 | -1.2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 18 |
| Rotatable Bond Count | 48 |
| Exact Mass | 761.45213306 g/mol |
| Monoisotopic Mass | 761.45213306 g/mol |
| Topological Polar Surface Area | 162Ų |
| Heavy Atom Count | 52 |
| Formal Charge | 0 |
| Complexity | 702 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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