
Azido-PEG15-azide
| Catalog Number | R14-0337 |
| Category | Azides |
| Molecular Formula | C₃₂H₆₄N₆O₁₅ |
| Molecular Weight | 772.88 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Azido-PEG15-azide is a polyethylene glycol (PEG)-based PROTAC linker. Azido-PEG15-azide can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | >95% |
| IUPAC Name | 1-azido-2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethane |
| SMILES | C(COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])N=[N+]=[N-] |
| InChI | InChI=1S/C32H64N6O15/c33-37-35-1-3-39-5-7-41-9-11-43-13-15-45-17-19-47-21-23-49-25-27-51-29-31-53-32-30-52-28-26-50-24-22-48-20-18-46-16-14-44-12-10-42-8-6-40-4-2-36-38-34/h1-32H2 |
| InChIKey | NWWZCYUFRXPNTG-UHFFFAOYSA-N |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | White waxy |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
Azido-PEG15-azide is a PEG-based, difunctional azide reagent designed for click chemistry workflows that require two azide handles on a single flexible polymer spacer. As a multivalent azide building block, it is commonly used in strain-promoted or copper-catalyzed azide–alkyne cycloaddition (CuAAC) strategies to introduce controlled spacing and modular attachment points in bioconjugation, surface functionalization, and molecular assembly. The long PEG chain and terminal azide groups make it particularly relevant when downstream constructs benefit from improved solubility, reduced nonspecific interactions, and defined multivalency for probe or material engineering.
1. Multivalent Probe Labeling
Azido-PEG15-azide is widely used to generate multivalent labeling reagents for chemical biology and molecular imaging toolkits, where two azide termini enable attachment to complementary alkyne-bearing partners. Researchers commonly incorporate it into probe design to increase effective local concentration of binding motifs, fluorescent dyes, or affinity tags while maintaining aqueous compatibility through the PEG spacer. The difunctional architecture supports stepwise assembly of complex conjugates, including dual-modality reporters or orthogonally addressable constructs when paired with appropriate alkyne handles.
2. Surface And Material Functionalization
Azido-PEG15-azide serves as a practical linker for functionalizing polymeric surfaces, nanoparticles, and biomaterial interfaces that require azide-rich capture points for subsequent click attachment. Materials groups often use it to create PEGylated, antifouling-friendly coatings before coupling to alkyne-functional ligands, enabling controlled presentation of reactive sites without introducing rigid linkers that can limit accessibility. This application is frequently adopted in research-grade surface chemistry workflows for building patterned or gradient functional materials, as well as for preparing clickable platforms for downstream sensor and assay development.
3. Protein And Biomolecule Conjugation
Azido-PEG15-azide is commonly employed in bioconjugation strategies to install PEG-mediated spacing between biomolecules and clickable moieties, improving conjugate solubility and reducing aggregation tendencies during labeling workflows. Bioconjugation teams use the two azide groups to create conjugates with defined multivalency, such as dual-tag protein constructs, affinity reagent assemblies, or branched biomolecule architectures formed via click coupling to alkyne-functional partners. Its PEG backbone is also leveraged to moderate steric effects, helping maintain accessibility of functional groups on large biomolecular targets.
4. Diagnostic Reagent And Assay Platforms
Azido-PEG15-azide is used to build clickable components for diagnostic reagent development and assay platform engineering, where multivalent attachment can enhance signal organization and reagent modularity. Developers often incorporate it into reagent schematics that require two-step assembly: first installing azide handles onto a scaffold, carrier, or capture surface, then coupling to alkyne-functional reporters or recognition elements. The PEG spacer supports robust handling in aqueous assay buffers and helps maintain consistent conjugate behavior across labeling batches, which is valuable for constructing reusable assay chemistries and multiplexed reagent sets.
Computed Properties
| XLogP3 | -0.2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 19 |
| Rotatable Bond Count | 48 |
| Exact Mass | 772.44296536 g/mol |
| Monoisotopic Mass | 772.44296536 g/mol |
| Topological Polar Surface Area | 167Ų |
| Heavy Atom Count | 53 |
| Formal Charge | 0 |
| Complexity | 741 |
| 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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