
Azide-PEG3-Sulfone-PEG3-azide | CAS 2055024-45-6
| Catalog Number | R14-0073 |
| Category | Azides |
| Molecular Formula | C₁₆H₃₂N₆O₈S |
| Molecular Weight | 468.53 |
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Product Introduction
Azide-PEG3-Sulfone-PEG3-azide is a polyethylene glycol (PEG)-based PROTAC linker. Azide-PEG3-Sulfone-PEG3-azide can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | 1-azido-2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethylsulfonyl]ethoxy]ethoxy]ethoxy]ethane; 3,6,9,15,18,21-Hexaoxa-12-thiatricosane, 1,23-diazido-, 12,12-dioxide |
| Purity | 98% |
| IUPAC Name | 1-azido-2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethylsulfonyl]ethoxy]ethoxy]ethoxy]ethane |
| SMILES | C(COCCOCCOCCS(=O)(=O)CCOCCOCCOCCN=[N+]=[N-])N=[N+]=[N-] |
| InChI | InChI=1S/C16H32N6O8S/c17-21-19-1-3-25-5-7-27-9-11-29-13-15-31(23,24)16-14-30-12-10-28-8-6-26-4-2-20-22-18/h1-16H2 |
| InChIKey | RBTZRBCQVZHOFS-UHFFFAOYSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
Azide-PEG3-Sulfone-PEG3-azide is a bifunctional, PEG-based click chemistry crosslinker featuring two terminal azide groups separated by a sulfone-containing linker. As an azide building block for copper-free or copper-mediated azide–alkyne cycloaddition workflows, it is widely used to introduce controlled, water-soluble spacing between reactive handles on biomolecules, polymers, and surfaces. The flexible PEG architecture and the sulfone core help maintain solubility and enable modular assembly of multivalent conjugates, including imaging and diagnostic reagent platforms that rely on orthogonal click-compatible chemistries.
1. Multivalent Probe Conjugation
Azide-PEG3-Sulfone-PEG3-azide is commonly used to build multivalent labeling reagents where two independent click handles are required on the same construct. Researchers incorporate this linker to connect azide-functional biomolecules to alkyne-bearing targeting ligands, affinity tags, or reporter moieties, enabling dense presentation of reactive groups that improves signal generation in assay formats. The PEG spacing helps reduce steric congestion and non-specific interactions, which is particularly valuable when assembling fluorescent, luminescent, or affinity-based probes for workflow development in chemical biology and molecular imaging.
2. Surface and Hydrogel Functionalization
Azide-PEG3-Sulfone-PEG3-azide is frequently selected for functionalizing materials with azide-reactive endpoints prior to downstream click coupling. In biomaterials research, it supports the preparation of PEG-rich hydrogels, coatings, and porous scaffolds that can be patterned or uniformly modified by subsequent reaction with alkyne-functional components such as peptides, cell-adhesion motifs, or imaging handles. The bifunctional design allows researchers to tune crosslinking density and spatial organization when integrating with polymer networks or surface immobilization strategies that benefit from water compatibility and linker stability.
3. PEG-Based Crosslinking Platforms
Azide-PEG3-Sulfone-PEG3-azide is used as a modular crosslinker precursor in polymer and conjugate engineering, where controlled connectivity between two click-reactive partners is needed. By installing azide termini with defined PEG spacing, teams can assemble networks, conjugated polymer architectures, or multicomponent assemblies that require reproducible linker length and hydrophilicity. This reagent is especially useful in research-grade development of clickable materials and reagent scaffolds where reproducibility of handle placement is critical for consistent downstream performance in screening and characterization workflows.
4. Diagnostic Reagent Building Blocks
Azide-PEG3-Sulfone-PEG3-azide is applied in the construction of diagnostic and analytical reagent components that rely on modular click assembly. Laboratory teams use it to connect azide-bearing capture elements, reporter conjugates, or assay-compatible scaffolds to alkyne-functional partners during reagent prototyping and optimization. The sulfone-PEG architecture supports aqueous compatibility and flexible spacing, which can help maintain accessibility of binding and reporting units in complex assay environments such as microarray formats, bead-based assays, and multiplexed analytical workflows.
Computed Properties
| XLogP3 | 0.5 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 24 |
| Exact Mass | 468.20023317 g/mol |
| Monoisotopic Mass | 468.20023317 g/mol |
| Topological Polar Surface Area | 127Ų |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 560 |
| 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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