
Propargyl-PEG4-S-PEG4-Boc | CAS 2055041-18-2
| Catalog Number | R01-0097 |
| Category | Alkynes |
| Molecular Formula | C₂₆H₄₈O₁₀S |
| Molecular Weight | 552.72 |
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Product Introduction
Propargyl-PEG4-S-PEG4-Boc is a polyethylene glycol (PEG)-based PROTAC linker. Propargyl-PEG4-S-PEG4-Boc can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Propargyl-PEG4-S-PEG4-t-butyl ester |
| Purity | 98% |
| IUPAC Name | tert-butyl 3-[2-[2-[2-[2-[2-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]ethylsulfanyl]ethoxy]ethoxy]ethoxy]ethoxy]propanoate |
| SMILES | CC(C)(C)OC(=O)CCOCCOCCOCCOCCSCCOCCOCCOCCOCC#C |
| InChI | InChI=1S/C26H48O10S/c1-5-7-28-9-11-30-13-15-32-17-19-34-21-23-37-24-22-35-20-18-33-16-14-31-12-10-29-8-6-25(27)36-26(2,3)4/h1H,6-24H2,2-4H3 |
| InChIKey | CQWOCVRYLDFSFI-UHFFFAOYSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
Propargyl-PEG4-S-PEG4-Boc is a PEG-based bifunctional click chemistry reagent featuring a terminal propargyl group for copper-catalyzed azide–alkyne cycloaddition (CuAAC) and a protected thioether-containing PEG segment for orthogonal handling during linker assembly. The molecule combines flexible polyethylene glycol spacers with an acid-labile Boc-protected functionality, making it well suited for constructing water-soluble conjugates, modular linkers, and surface-tethered materials where controlled spacing and solubility are important. Its propargyl handle enables reliable incorporation into azide-bearing biomolecules, polymers, and imaging or diagnostic scaffolds commonly used in chemical biology workflows.
1. PEG Linker Conjugation
Propargyl-PEG4-S-PEG4-Boc is used as a solubilizing, spacing, and modular conjugation linker in bioconjugation projects that require precise attachment to azide-functional partners via CuAAC. Researchers frequently incorporate the propargyl terminus into azide-containing targets such as PEGylated proteins, antibody fragments, peptides, or polymeric carriers to improve colloidal stability and reduce nonspecific interactions in downstream assays and probe development. The PEG4 spacers help maintain accessibility of the conjugated functional group, which is especially valuable when the conjugate is used in multistep labeling strategies or when the final construct must remain processable in aqueous buffers.
2. Surface Functionalization Chemistry
Propargyl-PEG4-S-PEG4-Boc supports the creation of functional surfaces and interfaces where click-ready attachment points are required for subsequent immobilization of azide-bearing ligands. Materials scientists and chemical biology groups use the reagent to introduce propargyl handles onto polymer films, hydrogel networks, or nanoparticle coatings, enabling later coupling to azide-functional biomolecules such as affinity reagents, targeting motifs, or reporter constructs. The PEG spacers contribute to antifouling-like behavior and improved wettability, which can be advantageous for building reproducible assay platforms, biosensing surfaces, and microscopy-compatible materials.
3. Molecular Imaging Probe Building
Propargyl-PEG4-S-PEG4-Boc is applied in the assembly of imaging and detection probes that rely on modular conjugation to azide-containing reporter scaffolds. Probe developers use the propargyl group to attach imaging moieties, affinity handles, or polymeric carriers through CuAAC, while the PEG4 spacing helps tune the hydrodynamic environment around the reporter for consistent labeling and handling. The Boc-protected functionality provides a convenient handle for staged construct assembly, allowing researchers to manage multicomponent workflows where the conjugate is built in steps and later integrated into a final probe format for microscopy, spectroscopy, or other analytical readouts.
4. Diagnostic Reagent Platforms
Propargyl-PEG4-S-PEG4-Boc is commonly used to prepare diagnostic reagent components that require robust, aqueous-compatible conjugation chemistry and predictable linker architecture. In research and industrial R&D settings, the reagent serves as a click-compatible linker to connect azide-bearing capture molecules, signal-generating reagents, or polymeric scaffolds used in assay development. The PEG-based design supports formation of stable conjugate mixtures and helps maintain accessibility of binding or recognition elements after coupling, which is important for building multiplexed reagent sets and standardized assay materials.
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