
Thiol-PEG4-tris-alkyne
| Catalog Number | R01-0266 |
| Category | Alkynes |
| Molecular Formula | C27H42N2O9S |
| Molecular Weight | 570.70 |
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Product Introduction
Thiol-PEG4-tris-alkyne is a multifunctional reagent featuring a thiol group and three terminal alkyne moieties linked through a polyethylene glycol (PEG) spacer. This compound is designed for applications in click chemistry, particularly enabling copper-catalyzed azide–alkyne cycloaddition reactions, where its multiple alkyne groups can facilitate the conjugation of azide-functionalized molecules. The PEG4 spacer enhances solubility and flexibility, making it suitable for bioconjugation processes, surface modification, and macromolecular assembly in various biochemical and synthetic chemistry contexts.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >90% by HPLC |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Oil |
Product Specification
| Storage | -20 °C |
Application
Thiol-PEG4-tris-alkyne is a PEG-based, multi-alkyne click chemistry reagent designed for copper-free and/or copper-mediated conjugation workflows where rapid, modular assembly is needed. The tris-alkyne functionality enables multivalent labeling and crosslinking, while the PEG4 spacer improves aqueous compatibility and reduces nonspecific interactions in biomolecular and materials contexts. This reagent is commonly used as a versatile handle for attaching biomolecules, building polymeric networks, and generating imaging or assay-ready conjugates through established click-compatible strategies.
1. Multivalent Biomolecule Labeling
Thiol-PEG4-tris-alkyne is used to introduce multiple alkyne groups onto biomolecular platforms such as proteins, peptides, and nucleic-acid-associated constructs, supporting high-density labeling for sensitive downstream readouts in research workflows. The PEG4 segment helps maintain solubility and dispersion in aqueous buffers, which is particularly valuable when preparing conjugates for microscopy, flow-based assays, or affinity reagent development. Researchers often select this tris-alkyne format to tune valency and spacing, enabling more robust conjugate architectures than single-alkyne reagents in multicomponent labeling schemes.
2. PEG-Based Hydrogel Crosslinking
Thiol-PEG4-tris-alkyne is applied in biomaterials research to form or functionalize PEG-containing networks where multiple reactive sites are advantageous for controlled gelation and surface modification. In hydrogel and coating development, the tris-alkyne motif supports incorporation of crosslinkable motifs that can be paired with complementary click handles to generate stable, tunable materials for cell-interaction studies and material characterization. The PEG4 linker contributes to water compatibility and helps produce uniform functional layers for consistent material performance in laboratory-scale fabrication.
3. Surface Functionalization For Assays
Thiol-PEG4-tris-alkyne is frequently used to functionalize assay surfaces and solid supports by providing a multivalent alkyne presentation that can be coupled with detection tags or capture elements bearing complementary click-reactive groups. This approach is common in diagnostic reagent development and analytical chemistry research, where spatially defined conjugation improves reagent organization and reduces variability across batches. The PEG spacer supports reliable handling during surface coupling steps and helps maintain accessibility of the reactive sites for subsequent labeling or probe attachment.
4. Molecular Imaging Probe Assembly
Thiol-PEG4-tris-alkyne serves as a modular building block for assembling imaging probes and labeled molecular tools that require multivalent attachment of fluorophores, affinity ligands, or other reporter moieties. The tris-alkyne architecture supports constructing probe formats with higher labeling density, which can be advantageous for generating well-defined conjugate structures used in imaging method development and instrument optimization. Its PEG4-based design supports aqueous compatibility during probe preparation, facilitating reproducible conjugation workflows for research-grade imaging reagents.
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