
m-PEG8-propargyl
| Catalog Number | R01-0114 |
| Category | Alkynes |
| Molecular Formula | C18H34O8 |
| Molecular Weight | 378.5 |
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Product Introduction
Propargyl-PEG8-methane is crosslinker with a propargyl group. It enables the formation of triazole linkage with azide compounds or biomolecules via copper catalyzed Click Chemistry.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | 98% |
Product Specification
| Storage | -20 °C |
Application
m-PEG8-propargyl is a methoxy-PEG functionalized with a terminal propargyl group, designed for copper-free and/or copper-mediated click chemistry workflows where a reactive alkyne handle is required. As a PEG-based click reagent, it combines bioconjugation-friendly solubility and stealth-like physicochemical tuning with a widely used alkyne moiety for strain-promoted cycloaddition or azide–alkyne coupling strategies. This makes m-PEG8-propargyl particularly relevant for preparing PEGylated probes, surface-modified materials, and modular biomolecular conjugates in chemical biology and materials research.
1. Protein And Peptide PEGylation
m-PEG8-propargyl is commonly used to introduce a short, hydrophilic PEG spacer onto proteins and peptides via azide–alkyne click conjugation, enabling researchers to generate PEGylated biomolecules for improved handling, stability, and reduced non-specific interactions in assay development. The terminal propargyl group provides a convenient orthogonal reactive handle that can be installed during reagent preparation and then coupled to azide-bearing biomolecules, affinity tags, or capture surfaces. In chemical biology workflows, this reagent is frequently selected when a compact PEG length is desired to modulate solubility and surface accessibility without substantially increasing molecular size.
2. Surface Functionalization For Biosensing
m-PEG8-propargyl is well suited for preparing functional coatings and sensor interfaces where alkyne-bearing PEG layers are used to control surface hydration, reduce fouling, and improve probe presentation. Typical workflows involve coupling m-PEG8-propargyl to azide-functionalized substrates, linker layers, or patterned surfaces, followed by attachment of azide- or alkyne-reactive recognition elements depending on the platform chemistry. Because the PEG spacer is short and flexible, it supports formation of stable, non-collapsing interfacial layers that are compatible with downstream binding assays, imaging-based readouts, and reagent automation in diagnostic-reagent development.
3. Hydrogel And Biomaterials Crosslinking
m-PEG8-propargyl is frequently applied in biomaterials science to incorporate clickable PEG segments into hydrogels and polymer networks, where PEGylated architectures help tune swelling behavior, diffusion, and mechanical properties. Researchers use the propargyl functionality to crosslink or assemble materials by coupling with complementary azide-functional crosslinkers, enabling modular fabrication of cell-compatible or assay-compatible matrices. The PEG nature of m-PEG8-propargyl supports reproducible material formation and helps create bioconjugation-ready scaffolds for embedding reactive sites that can later be used for immobilizing biomolecules or affinity ligands.
4. Modular Imaging And Probe Construction
m-PEG8-propargyl is widely used as a building block for constructing modular molecular imaging and detection probes that require an alkyne handle for late-stage conjugation. In many probe-development pipelines, the PEG spacer improves aqueous compatibility and helps manage probe aggregation and non-specific adsorption, while the propargyl group enables coupling to azide-functional fluorophores, targeting ligands, or scaffold molecules. This reagent is therefore a practical choice for assembling multi-component probe systems, including fluorescent labeling reagents and imaging-compatible conjugates used in molecular imaging and chemical biology research tool development.
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