
Propargyl-PEG18-alcohol | CAS 32199-97-6
| Catalog Number | R01-0183 |
| Category | Alkynes |
| Molecular Formula | C37H72O18 |
| Molecular Weight | 805.0 |
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Product Introduction
Propargyl-PEG18-alcohol is a crosslinker that can react with azide compounds under the catalyzation of copper to form stable triazole linkage. The hydrophilic PEG units increase the solubility of the molecule in aqueous environment.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Propargyl-PEG14-alcohol |
| Purity | 98% |
| Solubility | Water, DMSO, DMF, DCM |
Product Specification
| Storage | -20 °C |
Application
Propargyl-PEG18-alcohol is a PEG-based propargylated linker designed for copper-free and copper-mediated click chemistry workflows, enabling efficient installation of alkynes onto PEGylated platforms. Its long, flexible poly(ethylene glycol) chain and terminal propargyl alcohol functionality make it well-suited for solubilization, spacing, and bioconjugation-friendly surface or polymer modifications. Researchers commonly select this reagent to build clickable PEG handles for downstream conjugation to azide-bearing biomolecules, materials, and imaging reagents while maintaining colloidal stability and reduced nonspecific interactions.
1. PEGylated Bioconjugation Handles
Propargyl-PEG18-alcohol is widely used as a PEGylated alkyne building block to introduce a click-ready handle onto proteins, peptides, and other biomolecular scaffolds that are engineered to carry azide partners. The extended PEG spacer helps maintain accessibility of the reactive site and can improve aqueous compatibility during labeling workflows, which is particularly valuable when preparing conjugates for mechanistic studies, assay development, or multicomponent probe assembly. In typical research pipelines, the reagent is incorporated during linker installation steps to generate stable, well-defined alkyne-functional conjugates that can be rapidly coupled to azide-bearing targets using established click protocols.
2. Surface Functionalization For Materials
Propargyl-PEG18-alcohol supports click-based functionalization of polymeric and inorganic surfaces where PEG spacing is used to control interfacial presentation of ligands. By providing a terminal alkyne group on a long hydrophilic chain, it is commonly incorporated into coatings, hydrogel components, and surface-grafted layers to create clickable regions for subsequent attachment of azide-functional biomolecules, affinity ligands, or reporter tags. Materials scientists often rely on PEG18 length to reduce steric crowding and to tune surface wettability and nonspecific adsorption, enabling reproducible immobilization of clickable components for imaging, sensing, and platform screening.
3. Molecular Imaging Probe Construction
Propargyl-PEG18-alcohol is used to prepare alkyne-functional PEG linkers that serve as modular components in the construction of imaging and detection probes. The reagent’s flexible PEG chain provides a practical scaffold for attaching imaging moieties through click coupling to azide-containing reporter conjugates, allowing probe assembly with controlled spacing between the targeting/recognition element and the signal reporter. In molecular imaging reagent development, long PEG linkers are frequently selected to improve solubility and to help preserve the accessibility of binding or recognition domains after conjugation, supporting consistent labeling performance across probe formats.
4. Diagnostic Reagent And Assay Platforms
Propargyl-PEG18-alcohol is commonly employed in the development of assay reagents and diagnostic research tools that require modular, click-assembled components. The propargylated PEG handle enables straightforward coupling to azide-functional capture reagents, detection tags, or polymer supports, facilitating rapid generation of reagent libraries with matched linker chemistry and spacing. Within assay platform workflows, the PEG18 segment helps maintain reagent stability in aqueous buffers and can reduce background interactions, which is advantageous when preparing conjugates for multiplexing, standardized reagent panels, or scalable assay manufacturing processes that depend on reliable click coupling chemistry.
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