
Alkyne-PEG4-thioacetate
| Catalog Number | R01-0242 |
| Category | Alkynes |
| Molecular Formula | C13H22O5S |
| Molecular Weight | 290.38 |
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Product Introduction
Alkyne-PEG4-thioacetate is a specialized reagent featuring an alkyne group, a four-unit polyethylene glycol (PEG) spacer, and a thioacetate moiety. This compound is designed for use in click chemistry, particularly in copper-catalyzed azide-alkyne cycloaddition reactions, where the alkyne group facilitates precise bioconjugation with azide-functionalized molecules. The PEG4 spacer enhances solubility and flexibility, while the thioacetate can undergo further transformations, making it suitable for applications in linker design and surface modification.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >95% by HPLC |
| Solubility | THF, DCM, DMF and DMSO |
| Appearance | Oil |
Product Specification
| Storage | -20 °C |
Application
Alkyne-PEG4-thioacetate is a PEGylated alkyne-bearing click chemistry reagent designed for bioorthogonal conjugation workflows that commonly rely on strain-promoted or copper-catalyzed azide–alkyne cycloaddition. Its structure couples a terminal alkyne handle to a short, flexible PEG spacer while presenting a thioacetate functionality that can be used as a protected thiol motif in labeling and surface-modification contexts. This combination makes the reagent particularly relevant for constructing PEG-based linkers in chemical biology, biomaterials functionalization, and imaging/diagnostic reagent development where solubility, spacing, and modular attachment are important.
1. Surface PEG Functionalization
Alkyne-PEG4-thioacetate is used to introduce PEG-controlled spacing and improved aqueous compatibility onto material surfaces that will later be decorated with azide-bearing ligands, probes, or biomolecules via click conjugation. In biomaterials and interface engineering, the PEG spacer helps reduce nonspecific interactions and supports stable presentation of reactive handles for downstream assembly. The alkyne functionality provides a convenient attachment point for modular build-up of functional coatings, while the thioacetate motif supports workflows that benefit from a protected thiol group during intermediate steps.
2. Protein and Peptide Labeling
Alkyne-PEG4-thioacetate supports research-grade labeling strategies where a PEG spacer is desired between a biomolecular scaffold and a clickable attachment site. Chemical biology groups often incorporate this reagent into labeling pipelines to generate alkyne-functional conjugates that can be rapidly coupled to azide-containing tags, affinity handles, or reporter moieties. The PEG4 segment is particularly useful for minimizing steric hindrance and maintaining solubility during conjugation and purification, enabling reliable downstream click assembly for probe generation and multi-component construct building.
3. Molecular Imaging Probe Assembly
Alkyne-PEG4-thioacetate is applied in the preparation of imaging-oriented chemical probes that require modular attachment of fluorophores, affinity reagents, or signal-generating components through click chemistry. The reagent’s PEG spacer improves probe handling in aqueous buffers and can help tune the effective distance between the imaging label and the targeting or recognition element introduced later through azide–alkyne coupling. By providing a stable alkyne handle for orthogonal assembly, it fits common workflows used to generate libraries of clickable imaging reagents for microscopy, spectroscopy, and platform-based probe screening.
4. Diagnostic Reagent and Assay Platforms
Alkyne-PEG4-thioacetate is frequently incorporated into diagnostic reagent development workflows that rely on assembling multivalent assay components with defined spacing and reduced background. Researchers use the PEGylated alkyne handle to couple azide-functional reporters, capture elements, or secondary reagents onto assay surfaces and bead-based formats through click conjugation. The thioacetate functionality is compatible with intermediate processing steps where protected thiol chemistry is advantageous, supporting practical manufacturing-style assembly of clickable components for robust reagent construction and reproducible assay reagent generation.
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