
Propargyl-PEG1-acrylate | CAS 52436-42-7
| Catalog Number | R01-0118 |
| Category | Alkynes |
| Molecular Formula | C₈H₁₀O₃ |
| Molecular Weight | 154.16 |
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Product Introduction
Propargyl-PEG1-acrylate is a polyethylene glycol (PEG)-based PROTAC linker. Propargyl-PEG1-acrylate can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Propargyl-PEG2-acrylate |
| Purity | 98% |
| IUPAC Name | 2-prop-2-ynoxyethyl prop-2-enoate |
| SMILES | C=CC(=O)OCCOCC#C |
| InChI | InChI=1S/C8H10O3/c1-3-5-10-6-7-11-8(9)4-2/h1,4H,2,5-7H2 |
| InChIKey | QRAIBQFSMDTSQE-UHFFFAOYSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
Propargyl-PEG1-acrylate is a bifunctional PEG-based click chemistry reagent that combines a terminal alkyne handle for copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) with an acrylate group for polymerizable conjugation. The short PEG spacer supports aqueous compatibility and reduces nonspecific interactions, while the acrylic functionality enables incorporation into polymer networks and surface coatings. This reagent is commonly used in chemical biology and biomaterials workflows where orthogonal attachment points are needed to install bioorthogonal tags, linkers, or functional moieties onto PEG-containing materials.
1. Surface Coatings And Films
Propargyl-PEG1-acrylate is used to create functionalized surfaces and thin films where the acrylate group participates in polymerization or surface grafting, and the terminal alkyne provides a subsequent click handle. Research groups and materials labs employ this strategy to generate azide-reactive-ready interfaces for immobilizing biomolecules, affinity ligands, or fluorescent probes after the coating step. The PEG spacer helps maintain hydrophilicity and can improve accessibility of the alkyne for downstream CuAAC labeling, which is particularly valuable for multilayer assembly and patterned surface functionalization.
2. Hydrogel Network Functionalization
Propargyl-PEG1-acrylate supports hydrogel engineering by enabling incorporation of alkyne-bearing PEG units into acrylate-crosslinked networks, allowing later CuAAC conjugation to introduce imaging tags, capture elements, or cell-interactive motifs. Biomaterials researchers use this reagent to tune the density and distribution of clickable sites within hydrogels while leveraging the PEG segment to moderate protein adsorption and nonspecific binding. After gel formation, the alkyne functionality provides a convenient route to spatially or temporally control labeling of hydrogel-embedded components using azide-containing partners.
3. Bioconjugation Linker Platforms
Propargyl-PEG1-acrylate is applied as a modular linker precursor for constructing conjugate platforms in chemical biology, where the acrylate functionality is used to attach the PEG-bearing unit to polymeric carriers and the alkyne serves as a bioorthogonal attachment point. This approach is widely used to prepare reagent-ready materials for subsequent CuAAC coupling with azide-functional biomolecules such as peptides, glycans, or nucleic-acid analogs used as research tools. The reagent’s compact PEG1 segment supports water-compatible conjugation chemistry and helps maintain solubility during labeling workflows, making it useful for preparing standardized clickable intermediates.
4. Fluorescent And Imaging Probe Assembly
Propargyl-PEG1-acrylate is frequently used to build imaging-ready probe assemblies by first installing alkyne-containing PEG units into a polymer scaffold or surface, followed by CuAAC reaction with azide-bearing fluorophores or imaging reagents. Molecular imaging and assay development teams use this two-step design to decouple material formation from probe installation, improving flexibility when optimizing labeling density and reducing handling complexity. The acrylate handle supports integration into polymeric carriers, while the terminal alkyne provides a reliable clickable site for generating consistent probe conjugates for microscopy, flow-based assays, or imaging reagent screening.
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