
Propargyl-PEG2-Tos | CAS 145916-41-2
| Catalog Number | R01-0138 |
| Category | Alkynes |
| Molecular Formula | C12H14O4S |
| Molecular Weight | 254.30 |
| Catalog Number | Size | Price | Quantity |
|---|---|---|---|
| R01-0138 | 10 g | $998 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Propargyl-PEG2-Tos is a PROTAC linker containing a tosyl group and a propargyl group.
Chemical Information
Product Specification
Application
QC Data
Computed Properties
Patents
Chemical Information
| Synonyms | 2-(prop-2-yn-1-yloxy)ethyl 4-methylbenzene-1-sulfonate |
| Purity | 95% |
| IUPAC Name | 2-prop-2-ynoxyethyl 4-methylbenzenesulfonate |
| SMILES | CC1=CC=C(C=C1)S(=O)(=O)OCCOCC#C |
| InChI | InChI=1S/C12H14O4S/c1-3-8-15-9-10-16-17(13,14)12-6-4-11(2)5-7-12/h1,4-7H,8-10H2,2H3 |
| InChIKey | KTEIFCKZGZZTHP-UHFFFAOYSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
Propargyl-PEG2-Tos is a PEG-based propargylated tosylate click chemistry reagent designed to enable copper-free and/or copper-assisted alkyne-based conjugation workflows. As a small, water-compatible linker bearing a terminal alkyne and a tosylate leaving group, it is commonly used to introduce clickable handles onto amine- or thiol-containing biomolecules, surfaces, and polymeric materials under mild conditions. Its PEG spacer supports improved solubility and reduced nonspecific interactions, making it a frequent choice for preparing research-grade conjugates for chemical biology and materials imaging.
1. Biomolecule PEGylation
Propargyl-PEG2-Tos is used to install a terminal alkyne handle onto proteins and other biomacromolecules that contain nucleophilic residues, enabling subsequent conjugation to azide-bearing partners via widely used click strategies. The PEG2 spacer helps maintain aqueous compatibility and can reduce steric crowding around the reactive site, which is valuable when generating labeling reagents, affinity probes, or immobilized biomolecule constructs. Researchers in chemical biology and biomaterials frequently select this reagent when they need a compact, clickable modification that preserves functional binding or surface presentation in downstream assay formats.
2. Surface And Material Functionalization
Propargyl-PEG2-Tos supports the preparation of clickable polymer and surface coatings by introducing alkyne functionality onto material platforms that can be functionalized through tosylate-mediated substitution. This enables subsequent attachment of azide-tagged ligands, dyes, or capture elements for building patterned materials, biointerfaces, and microfabricated assay surfaces. Materials scientists and diagnostic reagent developers often use Propargyl-PEG2-Tos to create robust, chemically defined clickable layers that can be further processed without requiring extensive redesign of the upstream material synthesis.
3. Molecular Imaging Probe Building
Propargyl-PEG2-Tos is commonly incorporated as a linker reagent to generate alkyne-functional intermediates for assembling imaging and detection probes that rely on azide-bearing reporter components. The terminal alkyne provides a convenient handle for click conjugation to fluorophores, affinity tags, or imaging moieties, while the PEG2 segment improves dispersion and handling in aqueous labeling buffers. Molecular imaging and diagnostic chemistry teams use this approach to streamline probe synthesis workflows, especially when they need consistent clickable geometry across probe batches.
4. Targeted Affinity Reagent Conjugation
Propargyl-PEG2-Tos is used to produce alkyne-functional affinity reagents by appending a PEG-spaced clickable handle to nucleophile-containing targeting scaffolds such as peptides, antibodies, and binding proteins. After alkyne installation, the resulting conjugation-ready intermediates can be coupled to azide-functional reporters, capture handles, or multivalent constructs using click chemistry-compatible partners. This workflow is widely adopted in research reagent development because it separates the handle-installation step from the final assembly step, allowing flexible pairing with different azide-bearing components for screening and assay optimization.
QC Data
Computed Properties
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 6 |
| Exact Mass | 254.06128010 g/mol |
| Monoisotopic Mass | 254.06128010 g/mol |
| Topological Polar Surface Area | 61Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 352 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| US-2022131195-A1 | Electrolyte additives containing one, two, or more triple-bonded moieties for silicon anode-based li-ion batteries | 2020-10-28 |
| WO-2022093792-A1 | Electrolyte additives containing one, two, or more triple-bonded moieties for silicon anode-based batteries | 2020-10-28 |
| US-11539077-B2 | Electrolyte additives containing one, two, or more triple-bonded moieties for silicon anode-based li-ion batteries | 2020-10-28 |
| WO-2021213518-A1 | Compound for preventing or treating lipid metabolism-related diseases | 2020-04-23 |
| WO-2021011913-A1 | Tau-protein targeting compounds and associated methods of use | 2019-07-17 |
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