
TOSYL-PROPARGYL-DIETHYLENE GLYCOL > 95 % | CAS 1119249-30-7
| Catalog Number | R01-0135 |
| Category | Alkynes |
| Molecular Formula | C14H18O5S |
| Molecular Weight | 298.36 |
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Product Introduction
Tos-PEG2-O-Propargyl is a polyethylene glycol (PEG)-based PROTAC linker. Tos-PEG2-O-Propargyl can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Propargyl-PEG3-Tos;Propargyl-PEG4-Tos |
| Purity | 95% |
| IUPAC Name | 2-(2-prop-2-ynoxyethoxy)ethyl 4-methylbenzenesulfonate |
| SMILES | CC1=CC=C(C=C1)S(=O)(=O)OCCOCCOCC#C |
| InChI | InChI=1S/C14H18O5S/c1-3-8-17-9-10-18-11-12-19-20(15,16)14-6-4-13(2)5-7-14/h1,4-7H,8-12H2,2H3 |
| InChIKey | XOLBARIQCXNLPS-UHFFFAOYSA-N |
| Solubility | In Ethanol: 50 mg/mL (167.59 mM; Need ultrasonic) |
Product Specification
| Storage | Pure form, -20°C, 3 years; 4°C, 2 years; In solvent, -80°C, 6 months; -20°C, 1 month |
Application
TOSYL-PROPARGYL-DIETHYLENE GLYCOL > 95 % is a tosyl-activated propargyl ether designed for copper-free and copper-enabled click chemistry workflows, providing a protected propargyl handle for subsequent conjugation and surface functionalization. As a small-molecule click reagent, it combines a reactive terminal alkyne with an ethylene glycol spacer that improves solubility and reduces nonspecific interactions in labeling and materials studies. This reagent is commonly used to introduce alkyne functionality onto polymers, biomaterial surfaces, and labeling platforms that later undergo azide–alkyne cycloaddition for modular probe assembly.
1. Alkyne Functional Labeling
TOSYL-PROPARGYL-DIETHYLENE GLYCOL > 95 % is frequently selected to install terminal alkyne functionality on amine- or hydroxyl-bearing targets used in chemical biology and analytical labeling workflows. Researchers use the glycol spacer to maintain accessibility of the propargyl group, which supports efficient downstream azide–alkyne coupling for attaching fluorophores, affinity tags, or imaging handles. This reagent is particularly useful when a stable, ether-linked alkyne motif is desired to preserve labeling performance during wash steps and multi-step conjugation sequences.
2. Surface And Polymer Conjugation
TOSYL-PROPARGYL-DIETHYLENE GLYCOL > 95 % is widely used in biomaterials science to functionalize polymeric surfaces and coatings with clickable alkyne groups for subsequent immobilization of azide-bearing ligands or reporters. The ethylene glycol segment helps tune surface hydration and can mitigate aggregation on hydrophilic substrates, supporting reproducible probe presentation in microfabricated or membrane-based formats. Typical applications include creating clickable polymer films for multivalent binding assays, patterning surfaces for imaging workflows, and preparing alkyne-functional materials used in modular assembly of diagnostic reagents.
3. Probe And Imaging Reagent Assembly
TOSYL-PROPARGYL-DIETHYLENE GLYCOL > 95 % serves as a practical building block for preparing alkyne-containing probes that are later coupled to azide-tagged imaging components. Chemical biology groups commonly incorporate this reagent into labeling strategies to generate consistent clickable handles on small-molecule reporters, polymeric imaging agents, or assay-compatible conjugates. The glycol spacer supports probe solubility and helps maintain reactive-group accessibility, which is advantageous when constructing multi-component imaging reagents that require reliable azide–alkyne coupling in complex assay buffers.
4. Diagnostic Reagent And Assay Platforms
TOSYL-PROPARGYL-DIETHYLENE GLYCOL > 95 % is used to create alkyne-functional components for diagnostic reagent development and assay platform construction where modular azide–alkyne assembly is preferred. R&D teams employ alkyne introduction to enable controlled attachment of detection moieties, capture elements, or signal amplifiers onto solid supports and reagent cartridges. The reagent’s tosyl activation and glycol spacer make it convenient for preparing clickable intermediates that can be integrated into workflow-specific conjugate formats for high-throughput screening of assay chemistries and reagent performance under standardized lab conditions.
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