
Azide-PEG3-Tos | CAS 178685-33-1
| Catalog Number | R14-0193 |
| Category | Azides |
| Molecular Formula | C13H19N3O5S |
| Molecular Weight | 329.37 |
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Product Introduction
Azide-PEG3-Tos is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Azide-PEG3-Tos is also a non-cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | 2-(2-(2-Azidoethoxy)ethoxy)ethyl 4-methylbenzenesulfonate |
| Purity | >98.0% |
| Shelf Life | 0-4°C for short term (days to weeks), or -20°C for long term (months). |
| IUPAC Name | 2-[2-(2-azidoethoxy)ethoxy]ethyl 4-methylbenzenesulfonate |
| SMILES | CC1=CC=C(C=C1)S(=O)(=O)OCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C13H19N3O5S/c1-12-2-4-13(5-3-12)22(17,18)21-11-10-20-9-8-19-7-6-15-16-14/h2-5H,6-11H2,1H3 |
| InChIKey | PTOJCKLTCKYNFG-UHFFFAOYSA-N |
| Solubility | 10 mm in DMSO |
| LogP | 2.57736 |
Product Specification
| Storage | Store at -20 °C, keep in dry and avoid sunlight. |
Application
Azide-PEG3-Tos is a PEG-based aryl sulfonate click chemistry reagent that combines an azide handle with a tosylate leaving group for efficient conjugation workflows. As a multifunctional, linker-like building block, it is commonly used to introduce azide functionality onto surfaces, polymers, and biomolecule scaffolds while enabling subsequent copper-catalyzed azide–alkyne cycloaddition (CuAAC) labeling. The presence of the PEG3 spacer improves solubility and reduces steric constraints, making it useful in probe and material development where controlled attachment and downstream click compatibility are required.
1. Surface And Polymer Functionalization
Azide-PEG3-Tos is widely used to install azide functionality onto polymeric materials, coating layers, and solid supports that later undergo CuAAC-based attachment of fluorescent tags, affinity ligands, or imaging moieties. The tosylate group provides a practical reactive handle for nucleophile-driven substitution on compatible substrates, while the PEG3 spacer helps maintain accessibility of the azide for subsequent click labeling. This makes Azide-PEG3-Tos a common choice in materials chemistry and chemical biology laboratories building modular labeling platforms for surfaces and bulk polymers.
2. Biomolecule Labeling Workflows
Azide-PEG3-Tos supports azide introduction into biomolecule conjugates and bioconjugation intermediates used for downstream click chemistry. Researchers often employ it to generate azide-bearing protein, peptide, or nucleic-acid conjugates that can be selectively decorated with alkynyl probes via CuAAC, enabling consistent multicolor labeling and orthogonal assembly strategies. The PEG3 linker characteristic of Azide-PEG3-Tos helps reduce steric hindrance around the reactive site, supporting reliable probe attachment in labeling workflows.
3. Fluorescent Probe And Imaging Tagging
Azide-PEG3-Tos is frequently incorporated into the reagent toolbox for preparing fluorescent and molecular imaging tags that rely on azide–alkyne cycloaddition for final coupling. By providing an azide-bearing intermediate, it enables researchers to standardize probe synthesis: first functionalize the carrier or targeting scaffold with Azide-PEG3-Tos, then attach dyes or imaging reporters bearing terminal alkynes. The PEG3 spacer can improve dye conjugation efficiency and maintain optical labeling performance in probe construction for microscopy, flow-based assays, and imaging reagent development.
4. Diagnostic Reagent And Assay Platforms
Azide-PEG3-Tos is used to build azide-functional components for diagnostic and analytical assay platforms that depend on modular click coupling. In many workflows, azide-bearing capture reagents, scaffold polymers, or labeling polymers are prepared using Azide-PEG3-Tos and subsequently coupled to reporter conjugates through CuAAC to generate consistent assay formats. The reagent’s linker-like PEG3 architecture is particularly valuable when constructing multivalent or spatially controlled reagent assemblies for reagent development in research diagnostics and analytical chemistry.
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