
Trityl-PEG10-azide | CAS 877239-08-2
| Catalog Number | R14-0113 |
| Category | Azides |
| Molecular Formula | C₃₉H₅₅N₃O₁₀ |
| Molecular Weight | 725.87 |
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Product Introduction
Trityl-PEG10-azide is a polyethylene glycol (PEG)-based PROTAC linker. Trityl-PEG10-azide can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | Trityl-PEG9-N3; 2,5,8,11,14,17,20,23,26,29-Decaoxahentriacontane,31-azido-1,1,1-triphenyl-; 31-azido-1,1,1-triphenyl-2,5,8,11,14,17,20,23,26,29-decaoxahentriacontane; Trityl-PEG9-Azide |
| Purity | 98% |
| IUPAC Name | [2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy-diphenylmethyl]benzene |
| SMILES | C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)OCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C39H55N3O10/c40-42-41-16-17-43-18-19-44-20-21-45-22-23-46-24-25-47-26-27-48-28-29-49-30-31-50-32-33-51-34-35-52-39(36-10-4-1-5-11-36,37-12-6-2-7-13-37)38-14-8-3-9-15-38/h1-15H,16-35H2 |
| InChIKey | YGESYAKTEQEZFB-UHFFFAOYSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
Trityl-PEG10-azide is a PEG-based azide click chemistry reagent featuring a trityl-protected functional handle designed for robust conjugation workflows. As an azide component for strain-promoted or copper-catalyzed azide–alkyne cycloaddition platforms, it is commonly used to introduce PEG spacers and clickable termini into biomolecular, polymer, and surface-bound systems. The trityl-protected motif supports practical handling in materials and probe development, where controlled incorporation of an azide group is needed to build modular conjugates for research and industrial labeling.
1. Biomolecule PEGylation Handles
Trityl-PEG10-azide is widely used to install a PEG spacer and a terminal azide group onto biomolecules and biomolecular mimics, enabling downstream click conjugation to targeting ligands, reporter tags, or functional payloads. Researchers often select this reagent when they want to modulate solubility, reduce nonspecific interactions, and improve conjugate handle accessibility for multistep labeling strategies. The PEG10 length is particularly useful for creating a flexible distance between the biological scaffold and the next functional moiety, which is advantageous in probe formatting and assay reagent construction.
2. Surface And Material Functionalization
Trityl-PEG10-azide supports click-ready functionalization of polymeric materials, hydrogels, and solid supports where azide termini are required for subsequent attachment of dyes, affinity reagents, or imaging handles. Materials scientists use PEG-azide reagents to tune interfacial properties, improve wetting and biocompatible surface presentation, and create reproducible reactive sites for modular assembly. This reagent is also commonly incorporated into coating and scaffold designs for building libraries of surface-bound conjugates via standardized azide–alkyne coupling chemistries.
3. Molecular Imaging Probe Labeling
Trityl-PEG10-azide is used as a PEGylated azide building block for constructing imaging probes and diagnostic-reagent components that require a clickable handle for rapid attachment of fluorophores or other reporter units. Molecular imaging and chemical biology laboratories frequently rely on PEG spacers to enhance probe stability in complex labeling environments and to provide steric flexibility for maintaining reporter performance after conjugation. By providing a defined azide terminus, this reagent helps streamline the assembly of probe variants where consistent linker architecture is important for comparative studies and reagent optimization.
4. Diagnostic Reagent And Assay Platforms
Trityl-PEG10-azide is applied in the development of assay reagents and diagnostic research tools that benefit from modular conjugation chemistry and standardized linker presentation. Developers use PEG-azide reagents to prepare clickable components for coupling to capture reagents, signal-generating labels, or assay-compatible surface chemistries, supporting scalable workflows in reagent manufacturing and kit-style assay development. The PEG10 spacer and azide functionality are particularly useful when building multicomponent assay formats that require controlled spacing and reliable attachment points for downstream assembly steps.
Computed Properties
| XLogP3 | 4.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 34 |
| Exact Mass | 725.38874496 g/mol |
| Monoisotopic Mass | 725.38874496 g/mol |
| Topological Polar Surface Area | 107Ų |
| Heavy Atom Count | 52 |
| Formal Charge | 0 |
| Complexity | 805 |
| 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 |
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