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N-(Boc-PEG23)-N-bis(PEG3-azide)
| Catalog Number | R14-0049 |
| Category | Azides |
| Molecular Formula | C69H138N8O31 |
| Molecular Weight | 1575.9 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
N-(Boc-PEG23)-N-bis(PEG3-azide) is a aqueous soluble branched PEG linke. The azide groups enable PEGylation via Click Chemistry. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | 98% |
| IUPAC Name | tert-butyl N-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[bis[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethyl]amino]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate |
| SMILES | CC(C)(C)OC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN(CCOCCOCCOCCN=[N+]=[N-])CCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C69H138N8O31/c1-69(2,3)108-68(78)72-4-10-79-16-22-87-28-30-89-32-34-91-36-38-93-40-42-95-44-46-97-48-50-99-52-54-101-56-58-103-60-62-105-64-66-107-67-65-106-63-61-104-59-57-102-55-53-100-51-49-98-47-45-96-43-41-94-39-37-92-35-33-90-31-29-88-27-21-84-15-9-77(7-13-82-19-25-85-23-17-80-11-5-73-75-70)8-14-83-20-26-86-24-18-81-12-6-74-76-71/h4-67H2,1-3H3,(H,72,78) |
| InChIKey | JMLRZOZTYDSYNG-UHFFFAOYSA-N |
Product Specification
| Storage | -20 °C |
Application
N-(Boc-PEG23)-N-bis(PEG3-azide) is a PEG-based, bis-azide click chemistry reagent designed for copper-free and/or copper-mediated azide–alkyne cycloaddition workflows. The structure combines a Boc-protected PEG scaffold with two PEG3-azide termini, providing high aqueous compatibility, flexible spacing, and multivalent handle density for downstream conjugation. This reagent is commonly selected when researchers need efficient attachment of polymeric or biomolecular building blocks while preserving solubility and minimizing steric constraints in labeling, surface functionalization, and materials assembly.
1. Multivalent Biomolecule Labeling
N-(Boc-PEG23)-N-bis(PEG3-azide) is widely used to introduce two orthogonally addressable azide handles onto biomolecule conjugates, enabling multivalent labeling strategies for proteomics workflows, affinity reagent generation, and probe construction. The PEG-rich architecture helps maintain colloidal stability and reduces nonspecific aggregation during conjugation and subsequent handling, which is particularly valuable when working with dilute biological samples or complex mixtures. Researchers often incorporate this reagent to tune effective valency and spacing between reactive sites, supporting consistent performance in downstream click-based assembly of imaging or detection reagents.
2. PEG-Linker Polymer Conjugation
N-(Boc-PEG23)-N-bis(PEG3-azide) serves as a practical PEG linker for polymer–polymer and polymer–biomolecule conjugations where dual azide functionality is advantageous. The bis-azide termini allow sequential or parallel coupling to alkyne-bearing polymers, surfaces, or capture ligands, supporting the construction of brush-like architectures, amphiphilic conjugates, and modular macromolecular scaffolds. In materials research and chemical biology, this reagent is frequently used to improve solubility and circulation-like behavior of macromolecular constructs in vitro, while the flexible PEG spacer supports reproducible conjugate formation and easier downstream purification.
3. Hydrogel and Surface Functionalization
N-(Boc-PEG23)-N-bis(PEG3-azide) is used to functionalize hydrogel networks and polymer surfaces via click chemistry, providing a controlled route to install reactive azide groups that can be coupled to alkyne-modified crosslinkers or ligands. The PEG-based chain length and dual azide presentation are particularly relevant for creating uniform functional density across soft materials, where diffusion and steric accessibility can strongly influence coupling outcomes. This reagent is commonly selected for generating clickable biomaterial platforms used in cell-interaction studies, coating strategies, and responsive material designs that rely on modular post-functionalization.
4. Molecular Imaging Probe Assembly
N-(Boc-PEG23)-N-bis(PEG3-azide) is frequently incorporated into molecular imaging and diagnostic-reagent development pipelines as a solubilizing, multivalent azide building block for assembling alkyne-functional reporters. The PEG scaffold helps manage hydrophobicity and aggregation during probe synthesis and storage, while the two azide termini support higher loading of imaging moieties or attachment of multiple targeting/recognition components in a single construct. Researchers use this reagent to generate modular probe architectures that can be rapidly diversified by click coupling, facilitating iterative optimization of labeling density, linker length, and overall probe handling characteristics.
Computed Properties
| XLogP3 | -1.5 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 36 |
| Rotatable Bond Count | 98 |
| Exact Mass | 1574.9467996 g/mol |
| Monoisotopic Mass | 1574.9467996 g/mol |
| Topological Polar Surface Area | 338Ų |
| Heavy Atom Count | 108 |
| Formal Charge | 0 |
| Complexity | 1810 |
| 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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