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N-(acid-PEG24)-N-bis(PEG3-azide)
| Catalog Number | R14-0066 |
| Category | Azides |
| Molecular Formula | C67H133N7O32 |
| Molecular Weight | 1548.8 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
N-(acid-PEG24)-N-bis(PEG3-azide) is developed by BroadPharm as a branched crosslinker. it is aqueous soluble. The azide groups enable PEGylation via Click Chemistry. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU).
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | 98% |
| IUPAC Name | 3-[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]ethoxy]propanoic acid |
| SMILES | C(COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN(CCOCCOCCOCCN=[N+]=[N-])CCOCCOCCOCCN=[N+]=[N-])C(=O)O |
| InChI | InChI=1S/C67H133N7O32/c68-72-70-2-8-78-14-20-84-22-16-80-10-4-74(5-11-81-17-23-85-21-15-79-9-3-71-73-69)6-12-82-18-24-86-26-28-88-30-32-90-34-36-92-38-40-94-42-44-96-46-48-98-50-52-100-54-56-102-58-60-104-62-64-106-66-65-105-63-61-103-59-57-101-55-53-99-51-49-97-47-45-95-43-41-93-39-37-91-35-33-89-31-29-87-27-25-83-19-13-77-7-1-67(75)76/h1-66H2,(H,75,76) |
| InChIKey | LCYPYNCXKBLGQL-UHFFFAOYSA-N |
| Solubility | Water, DMSO, DCM, DMF |
Product Specification
| Storage | -20 °C |
Application
N-(acid-PEG24)-N-bis(PEG3-azide) is a multifunctional, PEG-based click chemistry reagent featuring an acid-anchored, long PEG24 scaffold terminated with two PEG3-azide groups. As an azide-bearing component, it is designed for copper-free or copper-mediated azide–alkyne cycloaddition workflows commonly used in bioconjugation chemistry, surface functionalization, and molecular imaging reagent assembly. The combination of dual azide handles and extended PEG spacers supports multivalent labeling strategies where spacing, solubility, and conjugation geometry are critical for downstream probe and material performance.
1. Dual-Azide Biomolecule Labeling
N-(acid-PEG24)-N-bis(PEG3-azide) is used as a versatile linker for introducing two independent azide reactive sites into biomolecule conjugates, enabling multivalent attachment to alkyne-functional targets such as peptides, proteins, antibodies, and aptamers. The PEG24/PEG3 architecture helps maintain aqueous solubility and reduces nonspecific interactions during conjugation and subsequent assay workflows. Researchers often select this reagent when they need controlled valency and improved accessibility of reactive handles, for example to build higher-order probe formats or to tune labeling density on complex biological scaffolds.
2. Surface And Hydrogel Functionalization
N-(acid-PEG24)-N-bis(PEG3-azide) supports azide installation on material surfaces and soft biomaterials where an acid-bearing PEG scaffold can be used to promote stable association with substrates prior to click coupling. Dual azide functionality is particularly valuable for creating crosslinkable or multi-point attachment architectures with alkyne-functional polymers, coatings, or network-forming components. This reagent is frequently incorporated into hydrogel and interface engineering pipelines to generate spatially defined functional layers for imaging probes, affinity ligands, or responsive material elements that require robust, water-compatible click chemistry handles.
3. Molecular Imaging Probe Assembly
N-(acid-PEG24)-N-bis(PEG3-azide) is commonly employed in the construction of imaging reagent conjugates that require modular attachment of fluorophores, radiolabeling chelators, or optical reporter motifs bearing terminal alkyne groups. The dual PEG3-azide termini allow researchers to vary labeling stoichiometry and to assemble multicomponent imaging constructs with improved solubility and reduced aggregation compared with shorter linkers. In molecular imaging and chemical biology workflows, this reagent is selected to provide click-ready azide functionality while the PEG spacers help maintain probe dispersion and accessibility for target-binding components or immobilized imaging platforms.
4. Multivalent Diagnostic Reagent Platforms
N-(acid-PEG24)-N-bis(PEG3-azide) is used to build multivalent diagnostic reagent platforms in which two azide handles enable sequential or combinatorial coupling to alkyne-functional capture reagents, reporters, or scaffold components. The PEG-based spacer design supports conjugate stability in aqueous buffers and helps preserve reactive-site accessibility during platform assembly and downstream handling. Teams developing research diagnostics and analytical tools often rely on dual-azide PEG linkers to control the geometry of multivalent binding architectures and to facilitate reproducible coupling onto nanoparticles, beads, or assay-compatible surfaces.
Computed Properties
| XLogP3 | -5.1 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 37 |
| Rotatable Bond Count | 99 |
| Exact Mass | 1547.8995151 g/mol |
| Monoisotopic Mass | 1547.8995151 g/mol |
| Topological Polar Surface Area | 346Ų |
| Heavy Atom Count | 106 |
| Formal Charge | 0 |
| Complexity | 1730 |
| 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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