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Tetra-(amido-PEG10-azide)
| Catalog Number | R14-0033 |
| Category | Azides |
| Molecular Formula | C105H204N16O48 |
| Molecular Weight | 2458.9 |
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Product Introduction
Tetra-(amido-PEG10-azide) is a multifunctional reagent featuring four azide groups attached to a polyethylene glycol (PEG) scaffold with amide linkages. This compound participates in copper-catalyzed azide–alkyne cycloaddition (CuAAC) reactions, facilitating the conjugation of biomolecules and synthetic polymers through the formation of stable triazole linkages. Its PEG10 chains enhance solubility and biocompatibility, making it suitable for applications in surface modification and bioconjugation strategies.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | 97% |
| IUPAC Name | N-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]-3-[3-[3-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethylamino]-3-oxopropoxy]-2,2-bis[[3-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethylamino]-3-oxopropoxy]methyl]propoxy]propanamide |
| SMILES | C(COCC(COCCC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])(COCCC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])COCCC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])C(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C105H204N16O48/c106-118-114-9-21-130-29-37-138-45-53-146-61-69-154-77-85-162-93-89-158-81-73-150-65-57-142-49-41-134-33-25-126-17-5-110-101(122)1-13-166-97-105(98-167-14-2-102(123)111-6-18-127-26-34-135-42-50-143-58-66-151-74-82-159-90-94-163-86-78-155-70-62-147-54-46-139-38-30-131-22-10-115-119-107,99-168-15-3-103(124)112-7-19-128-27-35-136-43-51-144-59-67-152-75-83-160-91-95-164-87-79-156-71-63-148-55-47-140-39-31-132-23-11-116-120-108)100-169-16-4-104(125)113-8-20-129-28-36-137-44-52-145-60-68-153-76-84-161-92-96-165-88-80-157-72-64-149-56-48-141-40-32-133-24-12-117-121-109/h1-100H2,(H,110,122)(H,111,123)(H,112,124)(H,113,125) |
| InChIKey | IKKIJAKFHVRGJA-UHFFFAOYSA-N |
Product Specification
| Storage | -20 °C |
Application
Tetra-(amido-PEG10-azide) is a multivalent, PEGylated azide click chemistry reagent designed for copper-free and copper-catalyzed azide–alkyne cycloaddition workflows. Its architecture combines four azide termini with amide-linked PEG10 spacers, enabling efficient spatial presentation of reactive handles on biomolecules, surfaces, and polymeric materials. This multivalent design is particularly relevant for researchers developing conjugation-ready probes, labeling reagents, and functionalized biomaterials where controlled loading and reduced nonspecific interactions are important.
1. Multivalent Biomolecule Labeling
Tetra-(amido-PEG10-azide) is used to install multiple azide groups onto proteins, peptides, and other biological macromolecules for subsequent click-based attachment of imaging tags, affinity ligands, or polymeric reporters. The PEG10 spacing helps maintain solubility and reduces steric congestion compared with densely packed azides, supporting more uniform downstream conjugation in complex labeling workflows. Multivalent azide presentation is also valuable for generating high-occupancy reagent conjugates used in mechanistic studies, assay development, and comparative labeling experiments across different biomolecule formats.
2. Surface Functionalization And Coatings
Tetra-(amido-PEG10-azide) serves as a building block for preparing azide-functional surfaces and thin films that can be patterned or uniformly functionalized prior to click coupling. Researchers use it to introduce reactive azide termini onto polymer coatings, hydrogel components, and material interfaces, enabling later attachment of fluorescent reporters, bioactive motifs, or capture chemistries through azide–alkyne cycloaddition. The amido-PEG10 architecture supports compatibility with aqueous processing and can improve functional group accessibility at the material interface, which is beneficial for reproducible surface labeling and downstream assay integration.
3. Hydrogel And Polymer Network Crosslinking
Tetra-(amido-PEG10-azide) is applied in the fabrication of PEG-based hydrogels and polymer networks where azide groups provide modular sites for click-mediated crosslinking or post-gel functionalization. In materials science and chemical biology, this reagent is commonly used to tune network connectivity and to incorporate defined reactive handles for orthogonal addition of fluorescent dyes, cell-interaction ligands, or analytical tags. The tetrafunctional nature supports higher crosslinking density options and enables multistage material assembly strategies that separate gel formation from final functional installation.
4. Imaging Probe And Diagnostic Reagent Building
Tetra-(amido-PEG10-azide) is widely used as a conjugation intermediate for constructing modular imaging probes and diagnostic reagent components that require controlled attachment of reporters via click chemistry. By providing four azide termini on PEG spacers, it can increase labeling density and improve aqueous compatibility of probe conjugates, which is advantageous when assembling multicomponent detection reagents such as fluorescent or luminescent imaging constructs. Many workflows leverage its multivalency to standardize reagent architecture across batches, supporting consistent performance in analytical and research imaging applications.
Computed Properties
| XLogP3 | -5.5 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 56 |
| Rotatable Bond Count | 152 |
| Exact Mass | 2458.4047471 g/mol |
| Monoisotopic Mass | 2457.4013923 g/mol |
| Topological Polar Surface Area | 580Ų |
| Heavy Atom Count | 169 |
| Formal Charge | 0 |
| Complexity | 2970 |
| 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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