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N-(Azido-PEG10)-N-PEG10-acid
| Catalog Number | R14-0100 |
| Category | Azides |
| Molecular Formula | C45H90N4O22 |
| Molecular Weight | 1039.2 |
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Product Introduction
N-(Azido-PEG10)-N-PEG10-acid features a dual-functional architecture with an azide group and a carboxylic acid, facilitating its role in bioorthogonal chemistry and surface modification applications. The azide moiety participates in copper-catalyzed azide–alkyne cycloaddition reactions, enabling the conjugation of biomolecules or polymers through a stable triazole linkage. Its PEG10 spacer enhances solubility and flexibility, supporting its incorporation into complex bioconjugation strategies and linker design for targeted delivery systems.
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-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethylamino]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid |
| SMILES | C(COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCNCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])C(=O)O |
| InChI | InChI=1S/C45H90N4O22/c46-49-48-4-8-55-12-16-59-20-24-63-28-32-67-36-40-71-44-43-70-39-35-66-31-27-62-23-19-58-15-11-54-7-3-47-2-6-53-10-14-57-18-22-61-26-30-65-34-38-69-42-41-68-37-33-64-29-25-60-21-17-56-13-9-52-5-1-45(50)51/h47H,1-44H2,(H,50,51) |
| InChIKey | MMVAMCAREJYWCU-UHFFFAOYSA-N |
| Solubility | Water, DMSO, DCM, DMF |
Product Specification
| Storage | -20 °C |
Application
N-(Azido-PEG10)-N-PEG10-acid is a PEG-based azide-containing click chemistry reagent designed for modular bioconjugation workflows. As an azide handle, it is commonly used in copper-free or copper-catalyzed azide–alkyne cycloaddition strategies to introduce hydrophilic PEG spacers onto biomolecules, surfaces, and materials. The reagent’s dual PEG character and terminal carboxylic acid support both conjugation-ready functionality and downstream coupling to amine/activated-carboxyl chemistries, making it a versatile building block for preparing stable, low-fouling conjugates and imaging/diagnostic reagent platforms.
1. Surface PEGylation
N-(Azido-PEG10)-N-PEG10-acid is frequently used to functionalize material surfaces with PEG layers that improve colloidal stability and reduce nonspecific adsorption in analytical and materials research. After installing the azide-bearing PEG spacer onto a surface through standard coupling chemistry involving the carboxylic acid, researchers can further attach targeting ligands, reporters, or capture moieties via azide-compatible click reactions. This approach is widely adopted in the preparation of microarrays, sensor coatings, and assay substrates where controlled surface presentation and minimized background signal are critical.
2. Probe And Reporter Conjugation
N-(Azido-PEG10)-N-PEG10-acid serves as a practical linker for generating PEG-extended probes and reporter conjugates used in chemical biology and molecular imaging tool development. The azide functionality enables rapid attachment of fluorophores, affinity tags, or other reporter groups through click-compatible partners, while the PEG spacers help tune solubility and reduce aggregation that can otherwise limit probe performance in complex media. The carboxylic acid also supports incorporation into multistep labeling schemes, enabling consistent linker length and improved handling for reagent manufacturing and assay prototyping.
3. Polymer and Hydrogel Functionalization
N-(Azido-PEG10)-N-PEG10-acid is commonly incorporated into polymeric systems and hydrogel matrices to introduce clickable PEG spacers that facilitate post-fabrication functionalization. Materials scientists use the reagent to create azide-functional networks that can be remodeled with alkynyl components, allowing modular installation of bioactive or binding elements while maintaining hydrated, low-interaction environments. The PEG architecture is particularly valuable when preparing responsive or heterogeneous materials where uniform distribution of functional groups and reproducible conjugation density are important for downstream research workflows.
4. Targeting Ligand Linkers
N-(Azido-PEG10)-N-PEG10-acid is used to build linker architectures for attaching targeting ligands to imaging or detection scaffolds in research reagent pipelines. By providing an azide-bearing PEG spacer along with a carboxylic acid handle, the reagent supports controlled conjugation design that separates bulky binding elements from the reporter or surface, helping maintain accessibility and reduce steric constraints. This makes it a common choice for constructing multicomponent labeling reagents used in biochemical assays, affinity-based detection formats, and platform development for molecular recognition studies.
Computed Properties
| XLogP3 | -5 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 25 |
| Rotatable Bond Count | 66 |
| Exact Mass | 1038.60467051 g/mol |
| Monoisotopic Mass | 1038.60467051 g/mol |
| Topological Polar Surface Area | 248Ų |
| Heavy Atom Count | 71 |
| Formal Charge | 0 |
| Complexity | 1070 |
| 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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