
t-Boc-N-amido-PEG10-azide
| Catalog Number | R14-0156 |
| Category | Azides |
| Molecular Formula | C27H54N4O12 |
| Molecular Weight | 626.8 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
t-Boc-N-amido-PEG10-azide is a polyethylene glycol derivative featuring an azide group, which participates in copper-catalyzed azide–alkyne cycloaddition reactions. Its t-Boc-protected amine functionality allows for controlled deprotection and subsequent conjugation to a variety of substrates, facilitating bioconjugation and surface modification applications. This reagent is commonly incorporated into linker design strategies due to its flexible PEG10 spacer, enhancing solubility and reducing steric hindrance in complex molecular assemblies.
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-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate |
| SMILES | CC(C)(C)OC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C27H54N4O12/c1-27(2,3)43-26(32)29-4-6-33-8-10-35-12-14-37-16-18-39-20-22-41-24-25-42-23-21-40-19-17-38-15-13-36-11-9-34-7-5-30-31-28/h4-25H2,1-3H3,(H,29,32) |
| InChIKey | YBOUOULSSCFNPI-UHFFFAOYSA-N |
Product Specification
| Storage | -20 °C |
Application
t-Boc-N-amido-PEG10-azide is a PEGylated azide building block designed for strain-free copper-free and copper-mediated azide–alkyne click chemistry workflows, commonly used as a functional handle for biomolecule and material conjugation. The reagent combines an azide reactive group with a PEG10 spacer and a protected amide (t-Boc), enabling flexible attachment strategies that help maintain solubility and reduce nonspecific interactions in complex aqueous environments. Its modular structure makes it a practical choice for generating clickable PEG linkers, surface-functional materials, and labeling reagents used across chemical biology, biomaterials, and imaging tool development.
1. PEG Linker Functionalization
t-Boc-N-amido-PEG10-azide is widely used as a PEG linker precursor for introducing azide functionality into research-grade conjugates, including PEGylated probes, affinity reagents, and polymer-bound constructs. The PEG10 spacer supports aqueous compatibility and can improve handling during labeling and downstream conjugation steps, while the t-Boc-protected amide provides a controlled functional motif for later derivatization or deprotection workflows. Researchers commonly incorporate this reagent when they need a robust, flexible distance element between a reactive biomolecular component and an azide for subsequent click labeling.
2. Biomolecule Labeling Probes
t-Boc-N-amido-PEG10-azide serves as an azide-tagging reagent for preparing click-compatible biomolecule probes used in chemical biology assays and molecular imaging research. The azide group enables straightforward coupling to alkyne-functional reporters, including fluorophores, biotin/streptavidin-compatible tags, and other detection handles, allowing modular assembly of labeling reagents. The PEG10-based architecture is particularly useful when probe solubility and reduced aggregation are important for consistent labeling in buffer-based experimental workflows.
3. Surface And Hydrogel Patterning
t-Boc-N-amido-PEG10-azide is used to introduce azide groups onto surfaces and soft materials such as polymer films and hydrogel matrices, enabling spatially controlled functionalization via click chemistry. By anchoring the PEG10-containing amide motif to a material scaffold, laboratories can generate clickable interfaces for subsequent attachment of imaging reagents, affinity ligands, or reporter molecules. This approach is frequently adopted in biomaterials research where stable, well-defined surface chemistry is needed for reproducible patterning and multicomponent material assembly.
4. Diagnostic Reagent Development
t-Boc-N-amido-PEG10-azide is commonly incorporated into the design of research diagnostic reagent platforms that rely on modular conjugation of detection elements through azide–alkyne click chemistry. The reagent’s PEG spacer supports conjugate solubility and can help maintain accessibility of the reactive site when assembling multicomponent assay reagents, such as probe–linker–reporter constructs used in analytical workflows. Teams developing labeling kits, assay reagents, and laboratory detection tools often select PEG10 azide linkers to streamline reagent assembly while maintaining compatibility with aqueous handling conditions.
Computed Properties
| XLogP3 | 0.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 35 |
| Exact Mass | 626.37382317 g/mol |
| Monoisotopic Mass | 626.37382317 g/mol |
| Topological Polar Surface Area | 145Ų |
| Heavy Atom Count | 43 |
| Formal Charge | 0 |
| Complexity | 652 |
| 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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