
t-Boc-N-amido-PEG11-azide
| Catalog Number | R14-0155 |
| Category | Azides |
| Molecular Formula | C29H58N4O13 |
| Molecular Weight | 670.79 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
t-Boc-N-amido-PEG11-azide is a PEG linker containing a protected amino group and an azide group. The azide group reacts with terminal alkynes and cyclooctyne derivatives via click chemistry.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | BocNH-PEG11-CH2CH2N3 |
| Purity | >97% |
| IUPAC Name | tert-butyl N-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate |
| SMILES | CC(C)(C)OC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C29H58N4O13/c1-29(2,3)46-28(34)31-4-6-35-8-10-37-12-14-39-16-18-41-20-22-43-24-26-45-27-25-44-23-21-42-19-17-40-15-13-38-11-9-36-7-5-32-33-30/h4-27H2,1-3H3,(H,31,34) |
| InChIKey | JGWSHTKKDWKMAY-UHFFFAOYSA-N |
Product Specification
| Storage | Store at 4°C |
Application
t-Boc-N-amido-PEG11-azide is a PEG-based azide building block designed for strain-promoted and copper-free click chemistry workflows, where the terminal azide enables efficient bioorthogonal conjugation to complementary click partners. The reagent combines a protected amide functionality with a long, flexible PEG spacer that helps control solubility, reduce nonspecific interactions, and provide a defined handle for downstream labeling, surface functionalization, or probe construction. Because PEG-azide motifs are widely used to tune hydrodynamic properties and presentation of reactive groups, this reagent is commonly selected for constructing conjugates for chemical biology, materials, and imaging reagent development.
1. PEGylated Probe Labeling
t-Boc-N-amido-PEG11-azide is used as a convenient azide-functional PEG linker for assembling labeling reagents and affinity probes in chemical biology workflows. Researchers incorporate this PEG spacer to improve aqueous compatibility and to modulate steric accessibility of the conjugated moiety, which is particularly valuable when attaching bulky dyes, reporter groups, or recognition elements. The protected amide handle supports controlled derivatization strategies, enabling consistent probe architecture when building multicomponent constructs such as imaging probes, pull-down tags, or assay-compatible molecular tools.
2. Biomolecule Conjugation Platforms
t-Boc-N-amido-PEG11-azide serves as an azide-bearing intermediate for generating PEGylated bioconjugation platforms used in research-grade labeling of proteins, peptides, and other biomolecule-derived scaffolds. In typical downstream workflows, the azide group provides a modular attachment point to complementary click-reactive partners, allowing users to install PEG spacers that can improve conjugate stability and reduce aggregation during handling and assay preparation. The long PEG chain is frequently selected to help preserve biomolecular recognition behavior while providing a reproducible conjugation geometry for comparative studies across probe batches.
3. Surface and Material Functionalization
t-Boc-N-amido-PEG11-azide is applied for introducing azide functionality onto polymeric or biomaterial surfaces, enabling subsequent click-based grafting of functional ligands, capture chemistries, or fluorescent reporters. The PEG11 spacer helps create a hydrated interface that can reduce nonspecific adsorption and improve compatibility with aqueous processing steps used in materials research. This reagent is therefore used in workflows that build functional coatings, hydrogel modifications, and surface-tethered molecular assemblies where a defined, flexible linker is required to present reactive groups away from the underlying substrate.
4. Molecular Imaging Reagent Building
t-Boc-N-amido-PEG11-azide is commonly used to construct imaging reagent components that require a bioconjugatable PEG linker and a terminal azide for modular assembly. Imaging-focused teams use PEG spacers to tune solubility and reduce background interactions, which can be important when preparing fluorescent or luminescent conjugates for microscopy, gel-based visualization, or analytical imaging assays. The protected amide functionality supports design flexibility for integrating additional chemical handles during probe synthesis, helping maintain consistent reagent performance across labeling batches.
5. Diagnostic Assay Reagent Design
t-Boc-N-amido-PEG11-azide is utilized in the design of diagnostic assay reagents as an azide-functional linker for creating assay-ready conjugates and labeling reagents. In common development workflows, the PEG11 chain provides a solubilizing and spacing element that supports reproducible conjugate formation and helps maintain reagent behavior under assay conditions. Teams developing research diagnostics and analytical kits often select azide-PEG building blocks to standardize linker length and presentation, enabling consistent coupling to complementary click partners for generating detection reagents, calibration components, and multiplex-ready assay formats.
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