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N-(t-Boc-N-amido-PEG10)-N-bis(PEG10-azide)
| Catalog Number | R14-0048 |
| Category | Azides |
| Molecular Formula | C71H142N8O32 |
| Molecular Weight | 1620.0 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
N-(t-Boc-N-amido-PEG10)-N-bis(PEG10-azide) is a heterobifunctional reagent featuring a tert-butoxycarbonyl (t-Boc) protected amine and dual azide groups connected through polyethylene glycol (PEG) chains. This molecular architecture allows it to participate in copper-catalyzed azide–alkyne cycloaddition (CuAAC) reactions, facilitating the conjugation of biomolecules or other alkyne-bearing compounds. The presence of the PEG linkers enhances solubility and flexibility, making it suitable for applications in bioconjugation, surface modification, and polymer functionalization.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | 95% |
| IUPAC Name | tert-butyl N-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[bis[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]amino]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate |
| SMILES | CC(C)(C)OC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN(CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C71H142N8O32/c1-71(2,3)111-70(80)74-4-10-81-16-22-87-28-34-93-40-46-99-52-58-105-64-67-108-61-55-102-49-43-96-37-31-90-25-19-84-13-7-79(8-14-85-20-26-91-32-38-97-44-50-103-56-62-109-68-65-106-59-53-100-47-41-94-35-29-88-23-17-82-11-5-75-77-72)9-15-86-21-27-92-33-39-98-45-51-104-57-63-110-69-66-107-60-54-101-48-42-95-36-30-89-24-18-83-12-6-76-78-73/h4-69H2,1-3H3,(H,74,80) |
| InChIKey | REQVISHIQSNENI-UHFFFAOYSA-N |
| Solubility | Water, DMSO, DCM, DMF |
Product Specification
| Storage | -20 °C |
Application
N-(t-Boc-N-amido-PEG10)-N-bis(PEG10-azide) is a multifunctional, PEG-based click chemistry reagent bearing two terminal azide groups for strain-promoted or copper-catalyzed azide–alkyne cycloaddition workflows. The structure combines a PEG10-azide “handle” architecture with an amide-linked PEG10 unit and a Boc-protected functionality, enabling solubility-friendly conjugation and modular bioconjugation strategies. This reagent is commonly selected when researchers need multivalent azide loading for constructing labeled biomolecules, PEGylated materials, and imaging or diagnostic reagent platforms with controlled spacing and reduced nonspecific interactions.
1. Multivalent Bioconjugation
N-(t-Boc-N-amido-PEG10)-N-bis(PEG10-azide) is used to introduce two azide functionalities onto biomolecule conjugates, supporting multivalent labeling strategies that improve signal density and enable multiplexed attachment of probes or affinity tags. In chemical biology and biomaterials workflows, the PEG10 spacing helps maintain accessibility of reactive termini, which is valuable when conjugating to bulky targeting ligands, polymer backbones, or surface-presented capture molecules. The Boc-protected component supports downstream handling and coupling logic in reagent assembly pipelines where orthogonal reactivity control is required.
2. PEGylated Surface Functionalization
N-(t-Boc-N-amido-PEG10)-N-bis(PEG10-azide) is well suited for functionalizing surfaces and interfaces with azide “linking points” for subsequent click attachment to coatings, nanoparticles, and sensor surfaces. Materials scientists and diagnostic reagent developers often use this type of PEG-rich azide scaffold to improve colloidal stability, reduce surface fouling, and create reproducible linker density for patterned immobilization of fluorescent dyes, affinity ligands, or recognition elements. The dual azide termini enable crosslinking or stepwise surface build-up when integrated with complementary alkyne-bearing components.
3. Molecular Imaging Probe Assembly
N-(t-Boc-N-amido-PEG10)-N-bis(PEG10-azide) supports the modular construction of imaging and analytical probes by providing two orthogonal attachment sites for click-compatible fluorophores, reporter groups, or scaffold components. In molecular imaging reagent development, PEG10-based linkers are frequently used to tune hydrophilicity and minimize aggregation, which helps maintain probe behavior during labeling and purification. The reagent’s multivalent azide design also enables systematic variation of labeling ratios and probe architecture when assembling probe libraries for research assays.
4. Diagnostic Reagent Platform Building
N-(t-Boc-N-amido-PEG10)-N-bis(PEG10-azide) is applied in the development of diagnostic and assay reagents where controlled conjugation chemistry is required for consistent reagent performance. By incorporating two azide handles, teams can build conjugate formats such as multivalent reporter constructs, bead- or membrane-associated labeling reagents, and reagent components for lateral flow or microarray-style workflows that rely on robust, high-yield click coupling to alkyne-functional partners. The PEG-rich scaffold supports compatibility with aqueous assay conditions and helps manage nonspecific interactions during reagent preparation and storage.
Computed Properties
| XLogP3 | -1.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 37 |
| Rotatable Bond Count | 101 |
| Exact Mass | 1618.9730144 g/mol |
| Monoisotopic Mass | 1618.9730144 g/mol |
| Topological Polar Surface Area | 347Ų |
| Heavy Atom Count | 111 |
| Formal Charge | 0 |
| Complexity | 1830 |
| 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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