
t-Boc-N-amido-PEG7-azide | CAS 206265-96-5
| Catalog Number | R14-0158 |
| Category | Azides |
| Molecular Formula | C₂₁H₄₂N₄O₉ |
| Molecular Weight | 494.58 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Boc-NH-PEG7-azide is a polyethylene glycol (PEG)-based PROTAC linker. Boc-NH-PEG7-azide can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Computed Properties
Patents
Chemical Information
| Synonyms | BocNH-PEG7-CH2CH2N3 |
| Purity | >97% |
| IUPAC Name | tert-butyl N-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate |
| SMILES | CC(C)(C)OC(=O)NCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C21H42N4O9/c1-21(2,3)34-20(26)23-4-6-27-8-10-29-12-14-31-16-18-33-19-17-32-15-13-30-11-9-28-7-5-24-25-22/h4-19H2,1-3H3,(H,23,26) |
| InChIKey | ZNEWYWROTJUFAM-UHFFFAOYSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
t-Boc-N-amido-PEG7-azide is a PEG-based azide building block designed for strain-promoted or copper-free click chemistry workflows, where the azide handle enables modular conjugation to complementary cyclooctyne or strained-alkyne partners. The reagent combines a protected amide functionality (t-Boc) with a flexible PEG7 spacer, which helps tune solubility, reduce nonspecific interactions, and provide controlled attachment points for biomolecular labeling and material functionalization. Its PEG-azide architecture is widely used in chemical biology and biomaterials research to introduce bioorthogonal reactivity while maintaining compatibility with aqueous assay conditions.
1. Biomolecule Labeling
t-Boc-N-amido-PEG7-azide is commonly used to install an azide functional group on proteins, peptides, and nucleic-acid conjugates as part of bioorthogonal labeling toolkits. Researchers leverage the PEG7 spacer to improve conjugate solubility and minimize aggregation during labeling and downstream purification, particularly when attaching bulky imaging or affinity tags. The t-Boc-protected amide motif provides a protected handle that can be carried through conjugation workflows and later adjusted during probe assembly, enabling consistent reagent-to-reagent performance in labeling pipelines.
2. Surface And Hydrogel Functionalization
t-Boc-N-amido-PEG7-azide supports azide-directed functionalization of polymer surfaces and hydrogel matrices for creating reactive biomaterial interfaces. In biomaterials science, the PEG7 chain helps present the azide group away from the surface, improving accessibility for subsequent click coupling to strained-alkyne crosslinkers, ligands, or detection moieties. This makes the reagent useful for building modular material platforms where the density and spatial presentation of reactive sites can be tuned to match the requirements of cell-interaction studies, affinity capture formats, or multicomponent material assemblies.
3. Molecular Imaging Probe Assembly
t-Boc-N-amido-PEG7-azide is used as a click-compatible linker component in the construction of molecular imaging probes, including fluorescent and luminescent reporters that require robust attachment chemistry under mild conditions. The azide handle enables straightforward coupling to strained-alkyne imaging partners, while the PEG7 spacer helps maintain probe water compatibility and reduces nonspecific binding that can complicate signal interpretation. In probe development workflows, this reagent is frequently selected to standardize linker length and to support modular swapping of targeting or reporter elements without redesigning the full conjugate.
4. Diagnostic Reagent And Assay Tools
t-Boc-N-amido-PEG7-azide is applied in the preparation of assay reagents and diagnostic research tools that rely on bioorthogonal conjugation to assemble multicomponent detection systems. The PEG7-based azide functionality is well suited for generating conjugates used in binding assays, separation workflows, and signal-generation formats where controlled spacing and improved solubility are important for reproducible reagent behavior. By providing a reliable azide moiety for click attachment to complementary assay components, the reagent integrates into platform-style development where assay chemistries are iteratively optimized by exchanging partners and linkers.
Computed Properties
| XLogP3 | 0.8 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 26 |
| Exact Mass | 494.29517893 g/mol |
| Monoisotopic Mass | 494.29517893 g/mol |
| Topological Polar Surface Area | 117Ų |
| Heavy Atom Count | 34 |
| Formal Charge | 0 |
| Complexity | 515 |
| 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 |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| US-2017355731-A1 | Amatoxin derivatives and conjugates thereof as inhibitors of rna polymerase | 2014-11-06 |
| US-9938323-B2 | Amatoxin derivatives and conjugates thereof as inhibitors of RNA polymerase | 2014-11-06 |
| WO-2016071856-A1 | Amatoxin derivatives and conjugates thereof as inhibitors of rna polymerase | 2014-11-06 |
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