
endo-BCN-PEG4-Boc-amine
| Catalog Number | R16-0009 |
| Category | BCN Reagents |
| Molecular Formula | C26H44N2O8 |
| Molecular Weight | 512.6 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
endo-BCN-PEG4-Boc-amine is a PEG linker containing a BCN group and a Boc-protected amine. The protected amine can be deprotected under mild acidic conditions. The BCN group can react with azide-tagged biomolecules.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | 98% |
| IUPAC Name | tert-butyl N-[2-[2-[2-[2-[2-(9-bicyclo[6.1.0]non-4-ynylmethoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate |
| SMILES | CC(C)(C)OC(=O)NCCOCCOCCOCCOCCNC(=O)OCC1C2C1CCC#CCC2 |
| InChI | InChI=1S/C26H44N2O8/c1-26(2,3)36-25(30)28-11-13-32-15-17-34-19-18-33-16-14-31-12-10-27-24(29)35-20-23-21-8-6-4-5-7-9-22(21)23/h21-23H,6-20H2,1-3H3,(H,27,29)(H,28,30) |
| InChIKey | XFUMWZYNWUSABX-UHFFFAOYSA-N |
Product Specification
| Storage | -20 °C |
Application
endo-BCN-PEG4-Boc-amine is a BCN (bicyclononyne)–based click chemistry reagent incorporating a PEG4 spacer and a Boc-protected amine handle. As a strain-promoted cycloaddition partner, BCN reagents are widely used for copper-free, bioorthogonal conjugation workflows where rapid labeling under mild conditions is advantageous. The PEG4 segment improves aqueous compatibility and reduces nonspecific interactions, while the Boc-protected amine enables downstream functionalization of the conjugated product in materials and chemical biology pipelines.
1. Bioorthogonal Target Labeling
endo-BCN-PEG4-Boc-amine is used as a BCN click handle for attaching PEGylated linkers, tags, and functional groups to biomolecules and biomaterial surfaces through strain-promoted cycloaddition. Research groups in chemical biology and molecular imaging value this reagent for building well-defined conjugates where labeling efficiency and compatibility with aqueous buffers are important. The PEG4 spacer supports uniform presentation of the reactive group on larger constructs such as polymers, nanoparticles, and protein conjugates, improving reproducibility across labeling experiments.
2. PEGylated Surface Functionalization
endo-BCN-PEG4-Boc-amine is commonly incorporated into surface modification strategies for creating BCN-functional coatings and interfaces that can later be addressed by complementary click partners. Biomaterials and materials science teams use this type of PEGylated BCN reagent to tune surface hydration and reduce unwanted adsorption while maintaining a reactive site for subsequent coupling. After conjugation, the Boc-protected amine provides a protected functional handle that can be converted into an active amine for further derivatization of the modified surface, enabling multi-step material assembly.
3. Linker Building for Conjugate Libraries
endo-BCN-PEG4-Boc-amine serves as a versatile building block in combinatorial chemistry and reagent development for generating conjugate libraries with consistent linker length and solubility. Molecular imaging and diagnostic reagent developers often rely on PEG spacers to improve handling and conjugate stability during probe synthesis and purification. The Boc-protected amine functionality supports orthogonal downstream modifications, allowing teams to diversify conjugate architectures while keeping the click-addressable BCN motif consistent across library members.
4. Polymer and Nanoparticle Engineering
endo-BCN-PEG4-Boc-amine is applied in polymer chemistry and nanoparticle engineering to introduce click-reactive BCN sites into PEG-containing macromolecular systems. Teams designing functional polymer carriers and particulate platforms use this reagent to create materials that can be selectively decorated with complementary click partners after formulation, supporting modular assembly of complex constructs. The PEG4 segment helps maintain colloidal compatibility and reduces aggregation tendencies, while the Boc-protected amine enables post-conjugation functional tuning for subsequent material processing steps.
Computed Properties
| XLogP3 | 2.4 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 20 |
| Exact Mass | 512.30976637 g/mol |
| Monoisotopic Mass | 512.30976637 g/mol |
| Topological Polar Surface Area | 114Ų |
| Heavy Atom Count | 36 |
| Formal Charge | 0 |
| Complexity | 694 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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