
N-(Azido-PEG3)-PEG4-t-butyl ester
| Catalog Number | R14-0097 |
| Category | Azides |
| Molecular Formula | C23H46N4O9 |
| Molecular Weight | 522.6 |
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Product Introduction
Azide-PEG-CH2CO2H, MW 5,000 is a click chemistry PEG polymer, azide undergoes click chemistry with alkyne group, such as DBCO or BCN molecules. Carboxylic acid can conjugate with amine containing molecules such as protein, peptide in the presence of coupling reagent, HATU or EDC to form a stable amide bond.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | 98% |
| IUPAC Name | tert-butyl 3-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethylamino]ethoxy]ethoxy]ethoxy]ethoxy]propanoate |
| SMILES | CC(C)(C)OC(=O)CCOCCOCCOCCOCCNCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C23H46N4O9/c1-23(2,3)36-22(28)4-8-29-12-16-33-20-21-35-18-14-31-10-6-25-5-9-30-13-17-34-19-15-32-11-7-26-27-24/h25H,4-21H2,1-3H3 |
| InChIKey | LUXGMTDJUGRSOT-UHFFFAOYSA-N |
Product Specification
| Storage | -20 °C |
Application
N-(Azido-PEG3)-PEG4-t-butyl ester is a PEG-based azide click handle designed for copper-free and bioorthogonal conjugation workflows. As an azide-functional reagent bearing an ester-protected PEG architecture, it is commonly used to introduce a stable, water-compatible azide moiety onto biomolecule conjugates, surfaces, and polymeric materials. Its PEG-rich structure supports solubility and spacing effects that are valuable in labeling, probe construction, and materials functionalization where controlled attachment chemistry is required.
1. Bioorthogonal Labeling Probes
N-(Azido-PEG3)-PEG4-t-butyl ester is widely used to incorporate an azide functional group into imaging and detection probes, including fluorescent tags, affinity reagents, and other labeling constructs that rely on subsequent click coupling. Researchers typically select this reagent when they need a hydrophilic PEG spacer to improve reagent handling in aqueous buffers and to reduce steric hindrance during downstream conjugation. The t-butyl ester protection is particularly relevant for workflows where the azide-bearing PEG unit must be carried through intermediate steps before being incorporated into a final conjugate format, enabling modular probe assembly for biochemical assays and molecular imaging reagent development.
2. Surface and Material Functionalization
N-(Azido-PEG3)-PEG4-t-butyl ester supports azide installation on polymeric and solid-phase platforms used in biomaterials research and diagnostic reagent manufacturing. The PEG-based design helps promote uniform presentation of the reactive azide at material interfaces, which is important for consistent labeling density and reproducible conjugation to capture ligands, polymers, or reporter molecules. In practice, teams use this reagent to prepare functional surfaces for affinity capture, to generate clickable linkers on hydrogel or resin systems, and to enable patterned or scalable construction of multi-component materials where azide–alkyne coupling is used to assemble final functional architectures.
3. Biomolecule Conjugate Building Blocks
N-(Azido-PEG3)-PEG4-t-butyl ester is commonly employed as a click-ready PEG linker for constructing azide-functional biomolecule conjugates used in chemical biology and molecular tool development. The reagent’s PEG spacing supports conjugation strategies that aim to preserve biomolecular recognition and reduce nonspecific interactions during probe preparation. By introducing an azide handle that can be carried into subsequent coupling steps, it enables flexible assembly of conjugates such as affinity reagents, nucleic-acid or protein-linked reporters, and multi-ligand constructs used to interrogate biomolecular systems in vitro.
4. Diagnostic Reagent and Assay Platforms
N-(Azido-PEG3)-PEG4-t-butyl ester is used to prepare clickable components for assay reagents and diagnostic research tools that require modular attachment of reporters, capture elements, or signal-generating moieties. The hydrophilic PEG framework is advantageous in reagent formulation because it supports aqueous compatibility and helps maintain functional accessibility of the azide group during conjugation. Many assay developers incorporate this type of azide-PEG building block into workflows that require controlled coupling to complementary click partners, facilitating batch-to-batch consistency when assembling multi-reagent assay components for research-grade diagnostic platform development.
Computed Properties
| XLogP3 | 0.5 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 29 |
| Exact Mass | 522.32647906 g/mol |
| Monoisotopic Mass | 522.32647906 g/mol |
| Topological Polar Surface Area | 117Ų |
| Heavy Atom Count | 36 |
| Formal Charge | 0 |
| Complexity | 544 |
| 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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