
Azido-PEG4-t-butyl acetate | CAS 864681-04-9
| Catalog Number | R14-0223 |
| Category | Azides |
| Molecular Formula | C14H27N3O6 |
| Molecular Weight | 333.38 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Azido-PEG4-t-butyl acetate is a PEG-containing bioorthogonal conjugation building block that provides an azide handle for modular click-chemistry workflows. The molecule can be used to introduce a click-reactive group onto an antibody, peptide, linker intermediate, or payload-containing component, depending on the chemistry of its second terminal functionality. Its additional reactive group is azide bioorthogonal handle; requires complementary click handle on the antibody. The structure includes peg4 spacer to provide hydrophilic spacing. Conjugation can be performed using spaac with dbco/bcn-functionalized partner or cuaac with terminal alkyne partner, depending the complementary handle. The sequence and orientation of the coupling steps should be selected according to the functional groups carried by the two conjugation partners.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Tert-butyl 14-azido-3,6,9,12-tetraoxatetradecanoate; Azido-PEG4-CH2CO2-t-Bu |
| Purity | >98.0% |
| Shelf Life | 0-4°C for short term (days to weeks), or -20°C for long term (months). |
| IUPAC Name | tert-butyl 2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]acetate |
| SMILES | CC(C)(C)OC(=O)COCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C14H27N3O6/c1-14(2,3)23-13(18)12-22-11-10-21-9-8-20-7-6-19-5-4-16-17-15/h4-12H2,1-3H3 |
| InChIKey | SIOLYQZSIFQODW-UHFFFAOYSA-N |
| Solubility | 10 mm in DMSO |
| Appearance | Solid |
| LogP | 1.15756 |
Product Specification
| Storage | -20°C |
Application
Azido-PEG4-t-butyl acetate, a versatile compound prominent in chemical biology and materials science, finds diverse applications across various domains. Here are four crucial applications of Azido-PEG4-t-butyl acetate:
Click Chemistry: Positioned at the core of click chemistry, Azido-PEG4-t-butyl acetate emerges as a crucial cornerstone driving reaction selectivity and efficiency. Its azide group engages in selective interactions with alkyne-containing molecules through the copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling the streamlined synthesis of intricate macromolecules, bioconjugates, and functionalized surfaces with unparalleled precision.
Bioconjugation: Within the realm of bioconjugation techniques, Azido-PEG4-t-butyl acetate assumes a pivotal role in linking biomolecules—be it proteins, nucleic acids, or small molecules—into hybrid entities for a myriad of applications ranging from targeted drug delivery to diagnostic imaging. The incorporation of Azido-PEG4-t-butyl acetate not only facilitates conjugation but also imparts enhanced solubility and reduced immunogenicity to the bioconjugates, courtesy of the polyethylene glycol (PEG) spacer.
Polymer Modification: Standing out in polymer chemistry, Azido-PEG4-t-butyl acetate showcases its utility in functionalizing and modifying polymer backbones with finesse. The presence of the azide functional group enables the introduction of reactive sites on polymers, paving the way for subsequent modifications like grafting or crosslinking. This transformative capability leads to the development of advanced materials tailored to exhibit specific properties suited for diverse applications ranging from biomedical devices to smart materials.
Surface Functionalization: Demonstrating its prowess in surface modification, Azido-PEG4-t-butyl acetate transforms surfaces by introducing functional groups that augment surface properties, paving the path for a multitude of applications. By binding to surfaces, it enriches them with new functional endings poised for further chemical reactions or biological interactions—a boon in devising biosensors, enhancing bio-adhesion, and crafting anti-fouling coatings for multifaceted uses.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry