
TCO-PNB ester | CAS 1438415-89-4
| Catalog Number | R15-0039 |
| Category | Trans Cyclooctene (TCO) |
| Molecular Formula | C₁₅H₁₇NO₅ |
| Molecular Weight | 291.30 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
TCO-PNB ester is a PROTAC linker, which is composed of alkyl chains. TCO-PNB ester can be used to synthesize a range of PROTACs.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | 95% |
| IUPAC Name | [(4Z)-cyclooct-4-en-1-yl] (4-nitrophenyl) carbonate |
| SMILES | C1CC=CCCC(C1)OC(=O)OC2=CC=C(C=C2)[N+](=O)[O-] |
| InChI | InChI=1S/C15H17NO5/c17-15(20-13-6-4-2-1-3-5-7-13)21-14-10-8-12(9-11-14)16(18)19/h1-2,8-11,13H,3-7H2/b2-1- |
| InChIKey | FJMMADPCDJNXAH-UPHRSURJSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
TCO-PNB ester is a strained trans-cyclooctene (TCO) click chemistry reagent presented as a PNB (p-nitrobenzyl) ester, enabling light-tunable handling and subsequent bioorthogonal conjugation workflows. As a TCO-based reagent, it is commonly used in strain-promoted inverse electron-demand cycloaddition (SPIEDAC) with tetrazines to rapidly label biomolecules, surfaces, and imaging constructs under mild conditions. The PNB ester functionality supports practical reagent storage and controlled activation, making TCO-PNB ester a frequent choice for researchers building modular conjugates for chemical biology, diagnostics research tools, and functional biomaterials.
1. Tetrazine-Based Target Labeling
TCO-PNB ester is widely used to generate tetrazine-reactive conjugates for rapid, catalyst-free labeling of proteins, peptides, and other targeting ligands. Researchers in chemical biology and molecular imaging workflows rely on the TCO handle to introduce fast-reacting sites that can be coupled to tetrazine probes, including fluorescent dyes, affinity tags, and imaging reporters. The PNB ester format is particularly useful when users want a practical ester-bearing precursor that can be incorporated into labeling strategies where controlled activation and subsequent click conjugation are advantageous for downstream handling and assay setup.
2. Bioorthogonal Imaging Probes
TCO-PNB ester supports the construction of bioorthogonal imaging reagents where strain-promoted click chemistry provides high labeling specificity in complex experimental mixtures. Molecular imaging and diagnostic reagent development teams use TCO-PNB ester to prepare tetrazine-compatible probe conjugates for fluorescence-based studies, microscopy labeling, and multimodal reporter platforms. By providing a robust TCO-bearing scaffold in an ester form, TCO-PNB ester helps streamline probe synthesis for researchers who need consistent conjugation chemistry across different imaging modalities and labeling targets, from small biomolecular ligands to larger macromolecular carriers.
3. Surface and Material Functionalization
TCO-PNB ester is used to functionalize polymeric materials, hydrogel surfaces, and biomaterial scaffolds with TCO reactive groups for subsequent tetrazine-mediated coupling. Biomaterials scientists and materials chemists incorporate TCO-PNB ester into surface modification workflows to create modular platforms that can be post-functionalized with tetrazine-tagged components such as fluorescent reporters, affinity ligands, or other reactive building blocks. The ester presentation facilitates practical incorporation into material chemistries where ester linkages or ester-reactive steps are compatible with the fabrication process, enabling researchers to design reusable or sequentially assembled material constructs.
4. Modular Conjugate Building Blocks
TCO-PNB ester is commonly adopted as a modular building block for assembling multi-component conjugates used in chemical biology tool development and research reagent pipelines. Teams creating libraries of labeled biomolecules, reagent standards, or tagging reagents use the TCO-PNB ester to introduce a defined click handle that can be coupled later to tetrazine-functional partners, supporting flexible experimental design and parallel synthesis. The combination of a strained-alkene click motif with an ester-bearing format helps users manage reagent workflows across different labeling campaigns, where consistent downstream coupling to tetrazine reagents is a key requirement.
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