
Methyltetrazine-PEG24-acid
| Catalog Number | R08-0053 |
| Category | Tetrazines |
| Molecular Formula | C60H108N4O27 |
| Molecular Weight | 1317.5 |
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Product Introduction
Methyltetrazine-PEG24-Acid is an aqueous soluble, monodisperse PEG reagent containing a click chemitstry group and terminal carboxylic acid. The acid (CO2H) can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. electron-donating properties of the methyl group enhances the stability of methyltetrazine-PEG4-Acid. Methyltetrazine enable fast click chemistry with TCO ((trans-cycloctene) under mild condition
Chemical Information
Product Specification
Application
Chemical Information
| Purity | 97% |
| Solubility | Water, DMSO, DCM, DMF |
Product Specification
| Storage | -20 °C |
Application
Methyltetrazine-PEG24-acid is a PEGylated methyltetrazine click chemistry reagent designed for bioorthogonal inverse-electron-demand Diels–Alder ligation with trans-cyclooctene (TCO) partners. The extended PEG spacer and terminal carboxylic acid enable robust conjugation to biomolecules, surfaces, and imaging platforms while maintaining favorable aqueous solubility and reduced non-specific interactions. This reagent is widely used in chemical biology and molecular imaging workflows where tetrazine–TCO labeling provides fast, selective attachment for assembling probes, materials, and multicomponent constructs.
1. Bioconjugation For Probes
Methyltetrazine-PEG24-acid is commonly used to introduce a tetrazine handle into antibody fragments, peptides, proteins, and other targeting ligands through its terminal carboxylic acid for subsequent coupling to amine-bearing biomolecules or solid supports. The long PEG24 chain helps preserve binding behavior and improves colloidal stability during labeling, which is valuable for creating well-defined probe conjugates used in receptor-binding studies, pathway mapping, and comparative labeling experiments. Researchers also rely on this reagent to build modular probe sets where tetrazine-functional components are paired with TCO-modified reporters, enabling flexible assembly of imaging or analytical reagents.
2. Molecular Imaging Labeling
Methyltetrazine-PEG24-acid supports the preparation of imaging reagents by enabling site-specific attachment of tetrazine-bearing components to TCO-functional imaging moieties or carrier platforms. The PEG spacer is particularly relevant for reducing aggregation and nonspecific adsorption when probes are formulated in complex buffers, supporting consistent labeling behavior across different imaging workflows. In practice, this reagent is used to generate conjugates for fluorescence and luminescence readouts, as well as for constructing multi-label imaging constructs where sequential or orthogonal conjugation strategies benefit from the tetrazine–TCO click pair.
3. Surface And Material Functionalization
Methyltetrazine-PEG24-acid is frequently applied to functionalize nanoparticles, polymeric surfaces, and biomaterial interfaces with tetrazine groups for downstream capture of TCO-tagged components. The carboxylic acid functionality provides a practical anchoring point for coupling to surface chemistries that present reactive groups, while the PEG24 spacer helps create a hydrated interface that can improve accessibility of the tetrazine for efficient labeling. This makes the reagent useful for building engineered materials used in sensing platforms, multivalent binding assays, and modular surface coatings where controlled presentation of reactive handles is critical.
4. Multicomponent Assay Construction
Methyltetrazine-PEG24-acid is used in assay development and chemical biology tool building to assemble multicomponent systems from tetrazine-bearing building blocks and TCO-modified detection elements. The PEGylated architecture supports aqueous compatibility and helps maintain reagent behavior in complex assay matrices, which is important for reproducible labeling across experimental batches. Teams designing multiplexed readouts often choose this reagent to create standardized tetrazine-functional intermediates that can be rapidly combined with TCO-functional reporters, enabling scalable workflows for constructing combinatorial probe libraries and structured reagent assemblies.
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