t-Boc-N-amido-PEG2-acid: High-Purity PEG Linker for Bioconjugation and Drug Delivery

Discover the advanced capabilities of t-Boc-N-amido-PEG2-acid, a premier PEG linker meticulously designed for superior performance in bioconjugation, peptide synthesis, and innovative drug delivery systems. As a trusted manufacturer and supplier, we provide this essential reagent to empower your research and development.

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Key Advantages of Using t-Boc-N-amido-PEG2-acid

Precise Bioconjugation

The dual functionality of t-Boc-N-amido-PEG2-acid makes it an excellent choice for precise bioconjugation. Researchers can buy this reagent for controlled attachment to proteins, peptides, or surfaces, optimizing molecular interactions and delivery profiles.

Streamlined Peptide Synthesis

In peptide synthesis, this reagent acts as a valuable building block. Its inclusion can introduce a hydrophilic spacer, improving peptide solubility and pharmacokinetic properties. Consider purchasing for your next peptide synthesis project.

Drug Delivery Enhancement

The PEG component significantly improves drug solubility and circulation half-life. As a dedicated supplier, we ensure you receive a high-quality product to advance your drug delivery research and development efforts.

Versatile Applications in Research and Development

Bioconjugation

Utilize t-Boc-N-amido-PEG2-acid to create antibody-drug conjugates (ADCs), protein-ligand pairings, or to functionalize nanoparticles. Its reactive ends are ideal for specific linkages.

Peptide Synthesis

Incorporate this PEG linker into peptide sequences to enhance solubility, modify pharmacokinetics, or create branched peptide structures. A must-have for peptide chemists.

Drug Delivery Systems

The hydrophilic PEG spacer improves the performance of drug delivery vehicles by increasing aqueous solubility and prolonging circulation time. Ideal for researchers looking to buy advanced formulation components.

Surface Modification

Passivate surfaces or create functionalized interfaces for biomaterial applications. The Boc group can be removed to allow further attachment of biomolecules to modified surfaces.