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m-PEG Acid Chlorides feature a reactive acid chloride group that forms stable amide bonds with amines. The PEG spacer boosts solubility, stability, and biocompatibility. Researchers use them for drug delivery, bioconjugation, and surface coating applications.

m-PEG Acid Chloride

Cat# Name Structure M.W. Purity Pricing
AP10149m-PEG2-CH2-acid chloride196.63≥95% Pricing
AP10147m-PEG2-acid chloride210.65≥95% Pricing
AP10150m-PEG3-CH2-acid chloride240.68≥95% Pricing
AP10148m-PEG3-acid chloride254.71≥95% Pricing

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    m-PEG Acid Chlorides are PEG-based compounds with a terminal acid chloride group, making them highly reactive for bioconjugation. The acid chloride forms stable amide bonds with amine-containing molecules, enabling the creation of drug delivery systems, antibody-drug conjugates (ADCs), and other bioconjugates. The PEG spacer improves water solubility, biocompatibility, and reduces immunogenicity.

    Key Features:

    • Reactive Acid Chloride Group: Forms strong amide bonds with amines for easy conjugation.
    • Solubility and Stability: The PEG spacer enhances water solubility, reducing aggregation and increasing stability.
    • Biocompatibility: Minimizes immunogenic responses, making it suitable for therapeutic applications.

    Applications:

    • Drug Delivery Systems: Used as a linker for prodrugs and ADCs, ensuring better drug stability and release.
    • Bioconjugation: Attaches proteins, peptides, and imaging agents for diagnostics and therapeutics.
    • Surface Modification: Coats surfaces like nanoparticles or polymers for biomedical applications.

    How to Use:

    • Storage: Keep at -20°C, away from light and moisture, for long-term stability.
    • Solubility: Dissolves well in organic solvents like DCM and THF for chemical reactions.

    Example Products:

    • m-PEG3-acid chloride (CAS: 66722-87-0): Reacts with amines in the presence of activators like EDC or DCC to form stable amide bonds.
    • m-PEG2-acid chloride: Works well in amide coupling reactions, boosting water solubility of final compounds.

    These versatile linkers are essential tools in pharmaceutical, diagnostic, and biotechnological research, supporting advanced therapeutic and material development.