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Bromo-PEGₓ-Amino tert-Butyl Ester (Br-PEGₓ-NHtBu, x=1-12) April 17,2026.

I. Product Overview
Bromo-PEG-Amino tert-Butyl Ester is a multifunctional, dual-functional PEG linker composed of a bromo terminus, an adjustable-length polyethylene glycol (PEG) chain, and an amino tert-butyl ester protecting group. This compound holds significant value in bioconjugation chemistry and drug development, playing a key role particularly in the emerging field of PROTAC technology.

II. Structural Features

  • Bromo terminus: Acts as an electrophile, reacting with nucleophiles such as thiols and amines for efficient conjugation.

  • Amino tert-butyl ester protecting group: Can be deprotected under acidic conditions to release a free amino group for subsequent functionalization.

  • Adjustable PEG chain length:

    • Number of PEG units: Customizable based on requirements.

    • Chain length effects: Solubility, steric hindrance, pharmacokinetic properties.

  • Excellent physicochemical properties:

    • Good solubility in both aqueous and organic solvents.

    • Enhances biocompatibility of conjugated products.

    • Reduces non-specific interactions.

III. Major Application Areas

  • PROTAC Development

    • Linker role: Serves as a connecting bridge between the E3 ligand and the target protein ligand.

    • Optimization properties:

      • Modulates cell permeability of PROTAC molecules.

      • Affects the formation efficiency of the ternary complex.

      • Regulates degradation activity and selectivity.

    • Structural advantages:

      • Bromo end for attaching the E3 ligand.

      • Deprotected amino end for attaching the target protein ligand.

      • PEG chain provides necessary flexibility.

  • Bioconjugation Chemistry

    • Functionalization of proteins/antibodies.

    • Modification of peptide compounds.

    • Attachment of fluorescent labels.

  • Materials Science

    • Polymer functionalization.

    • Surface modification.

    • Nanomaterial functionalization.

  • Drug Delivery Systems

    • Prodrug design.

    • Drug-carrier conjugation.

    • Improving drug solubility and stability.

IV. Detailed Description for PROTAC Applications

  • Design Advantages

    • Modular construction: The bromo and amino groups provide distinct conjugation points, facilitating modular assembly of PROTACs.

    • Adjustable length: The selection of 1-12 PEG units allows fine-tuning of the linker length to optimize degradation efficiency.

    • Protecting group strategy: The tert-butyl ester protection ensures the amino group remains stable during synthesis and can be selectively deprotected when needed.

  • Performance Implications

    • Short-chain PEG (1-4 units): Higher rigidity, suitable for targets requiring precise spatial positioning.

    • Medium-chain PEG (5-9 units): Balances flexibility and spatial constraint, suitable for most PROTAC designs.

    • Long-chain PEG (10-12 units): Maximum flexibility, suitable for targets requiring extensive spatial exploration.

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