2-Boc-amino-1,3-bis-propanoic acid
This Boc-protected amino acid derivative features an acid-labile tert-butoxycarbonyl (Boc) group on the amine and two terminal carboxyl groups. Its protected design supports orthogonal, stepwise synthesis, making it an especially valuable building block for peptide chemistry, drug discovery, and bioconjugation.
Key Features and Benefits:
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Boc-Protected Amine: Acid-labile protection for controlled deprotection and orthogonal synthesis.
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Dual Carboxyl Groups: Enable stable amide bond formation with amines.
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High Purity: Ensures reproducibility in peptide and synthetic chemistry workflows.
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Versatile Use: Supports peptide assembly, conjugation strategies, and scaffold design.
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Controlled Reactivity: Ideal for stepwise conjugation or protected intermediate use.
Applications:
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Peptide Synthesis: Serves as a protected intermediate for solid-phase or solution-phase methods.
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Bioconjugation: Enables controlled amine deprotection for stepwise functionalization.
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Drug Discovery: Useful in designing peptide-based therapeutics and linkers.
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Synthetic Chemistry: Provides orthogonal protection for multifunctional scaffold construction.
Storage and Handling:
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Storage: Store at –20 °C in a sealed, moisture-free, light-protected container.
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Handling: Use anhydrous solvents (e.g., DMF, DMSO) to maintain Boc and carboxyl stability.
This product provides a Boc-protected amine and dual carboxyl groups in a compact framework, making it an especially reliable tool for peptide synthesis, orthogonal chemistry, and advanced bioconjugation workflows.
AxisPharm offers 5000+ PEG Linkers with high purity. Different kinds of PEG Reagents may be available by custom synthesis.
