(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)succinic acid
EINECS 237-294-7
tert-butyloxycarbonyl-L-aspartic acid
BOC-ASP
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-
Boc-L-aspartic acid
L-Asparagine, N-[(1,1-dimethylethoxy)carbonyl]-, 4-nitrophenyl ester
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-aspartic acid
BOC-L-ASP
N-t-butyloxycarbonyl-L-aspartic acid
BOC-ASPARTIC ACID
N-BOC-L-aspartic acid
L-Asparagine, N2-((1,1-dimethylethoxy)carbonyl)-, 4-nitrophenyl ester
N-Boc-aspartic acid
N-tert-Butoxycarbonyl-L-aspartic acid
tert-Butoxycarbonyl-L-aspartic acid

Introduction: BOC-L-Aspartic Acid is a fundamental amino acid protecting agent widely employed in peptide synthesis. Derived from aspartic acid, BOC-L-Aspartic Acid plays a crucial role in protecting amino groups during the assembly of peptide chains. Renowned for its exceptional quality and reliability, BOC-L-Aspartic Acid has become a preferred choice among chemists and researchers involved in peptide synthesis.

Product Features: High Purity: BOC-L-Aspartic Acid is meticulously synthesized to ensure the highest level of purity, surpassing industry standards. Its exceptional purity guarantees minimal impurities, ensuring superior quality results and the synthesis of high-quality peptides.

Effective Amine Protection: BOC-L-Aspartic Acid acts as an efficient shield for amino groups, preventing undesired side reactions during peptide synthesis. By selectively protecting the amino group, it enables controlled and precise incorporation of amino acids into the growing peptide chain.

Compatibility with Various Synthesis Methods: BOC-L-Aspartic Acid exhibits excellent compatibility with a wide range of peptide synthesis methods, including both solution-phase and solid-phase synthesis. Its versatility allows chemists to utilize diverse strategies in peptide assembly.

Applications: Peptide Synthesis: BOC-L-Aspartic Acid is an essential component in solid-phase peptide synthesis (SPPS), the most widely used method for efficient peptide assembly. Its role as an amino acid protecting agent enables the stepwise addition of amino acids, preserving the integrity and controlled growth of the peptide chain.

Drug Development: BOC-L-Aspartic Acid finds significant application in the pharmaceutical industry for the synthesis of peptide-based drugs and drug candidates. It enables the incorporation of aspartic acid residues into peptides, allowing for the development of therapeutics targeting specific biological pathways or receptors.

Peptide Modifications: BOC-L-Aspartic Acid is employed in peptide modification strategies, such as the introduction of functional groups or attachment of tags to peptides. These modifications can enhance peptide stability, solubility, or target specificity, expanding their applications in drug discovery, molecular biology, and bioconjugation studies.

Market Outlook: The demand for BOC-L-Aspartic Acid is experiencing steady growth within the peptide synthesis market due to its reliable performance and compatibility with various synthesis methods. Pharmaceutical companies, academic research institutions, and contract manufacturing organizations (CMOs) heavily rely on BOC-L-Aspartic Acid for their peptide synthesis projects. With the increasing interest in peptide-based drugs, medicinal chemistry, and peptide modifications, there is a growing market for high-quality amino acid protecting agents.

Conclusion: BOC-L-Aspartic Acid stands as an essential amino acid protecting agent in peptide synthesis. Its high purity, effective amine protection, and compatibility with various synthesis methods make it an indispensable tool for chemists and researchers involved in peptide-based studies. With its wide range of applications in peptide synthesis, drug development, and peptide modifications, BOC-L-Aspartic Acid continues to drive advancements in drug discovery, molecular biology, and the development of innovative therapeutic strategies.

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