Synonyms
(2S)-2-[(tert-butoxy)carbonylamino]-3-methylbutanoic acid
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-valine
(S)-2-(Boc-amino)-3-methylbutyric acid
N-t-Butoxycarbonyl-L-valine
BOC-L-Valine
BOC-VALINE-OH
BOC-VAL-OH
L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-
BOC-VALINE
MFCD00065605
N-(tert-Butoxycarbonyl)-L-valin
Boc-L-Val-OH
(S)-2-(Boc-amino)-3-methylbutyricacid
Boc-L-Valine-OH
Product Description
Introduction:
BOC-L-Valine is a vital amino acid protecting agent widely employed in peptide synthesis. Derived from
valine, BOC-L-Valine plays a crucial role in protecting amino groups during the assembly of peptide
chains. Known for its exceptional quality and reliability, BOC-L-Valine has become a preferred choice
among chemists and researchers involved in peptide synthesis.
Product Features:
High Purity: BOC-L-Valine 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-Valine 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-Valine 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-Valine 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-Valine finds significant application in the pharmaceutical industry for the
synthesis of peptide-based drugs and drug candidates. It enables the incorporation of valine residues
into peptides, allowing for the development of therapeutics targeting specific biological pathways or
receptors.
Peptide Modifications: BOC-L-Valine 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-Valine 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-Valine 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-Valine 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-Valine continues to drive
advancements in drug discovery, molecular biology, and the development of innovative therapeutic
strategies.
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