Synonyms
Nα-tert-Butoxycarbonyl-L-glutamine
Boc-Gln-OH
EINECS 237-296-8
Nα-Boc-L-glutamine
MFCD00065571
TBOC-L-GLUTAMINE
5-Amino-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-5-oxopentanoic acid
N-Boc-glutamine
tert-butyloxycarbonyl-L-glutamine
Na-(tert-Butoxycarbonyl)-L-glutamine
N2-(tert-Butoxycarbonyl)-L-glutamine
Glutamine, N-[(1,1-dimethylethoxy)carbonyl]-
L-GLUTAMINE-N-T-BOC
(S)-5-Amino-2-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid
N-(tert-Butoxycarbonyl)-L-glutamin
Nα-(tert-Butoxycarbonyl)-L-glutamine
BOC-L-GLN
Boc-D-Gln-OH
Product Description
Introduction:
BOC-L-Glutamine is a highly valuable amino acid protecting agent widely used in peptide synthesis. Its
exceptional ability to protect the amine group during peptide chain assembly makes it an indispensable
tool in the field of peptide synthesis. With its high purity, reliability, and versatility,
BOC-L-Glutamine is the preferred choice for scientists and chemists engaged in peptide synthesis
projects.
Product Features:
High Purity: BOC-L-Glutamine is produced with meticulous care to ensure the highest level of purity,
minimizing impurities. Its superior quality guarantees the synthesis of peptides with excellent purity
and integrity.
Effective Amine Protection: BOC-L-Glutamine serves as a dependable protecting group for the amine group,
preventing unintended reactions during peptide synthesis. By selectively shielding the amine group of
glutamine, it enables controlled incorporation of glutamine residues into the growing peptide
chain.
Versatility and Compatibility: BOC-L-Glutamine demonstrates excellent compatibility with various peptide
synthesis techniques, including solid-phase synthesis and solution-phase synthesis. Its versatility
empowers chemists to employ different strategies for efficient peptide assembly.
Applications:
Peptide Synthesis: BOC-L-Glutamine plays a critical role in solid-phase peptide synthesis (SPPS), the
principal method for peptide construction. By safeguarding the amine group of glutamine, it ensures
precise integration of glutamine residues into the peptide sequence, facilitating the synthesis of
custom-designed peptides.
Peptide Modification: BOC-L-Glutamine is widely employed in peptide modification techniques, such as
N-terminal labeling or side chain functionalization. Its ability to protect the amine group allows
chemists to introduce desired modifications at specific sites within the peptide sequence, expanding the
possibilities for peptide customization.
Drug Development: BOC-L-Glutamine is essential for the synthesis of peptide-based drugs and drug
candidates. It enables the incorporation of glutamine residues into peptides, contributing to the
development of therapeutics targeting specific biological pathways or receptors.
Market Outlook:
The demand for BOC-L-Glutamine is steadily growing within the peptide synthesis market due to its
reliability and compatibility with various synthesis methods. Pharmaceutical companies, academic
research institutions, and contract manufacturing organizations (CMOs) rely on BOC-L-Glutamine for
peptide synthesis projects aimed at drug discovery, therapeutic development, and biochemical research.
With the increasing interest in peptide-based drugs and modified peptides, the market for high-quality
amino acid protecting agents like BOC-L-Glutamine is expanding.
Conclusion:
BOC-L-Glutamine is a versatile and reliable amino acid protecting agent that plays a crucial role in
peptide synthesis. Its high purity, effective amine protection, and compatibility with different
synthesis methods make it an indispensable tool for chemists and researchers in the field. The
applications of BOC-L-Glutamine in peptide synthesis, peptide modification, and drug development
contribute to advancements in therapeutics, peptide-based drugs, and biochemical research.
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