Synonyms
Carbamic acid, (2-hydroxy-1-methylethyl)-, 1,1-dimethylethyl ester, (s)-
Carbamic acid, N-[(1S)-2-hydroxy-1-methylethyl]-, 1,1-dimethylethyl ester
tert-Butyl [(2S)-1-hydroxypropan-2-yl]carbamate
tert-butyl N-[(2S)-1-hydroxypropan-2-yl]carbamate
MFCD00043121
N-Boc-S-alaninol
2-Methyl-2-propanyl [(2S)-1-hydroxy-2-propanyl]carbamate
Boc-Ala-ol
Boc-L-alaninol
Product Description
Introduction:
BOC-L-Alaninol is a vital amino acid protecting agent widely used in peptide synthesis. As an essential
component of the peptide chemist's toolkit, BOC-L-Alaninol plays a crucial role in protecting amino
groups during the assembly of peptide chains. Known for its versatility and reliability, BOC-L-Alaninol
has become a preferred choice among chemists and researchers involved in peptide synthesis.
Product Features:
High Purity: BOC-L-Alaninol is carefully synthesized to ensure exceptional purity, surpassing industry
standards. Its high purity guarantees minimal impurities, enabling the synthesis of high-quality
peptides and reliable results.
Effective Amine Protection: BOC-L-Alaninol serves as an efficient protective group for amino groups,
preventing undesired side reactions during peptide synthesis. By selectively protecting the amino group,
it facilitates the controlled and precise incorporation of amino acids into the growing peptide
chain.
Compatibility with Various Synthesis Methods: BOC-L-Alaninol exhibits excellent compatibility with a
wide range of peptide synthesis methods, including both solution-phase and solid-phase synthesis. Its
versatility allows chemists to employ diverse strategies for efficient peptide assembly.
Applications:
Peptide Synthesis: BOC-L-Alaninol plays a fundamental role in solid-phase peptide synthesis (SPPS), the
primary method for efficient peptide assembly. As an amino acid protecting agent, it enables the
stepwise addition of amino acids, ensuring the proper growth and preservation of the peptide chain's
integrity.
Drug Development: BOC-L-Alaninol finds extensive application in the pharmaceutical industry for the
synthesis of peptide-based drugs and drug candidates. It allows for the incorporation of alanine
residues into peptides, facilitating the development of therapeutics targeting specific biological
pathways or receptors.
Peptide Modifications: BOC-L-Alaninol is employed in peptide modification strategies, such as
introducing functional groups or attaching 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-Alaninol is steadily growing 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) rely on BOC-L-Alaninol
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-Alaninol stands as a versatile amino acid protecting agent in peptide synthesis. Its high purity,
effective amine protection, and compatibility with diverse 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-Alaninol continues to drive
advancements in drug discovery, molecular biology, and the development of innovative therapeutic
strategies.
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