Scientific Name and Aliases: Boc-D-Tyr-OH, also known as N-tert-Butyloxycarbonyl-D-tyrosine, is a synthetically derived amino acid. It is a derivative of tyrosine, an essential amino acid that plays a crucial role in various biological processes.
Chemical Structure and Composition: This compound features a bulky tert-butyloxycarbonyl (Boc) group attached to the nitrogen atom of the amino group. The Boc group is a common protecting group used in peptide synthesis to prevent unwanted reactions at the amino group during the synthesis process. The D-tyrosine portion of the molecule is the D-isomer of tyrosine, which is less common in nature compared to the L-isomer but is often used in research for its unique properties.
Historical Development and Research: The use of Boc-D-Tyr-OH has been extensively studied in the field of peptide chemistry. It has been a key component in the development of various peptide-based drugs and biomaterials. Its ability to be incorporated into peptides while protecting the amino group until the desired stage of synthesis makes it an invaluable tool for researchers in the pharmaceutical and biotechnology industries.
Market Position and Demand: In the global market for amino acid derivatives, Boc-D-Tyr-OH holds a significant position. Its demand is driven by the increasing need for high-purity amino acids in the synthesis of complex peptides and proteins. The compound is widely used in academic research as well as in the development of new therapeutic agents, making it a staple in many laboratories.
Boc-D-Tyr-OH