Unlock Peptide Synthesis: The Power of H-Orn(Tfa)-OH
Peptide synthesis is a cornerstone of modern drug discovery and biochemical research. Central to this process is the use of protected amino acids, which allow for precise control over the formation of peptide bonds. Among these crucial building blocks, N-delta-Trifluoroacetyl-ornithine (H-Orn(Tfa)-OH) stands out for its unique properties and wide applicability.
H-Orn(Tfa)-OH, also known by its CAS number 5123-49-9, is a derivative of ornithine where the delta-amino group is protected by a trifluoroacetyl (TFA) group. This protection strategy is highly valued in peptide synthesis because the TFA group offers excellent stability during the coupling steps of amino acids. It prevents unwanted side reactions at the delta-amino position, ensuring that peptide chains are built in a linear and defined manner.
The versatility of H-Orn(Tfa)-OH extends beyond mere protection. The trifluoroacetyl group can be selectively removed under specific acidic conditions, often using trifluoroacetic acid itself. This selective deprotection is critical for complex synthesis strategies, allowing chemists to reveal functional groups at precise stages of a reaction. This capability makes H-Orn(Tfa)-OH an indispensable chemical intermediate for synthesizing peptides with specific modifications or complex structures.
Researchers looking to buy N-delta-Trifluoroacetyl-ornithine often seek high purity and reliable suppliers. As a leading supplier in China, NINGBO INNO PHARMCHEM CO.,LTD. is committed to providing premium-grade H-Orn(Tfa)-OH, ensuring that your peptide synthesis projects benefit from the highest quality starting materials. Our dedication to quality supports advancements in areas like therapeutic peptide development and biochemical studies.
Incorporating H-Orn(Tfa)-OH into your research signifies a commitment to precision and efficiency in peptide synthesis. Whether you are exploring novel drug candidates or conducting fundamental biochemical research, this protected amino acid derivative will empower your scientific endeavors. For those engaged in advanced peptide synthesis, understanding the properties and applications of key building blocks like H-Orn(Tfa)-OH is paramount to success.
H-Orn(Tfa)-OH, also known by its CAS number 5123-49-9, is a derivative of ornithine where the delta-amino group is protected by a trifluoroacetyl (TFA) group. This protection strategy is highly valued in peptide synthesis because the TFA group offers excellent stability during the coupling steps of amino acids. It prevents unwanted side reactions at the delta-amino position, ensuring that peptide chains are built in a linear and defined manner.
The versatility of H-Orn(Tfa)-OH extends beyond mere protection. The trifluoroacetyl group can be selectively removed under specific acidic conditions, often using trifluoroacetic acid itself. This selective deprotection is critical for complex synthesis strategies, allowing chemists to reveal functional groups at precise stages of a reaction. This capability makes H-Orn(Tfa)-OH an indispensable chemical intermediate for synthesizing peptides with specific modifications or complex structures.
Researchers looking to buy N-delta-Trifluoroacetyl-ornithine often seek high purity and reliable suppliers. As a leading supplier in China, NINGBO INNO PHARMCHEM CO.,LTD. is committed to providing premium-grade H-Orn(Tfa)-OH, ensuring that your peptide synthesis projects benefit from the highest quality starting materials. Our dedication to quality supports advancements in areas like therapeutic peptide development and biochemical studies.
Incorporating H-Orn(Tfa)-OH into your research signifies a commitment to precision and efficiency in peptide synthesis. Whether you are exploring novel drug candidates or conducting fundamental biochemical research, this protected amino acid derivative will empower your scientific endeavors. For those engaged in advanced peptide synthesis, understanding the properties and applications of key building blocks like H-Orn(Tfa)-OH is paramount to success.
Perspectives & Insights
Nano Explorer 01
“It prevents unwanted side reactions at the delta-amino position, ensuring that peptide chains are built in a linear and defined manner.”
Data Catalyst One
“The trifluoroacetyl group can be selectively removed under specific acidic conditions, often using trifluoroacetic acid itself.”
Chem Thinker Labs
“This selective deprotection is critical for complex synthesis strategies, allowing chemists to reveal functional groups at precise stages of a reaction.”