High Purity N-delta-Trifluoroacetyl-ornithine: Synthesis, Applications, and Benefits

Discover the crucial role of N-delta-Trifluoroacetyl-ornithine in advancing peptide synthesis and organic chemistry. Learn about its unique protective properties and broad applications.

Get a Quote & Sample

Advantages Offered

Superior Protection

The trifluoroacetyl group on H-Orn(Tfa)-OH offers robust protection for the delta-amino group, enhancing the stability of the molecule during complex synthetic processes, thereby aiding in reliable peptide synthesis.

Controlled Reactivity

This derivative allows for controlled reactivity, enabling chemists to perform selective modifications and deprotections, which is crucial for crafting complex organic molecules and advancing biochemical research.

Enhanced Stability

The inherent stability of the trifluoroacetyl moiety ensures the integrity of the molecule throughout various chemical transformations, making it a dependable chemical intermediate for diverse applications.

Key Applications

Peptide Synthesis

N-delta-Trifluoroacetyl-ornithine is extensively used in solid-phase peptide synthesis to protect the ornithine side chain, enabling the incorporation of ornithine into therapeutic peptides.

Organic Chemistry

As a versatile building block, it serves as a valuable intermediate in the synthesis of complex organic molecules, pharmaceuticals, and fine chemicals, supporting organic synthesis pathways.

Biochemical Research

Researchers utilize this protected amino acid derivative in biochemical studies to investigate protein structure, enzyme mechanisms, and metabolic pathways, contributing to life sciences advancements.

Pharmaceutical Development

Its role as a key intermediate supports the development of novel drug candidates, particularly those involving modified amino acids or peptides, underpinning pharmaceutical development efforts.