Fmoc-Protected Amino Acids: Essential Reagents for Solid-Phase Peptide Synthesis (SPPS)
NINGBO INNO PHARMCHEM CO.,LTD. is a trusted supplier of high-quality reagents essential for modern biochemical research, with a particular focus on peptide synthesis. Among our extensive catalog, Fmoc-protected amino acids are foundational components for Solid-Phase Peptide Synthesis (SPPS), a revolutionary technique that has transformed the way peptides are produced. Fmoc-(S)-3-Amino-4-(4-trifluoromethyl-phenyl)-butyric acid exemplifies the critical nature of these specialized reagents.
Solid-Phase Peptide Synthesis (SPPS) relies on the strategy of anchoring the growing peptide chain to a solid support (resin). This allows for easy separation of the desired peptide from excess reagents and byproducts through simple washing steps. The Fmoc (9-fluorenylmethoxycarbonyl) group serves as the most widely used amine protecting group in SPPS. Its key advantage lies in its lability under mild basic conditions, typically using piperidine. This orthogonal deprotection strategy ensures that the growing peptide chain remains intact and is not cleaved from the resin during the Fmoc removal step. This compatibility with the SPPS workflow makes compounds like Fmoc-(S)-3-Amino-4-(4-trifluoromethyl-phenyl)-butyric acid indispensable.
The specific structure of Fmoc-(S)-3-Amino-4-(4-trifluoromethyl-phenyl)-butyric acid offers additional benefits within the SPPS framework. The trifluoromethyl-phenyl moiety can influence the solubility and physical properties of the resulting peptide, which can be crucial for purification and downstream applications. When researchers decide to buy such specialized amino acids, they are investing in the efficiency and success of their SPPS campaigns. The price of these high-purity reagents reflects the complex synthesis required and the crucial role they play in producing complex biomolecules for drug development and other scientific applications.
The iterative process of SPPS involves cycles of deprotection, coupling, and capping. Each amino acid is added sequentially to the N-terminus of the growing peptide chain. Having a reliable supply of Fmoc-protected amino acids, such as the specific chiral variants we offer, is vital for ensuring high coupling efficiencies and minimizing side reactions. This meticulous process allows for the synthesis of peptides with lengths and complexities previously unimaginable.
NINGBO INNO PHARMCHEM CO.,LTD. is committed to providing the chemical building blocks that enable breakthroughs in peptide science. Our range of Fmoc-protected amino acids, including those with unique functional groups like the trifluoromethyl substitution in Fmoc-(S)-3-Amino-4-(4-trifluoromethyl-phenyl)-butyric acid, supports researchers in achieving reliable and efficient peptide synthesis for drug discovery and other advanced applications.
Perspectives & Insights
Logic Thinker AI
“is a trusted supplier of high-quality reagents essential for modern biochemical research, with a particular focus on peptide synthesis.”
Molecule Spark 2025
“Among our extensive catalog, Fmoc-protected amino acids are foundational components for Solid-Phase Peptide Synthesis (SPPS), a revolutionary technique that has transformed the way peptides are produced.”
Alpha Pioneer 01
“Fmoc-(S)-3-Amino-4-(4-trifluoromethyl-phenyl)-butyric acid exemplifies the critical nature of these specialized reagents.”