Fmoc-N-Me-D-Leu-OH
- CAS No.103478-63-3
- GradeIndustrial / Pharmaceutical
- Availability● In Stock
Premium grade Fmoc-N-Me-D-Leu-OH designed for efficient peptide synthesis workflows and advanced pharmaceutical research applications.
Request a Quote & Full COAProduct Technical Details
Product Overview
Fmoc-N-Me-D-Leu-OH is a highly specialized N-protected amino acid derivative engineered for precision peptide synthesis. As a critical building block in the pharmaceutical and biotechnology sectors, this compound features a fluorenylmethyloxycarbonyl (Fmoc) protecting group on the nitrogen atom, combined with an N-methylated D-leucine backbone. This unique structural configuration offers distinct advantages in the construction of complex peptide sequences, particularly where steric hindrance and metabolic stability are paramount concerns.
Our manufacturing process ensures exceptional consistency and reliability, making this product an ideal choice for researchers and industrial manufacturers focused on developing novel peptide therapeutics. The D-configuration provides specific stereochemical properties required for mimicking natural biological structures or enhancing resistance against enzymatic degradation.
Technical Specifications
We adhere to rigorous quality control standards to guarantee the performance of every batch. The following table outlines the key physical and chemical parameters verified during our internal quality assurance protocols.
| Parameter | Specification |
|---|---|
| CAS Number | 103478-63-3 |
| Molecular Formula | C22H25NO4 |
| Molecular Weight | 367.44 g/mol |
| Appearance | White Powder |
| Purity | ≥98.0% |
| Density | 1.194 g/cm3 |
| Boiling Point | 537.3°C at 760 mmHg |
| Flash Point | 278.7±24.3 °C |
Industrial Applications
This protected amino acid is primarily utilized in solid-phase peptide synthesis (SPPS) and solution-phase synthesis. The N-methylation of the leucine residue is a strategic modification often employed to improve the pharmacokinetic profiles of peptide drugs. By incorporating this building block, chemists can enhance membrane permeability and reduce susceptibility to proteolytic cleavage.
- Development of cyclic peptides and peptidomimetics.
- Synthesis of constrained peptide analogs for drug discovery.
- Production of active pharmaceutical ingredients (APIs) requiring specific stereochemistry.
- Research into protein-protein interaction inhibitors.
Quality Assurance and Packaging
Every shipment is accompanied by a comprehensive Certificate of Analysis (COA) detailing batch-specific test results. We understand the importance of material integrity in sensitive synthesis reactions. Therefore, our packaging solutions are designed to maintain stability during transit and storage.
Standard packaging includes 25 kg drums, though we offer flexible customization to meet specific project requirements. Our logistics network ensures timely global delivery while maintaining the cold chain conditions necessary for preserving product quality.
Storage and Handling
To maintain optimal stability, this compound should be stored in a cool, dry environment at temperatures between 2-8°C. Containers must remain tightly closed to prevent moisture absorption, which could compromise the integrity of the Fmoc protecting group. Always handle with appropriate personal protective equipment in a well-ventilated laboratory setting.
