(2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoic acid

Advance your peptide synthesis and medicinal chemistry research with (2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoic acid (CAS No.: 73731-37-0, CAT No.: SRCF-013). This chiral amino acid derivative is protected at the amino group with the 9-fluorenylmethoxycarbonyl (Fmoc) moiety and features a hydroxyl group at the 3-position, making it a valuable building block for solid-phase peptide synthesis, stereospecific chemical modifications, and studies involving hydroxy-substituted amino acids.

It has a molecular formula of C₁₉H₁₉NO₅ and a molecular weight of approximately 329.36 g/mol. This compound typically appears as a white to off-white crystalline solid and is soluble in common peptide synthesis solvents such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO), and N-methyl-2-pyrrolidone (NMP), which facilitates its integration into diverse peptide synthesis protocols.

Product Highlights

Technical Features & Benefits

• Chiral Hydroxy-Amino Acid Derivative: Provides a stereospecific building block with 3-hydroxyl substitution, important for biochemical and structural studies.
• Fmoc Protection: Stable base-labile protection on the amino group, enabling stepwise solid-phase peptide synthesis with standard deprotection protocols.
• High Purity and Consistency: Manufactured under strict quality control to ensure reproducible research and synthesis outcomes.
• Excellent Solubility: Compatible with common peptide synthesis solvents for easy incorporation into automated and manual synthesis.
• Versatile Intermediate: Suitable for peptide modification, enzymatic assays, and development of hydroxy-substituted bioactive compounds.

Application Areas

• Building block for solid-phase and solution-phase peptide synthesis (SPPS).
• Studies on peptide structure and function involving hydroxyl amino acids.
• Synthesis of modified peptides, hydroxylated proteins, and bio-conjugates.
• Medicinal chemistry and drug development requiring stereospecific hydroxyl functionalities.
• Biochemical assays and enzymatic reaction studies involving hydroxy amino acids.

Safety & Handling

• Use appropriate personal protective equipment including gloves, lab coat, and safety goggles.
• Avoid inhalation, ingestion, and contact with skin or eyes.
• Store tightly sealed in a cool, dry, and well-ventilated place protected from light and moisture.
• Dispose of chemical waste in compliance with local, regional, and national regulations.

Why Choose SRIRAMCHEM Laboratories Pvt. Ltd.?

• Expert manufacturing with stringent quality control ensures high purity and reproducibility since 2013.
• Reliable supply of research-grade Fmoc-protected hydroxy-amino acid derivatives with detailed analytical documentation including COA, NMR, HPLC, and LC-MS.
• Custom synthesis and scale-up services tailored to specific research and industrial requirements.
• Responsive customer and technical support to assist throughout your research and development projects.

Request a Quote or Sample Today!
Enhance your peptide synthesis and medicinal chemistry research with SRIRAMCHEM’s premium (2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoic acid. Contact our expert team now for pricing, sample availability, or custom synthesis inquiries.