Overview
D-(-)-Threoninol is a stereospecific amino alcohol derived from threonine, featuring two chiral centers. It serves as a versatile chiral synthon in pharmaceutical and fine chemical industries. The compound's rigid structure and functional groups make it valuable for constructing complex molecules with defined stereochemistry. As a non-natural amino alcohol, it is typically produced through chemical synthesis or enzymatic resolution. Its demand has grown in recent years due to increased need for enantiomerically pure intermediates in drug development, particularly for antiviral and anticancer therapies.
Physical and Chemical Properties
D-(-)-Threoninol exhibits typical amino alcohol characteristics with both hydroxyl and amine functional groups. The crystalline solid has moderate hygroscopicity and should be protected from moisture absorption. Its melting point range indicates high purity material, while the solubility profile allows for flexible reaction conditions in both aqueous and organic media. The compound's chirality is its most critical property, with the (2S,3R) configuration enabling precise stereocontrol in synthesis. Optical rotation values ([α]D) typically range between -15° to -25° (c=1 in water), serving as an important quality control parameter. Stability studies show it remains intact under nitrogen at room temperature for extended periods.
Main Applications
In pharmaceutical manufacturing, D-(-)-Threoninol primarily functions as a building block for protease inhibitors and antiviral agents. Its structure mimics natural amino acids while providing synthetic flexibility, making it valuable for HIV and HCV drug development. The compound's chiral centers are often incorporated into drug molecules to enhance biological activity or reduce side effects. Beyond pharmaceuticals, it finds use in asymmetric catalysis as a ligand precursor and in biochemical research for modifying peptides and nucleic acids. Some agrochemical applications utilize its derivatives as chiral auxiliaries in pesticide synthesis. Recent studies also explore its potential in designing foldamers and supramolecular structures.
Safety and Storage
As an amino alcohol compound, D-(-)-Threoninol requires careful handling to prevent exposure. Standard laboratory PPE including gloves, goggles and protective clothing should be worn. The material may cause skin and eye irritation upon contact, and inhalation of dust should be avoided through proper ventilation or enclosed processing. Long-term storage recommendations include amber glass containers under nitrogen atmosphere at 2-8°C, especially for hygroscopic batches. Suppliers typically provide material safety data sheets (MSDS) detailing first aid measures and firefighting procedures. For large-scale industrial use, explosion-proof equipment may be necessary due to potential dust explosion hazards.
B2B Procurement Guide
When sourcing D-(-)-Threoninol commercially, buyers should prioritize suppliers with documented quality control processes. Key specifications to verify include chiral purity (typically ≥98%), residual solvent levels, and heavy metal content. Pharmaceutical-grade material requires additional documentation such as certificates of analysis (CoA) and GMP compliance statements. Lead times can vary from 2-8 weeks depending on order quantity and customization requirements. Bulk purchases (25kg+) often qualify for tiered pricing, though minimum order quantities may apply. For research quantities, some suppliers offer convenient small packaging (1g-100g) with purity guarantees. Always confirm shipping conditions, as some providers recommend temperature-controlled transport for optimal product integrity.
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