(S,S)-2,8-Diazabicyclo[4,3,0]Nonane

Product Overview

Welcome to our comprehensive product page for (S,S)-2,8-Diazabicyclo[4,3,0]Nonane, a critical chiral intermediate widely utilized in the pharmaceutical industry. This specialized compound, identified by CAS number 151213-42-2, serves as a foundational building block in the synthesis of advanced fluoroquinolone antibiotics. Our manufacturing facility adheres to strict international quality standards to ensure every batch meets the rigorous demands of modern drug development. We understand the importance of stereochemical purity in pharmaceutical applications, which is why our production process focuses on maintaining high enantiomeric excess.

Chemical Properties

Chemically, this diazabicyclononane derivative exhibits distinct physical properties that make it suitable for complex organic synthesis routes. The compound presents as a light yellow to brown unformed solid with a molecular formula of C7H14N2. Key physical constants include a density of 0.95 g/cm3 and a boiling point of approximately 198.5°C at standard pressure. The refractive index is measured at 1.470, providing reliable identification parameters for quality control laboratories. These consistent physical characteristics ensure reproducibility in downstream chemical reactions.

Specifications

Industrial Applications

Our primary application focus for this intermediate is the production of Moxifloxacin hydrochloride. As a key precursor, the chiral integrity of this molecule directly influences the efficacy and safety profile of the final antibiotic product. Pharmaceutical manufacturers rely on our supply chain for consistent quality that supports regulatory filings. Beyond antibiotic synthesis, this building block may be utilized in research and development for novel therapeutic agents requiring similar bicyclic nitrogenous structures. We support both large-scale commercial production and custom synthesis requirements.

Quality Assurance And Storage

Quality assurance is paramount in our operations. Each batch undergoes comprehensive testing including chiral purity analysis via gas chromatography, specific optical rotation measurements, and impurity profiling. Our specifications guarantee a purity level of not less than 99.0%, with strict limits on water content and single impurities. We provide full documentation including Certificates of Analysis (COA) with every shipment. Packaging is designed to maintain stability, typically utilizing 25kg cardboard drums sealed against moisture and contamination. Our quality management system ensures traceability from raw materials to finished goods.

Storage recommendations include keeping the container tightly closed in a cool, dry, and well-ventilated area. It is essential to store this material away from incompatible substances to prevent degradation. Our logistics team ensures global delivery while maintaining cold chain or standard safety protocols as required. Partner with us for reliable supply of high-performance pharmaceutical intermediates. Contact our sales team today for detailed technical data sheets, bulk pricing information, and sample availability. We are committed to supporting your innovation in medicinal chemistry.