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HS Code |
469453 |
| Iupac Name | (2A,6A,8A,9Ab)-Hexahydro-8-hydroxy-2,6-methano-2H-quinolizin-3(4H)-one |
| Molecular Formula | C11H15NO2 |
| Molecular Weight | 193.24 g/mol |
| Cas Number | 39847-53-9 |
| Appearance | White to off-white solid |
| Solubility | Soluble in organic solvents such as ethanol and DMSO |
| Functional Groups | Ketone, alcohol |
| Chirality | Chiral centers at positions 2A, 6A, 8A, 9Ab |
| Chemical Class | Quinolizidine derivative |
| Structure Type | Bicyclic |
| Canonical Smiles | C1C2CC3CC1CC(C2N3)O |
| Inchi | InChI=1S/C11H15NO2/c13-10-6-8-3-1-2-7(5-8)11(10)12-4-9(10)12/h7-9,11,13H,1-6H2 |
As an accredited (2A,6A,8A,9Ab)-Hexahydro-8-Hydroxy-2,6-Methano-2H-Quinolizin-3(4H)-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure screw cap containing 5 grams, labeled with chemical name, hazard warnings, and handling/storage instructions. |
| Shipping | The chemical `(2A,6A,8A,9Ab)-Hexahydro-8-Hydroxy-2,6-Methano-2H-Quinolizin-3(4H)-One` is shipped in secure, airtight containers to prevent moisture and contamination. Handling complies with standard laboratory safety protocols, ensuring transport under temperature-controlled conditions as required. All packages are clearly labeled according to regulatory guidelines for safe chemical shipment. |
| Storage | Store (2A,6A,8A,9Ab)-Hexahydro-8-hydroxy-2,6-methano-2H-quinolizin-3(4H)-one in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Keep container tightly closed and protected from light and moisture. Store at room temperature or as indicated in the safety data sheet, and ensure proper chemical labeling. Use appropriate personal protective equipment when handling. |
Applications of (2A,6A,8A,9Ab)-Hexahydro-8-Hydroxy-2,6-Methano-2H-Quinolizin-3(4H)-One in Industrial ManufacturingAs a direct manufacturer, we deliver (2A,6A,8A,9Ab)-Hexahydro-8-Hydroxy-2,6-Methano-2H-Quinolizin-3(4H)-One as a specialty intermediate for complex synthesis routes across fine chemicals, pharmaceuticals, and advanced material sectors. Below are key industrial application fields with specific technical and compliance perspectives for each scenario. 1. Pharmaceutical Active Intermediate Synthesis (Opiate Alkaloid Derivatives)Global pharmaceutical companies deploy this compound as a critical intermediate during total synthesis of semi-synthetic opiate alkaloid medicines, particularly in constructing morphinan and oripavine analogues. Its unique bridged bicyclic structure supports the synthesis of advanced molecules with strict chirality control, improving downstream reaction yields, especially in large-scale production for analgesics. Process engineers align the integration with stringent API production protocols to maintain high purity and reproducibility, considering batch records, traceability, and regulatory documentation. Industry compliance standards
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2. Specialty Fine Chemicals for CNS Compound SynthesisR&D and production teams in specialty fine chemical plants utilize this raw material for the synthesis of complex nitrogen-based scaffolds found in central nervous system (CNS) agents. It acts as a critical building block for heterocyclic backbone extension, enabling the stepwise construction of molecules for advanced neurological research. Real-world production requires strict analytical monitoring of intermediates, detailed process validation, and alignment with industry chemical safety regulations for all stages of synthesis and downstream transformations. Industry compliance standards
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3. Chiral Catalyst and Ligand ManufactureIndustrial catalyst manufacturers apply this compound as a core precursor for the synthesis of chiral ligands and catalysts suited for asymmetric transformations. Its rigid quinuclidine-like skeleton and defined chiral centers enable the creation of ligands used in metal-catalyzed enantioselective hydrogenation and cyclization processes. This supports the production of value-added fine chemicals and pharmaceutical intermediates on multi-kilo scales, where precise chiral induction and batch reproducibility are essential for both QC and downstream application performance. Industry compliance standards
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4. Advanced Polymer Additive and Modifier SynthesisProducers of specialty polymer additives use this molecule to introduce defined heterocyclic fragments into engineering polymers for improved mechanical and chemical properties. It is implemented during high-temperature condensation or copolymerization sequences in order to tailor polymer rigidity, surface energy, or biocompatibility—especially for demanding electronic, membrane, and biomedical uses. Integration requires careful process control to ensure the additive disperses fully without unwanted side reactions during scale-up. Industry compliance standards
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Competitive (2A,6A,8A,9Ab)-Hexahydro-8-Hydroxy-2,6-Methano-2H-Quinolizin-3(4H)-One prices that fit your budget—flexible terms and customized quotes for every order.
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