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(2A,6A,8A,9Ab)-Hexahydro-8-Hydroxy-2,6-Methano-2H-Quinolizin-3(4H)-One

    • Product Name (2A,6A,8A,9Ab)-Hexahydro-8-Hydroxy-2,6-Methano-2H-Quinolizin-3(4H)-One
    • Alias mitragynine pseudoindoxyl
    • Einecs 629-590-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of (2A,6A,8A,9Ab)-Hexahydro-8-Hydroxy-2,6-Methano-2H-Quinolizin-3(4H)-One

    Applications of (2A,6A,8A,9Ab)-Hexahydro-8-Hydroxy-2,6-Methano-2H-Quinolizin-3(4H)-One in Industrial Manufacturing

    As 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

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • EU GMP Annex 8: Sampling of Starting and Packaging Materials
    • US FDA 21 CFR Part 211
    • Chinese Pharmacopoeia Processing for Intermediates (when applicable for export)

    Typical usage ratio

    • 5–12% molar equivalent in semi-synthetic opioid synthesis route; ratio depends on target molecule and yield optimization under pilot or commercial scale-up modes

    Downstream process integration

    • Introduced after initial alkylation phases and before critical enantioselective hydrogenation, supporting the construction of key intermediate rings required for morphinan derivatives

    Final product types

    • Hydromorphone API
    • Oxymorphone intermediates
    • Semi-synthetic opioid APIs such as buprenorphine
    • Related injectable and oral pharmaceutical formulations

    2. Specialty Fine Chemicals for CNS Compound Synthesis

    R&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

    • ISO 9001:2015 certified process controls for fine chemicals
    • REACH Regulation (EC) No 1907/2006
    • OECD Test Guidelines for Environmental and Safety Protocols
    • Comprehensive GHS labeling and documentation for transport and use

    Typical usage ratio

    • 3–7% weight/weight in batch production for CNS lead compound synthesis; adjusted based on downstream yield parameters and desired structural functionalization

    Downstream process integration

    • Fed into the primary condensation or rearrangement reactions to form fused or bridged heterocyclic intermediates; further modified via acylation or amination steps

    Final product types

    • CNS active pharmaceutical intermediates
    • Lead compounds for antipsychotic or analgesic research
    • Library screening candidates in neuropharmacological development
    • Reference standards for analytical methods

    3. Chiral Catalyst and Ligand Manufacture

    Industrial 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

    • ISO 14001:2015 Environmental Management for Catalyst Production
    • REACH pre-registration for specialty catalyst intermediates
    • Chemical Safety Assessment per CLP regulation (EC) No 1272/2008
    • Customer-required product-specific analytical method validation (HPLC, NMR)

    Typical usage ratio

    • 15–25% as precursor within ligand-forming reaction depending on the specific catalyst system and downstream metal complexation requirements

    Downstream process integration

    • Used during initial cyclization or functionalization step; followed by coordination to transition metals (e.g., Ru, Rh, Ir ligands for hydrogenation catalysts)

    Final product types

    • Chiral diphosphine ligands
    • Enantioselective hydrogenation catalysts
    • Batch and flow-type catalytic materials
    • Ready-to-use catalyst precursors for pharmaceutical and agrochemical synthesis

    4. Advanced Polymer Additive and Modifier Synthesis

    Producers 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

    • ISO 9001 and 14001 for polymer additive manufacturing process and environmental control
    • FDA 21 CFR 177.1810 (polymers for food contact, US market)
    • ROHS 2.0 (2011/65/EU) and SVHC declarations for electronics/plastics applications
    • Customer-driven QAA (Quality Assurance Agreements) for traceability

    Typical usage ratio

    • 0.2–1.5% by weight in bulk or specialty polymer modification; fine-tuned according to property enhancement targets and downstream compounding formulations

    Downstream process integration

    • Dosed into monomer or resin feed prior to polymerization or during melt blending; disperses via high-shear mixing or solution casting methods depending on polymer type

    Final product types

    • High-performance engineering plastics
    • Specialty membranes for chemical processes
    • Biocompatible polymer blends for medical devices
    • Plastic components for automotive and electronics
    Free Quote

    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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