Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One

    • Product Name 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One
    • Alias 8-Chloro-11H-benzo[b][1,4]benzazepin-11-one
    • Einecs 629-235-6
    • 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

    780760

    Iupac Name 8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one
    Molecular Formula C13H10ClNO
    Molecular Weight 231.68 g/mol
    Cas Number 2558-30-7
    Appearance White to off-white solid
    Melting Point 153-155°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1CC2=C(C=CC(=C2)Cl)C(=O)C3=CC=CC=N13
    Pubchem Cid 5311604
    Inchi InChI=1S/C13H10ClNO/c14-10-6-5-8-3-1-2-4-11(16)13(8)12(10)7-9-15-9/h5-7,9H,1-4H2
    Storage Temperature Store at room temperature, away from light and moisture
    Hazard Statements May cause skin and eye irritation

    As an accredited 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 10g amber glass bottle with a tamper-evident cap, labeled with chemical name, formula, hazard symbols, and batch number.
    Shipping 8-Chloro-5,6-Dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one is shipped in secure, leak-proof containers compliant with chemical safety regulations. Packaging ensures protection from moisture, light, and physical damage. All shipments include necessary safety documentation and labeling, with transportation arranged according to local and international hazardous material guidelines to ensure safe handling and delivery.
    Storage Store **8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one** in a tightly closed container, in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling and access only to trained personnel. Always follow local, state, and federal regulations for chemical storage and handling.
    Application of 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One

    Applications of 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One in Industrial Manufacturing

    As a specialized manufacturer of 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One, we supply this intermediate for synthesis processes integral to the development of advanced pharmaceutical agents and agrochemical actives. Our industrial partnerships leverage the molecule’s chemical structure for high-value downstream transformations under strictly controlled, compliant environments. Explore the principal application scenarios where downstream producers validate and scale its integration.

    1. Pharmaceutical API Intermediate—Second-Generation Antipsychotics

    Pharmaceutical manufacturers rely on this compound as a key construction block in the controlled synthesis of second-generation antipsychotic active pharmaceutical ingredients, forming part of multi-stage processes for benzazepine derivatives. Downstream R&D and production teams require high purity and consistent composition for QC and regulatory registration, introducing the raw material in the late-stage cyclization or as a coupling precursor for finalizing the active molecule’s core structure.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211: cGMP for Finished Pharmaceuticals
    • Ph. Eur., USP, JP Monographs (as applicable for the final API registration)
    • European REACH for supply chain transparency

    Typical usage ratio

    • Typically 0.8–1.15 mol equivalent relative to the downstream coupling or cyclization reagent; exact loading calibrates to batch scale and impurity limits defined by the product specification file

    Downstream process integration

    • Charged after upstream condensation, often in a dry-stage reaction vessel adjoining hydrogenation steps, prior to the final purification and crystallization phases for API manufacturing

    Final product types

    • Olanzapine and structurally connected antipsychotic APIs
    • Bulk formulated oral tablets and injectables
    • Generic finished pharmaceutical forms registered in the EU, US, and Asia-Pacific
    • Stability-tested reference samples for regulatory submissions

    2. Fine Chemicals—Agrochemical Synthesis of Fungicide Scaffolds

    Agrochemical formulators employ this raw material as a scaffold precursor in the construction of cyclohepta-fused heterocyclic bases, utilized within multi-step synthesis for modern fungicidal agents. It integrates after specific halogenation or aromatic modification stages; traceability and impurity control enable compliance with environmental and worker safety restrictions in bulk synthesis environments.

    Industry compliance standards

    • ISO 9001:2015 for process and supply chain QA
    • EU Regulation (EC) No 1107/2009 on plant protection product safety
    • OECD Good Laboratory Practice (GLP) for regulated environmental chemistry
    • REACH substance registration files including toxicology profiles

    Typical usage ratio

    • Generally 5–10% w/w in target batch, referenced to downstream halogenated intermediate; ratio modulates with potency targets and step yield improvement protocols

    Downstream process integration

    • Fed in closed reaction systems following pre-functionalization of core benzene or pyridine ring, prior to inclusion in cross-coupling or oxidation reaction trains

    Final product types

    • Registered fungicide actives for broadleaf and cereal crop protection
    • Water-dispersible granules and suspension concentrate formulations
    • Packaged agrochemical technical concentrates (TCs)
    • GLP-certified environmental residue standards

    3. Pharmaceutical R&D—Process Development for Novel CNS Drug Candidates

    Drug discovery and process chemistry groups integrate this compound into exploratory synthesis programs when creating CNS agent analogues. Its unique ring system supports molecular diversification through custom substitution or regioselective modification, with analytical and pilot-scale teams monitoring input ratios tied to structure-activity relationship (SAR) studies. Materials enter prototype routes involving continuous flow or microwave-assisted synthesis for time- and yield-optimization.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for early-stage compound screening
    • EU Directive 2001/83/EC (as amended) for R&D-stage intermediates
    • Internal R&D quality systems for traceable reference material production
    • Company-specific impurity profiling and stability documentation

    Typical usage ratio

    • Ranges from 0.2 to 0.5 molar equivalents in base library synthesis libraries; ratio varies with intended analog structure, solubility testing, and scale-up batch targets

    Downstream process integration

    • Dosed at stepwise introduction points for scaffold creation or late-stage derivatization, supporting rapid iteration protocols in automated or semi-automated synthetic apparatus

    Final product types

    • Lead CNS compound analogues for IND-enabling studies
    • Stability and impurity test samples
    • Small-scale reference standards and analytical controls
    • Patent support substances for structure-activity investigation

    4. Custom Synthesis—Reference Standard Material Production

    Certified reference material providers utilize this intermediate in the preparation of pharmaceutical and agrochemical reference standards for analytical method development, impurity profiling, and batch validation. Custom synthesis operators require material with full traceability and certification under validated processing, using it for targeted side product generation or as the building block for isotopically labeled analogues under close process control.

    Industry compliance standards

    • ISO/IEC 17025:2017 for pharmaceutical and chemical testing laboratories
    • ISO 17034:2016 for production of reference materials
    • USP General Chapter <823> for pharmaceutical standard manufacturing
    • Pharmacopeial traceability and batch-specific CoAs

    Typical usage ratio

    • Most frequently employed at exact stoichiometric rates, typically 1.00 mol equivalent, determined by the reference standard's required identity and target impurity generation

    Downstream process integration

    • Charged into analytical-scale reaction setups, typically post-isolation and purification phases, with handling under inert conditions to prevent cross-contamination and ensure sample integrity

    Final product types

    • Pharmaceutical and agrochemical certified reference substances (CRS)
    • Secondary standards for method validation in QC labs
    • Isotopically labeled internal standards for MS and NMR
    • Qualitative and quantitative impurity reference mixtures
    Free Quote

    Competitive 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One: From Lab to Industry

    Deep Roots in Chemical Synthesis

    Over the years, we have seen a clear shift in the way pharmaceutical chemists and specialty chemical users evaluate their intermediate needs. The demands pour in for compounds with well-defined properties, robust performance profiles, and dependable supply. 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One, known in our production lines by its internal model, meets this challenge head-on thanks to a synthesis route we’ve perfected through persistent optimization.

    Unlike many intermediates that crowd the catalogs, this compound stands out because we oversee each stage of its lifecycle—planning, raw material sourcing, reaction monitoring, analytical checks, and batch-to-batch reproducibility. Our roots as a direct manufacturer let us bring an uncommon level of detail to every drum and kilogram we produce. Every scale-up tells a story; it teaches efficiency, and, sometimes, humility when a pathway refuses to cooperate. We have sharpened our process chemistry to achieve reliable purity levels and robust crystallinity, ensuring the final product fares well under analytical scrutiny.

    The Compound in Use

    Our product shines as a pharmaceutical intermediate and research tool. Many of our customers use it in the synthesis of central nervous system (CNS) active drug candidates, as its fused-ring scaffold features prominently in drug discovery programs focused on psychiatric and neurological conditions. The structure’s balance of rigidity and functionalization possibilities allows medicinal chemists to explore new analogues without entirely reinventing their synthetic wheels.

    In medicinal research settings, the stability of this compound in solution and its ability to survive a range of downstream transformations is a recurring theme in feedback we harvest from the field. Its unique ring fusion, the chloro substitution at position 8, and the reactive ketone allow for both fine-tuning of physicochemical profiles and exploitation in advanced cyclization or cross-coupling chemistry. There’s satisfaction in seeing shipments destined for discovery-stage work at research centers, as well as scale-out for early development manufacturing, since these confirm our focus on practical, real-world utility.

    Bridging Performance Gaps

    One question frequently comes up: how does this product differ from alternatives lining up in catalogs or those prepared in academic labs? Performance starts with consistency. We source our starting materials with a transparent trail back to their origin and verify each batch by GC, NMR, and HPLC before release. For the 8-chloro variant, the risk of minor impurities, particularly positional isomers or over-chlorination byproducts, separates the bulk producers from the careful ones. Our lot-to-lot variability sits within tight analytical windows, so clients know what spectral signatures to expect.

    Difference also arises in scale. Small-batch academic chemistry can deliver milligrams of a clean intermediate; scaling to kilogram or ton means exposures multiply—the risk of trace metals, the challenge of removing residual solvents, and the threat of reaction byproducts all ramp up quickly. We commit significant time to continuous flow processes and controlled crystallization, which protects yield and quality. Those seeking a clean, scalable input for medicinal chemistry, pilot plant work, or even initial toxicological batches look past the lowest price and toward long-run reliability.

    Refining What Matters Most

    Yields and purities only tell part of the story. Safe handling, reliable logistics, and deep knowledge of compound stability round out the package. Our team has rewritten process safety protocols to reflect not just regulatory requirements but also the lessons only years of handling this compound can teach. With a keen eye for moisture and light sensitivity, we choose drum liners and packaging based on real shipment experiences—not just the theoretical storage conditions. Our enclosed process lines and steady temperature control ensure minimal degradation from the plant to the customer’s bench.

    We also take pride in our responsiveness. When a solvent trace sneaks into a batch or a crystal habit changes due to an upstream tweak, our chemistry team holds live calls with partners to troubleshoot, share spectra, and advise on adjustments to downstream synthetic plans. This hands-on approach grew from early experience: tweaking a protocol for a Japanese pharmaceutical partner who needed a custom particle size and an especially tight impurity profile. The direct line from chemist to chemist—bypassing middlemen—means we translate bench-top needs into production-level execution.

    Why Structure Drives Value

    The structure of 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One gives it utility that goes beyond cosmetic differences. The rigid polycyclic platform provides a backbone stable to hydrolysis but open to late-stage functionalization. The aromatic chlorine opens up pathways to Suzuki or Buchwald-Hartwig coupling, meaning chemists can diversify efficiently from a shared precursor. Across several customer projects, these features have sped up analog synthesis, eliminated unnecessary protecting group chemistry, and supported the creation of new intellectual property in crowded drug classes.

    Sometimes, a structural variant, such as a non-chlorinated analogue, ends up less reactive or offers less selectivity in further transformations. In other cases, competing intermediates lack documentation or reveal surprises in the stability of intermediate tautomers or solvates. Real-world use has shown the predictable behavior of this compound both under elevated reaction temperatures and in storage over time, features that have helped customers cut troubleshooting cycles and clarify late-stage failures.

    Ongoing Challenges and Solutions

    Quality doesn’t stand still. The expectations keep rising, even for off-the-shelf intermediates. Our daily focus sharpens around several main topics: reduction of trace impurities, tighter control of residual solvents, and response to particulate or filtration problems in large-scale synthesis. Clients tell us these small differences often separate a project-ready intermediate from one they need to rework.

    We have tackled these issues by investing in new downstream cleaning technologies and adapting in-line analytics. For 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One, the persistent challenge is the removal of small amounts of side products from early-stage ring closure and chlorination steps. Our operator teams, trained hands-on with the plant’s quirks, have shortened reaction times and automated crystallization conditions to control these impurities—always balancing yield against ease of purification. Collecting two decades of process data, we’ve tailored our QC release parameters not just for regulatory compliance, but for real performance in the customer’s lab.

    Transparency matters as well. We share analytical raw data before shipment and explain any small deviations, making it easier for customers to avoid surprises when methods transfer to their own equipment. Forward-looking improvements—such as the introduction of green solvents and higher recovery rates—only happen because each customer dialogue brings new insight. Our next generation process, now in validation, aims to cut both energy use and solvent waste for this intermediate, inspired by client requests for cleaner and more sustainable chemistry.

    Building Reliability Batch by Batch

    Within any chemical supplier relationship, the big question always circles back to reliability. For us, this has meant taking old lessons from process upsets and batch failures and putting them to work each time we charge a reactor. Trust comes from shipping thousands of kilograms on tight timelines, but equally from pausing to run an extra impurity check when a color shift signals a deviation, no matter how slight.

    Clients come from across pharmaceutical, biotech, and research sectors, with diverse requirements for regulatory documentation and batch volumes. Working as a direct manufacturer shapes our interactions; supply chain interruptions or geopolitical shifts affect our raw inputs first, and we engineer our buffer stocks and backup suppliers accordingly. No outsourcing middlemen means when an unforeseen event impacts delivery, we bring alternatives to customers as fast as possible, sometimes delivering quantities from different facilities to meet commitments.

    Trust also grows from continuity among staff. Many of our team chemists began their careers amid the earliest process development for this compound. These hands, familiar with both triumphs and setbacks, now run continuous improvement programs. Internal know-how means troubleshooting a late-stage process hiccup or a new batch scaleup doesn’t start from zero but builds off years of plant and structure memory. Such institutional knowledge differentiates our offering from new entrants who source only on paper or lack hands-on manufacturing heritage.

    The Road Ahead: Sustainability and New Markets

    Sustainability now shapes every corner of modern chemical manufacturing. Preparing 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One isn’t immune to this reality. Our sustainability drive arose not from compliance but necessity—as waste streams piled up and raw material sources became uncertain, we had to chart smarter resource paths. New solvent recycling systems, in-process analytics, and greener reagents fuel process improvements instead of padding compliance reports.

    Opportunities keep expanding as researchers in new regions push into CNS-active compound exploration or tap into the advanced synthetic potential of this scaffold. Customers in South America and Southeast Asia now partner with us, drawing on our established documentation and consistent product availability. Each market comes with regulatory barriers, different shipping climates, and customs quirks, all of which our export team handles proactively, having experienced lost shipments, paperwork catch-ups, and language barriers first-hand.

    We’ve invited local partners to audit our facility, share their application needs, and suggest improvements which, more often than not, further enhance process and product quality. Our international ventures reinforce the need for real manufacturing roots behind export promises; only then do promises translate into actual product on a chemist's bench.

    Closing Thoughts on Shared Progress

    Years at the reactor face leave a clear lesson: progress is about persistent revision, learning, and partnership. 8-Chloro-5,6-Dihydro-11H-Benzo[5,6]Cyclohepta[1,2-B]Pyridin-11-One’s story at our facility is written by the evolution of process, the challenge of scale, and the insights shared by our customers. This compound brings together the tangible results of careful synthesis and the intangible benefits of trust and track record.

    From academic researchers needing milligram standards to high-volume pharmaceutical manufacturers requiring multi-kilo lots with ironclad documentation, we listen, adjust, and improve. The difference, in practice, grows from our willingness to examine each setback, communicate with openness, and apply hands-on plant experience to real-world goals. The road is long, but each batch adds another proof point, not just of chemical skill, but of shared ambition and resilience in building valuable materials for tomorrow’s medicines.