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3-Methoxy-2-Piperidone

    • Product Name 3-Methoxy-2-Piperidone
    • Alias 3-Methoxy-2-oxopiperidine
    • Einecs 629-051-1
    • 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

    158137

    Chemical Name 3-Methoxy-2-Piperidone
    Molecular Formula C6H11NO2
    Molecular Weight 129.16 g/mol
    Cas Number 6952-98-5
    Appearance White to off-white solid
    Melting Point 66-70 °C
    Solubility Soluble in water and organic solvents
    Purity Typically ≥98%
    Smiles COC1CCNC(=O)C1
    Inchi InChI=1S/C6H11NO2/c1-9-5-2-3-7-6(8)4-5/h5H,2-4H2,1H3,(H,7,8)

    As an accredited 3-Methoxy-2-Piperidone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 3-Methoxy-2-Piperidone packaged in a sealed, amber glass bottle with tamper-evident cap and clear labeling.
    Shipping **Shipping Description for 3-Methoxy-2-Piperidone:** 3-Methoxy-2-Piperidone is shipped in secure, chemical-resistant containers to prevent leakage and contamination. It is transported under controlled, ambient conditions, following all applicable regulations for chemical safety. Clearly labeled packaging includes hazard information and handling instructions, ensuring safe and compliant delivery to laboratories or authorized facilities.
    Storage Store 3-Methoxy-2-Piperidone in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and clearly labeled. Use appropriate chemical storage containers made of compatible material. Ensure proper secondary containment to prevent spills, and restrict access to trained personnel only.
    Application of 3-Methoxy-2-Piperidone

    Applications of 3-Methoxy-2-Piperidone in Industrial Manufacturing

    As a direct manufacturer, we supply 3-Methoxy-2-Piperidone for advanced synthesis needs across several high-value chemical industry sectors. Its defined reactivity and structural functionality allow precise adaptions in pharmaceuticals, specialty chemicals, and fine intermediates, supporting reliable output for further formulation and end-use integration.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies use 3-Methoxy-2-Piperidone as a building block in multi-step synthesis of piperidine-containing APIs and key intermediates. Typical applications occur in the construction of CNS drugs, anti-viral compounds, and new chemical entities for oncology pipelines. Chemists leverage its N-heterocycle for stereoselective reactions during core scaffold development. Custom process validation for each API maintains compliance across different jurisdictions, with in-process QC emphasizing trace impurity control and residual solvent monitoring.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • U.S. FDA 21 CFR Part 211 for finished pharmaceuticals production
    • European Pharmacopoeia (Ph. Eur.) monographs for relevant piperidine derivatives
    • Chinese Pharmacopoeia for intermediates (if exported to China)

    Typical usage ratio

    • 0.3 to 1.7 molar equivalents relative to target API backbone
    • Adjusted according to desired alkylation or acylation route and downstream purity demands

    Downstream process integration

    • Charged during initial batch reaction or as the N-heterocyclic source in cyclization steps
    • Incorporated in Grignard-based construction of functionally substituted piperidine rings
    • Introduced prior to final deprotection or side-chain extension

    Final product types

    • CNS therapeutic APIs (e.g., piperidine-based antidepressants)
    • Antiviral intermediate scaffolds
    • Experimental oncology compounds for clinical trial supply
    • Advanced pharmaceutical building blocks registered under INN program

    2. Agrochemical Intermediate Production

    Agrochemical formulators adopt 3-Methoxy-2-Piperidone for synthesizing active intermediates within insecticides, fungicides, and herbicidal agents that demand controlled nitrogen-heterocycle content for targeted bioactivity. Careful process scale-up ensures selective ring opening or substitution for high conversion rates and consistent batch-to-batch quality, helping meet seasonal field supply requirements and environmental compliance on pesticidal residues.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Technical Materials
    • ISO 9001-certified QC for active ingredient production
    • EU REACH Registration, Evaluation, Authorization, and Restriction of Chemicals
    • U.S. EPA pesticidal active ingredient registration system

    Typical usage ratio

    • 5–15% by mass in concentrated intermediate synthesis batches
    • Varying based on desired bioactivity spectrum and tolerance for secondary byproducts

    Downstream process integration

    • Dosed during stepwise nucleophilic substitution or amide coupling reactions
    • Enters at the heterocycle functionalization stage before final purification
    • Processed with phase-transfer catalysis in high-efficiency batch reactors

    Final product types

    • Nitrogenous insecticide intermediates
    • Precursors for proprietary fungicidal agents
    • Herbicide formulations based on piperidone core modifications
    • Seed treatment actives distributed for international agriculture markets

    3. Advanced Polymer Modifier Synthesis

    Specialty polymer manufacturers employ 3-Methoxy-2-Piperidone as a controlled monomer or chain extender in producing custom polyamides, epoxy hardener blends, or cross-linked polyurethane systems. Used primarily to introduce rigidity, steric hindrance, or chemical resistance, this raw material fits high-performance niche applications such as electronics encapsulation, membrane materials, and automotive under-the-hood plastics, where trace impurities and consistent functional group placement are mission critical.

    Industry compliance standards

    • ISO 14001 Environmental Management System for polymer factories
    • UL 94 flame retardancy protocols for polymer end-use
    • RoHS Directive (2011/65/EU) for electronics-related applications
    • ASTM D638 tensile property standards

    Typical usage ratio

    • 1 to 6 parts per hundred resin (phr) as reactivity modifier
    • Optimized based on target polymer architecture and end-use performance testing

    Downstream process integration

    • Added during polycondensation or prepolymer mixing
    • Enters main kettle at chain modification or as part of crosslinking step
    • Integrated with catalysts under temperature-controlled, inert atmosphere

    Final product types

    • Enhanced high-temperature-resistant polyamides
    • Epoxy-based electronic encapsulants
    • Custom-formulated polyurethane adhesives
    • Engineering plastics for electrical & automotive applications

    4. Fine Chemical Synthesis for Flavor & Fragrance Intermediates

    Producers in the flavor and fragrance sector apply 3-Methoxy-2-Piperidone as a precursor for specialty cyclic ketones and alcohols. These intermediates form essential backbones for high-impact aroma chemicals, musk fragrances, or green notes in complex formulations. Synthesis protocols emphasize total traceability and batch record maintenance per food safety programs, supporting compliance for use in food-contact or inhalation-safe products distributed globally.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • FCC (Food Chemicals Codex) for intermediates with downstream food contact
    • FEMA GRAS (Generally Recognized As Safe) program
    • ISO 9001:2015 quality management for batch traceability

    Typical usage ratio

    • 0.5–4% in multi-stage reaction streams, relative to target fragrance intermediate
    • Adjusted based on final compound purity and olfactory strength specification

    Downstream process integration

    • Incorporated during cyclization or selective reduction/oxidation reactions
    • Enters synthesis line before additional diketone or alcohol derivatization
    • Subjected to in-line GC and purity validation before downstream formulation

    Final product types

    • Complex aroma chemical intermediates (e.g., musks, ‘green note’ ketones)
    • Perfumery base molecules for blending
    • Flavoring agents used in beverage and confectionery products
    • Fragrance blends for household, personal care, and fine perfumery
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    Certification & Compliance
    More Introduction

    3-Methoxy-2-Piperidone: An In-Depth Look from the Manufacturer’s Bench

    Understanding 3-Methoxy-2-Piperidone in Daily Chemical Work

    Step into any modern pharmaceutical or specialty synthesis lab, and you notice certain molecules keep reappearing not for coincidence, but for reliability and strong downstream results. 3-Methoxy-2-piperidone is one of those foundational building blocks in our world of fine chemical manufacturing. From the moment we began refining its production process, our team witnessed high demand from research institutions and process developers aiming to push the frontiers of medicinal chemistry.

    In the real workday, choosing the right lactam makes all the difference. 3-Methoxy-2-piperidone carries a unique balance—a compact five-membered structure, a stable ether group at the third carbon, and a lactam backbone that doesn’t just wait to react but does so under both gentle and demanding conditions. The insight we’ve gained over years of producing this intermediate shines through most clearly in reaction efficiency: time and cost always matter, so minimizing purification headaches means a better product for us and for those relying on our output.

    Model Consistency and Batch Reliability

    Every batch we ship begins with a discussion about purity targets and analytical requirements among the shopfloor chemists and our quality group. Typical product coming off our line falls at 98%-plus purity, achieved through controlled crystallization from solvent blends we’ve tinkered with through hundreds of pilot and production runs. Water content, residual solvents, and stereochemical drift receive frequent in-process checks, since a stable 3-methoxy group is known to make or break functionalization downstream.

    Raw material variability is a constant challenge in chemical production. Over the years, we’ve learned that suppliers of piperidine and methoxylation agents can influence trace profile, so every incoming lot gets profiled with our own standards. The manufacturing team emphasizes clear, actionable feedback to our vendors—what’s out of line, shows up in our instrument room, sooner rather than later. This builds trust and keeps our product right for our partners, who run from gram-scale university groups to metric ton project leaders.

    Application Breadth in Pharmaceutical and Industrial Settings

    From the production side, it’s easy to see demand peaks trace back to early-stage drug discovery and generic molecule synthesis. Project teams working on central nervous system actives favor 3-Methoxy-2-piperidone for its ease in conversion to substituted piperidines, an essential motif in several leading therapeutics. The methoxy substituent speeds up certain nucleophilic additions, especially where a clean transition to tertiary amines is wanted, and saves hours against more protected piperidones or multi-step O-methylation work.

    We don’t see this material limited to pharma alone. Agrochemical developers have picked up its utility for constructing cyclic amides in herbicide candidates. The polymer world finds the rigidifying effect useful in modifying base resin structures for improved glass transition temperatures. Our own technical clients report the lactam is stable enough for aggressive catalytic conditions, often clocking higher yields without loss to side-reactions, a real value point when cost per kilo matters.

    Every application we’ve supported demands full control over byproducts like N-oxide or demethylated piperidone forms. In-house, we favoured a reflux-free workup, which replaced a legacy distillation that wasted solvent and energy. This shift improved both product profile and environmental impact, a win in every sense.

    Comparing 3-Methoxy-2-Piperidone to Its Relatives

    Plenty of labs stick with 2-piperidone, 3-hydroxy-2-piperidone, or 3-alkoxy variants. From a process chemist’s view, each has its place. For example, 2-piperidone lacks the electron-donating methoxy group and tends to stall in certain SN2 or SNAr coupling reactions. The hydroxy derivative offers reactivity but needs protection for multi-step workups, which adds cycle time and worker exposure to protective groups.

    The 3-methoxy twist shifts the balance: less prone to unwanted hydrogen bonding and easier to remove in post-reaction separations. Hydrogenation steps run cleaner, the intermediate turns more soluble, and yields trend higher—time and resource savings that only show up after years of routine production. One case from recent production involved a customer trying to build a substituted piperidine API core. They’d run into repeated bottlenecks with hydroxy and unsubstituted piperidone. Our batch of 3-methoxy-2-piperidone offered full conversion under milder conditions, cutting their cycle time. Results like this convince us to keep optimizing.

    Another striking difference appears in odor and handling. The parent 2-piperidone double-edges between unpleasant volatility and rapid hydrolysis on exposure. The methoxy group not only dials down the sharp smell but also holds the ring shut just long enough for careful manipulations during scale-up or continuous flow.

    Optimization Strategies and Safety Insights from the Shop Floor

    Piloting 3-Methoxy-2-piperidone production forced us to scrutinize every line in the synthesis. Early trials using old glass reactors ran into fouling from rapid methoxylation and variable pH control. Stainless steel brought corrosion, so our technicians developed a scheduling system—dedicated lines and timely cleaning using alcohol rinses, which minimize cross-contamination.

    On the ground, safety matters most, with lactams increasing the slip risk if mishandled. Small spills become a thing of the past with non-slip mats and regular team training. We keep every operator fluent with inhalation and dermal exposure precautions, which beats any theoretical safety protocol. Practical steps like pre-pouring secondary containers and enforced batch labeling have reduced incident rates to near zero in the past five years.

    Thermal stability studies pointed out a narrow range for safe storage. Most years, we rotate stock in temperature-controlled rooms to avoid degradation or polymer buildup, both problems which can stress reactors or trigger unplanned cleaning cycles. A reliable, stable intermediate means production runs without hold-ups, exactly what our customers and our facility want.

    Responding to Regulatory and Environmental Expectations

    The regulatory landscape demands constant adaptation, especially for intermediates that appear in controlled drug synthesis. Fresh attention from regulators drives ongoing analytical validation. Our batch records log every variable, from reagent quality to worker name—even for sub-batch sampling. This makes trace-backs possible if an issue emerges in downstream drug manufacture, which builds trust across the supply chain.

    On the environmental side, solvent reclamation stands out as our biggest improvement in the past decade. Modern waste processing turns previously discarded binary solvent systems into reusable feedstock, keeping overall emissions in check. The best improvements come from within—operator feedback on process bottlenecks routinely points out solvent drag or opportunities for water washing. This commitment works both for compliance and pure cost savings, making the entire operation more resilient in the face of changing waste handling requirements.

    Quality Control and Analytical Testing: Lessons Learned

    In our experience, even the slightest impurity quickly becomes apparent during scale-up. Each batch now passes through a battery of tests—NMR for structural confirmation, GC and LC for purity, and targeted testing for residuals based on reaction pathway. During a particularly challenging run, our technician noticed a subtle shift in retention time, picked up using a fresh column. That tiny detail flagged a supplier change we otherwise might have missed, saving a full day of troubleshooting.

    Documentation isn’t an afterthought; it’s integrated with our SOPs. Analysts record not just the numbers but the reaction history, so if product complaints arise, our team can point to the exact run, analytical data, and operator notes. Over time, this has cut down on returned product and batch inconsistencies—a benefit not only for us but for all users downstream.

    Responding to Customer Challenges and Requests

    No material leaves our facility without a clear story. Some of our best insights have resulted from dialogues with research chemists who face challenges unique to their own projects. One customer needed larger crystals for easier filtration in an ultrafast API development campaign. In response, we altered our crystallization solvent ratio, resulting in a product with improved filtration characteristics and more consistent yields.

    Another case came up with a customer needing reduced residual water for direct coupling steps. Our drying and storage adjustments, based on a customer’s feedback, allowed them to skip a lyophilization step, which improved their throughput. These iterative tweaks, driven by practical lab requests, shape both our finished product and our production know-how.

    Looking Ahead: Sustainable Production and Innovation

    Efficiency, safety, and waste minimization remain ongoing priorities. Recent experiments in continuous flow production for 3-Methoxy-2-piperidone have shown real promise. Early numbers point to reductions in solvent use, lower energy needs, and less manual intervention, with continuous analytical feedback ensuring spec remains tight. Our hope is to transition more of our volume through this process, so we can supply labs and plants with both greener and more affordable product.

    Our R&D group has also explored biocatalysis routes, targeting lower temperatures and alternative feedstocks. Challenges remain in enzyme stability and throughput, but each round of research adds experience. We believe the future of chemical manufacturing will stretch beyond incremental improvements as regulatory and environmental pressure grow—companies that can adapt and document every step in the chain will continue to lead.

    Why 3-Methoxy-2-Piperidone Remains a Key Choice in R&D and Production

    Long-term users recognize 3-methoxy-2-piperidone as a foundation for speedier synthesis and greater purity in downstream coupling steps. Each feature—electronic balance, stable ring, and clean conversion—comes as the result of years spent optimizing benchtop reactions and transferring knowledge to large-scale production. In our facility, we see the real-time benefits: shorter lead times, reduced scrap, and fewer surprises in the maintenance log.

    Synthetic chemists, process developers, and technical buyers rely on crisp, reproducible performance. The value of 3-methoxy-2-piperidone is born not from a single strength, but from the way its properties support both tactical breakthroughs in target synthesis and operational stability at scale.

    What We’re Watching in the Industry

    Every year, the need for novel intermediates rises as new therapies, materials, and fine chemicals emerge. We’ve noticed an uptick in requests for greener reagents and lower-impact processes. Staying ahead means listening closely—to frontline chemists, procurement specialists, and regulatory advisors, whose evolving requirements drive continuous product improvement.

    Plus, the pressure for traceability and batch accountability doesn’t just come from regulators—it’s echoed across customers who want absolute confidence in each shipment. Batch traceability and analytical transparency are now minimum expectations. That focus sits at the heart of the investments our facility continues to make, long after the first test batch of 3-methoxy-2-piperidone left our line.

    Final Thoughts from the Manufacturing Perspective

    There’s a real pride in sending out each shipment of 3-methoxy-2-piperidone—clear, reliable, and ready for the next idea a research or process team brings to life. Each year, tweaks and improvements in our workflow echo the problems and opportunities our customers bring. New technology, honest discussions, and a willingness to keep learning drive every improvement. For those of us who handle this molecule every day, it’s not just another jar in the storeroom—it’s a bridge between proven chemistry and the next round of innovation in synthesis.