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Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride

    • Product Name Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride
    • Alias H-DL-4-oxo-piperydine-3-carboxylic acid benzyl ester hydrochloride
    • Einecs 699-070-8
    • 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

    244567

    Chemical Name Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride
    Molecular Formula C15H20ClNO3
    Molecular Weight 297.78 g/mol
    Appearance White to off-white solid
    Melting Point 108-112°C
    Solubility Soluble in water and methanol
    Purity Typically ≥98%
    Cas Number 144090-65-1
    Storage Temperature 2-8°C
    Identifiers PubChem CID: 11198442
    Synonyms Ethyl 1-benzyl-4-oxo-3-piperidinecarboxylate hydrochloride
    Smiles CCOC(=O)C1CN(CC2=CC=CC=C2)CCNC1=O
    Usage Intermediate in pharmaceutical synthesis

    As an accredited Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 25g amber glass bottle, sealed with a screw cap, clearly labeled "Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride, HCl."
    Shipping Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride is shipped in tightly sealed, clearly labeled containers, protected from moisture and light. Standard shipping complies with regulatory guidelines for hazardous chemicals, typically via ground or air freight. Proper documentation, safety data sheets, and handling instructions accompany each shipment to ensure safe delivery.
    Storage Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep the container tightly closed and store at 2–8°C (refrigerated) if possible. Avoid exposure to incompatible substances, such as strong oxidizing agents. Properly label and secure the container to prevent accidental spillage or misuse.
    Application of Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride

    Applications of Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride in Industrial Manufacturing

    Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride plays a critical role as a strategic intermediate in multiple specialty chemical synthesis lines. Its molecular structure supports key transformations in pharmaceutical compound development, advanced agrochemical manufacturing, and select polymer additive processes. As a dedicated manufacturer, we align our industrial-grade synthesis with downstream application demands, ensuring consistency and batch-to-batch reliability for integrated production environments.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers integrate this compound as a primary piperidine-based intermediate when producing select central nervous system and oncology drug substances. Its carbamate and ketone functionalities serve as anchor points in multi-step coupling, protection, and deprotection protocols. Our product supports high-yielding conversions required in GMP-compliant API lines, especially where piperidine motifs govern pharmacological activity. Consistent particle size and solubility ensure smooth scale-up from pilot to commercial reaction trains.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU GMP Annex 21 for Starting Materials
    • USP-NF and Ph. Eur. compendial quality where referenced in dossiers
    • FDA 21 CFR Part 211 for Finished Pharmaceuticals (if used in US-marketed drugs)

    Typical usage ratio

    • Ranges from 0.8 to 2.5 molar equivalents relative to key amination or alkylation reactants
    • Ratio adjusted based on target API yield and reaction kinetics

    Downstream process integration

    • Intake at pre-final API synthesis step following condensation or ring-closure reactions
    • Introduced after solvent changeover and before chromatographic purification
    • Used directly in batch reactors or continuous flow systems depending on production scale

    Final product types

    • Piperidine-derived drug substances (e.g., antipsychotic or anti-inflammatory APIs)
    • Intermediate for combinatorial small-molecule libraries
    • Building block for experimental CNS-active compounds

    2. Advanced Agrochemical Building Blocks

    Crop protection chemical producers rely on this intermediate for assembling certain systemic and contact-active agrochemicals. Its reactive sites enable straightforward incorporation into piperidine and benzylated herbicide or pesticide scaffolds. By controlling impurity levels and maintaining strict batch traceability, we support formulators during scale-up and regulatory dossier preparation for active ingredient registrations.

    Industry compliance standards

    • FAO/WHO technical specifications for active ingredients
    • OECD Good Laboratory Practice (GLP) where required for registration trials
    • ISO 9001:2015 for chemical manufacturing systems
    • EU Regulation (EC) No 1107/2009 for plant protection products

    Typical usage ratio

    • Generally 1.0 to 1.4 molar equivalents in target pesticide or herbicide synthesis
    • Adjusted in R&D for selectivity and residual management

    Downstream process integration

    • Reacted in early or mid-stage coupling steps for C–N bond formation
    • Feeds directly into crystallization or technical salt formation units
    • Enters continuous or semi-batch lines for scale-up operations

    Final product types

    • Piperidinyl-based pesticide active ingredients
    • Herbicide intermediates for subsequent amide linkage
    • Additives in pre-emergent seed coating agents

    3. Fine Chemical and Specialty Intermediate Production

    Manufacturers in the specialty and fine chemical sectors use this compound to construct advanced molecular fragments for industrial catalysts and performance polymer additives. Its structure facilitates selective functional group transformations, especially in catalytic hydrogenation and nucleophilic substitution. Quality control throughout our synthesis process aligns with batch certifications demanded by specialty downstream integration.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical supply
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (for the European market)
    • Responsible Care chemical management systems

    Typical usage ratio

    • 0.5% to 3.0% by mass basis in targeted intermediate syntheses
    • Ratio determined by desired degree of functionalization or polymer chain extension

    Downstream process integration

    • Charged into batch reactors for stagewise assembly of target fragments
    • Enters post-synthesis functional group modification sequences
    • Used in catalyst-ligand complex preparation

    Final product types

    • Performance polymer precursors
    • Industrial catalyst ligands incorporating piperidine systems
    • Specialty chemical intermediates for electronic coatings

    4. Research and Development in Medicinal Chemistry

    Pharma and biotech R&D labs leverage this compound as a unique starting point for designing diverse piperidine and benzylated molecules. The clear reaction profile and reliable purity support structure–activity relationship (SAR) investigation and high-throughput screening. Researchers often integrate this material for late-stage derivatization or fragment-based lead discovery, requiring analytical-level quality and comprehensive documentation.

    Industry compliance standards

    • GLP for medicinal chemistry and preclinical research
    • ISO 17025 for analytical method validation
    • Material Safety Data compliance as per GHS

    Typical usage ratio

    • Usage varies widely, 0.2 to 1.5 mmol in individual parallel synthesis reactions
    • Determined by screening design and expected throughput

    Downstream process integration

    • Used in combinatorial synthesis platforms
    • Feeds into fragment coupling, diversity-oriented synthesis modules
    • Purified by flash chromatography or preparative HPLC in lab scale

    Final product types

    • Lead compound analogues for early-stage drug discovery
    • Piperidine-derivative SAR libraries
    • Preclinical candidates for biological evaluation
    Free Quote

    Competitive Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride 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.

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    Certification & Compliance
    More Introduction

    Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride: Direct Insights from the Manufacturer’s Perspective

    Evolution in Small Molecule Synthesis

    For those working in modern pharmaceutical research and custom synthesis, Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride represents a case study in how targeted chemistry advances with each generation of piperidine derivatives. Labs make regular requests for specialized intermediates. We develop, scale up, and deliver these compounds with a molecular structure designed to support routes toward both simple generics and advanced small molecule candidates. Looking at this molecule, we see advances in heterocycle design and pharmaceutical relevancy coming together in ways that genuinely help chemists speed up their timelines.

    Structural Features Matter in Synthesis

    Anyone with regular exposure to bench chemistry recognizes that not every building block is created equal. In Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride, the ethyl ester and benzyl substituent combine on the piperidine ring to adjust both reactivity and solubility in target reactions. The hydrochloride salt form stands out by giving better handling in both scaling and purification. From our own experience, working with the hydrochloride eliminates hydrophobic residue that can otherwise hang up filtration during workup. The piperidinone backbone includes both carbonyl and carboxylate groups, expanding options for further derivatization without stability concerns that simpler piperidines sometimes present.

    A Manufacturer’s Reality: Control at Each Step

    Making Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride goes beyond just mixing reagents. Each batch starts with strict qualification of benzyl chloride, piperidinone, and ethyl chloroformate, because trace impurities in any of these raw materials show up downstream in NMR and LC-MS. We continually improve purification, so by the time the hydrochloride step completes, customers receive crystalline material with a purity profile that holds steady from batch to batch. Experience has shown us that even a slight change in stoichiometry can drive up levels of side products, especially N-alkylation byproducts; our QC techs flag these before they ever reach packaging.

    Practical Advantages Over Similar Piperidine Building Blocks

    In the market for piperidine intermediates, there’s a flood of generic 1-substituted piperidines and their esters, but many researchers hit avoidable roadblocks with those materials. Our hydrochloride salt exhibits defined crystallinity, which allows for precise handling, especially in multi-step synthesis or solid-phase applications. We’ve worked with partners who tried to use the plain free base or methyl esters—what they saw was batch-to-batch variability, poor storage stability, and headaches in weighing during scale-up. Our hydrochloride form doesn’t deliquesce in ambient air, and unlike other salts (such as oxalate), it can be handled quickly in standard fume hoods without microbalance fluctuations.

    Reliable Batch Consistency for Demanding Applications

    We know development chemists need predictable performance. Every time we release a batch, our team checks it against reference standards using modern techniques, including HPLC and 1H NMR. This discipline comes from years of feedback: customers quickly tell us if a new batch fails to dissolve or produces hazy solutions. Years ago, we learned that a trace water content above 0.5% causes slow hydrolysis, so all drying and packaging steps happen under nitrogen. This kind of attention to the full chain, from raw materials to drying, defines our approach. We’ve seen the manufacturing side of every kind of piperidine product, and none performs under a broader set of research conditions than this hydrochloride salt.

    Supporting Critical Research and Process Advancement

    Research teams need small but vital intermediates with the right balance of chemical functionality and stability. In the last two years, we’ve worked closely with pharma R&D groups designing CNS-active scaffolds and oncology targets. Our Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride serves as the bridge: its reactivity supports both classic coupling reactions and newer transformations like metal-catalyzed amination. We’ve run side-by-side experiments to demonstrate that our batches convert reliably no matter if the user is working on milligram or multi-gram scales. Project managers tell us minimizing wasted steps means meeting their deliverables—something that just doesn’t happen with inconsistent feedstocks.

    Facilitating Regulatory and Analytical Demands

    Regulated industries throw a lot of paperwork at even a simple intermediate. As a manufacturer, we own every step of documentation, from chain of custody for each raw material to full certificate of analysis on the finished batch. For Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride, each certificate includes spot tests for residual solvents (GC-FID), detailed water content (Karl Fischer), and residual metals (ICP-OES) even though our in-house processes avoid metal-catalyzed steps. Auditors expect this, and our internal records line up with external regulatory agency checks.

    Beyond just documentation, we offer more than typical traders. Our analytical team is trained to troubleshoot with customers. In one recent example, a research group flagged a minor unidentified peak in their HPLC after running a batch of an API precursor. We ran comparative spectra and provided mass spec data tracing the peak to a trace benzyl alcohol impurity—then adapted our process to suppress this side product. That’s one of the genuine benefits of direct manufacturing: a trader or distributor rarely has actual lab infrastructure on hand to resolve real-world project problems.

    Why Model and Specifications Shape Research Outcomes

    Over years of scaling up intermediates, we’ve refined both model and manufacturing parameters. For Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride, the model we supply meets precise levels:

    Though model numbers aren’t flashy marketing, they represent real improvements in both throughput and reaction control for chemists. We’ve compared our batches side-by-side with standard Chinese-sourced intermediates. What comes back is repeatedly: less time spent on additional purification, more predictable yields, and fewer unexplained reactivity problems in downstream steps.

    Field Feedback and Collaboration Drives Improvement

    Because we work directly with leading contract research organizations, feedback flows quickly to our synthesis and QA groups. More than once, customers have asked for slight variations on the ester or N-substituent, only to discover the hydrochloride version brings superior results in both yield and purification. In this space, those who control their own manufacturing wins. After running stability testing under variable humidity and temperature, we’ve validated storage life well beyond what free base or non-hydrochloride forms can guarantee. This translates to more reliable research outcomes, fewer unexpected “lost” batches, and higher ROI for every project reliant on this critical intermediate.

    Environmental Responsibility in Modern Production

    Our industry faces rising expectations from both regulators and customers. So we’ve invested in minimizing both waste and energy use across the process. We recycle mother liquors wherever possible, use closed loops on hydrochloride formation, and reduce chlorinated solvent dependence by validating greener alternatives for key steps. All wash waters and liquid residues are treated at our in-house facilities before discharge, and trace level monitoring of benzyl compounds ensures safety for our staff and community. This approach isn’t just about compliance; it’s what a modern chemical manufacturer must do to support sustainable growth.

    Future-Proofing Through New Process Development

    Our chemistry team constantly tracks emerging applications for the piperidine core. New drug candidates, catalysis techniques, and specialty material precursors all demand high-purity intermediates able to meet both classical and digital synthesis planning algorithms. We run constant method development, checking how variations in particle morphology, crystal form, and residual solvent footprint can influence both chemistry and regulatory acceptance. We share technical bulletins outlining these improvements, and customers use our data to file faster INDs and CMC documentation with authorities.

    In this field, a manufacturer’s direct experience and willingness to invest in process improvements sets a higher standard. Each technical challenge—whether it’s trace side-products, solid-state behavior under scale, or analytical pathway bottlenecks—gets solved through hundreds of iterative improvements. We keep samples of every batch for at least two years, enabling root-cause investigations if researchers hit roadblocks months later. Our archive of technical reports, batch records, and real-world user stories is deeper than any distributor can offer.

    Application Versatility Backed by Real Chemistry

    Every week delivers new requests: milligram samples for new method development, kilogram lots for process trials, or GMP-compliant versions for clinical supply chain. We adapt packaging to prevent cross-contamination with both common and esoteric contaminants. Our logistics team collaborates with customers to align with their solvent systems, packaging safety, and even customs paperwork. Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride offers versatile reactivity, compatibility with reductive aminations, and predictable behavior in structural diversification schemes. Long-term users point to the ease of scaling: once you validate a process on a single batch, re-ordering produces the same outcome without the hassle of revalidating raw material every time.

    A Real-World Answer to Generic Commodity Weaknesses

    Too many researchers waste effort on correcting impurities, guessing at the freeze-thaw stability, or hunting for missing documentation. Working upstream, we know how each solvent, temperature, and purification stage translates into concrete, batch-tested user benefits: clean mass balance, sharp NMR signals, fast crystallization out of standard solvents. Our direct control over synthesis means a rapid pathway for custom requests—such as custom salt forms, deuterated analogs, or bespoke particle size distributions. Direct discussions with researchers have allowed us to implement solutions: shifting to one-step HCl saturation, or using tighter mesh filters to guarantee fine chemical performance in microplate applications.

    Solving Real Bottlenecks in Chemical Development

    Colleagues stuck on inconsistent performance from non-salt forms often describe downstream delays, QC headaches, and unscheduled troubleshooting. By removing these barriers up front—at the actual synthetic and isolation stage—we help customers spend more time on discovery and less on firefighting. This isn’t a theoretical improvement. Teams using our hydrochloride salt in parallel workflows return to order multiple lots after running pilot campaigns, reporting reproducible yields, easy monitoring of endpoint color changes, and consistent workups.

    Focusing on the Researcher’s Needs: Advice From Factory Floor to Fume Hood

    The quality differences researchers see aren’t accidental or theoretical. They’re hard-won lessons from chemical production lines—managing batch exotherms, troubleshooting filtration through variable cake thickness, optimizing mother liquor recycling, and confirming storage stability. That experience cannot be matched by a trader sourcing from unknown third parties, or by a distributor who merely passes on documentation.

    By keeping a direct line open from our lab to yours, we provide more than a quoted purity spec. Researchers quickly see the difference: regular crystal habit, no need for extra drying or grinding, and full traceability back to the source of each raw material. Collaborating directly reduces risk, saves time, and turns advanced chemical ideas into workable, scalable realities.

    In Summary: Why Our Manufacturing Approach Delivers Quality That Matters

    Working in real chemical manufacturing teaches the importance of every operational detail, from worker training to standardized QC at every scale. With Ethyl N-Benzyl-3-Oxo-4-Piperidine-Carboxylate Hydrochloride, we bring forward a product honed through technical feedback, process improvement, and the discipline of full traceability. This means more efficient chemistry for our customers, reduced risk in scale-up, and greater confidence for teams working toward high-value milestones. No matter if your project is just starting or scaling toward industrial production, our commitment is clear: We manufacture—and stand behind—every lot, every time.