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3-Carbethoxy-2-Piperidone

    • Product Name 3-Carbethoxy-2-Piperidone
    • Alias Ethyl 3-oxo-1-piperidinecarboxylate
    • Einecs 252-137-7
    • 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
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    VTB
    Specifications

    HS Code

    550241

    Chemical Name 3-Carbethoxy-2-Piperidone
    Molecular Formula C8H13NO3
    Molecular Weight 171.19 g/mol
    Cas Number 13754-49-1
    Appearance White to off-white crystalline powder
    Melting Point 74-76°C
    Solubility Soluble in organic solvents like ethanol and methanol
    Purity Typically ≥98%
    Smiles CCOC(=O)C1CCNC(=O)C1
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Synonyms 3-(Ethoxycarbonyl)-2-piperidone

    As an accredited 3-Carbethoxy-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-Carbethoxy-2-Piperidone is securely sealed in a labeled amber glass bottle, featuring hazard warnings and batch information.
    Shipping 3-Carbethoxy-2-Piperidone is carefully packaged in sealed, chemical-resistant containers to prevent moisture or contamination. It ships via regulated ground or air service, per hazardous material guidelines. Handling includes labeling with appropriate safety data. Delivery is prompt and traceable, ensuring compliance with transport regulations and maintaining product integrity during transit.
    Storage **3-Carbethoxy-2-piperidone** should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, ideally at 2–8°C (refrigerator). Avoid exposure to heat or direct sunlight. Proper labeling and adherence to chemical safety protocols are recommended during handling and storage.
    Application of 3-Carbethoxy-2-Piperidone

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

    3-Carbethoxy-2-Piperidone serves as a critical intermediate in multiple specialized industrial sectors. It enables precise molecular construction during the synthesis of active compounds, specialty chemicals, and advanced materials. Below we outline specific downstream applications adopted by industry leaders, highlighting compliance, usage ratio, process integration, and target finished products.

    1. Pharmaceutical API Synthesis (Antipsychotic and Anticonvulsant Drugs)

    Pharmaceutical manufacturers use this molecule for stepwise synthesis of piperidine-containing active pharmaceutical ingredients, particularly in the production of antipsychotic and anticonvulsant drugs. It supports the formation of core heterocyclic structures that determine activity profiles. Integration into multi-step reactions enables control over enantiopurity and impurity profile, essential for compliance and commercial competitiveness.

    Industry compliance standards

    • International Conference on Harmonisation (ICH) Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) specifications for APIs
    • U.S. Food and Drug Administration (FDA) 21 CFR Part 211
    • Current Good Manufacturing Practice (cGMP)

    Typical usage ratio

    • 0.85–1.05 molar equivalents relative to the primary amine or ketone reactant in coupling steps. Ratio adjusted for desired yield and process safety margin.

    Downstream process integration

    • Introduced at the cyclization step before N-functionalization
    • Incorporated into the amidation stage in cascade syntheses
    • Direct precursor in Michael addition or hydrogenation stages
    • Subjected to resolution or purification prior to final API crystallization

    Final product types

    • Quetiapine fumarate (antipsychotic)
    • Piracetam analogues (cognitive enhancer/anticonvulsant)
    • Other piperidine-based CNS drugs
    • Custom fine chemicals for innovative drug candidates

    2. Agrochemical Intermediate Manufacturing

    Producers of crop protection agents apply this material in the synthesis of heterocyclic intermediates for selective herbicides and insecticides. Use of this lactam facilitates the assembly of bioactive scaffolds and influences product selectivity. Meeting agricultural sector standards, accurate dosing and traceability guarantee regulatory acceptance across jurisdictions.

    Industry compliance standards

    • Registration, Evaluation, Authorization and Restriction of Chemicals (REACH, EU regulation)
    • U.S. Environmental Protection Agency (EPA) guidelines for pesticide chemicals
    • ISO 9001:2015 for chemical manufacturing quality systems
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.4–0.7 mole fraction, based on total heterocyclic component input, adjusted for targeted herbicide or insecticide performance

    Downstream process integration

    • Incorporated into Knoevenagel condensation with aldehydes
    • Used for cyclization in protected environment reactors
    • Subjected to functionalization before formulation into technical concentrates
    • Intermediate purification prior to large-scale blending

    Final product types

    • Piperidinyl-urea herbicides
    • Pyridine-based insecticides
    • Pre-emergent selective weed control agents
    • Nitrogen-functionalized seed treatment chemicals

    3. Specialty Polymer Modifier Synthesis

    Producers of advanced polymers employ this compound to introduce specific structural segments in specialty resins and engineering plastics. The piperidone base enables flexible molecular design, allowing for high-performance characteristics such as thermal stability and targeted reactivity. Manufacturers implement this ingredient in controlled-feed polymerization or post-polymer modification steps.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for polymer production
    • Directive 2011/65/EU (RoHS) for plastics in electronics
    • American Society for Testing and Materials (ASTM) D256, D638 for polymer performance testing
    • REACH SVHC registration for polymer additives

    Typical usage ratio

    • 0.5–2.0 wt% relative to main monomer feed; precise value determined according to polymer property targets and migration testing

    Downstream process integration

    • Fed into the monomer mix prior to ring-opening polymerization
    • Utilized as a building block for grafting side chains
    • Involved in functionalization of thermoset or thermoplastic resin matrices
    • Blended with catalyst systems for advanced copolymer production

    Final product types

    • High-impact structural resins for automotive and aerospace
    • Functionalized engineering plastics used in electronics enclosures
    • Customized coatings with chemical resistance
    • Polymer-based specialty adhesives

    4. Fine Chemical Building Block for Chiral Intermediates

    Fine chemical manufacturers use this compound as a backbone for constructing chiral intermediates, which serve pharmaceutical, agrochemical, and material science sectors. Stereocontrol during derivatization is central to this process. Formulators rely on high-purity input for predictable chirality outcomes, integrating this raw material into asymmetric synthesis under controlled conditions.

    Industry compliance standards

    • ISO 17025 testing certification for chiral resolution
    • ICH Q11 Development and Manufacture of Drug Substances
    • EU EudraLex, Volume 4: GMP Guidelines for intermediates
    • GHS chemical hazard communication standards

    Typical usage ratio

    • Stoichiometric 1:1 ratio in chiral catalyst-driven reactions; variance depends on enantiomeric yield targets and resin loading levels

    Downstream process integration

    • Serves as the starting lactam in enantioselective hydrogenation
    • Used in reductive amination processes for generating optically active centers
    • Integrated into multi-step cascade reactions for fine chemical assembly
    • Feeds directly into preparative chromatography or crystallization units for chiral separation

    Final product types

    • Chiral auxiliaries for pharmaceutical development
    • Key intermediates for bioactive alkaloids
    • Enantiomerically pure reagents for organic synthesis
    • Specialty intermediates for asymmetric organocatalysis
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    Certification & Compliance
    More Introduction

    3-Carbethoxy-2-Piperidone: A Maker’s Perspective on a Versatile Building Block

    Experience Forged in the Lab: Our Approach to 3-Carbethoxy-2-Piperidone

    Working in chemical synthesis brings a hands-on understanding of individual compounds that goes beyond catalogs or distribution lists. In the case of 3-Carbethoxy-2-Piperidone, our team has spent years refining its production, focusing on purity, reproducibility, and adaptability for end users in pharmaceutical and fine chemical manufacturing. Each batch gets our direct attention, not only because this molecule serves as a foundation for many complex syntheses, but because our own success is tied closely to the reliability we deliver to our partners.

    3-Carbethoxy-2-Piperidone often becomes a keystone in the creation of advanced piperidine derivatives. Its lactam structure and functionalized ester side group encourage chemists to explore a wide range of downstream reactions, such as alkylation, reduction, or amination. In our production line, we prioritize robust purification steps, because side products and trace impurities create challenges further downstream. Our in-house analytics, built up over decades of experience, reinforce this focus; we monitor for both common and rare contaminants with every lot, drawing on the cumulative feedback from years of direct customer dialogue about structure-specific pain points in actual synthetic pathways.

    Practical Attributes: What We’ve Learned Producing 3-Carbethoxy-2-Piperidone at Scale

    Scaling up from gram to kilogram production taught us the critical differences that show up once a process leaves the confines of a glass flask. Thermal stability, crystallization behavior, and handling characteristics shift in subtle ways. Through repeated observations, we noticed that maintaining strict thermal regimes limits unwanted ring-opening side reactions, which in turn keeps lot-to-lot properties consistent. Filtering and drying methods make a difference too; over-drying can encourage degradation, while small variations in filter grade can influence final product color and residue content. These lessons underpin the batch consistency that end-users value, since downstream syntheses in the pharmaceutical sector leave little room for surprises.

    Every laboratory and plant we’ve collaborated with brings distinct approaches to 3-Carbethoxy-2-Piperidone. The ester group, for example, makes selective modifications possible that would be difficult with a simple 2-piperidone. Research teams use this functionality to prepare N-alkyl, N-acyl, and reduced piperidine products, each needed for various active pharmaceutical ingredients. Feedback from development chemists highlighted the importance of a clear melting point and minimal residual moisture. To meet these standards, our process constantly evolves: we moved to closed-system crystallization and solvent recovery cycles to manage these finer points, increasing both yield and shelf stability.

    Differences from Related Piperidones and Esters

    Comparing 3-Carbethoxy-2-Piperidone with unfunctionalized 2-piperidone or other N-substituted analogs brings out several important distinctions. The carbethoxy group at the 3-position adds a layer of reactivity for synthetic chemists, allowing access to more complex products with fewer protection and deprotection steps. For instance, chemoselective reactions at the ester site offer access to C3-modified derivatives without affecting the lactam core, saving labs both time and resources.

    In direct contrast, many alternative piperidone derivatives lack this dual-function handle, necessitating longer and less efficient synthetic routes. Our clients in pharmaceutical process development specifically called out the time savings and improved yields enabled by this structure. For scale-up, this translates to fewer process steps, reduced solvent use, and smoother regulatory filings, as fewer intermediates require characterization. While some users initially gravitated towards other N-carbamoyl or simple alkyl piperidones, their feedback steered us to hone our process for the carbethoxy version, as the ester moiety opens pathways in medicinal chemistry that other compounds simply cannot match.

    Specifications: Going Beyond the Commonplace

    Daily operations in chemical manufacturing only succeed if specifications account for what actually matters at the bench or in the reactor. We don’t just post numbers; we tailor parameters based on collaborative exchange. Analytical data inform every decision. By pinpointing key physical characteristics—melting point stability, spectral purity via NMR and HPLC, and low water content—our process aligns closely with how researchers actually use 3-Carbethoxy-2-Piperidone.

    As a manufacturer, we’ve seen projects fail due to unpredictable polymorphs, too high an ash content, or invisible, low-level impurities that later poison a catalyst. Avoiding false economies pays dividends in the long run, so our specifications include not only minimum purity benchmarks but also tight controls on extractables and solution stability. Lab teams rely on these details to plan multistep programs, and our ongoing engagement with their process feedback helps us adjust protocols for changing needs.

    Usage: In the Trenches of Synthesis

    We talk to chemists every week whose work depends on clear, reproducible reaction outcomes. 3-Carbethoxy-2-Piperidone’s blend of ring stability and modifiable ester group attracts attention for synthesis of specialty pharmaceuticals, especially those built around the piperidine skeleton. Medicinal and process chemists find that this molecule enables rapid access to libraries of candidate compounds during drug discovery, and its manageable reactivity makes it a regular feature in scale-up batches destined for pilot plants and clinical supply.

    Through consistent use, we’ve watched as teams employ this compound for reductions to give 3-(carbethoxy)piperidine, for homologations, or for amide coupling reactions to yield more elaborate target molecules. The mature performance of this intermediate contributes crucially to companies developing new APIs, especially where regulatory compliance demands thorough characterization and traceability of every synthetic step.

    Adapting to Customer Realities: Tailoring Without Compromising Quality

    No process stays static; priorities shift as projects move forward, raw material logistics shift, or regulatory frameworks evolve. Our own journey with 3-Carbethoxy-2-Piperidone reflects this dynamic. Suppliers challenge us with batch-specific requirements—maybe a reduced trace amine specification for a sensitive catalyst run, or an extended particle-size distribution for an extrusion process. Many customizations arise through direct dialogue, followed by joint troubleshooting and trials on our pilot lines, rather than through one-size-fits-all product portfolios.

    Our quality system—built from internal audits and direct audits by partners—tracks each adjustment and the lessons learned from each deviation. Some routes require additional solid-phase purification, while others perform better with residue matched to a given solvent system. These incremental changes depend on trust developed over years of working shoulder to shoulder with the end users. Our production notes might seem over-detailed to outsiders, but any chemist, on examining the results, can appreciate the origins of a specification not found in generic product sheets.

    Meeting the Regulatory Burden: Knowledge and Documentation

    Modern pharmaceutical supply chains bring record-keeping and compliance requirements that shape every production decision. We’ve shepherded 3-Carbethoxy-2-Piperidone through audits and filing support for partners pursuing ANDA, DMF, or investigational new drug routes. This experience guides our data management and batch documentation practices. Each critical process parameter, impurity profile, and raw material source carries a paper trail to reassure both end users and regulators.

    Documentation isn’t only about box checking. Regulatory reviewers sometimes ask for data on carryover of solvents, residual elements, and process-related impurities. Years spent answering these queries drive continual process improvement; every data request we meet adds to the reference pool we draw on for the next challenge. We watch legislative changes in major markets, test for updates in analytical standards, and adjust our requalification intervals to accommodate the changing expectations. End users feel the benefits, as new projects can launch without months of new qualification, thanks to established records and real transparency about materials at source.

    Solving Technical Challenges: Pitfalls and Progress

    Working at scale with 3-Carbethoxy-2-Piperidone uncovers real-world challenges that don’t show up in textbooks. Temperature excursions during transport can affect solid form, or excess moisture uptake may lead to caking and variable reactivity. Some users arrived with concerns about polymorphic stability, especially when storing for extended periods. We adjusted packaging protocols, moved to sealed, low-permeability liners, and fine-tuned drying cycles based on practical evidence collected from fielded samples.

    Active troubleshooting runs through our operation. One project encountered catalyst poisoning during a selective reduction. After a root-cause analysis, carried out between our site and the user’s process chemists, it turned out that micro-level trace iron had slipped through from a batch of processing aids. We fixed the issue by switching suppliers and adding extra post-reaction chelation. Line operators now receive extra training, as the lessons learned on each project compound, influencing future workflow designs and ongoing audits.

    Working with innovators in specialty chemicals adds wrinkles. Each end use has quirks—like the demand for extremely tight particle size in continuous manufacturing lines, or solvent-specific performance for high-throughput flow reactors. We’re prepared to adjust grind size, packaging format, or supplier selection for solvents, based on a firm foundation of understanding how those changes ripple through downstream processes. This ‘from the shop floor up’ approach replaces guesswork with practical solutions every step of the way.

    Collaboration Drives Innovation

    Collaboration isn’t a buzzword when your entire operation depends on trusted relationships. The teams buying our 3-Carbethoxy-2-Piperidone return with honest feedback, frequently bringing ideas that improve things for everyone down the line. Process improvement often starts with practical concerns—an odd smell, a color difference, a foaming reaction that didn’t match expectations. We document these reports, return to the lab, and track down root causes, adjusting process steps, and updating work instructions. Over time, this cycle builds an evolving playbook that adapts fluidly to real industrial needs.

    Working closely with partners we’ve been able to extend our offering, introducing additional analytics and batch-to-batch tracking to support regulatory and scientific goals. Requests for different solvent fractions, alternative crystallization conditions, or intensified removal of byproducts often reveal new reaction mechanisms or bottlenecks. These discoveries translate into long-term product improvements, not just for one customer, but across all users relying on 3-Carbethoxy-2-Piperidone as a workhorse intermediate.

    Hands-On Integrity: What Sets Manufacturer Output Apart

    Chemists worth their salt know that the quality coming out of a manufacturer's own reactors doesn't compare to what gets passed from one warehouse to another. We invest in skilled staff, ongoing process R&D, and regular program reviews. Each operational shift carries out a full in-process control routine, with backup checks by analytical staff. That means every shipment gets a set of results straight from the production line, tracked by the same teams who put on lab coats and ran the reactors in the first place.

    Owning the supply chain puts us closer to the bench than anyone passing along a box of reagents. We can answer questions about particle size, flow properties, and moisture interaction without running up the line for permission or extracting an answer from a faceless spec sheet. That saves time for users piloting new scales or transferring processes from one site to another.

    Supporting Downstream Innovation

    Our history making 3-Carbethoxy-2-Piperidone supports both established commercial products and early-stage innovation. The compound enters the development pipelines of generics makers, specialty pharma innovators, and contract research organizations alike. Startup and established laboratories both encounter familiar questions about material behavior, solubility, and batch consistency in their day-to-day routines. Through continuous improvement and open technical lines with users, we adapt to support these goals with first-hand insight and a shared commitment to success.

    Some users configure automated synthesis equipment to test families of related compounds. In this rapidly evolving landscape, ensuring a consistent supply and clear, detailed supporting data boosts project speed and increases confidence in the results. For every new compound series made from our intermediate, the downstream innovation story depends on the upstream care we bring to production. We thrive on feedback—positive or otherwise—and see each question as a pointer towards the next layer of improvement.

    Future-Focused: Building the Next Generation of 3-Carbethoxy-2-Piperidone Applications

    Product development rarely stands still. As green chemistry gains traction, our plant teams work with process development chemists to identify lower-impact synthetic entries, alternative raw materials, and safer purification options for 3-Carbethoxy-2-Piperidone. Open discussions on solvent recovery, waste minimization, and greener energy inputs steer long-run upgrades and incremental in-process changes. The balance aims to reduce environmental load, advance safety, and retain the quality metrics that end users expect.

    Feedback from research partners moves us in new directions constantly—towards higher-purity lots, expanded analytical support, and batch arrays for rapid screening. The cumulative knowledge from these collaborations forms the backbone of our operation and the reason 3-Carbethoxy-2-Piperidone enjoys a place as a favored building block in many research programs worldwide.

    We manufacture 3-Carbethoxy-2-Piperidone, not as just another entry on a product list, but as a craft refined by every user partnership, every scale-up, every lab trial, and every batch made in the real world. Our long-term outlook stays grounded by these connections, as we continue to solve new problems and adapt to whatever the next round of discovery brings.