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Ethyl (3S)-Piperidine-3-Carboxylate

    • Product Name Ethyl (3S)-Piperidine-3-Carboxylate
    • Alias ethyl (S)-piperidine-3-carboxylate
    • Einecs 615-659-3
    • 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

    989983

    Name Ethyl (3S)-Piperidine-3-Carboxylate
    Molecular Formula C8H15NO2
    Molecular Weight 157.21 g/mol
    Cas Number 118982-15-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 93-95°C at 13 mmHg
    Density 1.05 g/cm³
    Optical Rotation [α]D20 +22° (c=1, CHCl3)
    Purity Typically ≥98%
    Smiles CCOC(=O)[C@@H]1CCCNC1

    As an accredited Ethyl (3S)-Piperidine-3-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g Ethyl (3S)-Piperidine-3-Carboxylate is packaged in a sealed amber glass bottle with a tamper-evident cap and label.
    Shipping Ethyl (3S)-Piperidine-3-Carboxylate is shipped in tightly sealed containers under cool, dry conditions. The packaging complies with chemical safety regulations to prevent leaks or contamination. All shipments include proper labeling and documentation for handling and transport. Avoid exposure to heat, direct sunlight, and incompatible substances during transit.
    Storage Store Ethyl (3S)-Piperidine-3-carboxylate in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Use appropriate chemical-resistant containers and ensure proper labelling. Follow all safety procedures when handling and avoid prolonged or repeated exposure to the atmosphere.
    Application of Ethyl (3S)-Piperidine-3-Carboxylate

    Applications of Ethyl (3S)-Piperidine-3-Carboxylate in Industrial Manufacturing

    Ethyl (3S)-Piperidine-3-Carboxylate plays a specialized role across advanced synthesis routes in several sectors, particularly pharmaceuticals, agrochemicals, and fine chemicals. As a direct manufacturer, we support the integration of this intermediate into demanding workflows, ensuring traceability, regulatory alignment, and batch consistency from the outset of each customer’s process chain.

    1. Active Pharmaceutical Ingredient (API) Intermediate for CNS Drugs

    Several modern central nervous system (CNS) therapeutic APIs utilize this compound as a key chiral building block. Medicinal chemists favor it due to the (3S)-stereochemistry, which serves as a foundational motif during the formation of piperidine-containing actives for neurological and psychiatric indications. Our material integrates directly into the first or second synthesis steps of key CNS API routes, with tight chiral purity requirements throughout multi-stage GMP processing. Large-scale manufacturers require consistent batch reproducibility and full upstream-downstream traceability, combined with precise stoichiometric and enantiomeric control at each handoff point.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU GMP Parts I/II
    • United States Pharmacopeia (USP) general chapters on chemical intermediates
    • EDQM/EMA guidelines for chiral pharmaceuticals

    Typical usage ratio

    • 0.7–1.1 molecule equivalents per API batch, adjusted for the target piperidine-containing API and route yield factor

    Downstream process integration

    • Entry as a chiral intermediate after initial amine protection or activation, before final ring-forming or substitution reactions
    • Subsequent coupling, deprotection, and purification steps under controlled GMP conditions

    Final product types

    • Antipsychotic and antidepressant active substances
    • Anticonvulsant APIs
    • Intermediates for anti-Alzheimer’s agents

    2. Chiral Ligand/Building Block in Agrochemical Synthesis

    The compound is valuable to agrochemical manufacturers developing novel crop protection agents that require asymmetric synthesis pathways. Its (3S)-enantiomer configuration aids in the formation of chiral piperidine rings found in advanced insecticides and fungicides. Downstream, our clients incorporate this intermediate early in heterocycle assembly or amidation workups, ensuring the final agrochemical’s bioactivity profile and field stability adhere to modern regulatory requirements. Lot records and residual solvent control remain crucial through every batch released for agricultural use.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing operations
    • FAO/WHO specifications for active substances in crop protection
    • REACH (EC No. 1907/2006) registration and safety data reporting
    • OECD principles for Good Laboratory Practice (GLP) in residue testing

    Typical usage ratio

    • 0.8–1.3 stoichiometric equivalents depending on desired product purity and route efficiency

    Downstream process integration

    • Supplied as a protected ester directly to the intermediate coupling stage, followed by hydrolysis or further ester exchange according to the agrochemical synthesis protocol
    • Handles under dry, inert conditions to prevent racemization prior to formulation

    Final product types

    • Chiral insecticide actives (e.g., neonicotinoids, piperidine-derived agents)
    • Selective fungicides targeting resistant pathogens
    • Seed treatment formulations

    3. Precursor in Synthesis of Specialty Polymers

    Fine chemical companies utilize this molecule in the custom synthesis of high-value specialty polymers, where the (3S)-piperidine motif imparts unique mechanical or optical properties. It enters as a monomer precursor in polyamide, polyurea, or polyimide production for niche markets, including electronics encapsulants and medical device housings. Polymer engineers require detailed incoming QC, including residual stereochemical impurity profiles, to prevent defects in the polymer matrix and ensure product traceability through all blending, extrusion, and curing operations.

    Industry compliance standards

    • ISO 9001 and ISO 14001 quality and environmental standards
    • RoHS Directive for polymer additives in electronics applications
    • FDA 21 CFR 177 for indirect food contact polymers (if applicable to downstream use)
    • IEC 60695 for flammability testing (electronics-grade polymers)

    Typical usage ratio

    • 1.0–10% by weight as co-monomer or chain modifier, depending on target mechanical/chemical profile

    Downstream process integration

    • Feeds into pre-polymer stage under controlled temperature, often via solution polymerization, before step-growth or chain-growth reactions
    • May undergo in situ hydrolysis or amide formation during upscaling

    Final product types

    • Functionalized performance polymers for electronics
    • Medical-grade polyamides
    • Specialty thermoset network polymers for industrial coatings

    4. Stereoselective Intermediate for Fine Chemical Synthesis

    Producers of advanced fine chemicals introduce this compound as a chiral auxiliary or precursor in multi-step synthesis of optical active molecules, including ligands, alkaloid derivatives, and functionalized heterocycles. Its controlled stereochemistry is particularly advantageous in enantioselective transformations, increasing downstream efficiency where yield and chirality maintenance are paramount. Custom synthesis customers require complete batch records, analytical certificates, and the ability to specify variant esters or salt forms for optimum route fit.

    Industry compliance standards

    • ISO 9001:2015 for supply chain traceability
    • REACH registered for laboratory and industrial chemical production
    • GMP guidelines (where produced for pharmaceutical or biotechnical intermediate use)
    • Analytical testing per ICH Q3A (Impurities in New Drug Substances) as requested

    Typical usage ratio

    • Batch-dependent, typically 0.5–1.5 molar equivalents based on downstream reaction design

    Downstream process integration

    • Applied in initial alkylation, acylation, or heterocycle construction steps, often followed by chiral separation or salt resolution
    • Used both as a direct reactant and as a precursor for further derivatization tailored for research or pilot manufacturing

    Final product types

    • High-purity enantiomeric ligands
    • Sterically defined alkaloid analogues
    • Functionalized heterocyclic building blocks for downstream contract synthesis
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    Certification & Compliance
    More Introduction

    Ethyl (3S)-Piperidine-3-Carboxylate: A Closer Look at a Key Intermediate

    Innovation Through Precision Chemistry

    Over the last decade, we have focused on crafting molecules that make the difference in active pharmaceutical ingredient development and advanced chemical synthesis. Among our catalog, Ethyl (3S)-Piperidine-3-Carboxylate stands out not just as another piperidine derivative but as a reliable backbone for complex transformations and chiral building block needs. The value of this compound starts with its stereochemical purity — the (3S) configuration controls both reactivity and downstream biological activity, factors that drive quality and performance in finished products.

    A Trusted Route for Stereoselectivity

    Manufacturing chiral intermediates challenges every plant engineer and synthetic chemist. Each batch must reflect precise controls, not only in reaction parameters but also in how solvents, catalysts, and raw materials interact across steps. During development of our Ethyl (3S)-Piperidine-3-Carboxylate line, extensive effort went into isolating the (3S) isomer to consistently reach over 98% e.e. (enantiomeric excess). Typical processes involve asymmetric hydrogenation, followed by rigorous purification to eliminate possible racemization. Tighter separation ensures predictable outcomes in later synthesis routes, a requirement we hear often from customers scaling from R&D to commercial manufacturing.

    Real-World Applications Across Industries

    Ethyl (3S)-Piperidine-3-Carboxylate gets requests from both custom synthesis and process chemistry teams for several reasons. Its chiral nitrogenous ring finds use in the synthesis of pharmaceutical agents where piperidine motifs play a functional role. We’ve seen requests for this intermediate spike as new research focuses on small-molecule drugs targeting CNS and anti-infective pathways. Its carboxylate ethyl ester makes it more versatile for further functionalization, such as amidation or hydrolysis, building out into various pharmacophores. Fine chemical users tap into this scaffold when exploring analogs where substitution on the nitrogen delivers new SAR data or tuning solubility for better drug-like properties.

    Preparation, Handling, and Quality Control

    Alkyl piperidines with defined stereochemistry require attention through every handling step. Even minor deviations in storage conditions or solvent residues introduce impurities that derail a synthesis campaign. Over time, we refined drying and storage setups that limit hydrolysis of the ester group and avoid amine oxidation. Our batches pass full NMR, HPLC, and chiral GC testing for each lot, giving users a transparent map of what the actual deliverable contains. Year over year, centralizing analytical oversight in-house rather than relying on third-party labs sped up troubleshooting and increased yield reliability by pushing issues back to synthesis teams in real time.

    How This Intermediate Stands Apart

    A crowded market offers many piperidine derivatives, yet subtle changes in purity, isomer content, or protecting group strategies often separate success on the bench from frustrating re-dos. Ethyl (3S)-Piperidine-3-Carboxylate distinguishes itself through reproducible chiral control and minimized impurities. While racemic esters (3R/3S mixtures) sometimes look like a discount option, labs relying on them face expensive downstream resolutions, yield loss, or uncertainty in biological assays. We’ve received validation feedback from partners who traced improved potency and fewer off-pathway metabolites back to this precise intermediate, demonstrating real-world distinctions that don’t show up on single-point specifications.

    Beyond Specifications: Meeting Process Needs

    Years of feedback from leading pharmaceutical and agrochemical research teams have shaped our strategy. Those running pilot processes need more than a certificate of analysis. We invest in understanding how reaction bottlenecks emerge, such as during acylation, hydrogenolysis, or cross-coupling steps. Sometimes a subtle shift in water content or trace catalyst presence hampers success during scale-up. To address this, we implement batch-to-batch logging stretching years backward so that any technical inquiry can be matched to production records within hours. This transparency builds trust and saves critical project time.

    Bridging Discovery and Production

    Our role as a manufacturer goes beyond providing a standard catalog. Customization doesn’t just pertain to packaging size or shipment urgency; it folds into how we tune starting material purity, choice of ester groups, or even alternate synthetic approaches to suit unique project constraints. Researchers often begin with milligram-scale samples for initial pharmacological screens, later ramping to multi-kilo quantities for preclinical supply. In several collaborative projects, availability of stereopure Ethyl (3S)-Piperidine-3-Carboxylate streamlined route scouting, derisked CMC plans, and cut timelines without requiring late-stage resourcing shifts.

    Troubleshooting Synthesis and Planning for Scale

    Scaling a chiral intermediate from bench to kilo-scale reveals lab-scale shortcuts that don’t hold up in reactors. Customers often point out issues such as incomplete reactions, emulsion formation, or unpredictable crystal formation during solvent switches. By working closely with process chemists, we’ve adjusted crystallization parameters, adjusted drying agents, and optimized filtration steps for this intermediate to manage these challenges. On more than one occasion, a route evaluation has steered a team away from alternative racemic piperidines after comparative cost/yield modeling and pilot reaction troubleshooting.

    Regulatory and Documentation Support

    As regulatory expectations grow for traceability and impurity profiling, every detail behind the scenes matters. We supply not only batch information but also impurity tracking, residual solvent history, and full characterization including stereochemical confirmation, IR, and MS data. Lately, requests for advanced documentation, including stability data and route-of-synthesis flowcharts, have become more common as projects head toward regulatory submission phases. Meeting these needs directly impacts a partner’s speed to market — and limits headaches during regulatory audits or due diligence reviews.

    Fine-Tuning Supply for Flexible Research and Production Cycles

    Our plant infrastructure lets us supply Ethyl (3S)-Piperidine-3-Carboxylate at diverse scales from early-stage milligram samples up through multi-kilogram batches. Over the years we have managed just-in-time demands when a research group hit unexpected success, and our buffer stocks are planned around typical project ramps. By controlling scheduling and purification, our output remains consistent even during seasonal or market-driven spikes in demand. Plant chemists coordinate closely with our commercial and logistics teams to minimize backorders or degrade lead time, learning from past bottlenecks and integrating those lessons into production workflow.

    Differences from Other Piperidine Esters

    Not all piperidine derivatives function equally in synthetic campaigns. Ethyl (3S)-Piperidine-3-Carboxylate’s defined stereochemistry and ester group carve a unique niche. In contrast, methyl and other alkyl esters adjust both solubility and reactivity, sometimes making downstream steps either easier or harder, depending on the coupling partner or protecting group strategy. Bulk racemic variants often fetch a lower price upfront, yet incur extra cost in purification and yield loss if optical activity matters in the target API. A large proportion of collaborations pivoted to the (3S)-variant only after unexplained result variation during scale-up, teaching teams the direct value of chiral precision here.

    Reliability Rooted in Manufacturing Practice

    Mistakes during chiral intermediate production quickly snowball to downstream partners. Recognizing this, our production crews monitor not only synthetic yields but also environmental controls, reagent integrity, and in-process impurity emergence at each step. An early investment in redundant analytical instrumentation and hands-on method development delivered stronger control points for each batch. Over time, these refinements turned a once exotic intermediate into a staple reference compound for research and pharmaceutical manufacturing teams. Customers appreciate knowing they can rely on uninterrupted supply, detailed batch records, and a responsive technical support team prepared to troubleshoot at any hour.

    The Value of On-the-Ground Experience

    Every project starts with a molecule, but successful deliveries require communication and adaptation. Supporting a custom synthesis partner once meant just sending a substance; now it means walking through downstream reactivity data, helping compare alternate synthetic pathways, and sharing hard-won process learnings. In the field, chemists demand more than a simple supply chain. Whether the issue stems from raw material drift, filter clogging at scale, or a misstep in workup conditions, real support means reaching the right expert who has run these reactions in practice — not a script or a general guideline. Many of our process chemists and technical advisors have spent years working with piperidine scaffolds, bringing hands-on troubleshooting experience rather than abstract advice.

    Continuous Improvement and Feedback Loops

    No synthetic campaign sits still. Unexpected turns show up, whether through regulatory review or changes to formulary designs. Our workflow involves tight feedback between production, quality control, and customer R&D teams. This way, each delivery of Ethyl (3S)-Piperidine-3-Carboxylate doesn't just represent a static offering but fits into a dynamic improvement cycle. Sometimes this means devising new purification runs to meet a new impurity threshold, other times it means adjusting packaging formats or shipping logistics to align with a customer’s protocol. These practical modifications make the difference during time-sensitive stages of pharmaceutical development or academic research.

    Supporting Sustainable Processes and Market Stability

    Raw material disruption, energy costs, and waste management have become daily concerns in chemical production. Our plant acts with sustainability goals in view, updating solvent recycling steps, adopting alternative reducing agents with lower environmental impact, and minimizing regulated waste output from every batch. Over the years, these investments allowed us to stabilize price points and delivery consistency, even as global supply chains fluctuated. We hear from customers how reliable partners enable better project planning and support internal sustainability targets set by their own organizations.

    Expanding Reach Through Collaboration

    Many synthesis and discovery teams now work across borders and industries, bringing together pharmaceutical, agrochemical, and academic needs. The significance of a high-quality chiral intermediate like Ethyl (3S)-Piperidine-3-Carboxylate stretches beyond standard orders. We have joined cross-functional collaborations, adjusting batch parameters to aid in method validation at partner sites and sharing stability results that inform formulation choices. This kind of hands-on cooperation lets users redeploy resources toward more ambitious R&D, knowing their intermediate stands up to close scrutiny.

    Looking Toward Future Demands

    With the growing complexity of target molecules and the increasing pressure from regulatory environments, researchers and process chemists face mounting technical and logistical demands. Ethyl (3S)-Piperidine-3-Carboxylate takes a key position within research pipelines thanks to its robust stereochemical profile and manufacturing pedigree. We stay alert to shifts in industry needs, regularly soliciting customer feedback, updating analytical suites, and investing in flexible equipment setups. These steps ensure our production keeps pace with evolving benchmarks for purity, safety, and traceability.

    Final Reflections

    Every batch of Ethyl (3S)-Piperidine-3-Carboxylate represents more than a chemical — it embodies the result of hands-on discovery, ongoing customer dialogue, and continuous refinement in response to the realities of large-scale synthesis. Our teams strive to minimize the gap between lab concept and plant reality, introducing practical technical support, data transparency, and adaptability to every partnership. As research accelerates and markets expect more from chemical suppliers, delivering a compound like this with reliability, traceability, and technical backup protects not just timelines and budgets but also the integrity of projects that depend on it. That practical commitment continues to shape both our product offerings and the collaborative relationships we value with the researchers and manufacturers counting on these building blocks.