|
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 | 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. |
Applications of Ethyl (3S)-Piperidine-3-Carboxylate in Industrial ManufacturingEthyl (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 DrugsSeveral 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
Typical usage ratio
Downstream process integration
Final product types
2. Chiral Ligand/Building Block in Agrochemical SynthesisThe 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
Typical usage ratio
Downstream process integration
Final product types
3. Precursor in Synthesis of Specialty PolymersFine 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
Typical usage ratio
Downstream process integration
Final product types
4. Stereoselective Intermediate for Fine Chemical SynthesisProducers 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
Typical usage ratio
Downstream process integration
Final product types
|
Competitive Ethyl (3S)-Piperidine-3-Carboxylate 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
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.