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HS Code |
947750 |
| Chemical Name | Ethyl 1-Benzylpiperidine-3-Carboxylate |
| Cas Number | 60446-37-1 |
| Molecular Formula | C15H21NO2 |
| Molecular Weight | 247.33 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 347.1°C at 760 mmHg |
| Density | 1.05 g/cm3 |
| Purity | Typically ≥98% |
| Smiles | CCOC(=O)C1CN(CC2=CC=CC=C2)CC(C1)N |
| Solubility | Soluble in organic solvents (e.g., ethanol, chloroform) |
| Storage | Store at 2-8°C, tightly closed |
| Refractive Index | 1.525-1.535 |
| Flash Point | 164.2°C |
| Synonyms | Ethyl 1-benzyl-3-piperidinecarboxylate |
As an accredited Ethyl 1-Benzylpiperidine-3-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of Ethyl 1-Benzylpiperidine-3-Carboxylate is supplied in a sealed amber glass bottle with a tamper-evident cap and labeled. |
| Shipping | Ethyl 1-Benzylpiperidine-3-carboxylate is shipped in secure, chemical-resistant containers, compliant with relevant transport regulations. The packaging ensures protection from moisture, light, and physical damage. Labels identify the product and hazards. Shipping documentation includes the safety data sheet (SDS). Only authorized handlers and carriers are used for domestic or international delivery. |
| Storage | Store Ethyl 1-Benzylpiperidine-3-Carboxylate in a tightly closed container, placed in a cool, dry, and well-ventilated area. Keep away from heat, sparks, open flames, and incompatible substances such as strong oxidizers. Protect from light and moisture. Ensure proper labeling, and limit access to trained personnel. Follow all relevant safety protocols and local chemical storage regulations. |
Applications of Ethyl 1-Benzylpiperidine-3-Carboxylate in Industrial ManufacturingEthyl 1-Benzylpiperidine-3-Carboxylate is a specialized intermediate widely incorporated in targeted chemical synthesis routes within the pharmaceutical and fine chemical industries. Below are the principal application scenarios where this material plays an essential role in industrial-scale production, each governed by unique compliance demands and process integration requirements. 1. Active Pharmaceutical Ingredient (API) Synthesis: Piperidine-Derived Drug MoleculesThis compound serves as a core intermediate for the preparation of substituted piperidine structures, especially in the synthesis of CNS-active pharmaceutical ingredients. Manufacturers employ it in multi-step processes leading to final APIs used in neurological disorder treatments. Consistently tight control over batch purity and traceability is required due to strict regulatory oversight. Industry compliance standards
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2. Fine Chemical Synthesis: Chiral Building Block ManufactureDownstream chemical manufacturers value this raw material as a stable starting point in the production of optically active piperidine derivatives, which are vital in asymmetric synthesis workflows. Its molecular structure supports enantioselective modifications employed in peptidomimetic and specialty amine projects where chirality is critical. Industry compliance standards
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3. Custom Synthesis for Contract Development & Manufacturing Organizations (CDMOs)CDMOs specializing in complex molecule construction incorporate this compound in client-specific synthesis routes, often as a protected piperidine segment supplying customized motifs for ongoing research or preclinical material production. Documentation and traceability in these projects emphasize strict adherence to client protocols and regulatory filing standards. Industry compliance standards
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4. Precursor for Specialty Agrochemical Active Ingredient SynthesisIn agrochemical production units, the molecule is employed as a key starting material in the synthesis of certain advanced piperidine-based herbicides and fungicides. Process technology teams rely on consistent physical and chemical performance to maintain reproducibility and meet agrochemical-grade specifications. Industry compliance standards
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5. Batch Raw Material for Diagnostic Reagent SynthesisChemical groups producing advanced diagnostic reagents—especially amine-reactive labeling compounds—utilize this molecule as a protected core in complex conjugation chemistry. High purity grades are essential to minimize interference in downstream diagnostic applications, and traceability reporting forms a required element of the supply chain. Industry compliance standards
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Drawing on years of hands-on experience managing the complex chemistry behind advanced specialty intermediates, it’s hard not to have a special respect for Ethyl 1-Benzylpiperidine-3-Carboxylate. This compound is much more than a string of syllables or a line in a catalog. Its structure—a piperidine ring with an ethyl carboxylate at the three position and a benzyl group at the one position—hints at both the depth of synthesis required and the value it brings to chemists who need a building block that behaves with reliability batch after batch.
In the manufacturing environment, we keep things concrete. Ethyl 1-Benzylpiperidine-3-Carboxylate, which often appears as a nearly colorless to slightly yellowish oil depending on minute levels of process impurity, comes to us through a precise, monitored process to guarantee structure and purity. Each batch leaves the reactor only after rigorous analysis, including nuclear magnetic resonance and chromatographic purity assessments. Typical purity on a dry weight basis goes north of 99 percent for most pharmaceutical and specialty chemical requirements.
Moisture presents itself as an unwelcome guest in many organic syntheses—our process holds residual water under strict limits, usually under 0.1%, measured by Karl Fischer titration. Each batch ships with current GC/MS data, not just a basic COA, so our customers can see what they're really getting. We don’t depend on generic qualification; instead, multiple stages of verification safeguard against cross-contamination or unreacted starting materials.
Experience in the synthesis plant has taught us that Ethyl 1-Benzylpiperidine-3-Carboxylate plays a pivotal role as an intermediate in the assembly of more complicated molecular scaffolds. Whether you are working in drug discovery, exploring analogues of CNS-active compounds, or mapping new reaction pathways in medicinal chemistry, this compound sits right at the crossroad of reactivity and selectivity.
Chemists appreciate its structure because the benzyl group serves both as a protecting group and, sometimes, a handle for further modification. The ethyl ester opens the door for simple hydrolysis or transesterification, depending on synthetic needs, while the piperidine ring forms the backbone for so many pharmacologically active molecules that its presence almost feels familiar in biochemistry circles.
The chemical’s performance during transformations such as reductive amination, nucleophilic substitution, or catalytic hydrogenation depends on starting with material that meets strict controls for side-products and residual solvents. In our own lab-scale and pilot runs, we have repeatedly seen yields and reproducibility improve when customers use our product, compared to inconsistent outcomes with material sourced through traders or outdated vendors. That reliability comes from direct manufacturer oversight, constant process verification, and a no-shortcuts approach.
Contaminants, especially those stemming from incomplete reactions or poor chromatography during purification, can halt a downstream process or mask a subtle analytical signal. In our experience, many hits during process development originate not from an exotic failure, but from trace byproducts that a trader might overlook. We run regular side-by-side trials using commercial samples from different origins. Time and again, in HPLC and NMR overlays, our tighter impurity thresholds correlate with cleaner end-products.
Process engineers on our floor tend to worry about more than analytical numbers. Stability during shipping, volatility, and container compatibility remain high-priority issues. Years ago, third-party drums arrived with surprising peroxide formation, likely due to temperature excursions and light penetration. We addressed that by investing in oxygen-scavenging liners for sensitive batches, and never shipping material in clear glass or unlined steel when off-site stability is a concern. These real-world precautions dramatically reduced off-spec complaints and boosted customer trust in our shipments.
A few clients still recall early years in the industry, when a shady, off-brand source delivered product with yellow-green tints and sticky residues that plugged up lines and sabotaged syntheses. Cleaning up after one inferior shipment cost days of labor and set the project timeline back a week. Since then, we introduced robust batch-tracing and full supply chain transparency. We never cycle off-standard material into commercial shipments. This approach adds cost but keeps our client relationships intact for the long term.
A superficial look might lump this molecule in with generic N-benzylpiperidine derivatives or with straightforward piperidine esters. Chemists who work with them soon learn that subtle differences in ring placement and ester chain length make or break a process. For example, methyl analogues sometimes produce higher volatility and increased migration during work-up, while the ethyl ester in this product grants a more manageable boiling point and easier liquid handling without clogging apparatus or hoses.
Compared with standard piperidine carboxylates lacking benzyl protection, our compound provides chemoselectivity advantages, especially for multi-step synthetic programs. Some customers pursue deprotection routes needing the benzyl group, while others design processes that exploit the group for stereoselective transformations.
Another distinction: Pharmaceutical-grade options are usually held to stricter trace-element standards than industrial makeshift batches. By excluding heavy metal catalysts from the final purification step, we keep transition metal traces near the lower detection limit—a key advantage during scale-up, particularly for regulated workflow. Our documentation backs these claims lot by lot, not just with vague supplier statements but detailed, third-party-certified results.
We manufacture Ethyl 1-Benzylpiperidine-3-Carboxylate with a view to both environmental stewardship and process efficiency. Solvent recycling forms part of every batch cycle, not simply because it saves money but because we recognize the volume of waste inherent to fine chemical manufacturing. The common pressure to reduce environmental footprint prompted us to redesign certain steps, replacing dichloromethane extraction with greener alternatives and introducing distillation-aided drying over salt beds that cut water use and reduced exposure risks in the plant.
Our waste management team monitors effluent streams closely, logging pH, conductivity, and organic load every shift. After a near-miss several years ago involving an overfilled holding tank, we invested in automated level monitors and tighter process controls. Problems serve as teachers. Auditors from international clients now find our logbooks and system records in order, and our operators stay empowered to take corrective action before outside regulators need to.
Worker training forms a core part of our quality. Operators know they aren’t just “making a chemical”; they are responsible for a medical building block with impact far beyond our walls. We run scheduled refreshers on spill management, PPE, and lockout-tagout to keep both staff and product safe.
Years on the production floor have shown that the cheapest input rarely achieves the lowest true cost in advanced synthesis. Quality shortfalls cascade: a sub-par ester translates to extra purification steps, higher solvent bills, and sometimes failed regulatory inspections. One illustrative event came up during a client’s ramp-up to GMP status. Their process failed valve cleaning because of polymeric contaminant carried through from a competitor’s product. They switched to our in-process controlled batches and eliminated the sticky buildup entirely. Documented downtime fell by nearly 40%.
Cost negotiations happen in every project, but our response remains consistent: cost control starts with robust upstream processing, not late-stage remediation. On more than one occasion, a buyer saw a price tag from a trader and asked us to match it. We explained the price reflects traceability, analytical rigor, and physical quality—not just “grams per dollar.” Some accepted it after running side-by-side trials and discovering less waste during work-up, fewer retests, and less operator frustration from batch-to-batch variability.
Collaboration sits at the center of our approach. Beyond supplying a molecule, we offer process feedback gleaned from hundreds of lab and pilot plant hours. We never hesitate to share our hard-won lessons, such as why certain filtration set-ups reduce clogging on recirculating loops, or which solvents best dissolve the final crude at scale. Feedback loops run both directions; a pharma client once identified a rare trace dimer on LC-MS. Our plant output underwent a minor adjustment, and current lots now meet both internal and external specs with margin to spare.
Chemists sometimes push back, wondering if Ethyl 1-Benzylpiperidine-3-Carboxylate just duplicates the function of other piperidine carboxylates already on their bench. We’ve run parallel synthetic tests and found several clear distinctions. Benzyl protection grants extra resistance to oxidative degradation under certain reflux conditions, minimizing impurity formation and residue deposits in final crystallization. The ethyl ester brings milder hydrolysis kinetics than methyl or isopropyl versions, resulting in better endpoint control for those running saponification-based deprotections.
Not all piperidine derivatives tolerate freeze-thaw cycles, drum transport, or long-term heated storage; our compound resists most cold-crystallization and tar formation due to the purity standards and impurity tightness enforced at every synthesis step. Through stability trials conducted during multi-month warehouse holding, we track shifts in purity, color, and reactivity. Our results consistently favor batches produced by direct synthesis and proprietary purification, compared to more generic or trader-brokered lots that too often lose spec ahead of expiry.
A manufacturer’s reputation rests not just on compliance filings but on the trail of results left in research and production projects. Looking across more than a decade of supplying Ethyl 1-Benzylpiperidine-3-Carboxylate, our proudest moments come from customer breakthroughs—novel CNS scaffold syntheses, successful patent submissions, and smooth, scalable process validations. Researchers demand flexibility: sometimes with new reactions, sometimes with analog development. Our material’s reproducibility and analytical support help innovators push forward, not battle upstream against unpredictable input chemistry.
Direct engagement with process teams builds trust. We encourage technical conversations—not just commerce—so that a customer never has to guess about lot compatibility, impurity profiles, or optimized handling. Our plant chemists listen to feedback and make PI-driven adjustments for yield improvements or impurity suppression, closing the loop between lab discovery and full-scale production.
After years turning raw materials into finished specialty products, we see patterns in customer needs and pain points. For those who need a building block that can support both medicinal chemistry screening and route development, Ethyl 1-Benzylpiperidine-3-Carboxylate brings substance, not shortcut. Production teams count on reliable supply and strong documentation to keep projects on track. Researchers bank on clean, predictable chemistry, not on halfway measures or gamble-sourcing from unknown brokers.
In feedback roundtables and after-action reviews, what sticks out isn’t just spectral purity or tidy drums; it’s the downstream gains: leaner process steps, sharper analytical peaks in QC, and faster scale-up. As direct manufacturers, we stake our standing on every outgoing batch. Whether the challenge lies in regulatory hurdles, scale-up bottlenecks, or tough selectivity, we’re in the trenches alongside our customers. Ethyl 1-Benzylpiperidine-3-Carboxylate remains a solid part of the modern chemical toolbox—shaped by hard-won know-how and a commitment to doing things right the first time.