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Ethyl 1-Benzylpiperidine-3-Carboxylate

    • Product Name Ethyl 1-Benzylpiperidine-3-Carboxylate
    • Alias H DEP 28
    • Einecs 696-310-1
    • 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

    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 & Storage
    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.
    Application of Ethyl 1-Benzylpiperidine-3-Carboxylate

    Applications of Ethyl 1-Benzylpiperidine-3-Carboxylate in Industrial Manufacturing

    Ethyl 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 Molecules

    This 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

    • ICH Q7 Good Manufacturing Practice for APIs
    • EU GMP Part II – Basic Requirements for Active Substances
    • USP <1058> Analytical Instrument Qualification
    • FDA 21 CFR Part 210–211 Current Good Manufacturing Practice

    Typical usage ratio

    • Ranges from 0.85 to 1.15 molar equivalents relative to the target API, finalized after pilot scale validation to optimize conversion rate and minimize downstream impurities.

    Downstream process integration

    • Introduced at the intermediate synthesis stage through an amidation or reductive amination reaction, followed by purification, crystallization, and API finalization

    Final product types

    • CNS-targeting drug active ingredients (tablets, capsules, injectable solutions)
    • Pharma grade intermediates for registered API dossiers

    2. Fine Chemical Synthesis: Chiral Building Block Manufacture

    Downstream 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

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC 1907/2006) for substances in Europe
    • Responsible Care® Initiative (Global Chemical Industry)
    • Chiral purity guidelines per European Pharmacopoeia (if targeting pharma)

    Typical usage ratio

    • Typically 5–15% by weight based on overall substrate input, with adjustment according to target enantiomeric ratio and catalyst system.

    Downstream process integration

    • Fed into batch reactors during the chiral transformation phase, combined with optically pure catalysts and monitored under in-process controls to achieve targeted isomer distribution before final separation.

    Final product types

    • Chiral fine chemicals for further synthetic elaboration
    • Amine-based building blocks exported to specialty chemical supply chains

    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

    • ISO 13485:2016 (for medical research substance development)
    • Client-specific process validation and audit protocols
    • Drug Master File (DMF) documentation standards (FDA, China NMPA, EMA)
    • Material Safety Data Sheet (MSDS) submission requirements

    Typical usage ratio

    • 2–10 mol% as a coupling or blocking group, depending on the length and complexity of the synthesis route; documented in project-specific batch records.

    Downstream process integration

    • Introduced as an isolated intermediate via automated or manual charge during stepwise assembly, supported by continuous in-line analytics and detailed electronic batch recording throughout contract synthesis workflows.

    Final product types

    • Research-grade intermediates supplied to biopharma development programs
    • Preclinical material batches for regulatory filing

    4. Precursor for Specialty Agrochemical Active Ingredient Synthesis

    In 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

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 17025 for internal labs (analytical method validation)
    • Local pesticide active ingredient registration standards (e.g., EU Regulation (EC) No 1107/2009)

    Typical usage ratio

    • Integrated at 8–20% of total reactor charge, tuned by reaction yield trials and dependent on specific agrochemical target molecule design.

    Downstream process integration

    • Charged at the ring functionalization stage prior to active ingredient formation, followed by multi-step derivatization and base neutralization before technical-grade crystallization.

    Final product types

    • Piperidine-derived herbicide actives for field crop treatment
    • Specialty fungicides for horticultural use

    5. Batch Raw Material for Diagnostic Reagent Synthesis

    Chemical 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

    • ISO 13485:2016 for medical devices and diagnostics
    • CLIA (Clinical Laboratory Improvement Amendments) for product release in the US
    • EN ISO 14971:2019 Risk Management for Medical Devices
    • Custom internal analytical QC specifications, validated for non-interference

    Typical usage ratio

    • Normally 1–3% by total precursor mass, with higher or lower ratios established in R&D by reactivity and labeling yield optimization.

    Downstream process integration

    • Added following initial scaffold assembly; enters amine protection and functionalization reactions before purification and final bio-conjugate formation steps.

    Final product types

    • Diagnostic assay reagents with active aminated groups
    • Calibrator solutions supplied for in vitro diagnostic platforms
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    Certification & Compliance
    More Introduction

    Ethyl 1-Benzylpiperidine-3-Carboxylate: A Closer Look from the Manufacturer's Perspective

    Real-World Insights into Ethyl 1-Benzylpiperidine-3-Carboxylate

    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.

    Practical Specifications and Batch Consistency

    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.

    The Value in Real Applications

    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.

    Why Purity and Analytical Rigor Matter

    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.

    How Ethyl 1-Benzylpiperidine-3-Carboxylate Stands Apart

    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.

    Sustainable Manufacturing and Process Evolution

    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.

    Quality, Cost, and Collaboration—Lessons from the Floor

    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.

    Real Differences from Standard Piperidine Esters

    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.

    Supporting Innovation, One Molecule at a Time

    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.

    A Manufacturer’s Word on Ethyl 1-Benzylpiperidine-3-Carboxylate

    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.