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(S)-1-N-Boc-Piperidine-2-Carboxamide

    • Product Name (S)-1-N-Boc-Piperidine-2-Carboxamide
    • Alias (S)-1-N-Boc-pipecolic acid amide
    • Einecs 851-709-2
    • 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

    519598

    Iupac Name (S)-tert-butyl 2-carbamoylpiperidine-1-carboxylate
    Cas Number 123332-58-1
    Molecular Formula C11H20N2O3
    Molecular Weight 228.29 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 80-85°C
    Solubility Slightly soluble in water; soluble in DMSO, methanol
    Optical Rotation [α]D20 ≈ +18° (c=1, CHCl3)
    Smiles CC(C)(C)OC(=O)N1CCCC[C@H]1C(=O)N
    Inchi InChI=1S/C11H20N2O3/c1-11(2,3)16-10(15)13-7-5-4-6-8(13)9(12)14/h8H,4-7H2,1-3H3,(H2,12,14)/t8-/m0/s1
    Chirality S-configuration at C2
    Storage Conditions Store at 2-8°C, protected from light
    Applications Used as a chiral intermediate in organic synthesis

    As an accredited (S)-1-N-Boc-Piperidine-2-Carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 10g amber glass bottle, sealed and labeled with chemical name, CAS number, batch number, and handling precautions.
    Shipping (S)-1-N-Boc-Piperidine-2-Carboxamide is shipped in tightly sealed containers, protected from moisture and light. It is handled as a non-hazardous organic chemical, usually transported at ambient temperature unless otherwise specified. Standard regulations for shipping laboratory chemicals apply to ensure safety and product integrity during transit.
    Storage (S)-1-N-Boc-Piperidine-2-Carboxamide should be stored in a tightly sealed container, protected from moisture and light. Keep at room temperature (15–25°C) in a dry, well-ventilated area, away from incompatible substances such as strong acids and bases. Avoid prolonged exposure to air. Follow local regulations for chemical storage to ensure safety and product integrity.
    Application of (S)-1-N-Boc-Piperidine-2-Carboxamide

    Applications of (S)-1-N-Boc-Piperidine-2-Carboxamide in Industrial Manufacturing

    As an established chemical raw material manufacturer, we supply (S)-1-N-Boc-Piperidine-2-Carboxamide to various specialized sectors. This chiral protected piperidine serves as a vital intermediate in multi-step synthesis, specifically in regulated pharmaceuticals and fine chemical production. Our material enables advanced industrial process control, precise dosage adjustment, and adherence to international norms.

    1. API (Active Pharmaceutical Ingredient) Synthesis for CNS Drug Development

    Our (S)-1-N-Boc-Piperidine-2-Carboxamide plays a fundamental role in the enantioselective synthesis of pharmaceutical intermediates used in central nervous system (CNS) medications, such as selective serotonin reuptake inhibitors (SSRIs) and antipsychotics. The product ensures high chiral purity critical for downstream active ingredient development. Our technical support covers integration with GMP lines, scaling from pilot to production, and batch-to-batch quality consistency.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – 21 CFR Parts 210 & 211 (FDA)
    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for chiral intermediates
    • USP <823> Sterile Drug Products compliance

    Typical usage ratio

    • 5–15% as step-specific intermediate by molar quantity in CNS drug synthesis; ratio varies according to target compound structure and protecting group retention.

    Downstream process integration

    • Introduced post-piperidine ring construction to deliver chiral protection prior to amide coupling and deprotection.
    • Used under controlled conditions (0–5°C) in batch reactor systems to prevent racemization.

    Final product types

    • SSRIs such as paroxetine intermediate
    • Antipsychotic compound precursors utilizing chiral piperidine frameworks
    • Other CNS-targeting active pharmaceutical ingredients with protected amide sidechains

    2. Peptide Synthesis for Biopharmaceuticals

    The Boc-protected piperidine-2-carboxamide is a favored chiral auxiliary in automated solid-phase peptide synthesis (SPPS) workflows. In this context, the raw material enhances enantiomeric control during amide bond formation, supporting scalable GMP biomanufacturing for therapeutic peptides and peptide-based APIs. Accurate delivery and side-chain management are standard in our supply for peptide pharmaceutical producers.

    Industry compliance standards

    • ICH Q11 – Development and Manufacture of Drug Substances
    • EMA Guideline on the Quality of Biological Peptides
    • ISO 9001:2015 Quality Management Systems for process traceability
    • EU Annex 13 – Investigational Medicinal Products GMP requirements

    Typical usage ratio

    • 3–10% relative to total protected amino acid inputs, adjusted per specific sequence length and protection group scheme.

    Downstream process integration

    • Loaded onto resin substrates after Fmoc/Boc strategy selection, enabling stepwise chiral incorporation.
    • Employed in intermediate coupling reactions prior to side-chain deprotection and cleavage for final peptide assembly.

    Final product types

    • Therapeutic peptides for metabolic and cancer indications
    • Chiral peptide intermediates for further backbone modification
    • Biotech APIs for injectable formulations

    3. Chiral Intermediate in Agrochemical Synthesis

    Agrochemical manufacturers rely on our product as a strategic chiral intermediate when developing advanced crop protection agents, especially those based on piperidine-derived scaffolds. Accurate chiral control is necessary for synthesizing active enantiomeric isomers, which are crucial for patented pesticide development and regulatory approval in the EU and North America. Our raw material undergoes intensive QC per shipment for this industry.

    Industry compliance standards

    • REACH Regulation (EU) No 1907/2006 for agrochemical intermediates
    • EPA 40 CFR Part 158 – Data requirements for pesticide registration
    • ISO 17025 – Laboratory Competence for residue testing
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • 8–20% of total intermediate inputs; ratio depends on the molecular design of the pesticide’s chiral centers and final formulation yield.

    Downstream process integration

    • Added post-ring formation during enantioselective synthesis of target pesticide intermediates.
    • Subject to controlled hydrolysis and derivatization prior to final API isolation.

    Final product types

    • Chiral herbicide and fungicide active ingredients
    • Crop protection compound intermediates with enhanced selectivity
    • Seed treatment products utilizing piperidine backbones

    4. Advanced Intermediate for Specialty Chemical Synthesis

    In specialty and fine chemical manufacturing, (S)-1-N-Boc-Piperidine-2-Carboxamide serves as a platform molecule for producing asymmetric building blocks. Fine chemical producers use it for advanced ligand synthesis and specialty reagents required in electronics and analytical standards. We deliver at technical grades suited for high-purity downstream demands, based on documented specifications and supply chain traceability.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing quality assurance
    • Responsible Care® Global Charter in chemical processing
    • Chemical Facility Anti-Terrorism Standards (CFATS) for specialty intermediates
    • IATA/ADR: Safe transport guidelines for fine chemicals

    Typical usage ratio

    • 2–7% weight fraction per batch, altered based on the complexity of the target ligand system or specialty reagent requirements.

    Downstream process integration

    • Introduced in multistep synthesis following key piperidine derivatization and Boc group stabilization.
    • Transferred to subsequent functionalization reactors for side-chain elaboration or cross-coupling.

    Final product types

    • Chiral ligands for asymmetric catalysis
    • Custom specialty reagents for electronic chemical processes
    • Reference analytical standards in instrumental labs
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    Competitive (S)-1-N-Boc-Piperidine-2-Carboxamide prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    (S)-1-N-Boc-Piperidine-2-Carboxamide: Craftsmanship and Character in Every Batch

    What Sets (S)-1-N-Boc-Piperidine-2-Carboxamide Apart

    Manufacturing (S)-1-N-Boc-Piperidine-2-Carboxamide means getting personally acquainted with the details that can make or break the results in your lab. This molecule isn’t just another intermediate; it’s a vital component for researchers and process chemists looking to build complicated targets with predictable stereochemical control. We don’t just see it as one more line in a catalog—each batch represents a chain of deliberate choices, from the way we start with high-purity raw piperidine to the last analytical checks before release.

    (S)-1-N-Boc-Piperidine-2-Carboxamide carries a chirality that impacts route selection and final compound character. Purity and precise control over enantiomeric ratio dictate the value of each shipment. Our experience in large-scale hydrogenations, careful Boc-protection, and amide couplings inform the outcome you see. We’ve worked closely with analysts during our own technology upgrades, which helped us spot how minute differences in crystallization conditions can leave an unexpected residue, even below the usual detection threshold. Over the years, chasing these small inconsistencies led us to adjust the temperature ramp patterns and recrystallization solvents, fitting the physical profile demanded by advanced synthetic processes.

    Specifications Backed by Experience

    Throughout our plant, every step contributing to the final (S)-1-N-Boc-Piperidine-2-Carboxamide passes rigorous oversight because mistakes here echo far down the chain. Purity measurements regularly exceed 99 percent by HPLC, and when the target is a pharmaceutical precursor, achiral and chiral checks matter equally. We never rely on a single chemist’s signoff; analytical teams cross-validate both melting points and specific optical rotations, establishing a fingerprint unique to each production run. Repeated feedback from partners confirms that subtle impurities, undetectable by routine protocols, can undermine subsequent couplings or final stage crystallizations. That’s why our equipment calibration schedule aligns with the latest quality benchmarks.

    Some projects call for kilograms rather than grams. Our scale-up follows the same logic and double-verification. Moving from a bench reactor to a 200-liter vessel tests not only our recipes but also the way solvents interact at larger volumes. It isn’t just about dumping more reactants into a bigger container; mixing efficiency and the length of temperature holds shift, affecting how crisp the isolated intermediate looks under NMR. We rely on decades of experience in industrial organic chemistry to decide which changes warrant further investigation. Our senior process team has traced origins of stubborn color impurities back to batch aging during winter, adjusting both protocol and warehouse layout to keep specifications in line.

    Product Applications Shaped by Chemistry Practice

    Research teams and commercial-process developers depend on (S)-1-N-Boc-Piperidine-2-Carboxamide as a building block for anything from experimental APIs to kilo-lab scale assembly of drug candidates. In our experience, its success in the field comes back to three factors: reproducibility, ease of downstream deprotection, and robustness in couplings. The Boc (tert-butoxycarbonyl) group keeps the nitrogen locked down, dodging side-reactions during subsequent transformations. After years spent working next to project managers in small molecule R&D, our chemists learned that a predictable and gentle Boc deprotection step spares major headaches later, especially when working with sensitive targets. Reports from external partners often come in the form of one-liners: “Good lot, no problems in coupling, saved time on work-up.”

    Amide functionality on the piperidine ring takes on special significance in medicinal chemistry. Its stability opens up options for custom functionalizations downstream, which our own teams have validated in gram and kilogram syntheses. Analytical chemists in our organization often point out where a slight shift from the amide position leads to entirely new impurity profiles, underscoring why sourcing well-characterized intermediates pays off. During technology transfer, our process engineers keep close records on batch homogeneity, since variable input quality can lead to bottlenecks in the flow of a multi-step synthesis. It’s these accumulated lessons—impossible to pull from a textbook—that allow us to troubleshoot unusual solubility issues or inconsistent assay results experienced by clients.

    Often, feedback loops add value before a molecule leaves our warehouse. Quality reports highlight performance in asymmetric syntheses, and internal conversations between our technical support and production chemists lead to small but significant tweaks in product drying or packaging protocols. In one case, a client flagged an unusual streak of discoloration after long ocean transport. Our teams took on batch-by-batch stability testing, uncovering issues related to micro-trace moisture trapped during vacuum drying. Now each drum is sealed under dry inert atmosphere—the types of refinements only possible when you’ve experienced the aftermath firsthand.

    Handling and Storage: What Works and Why

    Day-to-day handling of (S)-1-N-Boc-Piperidine-2-Carboxamide requires basic chemical hygiene, yet experience shapes the way we approach storage. We learned early that this product, once absorbed moisture, behaves differently both in dispensing and in downstream chemistry. Aggregation from re-absorbed traces of water slows down dissolution and, in unlucky cases, leads to partial decomposition. Because of this, we run regular in-process checks for water content and have introduced argon-flushed packaging for large shipments. For labs lacking glove-box infrastructure, extra drying protocols support product integrity—lessons shared directly with end-users who struggle with batch-to-batch inconsistency.

    Colleagues in scale-up recall the first time they spotted minor caking in a container stored near HVAC ducting. Prompted by this, storage at controlled temperatures away from vibration and pressure differentials became our house rule. A few grams left open on a bench for a weekend can look the same to the naked eye, but analysis post-exposure picks up formula changes no one wants to discover halfway through synthesis. This insight filtered into our educational materials and on-site briefings for repeat buyers.

    Differences from Other Intermediates

    As a manufacturer with decades in piperidine chemistry, we work with a portfolio dense with similar-seeming structures, including unprotected piperidine derivatives or analogues with alternative N-protecting groups. Each offers advantages, but (S)-1-N-Boc-Piperidine-2-Carboxamide occupies a unique place in the synthesis landscape. Clients seeking rapid protection group removal and reliable amide reactivity keep returning for this compound, having seen inconsistent results with alternatives, including simple methyl or benzyl-protected piperidines, where both selectivity and deprotection harshness raise barriers to scale-up.

    We have run direct comparisons under manufacturing conditions, testing our Boc-protected carboxamide against Fmoc and Cbz siblings. Boc delivers the right blend of protection power and gentle deprotection, often outperforming Cbz by eliminating multi-step removal setups and sidestepping the expensive hydrogenolysis hardware needed for other protection strategies. Between these compounds, minute differences in acid lability lead to big changes in downstream resource utilization—one reason our pilot plant logs track not only yields but solvent recovery and deprotection times as well.

    Chirality brings another layer of distinction. Our (S)-isomeric purity differentiates our compound from racemic or (R)-analogues, which have shown marked variances in biological activity during collaborations with discovery teams. In pharmaceutical assembly, only one stereoisomer fits the shape and function needed for top-tier drug candidates. We channel our own technical resources into confirming every batch’s stereochemistry, saving clients from potentially costly surprises at the API scaling stage.

    Alongside the flavor of the piperidine ring, subtle shifts in protection or amide configuration often introduce unpredictable solubility or reactivity behaviors. Over time, our teams catalogued how unprotected or differently substituted piperidines left customers with tough-to-resolve process issues or unexpected chromatographic tails. This close observation led us to refine not only our core product’s specification but the advisory support we provide, shaping a solution set rather than a menu of undifferentiated intermediates.

    The Path from Raw Materials to Reliable Intermediate

    Our production line begins with careful selection of feedstock. Reliable sources and full-spectrum impurity profiling for raw piperidine, Boc anhydride, and necessary coupling agents help us avoid surprises during scale-up. After early experiences with inconsistent purity grades, we shifted to a closed-loop supplier system, maintaining feedback between incoming quality and post-production analytics. Each lot’s journey through our reactors isn’t simply chemical; it embodies a history of adjustments, mishap avoidance, and lessons carried into each subsequent batch.

    Temperature, mixing intensity, and even spacer time between reagent additions receive close attention. Once, an uptick in dimer impurity caught us off guard—an extended hold at suboptimal agitation and a slight lag in heat-up contributed to the unwanted byproduct. Our team maintains robust batch logs and root cause analysis protocols, refining each cycle. Over the years, this attention to detail dramatically reduced out-of-spec returns, meaning end-users now see product performance matching their most demanding application.

    Beyond chemistry, our insights from cross-functional meetings lead to logistical improvements. Aligning production and shipping teams allows us to adapt packaging formats to different climates, addressing condensation risk on arrival. These operational lessons, informed by everything from lab coat stains to vessel-cleaning bottlenecks, circulate within the company as internal case studies—ensuring new team members learn from both fixes and fumbles.

    Continuous Improvement, Shared Knowledge

    We learned that every step in (S)-1-N-Boc-Piperidine-2-Carboxamide manufacturing builds on the previous cycle’s data and stories. The simplest lab observations—such as a sticky scoop or a slightly off smell—have led us to catch and correct potential pitfalls before they become major issues in customer hands. Experienced operators catch early signs of off-gassing or discoloration, triggering new holding protocols that later show up as bulletproof performance in pharmaceutical runs. These qualitative “checks” stand alongside instrument-based assurances, making both front-line staff and seasoned managers accountable for an intermediate’s life cycle.

    Over multiple years, we chart not just what worked but where challenges cropped up, feeding those chapters into formal continuous improvement recommendations. Once, an unexpected drop in total yield prompted a broader investigation that ultimately led to a new solvent filtration system—now standard for all high-value intermediates. Regular debrief sessions between the plant floor and R&D feed a closed feedback loop, ensuring new batches reflect hard-won experience and never just repeat standard operating procedures without reflection.

    In one notable case, input from an offshore process chemist prompted us to rerun our own shelf-life trials under real-world shipping conditions, exposing small flaws in vacuum seals. Real knowledge transfer like this makes further innovation possible, pooling the experience of global and local practitioners to reduce risk for everyone using our intermediates.

    Looking Beyond the Molecule

    Keeping pace with changing regulations and increasing expectations from pharmaceutical partners, we work to exceed standards not just in chemical analysis, but in every aspect of traceability and batch integrity. Auditors walking through our facility or reviewing our digital records see a culture where deviations aren’t swept aside but dissected and documented for system improvement. Compliance teams discuss lessons from (S)-1-N-Boc-Piperidine-2-Carboxamide as part of our ongoing efforts to challenge “business as usual.” Experience taught us that a comfortable status quo rarely delivers top shelf reliability or earns genuine confidence from advanced users.

    With growing demand for advanced chiral intermediates, we recognize that product traceability and open technical support define success now more than ever. Rather than handing over data sheets, our teams collaborate with buyers through their synthetic workflows, finding points of friction and offering modifications informed by thousands of batches. Proactivity pays off: by the time a challenge emerges in another lab, we have usually mapped a workaround from our internal history. We turn this hands-on expertise into lasting value for customers who face unforgiving timelines and budgets.

    End-users have high expectations for physical form, particle size, and reactivity, and we don’t leave those details to chance. We regularly train our operations and quality teams on new analytical methods and equipment upgrades, integrating the latest insights from the field. This investment isn’t abstract; it shapes everything from drum sealing techniques to HPLC run parameters.

    Conclusion: Experience Shapes Every Delivery

    Decades in chemical manufacturing taught us that details separate a good intermediate from a headache. Each batch of (S)-1-N-Boc-Piperidine-2-Carboxamide reflects that experience, from raw-material vetting through production, purification, and dispatch. We view problems as opportunities to learn, and share lessons openly within our network of clients and collaborators. With every shipment, our customers carry forward the benefit of hundreds of adjustments and troubleshooting steps made to keep the science predictable and the business sustainable. True confidence comes not from theory or paperwork, but from the hard-won groundwork that only hands-on manufacturing brings.