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N-Boc-2-Cyanopiperidine

    • Product Name N-Boc-2-Cyanopiperidine
    • Alias 2-Cyano-1-Boc-piperidine
    • Einecs 872-617-6
    • 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

    951751

    Product Name N-Boc-2-Cyanopiperidine
    Cas Number 870281-82-6
    Molecular Formula C11H18N2O2
    Molecular Weight 210.27 g/mol
    Appearance White to off-white solid
    Melting Point 75-79°C
    Purity Typically ≥98%
    Storage Temperature 2-8°C (refrigerated)
    Solubility Soluble in organic solvents such as DCM, methanol
    Smiles CC(C)(C)OC(=O)N1CCCC(C#N)C1
    Synonyms tert-Butyl 2-cyanopiperidine-1-carboxylate
    Inchi InChI=1S/C11H18N2O2/c1-11(2,3)15-10(14)13-7-5-4-9(8-12)6-13/h9H,4-7H2,1-3H3

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

    Packing & Storage
    Packing N-Boc-2-Cyanopiperidine, 25g, is packaged in a sealed amber glass bottle with a tamper-evident cap and safety labeling.
    Shipping N-Boc-2-Cyanopiperidine is shipped in tightly sealed containers, protected from moisture and light. It is typically packed in UN-approved packaging, labeled according to relevant hazardous material regulations. Shipping is conducted via ground or air by certified carriers, with all necessary documentation and safety data provided for secure and compliant transport.
    Storage N-Boc-2-Cyanopiperidine should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, well-ventilated area. It should be kept at temperatures between 2–8°C (refrigerator), and isolated from strong acids, bases, and oxidizing agents. Proper labeling and handling precautions should be maintained to ensure chemical stability and safety.
    Application of N-Boc-2-Cyanopiperidine

    Applications of N-Boc-2-Cyanopiperidine in Industrial Manufacturing

    N-Boc-2-Cyanopiperidine supports several high-value chemical industry sectors, primarily as a protected intermediate for demanding synthesis environments. The applications outlined below reflect established downstream processes in pharmaceuticals, fine chemical synthesis, and biotech pathways with strict quality requirements.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Research-based pharmaceutical companies and CMOs use N-Boc-2-Cyanopiperidine extensively in the multi-step production of advanced piperidine-derived APIs. Its N-Boc protection facilitates selective deprotection and conversion steps, particularly for CNS-active agents and anti-infective compounds, where precise functional group orientation is necessary for bioactivity. The compound enters early-stage API synthesis, enduring multiple purifications and derivatizations under tightly controlled GMP protocols. Engineers specify this material due to its high purity specification, low metal impurity profile, and favorable process economics for large-scale medicinal chemistry routes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters on starting materials for APIs
    • European Pharmacopoeia (Ph. Eur.) 2034 standards for pharmaceutical intermediates
    • FDA cGMP guidelines 21 CFR Parts 210/211 for API facilities

    Typical usage ratio

    • 5–20% w/w relative to total step reactants, depending on the target API’s core structure requirements and desired output mass; ratio adjusted for batch or continuous flow systems.

    Downstream process integration

    • Input for the protected piperidine nucleus formation, followed by stepwise deprotection, nitrile hydrolysis, and further functionalization before final API conversion.

    Final product types

    • Second and third-generation CNS drugs, piperidine-based antibiotics, specialty antivirals, complex anti-cancer agents, and clinical trial APIs.

    2. Specialty Peptide Synthesis

    Peptide contract manufacturing organizations integrate N-Boc-2-Cyanopiperidine as a safeguarded piperidine segment in non-standard amino acid residues. Its controlled reactivity allows for stepwise addition into solid-phase peptide synthesis (SPPS) protocols, usually in protected peptide elongation cycles where precise side chain and terminal modifications drive performance in therapeutic peptides and diagnostic reagents. The compound’s structure supports orthogonal protection strategies, particularly for high-purity, small-molecule peptide hybrids.

    Industry compliance standards

    • Peptide Synthesis GMP Standards (USP 1047, EMA Annex 2)
    • ISO 13485 for medical device peptides and diagnostics
    • ICH Q11 Development and Manufacture of Drug Substances

    Typical usage ratio

    • 0.2–2 mol equivalents per peptide chain elongation cycle, set by the sequence design and resin loading capacity; adjusted in custom protocols based on protected residue incorporation and desired coupling yield.

    Downstream process integration

    • Use during protected piperidine ring insertion onto resin or in solution synthesis; integrated early and removed at deprotection, prior to cyclization or final cleavage from resin support.

    Final product types

    • Modified therapeutic peptides, peptidomimetics, peptide drug conjugates, and high-specificity peptide labeling agents.

    3. Advanced Agrochemical Intermediate Manufacturing

    N-Boc-2-Cyanopiperidine functions as a protected building block in the synthesis of advanced agrochemical actives, particularly for next-generation piperidine-based insecticides and plant health compounds. Downstream processors value its N-Boc group for process safety and selectivity, aiding in multi-step conversion to final active substances where chemical selectivity in nitrile substitution and cyclization steps is critical for potent activity profiles. The material ensures consistent batch yield and process reproducibility, supporting regulatory compliance for active ingredient registration.

    Industry compliance standards

    • FAO/WHO technical guidelines for pesticide intermediates
    • REACH (EC 1907/2006) registration requirements for agrochemicals
    • ISO 9001:2015 Quality Management for chemical synthesis

    Typical usage ratio

    • 10–30% w/w of overall building block input in targeted active synthesis; proportion tuned to specific synthetic route and desired final active loading during formulation.

    Downstream process integration

    • Introduced prior to deprotection and cyclization steps, followed by controlled hydrolysis and functionalization for final technical-grade active substance isolation.

    Final product types

    • High-potency synthetic insecticides, fungicide development intermediates, and advanced plant growth regulator precursors.

    4. Chiral Building Block for Fine Chemical Synthesis

    Producers of optically pure fine chemicals employ N-Boc-2-Cyanopiperidine as a scaffold for enantioselective synthesis. The material’s protected nitrogen and cyano moieties provide synthetic flexibility, allowing downstream organic chemists to tailor asymmetric functionalization, perform regioselective reductions, or construct new heterocyclic frameworks. Its use is common in the assembly of advanced ligands, chiral auxiliaries, and specialty chemical intermediates, where high purity and trace impurity control are vital for advanced material applications.

    Industry compliance standards

    • Chemical Manufacturers Association Responsible Care® program
    • ISO 9001:2015 for batch fine chemical production
    • EU REACH compliance for specialty building blocks (EC 1907/2006)

    Typical usage ratio

    • 5–50% w/w, highly dependent on the downstream chiral or heterocyclic structure’s requirements; ratio determined by desired product throughput and chiral purity targets.

    Downstream process integration

    • Selected as the initial building block for ring assembly, chiralization, or molecule extension; frequently subjected to asymmetric hydrogenation, cyclization, or nucleophilic addition.

    Final product types

    • Chiral fine chemical intermediates, specialty ligands for catalysis, optically active scaffolds for high-value synthesis, and advanced electronic material precursors.

    5. Custom Chemical Intermediate for Contract Research and Development (CROs/CDMOs)

    Innovation pipelines at CROs and CDMOs rely on N-Boc-2-Cyanopiperidine as a foundational intermediate for custom synthesis programs in early discovery and preclinical research. Flexible molecular design necessitates materials with protected functional groups for versatile molecule modifications, efficient purification, and analytical verification. The compound supports convergent synthesis routes and high-throughput screening needs, serving clients engaged in lead optimization for pharma, agro, or specialty materials.

    Industry compliance standards

    • ISO 9001:2015 and ISO 17025 (testing and calibration) certified systems
    • OECD GLP principles for research-grade intermediates
    • Client-specific quality and documentation standards (CofA, MSDS, trace impurity reports)

    Typical usage ratio

    • 0.1–10 g per synthetic route, adjustable for pilot-scale batches; usage depends on molecule architecture and screening protocol requirements.

    Downstream process integration

    • Applied at the fragment assembly stage in route scouting or SAR exploration; subsequent exposures to diverse transformations such as reduction, alkylation, or amide coupling before bulk scale-up.

    Final product types

    • Screening libraries, HTS tool compounds, discovery-stage API candidates, and customized heterocyclic intermediates.
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    Certification & Compliance
    More Introduction

    N-Boc-2-Cyanopiperidine: Manufacturer’s Insight on Quality, Application, and Distinction

    Direct from the Source: Our Experience with N-Boc-2-Cyanopiperidine

    On the factory floor, every batch of N-Boc-2-Cyanopiperidine carries a story. For us, producing this compound is never just routine chemistry. It demands scrutiny at every step because the world of piperidine derivatives is crowded, and quality can be uneven in the wider market. Years of hands-on synthesis, purification, and control over handling have taught us where small details make a big difference—both in the final material and in how our clients use it out in the field.

    Model and Specifications: Why Purity and Traceability Matter

    Our N-Boc-2-Cyanopiperidine leaves the plant with a clear identity: a single, high-purity compound supported by a full analytical profile. Labs and production chemists across pharmaceuticals, research institutes, and specialty synthesis keep asking for that, and for good reason. Over time, even a small impurity or batch-to-batch variation can throw off downstream reactions, whether you’re assembling a complex active pharmaceutical ingredient or designing a new molecular scaffold. Because we run our entire synthesis—from the starting amines through Boc protection and cyanation—in a carefully tracked, closed environment, we cut out common sources of cross-contamination.

    We focus on reproducibility, which shows up in things like a consistent melting range and a sharp NMR fingerprint for every shipment. Beyond that, our team documents yield statistics, solvent residuals, and byproduct profiles over hundreds of batches. That data doesn’t stay locked in a database; it guides improvements and lets us respond fast when customers show us new analytical challenges.

    How N-Boc-2-Cyanopiperidine Fits Into Today’s Research and Manufacturing

    Over the years, the biggest adopters of N-Boc-2-Cyanopiperidine have come from drug discovery. Medicinal chemists like how the molecule offers a stable, protected piperidine that holds a reactive cyano handle, giving them an entry into constructing more complex nitrogen heterocycles. Unlike open-chain nitriles, the piperidine ring stabilizes the structure and the Boc group shields it from side reactions, so researchers have more control across multi-step synthetic routes. We’ve watched the product move from bench-scale library design straight into small-molecule pilot plants, supporting both screening campaigns and lead optimization for CNS and antiviral targets.

    Process engineers walk into our plant looking for a reliable building block with minimal risk of hydrolysis during storage or transport—especially when they scale up. The Boc group, in our experience, stands up well in bulk shipments and doesn’t slip off unless conditions get harsh, allowing efficient deprotection under acidic workups exactly when and where the chemist wants. That’s a practical advantage our clients talk about after firefighting with other protected piperidines or when they’re struggling to keep their feeds dry through multiple solvent changes.

    For contract manufacturers working under tight deadlines, every minute spent troubleshooting a reaction or comparing GC specs adds risk and cost. By maintaining in-house control of every kilogram, we eliminate those late-night phone calls about inconsistent product or out-of-spec color and viscosity.

    How Our Manufacturing Choices Set N-Boc-2-Cyanopiperidine Apart

    Not every supply on the market tells the full backstory—especially online, where intermediates often bounce between third-party brokers. Sometimes, buyers only discover differences after their process grinds to a halt or purification losses jump. Because we manufacture directly, it starts with detailed incoming material checks. Only specific grades of 2-piperidone and tert-butyl dicarbonate go into our system. We condition all solvents and reagents, monitor moisture, and run live assay checks through every critical phase.

    Any deviations in crystalline habit or color are flagged and investigated. We’ve reworked reaction times and conditions over the years—not just to boost yield, but to reduce side products that can complicate later steps. Instead of chasing maximum throughput or cutting costs at the expense of reliability, we put effort into optimizing the extraction and washing routines to leave behind less residue. Only material that clears a battery of identity and purity tests ever ships.

    Practical Lessons from Decades of Synthesis

    Looking back, some of the most important improvements in our process have come less from scaling bigger reactors and more from tightening process discipline. When we switched to in-line solvent drying and re-tooled our purification hardware, it wasn’t just a lab exercise. Those changes responded directly to customer feedback about variable performance when exposed to high-humidity environments or on storage shelves that saw seasonal temperature swings. The Boc group is robust, but careless handling can still degrade a batch and send traces of byproducts downstream. Our staff—many with a decade or more watching the same equipment—have helped us write the process guidelines that now keep problem runs to a bare minimum.

    Working as a direct manufacturer, we see firsthand how materials move from order to delivery. Our team inspects every lot of N-Boc-2-Cyanopiperidine before it goes out, knowing that small changes slip through in less controlled operations. Shipment temperature, time in transit, and compatibility with recipient labs all influence ultimate utility. Small things—like whether product remains dry and free-flowing or tends to clump—reflect how rigorously the upstream process has been managed. We’ve taken calls from customers who tried generic supplies, only to encounter slow dissolving or unexplained reactivity issues. In responding to those concerns, we’ve updated our own production methods, cutting down particle size variance and adjusting packing materials to better survive global shipping.

    Comparisons with Similar Piperidine-Based Compounds

    Working up close with N-Boc-2-Cyanopiperidine, our staff also tracks and studies related intermediates. Other Boc-protected piperidines without a cyano group offer different reactivity, but lack the versatility required by synthetic routes into certain active pharmaceutical ingredients and complex ligands. Some suppliers offer N-Boc-2-piperidone or N-Boc-piperidine without substitution, but these don’t offer direct access to a nitrile, which is crucial in coupling steps and as a precursor for amidine or amine transformations.

    We’ve compared many alternatives in our own plant. Products carrying bromine or other electron-withdrawing groups at the 2-position may work for some transformations, but the cyano group occupies a unique place by balancing electrophilicity with stability. This gives researchers more leeway in timing reactions and streamlining purification. Unprotected 2-cyanopiperidine exists as well, though its shelf life and risk of undesired side reactions limit large-scale applications. Having the Boc group present, in our direct experience, offers predictable deprotection and protects downstream yield profiles, reducing headaches for chemists under time pressure.

    Those looking at 2-cyanopiperidine hydrochloride as an alternative will see more sensitivity to moisture and an increased risk of degradation when carried through multiple synthetic steps, especially when exposed to base. N-Boc-2-Cyanopiperidine delivers a smoother path through complex synthetic trees, which is one reason our pharmaceutical partners keep returning to this intermediate.

    Supporting Reliability for Today’s Demanding Users

    Supplying N-Boc-2-Cyanopiperidine directly from our facility, we’ve grown familiar with the practical uses and sticking points across every scale—from milligram samples to full-kilogram lots powering fed-batch reactors. Medicinal chemists rely on the consistency of our material not just for bench chemistry, but also for early-stage toxicity studies and pilot plant expansions. The tight control we keep over trace metals, solvent residuals, and particle size directly reflects in fewer failed screens and smoother transitions to industrial production.

    Building a robust feedback loop helps as well. Our technical support team—drawn from the same group who produce the compound—receives real world process inquiries: does N-Boc-2-Cyanopiperidine dissolve well in your solvent mix? Does it hold up under the heat ramp in your purification column? Each answer shapes internal guidelines and process tweaks, helping future customers avoid old pitfalls.

    Many chemists remember frustrating delays after switching suppliers only to learn that what claims purity on a data sheet may still bring downstream headaches. Keeping synthesis internal, our staff pick up the phone and talk directly with R&D or manufacturing partners. Sharing tips on solvent selection, shipment timing, and storage conditions, we help protect expensive downstream campaigns and limit lost time from failed reactions.

    Traceability Drives Real-World Performance

    We believe every kilogram tells a story, which is why nobody on our team settles for just passing specification sheets between offices. Working hands-on with each batch cultivates familiarity that’s tougher to achieve across disconnected broker networks. If a defect arises, our lab sees it quickly and rolls out investigations before any material ever ships. This practice stands in sharp contrast to suppliers who broker from multiple sources without tying product history to each lot.

    Regular process reviews now pull in the latest analytic technologies, letting us spot new impurity trends before they rise to critical levels. Upstream, we field-test different reagent sources until we’re confident in every batch’s stability under normal usage and storage. Uninterrupted chain-of-custody not only provides security to our direct users, but also clarifies regulatory pathways for teams preparing filings anywhere from IND through NDA.

    This tight traceability grows more important as supply interruptions and quality concerns globally interrupt research progress. Where brokers sometimes gamble on mysterious stock or shipments delayed at customs, we maintain material provenance and offer rapid update cycles in response to new industry needs.

    Solutions Rooted in Direct Experience

    Every time an issue shows up in a client lab—like an unexpected filtration step or a dissolve problem—we use it as a springboard to refine our approach. For example, several years back, customers informed us about sporadic solubility hiccups when transferring material from cold rooms. After investigating, our team found the link tied to residual crystal water from a slightly tweaked crystallization step. We addressed it in real time, revising drying conditions and documentation. Since then, those calls have faded as the newly-tuned lots ship steadily across dozens of projects.

    We also observed that some alternative intermediates, while lower cost, introduce bottlenecks in automated scale-up reactors or require more aggressive purification. For those partners, we walked through their entire synthesis roadmap, identifying where a switch to our N-Boc-2-Cyanopiperidine cut out unnecessary side processing and improved reproducibility. Our support team stays tuned to this feedback, turning small tweaks into plant-wide gains.

    Direct relationships let us respond to uniqueness—if a customer specifies uncommon impurity cutoffs or a different packaging format, we can flex processes and documentation on the back end without endless negotiation. Because our crew works closely together, even unusual requests reach those who can act promptly, bridging the gap between request and delivery.

    How Market Trends Shape the Product We Deliver

    Global interest in N-Boc-2-Cyanopiperidine keeps shifting, driven by pharmaceutical innovation, changes in patent landscapes, and new classes of heterocyclic compounds. As new therapeutic areas demand robust, versatile intermediates, direct technical feedback helps us update not just production protocols, but also how we support customers building out their own chemistry platforms.

    Some clients pivot quickly, needing faster turnarounds as R&D teams start multiple programs in parallel. Others require long-term stability to feed multi-year projects. Sticking close to the synthesis allows us to keep inventory lean without risking outages or over-extended lead times. Throughout all cycles, clarity and speed in technical communications prevents mix-ups, which can cost days or weeks in high-stakes projects.

    As regulations tighten and demand grows for environmental responsibility, our plant continues to upgrade recovery, solvent recycling, and waste minimization. Most research groups pay attention when intermediates can help streamline downstream processing, cut emissions, and simplify compliance. Keeping control over every step lets us bake those improvements in, instead of reacting to changing requirements with band-aid fixes.

    Supporting the Next Generation of Chemical Synthesis

    The story of N-Boc-2-Cyanopiperidine doesn’t rest solely on purity numbers or throughput. It reflects a philosophy of hands-on manufacturing, where experience accumulates not just in the machines, but among the trained operators and chemists who interact with every run. Their hard-earned insights become tomorrow’s process improvements, building resilience and trust through consistent performance.

    From process troubleshooting to project-specific optimizations, the value of direct manufacture shows up not only in the product itself, but in the relationships that grow through each successful delivery and batch consultation. By listening to the evolving needs of customers and constantly reviewing process data, our team ensures N-Boc-2-Cyanopiperidine remains a reliable cornerstone for science that matters.

    Bringing this compound from raw material to finished form, we stand committed to upholding the standards that advanced chemical manufacturing demands today—rigorous data, hands-on feedback, and a commitment to continual improvement, grounded in real experience.