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4-(Piperidine-1-Carbonyl)Phenylboronic Acid

    • Product Name 4-(Piperidine-1-Carbonyl)Phenylboronic Acid
    • Alias Piperidine-1-carbonylphenylboronic acid
    • Einecs 820-724-7
    • 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
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    Specifications

    HS Code

    815688

    Product Name 4-(Piperidine-1-Carbonyl)Phenylboronic Acid
    Cas Number 1201909-72-5
    Molecular Formula C12H16BNO3
    Molecular Weight 233.08 g/mol
    Appearance White to off-white solid
    Purity Typically ≥97%
    Melting Point 185-190°C
    Solubility Soluble in DMSO, slightly soluble in water
    Smiles B(C1=CC=C(C=C1)C(=O)N2CCCCC2)(O)O
    Inchikey FFPZUFZCUUZMRK-UHFFFAOYSA-N

    As an accredited 4-(Piperidine-1-Carbonyl)Phenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed 5-gram amber glass vial with tamper-evident cap, labeled with chemical name, purity, CAS number, and safety warnings.
    Shipping The chemical 4-(Piperidine-1-Carbonyl)phenylboronic acid is shipped in tightly sealed containers to prevent moisture ingress. It is packaged according to regulatory standards, labeled appropriately, and transported under ambient conditions unless otherwise specified. Ensure compliance with local, national, and international shipping regulations regarding hazardous materials and chemical substances.
    Storage Store **4-(Piperidine-1-carbonyl)phenylboronic acid** in a tightly sealed container, protected from moisture and direct sunlight. Keep at room temperature (15–25°C) in a cool, dry, well-ventilated area. Avoid exposure to air and incompatible substances such as strong oxidizers. Handle under inert atmosphere if possible to maintain stability and prevent hydrolysis or degradation.
    Application of 4-(Piperidine-1-Carbonyl)Phenylboronic Acid

    Applications of 4-(Piperidine-1-Carbonyl)Phenylboronic Acid in Industrial Manufacturing

    As a specialized manufacturer of 4-(Piperidine-1-Carbonyl)Phenylboronic Acid, we supply this advanced boronic acid derivative for select downstream sectors where complex molecule synthesis and quality consistency are central to industrial production. Our technical input supports clients through strict compliance, integration into critical process steps, and stable quality management for demanding applications such as pharmaceutical R&D, active pharmaceutical ingredient (API) manufacturing, peptide coupling, and advanced agrochemical intermediate development.

    1. Pharmaceutical API Synthesis

    Major pharmaceutical plants utilize this boronic acid as a vital coupling agent and building block in the multi-step synthesis of high-value APIs, particularly for kinase inhibitors and next-generation oncology compounds. Due to strict traceability and complete documentation requirements, the raw material’s consistent purity and analytical profile are mandatory throughout development and scale-up, ensuring reproducible performance across process validation and manufacturing batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 1 and 21 CFR Part 210/211 (US FDA)
    • Ph. Eur., USP, JP for relevant finished APIs (as required)
    • DEA, EDQM, and local regulatory dossiers (where applicable)

    Typical usage ratio

    • Commonly 1.0–1.4 equivalents relative to the halogenated or pinacol boronate partner in Suzuki-Miyaura cross-coupling; may increase up to 1.8 equivalents for scale-up validation or poorly reactive substrates.

    Downstream process integration

    • Incorporated during C–C or C–N bond formation in key intermediate coupling stages; often handled under inert atmosphere in jacketed reactors, followed by aqueous or organic extraction and chromatographic purification under cGMP guidelines.

    Final product types

    • Small molecule kinase inhibitors
    • Pyridine-bearing antineoplastic agents
    • Advanced lead candidates for clinical trial supply
    • Late-stage drug substance intermediates

    2. Pharmaceutical Process Research and Lead Optimization

    Medicinal chemistry divisions at leading pharmaceutical firms and CROs employ this boronic acid in custom synthesis programs for rapid lead optimization, enabling structure-activity relationship (SAR) studies and derivatization of core pharmacophores. Its reliable reactivity profile aids chemists in minimizing byproduct formation during aromatic functionalization, which accelerates decision cycles from hit to candidate selection under GLP-compliant project management.

    Industry compliance standards

    • GLP (Good Laboratory Practice), OECD Principles of Good Laboratory Practice
    • Corporate QC and traceability guidelines (e.g., electronic lab notebook data integrity)
    • REACH/TSCA compliance for handling and documentation
    • Corporate safety assessment protocols (internal material safety documentation)

    Typical usage ratio

    • 0.8–1.5 equivalents, frequently modulated by structure complexity and required purity for next-step transformations; adjusted based on in-lab HPLC or NMR monitoring.

    Downstream process integration

    • Dissolved or suspended in polar aprotic solvents (e.g., DMF, DMSO) for parallel synthesis on mg–gram scale; introduced at late-stage coupling or diversity-oriented synthesis steps prior to analytical purification.

    Final product types

    • Novel heterocyclic scaffolds for SAR panels
    • Early-phase clinical lead compounds
    • Reference molecules for analytical standards
    • Fragment libraries for kinase and receptor screening

    3. Peptide and Peptidomimetic Drug Development

    Specialty peptide companies and custom synthesis CDMOs use 4-(Piperidine-1-Carbonyl)Phenylboronic Acid as a unique boronic moiety for peptide and peptidomimetic side-chain installation, offering non-standard backbone features required in targeted peptide medications and diagnostic agents. By facilitating the introduction of boron groups via chemoselective ligation, manufacturers expand the toolbox for novel conjugate and stabilizing motif production under auditable cGMP conditions.

    Industry compliance standards

    • US FDA Guidance for Industry: Peptide Drug Products
    • ICH Q11 (Development and Manufacture of Drug Substances)
    • ISO 13485 (for peptide-based IVD reagents)
    • EMA/FDA clinical supply chain traceability requirements

    Typical usage ratio

    • Typically 0.5–1.2 equivalents per coupling site; marginal increases up to 1.5 equivalents are sometimes applied for introducing boronic functionality to stabilized peptides with sterically-demanding environments.

    Downstream process integration

    • Applied during solid-phase peptide synthesis after primary chain assembly; boronic acid moiety is installed via post-synthetic coupling or incorporated into resin-bound sequences prior to cleavage and deprotection—integrated with in-process HPLC and LC/MS purity checks.

    Final product types

    • Boron-modified therapeutic peptides
    • Diagnostic peptide standards
    • Peptidomimetic APIs for clinical evaluation
    • Advanced intermediates for bioconjugation

    4. Agrochemical Intermediate Synthesis

    Major agrochemical companies and contract manufacturers incorporate this boronic acid as a functional arylboronic unit in the synthesis of advanced crop protection agents. Its role as an intermediate enables late-stage diversification and the assembly of heterocyclic active segments critical to the performance of modern herbicides and insecticides, while maintaining compliance with agricultural and environmental synthesis standards.

    Industry compliance standards

    • ISO 9001:2015 certified synthesis and QC procedures
    • FAO/WHO specification (active ingredient and impurity threshold)
    • Mandatory local agrochemical registration (EPA, EU Regulation 1107/2009)
    • OECD GLP for development of new active substances

    Typical usage ratio

    • Adopted at 1.0–1.5 stoichiometric equivalents relative to halide or triflate precursors in Suzuki-type couplings; process optimization may justify use of up to 2.0 equivalents to drive complete conversion at kilogram scale.

    Downstream process integration

    • Introduced during late-stage cross-coupling for aryl modification, under controlled solvent and base conditions, followed by aqueous workup and distillation or crystallization for intermediate isolation prior to active ingredient formulation.

    Final product types

    • Aromatic heterocycle-based herbicide intermediates
    • Advanced insecticidal active ingredient precursors
    • Seed treatment formulation intermediates
    • Chemical building blocks for patent-protected crop protection agents
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    Certification & Compliance
    More Introduction

    Introducing 4-(Piperidine-1-Carbonyl)Phenylboronic Acid: Our Perspective from the Production Floor

    Making Chemistry Work: What Sets Our Product Apart

    In today’s world, the demands on chemical manufacturers extend far beyond traditional production. As a producer of specialty boronic acids with decades of experience, every kilogram leaving our factory carries with it our commitment to purity, consistency, and innovation that meets the strictest standards of advanced industries. 4-(Piperidine-1-carbonyl)phenylboronic acid stands out in our product portfolio because it answers a recurring challenge for customers working in pharmaceuticals and advanced materials development: reliability in both synthesis and downstream transformations.

    The best way to describe this compound is to draw from the countless hours our chemists have spent perfecting its manufacturing process. We take raw materials through a complex route, tuning reaction parameters and purification schemes until the product crosses the finish line: a white to off-white powder, always characterized by tight control of moisture and residual solvents. Our facility focuses on batch traceability and integrated analytical control, so every drum we send comes backed by a full suite of data that matches precisely the laboratory’s expectations.

    Why 4-(Piperidine-1-Carbonyl)Phenylboronic Acid?

    In drug discovery, the reliability of a building block shapes how quickly and efficiently a project can move from the lab bench to research milestones. Medicinal chemists have faced spoiled experiments and inconsistent yields whenever small impurities or variable moisture levels sneak in. From our direct feedback with partners, one reality remains: purity never takes a back seat. For 4-(Piperidine-1-carbonyl)phenylboronic acid, we maintain HPLC purity over 98% and residual water well below 0.5%. Experience has shown us that when purity slips, reaction efficiency dwindles and impurities propagate throughout multistep syntheses, forcing reruns and driving up costs.

    Our technical staff still remember the story of a project halted by an unexpected contaminant that came with a lower-tier material: six weeks lost, resources spent, and confidence shaken. Fixing such setbacks means digging deep into the plant’s operational data to pinpoint if it came from the boronic acid’s production stage or a transfer issue. After hundreds of optimizations, every lot now comes with real transparency: LC-MS, NMR, and moisture reports that satisfy every customer audit.

    Other suppliers claim tight control, but as the producer, we know the truth rests in process histories. We use closed transfer lines for all moisture-sensitive intermediates, and our operators train annually in glovebox sampling for boronic acid derivatives. This attention to detail is not industry-wide, but we believe it is essential for products like 4-(Piperidine-1-carbonyl)phenylboronic acid, where air and trace water can rapidly ruin a batch.

    Downstream Use: Creating Value Beyond the Drum

    Our customers span pharmaceutical R&D teams and custom synthesis CROs working with palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura. For these critical transformations, the boronic acid component plays an outsized role: when defective or tainted by trace byproducts, it becomes the limiting factor. We take customer feedback seriously and have tailored both granularity and containerization based on their unique workflow requirements. Direct shipments to North America and Europe align with GMP documentation for clinical candidates, and our warehousing solutions guarantee that every order arrives with minimum transit-induced moisture exposure.

    The synthesis itself demands careful management of heat, reagent addition, and solvent recovery, since the piperidine ring and carbonyl group bring a new layer of sensitivity to the boronic acid’s usual handling characteristics. Considerations like these drive why we developed specialized drying processes, with in-line Karl Fischer titration as a routine step. Our operators regularly discuss these improvements with our process chemists, seeking further minimization of side reactions such as oxidation or boroxine formation—a recurring headache for those who cut corners at the factory level.

    Comparison: How Our Product Differs from Other Boronic Acids

    Creating 4-(Piperidine-1-carbonyl)phenylboronic acid in-house means more than just a change of functional group—this compound’s synthetic and purification steps present a greater challenge than lower-molecular-weight or non-heterocyclic boronic acids. The piperidine carbonyl group demands anhydrous conditions and sympathetic pH control to avoid hydrolysis or over-oxidation. From our laboratory’s perspective, standard phenylboronic acid often tolerates open air for storage and use; our specialized product does not, so we designed an inert-atmosphere packaging suite in response. Process-wise, yields fluctuate more in open reactors, so closed, continuously monitored reactors now handle almost every major intermediate, ensuring the profile meets what our customers expect for late-stage pharmaceutical intermediates.

    We often receive questions about whether generic boronic acids can substitute for this derivative in cross-coupling screens. Our experience is that the unique electronic influence from the carbonyl-piperidine system tunes its reactivity in ways other boronic acids cannot match. For instance, in lead optimization syntheses, medicinal chemists lean toward our compound for forming biaryl or heteroaryl linkages where additional polar or hydrogen bonding interactions enhance target selectivity. Cheaper or more generic options tend to fall short here, delivering either poor yields or inconsistent product distributions. We understand firsthand that switching to a less sophisticated boronic acid is not just a cost-saving maneuver; it often means risking an entire project’s timeline.

    Handling and storage differences may seem minor, but they shape the day-to-day routines for lab and plant personnel. Our boronic acid ships in argon-purged, high-barrier containers with full humidity trackers. Many commodity-grade boronic acids forgo such protection, focusing only on large-scale inorganic applications. As a manufacturer, we monitor these nuances through regular stability testing, assembling real-world shelf-life data so customers avoid surprises. Our data shows that, even under ambient conditions, product integrity holds for upwards of twelve months with proper storage, while substitutes suffer rapid color changes and loss of reactivity in a fraction of that time.

    Operational Insights: What Manufacturing Teaches Us About Quality

    On the production floor, watching a crew prepare, charge, and react these starting materials in precise order underscores how crucial in-process control is. Our team knows each operation’s rhythm: whether a batch needs a bit more drying under vacuum, or whether crystallization proceeds too rapidly under suboptimal cooling. The blend of years of muscle memory and modern process analytics means we catch the “invisible” process faults that competing facilities too often miss. Each operator’s diligence in monitoring and testing yields tangible benefits—projects keep moving, and we don’t hear about stalls due to poor raw materials.

    Compliance also stands as an unglamorous but non-negotiable marker of product trustworthiness. Our team submits every lot for third-party residual solvent analyses and upholds REACH and local health authority rules. Auditors increasingly scrutinize trace-level contamination and batch reproducibility. By taking ownership of sourcing our own starting materials and running end-to-end manufacturing under one roof, we create a transparent supply chain—a feature many traders and bulk resellers simply can’t offer.

    Beyond the numbers, we find constant learning through direct engagement with formulation scientists and project managers at major pharmaceutical and fine chemical companies. Whether they ask for grams for pilot studies or multi-kilogram quantities for clinical ingredient synthesis, the requests always carry the expectation: no loose ends, no late surprises. Any deviation, even down to slightly elevated residual halide content or crystallite size, triggers far-reaching effects on their downstream workflow. These conversations motivate internal improvements and have shaped the product’s evolution over the years.

    Troubleshooting and Solutions: Turning Setbacks Into Progress

    Every experienced manufacturer has confronted setbacks—reaction vessels foaming from trace amines, sticky crystals that won’t filter, NMR signals blurred by resin fragments. In the early days, inefficiencies forced line shutdowns until we tracked contamination to one particular transfer pump. Our maintenance crew and chemists convened, swapping out seals and modifying the pump’s contact surfaces to be inert to the boronic acid solution. Small technical corrections like this, rooted in deep process knowledge, have driven our track record of delivering a product with reliable batch-to-batch reproducibility.

    Customers sometimes face issues scaling up Suzuki couplings or hydrogenations with new boronic acid suppliers. The difference often traces to subtle process impurities—non-volatile bases, fine metal residues, or variable particle sizes. Because we manage every step from synthesis to packaging, we adapt on the fly: purging lines, tightening drying protocols, or onboarding new filtration media as new customer requirements surface. Their feedback closes a loop, leading to refinements in both process and product. For a product as finely tuned as 4-(Piperidine-1-carbonyl)phenylboronic acid, we view this dialogue as vital.

    We never approach challenges as isolated incidents. Instead, every batch history gets logged, audited, and mined for learnings that drive future improvements. This approach let us phase out problematic solvents, introduce more effective in-process controls, and improve environmental safety through closed-loop exhaust and waste treatments. Each lesson translates to measurable, actionable change—all benefits that partners see down the line in deliverable quality and reliable timelines.

    The Human Factor: Skill, Training, and Experience Behind Every Batch

    People make the difference between commodity-grade chemicals and truly reliable building blocks. Factory staff acquire skills not by rote but by working through real-world issues at the reactor, filtration, and drying stations. A seasoned operator might spot an off-color solution or a subtle odor, signaling a need for analytical review well before release. We back this intuition with rigorous, up-to-date training and invest in keeping operating manuals current with industry best practices—never letting process drift become anyone’s silent adversary.

    Mistakes sometimes slip through, but a culture of open reporting means problems rarely repeat. Each operator knows the stakes: one missed check can snowball into wasted batches or even liability for customers downstream. We encourage regular knowledge sharing—junior staff learn from veterans, and everyone understands not just the “how” but the “why” of process controls. For specialty products like 4-(Piperidine-1-carbonyl)phenylboronic acid, this experience forms the backbone of consistent production.

    Meeting Regulatory and Documentation Needs

    Pharmaceutical and biotech industries expect more than an acceptable certificate of analysis. Our internal documentation exceeds what auditors require. Each lot accompanies full NMR, HPLC, LC-MS, water content, and metals screening, along with a narrative batch record that details every deviation and corrective action. We keep digital records archived in secure data systems, and staff periodically review documentation to catch trends or recurring signals. Regulators now expect chain-of-custody visibility, and our plant answers that call without hesitation.

    Some may underestimate the challenge, but supplying authenticated analytical data for every shipment holds customers’ trust. Our in-house QA chemists collaborate closely with process teams to update specifications in light of any new findings—be it an environmental risk or a persistent minor impurity—ensuring customers never face compatibility surprises with evolving project requirements. Real-world compliance keeps our doors open and competitor claims honest.

    Continuous Improvement: Where We Go From Here

    The manufacturing environment never stays static. Equipment upgrades, procedural changes, and customer-driven variation become part of the daily landscape. We field inquiries about custom pack sizes, extended stability profiles, or new impurity thresholds, all of which feed back into how we plan and execute each campaign of 4-(Piperidine-1-carbonyl)phenylboronic acid. We run worst-case scenario stress tests and aging studies to inform storage protocols, and we continually pilot zero-waste and green chemistry approaches to minimize footprint where possible.

    Every new request or issue, whether it comes from a major multinational or a lean start-up, gets the same level of attention. Adaptability—backed by solid data, operator skill, and process control—lets us respond to market realities without cutting corners. From our perspective, the future of boronic acid manufacturing will depend on this balance between tight quality adherence and rapid process learning—not just adherence to old routines but true evolution guided both by experience and auditable results.

    Conclusion: Real Value from Direct Manufacturing Experience

    4-(Piperidine-1-carbonyl)phenylboronic acid embodies what it means to turn expertise, diligence, and pride into something greater than the sum of its molecular structure. As manufacturers, we stand behind every batch, guided by lessons only learned through hands-on chemistry and decades of meeting demanding customer standards. Our commitment traces from the first lab experiment to the last drum on the loading dock, with a steady eye on continuous improvement, transparency, and open communication with every stakeholder in the supply chain. From where we stand, that approach delivers more than just chemicals—it delivers confidence to keep unlocking new scientific possibilities.