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N-Boc-3-Piperidineacetic Acid

    • Product Name N-Boc-3-Piperidineacetic Acid
    • Alias N-Boc-3-(Piperidine)acetic acid
    • Einecs 680-348-4
    • 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

    389317

    Productname N-Boc-3-Piperidineacetic Acid
    Casnumber 218155-71-6
    Molecularformula C12H21NO4
    Molecularweight 243.30
    Appearance White to off-white solid
    Meltingpoint 70-76°C
    Purity ≥98%
    Storagetemperature 2-8°C
    Solubility Soluble in DMSO, methanol
    Synonyms tert-Butyl 3-(2-carboxyethyl)piperidine-1-carboxylate
    Smiles CC(C)(C)OC(=O)N1CCC(CC1)CC(=O)O
    Inchikey ZYJDMUYRRWUVAR-UHFFFAOYSA-N

    As an accredited N-Boc-3-Piperidineacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of N-Boc-3-Piperidineacetic Acid is packaged in a sealed amber glass bottle with a secure screw cap.
    Shipping N-Boc-3-Piperidineacetic Acid is shipped in tightly sealed containers to prevent contamination and moisture exposure. Standard shipping is conducted under ambient temperature conditions. For bulk or sensitive applications, secondary containment and cushioning may be used. Complies with chemical transport regulations, and includes appropriate safety labeling and documentation for safe handling during transit.
    Storage N-Boc-3-Piperidineacetic Acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong acids, bases, and oxidizers. Keep the container tightly closed when not in use. Store at room temperature or as specified by the manufacturer, and ensure proper labeling to avoid accidental misuse. Use appropriate protective equipment when handling.
    Application of N-Boc-3-Piperidineacetic Acid

    Applications of N-Boc-3-Piperidineacetic Acid in Industrial Manufacturing

    N-Boc-3-Piperidineacetic Acid functions as a key protected amino acid derivative in several advanced synthesis routes across the pharmaceutical, agrochemical, and specialty chemical sectors. As the direct manufacturer, we supply this intermediate for specialized process requirements in leading-edge industrial formulations and downstream product development.

    1. Active Pharmaceutical Ingredient (API) Intermediate for CNS Agents

    Major pharmaceutical companies integrate this material as a building block for developing central nervous system (CNS) agents, including selective receptor modulators and neuroactive compounds. It provides a piperidine scaffold with a removable Boc group for controlled reactivity in protected amination, essential during multistep synthesis of drug candidates. Chemists typically include this step prior to deprotection and subsequent coupling, ensuring robust batch control according to validated protocols. Final therapeutic molecules undergo full traceability and impurity profiling, with our raw material supporting consistent downstream outcomes.

    Industry compliance standards

    • ICH Q7 and Q11 guidelines for GMP starting materials
    • Current Good Manufacturing Practice (cGMP, 21 CFR Part 210/211)
    • European Pharmacopeia suitability for API manufacturing
    • FDA Drug Master File (DMF) support on request

    Typical usage ratio

    • 0.2–0.5 mol equivalent relative to core active intermediate; adjusted as per route optimization and batch size scaling from clinical evaluation to commercial supply

    Downstream process integration

    • Added during the synthesis of protected intermediates prior to Boc deprotection and subsequent coupling, used in stepwise CNS small molecule formulation pipelines

    Final product types

    • Antipsychotic and antidepressant APIs
    • Cognitive enhancer APIs for nootropic development
    • Bulk intermediates for neuroreceptor ligand synthesis

    2. Chiral Synthesis for Peptidomimetic Drug Discovery

    Research and development divisions in peptide and peptidomimetic production rely on this raw material to insert a piperidine ring at the γ-position during fragment assembly. Its Boc protection ensures selectivity in stereocontrolled steps, critical for the structural fidelity of peptidomimetic scaffolds. Our compound supports efficient scale-up from milligram-mole screening experiments to pilot batch campaign manufacturing under strict analytical control to minimize racemization and batch-to-batch variation.

    Industry compliance standards

    • USP <1047> for compounding nonsterile drug products
    • GMP requirements from EudraLex Volume 4 Chapter 5
    • Synthetic peptide guidance (FDA and EMA)
    • Quality control by chiral HPLC and NMR verification

    Typical usage ratio

    • 0.9–1.0 mol equivalent per peptide segment in solid-phase or solution-phase assembly; variable to segment length and protecting group strategy

    Downstream process integration

    • Inserted at elongation or cyclization stages for γ-piperidine ring incorporation before global deprotection and purification of peptidomimetics

    Final product types

    • GPCR ligand leads for pharmaceutical screening
    • Protease inhibitor libraries
    • Specialty cyclic peptide scaffolds

    3. Agrochemical Intermediate Synthesis (Herbicide and Fungicide Research)

    Our plant-scale clients in agrochemical production incorporate this material as a precursor in the synthesis of piperidine-containing crop protection compounds. Its use as a masked amine intermediate supports selective N-alkylation and conjugation chemistries, which are essential for generating lead structures during herbicide and fungicide candidate optimization. Quality screening for environmental and residual profiles remains central to downstream product registration and compliance.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) Principles
    • FAO/WHO pesticide specification guidelines
    • REACH registration for intermediate transfer
    • ISO 9001:2015 quality management for raw materials

    Typical usage ratio

    • 5–20% by weight of total batch intermediates; dependent on lead structure complexity and scale, recalculated based on candidate molecular design

    Downstream process integration

    • Introduced during the masked amination step, then followed by deprotection and coupling for lead candidate synthesis and field trial production

    Final product types

    • Pre-emergent herbicide actives with piperidine cores
    • Pesticide candidate libraries for regulatory review
    • Fungicide trial substances for field-testing

    4. Protected Intermediate for Specialty Fine Chemical Synthesis

    Manufacturers of specialty fine chemicals and advanced materials utilize N-Boc piperidineacetic acid in high-purity synthesis where controlled reactivity is required. It enters modular organic synthesis workflows, particularly for crafting functional piperidinyl units in dyes, organic electronic materials, or ligands for transition metal catalysis. The Boc group endows synthetic flexibility, while our batch-level quality and impurity monitoring guarantee consistency and traceability essential for downstream quality-critical applications.

    Industry compliance standards

    • ISO 9001:2015 for quality management in fine chemical manufacturing
    • RoHS and REACH for environmental and safety compliance
    • Supplier audits and traceability (customer-specific requirements)
    • Batch COA aligned with end-user technical specification sheets

    Typical usage ratio

    • 1.5–10 mol% as core building block; adjusted for target molecule ring density, functional group number, and scale of production

    Downstream process integration

    • Fed during condensation or amide bond formation steps, often prior to deprotection and subsequent derivatization within custom organic synthesis schemes

    Final product types

    • Colorimetric and fluorescent dyes with piperidine units
    • Ligands for homogeneous catalysis
    • Organic semiconductors and advanced materials

    5. Intermediate for Pharmaceutical Impurity Profiling and Reference Standards

    Analytical standards suppliers and QC laboratories request this compound as a reference for impurity and metabolite profiling in drug substance development and release testing. It supports the preparation of impurity markers and serves as a qualified comparator for routine quality control, stability studies, and regulatory submission batches, with all specifications traceable to manufacturing documentation and full analytical profiling for trace-level quantification in finished pharmaceutical products.

    Industry compliance standards

    • ICH Q3A/B (Impurities in New Drug Substances and Products)
    • Pharmacopeial impurity reference standard validation (USP, EP, JP)
    • ISO/IEC 17025 for chemical testing and calibration labs
    • GMP-compliant documentation and audit trail support

    Typical usage ratio

    • 0.1–1.0 mg per analytical batch for calibration and method validation; scale based on detection limit and methodology used (e.g., HPLC, LC-MS)

    Downstream process integration

    • Dissolved or spiked into reference mixtures and calibration curves for use in routine and regulatory-release analytical workflows

    Final product types

    • Pharmaceutical impurity reference standards
    • Certified reference materials (CRMs) for drug release
    • Analytical control standards for QC labs
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing N-Boc-3-Piperidineacetic Acid: A Chemist’s Building Block

    Genuine Experience in Synthesis Drives Our Production

    Working with N-Boc-3-Piperidineacetic Acid on a daily basis brings insight that doesn’t come from handling catalog samples or mere descriptions on data sheets. Every batch provides us with firsthand knowledge of its behavior, solubility, and consistency across reactions. We see beyond purity figures. Our team recognizes the quirks and strengths this protected acetic acid derivative brings to different synthetic routes. Chemists crafting APIs or intermediates rely on materials which behave predictably under scale-up, and this product delivers that stability.

    Model, Specifications, and Analytical Experiences

    Our batches align with the industry’s need for consistent quality. Molecular formula C12H21NO4 provides a foundation for accurate identification, yet what matters in actual chemistry is how reliably the product performs and remains free from troublesome contaminants. We routinely analyze each production lot with HPLC and NMR—beyond common mass spectrum checks—to ensure there’s no trace of unprotected amine or decomposed byproducts. Moisture content, residual solvents, and trace metals all get scrutinized because these issues cause headaches during scale-up. From crystallinity to melting point, details are not mere certificate numbers; they shape how smoothly downstream processing flows.

    Some requests call for customization of particle size or for reducing certain impurities below typical detection levels. We have integrated both manual and automated controls at several points, allowing us to adapt output for pharmaceutical as well as fine chemical applications. Having seen both bottlenecked filtration and over-reactivity at pilot scale, we focus sharply on tight pH profiles and precise temperature control during boc protection and ring functionalization.

    Usage in Modern Laboratories and Manufacturing Sites

    N-Boc-3-Piperidineacetic Acid often enters the scene as a protected intermediate, especially in the construction of complex nitrogen heterocycles. Process chemists value the stability the Boc group brings, keeping the piperidine amine untouched through diverse steps—alkylation, peptide coupling, or reductive amination—until needed. We’ve supported both discovery projects crafting new CNS and oncology targets, and GMP campaigns where reactivity and purity determine route viability. Our own development group uses this molecule to build piperidine frameworks, peptidomimetics, and linkers for conjugates, so we produce what we prefer working with ourselves.

    Solubility and compatibility come up repeatedly as deciding factors. This acid dissolves well in many organic solvents—DMF, DCM, and THF included—yielding solutions that facilitate clean couplings and easy workups. We’ve tackled stubborn emulsion problems and provided adjustments to particle characteristics so developers downstream see faster phase separations or easier crystallizations. That level of tuning only comes through pressing real materials through real reactions, not hypothetical “typical” values.

    What Sets Our N-Boc-3-Piperidineacetic Acid Apart

    We’ve handled derivatives from more suppliers than we can recall, often uncovering batch inconsistency, off-color residues, or erratic melting points. Those touches aren’t trivial—they reveal impurities from incomplete reactions or careless purification. Our batches present uniform white crystalline powder, always sharp in appearance, and never leaving doubts about process fidelity. Such quality stems from relentless oversight at each synthetic stage, not just at the packing bench.

    Trace element contamination, especially from older glassware or aging catalyst lots, can sabotage a large-scale coupling or generate regulatory delays. We embrace metal-catalyst scavenging and extra-wash steps for this reason. There’s a marked difference between a casually protected piperidine acid and one produced with repeated attention to sub-ppm impurity profiles. We hear from researchers who’ve suffered from stubborn side products only to find our acids run cleaner and without unexplained NMR signals.

    This compound’s protected acid functionality avoids unwanted deprotection and side reactions common in less robust intermediates. Other piperidine acids, lacking Boc or built on less stable scaffolds, require extra steps to shield the amine or to strip protecting groups at inconvenient points. We take pride in offering a compound that avoids the time sinks and purification headaches seen with less selective alternatives.

    Supporting Real-World Drug Discovery and Process Development

    N-Boc-3-Piperidineacetic Acid plays a key role in early medicinal chemistry, especially where nitrogen-rich scaffolds spark new SAR campaigns. Medicinal chemists appreciate how the intact Boc group travels untouched through demanding transformations. We’ve seen teams lose days to amine protection issues when using less stable alternatives, causing delays in route optimization. Feedback from client labs points to easier workups, fewer byproducts, and more direct in-process analytics when compared to related amine acids.

    For process chemistry scale-ups, reproducibility is everything. We control every batch to support kilo- and multi-kilo manufacturing. Engineers have flagged the importance of having spectral and chromatographic records for every lot. Many asked for extra aliquots for parallel route scouting, and we’re prepared for that level of engagement. Our team collaborates directly with process scientists to balance throughput, robustness, and compliance needs in active ingredient manufacturing.

    Handling also matters at scale. Our material flows well, resists caking, and reacts cleanly in batch or continuous settings. With certain generic versions, we’ve seen clumping or unexplained wetness—often traced back to overlooked moisture pickup or poor post-crystallization handling. Our in-house drying and final packing routines guard against those frustrations.

    Manufacturing Integrity and Audit Readiness

    Over the years, auditors drilling into traceability and data integrity have pushed our production standards higher. Every batch, from initial raw piperidine source to Boc-protection and carboxylation, follows validated SOPs tied directly to our electronic batch manufacturing records. Documentation runs complete, and all analytical results are stored and accessible for future assessments. This means process chemists and regulatory teams receive what they need without chasing paperwork or piecing together loose ends. Having worked with numerous auditing teams, both local and international, we anticipate the kinds of questions that matter—be it trace impurity evidence, reagent provenance, or lot sample reserves.

    We invest in GC and LC-MS access at multiple points, not just for end-product release, but for tracking byproducts through every critical stage. Knowing which side-products exist, even if benign, helps prevent scale-up surprises or regulatory rework. Those lessons stem from years of internal route extension projects, not just theoretical risk assessments. If a customer encounters a downstream incompatibility, we support troubleshooting, not by referring back to literature, but by running split tests and benchmarking solutions in our own labs.

    Supporting Innovation with Consistent Supply

    Our supply chain avoids the typical bottlenecks and surprises that come with relying on outside parties for raw piperidine sourcing. By handling Boc-activation and acetic acid extension ourselves, we guarantee direct oversight on inventory and batch reserves. This matters during tight timelines—our customers count on immediate access to the lots they need, with pre-shipment samples sent within days rather than languishing in transit or customs.

    On more than one project, a stock-out or shipping hold elsewhere would have halted critical medicinal chemistry. With us, the direct line from production vessel to custom packaging protects clients from those delays. Years of experience managing scale-up, regulatory requests, and customs challenges underpins our ability to keep timelines on track, whether for a bench-scale method scout or a commercial delivery.

    Environmental Considerations and Process Sustainability

    Years ago, process improvements felt incremental. Recent changes in regulation and pressure for greener approaches have changed that. We’ve adopted less hazardous solvents and optimized Boc-protection steps to reduce waste and lower process mass intensity. Reusing filtered solvents and capturing emissions isn’t just regulatory—recycling helps manage costs, improves safety, and meets client sustainability demands. Solvent minimization and careful pH control also allow for safer waste stream disposal, both for us and for our customers during scale-up and production runs.

    We monitor carbon, nitrogen, and phosphorus waste at every release stage, not out of obligation but because previous overlookings led to downstream headaches. Our local environment, especially water treatment, has benefited from these adjustments. We know that for many sites making the next API or development candidate, environmental audits can halt or delay progress with little notice. By documenting and minimizing process byproducts and demonstrating solvent recovery practices, we help smooth the path for both pilot and commercial launches.

    Differences from Related Piperidine Acids and Boc-Protected Variants

    We often see confusion between N-Boc-3-Piperidineacetic Acid and its close relatives—unprotected acid, 4-piperidineacetic acid, or higher homologues. Our product stands out by providing selective protection on the nitrogen while keeping the primary acid accessible. Unprotected acids create route complications, inviting premature functionalization or the need for extra safety measures. Other Boc-piperidines, whether 2- or 4-substituted, often shift regioselectivity. Experimental findings demonstrate how the 3-acetic acid configuration offers distinctly different coupling outcomes, sometimes altering the final stereochemistry or adding steps later in the synthesis flow.

    Boc-protected analogs lacking a carboxylate group cannot serve as linkers or intermediates where further chain extension or peptide synthesis matters. We also see requests for derivatives with both amine and acid unprotected, but the unpredictability of downstream functionalization makes those versions unreliable for tight SAR work or scale-up. Our product’s dual protection and positioning prevent the common yield drops and rework cycles that plague less specific intermediates.

    Collaborative Troubleshooting and Process Support

    In daily operations, issues arise—whether in process development or analytical. Our background in both manufacturing and applied chemistry allows us to support partners through stumbling blocks. We don’t just ship out bulk product and wait for feedback. Our technical team carries experience in bench chemistry, pilot verification, and regulatory filings. Whether the challenge involves solubility, chiral resolution, or purification, we walk through problems in our own facility before proposing solutions.

    Researchers have hit snags with sequence coupling yield or protecting group removal—often a small adjustment, such as slower Boc cleavage or a better choice of coupling reagent, resolves these bumps. We’ve even run comparisons using different bases, solvent loads, or crystallization temperatures to replicate clients’ outcomes and recommend real, workable improvements. If a team needs to track down a source of unexplained impurity, we draw on internal records from every batch made since our first supply, using actual data to map potential root causes.

    Responding to Market Demands with Transparency

    Industry shifts, such as tightened API manufacturing regulations and increased focus on trace contaminants, have shaped our ongoing improvements. Direct conversations with quality assurance teams taught us that even small inconsistencies—color changes, off-odors, microdroplets of unknown liquid—undermine confidence. We hold detailed lot histories for every client and continue updating them as production, purification, and packaging practices evolve.

    Customers come back asking not for the lowest cost, but for the reliability and traceability proven in practice. Shortages, batch retesting, and process upsets all disrupt research and production cycles. That’s why we provide open access to analytical data, answer specific questions about reagent origins, and support flexible lot segmentation for different process pathways, whether for early research quantities or commercial campaigns.

    Looking Forward: Shaping the Next Chapter in Protected Piperidine Chemistry

    With regulatory scrutiny intensifying and performance demands outpacing legacy intermediates, we see growing reliance on robust, multipurpose building blocks like N-Boc-3-Piperidineacetic Acid. Practice teaches what theory cannot: details matter, shortcuts multiply problems, and ongoing dialogue with users yields superior results. It’s not only about what goes right, but how quickly and accurately we solve the occasional difficulty. Our commitment—shaped by years spent in the lab, years spent debugging scale-ups, and years learning from customer feedback—brings the kind of material you can bet your next synthesis on.

    Every gram of N-Boc-3-Piperidineacetic Acid leaving our facility reflects those lessons. The finished product is not just a commodity, but a tested, trusted intermediate on which entire discovery and development campaigns depend. We stand behind every batch with the transparency, reliability, and spirit of partnership that only a manufacturer rooted in hands-on chemistry can offer.