Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
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Nipecotic Acid

    • Product Name Nipecotic Acid
    • Alias Gabitril
    • Einecs 212-753-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    949018

    Cas Number 498-95-3
    Iupac Name Piperidine-3-carboxylic acid
    Molecular Formula C6H11NO2
    Molar Mass 129.16 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 246–250°C
    Solubility In Water Soluble
    Pka 4.4 (carboxyl), 10.6 (amino)
    Boiling Point Decomposes before boiling
    Synonyms Nipecotinate, 3-Piperidinecarboxylic acid
    Storage Conditions Store at 2-8°C
    Pubchem Cid 9867

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

    Packing & Storage
    Packing Nipecotic Acid is supplied in a 25g amber glass bottle with a tamper-evident cap, labeled for laboratory use.
    Shipping Nipecotic Acid is shipped as a solid chemical in tightly sealed containers to prevent moisture absorption and contamination. It is stored and transported under cool, dry conditions, away from incompatible substances. Proper hazard labeling and handling procedures are observed in accordance with regulatory and safety guidelines for chemical shipments.
    Storage Nipecotic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep the container protected from moisture and direct sunlight. Store at room temperature, typically between 15–25°C (59–77°F). Ensure proper labeling and prevent accumulation of dust to minimize exposure and contamination risks.
    Application of Nipecotic Acid

    Applications of Nipecotic Acid in Industrial Manufacturing

    Nipecotic Acid serves as a specialized intermediate in industrial manufacturing for active pharmaceutical ingredients and fine chemicals. Our integrated production supports regulatory-driven applications requiring strict purity, controlled handling, and traceable quality parameters across diverse downstream sectors.

    1. Active Pharmaceutical Ingredient Synthesis (Anticonvulsant APIs)

    Pharmaceutical producers widely adopt Nipecotic Acid as a core precursor in the synthesis of new-generation anticonvulsant drugs, including certain gamma-aminobutyric acid uptake inhibitors. Chemists incorporate it into multi-step processes to modulate GABA-ergic pathways with precise control of stereochemistry and impurity profiles. Manufacturers demand consistent batch records to maintain compliance with finished dosage regulations for regulated markets, driving repeat-use in API manufacturing and validation batches.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredients
    • United States Pharmacopeia (USP) and European Pharmacopoeia (EP) monograph impurity limits
    • FDA 21 CFR Part 211 cGMP for finished pharmaceuticals
    • Audit traceability under PIC/S guidance for pharmaceutical intermediates

    Typical usage ratio

    • Intermediary step using 0.3–0.75 mole Nipecotic Acid per mole of target compound, adjusted by stoichiometry
    • Optimized in pilot scale to 98–102% material utilization for API purity

    Downstream process integration

    • Introduced at early condensation or coupling stage in API route
    • Requires controlled-temperature and pH conditions with monitored addition speed
    • Critical for chiral purity, checked by HPLC or GC in process controls

    Final product types

    • Antiepileptic bulk APIs (e.g., tiagabine)
    • Research compounds for CNS modulation
    • Regulated pharmaceutical intermediates for licensing partners
    • Clinical trial material for neuropsychiatric drug programs

    2. Research Reagent Manufacturing for Neuroscience

    Referencing peer-reviewed studies, laboratory reagent suppliers source Nipecotic Acid for downstream formulation into analytical and preclinical assay kits that analyze neurotransmitter modulation and GABA transport. Product consistency and absence of interfering byproducts remain essential for data reliability, pushing demand for high-purity lots and documented syntheses validated by independent laboratories. Contract manufacturers prioritize secure chain-of-custody and rapid batch-release under signed quality agreements to support regulated global research.

    Industry compliance standards

    • ISO 9001:2015 quality management for analytical reagent suppliers
    • OECD Good Laboratory Practice (GLP) for preclinical testing
    • REACH registration for import and distribution in the EU
    • Safety Data Sheet (SDS) provision per GHS for laboratory use

    Typical usage ratio

    • Standard formulation at 1–10 mM stock concentrations in buffer solutions
    • Precision weighed quantities, typically 5–100 mg per kit depending on application

    Downstream process integration

    • Dissolved directly into buffer or cell culture medium for in vitro assays
    • Used in receptor-binding, enzyme inhibition, and uptake measurement workflows
    • Packaged in aliquots with batch-specific CoAs in temperature-stable transport

    Final product types

    • GABA transporter inhibition assay kits
    • Reference reagents for CNS research services
    • Custom-labeled preclinical screening products for CROs and academic labs
    • Specialty analytical solutions for regulated neuroscience trials

    3. Intermediate for Advanced Organic Synthesis

    Nipecotic Acid supports custom synthesis houses and fine chemical manufacturers producing complex heterocyclic scaffolds for specialty molecules. Its cyclic amine structure offers versatile reactivity in multi-step syntheses for contract research and industrial-scale custom chemical production. Sourcing at scale requires clear material provenance, impurity tracking, and adherence to customer-specific material specifications integrated into confidentiality-driven technical agreements.

    Industry compliance standards

    • ISO 9001:2015 quality management for fine chemical supply
    • Customer-defined impurity and residual solvent limits
    • Controlled substance precursor tracking policies as needed
    • Material tracing to original batch through lot-coded documentation

    Typical usage ratio

    • 0.1–1.0 equivalents based on downstream heterocycle formation target
    • Reaction stoichiometry tuned by project-specific reaction pathway

    Downstream process integration

    • Introduced as a ring-building block in transition-metal catalyzed reactions
    • Functional group transformations by acylation, alkylation, or reductive amination
    • Reaction monitoring by NMR or LC-MS to ensure target molecular integrity

    Final product types

    • Specialty heterocyclic intermediates for agrochemical development
    • Building blocks for photoinitiators and fine chemicals
    • Custom molecules for contract research organizations (CROs)
    • Functionalized scaffolds for advanced material science prototyping

    4. Precursor in Peptide Mimetic Synthesis

    Peptide and peptidomimetic manufacturers utilize Nipecotic Acid to introduce conformational stabilization in peptide analogues for drug discovery and biochemical exploration. Its rigidified piperidine core modulates bioactivity, solubility, and metabolic pathway engagement. Our supply teams meet the rigorous demands for high-purity, low-residual-metal, and documented origin mandated by regulated peptide production protocols.

    Industry compliance standards

    • ISO 13485 for medical-grade peptide manufacturers (when required)
    • USP/NF guidelines for peptide API precursors
    • Supplier qualification and traceability audits under cGMP for pharma use
    • REACH compliance for distribution to European processors

    Typical usage ratio

    • 0.5–1.2 equivalents per peptide chain, depending on designed sequence and coupling efficiency
    • Loading based on solid phase synthesis resin functionalization and desired yield

    Downstream process integration

    • Incorporated during solid-phase or solution-phase peptide elongation
    • Activated in situ by coupling agents such as HATU or PyBOP
    • Cleaved and isolated for analytical matching to structure-activity requirements

    Final product types

    • Bicyclic or constrained peptide analogues for drug lead libraries
    • Bioactive peptide conjugates for in vivo and in vitro research
    • Investigational peptide APIs in preclinical development
    • Diagnostic peptide standards for reference laboratories
    Free Quote

    Competitive Nipecotic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Nipecotic Acid: Supporting Advanced Synthesis in Modern Chemical Manufacturing

    Understanding Nipecotic Acid From the Manufacturer’s Perspective

    Nipecotic acid has played a key part in chemical synthesis for decades. In our production lines, we encounter nipecotic acid most often as a white crystalline powder, recognized for its purity and stability under normal handling. We have spent years fine-tuning our process to ensure every batch meets lab-grade expectations. What sets our nipecotic acid apart rests on foundational experience and ongoing improvement, not just adherence to a formula or checklist.

    Structurally, nipecotic acid falls within the family of piperidine carboxylic acids, commonly referenced by its IUPAC name: piperidine-3-carboxylic acid. Our main production model focuses on the racemic form, which offers broad compatibility for both research and industrial applications. Chemists in pharmaceuticals and neuroscience target nipecotic acid for its unique action as a γ-aminobutyric acid (GABA) uptake inhibitor. This makes it indispensable for anticonvulsant research and the development of new neurological therapeutics.

    Getting precise, high-purity nipecotic acid takes practical commitment. We control every step, from raw piperidine input to the last crystallization and drying stage. Years on the floor showed us small deviations in temperature or solvent handling can impact final purity. Over many cycles, we developed a protocol that maintains batch consistency, supported by in-house analytics and experienced teams. Every kilogram leaving our plant reflects decades honing the craft of purification, so users count on reproducible results and reliable traceability.

    Getting Quality Right: Beyond Simple Specifications

    A common question: What’s different about the nipecotic acid coming out of this plant, compared to alternatives? Real answers surface in the lab, not just from a certificate of analysis. From our earliest days, we learned high-grade nipecotic acid responds to quality control, not just paperwork. We focus on two main markers—assay purity and low moisture. Our typical batches exceed 99% by HPLC, with moisture tracked closely using Karl Fischer titration. Retained solvents, if present, fall under strict international thresholds. NMR, IR, and LC-MS support each batch release.

    Other producers may match this on paper, but our process brings deep-rooted stability, even in high-throughput manufacturing. Over time, partners told us that minor variations in impurity profiles, or subtle inconsistencies from batch to batch, can disrupt sensitive syntheses. To avoid these pitfalls, our operators have learned to read not just numbers but the products themselves. We won’t release a lot unless we’d use it in our own in-house development. The result is long-term trust from regular clients, whether their work sits in advanced neuroscience, pharmaceutical development, or fine chemical synthesis for further derivatization.

    Application In Research and Industry

    Most nipecotic acid flows into pharmaceutical R&D, where it serves as a precursor or reference ligand. It supports work aiming to regulate GABAergic transmission in neurological disorders. In our own collaborations, we’ve seen nipecotic acid feeding into research on epilepsy, neuroprotection, and cognitive modulation. Its unique ring structure and carboxylic acid group link directly into synthetic strategies—such as the construction of analogs for drug evaluation or the formation of complex heterocycles.

    Our R&D department often runs custom syntheses, leveraging nipecotic acid as a versatile building block. Its amine and acid groups provide two reactive handles for coupling, alkylation, or amidation. N-protection and subsequent derivatization follow with predictable yields, a result of consistent input purity. Nipecotic acid’s robustness during these steps, without unwanted side reactions, saves time and reduces waste. Our in-plant experience checks out lab-scale claims in real-world tonnage, closing the loop between small-scale and manufacturing needs.

    Comparisons With Related Compounds

    Clients often ask how nipecotic acid stacks up to similar piperidine derivatives. Pipecolic acid, for example, shares a similar backbone but targets separate biochemical pathways. Pipecolic acid enters biosynthetic routes for plant and microbial metabolites, while nipecotic acid stays more directly connected to GABA-related research. Piperidine itself, as a simple heterocycle, offers usefulness but without the selective binding or blocking capabilities nipecotic acid provides in neurochemistry.

    Compared to analogs like guvacine or tiagabine intermediates, nipecotic acid’s profile offers balance between synthetic accessibility and receptor specificity. Guvacine, with its own GABA transport inhibitory action, introduces a rigid cyclopentene structure, shifting pharmacological action. Nipecotic acid’s six-membered ring ensures stability and metabolic flexibility in further transformations. Downstream, it enables new derivatives for patent filings, without restrictive sourcing or byproduct complications that sometimes complicate other pathways.

    Experience With Scaling and Customization

    Production experience counts most during scale transitions. In the early 2000s, our team moved from 10-gram to 100-kilo production. Several lessons stuck. During upscaling, solvent recovery, filtration rates, and temperature control shift dramatically. Minor solvent impurities become problematic at scale, which our QC flagged early. Through these years, risk mitigation meant building redundancy into distillation lines, updating filter media, and repurposing older vessels for intermediate holding to minimize contamination.

    In custom syntheses, our flexibility rests not just on plant size, but on cross-training. Small teams carry out checks with full knowledge of the properties and reactions. If a client needs nipecotic acid with specific stereochemistry, such as enantiopure samples for advanced SAR work, we introduce resolution steps or contract with partners for chiral precursors. This saves clients significant time, instead of forcing downstream purification at their own facilities. We routinely accommodate requests for nipecotic acid with specialized impurity profiles for toxicological or metabolic pathway studies. Fast communication with purchasing and R&D ensures material meets demand, not an off-the-shelf minimum.

    Trust Built on Consistency and Validation

    True reliability flows from repeated performance, not single-run perfection. Over multiple audit cycles, regulatory and GMP authorities scrutinize our record-keeping, production batch logs, and analytical tracebacks. Each nipecotic acid lot includes full spectral records, chromatographs, and origin data for critical precursors. We maintain reference samples for tracking shifts in impurity profiles. If a synthetic chemist or regulatory auditor requests historical data for a specific lot, it’s already archived and accessible.

    Our operators and QC staff invest heavily in preventive maintenance and calibration. Equipment used for final crystallization or drying receives regular checkups. Any deviation flags an internal review, with corrective measures implemented before further release. Analytical tools get recalibrated following manufacturer schedules, and personnel undergo refresher training throughout the year. This discipline keeps our production output consistent, year by year. Final product packs in double-lined bags within tamper-evident drums, indexed by unique identification codes linking back to full batch histories.

    Bridging Warehouse and Research Bench

    As a manufacturer, our split attention between industrial buyers and research institutions shapes our distribution philosophy. Bulk shipments often head to pharmaceutical formulators, who require steady deliveries for process validation and early-phase drug manufacture. Meanwhile, universities and biotech startups order in gram-scale, prioritizing rapid turnaround over sheer volume. Both groups benefit from continuous feedback loops. If a client reports an issue, our technical support links directly to the production teams, not intermediaries.

    Freight reliability and climate considerations remain top-of-mind, especially for global destinations. Every drum receives monitoring for temperature excursions during shipping. Some partners request additional documentation—such as certificates for controlled substance import, customs codes, or assurance statements addressing specific local regulatory requirements. We supply these using our own compliance officers, who maintain up-to-date knowledge of import/export standards for our markets in North America, Europe, and East Asia.

    Challenges in the Market and How We Address Them

    Market volatility for raw materials sometimes impacts pricing and availability. Over two decades, we’ve faced disruptions in the global supply chain, ranging from piperidine precursor shortages to international regulatory shifts affecting material classification. Our solution: establish second-source agreements with vetted suppliers and maintain buffer stocks in dedicated storage. This allows us to absorb temporary shocks without passing disruption downstream. During recent transportation crunches, advanced notification on delivery timelines and honest forecasting helped partners adjust schedules or modify orders proactively.

    Competition from lower-cost sources surfaces regularly. Some labs bring in nipecotic acid from offshore producers chasing minimal price points. Clients report occasional issues—like unexpected side products or mismatched impurity levels—which led them back to us for critical projects. Our response stays simple: focus on verifiable quality, responsive support, and product integrity. Long-term, this builds a reputation that price alone can’t displace.

    Environmental Stewardship and Process Safety

    Running a modern manufacturing operation brings environmental responsibilities. Waste minimization and solvent recovery anchor our daily routines. Closed-system extraction and solvent recycling recover over 80% of organics, reducing both costs and emissions. Safe disposal chains for spent acids and mother liquors comply with local and international requirements. Plant effluents get adjusted and tested before any discharge. As technology improved, we redirected some byproducts for use in adjacent fine chemical pathways, converting potential waste into value streams.

    From the training floor to the control room, safety guides our practice. Each operator completes periodic refreshers on materials handling, emergency protocols, and chemical risk awareness. Real-world scenarios and drills keep readiness high. Sensor arrays monitor critical reaction stages, triggering automatic shutdown if conditions drift out of safe range. This focus on process safety didn’t just grow from regulations—it emerged naturally from decades navigating practical challenges with batch chemistry under real pressures.

    Nipecotic Acid for the Next Generation of Research

    In recent years, requests have shifted toward nipecotic acid with tighter impurity profiles, custom chiral purity, and enhanced documentation for regulatory submissions. As the bar rises for preclinical and clinical research, so does our investment in more sensitive analytical tools and documentation processes. We now offer optional services—like origin tracing for all raw materials, restricted-substance declarations, and advanced storage tracking for compliance needs in regulated markets.

    As research builds on GABAergic mechanisms and neurological control, chemists look for flexibility in sourcing—not just bulk quantity. Whether developing novel CNS drugs, studying transport inhibition, or mapping metabolic breakdown, researchers count on reliable input. Our willingness to share process data, support method transfer, and tailor deliveries to new project designs has cemented long-term partnerships with universities, pharma, and contract research organizations worldwide.

    Looking Forward: Innovation and Responsiveness

    The field keeps shifting. New automation tools, digital batch logs, and portable on-line analyzers streamline production tracking and real-time QC. Recently, we rolled out digital signatures and layered barcoding for tighter inventory controls. Clients can now access release data portals linked directly to our quality management systems, cutting paperwork and administrative lag.

    Feedback from customers continues to drive improvements. In response to growing focus on green chemistry, we invest in alternative solvents and synthetic strategies that trim hazardous byproducts. Recently, we piloted a more energy-efficient heating regimen for critical steps, reducing emissions and operating costs alike. Instead of treating sustainability as marketing, we treat it as a practical necessity that strengthens both product quality and regulatory acceptance.

    Collaborative Spirit Strengthens Delivery

    Day to day, our plant engineers, chemists, and support staff work alongside clients and researchers at each phase: from first inquiries to troubleshooting application issues. This close-knit collaboration makes real-time adaptation possible. Whether adjusting a batch to meet new regulatory standards or fine-tuning a custom lot for a specific analytical threshold, openness at every step keeps projects moving forward.

    We’ve seen firsthand that supporting scientific progress relies on more than materials—it flows from shared knowledge, transparency, and trust built on thousands of exchanged emails, phone calls, and site visits. Our knowledge grows from success and occasional mistakes, always shared back with the people who use our products. This builds resilience and agility throughout our organization and our customers’ research pipelines.

    Conclusion

    Nipecotic acid forms just one part of the complex world of chemical building blocks, but at our plant, it represents decades of craftsmanship, responsiveness, and scientific engagement. We make every effort to deliver what matters most: purity, consistency, comprehensive support, and an open ear to new challenges. In a market hungry for reliability and advancement, experience counts—and our story continues alongside each researcher and developer who depends on nipecotic acid to unlock the next discovery.