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Kainic Acid

    • Product Name Kainic Acid
    • Alias Dkainic
    • Einecs 205-525-5
    • 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
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    Specifications

    HS Code

    409314

    chemical_name Kainic Acid
    cas_number 486-85-1
    molecular_formula C10H15NO4
    molecular_weight 213.23 g/mol
    appearance White to off-white crystalline powder
    solubility Soluble in water and methanol
    melting_point 225-230°C
    synonyms Domoic kainic acid, Kainate
    storage_temperature Store at 2-8°C
    usage Glutamate receptor agonist
    purity Typically ≥98%
    iupac_name (2S,3S,4S)-3-(carboxymethyl)-4-isopropenylpyrrolidine-2-carboxylic acid
    stability Stable under recommended storage conditions
    hazard_statements Harmful if swallowed, causes serious eye irritation

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

    Packing & Storage
    Packing Kainic Acid is packaged in a 100 mg amber glass vial, sealed with a screw cap, and labeled with hazard information.
    Shipping Kainic Acid is shipped in tightly sealed, leak-proof containers, typically under ambient conditions unless otherwise specified. It is packed and labeled according to regulatory guidelines for hazardous chemicals. Shipping documentation includes safety data sheets (SDS), and all packages are handled to prevent exposure, damage, or contamination during transit.
    Storage Kainic Acid should be stored in a tightly sealed container, protected from light and moisture, at a temperature of -20°C. It should be kept in a well-ventilated, dry area, away from incompatible substances such as strong oxidizers. Proper labeling and secure storage are essential to prevent unauthorized access, as it is a neurotoxic compound used primarily for research purposes.
    Application of Kainic Acid

    Applications of Kainic Acid in Industrial Manufacturing

    Kainic Acid is a high-purity amino acid derivative primarily utilized in specialized pharmaceutical and life science sectors. As a direct manufacturer, we support leading research institutions, pharma process developers, and analytical reagent producers with industrial-scale grade and traceability. Below are the major downstream applications validated in genuine B2B production environments.

    1. Pharmaceutical Intermediates for CNS Drug Research

    In drug discovery and preclinical manufacturing, Kainic Acid functions as a critical intermediate to model excitotoxic neural injury and test neuroprotective compounds. Formulation chemists and pilot plant managers require high batch reproducibility and strict impurity profiles to maintain consistency in CNS-targeted compound development. Larger batches for GLP or GMP environments must demonstrate traceable quality through internal systems and third-party audits. Raw Kainic Acid enters process streams as a base material in the synthesis of receptor agonists and analytical standards for pharmacological assays.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211: Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs
    • USP: Reference for analytical standard materials
    • REACH (EU) registration and safety data compliance

    Typical usage ratio

    • Batch-dependent; from 0.01% to 0.5% by weight in model compound syntheses, adjusted based on target pathway and scale-up requirements

    Downstream process integration

    • Introduced after initial solvent charging and before main condensation reactions in CNS ligand synthesis
    • Weighing and dissolution step under nitrogen or inert gas to prevent degradation
    • Post-reaction chromatographic purification as a quality control checkpoint

    Final product types

    • Reference CNS pharmacological compounds
    • Validated analytical standards for preclinical testing
    • Neurotoxicity research reagents for academic/industrial labs

    2. Analytical Reagents for High-throughput Neurochemical Screening

    Analytical laboratories and OEM reagent suppliers apply Kainic Acid in manufacturing neuroactive screening kits. These kits enable quantification and modulation of glutamate receptor activity within biopharmaceutical quality control and neuroscience R&D. All inputs must demonstrate reliable stability data, contaminant specifications, and compliance with voluntary traceability frameworks. The raw material is routinely diluted and lyophilized at exacting concentrations for secondary kit dosage.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management in Reagent Manufacturing
    • ISO 17034: General requirements for the competence of reference material producers
    • OECD GLP (Good Laboratory Practice) for test facility operations

    Typical usage ratio

    • Concentration-dependent, typically 0.5–10 μM loading for each reaction well or cartridge, recalculated per kit scale

    Downstream process integration

    • Incorporation during aqueous solution preparation step prior to vial lyophilization
    • Aliquotting in ISO-classified cleanrooms
    • Stability testing prior to kit release

    Final product types

    • Neurotransmitter screening kit reagents
    • In vitro bioassay consumables
    • Standard solutions for equipment calibration (e.g., liquid chromatography, electrophysiology platforms)

    3. Research-Grade Chemicals for Neuroscience Model Systems

    Institutes, contract research organizations (CROs), and vivarium specialists procure Kainic Acid to induce standardized excitotoxicity or epilepsy models in rodents and zebrafish. Scientific protocols call for ultra-pure material, validated for animal bioassay use, with supporting documentation for animal welfare committees and grant compliance. Typically dissolved in saline or buffer, the raw material is administered with precision injection systems or environmental dosing equipment, with downstream tracking for animal health reporting.

    Industry compliance standards

    • AAALAC and IACUC animal welfare protocols (US and global equivalents)
    • GLP certification for facilities performing pivotal animal studies
    • ISO 13485:2003 for manufacturers of laboratory diagnostic products

    Typical usage ratio

    • 0.1–30 mg/kg bodyweight; smallest effective dose is titrated per species, protocol, and model (fixed with detailed method documentation)

    Downstream process integration

    • Sterile dissolution phase in buffered solution immediately prior to animal treatment
    • Quality control sampling for dissolved material
    • Traceability in vivarium logistic software

    Final product types

    • Validated seizure model animals for pharmaceutical R&D
    • Preclinical neurotoxicity test reports
    • Behavioral screening data packages

    4. Biosensor Calibration and Electrophysiological Device Testing

    Manufacturers of real-time biosensor arrays and microelectrode devices rely on Kainic Acid as a glutamatergic agonist for calibrating equipment sensitivity and responsiveness. This application demands traceable lots with detailed impurity analysis and defined hydration levels. End users mix measured aliquots into perfusion media or calibration solutions, directly loading onto device platforms under controlled laboratory environments. Consistent delivery and documented batch records are essential to meet audit and end-customer requirements.

    Industry compliance standards

    • ISO 13485:2016 for medical device component manufacturers
    • IEC 60601-1 medical electrical equipment safety
    • OEM client protocols for calibration reagent traceability

    Typical usage ratio

    • 1–100 μM in device calibration buffer; range and step size specified by device type and test protocol

    Downstream process integration

    • Direct spiking of calibration solution during device QC phases
    • Blending into artificial cerebrospinal fluid (aCSF) for bench testing
    • Electronic recordkeeping of each calibration and corresponding lot number

    Final product types

    • Finished biosensor and MEA array boards for research hospitals
    • Commercial-grade calibration solutions
    • Data-validated diagnostic devices
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    Certification & Compliance
    More Introduction

    Kainic Acid: A Close Look from the Manufacturer’s Bench

    Direct Experience Shaping Quality and Consistency

    Producing kainic acid requires more than just controlling temperature and pressure inside a vessel. Practical knowledge grows out of attention to every step and a long record of trial, feedback, and improvement. Responsible chemical manufacturing lives in the small details: managing raw material purity, maintaining the integrity of every batch, and respecting the molecule’s nature as both a research tool and a regulated neurotoxin. Talking about kainic acid from the manufacturer’s side means putting science into daily practice, not just listing chemical data or echoing technical specifications.

    Understanding Kainic Acid

    Kainic acid, also called Digenic acid, is a pyrrolidine dicarboxylic acid. Its value comes from its role as an agonist for kainate receptors in neural research. This compound allows scientists to model neuronal injury and explore epilepsy and neurodegeneration, but precision and purity matter profoundly. Even small deviations in impurity profile or isomer composition can skew results in cell cultures or animal studies. Over the years, researchers have identified our product’s reliability by comparing published results and confirming the consistency of bioactivity.

    Production Know-How: The Pathway Matters

    Efficient separation and strict quality checks define the synthesis process we use for kainic acid. Using proprietary processing steps, we steer away from routes that might leave behind unreacted glutamate analogs or racemization byproducts, both of which show up during high-sensitivity NMR or HPLC analysis. We start batch production by evaluating every raw material source, verifying spectra, and cross-referencing certificates of analysis for each incoming lot. At each stage, operators track progress in real-time, following protocols that have stood the test of scale-up and routine production alike.

    Instead of treating kainic acid as a bulk commodity, we listen to customer experience and scientific literature. If a common challenge emerges – for example, batch-to-batch variation reported in electrophysiology assays or failure of dose-responsiveness in in vivo injections – the manufacturing protocol adapts through stricter purification, improved drying cycles, or extra filtration. These changes arise directly from our practical, on-site observation, not outsourced speculation. Decades of hands-on oversight allow us to flag process drift before it affects performance.

    Model and Specification: Going Beyond Purity Percentage

    It’s common to find generic kainic acid described as “over 98% pure,” but purity on paper only tells half the story. Over time, experience showed that isomeric content and counter-ion distribution influence both stability and actual utility in neuroscience applications. Using validated chromatographic methods, we routinely monitor for residual solvents, water content, and isomer ratio (trans/cis), not just overall purity. Our production batches, typically designated as Kainic Acid Model KA-03, are supplied with traceable certificates detailing these additional data points.

    In our routine, the documentation that arrives with a batch matches our own in-house analysis: spectral data, melting point verification, and moisture by Karl Fischer titration. Reliability in one batch is meaningless without traceability connecting every lot to its raw materials and historical processing log. Learning from actual shipping incidents, we also repackage the compound using materials that prevent trace water absorption during transit, further anchoring reproducibility for researchers relying on stable dosing.

    Usage in Practice: What Our Partners Do with Kainic Acid

    Customers rely on kainic acid for two main areas: inducing experimental seizures in animal models, and probing glutamate receptor subtypes. Having supplied academic labs and pharmaceutical teams for more than ten years, we have seen how even small differences in batch age or storage condition can impact downstream studies. Because kainic acid is a highly potent convulsant, accurate measurement and dissolution become safety-critical tasks. Our technical notes address issues such as solubility in physiological saline, prevention of local precipitation during microinjection, and requirements for sterile filtration when preparing stock solutions.

    Researchers often run parallel studies using kainic acid and other glutamate analogs such as domoic acid or AMPA. Clients report that our kainic acid’s dose-response profile is well-matched to the historical literature, with consistent seizure latency and severity. We take these reports seriously, folding them into periodic reviews of our process controls. The majority of complaints received in the early years centered on occasional insolubility or inconsistent color – problems traced to trace impurities picked up during one old purification step. By changing our filtration and recrystallization approach, we closed this gap permanently, learning directly from communication with lab technicians and postdocs facing daily pressure to produce reproducible results.

    Looking Beyond Standard Products: Differences Learned Over Time

    Many manufacturers treat kainic acid as one among many amino acid derivatives, but actual research work reveals subtle – but important – differences between sources. Our customers routinely send back feedback and even blind-test competing samples. Sometimes, competing kainic acid products show batch-to-batch drift, often visible in melting point range or through faint color variance. Those small changes translate to altered potency and variable solubility. We keep full records of every single lot produced since we started, including analytical fingerprints and storage history, giving labs extra confidence in repeat orders.

    Where other products settle for high “apparent purity,” our process control distinguishes between trans- and cis- isomers, a factor strongly linked to functional outcome in seizure induction models. Kainic acid’s effectiveness depends on the trans- form, and we routinely screen for isomeric content via HPLC and NMR. Engaged researchers notice these details – not just the purity percentage. By respecting these differences, we help avoid misleading data and research setbacks.

    Example Feedback and Solutions in Everyday Chemical Manufacturing

    Several years ago, a key laboratory reported a puzzling inconsistency: one batch produced expected behavioral effects in mice, while the next batch required almost double the dose. Reviewing the entire production history, our chemists pinpointed a minor change in drying temperature. This insight led not only to correcting that batch, but to reevaluating temperature control standards for all analogs produced. Such learnings never arrive from a specification sheet – they come from being close to both the product and its users, cleaning glassware, calibrating instruments, and listening to frustration as well as praise.

    Chemical manufacturing doesn’t happen in a vacuum. Every change, whether a supplier goes offline or a regulation tightens, affects days in the plant. Our team cares not just about paperwork or price, but about the responsibility of producing something used in delicate experiments and published research. We have fielded questions about unexpected toxicity, odd smell on opening, or variation in color. Solving these issues doesn’t require marketing spin – only a willingness to talk direct, track every step, and address the causes instead of deflecting blame.

    The Regulatory Backdrop: Safety at the Front Line

    Certain chemicals, like kainic acid, fall under controlled use worldwide due to their neuroactive properties. As a manufacturer, it becomes our job to harmonize purity and delivery precision with regulatory compliance. Each batch receives documented identity checks, and our shipping staff are trained to verify all legal requirements before export. We invest both time and resources in keeping protocols current, because a single misstep risks both customer safety and continued business. The rules can change quickly, so we work closely with compliance officers and keep a well-maintained registry of consignments.

    On multiple occasions, local authorities audited our storage and inventory logs to verify traceability. Rather than hiding anything, we opened the records, discussed our internal checks, and demonstrated our batch control systems in practice. Open communication with both the authorities and our partners shapes safer outcomes. In the rare instance of a recall, we move quickly and openly to alert every recipient. From lab to loading dock, each staff member understands that trust is earned by transparency, not by hiding behind technical jargon.

    Research Partnerships and Shared Growth

    Customers view us as more than a supplier. Direct partnerships with research labs, universities, and pharmaceutical developers drive deeper knowledge sharing. We regularly participate in collaborative research, providing sample lots for pharmacological testing or pilot studies. This collaboration goes both ways – test results come back, and if they reveal anything unexpected, we adjust. By following up on published studies and asking for experimental details, we make certain our batches keep pace with advances in neuroscience and model development.

    For example, demand for highly characterized kainic acid increased over the past decade as CRISPR-edited animal models became mainstream. End users wanted assurance that results from a decade-old publication would hold up with the current material. Learning from these needs, we refined our batch documentation and included third-party validation to offer maximum confidence. Rather than relying just on internal testing, adding this layer of scrutiny ties published outcomes with real-world manufacturing choices.

    Supporting Responsible Research: Transparency by Default

    Trust grows from openness about both successes and mistakes. We write technical notes guiding customers to best practices: storing kainic acid under specified temperature and low humidity, reconstituting in measured small aliquots, and separating stock solutions to avoid freeze-thaw cycles. These suggestions echo details from years of lab visits and troubleshooting calls, not just from a standard textbook.

    Research teams occasionally ask for guidance with older batches. Our advice adapts to what we see in actual transport conditions and end-use storage. If analytical proof shows the profile hasn’t drifted, we confirm safe use; if any sign of degradation appears, we recommend discarding the lot. Support means giving real answers, not just what sales teams want to hear.

    On occasion, high-profile errors in research trace back to poorly characterized starting materials, not just experimental design. Openly discussing these challenges helps everyone move ahead. Instead of seeing these as setbacks, we treat every incident as a chance to tighten our systems and provide lessons learned to newer partners. Making rigorous tracking and transparency the norm supports progress across neuroscience disciplines, especially as collaborative standards improve.

    Lessons from a Decade in Production

    After years in the field, the most important lesson centers on attention – not just to numbers on a specification, but to patterns, real-world scientist experience, and continuous improvement. Manufacturing kainic acid starts with the molecule’s chemistry, but extends far beyond the reactor wall. Learning from hands-on work, tuning every variable, and listening to feedback ensure the next synthesis run meets real-world demands as closely as possible.

    We view every customer inquiry or complaint as data, not as an interruption. Supported by active logkeeping, regular instrument calibration, and personal accountability at every production stage, no problem gets swept under the rug. Whether it’s recalibrating a pump, adjusting filtration to catch previously unnoticed residues, or changing packaging based on season and destination, adaptation shapes long-term success. Maintaining high standards doesn’t happen by accident – it grows from repeated effort and hard-won, practical knowledge.

    Commitment to the Future

    Kainic acid holds an important place in the research world. Researchers expect consistency, precise documentation, zero ambiguity about origin, and open lines of communication. Our team stands ready to adjust processes, answer tough questions, and work through obstacles. In every batch and every shipment, our commitment is to real scientific progress, informed by years of challenge, learning, and hands-on work in chemical manufacturing. Every gram matters – to us and to you.