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Kynurenic Acid

    • Product Name Kynurenic Acid
    • Alias KYNA
    • Einecs 225-248-4
    • 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

    108562

    Name Kynurenic Acid
    Cas Number 2387-39-1
    Molecular Formula C10H7NO3
    Molecular Weight 189.17 g/mol
    Appearance White to yellowish powder
    Melting Point 315-316 °C (decomposes)
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Temperature 2-8°C (refrigerated)
    Synonyms KYNA, 4-Hydroxyquinoline-2-carboxylic acid

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

    Packing & Storage
    Packing Kynurenic Acid, 25g, is supplied in a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping Kynurenic Acid is shipped in tightly sealed containers, protected from light and moisture, and handled according to standard regulations for chemicals. Packaging follows safety standards to prevent leaks or contamination. Appropriate hazard labeling and documentation are included, and the shipment is transported by certified carriers in compliance with relevant transportation regulations.
    Storage Kynurenic Acid should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerator temperature). Avoid exposure to heat and incompatible substances. Ensure proper labeling and follow standard laboratory safety procedures to prevent contamination or degradation of the chemical.
    Application of Kynurenic Acid

    Applications of Kynurenic Acid in Industrial Manufacturing

    Kynurenic acid is a key intermediate and functional ingredient across several advanced industrial fields. As the direct manufacturer, we supply material that meets stringent requirements demanded by sectors involved in pharmaceutical synthesis, veterinary preparations, neurological research, agricultural biotechnology, and specialty analytical reagents. Our formulations support process reliability and regulatory compliance in each application below.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Neurological Drugs

    Manufacturers use kynurenic acid as an essential precursor in producing pharmaceutical compounds targeting neurodegenerative diseases, including novel anti-epileptic and neuroprotective drugs. This material supports synthesis under strict quality and traceability programs, forming a controlled step in the multi-stage development of finished actives where purity, batch uniformity, and impurity profiling are critical. Its integration requires validated methods to maintain pharmacopoeial standards, especially within GMP-compliant facilities.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) monograph for API intermediates
    • FDA 21 CFR Part 210/211
    • ICH Q3A (Impurities in New Drug Substances)

    Typical usage ratio

    • Determined by synthesis protocol; typically 0.1–1.0 molar equivalent relative to target active, adjusted by reaction optimization and required purity.

    Downstream process integration

    • Introduced at early or mid-stage of chemical synthesis for small molecule drug candidates via amidation, condensation, or coupling reactions.

    Final product types

    • Neuroprotective small molecule APIs
    • Experimental anti-epileptic formulations
    • Kynurenine pathway modulators for CNS indications
    • Bulk intermediates for further synthetic modification

    2. Reference Standard and Diagnostic Reagent Production

    Laboratories and diagnostic solution manufacturers apply kynurenic acid as a high-purity standard for instrument calibration, quantification, and quality assurance in bioanalytical assays, especially for LC-MS/MS and HPLC detection of kynurenine pathway metabolites. Selection of traceable material is necessary to achieve consistent analytical results and documentation suitable for accrediting authorities in clinical labs and contract testing organizations.

    Industry compliance standards

    • ISO 17025:2017 (Testing and Calibration Laboratories)
    • USP Reference Standard requirements
    • CLSI guidelines for diagnostic assay validation
    • ISO 15189 (Medical Laboratory Quality)

    Typical usage ratio

    • Prepared into calibration solutions of 10–500 ng/mL for LC-MS/MS controls; exact concentration based on instrument protocol and target detection range.

    Downstream process integration

    • Weighing and dissolution at reagent preparation stage, followed by validation as part of the assay master mix or calibration/quality control panel.

    Final product types

    • Certified reference materials for clinical validation
    • Quality control kits for laboratory assay development
    • Standard curve solutions for HPLC and mass spec quantification
    • Diagnostic reagent kits for medical and research use

    3. Veterinary Pharmaceutical Formulations

    Producers in the veterinary health sector incorporate kynurenic acid within specialized drug products for companion and livestock animals, particularly in experimental therapies aimed at inflammation control and neuroregulation. Veterinary use demands compliance with pharmaceutical standards for animal health and detailed documentation of mixing procedures, trace elements, and cross-contamination control, following regional regulatory frameworks.

    Industry compliance standards

    • Veterinary Medicinal Products Directive 2001/82/EC (Europe)
    • VICH GL43 (Pharmaceutical Quality of Veterinary Drugs)
    • US FDA Center for Veterinary Medicine (CVM) guidance
    • Good Manufacturing Practice for Veterinary Drugs (China, GB/T 17224)

    Typical usage ratio

    • Commonly 0.01–0.2% w/w in medicated premixes or injectable solutions; ratio set by animal species, target condition, and pharmacokinetic study outcome.

    Downstream process integration

    • Dosed during formulation blending or solution preparation, then homogenized with other actives/excipients before final filling and packaging.

    Final product types

    • Oral suspensions for livestock therapy
    • Injectable animal health solutions
    • Veterinary premix powders
    • Adjunct ingredient for clinical veterinary trial supplies

    4. Biotechnological Research and Agricultural Stress Modulator Development

    Research entities and agri-biotech firms apply kynurenic acid in controlled experiments to analyze plant stress physiology and signaling, as well as to develop specialty products modulating biotic and abiotic responses. Trials frequently require narrowly defined purity levels and batch specifications to maintain experiment reproducibility and regulatory compatibility for eventual scaling to biostimulant product registration.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) Principles
    • ISO 9001:2015 (Quality Management Systems)
    • REACH Regulation (if product enters EU agritech market)
    • FAO/WHO specifications for biostimulant analytical reference

    Typical usage ratio

    • Applied at 5–100 mg/L concentration for in vitro or greenhouse assays; scale-up studies adjust based on plant type, endpoint, and delivery method.

    Downstream process integration

    • Added to nutrient media, spray solutions, or root drenches during experimental design or pre-formulation screening of candidate biostimulant blends.

    Final product types

    • Plant growth regulator prototypes
    • Advanced biostimulant R&D samples
    • Experimental foliar spray formulations
    • Custom research reagents for plant stress studies
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    More Introduction

    Kynurenic Acid: A Closer Look from a Manufacturer’s Perspective

    Introduction to Kynurenic Acid: More Than a Tryptophan Derivative

    Inside our factories, the journey of kynurenic acid begins long before it reaches a bottle or container. We have spent years developing processes that reliably convert starting materials into a stable, high-purity crystalline product. Each batch reflects careful attention to pH, temperature, and purity control. We know kynurenic acid as more than just a compound. For us, it represents research, hard work, and technical innovation brought into practical use.

    Kynurenic acid comes from the tryptophan metabolic pathway. Over the years, scientists and industrial partners have turned to our facilities for consistent, well-characterized material. Some may recognize kynurenic acid for its unique role in the brain, acting as an antagonist at specific glutamate and nicotinic receptors. Others encounter it in fields ranging from analytical chemistry to food testing and pharmaceutical research. Our plant operators and QC teams remain equally comfortable in all these domains, maintaining strict standards for contaminant levels, particle size, and storage stability.

    Product Model and Available Specifications

    Specifications shape the way our kynurenic acid enters the market. Most of the material leaves our plant as a fine, off-white to light yellow powder, typically with a purity above 98%. Our typical product grades include KYNA-98, which has become a staple for researchers who require high analytical performance and batch-to-batch reliability.

    Particle size matters for some clients, especially those preparing standards or analytical solutions. We pay close attention to sieve analysis and fine-tuning milling parameters to produce powders that dissolve quickly or suspend cleanly, depending on the application. We measure moisture content regularly, because water can cause kynurenic acid to deteriorate over time or clump when handled. Our QA protocol keeps moisture consistently below 1%.

    How the Manufacturing Process Shapes Quality

    Producing kynurenic acid consistently requires more than buying good raw materials. Every step, from starting chemical selection to the fine points of purification, influences the final product. Years ago, our team abandoned older methods that introduced chemical byproducts difficult to remove downstream. We use a modern synthesis that streamlines conversion and makes purification more manageable.

    Filtration, washing, recrystallization—these are not generic steps for us. Operators oversee each one directly. If the color starts shifting, or if crystals crowd together, we slow down, analyze, and correct. Strict process control pays off in improved spectral purity and reduced ambiguity in NMR and HPLC assessment. This matters because many clients use kynurenic acid as a standard substance, where clarity and assay precision play a critical role.

    Understanding the Differences: Kynurenic Acid Compared to Other Analogs

    Kynurenic acid stands apart from other tryptophan metabolites and glutamate antagonists. Many chemicals in this field—such as quinolinic acid or 3-hydroxykynurenine—carry different risks and reactivity. For instance, kynurenic acid shows lower oxidative potential than 3-hydroxykynurenine. This makes storage and handling less complicated, reducing the risk of uncontrolled side reactions in analytical settings.

    We see clients switching to our kynurenic acid grades to avoid inconsistencies they encounter elsewhere. Some other products, even with high nominal purity, cause headaches in chromatography or spectroscopic assays because of trace impurities, solvates, or variable crystal forms. Our stability and quality control steps lead to fewer chromatogram peaks and cleaner background in MS and NMR spectra.

    In some research fields, scientists prefer kynurenic acid over related compounds due to its more selective biological action. Kynurenic acid antagonizes the glycine-binding site of the NMDA receptor, while analogs like quinolinic acid act as agonists and trigger different outcomes. These subtle differences mean a lot in pharmaceutical research. The feedback we receive emphasizes reproducibility and the absence of background interference—a direct result of our manufacturing discipline.

    Applications Across Industries and Research

    Kynurenic acid travels far beyond the chemical plant gates. Our clients include academic researchers studying the central nervous system, pharmaceutical firms investigating new neuroactive drugs, and analytical laboratories developing robust assays. Some nutritional research groups use kynurenic acid as a reference marker in the exploration of tryptophan metabolism in foods, grains, and health supplements.

    For every sector, we direct routine technical support and advise on preparation, solubility, and compatibility with solvents and buffers. Most analytical chemists dissolve our kynurenic acid in alkaline aqueous solutions or buffer systems. Dissolution goes smoothly due to the controlled particle size and absence of hydrophobic aggregate formation.

    Pharmaceutical researchers pay close attention to batch records and certificates of analysis. Our in-house documentation tracks every production variable, linking each gram to comprehensive chromatographic and spectrometric testing. We do not treat this as a box to tick; our technical team works with researchers when transitions between lots occur, minimizing experimental deviation.

    Environmental scientists and food safety specialists also turn to kynurenic acid as a biomarker. Reliable quantitation in complex matrices depends on authentic, uncontaminated standard material. We provide both neat compound and pre-weighed sealed ampoules, preventing accidental moisture uptake and cross-contamination.

    Challenges and Opportunities in Quality Control

    Achieving confidence in kynurenic acid’s purity is about more than passing a single HPLC or NMR analysis. Some impurities remain silent until subjected to accelerated stability testing or harsh extraction conditions, which appear in real-world laboratories. Our team uses a suite of analytical techniques—HPLC, GC-MS, FTIR, and sometimes even LC-MS-MS—to verify both organic and inorganic impurity profiles. So far, our results show that even minor changes in crystal growth environment can shift purity levels and cause batch failures.

    Legacy processes, if left unchecked, introduce metal ions or residual solvents. Our routine batch reviews spot such trends before scale-up stages. This not only minimizes internal waste but also heads off customer complaints downstream. Our chemists prefer over-communicating non-conformance and sharing suggested analytical corrections with clients. This keeps trust high, and we see better research results published as a consequence.

    Logistics present another layer of complexity. Extreme heat or humidity during storage or shipping can cause degradation or partial hydrolysis. We invest in moisture-barrier packaging and real-time environment monitoring that record both storage temperatures and humidity levels. Recent feedback and returned samples confirmed that unprotected product left at 35°C for a week lost more than 10% of its active component. We redesigned our warehouse and distribution protocols to block these problems before the product leaves our hands.

    Kynurenic Acid’s Place in Green Chemistry and Regulatory Trends

    Sustainable manufacture sits at the intersection of cost, safety, and operational integrity. Traditional kinurenic acid production generates solvent waste and acidic byproducts. Our latest manufacturing lines recycle more than 80% of process water and neutralize acidic streams with minimal waste generation. These methods cut disposal costs and promote a safer factory environment. Where possible, we re-engineer steps to require less energy, especially at purification and drying stages.

    New customers frequently ask about compliance with REACH, California Proposition 65, or specific FDA and EMA specifications. While kynurenic acid seldom appears on restricted lists, trace metallic and organic impurities must remain tightly controlled. We issue full analytical reports with every lot, including specific test results for lead, mercury, cadmium, and arsenic, plus expanded organic impurity screening per recent regulatory guidance. These efforts reflect both regulatory compliance and our broader commitment to community health and transparent operations.

    Comparisons with Common Market Alternatives

    Cheap kynurenic acid can tempt buyers. We understand the market, and we regularly analyze off-the-shelf samples from overseas and unregistered vendors. These products carry risk—higher levels of residual solvents, polymorphic contamination, inconsistent particle size—which compromise experimental results and may even risk laboratory safety. One sample from a global web-based supplier contained unidentified fluorescent contaminants and decomposed on exposure to light. Such issues rarely result from malicious intent, but rather from under-resourced facilities, poor process documentation, or inattention to solvent and material compatibility.

    We see that our long-term clients rarely switch suppliers after seeing the impact on their research reproducibility. By being transparent about our manufacturing process, routine re-validation, and live technical support, we encourage critical evaluation and feedback. In many cases, our high-purity product leads to higher yield and sensitivity in downstream couplings, derivatizations, or secondary syntheses. For assay laboratories, blank controls stay blank—and standards do not shift during storage or under standard light conditions.

    Technical Support: Bridging the Manufacturer-Scientist Gap

    Supplying a specialty chemical does not end at shipment. Our technical support operates side by side with the manufacturing floor and QC lab. Questions about solubility, storage, and batch variation come up often. Recently, a customer running a new LC-MS protocol found that another brand introduced unknown peaks in their spectra. Our technical group ran side-by-side analyses and identified the impurity source, then provided the customer with detailed cleaning and reconstitution directions.

    These interactions go both ways. Feedback from end-users helps us refine particle size targets and test solubility in popular buffer systems. On occasion, university groups approach us about custom specifications—a slightly larger particle size for unique suspension needs, or a sealed sterile grade for preclinical testing. Having synthesis and packaging under one roof lets us implement these changes quickly, unlike distributors who may be locked into preset lot structures.

    Our daily work reflects the practical needs of the chemical and medical research communities. If new regulatory requirements arise or clients propose new stability protocols, we respond without the inertia and disconnect seen in more bureaucratic supply chains. Our familiarity with every step, from raw material to analytical confirmation, puts us on solid ground for adapting our kynurenic acid grade to future research and regulatory needs.

    Looking Forward: Investment in Research, Safety, and Quality

    The chemical world does not sit still. Demand patterns change as new biological insights emerge. Kynurenic acid, once the focus only of a few neurobiology labs, now appears in nutritional science, animal feed testing, and early biomarker screening. We invest in ongoing metabolite research, working with university and corporate laboratories to map degradation, reaction mechanisms, and new solubility enhancement options.

    Process safety remains a front-line commitment. Our onsite teams conduct ongoing risk analysis for every solvent, acid, and piece of equipment that enters a process stream. New methods focus on eliminating single-point failures and reducing environmental hazards. The impact shows up not only in more robust products but in fewer worker injuries and lower insurance costs. By keeping safety and environmental records open to client review, we welcome scrutiny and continual improvement.

    Our investment in automation has not come at the cost of human expertise. Continuous monitoring, digitally logged batch records, and automated purity testing free up chemists for problem-solving and technical support. Faster feedback loops in process optimization contribute directly to higher quality and more responsive service. Even as we automate, human judgment stays central, especially when dealing with ambiguous analytical signals or troubleshooting odd product requests.

    The Role of Authenticity and Traceability

    Traceability has grown in importance as the regulatory burden on scientific suppliers increases. Each shipment of kynurenic acid carries a unique batch code tied to a full history of reagents, processing conditions, and analytical oversight. Our documentation tracks environmental content, operator interventions, and third-party laboratory confirmations.

    To ensure authenticity and combat counterfeiting, we have begun incorporating tamper-proof seals, serialized packaging, and in some cases, blockchain-based tracking visible to customers. These investments respond directly to both end-user demand and the realities of global supply chain complexity. Untraceable and misidentified products not only disrupt research but create risks for regulatory violations and publication retractions.

    We encourage new and existing partners to request detailed COA documentation, method validation data, and insight into packaging changes. This transparency has helped us catch labeling and storage errors before they reach market and builds trust that the product within the package matches its analytical claims.

    Challenges in Scaling Up Kynurenic Acid Production

    Scaling up specialty organic chemicals like kynurenic acid does not just mean running reactors longer. Heat transfer, mixing times, and impurity profile all shift with larger batch volumes. Our engineering team redesigned reaction vessels to ensure rapid, uniform mixing and efficient reagent dispersion. Samples from pilot scale runs often uncover problems missed on laboratory equipment. This is where experience counts—a small deviation during pH adjustment on a 5 kg batch magnifies defects that might be invisible at 50 g scale.

    We found that downstream purification required additional filtration and centrifugation steps at scale to maintain product consistency. In one instance, unstable intermediate formation at higher batch concentrations produced colored tars that complicated crystallization. Our engineering chemists tracked the problem to temperature control lag and implemented both real-time temperature sensors and more rapid cooling systems.

    Clients working at gram or milligram scale seldom anticipate these problems, so we share our experience to anticipate and troubleshoot these larger volume challenges. This cooperative approach has proven essential as new nutritional, environmental, and pharmaceutical applications create surges in demand that traditional commodity chemical infrastructure cannot handle with accuracy.

    Investing in Long-Term Partnerships

    Most of the feedback we value arrives post-sale. Research partners test our kynurenic acid in ways we do not anticipate, exposing it to everything from harsh oxidative conditions to exotic solvents. Some results return as questions or data requests. We embrace this, learning from client experience and adopting new best practices suggested by end-users. Supporting open data sharing and technical dialogue opens the door to continuous product and process improvement.

    For some research groups, the appeal of our product relates less to an abstract notion of purity and more to the reliability of each successive order. They want the same batch-to-batch performance today as they will next year. For this reason, we routinely archive reference samples from every batch and test past material alongside newly produced lots. This minimizes drift and lets us address drift or unexpected backward incompatibility in analytical performance.

    We also see a growing demand for co-development: initiatives where we work alongside the client to establish new product standards, custom grades, or packaging formats. Our flexibility as a manufacturer—not a reseller or middleman—allows us to innovate quickly. From rapid prototype lots to regulatory submission support, we see each new challenge as a chance to strengthen long-term partnership, rather than merely close a transaction.

    Final Thoughts on Kynurenic Acid’s Place in Today’s Chemical Landscape

    Making kynurenic acid is a daily demonstration of careful craft, scientific discipline, and responsible business practice. Our commitment comes from seeing this compound in the hands of researchers breaking new scientific ground and industries developing safer, more consistent products. Whether the end use lies in foundational neuroscience, food science, or the early stages of drug development, the story behind every batch reflects thousands of hours of process optimization, quality control, and collaboration with the world’s most demanding scientists.

    We take pride in every request for technical support, each returned archive sample for benchmarking, and every publication that cites our product. Our work never finishes because needs and challenges shift. From upgrading plant infrastructure to adapting new green chemistry standards, we push to advance not only the performance of kynurenic acid but also the deep trust placed in its quality, origin, and technical backing.