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Chelidamic Acid

    • Product Name Chelidamic Acid
    • Alias 4-Pyridinecarboxylic acid, 2,6-dihydroxy-
    • Einecs 207-490-2
    • 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

    149471

    Cas Number 1910-18-9
    Molecular Formula C7H5NO4
    Molar Mass 167.12 g/mol
    Iupac Name 4-pyridinecarboxylic acid-2,6-dione
    Appearance White to off-white crystalline powder
    Melting Point 224-226 °C
    Solubility In Water Slightly soluble
    Synonyms 6-Carboxyuracil, 2,6-Dioxo-1,6-dihydropyridine-4-carboxylic acid
    Storage Temperature Store at 2-8°C
    Pka 1.30 (carboxylic acid), 9.35 (pyridine nitrogen)

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

    Packing & Storage
    Packing Chelidamic Acid is packaged in a 25-gram amber glass bottle with a secure screw cap and detailed safety labeling.
    Shipping Chelidamic Acid is typically shipped as a solid powder in tightly sealed containers to prevent moisture absorption and contamination. It should be transported in compliance with relevant regulations, away from incompatible substances, and stored in a cool, dry place. Appropriate labeling and documentation accompany the shipment to ensure safe handling.
    Storage Chelidamic acid should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Store at room temperature, ideally between 15-25°C. Ensure the container is clearly labeled and avoid exposure to extreme temperatures. Follow all relevant safety regulations for storage of chemicals.
    Application of Chelidamic Acid

    Applications of Chelidamic Acid in Industrial Manufacturing

    Chelidamic acid, a pyridinedicarboxylic acid compound, plays a specific technical role in several industrial sectors due to its well-defined chelation properties, reactivity, and compatibility with high-performance chemical syntheses. As a manufacturer, we supply chelidamic acid strictly for qualified downstream markets where its functional advantages are critical to formulation integrity, process consistency, and finished product performance.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers employ chelidamic acid as a key intermediate in the synthesis of specific pyridine-based active pharmaceutical ingredients (APIs), notably for drugs that require carboxyl functional group modifications or pyridine scaffolds. Its purity and stability are crucial for multistep syntheses routed through condensation or cyclization. The acid often appears during building block assembly or heterocycle formation, where precise stoichiometric control and process validation are mandatory under cGMP environments. Formulators optimize the input ratio depending on the molecular weight targets and sequence yield requirements established during route selection.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) for Intermediates
    • U.S. FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • SOPs for Qualified Intermediate Handling

    Typical usage ratio

    • 1.1–1.5 equivalents relative to the pyridine-derived API’s target moiety; exact ratio adjusted based on conversion efficiency and process validation yields

    Downstream process integration

    • Added in batch synthesis or semi-continuous reactors at the stage of carboxylation or cyclization to form pyridinedicarboxylic derivatives; introduced after solvent loading and before the primary condensation step

    Final product types

    • Pyridine-based antihypertensives, anti-inflammatory agent intermediates, API building blocks for generics

    2. Specialty Metal Chelate Formation for Analytical Reagents

    High-purity chelidamic acid finds its principal downstream use in the preparation of specialty metal chelates applied in laboratory and industrial analytics. Its unique complexing ability with transition metals, especially in pH-controlled aqueous media, supports sensitive colorimetric and spectrophotometric assays. Laboratory reagent producers process chelidamic acid during chelate synthesis steps, ensuring metal ion selectivity critical to reagent batch reproducibility and shelf stability. The precise acid-to-metal molar ratio depends on the endpoint color stability and detection sensitivity requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for Analytical Reagent Production
    • JIS K 8001: Analytical Reagent Standards
    • REACH Regulation (EC No 1907/2006)
    • Internal QC specifications for chelate purity and stability

    Typical usage ratio

    • 1:1 molar ratio with target metal ion (e.g., Cu2+, Fe3+); adjusted up to 1.2:1 to ensure complete chelation depending on trace impurity profile

    Downstream process integration

    • Dissolved into aqueous buffer and added to pre-treated metal ion solution, followed by controlled pH adjustment; isolation of the resultant chelate occurs before formulation of analytic kit components

    Final product types

    • Trace metal colorimetric assay kits, titration indicators, standards for water quality analysis

    3. Catalyst Precursor in Polymerization Processes

    Polymer and resin producers use chelidamic acid as a ligand precursor in the manufacture of specialized homo- and co-polymerization catalysts. Its dual carboxyl group coordinates with metallic centers, facilitating homogeneous catalyst formation and improved control over polymer chain branching. Chelidamic acid enters the catalyst preparation during complex assembly, where engineers optimize concentrations to balance activity and thermal stability requirements for each polymer system. Catalyst formulation processes must adhere to strict batch documentation and residual ligand validation for end-use regulatory compliance in food-contact and technical-grade polymer resins.

    Industry compliance standards

    • FDA 21 CFR 177 (Indirect Additives for Food Contact Plastics)
    • ISO 14001:2015 (Environmental Management in Polymer Manufacturing)
    • EU Regulation (EC) No 2023/2006 on GMP for Materials Intended to Come into Contact with Food
    • Corporate QA/QC procedures for catalyst purity

    Typical usage ratio

    • 0.05–0.2 mol% relative to total catalyst metal; adjusted via pilot plant trials based on polymerization kinetics and final molecular weight distribution objectives

    Downstream process integration

    • Introduced during catalyst ligand exchange in solvent or melt phase, before catalyst activation; follows precise chrono-temperature ramp scheduling for active site stabilization

    Final product types

    • Polyamide specialty resins, advanced engineering plastics, custom block polymers for extrusion and injection molding

    4. Fine Chemical Building Block for Dye and Pigment Synthesis

    Chelidamic acid forms an essential building block in the synthesis of high-performance azo and pyridine-based dyes, especially those requiring multiple carboxyl functional groups to achieve thermal or photochemical stability. Producers in the fine chemical industry perform esterification or amidation reactions involving chelidamic acid to introduce key linkages within dye molecular structures. The loading level is determined during laboratory scale-up to ensure consistent chromophore yield and fastness ratings in the final pigment or dye. Process chemists monitor purity and conversion rates using in-line analytical controls as required for global regulatory acceptance in textile and plastic coloration.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Chemicals for Textile Applications)
    • REACH Annex XVII (Restrictions on Dye Chemicals)
    • ISO 9001:2015 (Quality for Fine Chemical Manufacturing)
    • GOTS 6.0 Input Approval (for textiles)

    Typical usage ratio

    • 5–20% by weight of total dye intermediate mixture, dependent on desired chromophore type and degree of molecular substitution; adjusted after synthetic optimization

    Downstream process integration

    • Added to the synthesis reactor with coupling agents and solvent system, generally before the primary diazotization or coupling stage; excess neutralized downstream using base to ensure residual compliance with output requirements

    Final product types

    • Synthetic textile dyes, plastic pigment masterbatches, technical colorants for paper and printing ink industries
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    Certification & Compliance
    More Introduction

    Introducing Chelidamic Acid: Practical Experience from the Plant Floor

    Shaping Our Approach to Chelidamic Acid Production

    On any thriving chemical production line, every compound tells its own story. Chelidamic acid, with Chemical Formula: C7H5NO5, stands out in our product list mainly due to the ways it meets the demands of specialty applications. Our process begins far from a desk; it starts in the blending tanks, where purity control and reproducibility challenge us each production run. Success depends on practical skill, refined procedures, and understanding the ways this organic acid interacts in real workflows. That ongoing, hands-on effort is what customers lean on, not just certificates of analysis.

    What Makes Chelidamic Acid Special in the Field

    Chelidamic acid (4-pyridone-2,6-dicarboxylic acid) carves out its place among other pyridine derivatives because of its specific reactivity profile. The molecular structure is defined by the two carboxylic acid groups positioned at the 2 and 6 spots on the pyridine ring. From hands-on work in the reactor hall, we see the importance of tight control here—missteps in synthesis or an off-balance in temperature quickly show up in product color, solubility shift, or yield drop. The knowledge required to address these issues does not come from theory alone but from years of course-correcting in real time.

    Unlike generic benzoic acids or nicotinic derivatives, chelidamic acid features a higher chelating potential. We work with researchers who point out its unique metal ion binding ability. In the lab, clear differences come up during titration: chelidamic acid shows stronger complexation with ions like calcium and magnesium than simpler analogs. The downline effect means greater efficiency for users in areas from analytical reagents to pre-catalyst formulations, which often depend on tight control of trace metals.

    Interest comes mostly from professionals in chemical research, advanced material synthesis, and specialized analytical testing. Over the years, collaborations with university chemistry departments and industrial customers have highlighted the value of a material that brings predictability to synthesis work. Consistency in spectral data—clean, strong signals in NMR, IR, and HPLC runs—reflects the process adjustments we have made based on years of customer feedback and hands-on observation at the plant.

    Comparison to Similar Compounds and Applications

    In conversations with application specialists or process chemists, the discussion quickly turns to how chelidamic acid stacks up to similar compounds. We have processed batches of isonicotinic acid, picolinic acid, and even aromatic polycarboxylic acids, so our perspective is grounded in compound-to-compound differences. Chelidamic acid’s second carboxyl group on the pyridone ring dramatically changes how it interacts in both metal chelation and organic transformations.

    Colleagues in formulation research have noted that, compared to isonicotinic acid (which only has one carboxylic acid at the 4–position), chelidamic acid provides dual-point binding. This two-point interaction allows for more robust chelation—something easily demonstrated during pH titrations and analytical extractions. Other chemistries, such as use in cyclization reactions or as ligands in coordination chemistry, benefit from the same structural features. In our own testing, reaction rates or selectivity often shift measurably, prompting development of protocols that take full account of the distinctive acidic and chelating properties.

    In practice, product users value these distinctions. Whether the end aim involves creating new organic frameworks, studying metal-ligand interactions, or preparing pre-catalysts, customers report stronger results with a clean, reliable supply. We tailor our purification and drying steps to prevent contamination by unintended isomers or byproducts, since these can complicate downstream reactions. Years on the factory floor have shown that even minor impurities can disrupt complex synthesis or throw off an entire run, requiring costly troubleshooting or repeated purification steps.

    Technical Observations and Route Selection

    In our facility, we draw on practical lessons to choose production routes. One method starts with a condensed pyridine ring system, using established oxidative pathways. Our teams have experimented with various oxidizing agents: potassium permanganate, nitric acid, and, in some pilot runs, milder options for reducing waste. Reaction order, solvent choice, and temperature play crucial roles. The difference between a yield above 95% and a run that tops out at 88% often comes down to subtle tweaks—modifying agitation speed or adjusting intermediate wash stages, all guided by batch-to-batch performance data.

    Handling chelidamic acid post-reaction presents its own set of demands. In humid seasons, the compound draws moisture, so controlled-atmosphere drying is essential. Material flow changes when humidity creeps above 60%. Over time, we moved from simple tray drying to sealed rotary dryers, then to vacuum ovens for large-scale production, as those brought us the low moisture levels customers needed for consistent performance.

    Specifications That Make a Difference to the End User

    What does this look like on the datasheets? For us, the targets have shifted over the years as end uses have changed. Today, purity levels consistently run above 99.5% by HPLC and NMR, with minimal trace metals—typically below 10 ppm. Visual inspection matters just as much: off-white, free-flowing crystalline powder is standard now due to improvements in filtration and drying lines. Bulk density, particle size, moisture content—each of these is monitored by operators who understand how downstream process compatibility depends on tight tolerances.

    Nonvolatile residue and the freedom from organic solvents are essential concerns, especially for fields like pharmaceutical research or advanced materials work. More than once, we’ve been called on to troubleshoot customer syntheses, only to trace the problem back to an off-brand chelidamic acid laden with solvent residues. That sends a clear message: a manufacturer’s attention to purification steps really does ripple outward, affecting not just laboratory reactions but the reliability in a researcher’s entire workflow.

    Insights Into Usage Based on Field Experience

    Direct customer interaction is the true gauge of any chemical’s market fit. Scientists handling chelidamic acid often need microgram-scale precision, such as in trace metal analysis, or gram-to-kilogram volumes for pilot-scale syntheses. What matters most in these contexts is not just a clean chemical record but also predictable functional performance. A tight melting point range (usually 280–283°C, with slight batch-to-batch variation), consistent solubility profiles, and reliable metal chelation properties matter more than brochure adjectives.

    In catalysis, the compound serves as a scaffold for ligands, bringing uniform coordination around transition metal centers. Materials scientists report beneficial effects on crystal growth when chelidamic acid replaces more volatile or less robust chelating agents. For analytical chemists, especially those running calibration standards in trace metal or complexometric titrations, the difference is clear: signal precision increases, background interference drops. These are measured, testable outcomes, not just seller’s pitches.

    Organic synthesis groups find the acid a reliable building block in reactions that require introduction of carboxyl functionalities, ring modifications, or controlled metal complexation without unwanted side reactions. During discussions at technical meetings, customers have shared details of research where chelidamic acid’s lower background reactivity eliminates interference seen with other diacidic pyridine compounds. The upshot: more usable product, fewer column purifications, and time saved in subsequent processing steps.

    Process Improvements Backed by Real-World Results

    The cost and effort behind each drum of chelidamic acid trace back to hundreds of tweaks over years of production. Early runs saw unpredictable yield loss during crystallization or unwanted color changes from over-oxidation. Stepwise refinements came from inspecting intermediates, logging granular temperature data, and interviewing chemists about where previous suppliers had let them down. For those of us in production, nothing replaces feedback from a customer whose research or manufacturing hinges on a single consistent source.

    Recent investments have improved throughput and quality assurance. Multiple chromatography steps now monitor both final product and intermediates for isomer splits and byproduct retention. These upgrades came about not from external audit recommendations but from in-the-field trial and error. Our operators now work alongside lab analysts, discussing the meaning of each retention time and spectral anomaly. SOPs have evolved to reflect these learned lessons, making today’s batches safer and more uniform than those from a decade ago.

    Our logistics team ensures that each package—be it 100 grams or a multi-ton bulk tote—arrives free from extraneous moisture or contamination, and with robust packaging to survive global shipping. We have reduced claims of caked or degraded lots by adjusting not just the inner bagging and drum lining but also coordinating shipment schedules to avoid exposure during rainy and high-humidity seasons. Customers tell us that material that performs after months in storage, even after a cross-ocean journey, points to diligence on the manufacturing side.

    Responsiveness to Customer Feedback and Industry Trends

    The chelidamic acid market has its cycles. As researchers identify new uses in supramolecular chemistry or as precursors in more complex ligands, our production priorities shift accordingly. Batch campaigns are sequenced based on demand surges from government R&D contracts, scaling specialty polymers, or changes in regulatory compliance, such as restrictions on certain process byproducts.

    Feedback flows both ways. A polymer manufacturer alerted us to a purity concern that surfaced only under specific high-temperature extrusion conditions. Our QA found a trace impurity below typical detection limits, prompting a process overhaul: more frequent sampling of mother liquor, longer purge times at the filtration stage, and a new staff training round. This experience directly improved product quality for other customers, as evidenced by tighter analyte peaks and smoother product consistency.

    Academic researchers often approach us with experimental methods that stress-test the limits of our product: applying chelidamic acid in novel ligation reactions, metal-organic frameworks, or as a custom reagent in biochemistry. Each request adds a new dimension to our knowledge base. Instead of generic assurances, we prefer to share findings from those field tests, openly discussing melting behavior under vacuum, long-term storage stability, or material flow through micro-dispensing systems.

    Challenges and Sustainable Processing Priorities

    Environmental priorities are not just talking points for our operation. Waste minimization and solvent recovery have driven recent process changes. In the past, oxidative steps generated greater volumes of organic waste. Over the past five years, new capture and recirculation systems have cut solvent usage by over a third. On multi-ton runs, this means not just material savings but less environmental impact—a crucial factor in long-term supplier relationships, particularly with multi-national clients who track “green chemistry” metrics.

    Solid waste from crystallization and filtration used to be a disposal bottleneck. This prompted us to adopt new washing protocols, improving yield while scrubbing out more impurities. These improvements came through the resourcefulness of our operations team—technicians who understood where material loss was occurring and worked side-by-side with R&D chemists to refine every step. Outcome: better utilization rates, less scrap, and lower energy consumption during drying cycles.

    Staff safety also gets top billing. Operators working with strong acids, high temperatures, and vacuum lines are at the frontlines of chemical production. Our training programs and equipment upgrades come directly from their feedback on what really works versus what looks good on a checklist. Nothing we do in the pursuit of purity and performance ignores the need to protect those hands doing the work.

    Direct Relationships with End Users

    Buying from a manufacturer connects customers directly to experience, not just inventory. We receive requests to tweak mesh size, adjust packaging, or meet unusually tight lead times for R&D deadlines. Because we manage the process from raw pyridine through the last drum out the door, adjustments happen quickly and questions receive answers from people who know, not just read a script. We recognize most major customers by project, not by PO number, and know how far samples from pilot runs make it into multi-year downstream programs.

    Those relationships shape the product in tangible ways. A university chemistry department requested a lower metal content for sensitive complexation studies. We responded with a dedicated clean room crystallization step. An industrial customer developing new water treatment processes asked for finer particle sizing for better dissolution—so we set up a trial micronizing run. Real-world chemistry does not fit a catalog, and neither can production lines set in their ways. Rather than produce whatever fits standard equipment, we tune output to persistent customer challenges.

    Continuous Learning and Looking Forward

    Standing over the reactor’s sight glass, hearing feedback from field researchers, following up on every claim returned—these make production of chelidamic acid a craft, not just an operation. Every specification reflects hard-earned trust and an openness to change. While market dynamics and application fields keep evolving, the foundation stays the same: make each batch better than the last, learn not just what works for us but what customers prove works for them. That synergy, from plant floor to lab bench, has shaped chelidamic acid’s place as a go-to option for those who refuse to compromise with uncertainty.