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HS Code |
441536 |
| Iupac Name | 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid |
| Molecular Formula | C7H5NO5 |
| Molecular Weight | 183.12 g/mol |
| Cas Number | 55210-06-3 |
| Appearance | White to off-white solid |
| Melting Point | Approximately 270°C (decomposes) |
| Solubility In Water | Slightly soluble |
| Pka1 | Approximately 2.1 |
| Pka2 | Approximately 3.4 |
| Boiling Point | Decomposes before boiling |
| Chemical Class | Pyridine dicarboxylic acid derivative |
| Smiles | O=C1C(=O)NC=CC1(C(=O)O)C(=O)O |
| Inchi | InChI=1S/C7H5NO5/c9-5-2-1-3-8-6(5)7(13)4(10)11/h1-3H,(H,8,9)(H,10,11)(H,12,13) |
| Synonyms | Quinolinedicarboxylic acid, pyridone-2,6-dicarboxylic acid |
As an accredited 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, tightly sealed plastic bottle containing 25 grams of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid, labeled with hazard and handling information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packaged 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid in drums or bags, maximizing container capacity. |
| Shipping | 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid is shipped in sealed, airtight containers to protect it from moisture and contamination. The packaging complies with chemical safety regulations, and the product is labeled according to hazardous material guidelines. Transport is carried out by certified carriers with appropriate documentation and temperature control, if required. |
| Storage | 4-Oxo-1,4-dihydropyridine-2,6-dicarboxylic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally at 2–8 °C (refrigerated) unless otherwise specified. Ensure the storage area is well-ventilated and that the chemical is segregated from incompatible substances. Label clearly and handle using proper personal protective equipment. |
| Shelf Life | 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid is stable when stored dry and protected from light at 2–8°C. |
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Purity 99%: 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid with a purity of 99% is used in pharmaceutical synthesis, where it ensures high yield and reproducibility of active compounds. Melting Point 260°C: 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid with a melting point of 260°C is used in high-temperature reaction protocols, where it provides thermal stability during process scale-up. Particle Size <10 µm: 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid with a particle size below 10 µm is used in solid formulation development, where it improves dissolution rates and bioavailability. Molecular Weight 199.13 g/mol: 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid with a molecular weight of 199.13 g/mol is used in analytical standards preparation, where it ensures precision in quantitative assays. Stability up to 150°C: 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid stable up to 150°C is used in polymer modification, where it maintains structural integrity under processing conditions. Water Solubility 50 mg/mL: 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid with water solubility of 50 mg/mL is used in aqueous formulations, where it enables uniform dispersion and consistent product quality. Assay ≥98%: 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid with assay ≥98% is used in biochemical pathway research, where it provides reliable substrate concentration in enzymatic studies. |
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Many years in the business of synthesizing heterocyclic compounds have led us to appreciate the nuances of each intermediate we produce. Among our most technically distinctive molecules, 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid has shown a unique balance of reactivity and selectivity. The compound’s structural features, particularly its dicarboxylic acid groups at positions 2 and 6 and the ketone functionality at the fourth carbon of the pyridine ring, set the stage for a surprising range of downstream transformations. In practice, this translates into cleaner yields for our customers working on complex syntheses. The beauty of this molecule is in its dual acid groups, offering straightforward derivatization options, which directly impact research and scale-up settings, especially where purity can make or break the outcome.
Over time, we’ve seen clear patterns in the use of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid. Researchers in pharmaceuticals and advanced material science gravitate to intermediates that provide flexibility—a feature this molecule continuously delivers. For scientists aiming to develop small molecule drugs, the scaffold offers pathways for lactam and pyridine derivatives. Its behavior under mild or stepwise functionalization broadens its application into the more specialized world of pharmaceutical lead compound development, where every group added or removed tells you something vital about the larger synthetic target. That has been the heart of its value for medicinal chemists.
Since this acid features both a highly conjugated pyridine core and distinct carboxyl sites, it’s also found a role in creating coordination complexes with metals. These complexes often display catalytic or fluorescent activity, making the compound not just a building block but a pivot point in both organic and inorganic synthesis. Years of feedback from our academic and industrial partners confirm that fewer byproducts and easier purification facilitate not just lab-scale work but industrial reproducibility.
We commit to consistent, high-purity batches. Our current model delivers material at a minimum purity of 98%, verified by standardized HPLC and NMR methods. This benchmark did not arrive by chance. It came from hundreds of batch iterations, methodical troubleshooting, and a feedback loop with the chemists using our product day in and day out. The presence of those two carboxyl functions introduces the risk of decarboxylation or side product formation under less controlled conditions, but our process gives us control over both yield and impurity profiles.
Every manufacturer faces the challenge of batch variation. Even trace contaminants can complicate product purification or analytic results downstream. Through control of precursor sourcing, solvent grades, and reaction atmosphere, our staff keep impurity levels to a minimum. Lots come with full chromatographic and spectroscopic data because the analytical challenge for heterocycles with multiple substitution patterns remains real; without full transparency, failures can show up late and cost time and money.
Experience tells us most heterocyclic carboxylic acids present similar problems—poor solubility in common solvents, rapid hydrolysis, or difficulties in crystallization, for example. In the case of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid, our method minimizes these headaches. We have learned not to cut corners, especially with drying and temperature control, as the hydrate forms can mislead even trained chemists during weighing and storage. Over the years, we developed a protocol for solvent selection and post-crystallization handling that helps users avoid subpar results or degradation.
The feedback we’ve received from process chemists is underscored by one theme: no time for rework due to poor material quality. We tightly monitor our final step purification, using both recrystallization and column methods in parallel when needed, to guarantee color, texture, and purity fall within spec. The product’s solid state—typically as a white to off-white powder—makes it easy to handle in both laboratory and pilot-plant environments, providing practical traction for scale-up work. No unnecessary fillers, extenders, or anti-caking agents ensure there are no hidden variables in reaction optimization.
Our compound serves as a starting material in several synthetic directions. Chemists using it for condensation reactions, or for ring-closure steps in the synthesis of fused heterocyclic products note its clean conversion rates and minimal side product formation, even with sensitive nucleophiles or under basic conditions. We’ve followed collaborations with universities where the product’s utility in fine-tuning the electronics around the pyridine ring made the difference between a stalled project and a published paper. The dicarboxylic acid motif opens access to both amide and ester derivatives without excess protection or deprotection steps, improving efficiency in iterative synthesis workflows.
Customers tackling transition metal binding studies have reported that the binding constants and chromophore properties of complexes derived from our material remain consistent across batches. That predictability comes not just from the core purity, but also from our care with moisture and ion content. Metals can form unwanted salts with poor grade acids, throwing off stoichiometry and making scale-up nearly impossible. By providing well-characterized batches, we reduce surprises—saving valuable laboratory resources.
Plenty of dicarboxylic acids see use in the chemical and pharmaceutical industries. What we see from direct side-by-side testing is that 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid occupies a distinct niche thanks to its conjugated aromatic core and functional group positioning. Simple aliphatic dicarboxylic acids, like succinic or glutaric acid, cannot offer the same platform for aromatic modification, electronic effects, or heterocycle fusion. Other comparably functionalized aromatic acids—such as pyridine-2,6-dicarboxylic acid—lack the crucial 4-oxo group, which controls reactivity towards both electrophiles and nucleophiles, aiding in selective transformations.
This 4-oxo-1,4-dihydropyridine framework acts as a useful compromise between stability and chemical reactivity. While comparable molecules often force chemists to use harsher reagents or more complex protection strategies, our compound can undergo chemoselective reactions, simplifying purification and improving atom economy. This difference may appear subtle on paper but means a great deal in practice—less waste, fewer impurities, and more control at each synthetic stage. In one project involving fused bicyclic heterocycles, a client found that switching to our compound reduced time spent troubleshooting side products by over forty percent, dramatically improving throughput in their R&D pipeline.
We have heard too often from customers who tried to use less pure, off-spec materials from other sources. Their feedback always circles back to difficult filtration, erratic solubility, or batch-to-batch color changes. These seemingly small issues accumulate into major inefficiencies over long timelines. Our consistency helps teams working to demanding project schedules, where unpredictable results can block key deliverables or regulatory submissions.
Unlike generic trading houses, we set specification controls at every step—analytical data is more than a paperwork exercise. Moisture content, residual solvent load, and micro-impurities receive full quantitation to ensure that the compound’s reactivity and storage life remain uncompromised. Because 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid can form hydrates and sodium or potassium salts readily, we keep our environmental humidity and raw material source water tightly regulated. Every kilogram goes through loss-on-drying and melting point checks, assuring no surprises in thermally sensitive transformations.
Particle size has surfaced as a quiet but critical parameter too. Finer control over milling enables reproducible dissolution rates and faster reaction set-up, especially in automated or continuous flow chemistry platforms. Our material comes as a free-flowing powder by default but can be custom-milled for those working in specific dispersion environments. In peptide synthesis, for example, small differences in acid handling matter; our granular and powder batches perform equally well by the feedback gathered through client process validation studies.
Sourcing, manufacturing, and delivering high-purity dicarboxylic acids means operating with respect for both laboratory safety and broader environmental stewardship. This compound, while not classified as acutely hazardous, deserves care in handling due to potential respiratory or skin sensitization. We recommend the use of conventional PPE, as experience shows that even robust process lines can become challenged by dust generation or accidental spills. Our workforce receives ongoing training—no shortcuts make their way into shipping.
On environmentally conscious production, waste minimization sits front and center in our workflow. We have moved away from volatile organic solvent-heavy reactions wherever possible. Purification by crystallization tends to reduce the mass of solvent waste, and recycling protocols in our plant push residual organic solvents into recovery streams, not outflow. Our wastewater meets or beats regulatory guidelines, and every year brings another round of internal audits looking for areas to squeeze down environmental impact even further.
Transport of any fine organic acid requires appropriate packaging to guard against both moisture ingress and dust tracking. Our QA staff check seals and liners on every barrel or drum before dispatch. That extra step may seem redundant but has prevented more than one lost lot during humid seasons. In practice, well-packaged, high-purity acid avoids surprises—giving our customers confidence that the material will perform as expected from the minute it leaves our doors to the moment it enters their reactors.
Researchers developing new ligands and pharmaceutical intermediates look to partners who can share both reliable products and accurate technical guidance. Over three decades, we have supported everything from milligram-scale academic syntheses to multi-ton GMP campaigns. This longevity lets us recognize when an issue traces back to the material, not the process. Calls from synthetic chemists asking about reactivity trends, solubility, or storage stability get answered by staff who know both the theory and the practice, not just sales reps reading paperwork.
We believe clear and direct communication saves everyone time. If a batch appears off, our first step involves checking the operator’s handling procedures and environmental factors, rather than jumping to conclusions. Real-world chemistry rarely matches textbook scenarios; environmental humidity, aging solvents, or even instrument calibration can complicate data. Our customers appreciate candid assessments of both strengths and limits, instead of canned guarantees.
Through feedback loops with end users, we’ve revised filtration techniques, adjusted particle size, and even modified package types to better meet customers’ workflows. Those changes didn’t originate from market surveys, but from hands-on experience, with direct input from synthetic and analytical chemists who depend on consistency. In one instance, a customer’s request for a special milling finish led to a new product line, now standard for clients running high-throughput screens.
Working extensively with pyridine-based dicarboxylic acids means facing concrete challenges regularly: sensitivity to moisture, degradation under strong base, batch-to-batch color variation, and sometimes short shelf-life under ambient storage. We found that triple-sealed, opaque packaging mitigates most light and humidity risks. Refrigerated storage further extends shelf life, though many customers report satisfactory stability under dry, room-temperature conditions for several months.
Oxidative degradation remains the greatest threat in long-term storage. To counteract that, our technical staff maintain strict anaerobic conditions during bulk packaging. On the process end, slow trickle feeding during reactions gives better yields than dumping the whole charge at once, a tip passed down from one process chemist to another. Both solvent selection and pH control have proven especially important, as the carboxyl groups respond differently to protic and aprotic conditions.
Occasional off-odors or slight discoloration—common in heterocyclic carboxylic acids—sometimes signal sub-threshold decomposition. Instead of leaving customers guessing, we run extended stability studies and provide plain-language analysis summaries. Our willingness to discuss and resolve real-world problems, not just sell product, builds trust within a field where reliability trumps all else.
Over the years, we have watched the demands for advanced intermediates grow, especially as pharmaceutical and materials scientists push towards more complex, functionally rich agents. Molecules like 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid stand out in this context—acting as connectors between what used to be separate fields, including catalysis, supramolecular assembly, and medical chemistry.
Our direct engagement in scale-up projects has revealed industry trends before they appear in journals. For example, more teams shift toward continuous flow processing, seeking compounds with solubility and stability profiles that support these advanced systems. Knowing this, we offer technical support on solvent and process compatibility, including guidance drawn from our own continuous pilot runs.
From our vantage point, regulatory standards for pharmaceutical intermediates have become more stringent, with greater emphasis on traceability and reproducibility. We see our role as a partner in compliance, offering thorough documentation alongside our products. It’s not just about ticking off regulatory boxes; it’s about empowering chemists to move quickly from bench to plant without unexpected roadblocks.
A chemical manufacturer’s true mark lies not in price or volume, but in sustained relationships rooted in technical credibility. From the raw material supplier to the research scientist at the lab bench, we share a common goal: to keep processes moving, reliability high, and innovation possible. Experience with compounds like 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid gives us hands-on knowledge about real production pain points, but also about where careful synthesis can unlock downstream possibilities.
We welcome technical discussions, process walk-throughs, and problem-solving collaborations. The ongoing exchange with the scientific community keeps us sharp, honest, and resilient in a rapidly changing field. Each kilogram shipped reflects not only quality chemistry, but the shared expertise of countless professionals along the supply chain.
Every lot of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid carries the weight of our company’s history, dedication, and learning. Its consistent performance, versatility, and reliability make it more than just a building block—it's a testament to what can result from close partnership, technical rigor, and a practical grounding in chemical manufacturing. Combining smart process design with careful attention to end-user needs ensures this compound remains a valued resource for laboratories and production plants around the globe.