6-oxo-1,6-dihydropyridine-3-carboxylic acid

    • Product Name: 6-oxo-1,6-dihydropyridine-3-carboxylic acid
    • Chemical Name (IUPAC): 6-oxo-1,6-dihydropyridine-3-carboxylic acid
    • CAS No.: 5444-14-8
    • Chemical Formula: C6H5NO3
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    253270

    Chemical Name 6-oxo-1,6-dihydropyridine-3-carboxylic acid
    Molecular Formula C6H5NO3
    Molar Mass 139.11 g/mol
    Cas Number 2886-80-0
    Appearance White to off-white solid
    Melting Point 216-220 °C
    Solubility In Water Slightly soluble
    Iupac Name 6-oxo-1,6-dihydropyridine-3-carboxylic acid
    Pubchem Cid 2763548
    Smiles C1=CC(=O)NC=C1C(=O)O
    Inchi InChI=1S/C6H5NO3/c8-5-2-1-4(6(9)10)3-7-5/h1-3H,(H,7,8)(H,9,10)
    Storage Conditions Store at room temperature, tightly closed, protected from moisture

    As an accredited 6-oxo-1,6-dihydropyridine-3-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A white, sealed 25g HDPE bottle labeled "6-oxo-1,6-dihydropyridine-3-carboxylic acid, CAS 1119-68-4, for research use only."
    Container Loading (20′ FCL) Container Loading (20′ FCL): 6-oxo-1,6-dihydropyridine-3-carboxylic acid is packed securely in drums or bags, optimizing full container capacity.
    Shipping Shipping of **6-oxo-1,6-dihydropyridine-3-carboxylic acid** requires tightly sealed packaging to protect from moisture and light. It is shipped as a solid, typically at ambient temperature, and classified as a laboratory chemical. Appropriate labeling and documentation are included, ensuring safe handling in compliance with regulatory and safety guidelines during transit.
    Storage 6-oxo-1,6-dihydropyridine-3-carboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated place, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect it from moisture and light. It is advised to keep the chemical in a clearly labeled container and follow standard laboratory safety protocols.
    Shelf Life **6-oxo-1,6-dihydropyridine-3-carboxylic acid** is stable for at least 2 years when stored at 2–8°C, protected from light.
    Application of 6-oxo-1,6-dihydropyridine-3-carboxylic acid

    Purity 99%: 6-oxo-1,6-dihydropyridine-3-carboxylic acid with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and contaminant-free product formation.

    Melting point 182°C: 6-oxo-1,6-dihydropyridine-3-carboxylic acid with a melting point of 182°C is used in solid-state drug formulations, where it facilitates precise thermal processing and stable dosage forms.

    Molecular weight 153.13 g/mol: 6-oxo-1,6-dihydropyridine-3-carboxylic acid with a molecular weight of 153.13 g/mol is used in analytical reference standards, where it guarantees accurate quantification in HPLC analysis.

    Particle size D90 < 50 μm: 6-oxo-1,6-dihydropyridine-3-carboxylic acid with a particle size D90 below 50 μm is used in tablet manufacturing, where it enhances uniform blending and optimal compaction.

    Stability temperature up to 120°C: 6-oxo-1,6-dihydropyridine-3-carboxylic acid with stability up to 120°C is used in controlled thermal reactions, where it maintains structural integrity and reaction consistency.

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    Certification & Compliance
    More Introduction

    6-oxo-1,6-dihydropyridine-3-carboxylic Acid: A Practical Overview from Our Production Line

    A Behind-the-Scenes Look at Our Daily Work

    Anyone working in the fine chemicals sector knows life on the production floor has little room for shortcuts. Every batch poured, every tank cleaned, every shift clocked in, puts hands and eyes right next to the actual compounds. In our facility, 6-oxo-1,6-dihydropyridine-3-carboxylic acid – informally known among the line crew as “6-oxo-pyridine acid” – has gained a certain familiarity. Over the past five years, its synthesis has become a regular fixture, often scheduled for both early-morning start-ups and overnight runs.

    This isn’t just another catalog item: the technical team has watched it move from an experimental stage to a routine operation. Hands-on experience has revealed a lot about its quirks, physical attributes, and consistency across runs. There is no substitute for pouring solvent yourself, seeing the reaction progress, and watching the color changes as this molecule takes shape in the reactor.

    Specifications Arising from Real-World Operations

    Most chemical buyers expect technical data—molecular weight, melting point, purity. Those metrics tell part of the story, but they don’t capture the texture, the scent, or the tolerance for storage conditions. Start with the basics: this solid presents as a white to off-white powder, usually very fine, occasionally more crystalline if the temperature and mixing are just right. Its melting point centers around 250 degrees Celsius, with purity pushed above 98%, measured every shift by HPLC – not because the brochure says so, but because every experienced worker has dealt with what happens when these details slip.

    Purification for this compound relies on tried-and-tested crystallization steps, but the yield often hinges on environmental controls. Humidity above 65% in the work area throws off evaporation; under-dried product tends to clump, pulling handling speeds down during large-volume packaging. The batch size runs between 25 and 150 kilos per cycle—interesting to note for those scaling up a process or timing a pilot run.

    Use Cases Learned from Years on the Synthesis Floor

    Experienced process chemists or R&D specialists likely look to 6-oxo-1,6-dihydropyridine-3-carboxylic acid as a tool for building larger, more complex molecules. Its core structure lends itself well to heterocyclic synthesis, which plays a critical role in pharmaceuticals, pigments, and intermediates relevant to electronics and advanced materials. The close positioning of the keto and carboxylate groups influences reactivity, and this behavior gets discussed almost weekly in our troubleshooting sessions. Anyone planning to introduce it into a route involving nucleophilic or electrophilic attacks should make a note: side reactions, if the process air is not kept dry enough, may impact overall yields.

    One of the significant strengths, and a regular talking point in our scale-up meetings, comes from the versatility of the 3-carboxylic acid moiety: it opens direct access to amide coupling. Straightforward conjugation to amine-functionalized molecules has supported several projects, especially within development teams exploring library syntheses or custom intermediates. Feedback from long-term partners often mentions batch-to-batch reliability, a direct result of the rigorous QC protocols we’ve put in place. Without strict temperature monitoring during reaction and neutralization, yields slide noticeably.

    We have seen increased interest from researchers exploring ligand frameworks, particularly in metal-organic coordination and catalysis. Since the molecule supports modifications on both the pyridine ring and at the carboxylic acid, developers benefit from this dual-point functionalization, leading to new analogs or block building in medicinal chemistry pipelines.

    How 6-oxo-1,6-dihydropyridine-3-carboxylic Acid Stands Apart

    Within our own product lineup, plenty of pyridine-based acids and related intermediates have hit the packing tables. What stands out about this molecule—both from feedback and internal observations—comes from its less common arrangement of the functional groups. The oxo group at the 6-position shifts its reactivity profile compared to more standard 2- or 4-oxo derivatives.

    Over time, we have fielded inquiries from specialists using other pyridine carboxylic acids who later found reaction rates or selectivity favor this variant for their synthetic assignments. Teams developing new medical agents focus on subtle changes in starting materials, sometimes observing significant impacts in downstream activity. From our point of view, those shifts get traced to the presence of the 6-oxo substitution, which alters both solubility and activation patterns. During workshops, several in-house chemists pointed out that hydrogen bonding and resonance effects shape the outcome in coupling reactions, offering routes that simpler pyridine acids don't provide.

    Another edge emerges in purification: unwanted byproducts formed with 2-oxo or 4-oxo analogues tend to have similar polarity, complicating separation. 6-oxo substitution gives a distinct Rf value during chromatography, making it easier to spot and isolate using standard silica columns, a detail that saves time on the bench and lowers solvent bills.

    We often have requests comparing our 6-oxo-1,6-dihydropyridine-3-carboxylic acid to isomeric analogues that come with different arrangements of the same core ring. The working consensus around our plant floor: the 6-oxo isomer presents fewer complications during aqueous workup and shows less tendency to form stubborn emulsions, especially in gram-scale preparations.

    Quality Under the Microscope

    Real-world chemical manufacturing means grappling with the fine details of quality. Any variation in the input raw materials, operator judgment, even simple differences in reactor agitation, can cascade into the way a batch turns out. Staff here spend as much time cross-checking calibration as they do in the actual weighing of starting reagents.

    We do not compromise on drying parameters. Clumped material from rushed processing ends up as rework, costing overtime and pushing back other schedules, and this lesson has improved our repeatability statistics over several quarters. Every container that leaves the warehouse gets tracked; data logging identifies not just lot numbers but also specifics of the operator and ambient conditions when the material left the suction filter.

    For customers running GMP or requiring documentation trails, these packaging and analytic steps ease tech transfer or method validation. Hands-on chemists appreciate knowing whether last month’s batch saw an unusual room temperature fluctuation, not just purity statistics from the printout. Our records keep that chain of custody clear—from operator initials on control sheets to real-time pictures from the drying oven.

    Listening to Researchers and Adjusting Process Routines

    It pays to pay attention to the people on the other end of the supply chain. Sometimes, that means working directly with synthetic chemists at partner firms or academic labs, double-checking the finishing step, or providing early samples with co-packed desiccant to support those running moisture-sensitive routes. We have adapted our filtration and drying packages at least twice in response to suggestions from long-term users whose reactions improved with tighter moisture thresholds.

    A university development group once ran into a persistent filtration problem and reached back to us. After a run-through on both sides, we deployed a finer pore membrane in our set-up, which solved both the upstream clumping and improved yield upon re-crystallization at their facility. This collaborative feedback loop refines operational habits and sometimes even sparks broader improvements across unrelated lines.

    Supporting Innovation in Synthesis: The Value of Reliable Intermediates

    Walk through our plant’s shipping bay any month, and you’ll see large drums and small bottles for dispatch, marked for research use in new drug discovery, custom monomer development, or specialty pigment work. Experience shows that in fields where researchers juggle multiple parallel syntheses, a hiccup in intermediate supply causes delays that echo through entire projects. We have watched R&D teams lose weeks waiting for a missed shipment or trying to substitute a slightly different intermediate when their process depends on a specific oxo-position.

    We’ve designed our restocking strategy around the predictability that chemists need, especially now that project cycles tighten and time-to-proof-of-concept grows shorter. By keeping a portion of every batch in reserve, we respond faster to sudden needs, which sometimes emerge when a research team discovers something unexpected late on a Friday. Nothing in this trade is more satisfying than providing a rush order that lets someone secure a breakthrough or file the next round of patent claims.

    Why We Focus on Practicality and Communication

    It’s easy to find technical write-ups or supplier catalogs that cover the theoretical value of chemical intermediates. Daily reality involves weathering power supply interruptions, training new hires about careful addition procedures, or adjusting the timeline when a valve gasket fails at 3 AM. We have learned to communicate the state of each batch honestly, staying clear of the false promises that cloak inevitable variability.

    We favor direct language in reporting problems or changes to regular customers, maintaining trust built from years of open conversations. Regulars know to expect complete Certificate of Analysis documents, detailing not only chemical parameters but also key notes—viscosity, color, even odor—since subtle irregularities sometimes signal more meaningful process drift than a formal assay can capture.

    No product, not even this versatile pyridine acid, meets every synthetic challenge. Situations arise where reactivity or solubility mismatches need a pivot, and in those cases, we pivot with users. Over the years, sharing experiences—both setbacks and triumphs—has deepened industry relationships and encouraged technical improvements that benefit new customers and veterans alike.

    Environmental Responsibility and Process Safety

    Our experience producing 6-oxo-1,6-dihydropyridine-3-carboxylic acid consistently reinforces how environmental attention influences the most basic planning choices. Efficient solvent recovery and energy management played a major role in the current configuration of our production lines. Some organic syntheses come with aromatic odors or require robust scrubbing equipment. During scale-up, keeping discharge within regulatory requirements required investment in both automation and operator safety training, which pays off with higher yield and less rework.

    Bundling responsible waste disposal into plant routines not only fulfills legal obligations—it also guards against discarded byproducts fouling subsequent runs. In the early years, trace contamination led to inconsistent color and purity results, both noticed by customers and flagged internally. Refined disposal and air-handling routines now standardize the process, so each fresh batch runs on genuinely clean kit.

    We track near-miss incidents and analyze process hazards with equal attention, aiming for improvements that support both the safety of onsite teams and the confidence of users who trust the material to be consistent.

    Commitment to End-User Success

    For those invested in new chemical synthesis or responsible for scale-up in pharma, dye, or advanced material contexts, stable intermediates mean fewer interruptions and smoother transitions between research and manufacturing phases. This reliability doesn’t result from printed promises but from repeated, careful observation and ongoing investment in people and process.

    The plant’s internal culture relies on cross-training: every new hire learns about 6-oxo-1,6-dihydropyridine-3-carboxylic acid during the first few months on the job, and nobody signs off on a shipment before understanding what small mistakes in drying or weighing can do to reaction performance. Quality reflects not just instrumentation and batch reports, but people who track trends and patterns month to month. Problems get discussed in regular crew meetings, with direct feedback loops from warehouse to lab.

    Over countless batches, process stability and transparency have proven to be more valuable than chasing marginal cost cuts at the risk of losing trust. The chemistry behind 6-oxo-1,6-dihydropyridine-3-carboxylic acid has complexity, but the priority remains serving real-world needs. Solutions to small process headaches—be it odd particle size variation or a tricky dissolution—arise from actually running and adjusting the process with user feedback.

    Building Trust Through Real Experience

    What makes this molecule interesting isn’t abstract potential, it’s the record of successful reactions, the trust our regulars place in every bottle leaving the packing room, and the understanding that nothing about chemical manufacture happens by accident. We keep learning every time a new requirement emerges or a repeat client requests a tweak in particle size or residual solvent.

    Watching shipments of 6-oxo-1,6-dihydropyridine-3-carboxylic acid leave for diverse laboratories and seeing the end-use applications broaden confirms one core lesson: true expertise grows on the production floor, where theory meets practice. We take pride in turning that practical expertise into material that researchers and commercial innovators can depend on, batch after batch.