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HS Code |
965116 |
| Iupac Name | 2-oxo-1,2-dihydropyridine-3-carbonitrile |
| Molecular Formula | C6H4N2O |
| Molecular Weight | 120.11 g/mol |
| Cas Number | 30743-54-1 |
| Appearance | White to off-white solid |
| Melting Point | 164-166°C |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC(=C(C=N1)C#N)C=O |
| Inchi | InChI=1S/C6H4N2O/c7-3-4-1-2-8-6(9)5-4/h1-2,5H,(H,8,9) |
As an accredited 2-oxo-1,2-dihydropyridine-3-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a sealed amber glass bottle, labeled, containing 5 grams of 2-oxo-1,2-dihydropyridine-3-carbonitrile powder. |
| Container Loading (20′ FCL) | 20′ FCL loads ~12 metric tons of 2-oxo-1,2-dihydropyridine-3-carbonitrile, packed in fiber drums or PE-lined bags. |
| Shipping | 2-Oxo-1,2-dihydropyridine-3-carbonitrile is shipped in tightly sealed containers, protected from moisture and direct sunlight, and stored at controlled room temperature. The chemical is packaged according to regulatory guidelines for safe transport, with appropriate labeling and documentation. Ensure handling by trained personnel using proper personal protective equipment (PPE). |
| Storage | 2-oxo-1,2-dihydropyridine-3-carbonitrile should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protected from moisture and direct sunlight. Store at room temperature or as otherwise specified by the manufacturer. Always use appropriate personal protective equipment when handling. |
| Shelf Life | 2-oxo-1,2-dihydropyridine-3-carbonitrile typically has a shelf life of 2–3 years when stored in a cool, dry place. |
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Purity 98%: 2-oxo-1,2-dihydropyridine-3-carbonitrile with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures optimal reaction yield and product consistency. Melting Point 142°C: 2-oxo-1,2-dihydropyridine-3-carbonitrile with a melting point of 142°C is applied in organic synthesis processes, where thermal stability enhances process reliability. Particle Size <10 μm: 2-oxo-1,2-dihydropyridine-3-carbonitrile with particle size less than 10 μm is utilized in medicinal formulation development, where fine particle distribution improves solubility and bioavailability. Stability Temperature Up To 120°C: 2-oxo-1,2-dihydropyridine-3-carbonitrile stable up to 120°C is used in high-temperature reactions, where it maintains molecular integrity during processing. Moisture Content <0.5%: 2-oxo-1,2-dihydropyridine-3-carbonitrile with moisture content below 0.5% is incorporated in analytical research, where low water content preserves compound reactivity and analytical accuracy. Molecular Weight 134.13 g/mol: 2-oxo-1,2-dihydropyridine-3-carbonitrile of 134.13 g/mol is used in custom chemical synthesis, where defined molecular weight supports predictive formulation and purity control. Assay (HPLC) ≥99%: 2-oxo-1,2-dihydropyridine-3-carbonitrile with HPLC assay not less than 99% is used in reference standard preparation, where high assay ensures analytical reliability. Low Heavy Metal Content <10 ppm: 2-oxo-1,2-dihydropyridine-3-carbonitrile with heavy metal content less than 10 ppm is adopted in sensitive biotechnological applications, where low contamination levels secure safety and compliance. |
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Working in the chemical manufacturing field, we see firsthand how the details in synthesis steps turn into tangible results in labs, pilot plants, or on production floors. Among the compounds we’ve produced for years, 2-oxo-1,2-dihydropyridine-3-carbonitrile brings a few special challenges and advantages. Our team gets directly involved with everything from raw materials to the final tests before shipping out the finished product. Day to day, our own equipment fills, blends, purifies, and tests every batch. That level of hands-on control lets us talk honestly about what makes this molecule stand out and where it finds a place in real-world applications.
This compound, built on a pyridine ring with a cyano group at the third position and a carbonyl next to the nitrogen, sits at an intersection in organic chemistry. The balance between its aromatic ring, nitrile, and carbonyl functions leads to unique reactivity. You won’t find many intermediate molecules that offer such a straightforward path to both heterocyclic and aromatic transformations. Pharmaceutical labs often reach for it when building more complex scaffolds. Its core structure serves as a launching point for several bioactive molecules—some leading to finished drug candidates, others for agricultural chemistry or advanced materials.
We’ve seen our 2-oxo-1,2-dihydropyridine-3-carbonitrile head off to medicinal chemistry labs, where it forms a piece of anti-inflammatory or antiviral lead compounds. Sometimes, agrochemical developers ask for this intermediate to chase new approaches to pest management—the cyano and carbonyl groups allow for versatile functionalizations. Our batch records show orders from pigment projects as well. Cyclization, alkylation or further condensation reactions with this building block get mentioned in reaction schemes from synthetic chemists who want options not available with simpler pyridine derivatives.
Producing this compound in large volume brings a few hurdles you only understand if you’ve run a production line yourself. It’s easy to make a gram in a research lab, balancing reagents under a fume hood, using small-scale glassware. We take it to the next stage: handling tens or hundreds of kilograms at a time under high-throughput reactions. Careful selection of solvents, temperature control, and pure starting materials become critical. Our plant routinely verifies every batch for chemical purity—especially the isomeric purity, which can influence downstream outcomes. Sometimes minor side-products or impurities at the part-per-million level can derail an entire synthesis run for a pharmaceutical client. That’s the kind of control we enforce by linking analytical instruments at every production checkpoint.
Customers often ask about polymorphic forms or about maintaining a particular crystal habit for their own downstream steps. During years of repeated batches, our team has dialed in drying temperatures and solvent choices that keep the product needle-shaped or fine-powdered, depending on the needs. Moisture content gets tracked tightly, as even small changes influence reactivity in subsequent reactions. Nothing highlights the difference between laboratory chemistry and plant-scale work quite like watching a run go off-spec because of overlooked process water or batch aging.
The specifications in our technical sheets come directly from decades of digging into the sources of process hiccups. Purity targets—typically above 98%—do not spring from tradition. They follow from batches where 95% purity led to uncontrolled byproducts or failed downstream steps. We control residual solvents and inorganics because we’ve seen what trace acidic or basic impurities do to later reactions. For shipments headed to active pharmaceutical ingredient syntheses, we push for absolute tightness in impurity control, using chromatography and spectroscopy to track possible decomposition products.
Appearance matters too. Some users prefer a bright white, free-flowing powder for easier weighing and dispensing. Others need finer crystals to dissolve quickly in synthesis steps. We respond by tailoring drying and crystallization conditions, not just to chase technical bullseyes but to match real users’ workbench habits. It’s routine for our shift supervisors to check the actual product flowing out of the blender against both lab specs and customer feedback. Over time, that’s how we’ve learned that “appearance” isn’t just cosmetic—it impacts metering, mixing, and the consistency of reaction outcomes in entirely different manufacturing environments.
The synthetic world holds dozens of pyridine-based intermediates. Some at first glance resemble 2-oxo-1,2-dihydropyridine-3-carbonitrile. The isomer positions make all the difference once you get into multi-step synthesis. For example, compare it to 2-pyridone or plain nicotinonitrile. The introduction of a carbonyl directly next to the nitrogen atom changes polarity and electronic distribution. Reagents react differently—electrophiles and nucleophiles approach distinct positions, and the resulting products branch into separate chemical families. Downstream, that flexibility lets medicinal chemists or industrial formulators either retain the heterocycle or modify it, opening the door to a bigger spectrum of analogs.
In our process logs, we see requests from clients accustomed to working with standard pyridone intermediates who need increased reactivity at the third position—or conversely, want precisely to block specific transformations by placing the cyano group there. Many of these subtle distinctions show up only in later synthetic steps, but they begin with the initial choice of reagent. In our experience, skipping from one pyridine intermediate to another often creates surprising bottlenecks due to changed reactivity, reduced solubility, or altered crystallization properties. Treating 2-oxo-1,2-dihydropyridine-3-carbonitrile as a simple “swap-in” rarely succeeds—actual synthetic routes respond dramatically to these structural shifts.
We’ve shipped this molecule in small bottles for early-stage medicinal screening, and in lined drums for large process optimization runs. Each time, the requirements and intended use shape our approach to batch release. One week it’s checked for trace metals for pharmaceutical compliance; the next week we’re adjusting quality on the fly for a team making new organic semiconductors. Our in-house chemists regularly attend review calls or visit industrial partners when scale-ups hit roadblocks. Both troubleshooting and optimization become easier once real feedback flows both ways—our technical support spent as much time helping solve end-stage solubility issues as they do answering questions about the initial synthesis.
Over the years, we’ve tracked how feedback from users drove changes in batch protocols. Originally, our drying schedules ran longer; this led to slightly different polymorph distributions. Input from a customer about changes in melting point recovery drove a revision to the crystal seeding process. By focusing on how people actually use our chemical—rather than just producing a number on a spec sheet—we’ve nudged both our process and others’ syntheses toward more reliable results.
Market swings, raw materials shortages, and shipping obstacles form a constant part of the manufacturing world. Our sourcing experts deal directly with supply-chain uncertainty. One year, a key precursor saw price spikes due to upstream plant shutdowns. Volume customers got hit, and suddenly we were retooling to buffer stock and adjust order schedules. This is not just about making up numbers on inventory—it’s about working with both upstream suppliers and downstream users to smooth volatility. We keep extra raw material on hand only if we know clients need steady delivery, because dead stock raises costs for everyone along the chain.
On the scale-up side, pressure to deliver larger lots means full transparency for any process change. Our auditors regularly trace every step from raw material input through reaction and purification to final QC. Customers running regulatory submissions—especially in pharmaceuticals—rightly demand full data packages and chain-of-custody documentation. Over the years, these demands have kept us vigilant about data integrity in both process economics and product traceability. Every batch that leaves our warehouse gets its own paper trail, ready for scrutiny under the toughest compliance rules.
Waste management and green chemistry principles have never been side issues for us—they are daily realities. The process for making 2-oxo-1,2-dihydropyridine-3-carbonitrile generates residues, spent solvents, and wash water that demand careful handling. Rather than treat waste reduction as an afterthought, we invest in recapture systems for both solvents and process water. Several years ago, a plant upgrade allowed us to cut solvent losses by more than 30%, both saving money and reducing environmental risk. All effluents pass through in-house treatment before leaving our gates.
We pay attention to worker safety as much as to environmental releases. Our teams operate under strict air-quality monitoring, personal protective measures, and exposure limits set even tighter than official guidelines in several jurisdictions. Direct knowledge of how small leaks, poor drum seals, or subpar ventilation affect both product and people keeps us focused on improvement. As process chemists ourselves, we know that a healthy and safe workplace isn’t optional—it’s vital for maintaining skilled staff and building lasting expertise.
Final delivery, whether in kilogram or ton scale, depends on details too often missed in theory. We’ve watched shipments arrive after weeks in humid conditions with clumped crystals, which impacts user performance at the bench. That led to investment in moisture-resistant liners, added drying agents, and improved packaging QA. Advice from long-term users about their specific storage conditions helped us develop guidelines for shelf-life and reactivity maintenance under varying climates—practical details that make a measurable difference in how the product behaves when it reaches its destination.
Documentation is more than a formality for us. Each shipment comes with batch records, analysis certificates, and documented packaging history matching exactly the actual batch made in our facility. We aren’t brokers moving material through distant hands; everything carrying our label passes under the eyes and hands of our own staff. Having resolved dozens of “mystery” issues by retracing shipments or reviewing handheld logs confirms the value of this close-knit approach.
Real-world chemistry often resists easy answers. Users sometimes run into solubility challenges, unexpected side-product formation, or instrument-detected trace impurities. Any chemist who’s had a reaction fail after a perfect run on paper understands the black box of chemical behavior. Our support doesn’t stop at batch release. If an issue arises in a user’s hands, we pull archived samples, repeat analyses, and arrange sample splits to compare their findings with our own. This troubleshooting mindset grows out of direct manufacturing experience—your own process rarely stays static for long. Over the years, collaboration between end users and our plant staff has solved a range of problems, from finding preferred recrystallization solvents to identifying rare contaminants introduced by downstream handling.
The long arc of process improvement keeps us moving forward. Input from users pushes us to refine batch consistency, extend shelf-life, and trim down trace impurities. Internally, we focus on upgrading production vessels, switching to cleaner energy sources, and further automating batch records for improved transparency. The greater the scrutiny from pharmaceutical, agricultural, or technological clients, the higher we set our own bar for performance. In practical terms, our business lives or dies on repeat orders and word of mouth from working chemists—consistent results matter more than glossy marketing sheets.
We see demand growing for this compound in both established markets and newer fields. As biotechnology, advanced materials, and pharmaceutical research evolve, the chemistry community keeps pushing for tighter tolerances, more sustainable manufacturing, and customized properties. Investing in production flexibility, quality control, and technical expertise keeps us ready for shifts in regulatory needs, customer preferences, or supply-chain volatility.
Our facility commits to ongoing improvements, both in core batch production and support for the people who actually work with these molecules each day. By keeping our focus on hands-on involvement, clear communication, and rigorous control of every step, we help our customers not just get product, but to succeed in their own innovation. Each lot of 2-oxo-1,2-dihydropyridine-3-carbonitrile leaving our doors reflects years of accumulated knowledge—not just chemical know-how, but the insight that comes from running a manufacturing operation with real end users in mind.
From the first kilo we made to the latest multi-ton batch, we’ve witnessed how this molecule enables progress in dozens of projects. Every improvement, every challenge, and every feedback loop strengthens both our process and our partnerships with the chemists, engineers, and project teams who rely on our work. Looking forward, we continue to approach chemical manufacturing not as a distant supplier, but as active participants in the chain of discovery, development, and successful application that underpins progress in science and industry. For us, every step in making and delivering 2-oxo-1,2-dihydropyridine-3-carbonitrile carries that responsibility—a responsibility shaped by real-world experience, guided by respect for those who put our products to work.