|
HS Code |
949464 |
| Iupac Name | 1,2-dihydro-4-methyl-6-(trifluoromethyl)-2-oxo-3-pyridinecarbonitrile |
| Molecular Formula | C8H5F3N2O |
| Molecular Weight | 202.14 g/mol |
| Smiles | CC1=CC(=O)NC(=C1C#N)C(F)(F)F |
| Inchi | InChI=1S/C8H5F3N2O/c1-4-2-6(8(9,10,11)3-12)13-7(14)5(4)15/h2H,1H3,(H,13,14) |
| Appearance | Solid, crystalline |
| Melting Point | Approx. 162-165 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Boiling Point | Decomposes before boiling |
| Cas Number | 32260-15-6 |
As an accredited 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams, labeled with chemical name, hazard warnings, lot number, and manufacturer’s information. |
| Container Loading (20′ FCL) | 20′ FCL container typically holds 12–14 metric tons of 3-pyridinecarbonitrile, securely packed in 25 kg fiber drums or bags. |
| Shipping | Shipping of **3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)-** requires secure, chemical-resistant packaging, proper labeling, and adherence to all hazardous material transport regulations. The substance should be shipped under ambient temperature, away from incompatible materials, with safety data sheets provided. Ensure compliance with local and international chemical shipping guidelines. |
| Storage | Store **3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)-** in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizers and strong acids. Protect from direct sunlight and sources of ignition. Use secondary containment to prevent leaks or spills, and ensure storage area is labeled and restricted to trained personnel. |
| Shelf Life | Shelf life of 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- is typically 2–3 years when stored properly. |
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Purity 99%: 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- with Purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal by-product formation. Melting Point 120°C: 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- with Melting Point 120°C is used in agrochemical development, where it provides optimal processing stability during formulation. Molecular Weight 230.17 g/mol: 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- with Molecular Weight 230.17 g/mol is used in fine chemical manufacturing, where it allows accurate stoichiometric calculations for synthesis. Particle Size <10 μm: 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- with Particle Size <10 μm is used in catalyst production, where it increases surface area for enhanced reactivity. Stability Temperature up to 200°C: 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- with Stability Temperature up to 200°C is used in high-temperature organic reactions, where it maintains structural integrity and consistent conversion rates. Water Content ≤0.2%: 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- with Water Content ≤0.2% is used in moisture-sensitive compound synthesis, where it prevents hydrolytic degradation of reactants. Chromatographic Purity ≥98%: 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- with Chromatographic Purity ≥98% is used in analytical standard preparation, where it assures precise calibration and reproducible results. |
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On any given day in our production facility, the talk often turns to the finer points of 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)-. It’s a mouthful, but to those who spend their days mixing, filtering, distilling, and testing chemical intermediates, this compound stands out as a clear workhorse. Over years of manufacturing, we’ve learned to judge the subtle details that turn a routine production batch into a top-tier product relied upon across several demanding sectors. It starts not in a boardroom, but right on the factory floor, from the pressure gauge readings to the sight of a clear crystalline sample held up to the light.
For those of us who focus on pyridinic compounds, the difference between good and great often comes down to habit, patience, and experience with fine margin settings. It’s always important to recognize a product not as an entry in a database but as the sum of the daily efforts behind each drum and bottle.
Chemistry isn’t about theoretical tables or digital simulations in our world—it’s about repeatable results in a real reactor. This chemical, marked by the pyridine backbone fused to nitrile and uniquely structured with a methyl group on the fourth position and a trifluoromethyl at the sixth, finds appreciation among those who need consistent, predictable intermediates for further reaction steps. It seems easy to overlook at a glance, but anyone who has dealt with unstable intermediates or impure starting materials can appreciate the consistency and stability our approach delivers.
Through the years, we noticed the difference between batch-to-batch consistency and measurable specifications is more than numbers. Our chemists take regular samples, not just at the end but throughout the process, looking out for subtle shifts in color, odor, and even the feel of a solution as it flows through custom glass columns. It’s these hands-on experiences that turn a line item into an asset. We observed that a single small change—say, a degree or two in temperature or a slightly different rate of addition—translates down the line to purity and performance during customer synthesis. Sometimes that spells the difference between a successful active pharmaceutical ingredient (API) synthesis and a troubled batch that needs costly rework.
Discussions about pyridines often reach the same crossroads: available derivatives outnumber the applications. There’s a tendency to view every substitution as just another chemical tweak, but as producers, we know not all changes are created equal. The 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl) motif offers a distinct chemical profile you won’t find in simpler nitrile pyridines.
We have learned over years of manufacturing that trifluoromethyl groups in the sixth position give more than just a higher molecular weight. They boost hydrophobicity and serve as practical handles for those working in medicinal chemistry or advanced material science. Unlike other pyridinecarbonitrile variations, this one creates an electron-deficient environment on the heterocycle, which shapes both how it reacts in coupling and how easily it’s incorporated into larger target molecules. From our side, it means we keep a close eye on the fluorinated precursor’s source and inventory, since variations at that level can ripple through to the customer’s end results.
We handle a range of pyridine compounds, and the neighbors to this product—like simple 4-methylpyridinecarbonitriles or those lacking the trifluoromethyl addition—don’t deliver the same performance in cross-coupling reactions or hydrogenations. A few years ago, one of our customers struggled with repeated side-product formation and fouling in a similar synthetic route, only to realize after in-depth consultation with our technical team that they needed the electron-withdrawing effect built into this structure. The replacement solved weeks of troubleshooting in one cycle, all because of this product’s ability to guide selectivity and suppress undesired reactivity.
Specifications in our operation run deeper than a certificate of analysis. That might appear as an administrative formality, but behind every percentage sits hours of distillation, drying under reduced pressure, and fine-tuning of filtration rates. This compound’s finished product specifications might read plainly to outsiders, but in the plant, there’s a living sense of achievement behind a 99% purity or an impurity threshold held reliably below 0.1%. Even scaling up doesn’t excuse quality slippage. Several times, we went back to recalibrate reactor dwell times or solvent ratios, particularly when reaction volumes grew in response to larger customer orders. Our staff still keeps the initial trial run data around as a constant reminder that those first, finicky experiments set the tone for everything that follows.
Chemists new to this field sometimes ask why a methyl at C4 and a CF3 at C6 matter so much; to them, a nitrile is a nitrile. In practice, even subtle electronic tweaks influence both physical properties and the route's robustness. We found in repeated HPLC checks and NMR runs that these substituents can shield reactive intermediates from moisture and background acidity, resulting in far less decomposition than in unsubstituted variants. Over time, this leads to longer shelf lives—something anyone responsible for bulk inventory learns to value deeply.
Years of feedback from process chemists and R&D teams taught us something simple but true: reliability counts most when every step in the synthesis has to work the first time. In our routine conversations with buyers, no one asks for an intermediate just to fill a stockroom. They need a material that runs straight through their synthetic plan, whether they’re working on new pharmaceutical candidates, specialty agrochemicals, or custom polymers.
We often ship this compound into hands-on labs working under tight project deadlines. In one memorable case, a pharmaceutical company racing to file a patent requested weekly updates on impurity profiles and moisture content for every lot. The clarity of our answers gave their regulatory team confidence—not because of abstract promises but due to a track record shaped by hundreds of hands-on, repeatable production runs. A smooth-running synthesis not only saves on solvent and catalyst; it lets customers avoid technical delays and setbacks, which in this field translates directly to competitiveness and reputation.
Our ongoing dialog with formulators and scale-up chemists revealed something else: Unexpected side reactions and off-target products crop up much less often when the 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl) variant is used, compared to those lacking the electronic influence from strong electron-withdrawing groups. This is not trivial for operations that run around the clock, where down time means missed targets and lost revenue. It’s these practical insights that help us improve, batch by batch.
In manufacturing, the best product is the one that delivers even when supply chains get complicated. We’ve lived through volatile periods—material shortages, regulatory changes on certain solvents, and spikes in demand from downstream industries. Through it all, our persistent focus has been on stock stability and process adaptability. Reactors don’t pause when orders flood in, nor do they wait for market shifts. Here, quick decisions and resilience under pressure make the difference.
This chemical’s handling may look routine on a paper form, but our operators developed a sixth sense for the subtle signals that indicate minor shifts in shelf conditions or drum headspace. Once, a tiny rise in humidity after a shipping container sat in an exposed port nearly led to a suspected loss of product quality. Only a careful dry-room reprocessing prevented a handful of lots from slipping below spec—a lesson we now bake into tighter delivery arrangements. Nothing replaces an experienced eye or a commitment to intervention before issues grow.
Customer feedback from scale-up trials or pilot plant phases feeds directly back into future runs. We’ve adopted shift schedules and tightened our lot-tracking so clients receive detailed histories on each batch. This isn’t bureaucracy; it’s a direct outgrowth of years responding to the needs of high-stakes R&D, custom manufacturing, and emerging science fields pushing for ever stricter purity thresholds and documentation.
What we see from the manufacturing side is that 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)- frequently serves as an early step in a much longer, multi-step synthetic flow. Intermediates in this family often play supporting roles, providing the core building blocks for more elaborate structures. Over the years, our partners investing in new active pharmaceutical ingredients or pesticide leads have shared their experiences converting this compound into advanced fragments or step-up intermediates. The consistent message: A trusted supply transforms ambitious synthetic schemes from ideas into reality.
On the plant side, the chemistry isn’t always glamorous. Grinding, stirring, filtering—these daily chores ensure a product free from unwanted isomers or side-products. Automated systems only get us so far. For the critical steps, hands-on monitoring, temperature logging, and the discipline of regular titrations still carry as much weight as any controller display.
We have witnessed chemists move from gram-scale proof-of-concept work to large-scale production orders as projects shift from discovery to commercialization. Each step up in bulk demand means reviewing our process from the ground up, re-confirming solvent recovery rates, and stress-testing purification protocols. Only after multiple scale-up runs, each checked by both classic wet-chemistry assays and modern analytical tools, do we sign off on a process revision. The compound has to deliver at both the lab bench and on the warehouse dock.
A recurring topic among our staff meetings concerns sourcing of certain fluorinated raw materials. The industry as a whole grapples with tightening global regulations on emissions, hazardous waste, and supply chain transparency. For us, this translates into diligent supplier vetting, frequent audits, and a willingness to adapt technical recipes as upstream sources evolve. A decade back, it might have been enough to rely on large, well-known suppliers. Today, constant change prompts us to maintain deeper relationships with multiple partners, cross-checking quality and reliability through each batch. Mistakes rarely stay isolated; even a minor slip at the procurement level carries direct quality consequences downstream.
Environmental compliance is now a baseline, not an afterthought. Our waste management team developed solvent recycling protocols and adopted high-efficiency capture techniques for fluorinated off-gasses. This was no small investment, but over repeated trial runs and audits, we found it leads to better operational predictability and lower both short- and long-term disposal costs. This is as much about responsibility as it is about protecting years of accumulated manufacturing experience from regulatory interruption.
Outside observers sometimes flatten specialty chemical manufacturing into a numbers game—capacity in tons or liters, orders filled against a deadline—but those in the trenches know there’s more. The ability to hit the same tight purity targets in small and large batches alike doesn’t happen overnight. Our line operators train under experienced supervisors for months, learning not just the textbook procedures but how to recognize the almost invisible signals that hint at tiny shifts in product quality or process drift.
Our internal debate about continuous improvement never stops—debates about inlet drying, the right grade of glass for specific distillations, or how to balance throughput against the careful cooling cycles that preserve product structure. Sometimes, this means pushing back against outside pressure for quicker, cheaper runs. Every shortcut invites long-term headaches—so the focus remains on reliability over speed.
In the case of 3-pyridinecarbonitrile, 1,2-dihydro-4-methyl-2-oxo-6-(trifluoromethyl)-, the extra steps pay off through greater acceptance in quality-focused fields, especially where rigorous documentation and batch history are required. We’ve had third-party audits run through every process step, confirming that our hands-on philosophy works through every kilogram we produce.
We don’t just stay in the factory; a lot of our applied learning comes from customer feedback. Some of the most interesting technical discussions involve the role of this compound in Suzuki couplings, Sonogashira reactions, and other modern palladium-catalyzed cross-couplings. Clients developing active pharmaceutical compounds report increased yields and lower byproduct levels than those using non-fluorinated analogues. On the agrochemical side, the compound’s robustness to trace moisture and oxygen means fewer failed syntheses, a crucial edge in process development campaigns battling for tight patent windows.
Another point of feedback from application teams involves its direct conversion into more advanced fragments. Those working in materials science have also used the compound’s unique electronic characteristics to manipulate the conductivity or optical properties of advanced polymers. Our technical staff regularly reviews application notes and literature, sharing findings and collaborating to refine not just product purity but also pre-shipment testing regimens based on specific end-use needs.
If there’s a lesson that looms large after decades in this sector, it’s that adaptability and mutual trust matter as much as process control. Every improvement we’ve made—whether in drying, purification, or documentation—has come in response to the real, daily challenges of those who take delivery of our products. We listen, adapt, and refine every step because we know the stakes: people’s careers and reputations turn on the outcome of every key intermediate.
Our records over the past years give a panoramic view of how high-quality intermediates enable companies to advance faster, take bigger chances, and pull off complex campaigns that would otherwise lose time to uncertainty or rework. The product may sound like another molecule, but the true value comes from hands-on commitment to transparency, flexibility, and a willingness to get every step right. It’s an ongoing process. Today’s batch becomes tomorrow’s benchmark, and each success raises expectations for everyone—including those of us who make it.