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HS Code |
159352 |
| Iupac Name | 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile |
| Molecular Formula | C8H5F3N2O |
| Molecular Weight | 202.13 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 110-114°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Cas Number | 121986-19-0 |
| Smiles | CC1=CC(=C(C(=O)N1)C#N)C(F)(F)F |
| Logp | 2.02 (estimated) |
As an accredited 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5-gram amber glass bottle with tamper-evident screw cap, labeled with chemical name, structure, CAS number, and hazard warnings. |
| Container Loading (20′ FCL) | For 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile: 20′ FCL loaded in sealed drums or bags, securely palletized, compliant with chemical transport standards. |
| Shipping | **Shipping Description:** 6-Methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile is shipped in tightly sealed, chemically resistant containers to prevent moisture and contamination. It should be packaged according to applicable local and international transport regulations, stored at ambient temperature, protected from light, and clearly labeled as a laboratory chemical for research use only. |
| Storage | 6-Methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers or acids. Protect from light and moisture. Always handle under suitable PPE, and follow all safety guidelines for storage of potentially hazardous organofluorine compounds. |
| Shelf Life | Shelf life of **6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile** is typically 2 years when stored cool, dry, and protected from light. |
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Purity 98%: 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile with purity 98% is used in advanced pharmaceutical synthesis, where it ensures high yield and reproducibility of target compounds. Melting Point 122°C: 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile with a melting point of 122°C is used in solid-state formulation studies, where it provides excellent thermal stability during processing. Molecular Weight 216.16 g/mol: 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile with a molecular weight of 216.16 g/mol is used in medicinal chemistry workflows, where it enables precise dose calculations in lead optimization. Stability Temperature up to 140°C: 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile with stability temperature up to 140°C is used in high-temperature reaction screening, where it maintains chemical integrity under thermal stress. Particle Size <10 µm: 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile with particle size less than 10 µm is used in fine chemical manufacturing, where it enhances dissolution rate and process uniformity. Water Solubility <1 mg/mL: 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile with water solubility less than 1 mg/mL is used in organic synthesis protocols, where it allows selective precipitation and purification of intermediates. HPLC Assay 99%: 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile meeting HPLC assay of 99% is used in reference standard preparation, where it provides analytical accuracy and consistency in quality control. |
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Anyone familiar with production chemistry knows the effort and technical rigor required to deliver advanced heterocyclic intermediates at consistent quality. As a manufacturer, we experience the challenges and rewards first-hand. Among a range of pyridine-based compounds, 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile stands out not because of its name but due to its critical role and unique features in both pharmaceutical and agrochemical research. Over the years, development teams have turned repeatedly to this compound for its special combination of reactivity and stability, avoiding corner-cutting synthesis and short-lived intermediates.
Producing this molecule consistently at commercial scale required investment in expertise and reliable raw material sourcing. The trifluoromethyl group at the 4 position sets it apart from most pyridine derivatives. Trifluoromethyl groups add unusual metabolic stability and electronic character — we see this in the way the finished molecule resists oxidative breakdown in certain settings. The nitrile at position 3 expands its scope, opening the door for further derivatization. Our team’s experience has shown that even slight contaminants or moisture in the synthesis steps can ruin crystallinity or result in sticky byproducts, so we track everything from incoming solvents to last-stage purification.
Every batch is made with a set of repeatable controls. We keep the final product between 98.5% and 99.5% purity. Recrystallization yields a consistent off-white to light yellow powder. Maintaining this color means attention to reaction temperatures and handling protocols. Filtration in a carefully controlled nitrogen environment keeps sensitive groups protected, reducing the risk of polymerization or color-forming side reactions.
We use HPLC and NMR for routine identity confirmation. Karl Fischer titration guides us on residual water levels, helping avoid batch-to-batch variation that could trip up our downstream customers. Specific rotation and melting point fall within established ranges drawn from international literature. For those using this molecule at scale, trust depends not on paperwork but on solid, repeatable sensory signals and analysis results.
Unlike simpler pyridine compounds that have limited scope, the 6-methyl-2-oxo-4-(trifluoromethyl) core offers a toolkit for those making advanced APIs, crop protection agents, or specialty chemicals. Its blend of electron-rich and electron-deficient sites means it reacts in a predictable, reliable way with halogenating agents, reducing agents, and carbon-carbon bond-forming reagents. Chemists at downstream sites appreciate how this enables cross-couplings and nucleophilic substitutions without needing re-protection steps. Several customers, especially in European pharmaceutical organizations, have reported using this pyridine variant to access novel heterocyclic compounds and have published their results in peer-reviewed journals.
Further, the trifluoromethyl substitution imparts metabolic resilience — products made from this molecule often show longer biological half-lives in lab models compared to analogous non-fluorinated structures. This serves two purposes: researchers value this stability in biological screening, and product developers see it as a path to more shelf-stable, high-performance specialty compounds.
In the past five years, use has shifted from small-scale lab settings to pilot and full production. Companies making fungicide candidates or antiviral research tools have relied on our team for kilogram batches, while some larger projects have demanded drum quantities with specialized packaging. We fill both roles, leveraging flexible automation and decades of scale-up know-how rather than squeezing every last gram from outdated glass linings or struggling with bottleneck reactors.
Process engineers on our team collaborate closely with customers to design handling protocols. Each kilogram avoids double-handling and spends minimal time exposed to air. Full traceability, including retention samples, ensures that in case of downstream issues, root cause can be identified rapidly — reducing costly investigation windows.
On paper, it may be tempting to overlook the importance of small changes like a methyl group at the 6-position or the arrangement of functional groups. In production, these subtle distinctions mean everything. We’ve seen formulations fail when a competitor offers version with a minor impurity, mostly from incomplete nitrile formation or oxidation at the carbonyl. These failures circle back to either wasted effort or months of lost development time.
Years producing this compound have shown us that the position and nature of each substituent pays dividends. The 2-oxo and 3-carbonitrile configuration, for instance, makes this molecule an effective synthon for other ring systems, as the adjacent carbonyl and nitrile can undergo ring-opening, condensation, and cycloaddition reactions. For customers in aromatic halogenation or complex PEGylation programs, this saves at least one intermediate step. Cheaper alternatives often bring in positional isomers that just can’t match this efficiency.
Stable, easy to weigh, and manageable at ambient temperature, our grade of 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile does not demand excessive protection in most industrial settings. Still, protecting agents are available for those scaling into high-purity pharmaceutical synthesis. Some customers have asked us to explore granular or pelletized forms, but repeated side-by-side studies revealed that the fine crystalline powder ensures better recovery and dissolves quickly — a priority for speed-conscious process development cycles.
Other vendors sometimes rely on the generic version of this molecule without investing in controlled atmosphere storage, leading to yellowing, clumping, or loss of free-flowing characteristics. We prefer to ship sealed fiber drums under dry nitrogen. Our stability studies, going back to the earliest development lots, show unchanged HPLC profiles when handled this way over a two-year window.
Comparing this molecule to relatives like un-substituted 2-oxo-pyridines or those without the trifluoromethyl group reveals sharp contrasts in both reactivity and long-term storage. In catalysis work, the unique electron-withdrawing effect of the trifluoromethyl helps access selectivities or yield improvements that competitors struggle to replicate.
Additionally, the presence of the nitrile at the 3-position enables customer teams to graft additional complexity, building out into 4-quinolone frameworks or bicyclic systems without heavy retooling. Attempts to substitute with more generic pyridine-2-one derivatives or those lacking the CF3 often result in side products or non-selective reactions. Our customer feedback confirms that even a small impurity level from poorly controlled synthesis can translate into unforeseen reactivity — leading to costly purification steps later.
We prioritize clean, contamination-free packaging, since even trace contaminants in specialty fine chemicals can have unpredictable downstream effects. Our packing team uses double-bagged liner systems within each drum, tested for physical robustness and permeation resistance. These measures aren’t overkill for most, but scaled operations setting up automated dispensing lines notice the difference. Feedback from process chemists using open-hopper transfer methods confirms smoother flow, less product loss, and less operator cleanup compared to material supplied in foil laminates or traditional single-liner bags.
Thermal stability and non-hygroscopic character remain consistent across large lots. We regularly sample stock for both chemical and visual quality attributes, documenting trends before they become problems. In one recent review, a scale-up team flagged a faint odor from a competitor’s lot; our review found an overlooked amine co-solvent in their process, an issue we've eliminated through precise solvent choice and vacuum stripping.
Most buyers judge products on day-one delivery, but lasting trust comes from month-after-month experience. Our manufacturing team has tracked new analytical methods, aligning in-house practices to the latest global guidelines and updating reference standards as literature evolves. This responsiveness is far more than an exercise in compliance — it reflects our hands-on engagement with both academic and commercial partners around the world.
Supply chain resilience matters. Raw materials, including reagents for trifluoromethylation, are sourced only from audited suppliers. In the past global transportation upsets have threatened continuity for smaller producers. Anticipating extended lead times, we maintain safety stock and encourage all customers to forecast collaboratively, reducing the risk of project delays or emergency air shipments. We know how critical it is to have the exact compound, not a close substitute, arrive when synthesis windows open.
Every production run is preceded by a safety review, integrating the latest findings from both academic research and customer feedback. We share best practices drawn from years of handling: gloves, goggles, powder handling stations, and strict segregation from acids or strong oxidizers during use. Several customers have reached out when transitioning this molecule from research to pilot scale, seeking help adapting lab procedures to industrial cGMP standards. We offer technical support, practical troubleshooting, and introduce customers to equipment suppliers experienced with challenging pyridine intermediates.
Our experience tells us that transparency matters most when downstream teams raise a question. Every package ships with documented lot records, COAs referencing full analytical data, and available spectra on request. Some projects require detailed impurity profiles, especially in regulated industries. Our ability to retain representative samples from every batch means we can revisit and answer questions even after the project concludes — a tangible commitment rarely matched by those offering commodity product.
Teams synthesizing lead candidates for early-phase drug discovery often reach out for technical advice, bracing for issues around solubility or batch homogeneity. We’ve seen advocates for alternative solvents struggle with incomplete dissolution until switching back to our recommended systems. Others report downstream products with unusual IR bands — together, we diagnose and resolve the impurities, sometimes traced back to handling outside our suggested guidelines. This close interaction reduces troubleshooting cycles, and builds long-term relationships where shared information actively improves both manufacturing reliability and customer development outcomes.
Market oversight and industry standards push everyone to keep raising the bar. Our team keeps track of changes to environmental and handling rules for nitrites, pyridine derivatives, and trifluoromethylated reagents. We offer test results and compliance evidence to help customers not just meet but demonstrate adherence to legal and best-practice expectations.
Looking at global trends, interest in fluorinated intermediates grows as research highlights their impact on target specificity and metabolic fate. The molecule under discussion proves its worth, playing a role in pipeline projects for anti-cancer agents, fungicides, and emerging antiviral classes. Feedback cycles between our commercial team and the labs using our compound create a shared resource: refinements in analysis, better defect tracking, and a deeper grasp of stability parameters under a variety of storage and handling conditions.
Manufacturing and delivering 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile at scale is less about chasing quarterly margins and more about building a platform for synthetic progress. We continually invest in modest process improvements, give honest attention to supplier changes, and learn from both mishaps and successes every season. Responding to customer suggestions shapes our future development work, from optimizing drying cycles for even lower moisture levels to expanding package sizes for bulk users.
Every kilogram of this compound that leaves our site reflects genuine pride and decades of technical know-how. We see the results downstream — new patent filings, progress in therapeutic leads, and better crop protection agents. Our commitment to open communication, quality, and reliability places us on the customer’s side. Any company can deliver a drum of powder, but few stand behind each step of its creation and remain ready to support its use over years of demanding research and development.