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HS Code |
437038 |
| Chemical Name | 4-(Trifluoromethyl)nicotinonitrile |
| Molecular Formula | C7H3F3N2 |
| Molecular Weight | 172.11 g/mol |
| Cas Number | 349-76-8 |
| Appearance | White to off-white solid |
| Melting Point | 46-48°C |
| Boiling Point | 203-205°C at 760 mmHg |
| Density | 1.37 g/cm3 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CN=CC(=C1C#N)C(F)(F)F |
| Inchi | InChI=1S/C7H3F3N2/c8-7(9,10)5-1-2-12-3-6(5)4-11/h1-3H |
| Synonyms | 4-(Trifluoromethyl)pyridine-3-carbonitrile |
As an accredited 4-(Trifluoromethyl)Nicotinonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g quantity of 4-(Trifluoromethyl)nicotinonitrile is packaged in a sealed amber glass bottle with a secure screw cap. |
| Shipping | 4-(Trifluoromethyl)nicotinonitrile is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be transported according to local and international regulations for chemicals, typically as a non-hazardous or limited-quantity substance. Ensure the package is clearly labeled, and all safety data sheets (SDS) accompany the shipment for safe handling. |
| Storage | **4-(Trifluoromethyl)nicotinonitrile** should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from direct sunlight. Store at room temperature, and ensure proper segregation from food and drink. Clearly label storage containers and follow all relevant safety protocols and regulations. |
Applications of 4-(Trifluoromethyl)Nicotinonitrile in Industrial ManufacturingAs a specialized manufacturer, we supply 4-(Trifluoromethyl)Nicotinonitrile for a range of advanced downstream sectors. Our technical teams collaborate with producers in pharmaceutical synthesis, agrochemical development, specialty material production, and fine chemical manufacturing. Below we detail application scenarios, typical industrial formulations, and established compliance standards based on real-world customer practices. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers rely on this intermediate for pyridine-based API synthesis, serving as a building block in small-molecule drug R&D and production. The compound’s electron-withdrawing trifluoromethyl group influences pharmacokinetic properties and metabolic stability in target molecules. Synthesis routes frequently involve Suzuki-Miyaura and nucleophilic substitution, with our technical support ensuring controlled quality and batch reproducibility for downstream GMP processes. Industry compliance standards
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2. Crop Protection Actives ManufacturingAgrochemical formulators use this raw material as an intermediate for synthesizing trifluoromethyl-substituted nicotinic insecticides. The compound enters the process at early-stage nitrile coupling, contributing to the selectivity and bioavailability of final active ingredients. Producers focus on stability, regulatory-mandated impurity limits, and scale-up parameters to meet global registrations for field application products. Industry compliance standards
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3. Specialty Materials and Electronic ChemicalsProducers in specialty materials use the compound for custom synthesis of functional building blocks in advanced polymers, electronic materials, and high-performance coatings. The fluorinated moiety imparts chemical resistance, thermal stability, and tuned dielectric constants, which are crucial for semiconductor precursor or photoresist resin manufacturing. Stringent process controls and raw material traceability are essential for end-user validation in electronics fabrication. Industry compliance standards
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4. Fine Chemical Synthesis for Analytical ReagentsProducers of analytical and diagnostic reagents use this compound as a reference standard or reactant for labeled molecular probes. Its chemical structure allows for the design of compounds with high sensitivity and selectivity in chromatographic and spectroscopic applications. Customers require precise batch documentation and reference material traceability for use in regulated testing environments. Industry compliance standards
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5. Synthesis of Veterinary PharmaceuticalsThis compound is applied as a core intermediate in the synthesis of veterinary drug candidates, particularly for companion animal parasite control products. Processes involve nucleophilic aromatic substitution, with careful control of reagent purity and formation of downstream biologically active molecules. All batches meet quality assurance standards for subsequent blending and formulation at animal health manufacturing facilities. Industry compliance standards
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In the fine chemical industry, we often find that demand for specific pyridine derivatives like 4-(Trifluoromethyl)Nicotinonitrile keeps growing alongside new pharmaceutical and agrochemical research. At our plant, every day brings a constant effort to maintain product consistency for such advanced intermediates. The team monitors every stage, starting with purification and carrying through the final nitrogen testing, to confirm both purity and moisture stay within strict boundaries. The product carries a formula of C7H3F3N2, with a molecular weight of 172.1.
Chemists in the laboratory and operators at the reactors both recognize 4-(Trifluoromethyl)Nicotinonitrile’s value. Unlike basic nitriles or simple pyridines, the presence of both a cyano group and a robust trifluoromethyl substituent at the 4-position delivers unique chemical reactivity and increased metabolic stability, often favored for new drug candidates or crop protection agents. Products shipping from our reactors consistently reach a minimum purity exceeding 99%, confirmed by HPLC, and all meet tight controls on residual solvents and heavy metals.
In research and commercial settings, this compound often becomes a preferred intermediate when a project calls for greater fluorine content, reliable electron-withdrawing functionality, and robust pyridine backbone stability. The sequential difference made by trifluoromethylation separates this molecule from simpler pyridine-based nitriles such as 4-cyanopyridine or 3-(trifluoromethyl)pyridine. Our experience shows that the increased lipophilicity and electron-withdrawing strength from the trifluoromethyl group can make a remarkable difference in properties such as bioavailability or resistance to enzymatic degradation. Teams developing kinase inhibitors or investigating new herbicide scaffolds frequently cite the benefit of this structure compared to less substituted analogues.
Movements in pharmaceutical R&D set new bars for both efficiency and safety, prompting renewed appreciation for specialty intermediates like 4-(Trifluoromethyl)Nicotinonitrile. As global demand shifts and programs compete to bring new molecules to market, batch reproducibility has gained even more importance. We design our synthesis to scale, and our operators bear in mind raw material traceability, minimizing impurities that might complicate downstream transformations. The feedback loop between our plant floor and customer laboratories continues to direct focus on minimizing process impurities (including isomers and over-oxidized byproducts), which could otherwise frustrate scale-up or lead to batch failures.
No matter how elegant a chemical structure might appear on paper, it can become irrelevant without the muscle of reliable manufacturing and thoughtful logistics. Years of micro-adjustments to reaction conditions—temperature controls, solvent swaps, agitation speeds—have gradually led us away from less selective methods, such as uncontrolled trifluoromethylations or oxidation runs that strip away yield and generate difficult-to-remove tars. The right process design keeps our operators safe, our batch records clean, and our customers confident in the lot-to-lot uniformity. We document each cycle, retain retention samples, and engage in regular audits, following the sort of practices demanded by regulated pharmaceutical supply chains, not just chemical catalogs.
Reactivity patterns for 4-(Trifluoromethyl)Nicotinonitrile often surpass more basic nitrile analogues, mainly because the electron-withdrawing group draws attention where medicinal chemists want it—helping with targeted C–H activation, selective coupling reactions, and smooth late-stage modifications. This sort of reliability enables research groups to avoid surprises, whether in the medicinal chemistry wing or in agrochemical formulation labs. We’ve watched customers struggle with batches from traders who source from inconsistent origins or repurpose material originally destined for less demanding sectors. That route rarely holds up, as even trace levels of byproducts or unexpected water sensitivity can risk entire development timelines.
Within our walls, the team’s expectations constantly rise. The daily pressure to produce means continually evaluating process chromatography, fine-tuning quenching stages, and record-keeping every pH swing in the reactor profile. Each operator learns to spot trouble before it becomes waste. Our final batch release only happens after confirmation from a trained analyst using validated HPLC and GC methods. UV/Vis spectra and NMR scans have become so routine that for certain lots we’ve adopted stricter impurity cut-offs than industry norms suggest. For customers operating under GMP or developing regulated substances, this extra layer means fewer surprises and better yields in downstream chemistry.
The 4-(Trifluoromethyl)Nicotinonitrile leaving our plant ships in tightly sealed HDPE containers with pre-shipment desiccant checks—minimizing water ingress, which could hydrolyze the nitrile or affect subsequent transformations. Storage recommendations come from direct experience: low moisture, moderate temperature, and minimal exposure to acidic fumes. The product packs efficiently in drums for larger scale, or smaller units for lab consumption; this plan is born out of years listening to customers whose projects depend on immediate access to high-purity material, right when the next synthetic step opens up.
Compared to simple pyridine nitriles, the trifluoromethyl group at the 4-position in this product triggers tangible differences during both chemical synthesis and application testing. Its electron impact raises differences in pKa by up to two orders of magnitude, and the presence of fluorine helps medicinal chemists create molecules resistant to oxidative metabolism. Often, we compare the reactivity of 4-(Trifluoromethyl)Nicotinonitrile with its close cousin, 2-(trifluoromethyl)nicotinonitrile; the 4-substituted version usually enables slightly better regioselective coupling and can deliver higher yields of desired products with fewer overreaction byproducts.
Most standard 4-cyanopyridine grades lack the chemical stability under harsh reaction conditions, where the trifluoromethylated analog endures. Process chemists report higher success rates when pairing this intermediate with transition metal catalysts, including palladium-catalyzed Suzuki or Buchwald coupling. Substitution on the pyridine ring prevents complications that often interrupt routes using more reactive, less robust aromatic ring systems. Unlike certain halogen-substituted pyridines, which might provoke regulatory hurdles or unwanted side reactions, we find the trifluoromethyl group provides greater synthetic latitude with less toxicological baggage.
Several years back, a customer in crop protection development approached us after repeated failures using a non-fluorinated analog. Their starting material exhibited poor shelf stability and required strict refrigeration. Simple contamination by trace water led to significant yield drops and color formation in final active compounds. Our 4-(Trifluoromethyl)Nicotinonitrile, in contrast, carries a robust trifluoroalkyl group, providing shelf life approaching two years under optimal storage, with minimal signs of polymerization or discoloration. The product's lower inclination toward side reactions has allowed these teams to streamline workflows—minimizing extra purification steps or secondary drying cycles.
An innovation on our production line, including fully inert transfer under nitrogen and frequent microfiltration, dramatically reduced residual sodium or iron from raw materials. This seemingly small improvement quietly increased customer batch yield by over 4%, and reduced the need for labor-intensive post-processing on the client’s end. Such continuous improvements don’t appear in catalogs but have become bedrock for researchers and formulators seeking high success rates during regulatory trials or pilot production.
Environmental and regulatory pressures keep increasing; our team responds by retooling process waste water management and adopting low-residue solvents. We use closed-loop solvent recovery systems, sharply cutting effluent and improving recyclability. Our compliance records cover all typical European and North American expectations, thanks to regular external audits. Continuous improvement remains a production mindset rather than just a reporting item for regulatory filings.
By-product streams now get routed for energy reclamation or sold to secondary users, which reduces landfill and promotes secondary value creation. Our experience shows solvents and reagents posing the highest environmental risk also carry higher risk for unfiltered process impurities. Close supplier relationships and active material qualification help us catch issues before they ripple down to our reactor floor—or the customer’s.
During feedback calls, formulation chemists regularly mention how 4-(Trifluoromethyl)Nicotinonitrile simplifies their synthetic planning. They can count on the trifluoromethyl group to push electron density toward selective positions on the pyridine ring, opening up coupling or acylation steps otherwise burdened by competitive side reactions. One client, running a medicinal chemistry project targeting resistant bacterial strains, described how the intermediate seamlessly merged into their late-stage pipeline. Their analytic team stressed that side products appeared less frequently, so their need to run extra column purifications dropped. In agricultural applications, similar stories appear, with the compound’s robust profile giving superior stability in the presence of complex matrices, dirt, oxidizing agents, or sunlight.
We encourage open communication from customers about experiences with their own catalytic systems, reaction scales, and purification hurdles. Genuine partnership has helped us identify where certain batches, after transportation or extended storage, might begin to pick up trace hydrolysis byproducts. By refining our packaging and lowering moisture permeability, we responded quickly; improved product shelf life now ranks high among points our partners emphasize in repeat feedback.
Manufacturing works best as a living system, not a static checklist. Over the years, we noticed product performance differences often sprang not from the molecular structure but from how different manufacturing routes impacted residuals or fine particulate content. To combat this, our plant adopted real-time monitoring—collecting sample spectra in-process and correlating findings with customer application yields. Small shifts in temperature or residence time sometimes led to micro-impurities, only detectable by LC-MS but affecting downstream reactions, especially scale-ups. Recognizing this, we altered several batch control points and added high-purity filtration steps.
Such process modifications reduced complaints and increased repeat batch volumes. In the rare event a batch didn’t meet customer specs on delivery, we traced it back to actionable plant-floor data in minutes. By proactively addressing root causes, we side-stepped recurring issues while giving customers credible, data-driven explanations along with corrected product—no excuses or stalling.
In recent years, market requirements have grown tougher, especially as pharmaceutical and agrochemical synthesis races to deliver ever more specialized molecules. Project managers and senior chemists describe compressed development timelines and rising expectations for analytical transparency. For many teams, persistent failures with standard-purity intermediates send work back to the drawing board; delays become expensive quickly. Our years of work with 4-(Trifluoromethyl)Nicotinonitrile fit this environment, where unplanned rework isn’t an option. Reproducibility and documented batch lineage matter much more than textbook reaction yields or theoretical purity claims.
We hear repeatedly from purchasing teams and development chemists about hidden pitfalls with intermediates from less established sources—moisture issues, solvent residues, even unexplained color changes on storage. By building robust feedback cycles into our order management, and integrating technical sales with process engineering, we bridge gaps long before something goes wrong at the point of use. This interconnectedness shapes all continuous improvement efforts, translating real laboratory needs into focused plant upgrades. Many traders or generalized distributors miss this detail; but as the actual manufacturer, on-the-ground know-how shapes our standards at every touchpoint.
Traders and resellers rarely track feedback about purification, real shelf life, or the nitty-gritty details faced by formulation scientists. From the factory floor, everything comes down to authentic process knowledge, fault diagnosis, and the hard lessons from batches that didn’t go as planned. We’ve spent years learning to work up from the molecular specifications to application performance—not just selling a synthetic puzzle piece but supplying a real-world solution that fits the entire workflow.
4-(Trifluoromethyl)Nicotinonitrile doesn’t just represent another intermediate in the catalog; it signals a shift toward smarter, more robust synthetic design. Its distinct features—notably the strong electron-withdrawing power, chemical stability, and proven track record in regulated and non-regulated industries—reflect what real-users look for when the margin for error shrinks. We use plain feedback from lab partners, not just internal numbers, to rate success and steer new improvements. Plant managers, laboratory heads, and R&D chemists all contribute to defining which specifications matter most; nothing stays theoretical for long.
In every step from procurement to final product integration, reliability and collaborative improvement drive our approach. Unlike distributors, our team sits directly with process data and application outcomes—bridging the documentation gap and ensuring every inquiry gets an experienced answer rooted in plant performance and customer success rates. While other players might chase the lowest cost or broadest reach, real-world experience at every scale—bench, kilo lab, or full plant—shapes our standard operating procedures and customer engagement.
The path forward for 4-(Trifluoromethyl)Nicotinonitrile isn’t static. As chemistries evolve and regulatory frameworks adjust, needs shift fast. Customer-driven batch qualifications now push our own internal R&D to unearth even more selective catalysts, smarter purification cycles, and packaging tweaks for global climates. None of these advances comes from guessing or speculation; they emerge from honest feedback and hands-on knowledge. Every lot delivered forms a link in a much larger chain, joining supplier, end-user, and regulator in a collaboration that pushes boundaries and sets new benchmarks for performance.
Stepping beyond the basics, we see in 4-(Trifluoromethyl)Nicotinonitrile a real-world tool for chemists under pressure to deliver next-generation medicines, advanced crop protectants, or specialty materials. Its robustness and unique substitution pattern set tangible advantages, but it’s the honesty and technical depth of manufacturing that defines end-user experience. Bringing the combined insight of the entire production crew—plant managers, quality analysts, logistics professionals, and technical partners—makes the difference between theoretical compliance and real-world trust.
We choose to operate in this space because every day uncovers another opportunity for genuine improvement. Our team stays connected not through buzzwords or perfunctory metrics, but by knowing every bottle, drum, and process step represents a tangible promise to our partners. As researchers push further into new targets, and scale-up hurdles challenge even seasoned chemists, we remain committed to backing every order with hard-won experience, transparent data, and straightforward solutions—keeping 4-(Trifluoromethyl)Nicotinonitrile a step ahead in both innovation and dependable service.