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HS Code |
591100 |
| Chemical Name | 4-(trifluoromethyl)pyridine-3-carbonitrile |
| Molecular Formula | C7H3F3N2 |
| Molecular Weight | 172.11 g/mol |
| Cas Number | 87482-80-2 |
| Appearance | White to off-white solid |
| Melting Point | 68-72 °C |
| Smiles | C1=CN=CC(=C1C#N)C(F)(F)F |
| Inchi | InChI=1S/C7H3F3N2/c8-7(9,10)6-4-12-3-5(1-11)2-6/h2-4H |
| Solubility | Soluble in organic solvents (e.g., DMSO, DMF) |
| Storage Conditions | Store at room temperature, in a tightly sealed container |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 4-(trifluoromethyl)pyridine-3-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams, sealed with a screw cap, labeled with chemical name, hazard symbols, and handling instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-(trifluoromethyl)pyridine-3-carbonitrile: Securely packed, palletized drums or bags, maximizing space, ensuring safe international chemical transport. |
| Shipping | 4-(Trifluoromethyl)pyridine-3-carbonitrile should be shipped in tightly sealed containers, protected from moisture and light. It must comply with all applicable local and international regulations for shipping chemicals, including appropriate labeling. Recommended shipping methods include ground or air transport in accordance with hazardous materials guidelines to ensure safety and product integrity. |
| Storage | Store **4-(trifluoromethyl)pyridine-3-carbonitrile** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition or heat. Protect from moisture and direct sunlight. Keep separated from incompatible substances such as strong oxidizing agents and strong bases. Use appropriate personal protective equipment (PPE) when handling to avoid inhalation, ingestion, and contact with skin or eyes. |
| Shelf Life | Shelf life of 4-(trifluoromethyl)pyridine-3-carbonitrile is typically 2-3 years when stored in a cool, dry, and airtight container. |
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Purity 99%: 4-(trifluoromethyl)pyridine-3-carbonitrile with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal side reaction formation. Melting point 92°C: 4-(trifluoromethyl)pyridine-3-carbonitrile with a melting point of 92°C is used in agrochemical research, where it enables consistent crystallization and reproducible batch production. Molecular weight 172.11 g/mol: 4-(trifluoromethyl)pyridine-3-carbonitrile at a molecular weight of 172.11 g/mol is applied in medicinal chemistry projects, where precise reagent quantification supports reaction predictability. Stability temperature up to 120°C: 4-(trifluoromethyl)pyridine-3-carbonitrile with stability temperature up to 120°C is utilized in heated reaction protocols, where it maintains compound integrity during process development. Particle size <50 μm: 4-(trifluoromethyl)pyridine-3-carbonitrile with a particle size below 50 μm is deployed in formulation science, where enhanced dispersion improves solubility in target matrices. |
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In the chemical business, understanding a compound’s backstory from those who actually manufacture it makes a difference. Our team at the synthesis plant has spent years working with 4-(trifluoromethyl)pyridine-3-carbonitrile, a building block that bridges fundamental science with practical application. What we offer isn’t just a commodity shipped off a warehouse shelf. Our experience with the chemistry and scaling of this compound stretches beyond data sheets and typical reports. Here, we put together a straightforward introduction to this specialized intermediate, drawing on the team’s hands-on knowledge and observations from daily production.
4-(Trifluoromethyl)pyridine-3-carbonitrile is a pyridine derivative, notable for its electronegative trifluoromethyl group attached to the fourth ring position, and a cyano group located on the third. Its structure brings together two critical functions: the strong electron-withdrawing -CF3 and the nitrile -CN. These features drive its behavior in organic synthesis, particularly for customers developing pharmaceutical leads, agrochemical candidates, and specialty materials.
This isn’t a compound you find everywhere. Every batch starts with aromatic halides and employs fluorinated intermediates, demanding strict control in our reactors. Only skilled technicians—people who’ve handled both the raw halides and tricky fluoride sources—can keep the process consistent. We use high-purity solvents and reactors lined for resistance to aggressive conditions during the trifluoromethylation and subsequent cyanation stages. Every step gets scrutinized for completion and selectivity before moving forward. These measures aren’t bells and whistles; they’re the product of real production-time headaches, uncooperative intermediates, and years of hands-on experience with leaks, off-gassing, and temperature swings.
Our most in-demand model carries a molecular formula of C7H3F3N2, with a molecular weight you’ll find reported as approximately 172.1. Across years of shipments and customer feedback, we have settled on a technical standard that hits the sweet spot between purity and process efficiency. Our standard material leaves the plant at a minimum assay of 98 percent, measured by both HPLC and NMR, with controlled residual water and minimal organic solvents.
Physical form depends on temperature and humidity during finishing. The product typically appears as an off-white to pale yellow crystalline solid. Handling losses and caking once plagued our earliest production runs, so we revamped drying procedures and packaging. There’s a noticeable stability now in warehouse conditions and during extended shipping, with no unpredictable clumping or melting hazards under standard storage.
Much of the 4-(trifluoromethyl)pyridine-3-carbonitrile leaving our site ends up in research and production labs developing new pharmaceuticals. Medicinal chemists favor the compound because that -CF3 group, stubbornly electron-withdrawing, influences pharmacokinetic properties including metabolic stability and binding. Our own technical support team fields regular questions about optimizing its use in Suzuki-Miyaura and other cross-coupling protocols. The large-scale reactors at our plant have seen firsthand how selectivity changes when using boronic acids, stannyl derivatives, or organozinc reagents. The experience with isolation issues and purification prompts us to keep technical supports open to buyers—a corner often cut by intermediaries, but which ensures safer, more predictable reactions for the user.
Another large customer base works in the agrochemical field. In synthesis routes for fungicides, insecticides, or herbicide re-engineering, research teams—sometimes at major brands, more often at fast-moving startups—adopt this compound to introduce unique molecular scaffolds. Often, the team at our plant hears about application in late-stage diversification steps, especially when the final candidate must show both biological activity and resistance to breakdown in the field. Our consistency in specification gets tested here, as margins for by-product tolerance in agrochemical formulations are razor thin.
A handful of customers use this building block for specialty materials: sometimes for advanced dyes, sensors, or even organic electronics. Here, subtle impurities can derail downstream properties, so technical teams often ask for custom specifications or even joint R&D. We’ve learned how minor changes in synthesis (adjusting crystallization temperatures or switching purification routes) can impact electrical or spectral properties—details invisible to a basic Certificate of Analysis.
Compared to related pyridine derivatives or trifluoromethyl-substituted aromatics, this compound stands apart in a few key respects. For those of us on the plant floor, the biggest difference lies in process sensitivity. Unlike simple trifluoromethylpyridines, the combination with a cyano group here demands more care during every operation. Purification by crystallization or preparative chromatography requires ongoing monitoring. Our team found early on that loosely defined crystallization points caused variable melting points and unpredictable purity once the product reached customers. We have since added in-line monitoring and improved process timing to nail down these bottlenecks.
Downstream, many customers have told us that 4-(trifluoromethyl)pyridine-3-carbonitrile outperforms other pyridine nitriles in substitution reactions, especially where steric hindrance plays a role. The trifluoromethyl group changes reactivity just enough to enable selective transformations that fail with regular nitrile-substituted pyridines. Feedback from process chemists driving kilo-lab and pilot-plant runs prompted us to maintain batch-to-batch uniformity, since even slight shifts in composition impacted overall process yields.
Compared with simpler trifluoromethyl aromatics lacking a pyridine nitrogen, this compound carves out a niche for those needing the added hydrogen bond acceptor and electron-deficient ring. The N atom at the right ring position matters when customers need to leverage pyridine-based metal ligation or deliberate modulation of basicity—for example, in catalytic cycles relevant to C-H activations or heteroaromatic substitution routes.
Scaling production of 4-(trifluoromethyl)pyridine-3-carbonitrile has provided our chemists and operators with more than a few stories. Years back, early attempts at direct trifluoromethylation saw runaway reactions and spotty yields. Drum heating and temperature probes kept the process within safe, productive limits. Workers learned the hard way how a few degrees swing transformed a manageable exotherm into a foaming mess—and how off-gassing changed product properties if not controlled. Through several process hazard analyses, we swapped glass reactors for jacketed steel lined vessels, boosting both throughput and quality.
Dust control and handling have brought their own set of challenges. The compound’s crystalline powder form calls for enclosed transfer systems and static controls, especially in dry winter months. Our team invested in both local exhaust solutions and batch weighing systems shielded from the main production area. This reduced cross-contamination with other pyridine derivatives, making operator health complaints far rarer. Anyone familiar with chemical manufacturing understands the persistent process improvements driven by frontline staff, not just outside auditors or consultants.
Waste management stands as a constant concern. Byproducts and spent solvents from production of fluorinated nitriles need careful tracking. Over the years, our facility management switched from on-site neutralization to certified waste partners, making sure routine site audits catch nothing out of order. We now reclaim much of the spent solvent stream in-house—something both the production engineers and sustainability team see as a pride point. The same teamwork that keeps environmental compliance on point also keeps neighbors and local agencies informed and supportive.
Many customers, particularly those running demanding reaction screens, send us questions before ordering. Sometimes these queries relate to solubility in lesser-used solvents, other times about compatibility in late-stage Suzuki or Buchwald reactions. Our technical support team—mostly drawn from the plant chemists—relies on decades of data, including actual failed reactions, not just supplier brochures. We’ve sent out experimental runs in DMSO, DMF, THF, and even more obscure solvents, logging how the compound holds up or degrades. The feedback loop we enjoy with both buyers and our internal QA team improves the consistency of every next kilo. Our own in-plant R&D staff continually test for trace contaminants and build improved synthetic routes based on this direct user feedback.
Once, a customer flagged an unexpected impurity detected during late-stage process scale-up. Our analytical chemists dug into batch records, tied the impurity profile to a subtle process change, and supported a short production run to confirm the fix. Faster than regulatory authorities could step in, our team implemented a modification, saving the customer both time and regulatory headaches. These real-world collaborations don’t get written up in glossy reports, but they make a genuine difference to both producer and end-user. That’s how our process improvements keep moving: learning from shared experience rather than static product specifications.
A customer’s work doesn’t operate in a vacuum. Researchers and process chemists want reliable, relevant technical details—not a wall of boilerplate or recycled catalogue copy. From this side of the factory doors, direct relationships with users uncover the details distributors miss. Shipping temperature, solvent traces, and repackaging risks mean more than market gloss. We’ve seen research projects saved by a production manager picking up the phone, clarifying a batch question, and relaying advice from someone who actually weighed out a drum—not just a sales agent. Our plant team prefers this hands-on connection, building ongoing trust as teams troubleshoot both successful and failed reactions together. In tricky fields like fluorinated intermediates, that makes the difference between process safety and unnecessary setbacks.
Transparency on sourcing stands as another matter our customers value. Supply disruptions, global price shocks, and regulatory hurdles hit smaller intermediates regularly. From this manufacturing perspective, we mitigate these risks by forward-contracting raw fluorinated feedstocks, maintaining in-house analytics, and managing our supply chain directly. The result for our customers: fewer surprises, cleaner supply, and dependable technical communication. Our focus on direct feedback from the floor—not layers of resellers—keeps both quality and trust intact. Each kilo shipped carries advice refined through decades of actual production, meeting requirements without inflated promises or shortcuts.
Customers in regulated fields, especially pharmaceuticals and agrochemicals, face heightened regulatory review. Our manufacturing workflows have evolved alongside these demands, embedding tight documentation and traceability from every shipment. There’s no hiding behind vague language; someone from our quality assurance team checks each lot and keeps “out-of-spec” material from reaching customers. These lessons came at a cost—missed deliveries in our early days taught us how regulatory non-compliance quickly halts supply and damages reputations. Now, with rigorous certificates, full chromatograms, and validated test methods, the plant anticipates both customer and regulator concerns instead of reacting late in the chain.
Customization stands as another core advantage. Sometimes a process chemist needs tighter control on residual solvents, or a different crystalline form for downstream processing. We’ve worked directly with buyers to set up custom drying, tailored sieving, and alternate crystallization. Each adjustment feeds back into plant routines, training, and in-lab documentation, boosting both customer satisfaction and internal know-how.
The story of 4-(trifluoromethyl)pyridine-3-carbonitrile doesn’t stop with each shipment. User needs keep evolving; regulatory standards shift; new synthetic routes pop up in research journals and at customer sites. Plant teams have adapted by investing in new reactor controls, dust-free transfer technology, and better analytics for trace impurity tracking. The future may bring greener fluorination chemistry, new purification approaches, or expanded applications in materials science. Engaging directly with research chemists and downstream users gives our plant real insight into these shifts before they become industry norms.
Feedback—positive and negative—drives every improvement, from reactor upgrades to operator training. We keep open lines of communication with customers, building relationships based on shared wins and tough challenges solved together. This level of support only grows stronger as we see our intermediate powering new research leads, better crop protection, or improved specialty materials. Ownership of the whole process, grounded in years of hard lessons at the bench and in the plant, sets the direct manufacturer’s approach apart. We look forward to tackling every next challenge, one batch at a time, with the same blend of experience and transparency that’s defined our journey with 4-(trifluoromethyl)pyridine-3-carbonitrile so far.