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HS Code |
847686 |
| Cas Number | 151605-02-0 |
| Molecular Formula | C7H3F3N2 |
| Molecular Weight | 172.11 |
| Iupac Name | 5-(trifluoromethyl)pyridine-2-carbonitrile |
| Appearance | White to pale yellow solid |
| Boiling Point | 236-238°C |
| Melting Point | 34-38°C |
| Density | 1.38 g/cm3 (approximate) |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically >98% |
| Smiles | C1=CC(=NC=C1C#N)C(F)(F)F |
| Storage Condition | Store in a cool, dry place, tightly closed |
As an accredited 5-trifluoromethyl-pyridine-2-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25g of 5-trifluoromethyl-pyridine-2-carbonitrile with tamper-evident screw cap and hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL container holds 12 MT of 5-trifluoromethyl-pyridine-2-carbonitrile, packed in 25kg fiber drums, securely palletized. |
| Shipping | 5-Trifluoromethyl-pyridine-2-carbonitrile should be shipped in tightly sealed containers, protected from light and moisture. Special attention must be paid to ventilation, and containers should be clearly labeled according to hazardous material regulations. Transport should adhere to local and international chemical shipping guidelines to ensure safety and compliance. |
| Storage | 5-Trifluoromethyl-pyridine-2-carbonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition. Protect from moisture, heat, and direct sunlight. Store separate from incompatible materials such as strong oxidizers and acids. Ensure proper labeling and restrict access to trained personnel. Follow relevant local regulations for hazardous chemicals. |
| Shelf Life | 5-Trifluoromethyl-pyridine-2-carbonitrile is stable under recommended storage conditions; shelf life is typically 2–3 years in a cool, dry place. |
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Purity 99%: 5-trifluoromethyl-pyridine-2-carbonitrile with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-products. Molecular Weight 156.1 g/mol: 5-trifluoromethyl-pyridine-2-carbonitrile with molecular weight 156.1 g/mol is used in organic reaction scale-up, where it provides predictable reaction stoichiometry. Melting Point 38°C: 5-trifluoromethyl-pyridine-2-carbonitrile at melting point 38°C is used in chemical process optimization, where it allows efficient temperature-controlled reactions. Stability Temperature 120°C: 5-trifluoromethyl-pyridine-2-carbonitrile with stability temperature up to 120°C is used in agrochemical production, where it maintains structural integrity under process conditions. Water Content <0.5%: 5-trifluoromethyl-pyridine-2-carbonitrile with water content below 0.5% is used in moisture-sensitive synthesis, where it prevents unwanted hydrolysis and degradation. Particle Size <20 µm: 5-trifluoromethyl-pyridine-2-carbonitrile with particle size less than 20 µm is used in high-dispersion formulation, where it enables uniform mixing and enhanced reactivity. GC Assay ≥98%: 5-trifluoromethyl-pyridine-2-carbonitrile with GC assay of at least 98% is used in analytical reference standards, where it ensures accurate calibration and reliable analytical results. Residual Solvents <100 ppm: 5-trifluoromethyl-pyridine-2-carbonitrile with residual solvents under 100 ppm is used in fine chemical manufacturing, where it minimizes contamination risks and ensures product compliance. |
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We have watched the pharmaceutical and agrochemical sectors change as innovations demanded more from intermediates. Over the years, we have produced 5-trifluoromethyl-pyridine-2-carbonitrile at scale and have seen firsthand how its distinctive combination of the trifluoromethyl group and pyridine ring opens doors to reaction pathways not achievable with plain nitriles or other halogenated analogues. Crafting this molecule in purity batches for years, with consistency in lot-to-lot synthesis, has taught us about its vital role in process reliability. Chemical engineers, formulation specialists, and medicinal chemists often remark on the value of that reliability. In our experience, every time a research team transitioning from lab scale to pilot scale chooses this compound, it is never solely about purity. The value is in how our process removes hidden, low-level contaminants that would otherwise complicate downstream hydrogenations or halogenations. This is learned not from certifications but from batches that reacted as expected and saved clients days of troubleshooting.
The trifluoromethyl group, attached at the 5-position of the pyridine, creates a molecular structure that challenges ordinary synthesis. Fluorine atoms increase the electron-withdrawing capability, which in turn affects not just reactivity but eventual pharmacokinetics or efficacy in agricultural chemicals. Over hundreds of synthesis cycles in our reactors, we have learned conditions that keep byproducts at bay and ensure that the nitrile group isn’t degraded. Colleagues in custom synthesis have commented that the sharp NMR signals for the trifluoromethyl protons are a confirmation of clean process flows, a testament to disciplined housekeeping in our plant.
Some formulas demand this structure because the electron distribution from CF3 groups at the 5-position blocks metabolic pathways that would otherwise deactivate the molecule too soon or make purification too costly. Feedback from partners running preclinical tests confirms that this stability reduces downstream variability—a difference only experienced once a full batch fails due to trace impurities.
Through years of hands-on manufacturing, we standardize batches to meet specifications—typically offering 5-trifluoromethyl-pyridine-2-carbonitrile in purity grades above 98 percent. Each batch is verified using a combination of HPLC and NMR, double-checked on the production line before dispatch. We do this not to fill out paperwork, but because small deviations—from a faint yellow tint to a slight shift on GC analysis—often signal trouble in later synthesis steps, whether in Grignard additions or amidation routes.
From the operator’s perspective, batch consistency starts with handling the raw trifluoroacetic sources and builds through every control valve adjustment. Only someone who has monitored a column all night, keeping an eye on the exotherms during cyclization, really understands how small variations can haunt a scale-up. So, our specifications emerged not from a marketing department, but from years of troubleshooting and listening to real users who once had whole shipments rejected for being out-of-spec.
We maintain an open dialogue with users in both pharma innovation and large-scale agrochemical reactions. Their feedback shaped improvements such as tighter water controls, improved filtration, and a fully documented residual solvent program. It has shaped our process techniques and the way we train the next generation of chemical engineers.
Chemists developing active pharmaceutical ingredients report smoother overall yields, a reduction in side product bands when moving to multi-step syntheses, and even decreased time spent on final purification columns after switching to our grade. There have been stories of how a single source of trace metals from a competitor batch ruined weeks of downstream coupling reactions; such stories push us to continuously review raw material vendors and refine cleaning protocols inside reactors and transfer lines.
Colleagues in formulation sometimes assume this compound serves as an interchangeable substitute for less fluorinated nitrile-pyridines. This is almost never the case for challenging syntheses. The three fluorine atoms deliver more than increased lipophilicity: they drive up the stability of the molecule against oxidation, making it suitable for intermediates meant for extended-release pharmaceutical profiles or slow-degrading crop protection agents.
Comparisons with analogous compounds—such as 2-cyanopyridine without the CF3 group or halogenated pyridines lacking the nitrile—reveal marked differences in regulatory registrations, synthetic flexibility, and downstream cost. One agricultural partner demonstrated in the field that formulation stability doubled after switching to the trifluoromethyl version. Other manufacturers have seen similar improvements in shelf life and metabolic half-life when using our compound as a building block.
In pharmaceutical development, the difference sometimes boils down to small-scale batch quality visible only under significant analytical scrutiny. Our customers increasingly share data on how our version reduces anomalous spots in LC-MS traces—indicating that specific synthetic control at manufacturing, not just at point-of-use, is crucial. Years of talking with process chemists taught us that choosing the right synthetic route early conserves resources later. This is a lesson we reinforce on every batch, not because it’s industry best practice, but because some team member remembers the day a costly pilot was lost on account of a poorly sourced intermediate.
We have watched this compound find its way into many sectors, but most applications share a need for high purity and strict contaminant thresholds. Pharmaceutical teams typically use it as a key intermediate in stepwise arylation or selective hydrogenation reactions where unwanted reactivity from impurities produces costly byproducts.
In crop protection R&D, teams select the trifluoromethylated pyridine structure to increase the environmental stability and bioavailability of active compounds. Chemical engineers at major protection developers prefer its profile over simpler pyridines, citing resistance to UV breakdown and improved dispersion in common suspensions.
Some clients purchase our product as a coupling partner in small molecule libraries, leveraging the electron-withdrawing trifluoromethyl to tune the reactivity or binding affinity in early-stage drug screens. Researchers in advanced materials appreciate the molecule’s role in producing fine-tuned, fluorinated polymers required in electronics or specialized coatings.
While the molecule enters many synthetic paths, repeated customer feedback points to a single common factor: every additional percent of purity achieved at our production site saves multiple hours in downstream analytical purification. Teams in process chemistry have shared year-over-year data with us, showing direct cost savings on column media, solvent consumption, and staff time after switching from lower-grade imports. Some have even detailed how a reduction in trace mineral content, as achieved through our filtration steps, lessened the number of regulatory compliance filings.
Producing 5-trifluoromethyl-pyridine-2-carbonitrile effectively at scale requires more than just running a reliable reaction. Raw material volatility impacts not only yield but also downstream stability. There have been times, particularly during global supply chain squeezes, when sourcing reliable trifluoroacetic acid derivatives became a daily concern. Prices spiked, and we felt pressure to cut corners, yet our team decided against this time and again to safeguard the integrity of future batches.
Safety considerations extend far beyond paperwork and audits. During synthesis, the exothermic cyclization step poses real thermal risks, and failing to monitor scrubbers and jacket temperatures can throw an entire run out of spec. Our staff has gone through rigorous training to react rapidly to early signs of deviation—something a producer appreciates much more than an external observer. Investments in sealed system upgrades, real-time digital monitoring, and secondary containment have paid off, evidenced by the decade-long absence of major incidents on our line.
Waste management ranks high for us. Developing a protocol for fluorinated waste stream collection required negotiation with regulators, upgrading wastewater treatment, and persistent investment in newer catalyst technologies that generate fewer persistent organofluorine traces. Down the road, this has spared us hefty penalties as environmental rules have tightened worldwide.
Clients often come to us after a run-in with inconsistent overseas production or a shipment held up by compliance irregularities. What they want from us, beyond COAs and test reports, is a sense that their own production will not grind to a halt. Years of open-door audits, detailed batch logs, and the willingness to custom-produce documentation for unusual requests have convinced even skeptical buyers to switch from brokered sources to direct supply.
Feedback loops between our production teams and end-user technical staff mean we can adjust particle size distribution, optimize for solubility in atypical solvents, or fine-tune drying procedures to meet distinct project needs. We have made countless small adaptive changes suggested by these users, ranging from custom packaging (to prevent peroxide formation in shipment) to specialty storage conditions based on project parameters.
Continuity of supply isn’t just about safety stock and logistics planning. Our buyers have often revealed how one missed shipment or offgrade batch can bring a project pipeline—years in the making—to a standstill. We know from experience that reputation builds on doing what is promised, batch after batch, without substitution, dilution, or unexplained quality changes.
It takes serious investment to maintain safety protocols, quality controls, and environmental stewardship while producing a molecule as challenging as 5-trifluoromethyl-pyridine-2-carbonitrile. No process is ever truly “finished,” because regulatory expectations evolve and user requirements grow more sophisticated. Our technical team, informed by years of real-world production, meets regularly to review every deviation, every unexpected test result, and every bit of customer feedback.
We do not shy away from sharing details—failures, successes, improvements. The science is open, the process refined by honest mistakes and sharper oversight. Process transparency serves our users, who demand not just product, but partnership. They bring us ideas, new applications, and tougher specifications. We respond not by reciting literature values, but by opening our production records, investing in advanced analytical gear, and inviting on-site visits.
By listening closely to those who run the downstream reactions, we gain knowledge unavailable from specification sheets alone. They show us how even subtle differences in impurity profiles impact crystallizations or change compound longevity in finished products. This feedback loop allows us to improve and customize, always aiming to preempt problems rather than just react.
Every batch of 5-trifluoromethyl-pyridine-2-carbonitrile we ship carries with it the lessons of past errors and customer-driven improvements. Facing challenges—from raw material volatility to increasing regulatory scrutiny—means being present, not distant. It means someone from the manufacturing floor can explain every aspect of a batch, from why a minor byproduct arose to what corrective step will keep the next batch clean.
We see demand heading further toward traceability, real-time digital controls, and lifecycle analysis with greater granularity. We continue to implement more rigorous in-line monitoring, reinforcing quality by design, not just by final checkpoint. We build resilience against supply shocks by qualifying secondary supply chains and collaborating directly with raw material producers to keep quality non-negotiable. We test every “green chemistry” advance in pilot runs before plant-wide adoption, refusing to jeopardize consistency for the sake of buzzwords.
Ultimately, 5-trifluoromethyl-pyridine-2-carbonitrile is more than a line on a chemical catalog—it is a result of thousands of hours managing safety, efficiency, and continuous improvement. Those who have run pilot plants, managed supply crises, or rectified failed reactions know the value of a reliable partner in specialty chemicals. Our approach rests on openness, humility, and technical mastery developed in practice.
Rather than promising all things to all users, we engage closely, respond promptly, and refine obsessively. This approach drew long-standing partners into returning year after year, requesting ever tighter specifications and more complex customizations. Each request stretches us, and each challenge advances not only our technical capabilities but the standards by which this challenging molecule is measured in labs and manufacturing plants worldwide.