|
HS Code |
672008 |
| Chemical Name | 2-Trifluoromethyl-4-chloropyridine |
| Cas Number | 89831-20-1 |
| Molecular Formula | C6H3ClF3N |
| Molecular Weight | 181.54 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 174-176°C |
| Density | 1.41 g/cm3 (at 25°C) |
| Refractive Index | 1.490 (at 20°C) |
| Flash Point | 63°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Synonyms | 4-Chloro-2-(trifluoromethyl)pyridine |
| Smiles | C1=CN=C(C=C1Cl)C(F)(F)F |
| Inchi | InChI=1S/C6H3ClF3N/c7-4-1-2-11-5(3-4)6(8,9)10 |
As an accredited 2-trifluoromethyl-4-chloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 g of 2-trifluoromethyl-4-chloropyridine supplied in a sealed amber glass bottle with hazard labels and tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-trifluoromethyl-4-chloropyridine includes secure drum packaging, careful palletizing, and compliance with chemical safety transport regulations. |
| Shipping | 2-Trifluoromethyl-4-chloropyridine is typically shipped in sealed, airtight containers made of compatible materials (e.g., glass or HDPE). It is packed to prevent leaks, moisture, and light exposure. The package is clearly labeled with hazard information and follows relevant regulations for the transport of hazardous chemical substances. |
| Storage | **2-Trifluoromethyl-4-chloropyridine** should be stored in a tightly sealed container, away from moisture and incompatible materials such as strong oxidizers. Keep in a cool, dry, and well-ventilated area, preferably in a dedicated chemical storage cabinet. Protect from direct sunlight and sources of ignition. Clearly label all containers and ensure good laboratory practices are followed when handling and storing this compound. |
| Shelf Life | 2-Trifluoromethyl-4-chloropyridine has a typical shelf life of 2 years when stored in a cool, dry, and dark place. |
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Purity 98%: 2-trifluoromethyl-4-chloropyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield formation of target compounds. Boiling Point 172°C: 2-trifluoromethyl-4-chloropyridine with a boiling point of 172°C is used in agrochemical manufacturing, where it allows for efficient solvent recovery during distillation. Moisture Content <0.5%: 2-trifluoromethyl-4-chloropyridine with moisture content below 0.5% is used in catalyst preparation, where it prevents hydrolysis and assures catalyst performance. Melting Point 28°C: 2-trifluoromethyl-4-chloropyridine with a melting point of 28°C is used in fine chemical synthesis, where its low melting point permits easy processing under mild conditions. Particle Size <50 microns: 2-trifluoromethyl-4-chloropyridine with particle size under 50 microns is used in solid formulation processes, where it ensures homogeneous blending and improved dissolution rates. Chemical Stability up to 120°C: 2-trifluoromethyl-4-chloropyridine with chemical stability up to 120°C is used in industrial-scale batch reactions, where it maintains reactivity and product integrity during thermal processing. Residual Solvent <500 ppm: 2-trifluoromethyl-4-chloropyridine with residual solvent content below 500 ppm is used in electronic material synthesis, where it avoids contamination of sensitive devices. |
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Our experience with 2-trifluoromethyl-4-chloropyridine stretches across process development, production scale-up, and practical use in demanding chemical syntheses. This is a compound that brings sharp differentiation to the table. Produced at our integrated facility, every batch comes off the line after careful adherence to protocols born from years of pyridine chemistry. The structure—bearing both a trifluoromethyl group at the 2-position and a chlorine at the 4-position—is no accident. This substitution pattern shapes how our product behaves in downstream synthesis, particularly as a key intermediate for pharmaceutical and agrochemical manufacturing.
In our plant, achieving the correct substitution on the pyridine ring calls for experienced handling of halogenation, fluorination, and rigorous purification. Impurities such as unreacted starting material, isomers, or hydrolyzed byproducts are tracked at each step because these can derail late-stage reactions for formulators. We run in accordance with tight specifications, keeping water below 0.2% and single-digit ppm on key metal contaminants. These are not arbitrary numbers for us—they are hard-won targets shaped by projects where a single contaminant cost a week’s work in multi-step synthesis. The material exits our reactor with a melting range commonly just above room temperature, which we monitor through both traditional and modern analytical techniques.
In contrast to our experiences with simple 4-chloropyridine or unsubstituted trifluoromethyl pyridines, the dual-substituted 2-trifluoromethyl-4-chloropyridine demands a different approach to process safety and storage. We learned that in larger reactors, traces of acidic gas formation rose unless pressured venting was controlled. That led us to spec out heavy-duty filtration and specific polymer-lined containment. By elbows-deep work in optimizing these factors, we can deliver consistent product without batch-to-batch variation that disrupts end-use consistency.
We have seen 2-trifluoromethyl-4-chloropyridine perform as a crucial building block in medicinal chemistry programs. Researchers lean on it to introduce both strong electron-withdrawing functionality and halogen reactivity into their scaffolds. Our collaborations with process chemists show that even slight differences in the impurity profile of this intermediate cause headaches at the coupling stage. With older, outsourced supply streams, partners encountered side-reactions during Suzuki and Negishi cross-couplings—often traced back to halide carryover. Our controlled process slashes these problems. By running this compound through continuous chromatography, we took out unpredictable trace impurities that became obvious issues only in late-stage API synthesis.
For anyone scaling up a lead candidate, reproducibility means everything. Our team understands that commercial lots need to behave exactly like milligram lab samples, even over many months in storage. We conducted stability trials over a three-year window; the product retained its halogen content, did not develop high levels of decomposition, and maintained reactivity in both aromatic substitutions and amidation reactions. Involving the same operators, the same glass-lined vessels, and the same internal standards as our early laboratory runs protects end users from lot-to-lot drift—a difference born from direct manufacturing, not just spec paperwork.
Working with innovators in crop protection, we have seen firsthand that the combination of a trifluoromethyl and a chloro group on the pyridine nucleus opens up a rich spectrum of bioactivity. Field chemists and patent teams routinely search for molecules that resist biodegradation while hitting target pest species with precision. Our 2-trifluoromethyl-4-chloropyridine fits right into streamlined development programs for new fungicidal and insecticidal agents. By generating this intermediate at large scale under strictly regulated conditions, we reduce regulatory project delays caused by off-spec byproducts.
Handling and formulation teams appreciate that our material dissolves without noticeable residue in a range of solvents, a result of drying and filtration steps we have optimized over multiple years. Clogging and injection pump failures used to be common complaints from early adopters using lower-grade materials from secondary refining. Our process eliminates the particulate issue at source—less downtime in application means more uptime on field trials. These details may not make it onto the package, but they make all the difference for teams on a tight schedule.
Our direct knowledge with allied pyridine intermediates—such as 2-chloro-4-trifluoromethylpyridine or the parent trifluoromethylpyridine—gave us a clear view of the unique chemistry this compound enables. Cross-comparisons in nucleophilic aromatic substitution reveal distinct reactivity profiles: the order and nature of substitution determine electrophilicity and stability under common conditions. We have run side-by-side trials; 2-trifluoromethyl-4-chloropyridine displays higher selectivity in metal-catalyzed coupling, making it well suited where both yield and purity are business-critical. The presence of the electron-withdrawing trifluoromethyl group makes this intermediate less prone to unwanted side reactions than its mono-substituted or non-fluorinated cousins.
In scaling up other dichloropyridines or mono-halogenated trifluoromethylpyridines, we encountered more baseline reactivity and less functional group tolerance at higher temperatures. With the product at hand, we managed cleaner conversions and much-improved mass balance, sparing customers from byproduct-related troubleshooting. We often share these practical differences up front with partners who look for fit-for-purpose intermediates, not just catalog entries.
We have watched 2-trifluoromethyl-4-chloropyridine bridge the worlds of laboratory research and full-scale production. Early in a project’s life cycle, it might help med chem teams quickly build new heterocycles by acting as a versatile synthon. The combination of halide and fluoroalkyl handles opens up direct access to growing families of kinase inhibitors and crop protection candidates. Down the supply chain, process engineers choose our material for batchwise or continuous reactions. The clean GC and HPLC spectra make for straightforward process control, and chemists spend less time troubleshooting filter blockages or color-forming byproducts.
Packing and storing this product calls for specific protocols—our teams moved away from ordinary HDPE storage after discovering trace leaching at elevated temperatures. By now, our drumming procedures use lined steel to prevent cross-contamination and preserve physical integrity over extended warehouse holds. It took being the manufacturer to learn what survives both summer and winter cycling, saving users from receiving problematic batches. We established a model for labeling and chain of custody, critical for regulated customers in pharmaceuticals and crop science.
Innovation in pharmaceuticals or agriculture leans heavily on predictable access to high-purity raw materials. Our history has taught us that a missed delivery or an out-of-spec batch can grind a discovery program to a halt. Over the years, we have invested in backup reactors and contingency plans for the production of 2-trifluoromethyl-4-chloropyridine. Our supply agreements allow committed customers to secure annual volumes, backed by traceable release documentation and certificates showing what truly left the factory.
It’s one thing to read the assay on a certificate; quite another to work with a supplier who runs an extra impurity scan after every maintenance shutdown. We do this not just to hit a number, but because in our experience, trace contamination from a swapped gasket or minor temperature drift at a critical point can undo months of downstream process development. As the original manufacturer, we hold onto full records, sample retention, and analytical logs so that projects encountering surprises downstream get answers, not excuses.
Compliance with environmental and occupational health rules stands as a non-negotiable part of our business. Regulations have grown tougher; audits walk through our production and fill lines with an eye for risk. Decades of real experience led us to design air handling and secondary containment for worst-case scenarios, rather than waiting for an incident to force improvement. This attitude protects both our teams and our customers’ risk profiles.
For clients bound by REACH, TCSA, or similar laws, the provenance of each lot matters. Because we keep production and purification in-house, we provide full chain traceability and rapid document turnaround for notifications or due diligence requests. Our team includes compliance specialists who handle complex customer questionnaires, not just by copying boilerplate answers, but with analytical backup and historic batch data. The effect is that risk managers, not just technical staff, can trust the product to meet both legal and operational requirements.
Even in the best run facilities, we see challenges. Both batchwise and continuous processes sometimes exhibit variable reactivity due to minor differences in incoming raw material quality. Rather than just complain about it, we built longer-term contracts with raw material suppliers, fostering communication and problem solving over blame games. Our laboratory evaluates every lot before large-scale production. From this, we have eliminated disruptions in reaction kinetics or downstream purification compared to less predictable purchasing models.
Shipping and storage conditions can cause headaches. To solve for these, we adopted temperature data logging on every drum and implemented quarterly transport reviews. From these audits, we found that minor delays in customs clearance could expose product to temperature swings—enough to affect color and reactivity. By tightening our export chain and working closely with certified forwarders, we keep product within optimal parameters through the supply chain. These actions evolved from challenges faced in practice, not just checklists on a logistics plan.
Customers rarely use our 2-trifluoromethyl-4-chloropyridine in isolation; it almost always forms part of a larger synthetic plan. From countless technical discussions, we see that needs evolve fast: from research phase kilo-quantities for structure-activity studies to regular multi-ton deliveries as the compound moves into pilot or production scale. As the manufacturer, we draw on direct project experience to provide batch customization, varied fill sizes, or just-in-time shipments. One project called for extra analysis because their formulation detection method was unusually sensitive to a narrow class of trace aromatic impurities—our technical group provided high-resolution spectra and extra QA checks, solving a problem before it became a showstopper.
Direct communication between our laboratory and the end user cuts down on noise and paperwork. Practical advice for the first synthesis or scale-up run comes not from generic spreadsheets, but from colleagues who have handled the same reagents on the shop floor. Their hands-on stories and troubleshooting become part of the support we deliver, long after the material has left the warehouse.
The true value of 2-trifluoromethyl-4-chloropyridine comes not merely from its molecular properties, but from the accumulated technical knowledge and disciplined manufacturing process behind each batch. By anchoring supply, keeping specifications based on real-world results, and investing time in direct dialogue with customers, we empower innovation while reducing risk and uncertainty downstream.
Each molecule we deliver reflects years of direct technical learning, investment in plant equipment, and day-to-day hard work by our teams. For formulators, process chemists, and R&D leaders, this means not just access to a compound, but a partnership that understands what it takes to deliver reproducible, project-ready intermediates to fuel the next breakthrough.