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HS Code |
419716 |
| Product Name | 2-Chloro-6-(trifluoromethyl)pyridine-4-carbonitrile |
| Molecular Formula | C7H2ClF3N2 |
| Molecular Weight | 206.55 g/mol |
| Cas Number | 874637-12-2 |
| Appearance | White to off-white solid |
| Melting Point | 61-65°C |
| Density | 1.54 g/cm3 (estimated) |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=NC(=C1C#N)Cl)C(F)(F)F |
| Inchi | InChI=1S/C7H2ClF3N2/c8-6-3-5(7(9,10)11)2-1-12-6(4-13)7/h1-3H |
| Storage Temperature | 2-8°C |
| Hazard Statements | May cause irritation to skin, eyes, and respiratory tract |
As an accredited 2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE-4-CARBONITRILE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle with a tamper-evident cap and a clear hazard label for safety. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 12MT packed in 480 x 25kg fiber drums lined with polyethylene bags, ensuring safe chemical transport. |
| Shipping | 2-Chloro-6-(trifluoromethyl)pyridine-4-carbonitrile should be shipped in tightly sealed, clearly labeled containers, protected from light and moisture. Transport must comply with applicable regulations for hazardous chemicals, ensuring compatibility with shipping materials and safety protocols. Appropriate documentation, including safety data sheets (SDS), should accompany the shipment for proper handling and emergency response. |
| Storage | Store **2-chloro-6-(trifluoromethyl)pyridine-4-carbonitrile** in a cool, dry, well-ventilated area away from heat sources and incompatible substances such as strong oxidizers. Keep the container tightly closed, clearly labeled, and protected from moisture. Use in a chemical fume hood, and avoid exposure to light. Follow all relevant safety protocols and regulations for handling hazardous chemicals. |
| Shelf Life | 2-Chloro-6-(trifluoromethyl)pyridine-4-carbonitrile is stable for at least 2 years when stored in a cool, dry, dark place. |
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Purity 99%: 2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE-4-CARBONITRILE with 99% purity is used in pharmaceutical intermediate synthesis, where high product consistency is ensured. Melting Point 89°C: 2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE-4-CARBONITRILE with a melting point of 89°C is used in agrochemical formulation, where ease of solid-state processing is achieved. Moisture Content <0.5%: 2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE-4-CARBONITRILE with moisture content below 0.5% is used in API development, where degradation and impurity formation are minimized. Molecular Weight 222.56 g/mol: 2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE-4-CARBONITRILE with molecular weight of 222.56 g/mol is used in fine chemical production, where precise stoichiometric control is required. Particle Size D90 <50 µm: 2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE-4-CARBONITRILE with a particle size D90 below 50 µm is used in catalyst application, where improved dispersion in reaction media is obtained. Stability Temperature ≤130°C: 2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE-4-CARBONITRILE with stability temperature up to 130°C is used in polymer additive manufacturing, where integrity under processing heat is maintained. Assay ≥98%: 2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE-4-CARBONITRILE with assay not less than 98% is used in laboratory research, where reproducibility of experimental results is supported. Refractive Index 1.532: 2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE-4-CARBONITRILE with a refractive index of 1.532 is used in optical material synthesis, where controlled optical clarity is required. |
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Manufacturing specialty pyridine derivatives like 2-chloro-6-(trifluoromethyl)pyridine-4-carbonitrile takes more than precise chemical synthesis. It asks for a full grasp of what chemists in the field need to solve their toughest problems, from custom intermediates to highly selective reagents. As a direct manufacturer, seeing firsthand how this molecule fits the day-to-day work in pharmaceutical, agrochemical, and fine chemical labs gives useful insight, beyond what data sheets or distributor write-ups describe.
Working in this business, I’ve watched how the trifluoromethyl and cyano groups on the pyridine ring change the game for organic transformations. Introducing a trifluoromethyl group adds metabolic stability and strong electron-withdrawing power, something synthetic chemists value when mapping out medicinal molecules. The cyano group, sitting across the ring, gives another handle for further modifications—adding diversity through straightforward nucleophilic or palladium-catalyzed substitutions.
Each batch that leaves our reactor tells a story of development. Scaling up 2-chloro-6-(trifluoromethyl)pyridine-4-carbonitrile didn’t just mean getting yield. It meant tuning reaction times, extraction steps, and crystallization to reach purity levels that truly deliver in downstream syntheses. Customers who visit our plant often want to see more than a property sheet; they ask about real-world handling, shelf stability, and how smoothly the compound dissolves in acetonitrile or DMF. We listen—every answer shapes the next batch.
Most end users ask for a minimum purity of 98 percent by HPLC, though some advanced applications rely on purities closer to 99.5 percent. Achieving this consistently means hands-on refining—washing with optimized solvent grades, controlling pH in the work-up, and using updated filtration. Analytical teams in our facility run NMR, GC-MS, and LC-MS for every batch. These aren’t just checkboxes or regulatory chores. They reveal clues about hard-to-remove impurities, making it easier to prevent issues with cross-coupling or nucleophilic substitutions later down the line.
Users expect the compound to arrive as stable, white to off-white crystals, and to resist moisture and air when stored tightly sealed. Over years of shipping this material globally, we found moisture control in packaging—using multilayer barrier bags and desiccants—cuts the chances of trace hydrolysis and discoloration far more reliably than a simple drum lined with plastic. Many pharma partners credit our tight containment approach for saving critical time on stability studies.
Our technical sales and process chemists spend time with teams who compare this compound to several other pyridine nitriles. The difference comes down to how the combined trifluoromethyl and chloro pattern impact both reactivity and selectivity. The electron-withdrawing power from the CF3 group on the 6-position shifts the electronics of the whole ring, making certain substitutions at C-4 or C-2 possible, even with relatively mild bases or during metal-catalyzed couplings.
Without that CF3 group, pyridine-4-carbonitriles lose much of their ability to resist hydrolysis and oxidation—this stability opens doors in late-stage functionalization or when adding the pyridine core to complex heterocycles. The chloro group assists in Suzuki or Buchwald-Hartwig aminations, where direct arylation without need for harsher halides is essential for fragile substrates. Colleagues in pharmaceutical research reach for this specific pattern because even small changes in substitution can mean the difference between a lead compound and a failed reaction route.
Visiting the pilot plant of a long-term customer, I saw firsthand how our product enters their synthesis line for agrochemical intermediates. The 2-chloro unit, paired with trifluoromethyl stabilization, lets their team introduce amines, alkoxides, or other functional groups in single-step couplings. The cyano group leaves further room for constructing bi-cyclic or tri-cyclic scaffold cores, critical for new patented active ingredients. What felt like a simple upstream building block over the years has become a quiet backbone in seed treatment agents, insecticides, and herbicides world-wide.
On the pharma side, teams working on kinase inhibitors or anti-infective scaffolds use the same core structure to enable high selectivity, often running test reactions late in the drug discovery process. They rely on precisely the right regiochemical pattern so candidates clear regulatory hurdles without needing major downstream changes. Getting the building block right, batch after batch, means these teams avoid wasted weeks troubleshooting unknown impurities.
As a manufacturer, uncovering hidden reaction variables shapes how we talk about this molecule. Even slight variability in trace metals or water content from raw solvents can interfere with cross-coupling yields, often surfacing only in scale-up. Years ago, we started a policy of using freshly distilled solvents, not just for our own peace of mind, but because feedback from customers showed even 0.2 percent extra water throws off the Suzuki couplings. Sometimes, chemists call us less to chase documentation, more to ask about freeze-thaw stability or sticky residues after evaporation.
Hearing this in real-time honed our process. For instance, on discovering off-odors in a summer batch, we traced the issue to a specific grade of acetonitrile supply, switching suppliers and setting up an incoming solvent QC inspection that cut complaints to zero. Many problems only surface when batch scale grows, so we stress keeping testing and records live, not out of regulatory obligation, but to react fast when partners push projects from kilo-lab to pilot line.
Many customers ask me about “model” numbers for our material. In practice, each facility may list the batch under their own code. Ours matches structure and purity, with every drum traceable to its reactor and date. True consistency means knowing exactly where each kilogram came from and what variables shifted that day—so if a downstream synthesis shifts, both our teams review the same data set.
Global users say product from different manufacturers looks identical on paper, but experienced chemists see real-world difference in solubility, color, and “feel” during charging into reactors. Even a slightly gritty or clumpy sample can signal poor crystallization or lingering solvent. A batch that dissolves smoothly, pours cleanly, and leaves no sticky residues keeps lines running without jam-ups or lost time.
Specification sheets rarely capture subtleties like static buildup from dry air handling or changes in flowability on humid days. Over years, we’ve refined drying cycles, sieving steps, and final pack-down to balance rapid charging with minimal dust in user plants. It might sound basic, but details like these separate trouble-free routine use from calls about clogged filters or lost batch yield.
Manufacturing 2-chloro-6-(trifluoromethyl)pyridine-4-carbonitrile brings responsibilities—especially to the environment. In the past, common procedures involved chlorinating reagents with high volumes of hazardous solvents. Over the past decade, tightening regulations and rising solvent recovery costs have driven our team to pilot lower-emission syntheses. Waste reduction now plays as important a role as conversion yield.
A few years ago, we invested in a closed-loop solvent recycling unit, which allowed us to cut down fresh solvent usage by over half. The newer process steps rely on catalytic, rather than stoichiometric, quantities of reagents where possible, and purification by aqueous washes rather than repeated organic extractions. Improvements like these came not just by choice, but through direct feedback from international buyers who must meet ever tougher “green label” standards.
Continuous feedback led us to design waste stream tracking for each batch. This means we observe not just how much product leaves the plant, but where every kilogram of by-product ends up. Engineers watch for losses at every juncture—low-yield side paths, solvent evaporation, even filter cake moisture. By catching these small inefficiencies, we improve not just costs, but the overall sustainability record buyers have to log when importing our product to Europe, Japan, or North America.
Customers and researchers seeking this compound aren’t just buying a chemical—they’re investing in every step behind it. On our side, engineers, QC chemists, and operations managers contribute insight gathered through years of running plants. Routine morning debriefs after night shifts often turn into problem-solving sessions, where issues from one client’s process run lead to small tweaks in ours. By the next shipping window, improvements show up in cleaner spectra, more uniform crystals, or faster filtration.
Sharing technical data with key partners helps them plan their reactions more confidently. Instead of waiting for complaints, we encourage open calls and visits. One team recently joined us onsite to troubleshoot a crystallization bottleneck on their side, only to discover subtle differences in humidity and cooling rates at bulk scale. By testing samples from both sites under matched conditions, we isolated the cause—saving weeks of frustration and helping both sides avoid similar problems later.
Working this closely does more than solve short-term issues. It cements trust—letting both teams invest less time on redundant checks and more on moving new products forward or qualifying new processes.
Years ago, only a small number of pharmaceutical and agrochemical innovators sought highly substituted trifluoromethyl pyridine nitriles. It felt like an exotic request, usually for research or early proof-of-concept studies. As the benefits of this scaffold—especially in metabolic resilience and selectivity—became proven, volume requests multiplied. What began as a multi-step flask procedure in a lab hood matured to a multi-metric ton process, pushing facility upgrades and more robust QC.
Research partnerships fostered new application spaces—fine chemicals, specialty dyes, performance additives—each one demanding a fine-tuned material tailored for rapid development or stable long-term formulations. Alongside these applications, our own understanding of work-up bottlenecks, environmental variables, and packaging weak spots deepened, leading to a tighter overall operation.
Uprating reactor volume or introducing parallel lines means more than just increasing output; it sends every step back through process safety reviews, raw material controls, and equipment tuning. Any new source of 2-chloro-6-(trifluoromethyl)pyridine-4-carbonitrile has to match the tightest standards for impurity content, color, and microbiological status—down to parts per million on each spec. Customers often trial small pilot batches with deliberate failure points to stress-test robustness before scaling up.
Every new process route uncovers a few surprises. Whether a filtration behaves differently at 200L versus 2000L, or a minor impurity shifts crystallization, each lesson gets logged in site manuals for the team and shared in confidence with long-time partners.
Whenever a support request arises—say, unexpected polymerization during solvent recovery—our internal review covers not just the batch in question, but other batches run under similar conditions. We drill down to raw materials, environmental logs, even staff handover notes, so improvements stick over time, instead of being band-aids.
In today’s global procurement landscape, end users have dozens of choices for specialty pyridine derivatives. What sets one supplier apart aren’t only numbers on a spec sheet, but the reliability of every delivered drum and the depth of traceability offered. Our reputation took root on the willingness to let customers examine production logs, question analytical runs, or suggest tweaks for upcoming campaigns.
Comparisons with other suppliers often come down to how consistently the material works across different reaction schemes, not just initial cost or paperwork. Labs under tight project timelines value fewer “out-of-spec” surprises, faster loading, and stable appearance batch after batch. Our site’s investment in both people and equipment pays back with more predictable downstream yields and less waste disposal.
One customer, looking to avoid frequent source changes for regulatory filings, tracked the cumulative impact of switching to our compound: less lost time on failed reactions, fewer customer complaints, and smoother validation for their compliance checks. Those tangible savings, multiplied by thousands of kilograms and regulatory hours, outweigh trivial price gaps from competitors.
Ongoing process innovation doesn’t happen in isolation. We draw on real stories and pain points from every user. Some suggest tighter sieving for ultrafine powder use in continuous feed processes. Others prompt us to try new solvent or reagent combinations that could further boost sustainability. Each comment forms the ladder for the next round of improvement.
As the regulatory landscape gets tougher worldwide, buyers ask for transparent documentation on everything—trace metals, residual solvents, even carbon footprint. We took this as a cue to overhaul our own data capture, automating batch records and adding new checkpoints. A simple QC slip now carries detailed traceability from raw material batch to final out-loading. This hasn’t just improved compliance; it tells our customers we care about the entire lifecycle of the molecule, from synthesis to use and beyond.
Every part of the journey with 2-chloro-6-(trifluoromethyl)pyridine-4-carbonitrile reflects the core value of reliability. Whether it’s the reproducibility of coupling reactions, the absence of out-of-spec crystals, or the sustainability baked into each item, the real value comes from the accumulated lessons inside every drum. Through decades in this field, we’ve come to see this compound not just as another addition to the catalog, but as a testament to the careful balance between innovation and daily diligence in manufacturing.