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HS Code |
822300 |
| Iupac Name | 2-chloro-6-(trifluoromethyl)pyridine-3-carbonitrile |
| Molecular Formula | C7H2ClF3N2 |
| Molecular Weight | 206.56 g/mol |
| Cas Number | 39890-94-3 |
| Appearance | White to off-white solid |
| Melting Point | 53-57°C |
| Density | 1.51 g/cm³ (estimated) |
| Solubility In Water | Low |
| Smiles | C1=CC(=NC(=C1C#N)Cl)C(F)(F)F |
As an accredited 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- is supplied in a sealed amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- ensures secure, moisture-free bulk shipment in sealed drums or containers. |
| Shipping | The shipping of 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- should comply with all local, national, and international regulations for hazardous chemicals. The chemical must be packed in tightly sealed containers, labeled correctly, and protected from moisture and incompatible substances during transport. Use appropriate safety documentation, including the Safety Data Sheet (SDS). |
| Storage | 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Avoid exposure to moisture and direct sunlight. Store at a controlled room temperature and prevent contact with skin or eyes by using appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life of 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)-: Typically stable for 2-3 years when stored properly, protected from moisture. |
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Purity 98%: 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- with purity 98% is used in pharmaceutical intermediate synthesis, where it enables efficient drug candidate development. Melting Point 48°C: 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- with a melting point of 48°C is used in fine chemical manufacturing, where it facilitates easy handling and processing. Molecular Weight 210.56 g/mol: 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- at molecular weight 210.56 g/mol is used in agrochemical formulation, where it provides precise dosing for active ingredients. Stability Temperature 120°C: 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- stable up to 120°C is used in high-temperature organic synthesis, where it maintains structural integrity under reaction conditions. Particle Size <10 µm: 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- with particle size less than 10 µm is used in catalysis research, where it ensures enhanced reactivity due to increased surface area. |
Competitive 3-Pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl)- prices that fit your budget—flexible terms and customized quotes for every order.
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At our manufacturing plant, we know the pressure that comes from running modern synthesis routes for pharmaceuticals and agrochemicals. Every day, our colleagues come to work focused on materials science, yield optimization, safety, batch integrity, and strict adherence to regulatory standards. Few intermediates play a bigger role in cutting-edge molecule construction than 3-pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl). For years, our production teams have supported the life sciences sector with this specific compound, which demands high process control and consistent purity. Many of our partners rely on our plant output to keep their critical product timelines on schedule.
The molecular scaffold of 2-chloro-6-(trifluoromethyl) 3-pyridinecarbonitrile offers synthetic chemists both versatility and unique reactivity. Our experience in the plant tells us that this compound’s electron-withdrawing trifluoromethyl and nitrile groups steer selectivity in cross-coupling, nucleophilic substitution, and ring transformation reactions more reliably than analogous structures. The chloride at the 2-position invites diverse substitutions, letting research teams build extensive libraries targeting kinase inhibitors, anti-infectives, herbicidal agents, and imaging probes.
Manufacturing at multi-ton scale grants us a unique vantage point. Materials from our own reactors head straight to packaging right at the origin, so there are no unknowns from “grey market” transshipment or repackaging. That transparency matters for teams where downstream analytical results, QbD initiatives, or regulatory compliance reviews can hit a snag when intermediates arrive with ambiguous provenance or mixed purity. In our facility, 2-chloro-6-(trifluoromethyl) 3-pyridinecarbonitrile never changes hands or labels before it gets boxed and shipped. That consistency can mean peace of mind for a technical director worried about risk in the supply chain.
Our compound, 2-chloro-6-(trifluoromethyl) 3-pyridinecarbonitrile, rolls out of synthesis with high GC and HPLC purity. We use in-line analytical controls that allow continuous detection of key byproducts, chlorides, and residual solvents. Our product’s typical purity levels exceed 98%, and trace metal screening ensures suitability for downstream catalytic steps. As with all pyridine derivatives, we learned early in scale-up that trace water and low-level oxygen exposure can invite hydrolysis or colouration over time, so we moved to nitrogen-sealed packaging more than a decade ago. Shelf stability improved markedly, and incoming COA complaints dropped away almost entirely.
We have also logged meticulous records of bulk properties such as melting point and moisture content. Our in-process samples consistently measure a melting range of 75–78°C, and Karl-Fischer titrations rarely exceed 0.1% water. This matches what our R&D partners expect, especially because fluctuation in melting point usually signals impurities or polymorphic variation that can create headaches later in formulation. Our process keeps those risks low, so our customers see very tight batch-to-batch reproducibility.
Most clients prefer drum or lined fiber packaging due to the compound’s low volatility and manageable hazards, but for those running high-throughput routes that need precision-dosed solids we offer small-pack formats, delivered with full traceability down to batch and lot-date. We take enormous care in documentation—right down to technician logs and reactor loading schedules. Full batch records with chromatograms, NMR, and FT-IR confirmatory spectra are standard on request.
Decades ago, 3-pyridinecarbonitrile, 2-chloro-6-(trifluoromethyl), mostly showed up as a boutique intermediate for medicinal chemistry screens. Recent advances in route engineering opened up scalable processes where this molecule fits perfectly as a scaffold in a range of therapeutic areas. In our synthesis halls, we've watched our product move from grams for seed research, up to multi-metric ton shipments for ongoing clinical supply or active herbicidal ingredient runs.
Partners in the pharmaceutical sector value this compound’s resilience to high-pressure hydrogenation, its selectivity in Suzuki, Buchwald-Hartwig, and SNAr conditions, and the ease of downstream cross-coupling chemistry. Many times, a team will reach out with a question: how does the trifluoromethyl group affect their metal-catalyzed amination sequence, or how much chloride remains after typical purification? Only manufacturers with direct technical oversight can give precise answers. In our facility, we run real-world process checks and pilot plant studies that let us provide data-driven recommendations, not guesses or literature data. For a chemist charged with beating an API launch deadline, having that bench-to-plant continuity can resolve workflow headaches and reduce wasted cycles.
Agrochemistry calls on this intermediate for very different reasons. The 2-chloro-6-(trifluoromethyl) pyridine backbone offers strong UV stability, which can translate into longer residuals in target applications. Our engineers collaborated with several partners to optimize the polymorphic form and particle-size distribution, which improved wettable powder blends and reduced clumping in their grinds. Real production insight, not hypothetical lab data, helped those clients reach their regulatory and product performance targets in tight timelines.
Our direct plant experience gives us a weekly view into how 2-chloro-6-(trifluoromethyl) 3-pyridinecarbonitrile compares to other building blocks on the market. Pyridine derivatives with halogen substitutions are common in both fine and specialty chemistry, but most lack either the electron strength or the synthetic flexibility that comes from this specific molecule’s constellation of nitrile, chloride, and trifluoromethyl groups.
Take 3-cyanopyridine as a base case. Its single nitrile allows certain transformations, but in high-throughput screening for pharma or crop protection leads, libraries made from unhalogenated homologs just do not deliver the reactivity spread or potency of the 2-chloro-6-(trifluoromethyl) analog. Similarly, direct fluorination or methylation at the 6-position shifts both toxicity and metabolic stability, altering project viability compared to the trifluoromethyl derivative. Other manufacturers sometimes cut corners by mixing or blending batches of simpler mono-substituted pyridines. As a plant operator, I can see and test those shortcuts instantly—they show up as broader melting range, yellowing, and peak splitting on QC traces.
Naturally, 2-chloro-3-cyanopyridine and related dichloro variants have their applications, but across years of manufacturing, we see that trifluoromethyl substitution at the 6-position improves material handling, increases downstream synthetic yields, and sharpens deposit stability in field applications. Every batch that leaves our site bears the fingerprint of this structure—recognizably different from anything that uses isosteric substitution or hybridized sources. For a process developer, that means fewer worries about carry-over of closely related impurities into late-stage steps, especially when regulatory filings call for meticulous impurity mapping and analytical traceability.
As direct producers, we swim in the nitty-gritty details every day. We calibrate flow controllers on the chlorination units, monitor jacketed reactors for exotherms, and log every finishing batch through our LIMS platform. These steps take time and cost money, so fly-by-night traders rarely bother. But as we’ve learned through long-term commitments with global partners, any slip in process control gets revealed in customer returns, failed pilot campaigns, or downtime when regulatory bodies come to inspect.
Years of hands-on production have taught us one central lesson: knowing the upstream chemistry lets you anticipate possible impurities before they become QC problems. Early in scale-up, we noticed a tendency for trace dimers or incomplete chlorination byproducts when jacket temperatures varied by more than 3°C at loading. As a result, our control room tracks and alarms those parameters, and our shift leads get live trending data every hour. That’s how we keep performance sharp and avoid costly reworks or product recalls for our clients. Our compliance team has hosted multiple regulatory site visits, and they use our tested protocols as a benchmark for traceability and chain-of-custody audits.
End-user companies want more than a reliable source—they need resilience. Every year brings surprises: variations in global fluorochemical feedstocks, unpredictable shipping delays, or changing regulatory landscapes. As a primary producer, we have the ability to buffer against these shocks by sourcing our own starting materials in advance and maintaining safety stocks for essential intermediate runs.
In contrast, third-party traders and some bulk distributors operate with thin inventories. They pitch attractive low prices, but as soon as upstream delays or transport hiccups hit, their customers hear only excuses and get little real support. Our site continues running through those disruptions, as our plant managers build margin into our production plans and maintain close ties with core suppliers. Our priority is getting our partners what they need, when they need it—not making excuses.
Last year, when fluoroaromatic raw material supply dipped due to a major producer’s shutdown, our facility had prepared enough in advance to ride through the crunch without any order cuts. Clients needing 2-chloro-6-(trifluoromethyl) 3-pyridinecarbonitrile for late-stage clinical synthesis or critical herbicide pilot runs faced no delays. Our reliability isn’t an accident; it’s a direct result of years of planning, forecasting, and learning from earlier supply interruptions.
Producing highly functionalized pyridine derivatives brings genuine hazards. Chlorinated intermediates need careful handling, both for personnel and the environment. We run full Material Safety Data reviews for every process stage and regularly update training for our operators. Because hydrolytic or byproduct residues can affect both safety and product stability, our technical and EH&S teams run root-cause investigations on any deviation reports. Over years of iterative safety improvements, unplanned releases and reportable incidents have dropped well below industry averages at our site.
When regulators inspect or audit, we open all records—the protocols, cleaning logs, environmental monitoring, emissions records, and downstream transport tracking. Customers gain the benefit of a supply partnership not just from a transaction, but from a direct relationship with an entity that understands and mitigates real chemical risk. For those filing regulatory dossiers, access to true manufacturer-level transparency can save months of back-and-forth and reduce the risk of questions from health or environmental agencies.
Direct communication with our R&D and production chemists gives our partners a real advantage. Anyone can copy-paste a data sheet, but only a hands-on producer can advise clients on subtle issues of solubility in mixed systems, optimized process filtration, or impurity challenges when pulling intermediates through new catalytic methods. We hear regularly from project chemists who face shifting parameters or route changes in the middle of a campaign. Our own staff can pull historical batch data or suggest tweaks based on what we’ve seen in our own pilot plant—the insights gained from years of scaling and troubleshooting, not just what an MSDS or textbook specifies.
Over time, we’ve worked with start-ups developing novel kinase inhibitors, established pharma plants building risk mitigation into their routes, and crop science firms seeking sharper stability under field conditions. These collaborations go beyond transactional supply; they ground themselves in open discussion, technical troubleshooting, and truly science-first problem solving. That’s possible only because our perspective comes from actual manufacturing, not intermediary sales offices.
As the team responsible for putting 2-chloro-6-(trifluoromethyl) 3-pyridinecarbonitrile into the hands of advanced synthetic teams, we know that every kilogram we ship is headed toward world-changing science—new medicines, vital crop protection, advanced imaging. We do not gamble with batch quality or provenance; we protect our client’s timelines and reputations because we work at the source, with full control from synthesis to shipping.
Choosing a direct producer means open lines to real scientists, repeatable batch results, continuity in supply, and answers grounded in day-to-day production experience. It’s not just about buying a chemical; it’s about building reliable processes, reducing headaches, and meeting the standards that global science demands. For every gram, kilo, or drum that rolls out our doors, we put our expertise and dedication behind it—just as we have, year after year, for partners worldwide.