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HS Code |
885855 |
| Chemical Name | 2-chloro-4-iodo-6-(trifluoromethyl)pyridine |
| Molecular Formula | C6H2ClF3IN |
| Cas Number | 886372-39-0 |
| Appearance | Pale yellow to light brown solid |
| Melting Point | 47-51 °C |
| Purity | Typically >97% |
| Solubility | Soluble in organic solvents (e.g., DMSO, methanol) |
| Smiles | C1=CC(=NC(=C1I)C(F)(F)F)Cl |
| Inchi | InChI=1S/C6H2ClF3IN/c7-4-2-3(11)5(6(8,9)10)12-1-4/h1-2H |
| Storage Conditions | Store at 2-8°C, protect from light |
As an accredited 2-chloro-4-iodo-6-(trifluoromethyl)pyridine 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 of 2-chloro-4-iodo-6-(trifluoromethyl)pyridine, with tamper-evident cap and hazard labels. |
| Container Loading (20′ FCL) | 20′ FCL container holds ~10-12 MT of 2-chloro-4-iodo-6-(trifluoromethyl)pyridine, packed in sealed, chemical-safe drums. |
| Shipping | 2-Chloro-4-iodo-6-(trifluoromethyl)pyridine shipping is conducted in accordance with all relevant safety regulations. The chemical is securely packaged in sealed, chemical-resistant containers, labeled appropriately, and shipped by certified carriers. Transport follows UN hazardous materials guidelines to prevent exposure, contamination, and environmental release throughout transit. |
| Storage | 2-Chloro-4-iodo-6-(trifluoromethyl)pyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep away from incompatible substances, such as strong oxidizing agents. Store at room temperature and protect from moisture. Clearly label the container and handle under an inert atmosphere if sensitive to air or moisture. |
| Shelf Life | 2-chloro-4-iodo-6-(trifluoromethyl)pyridine typically has a shelf life of 2 years when stored cool, dry, and protected from light. |
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Purity 98%: 2-chloro-4-iodo-6-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low impurity formation. Melting point 57-60°C: 2-chloro-4-iodo-6-(trifluoromethyl)pyridine with a melting point of 57-60°C is used in solid state formulation processes, where it provides ease of handling and stable formulation. Particle size <50 µm: 2-chloro-4-iodo-6-(trifluoromethyl)pyridine with particle size less than 50 µm is used in fine chemical blending applications, where it enables uniform dispersion and optimal reaction efficiency. Stability temperature up to 120°C: 2-chloro-4-iodo-6-(trifluoromethyl)pyridine with stability temperature up to 120°C is used in high-temperature coupling reactions, where it maintains structural integrity and consistent reactivity. Moisture content <0.3%: 2-chloro-4-iodo-6-(trifluoromethyl)pyridine with moisture content below 0.3% is used in moisture-sensitive organometallic synthesis, where it prevents side-reactions and increases product purity. |
Competitive 2-chloro-4-iodo-6-(trifluoromethyl)pyridine prices that fit your budget—flexible terms and customized quotes for every order.
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Handling 2-chloro-4-iodo-6-(trifluoromethyl)pyridine day after day, we’ve learned that the smallest shifts in quality control or process adjustment can tip the final product in ways that ripple through downstream syntheses in pharmaceuticals and agrochemicals. This isn’t a molecule that serves as a basic flavoring—it springs up where functional complexity and elemental precision act as the driving forces.
Our production lines have remained steady through market disruptions because our operators and process chemists understand the stakes. Every gram of this pyridine derivative reflects attention not only during batch reactions but also at each workup stage. Chlorination, iodination, and the careful introduction of the trifluoromethyl group involve a dance of reagents where temperature, agitation, and concentrations matter just as much as the source material. We have tuned our multiple reactors for stability, not just speed, because we’ve seen what happens when a reaction runs too hot or impurities sneak past filtration. Purity impacts both the final functionality and the liability that rides on each shipment leaving our dock.
We manufacture this compound to meet specs—not the kind posted on a generic product sheet, but those pulled from real-life process feedback and regulatory compliance requirements. Moisture content stays low because water and pyridine analogs rarely play nicely during coupling and cyclization reactions. Our analytical teams keep an eye out not only for direct impurities but also for structurally related isomers. By the time a batch is packed, the content of the primary compound usually exceeds 98 percent by HPLC, and all measured metals drop below limits that could poison hybridization or inhibit further functionalization.
In our hands, the physical appearance of this pyridine is neither incidental nor cosmetic. Slight color changes often hint at problems during halogenation. Our staff learned to spot off-notes before formal analysis even begins. This practical vigilance goes upstream and downstream; we check that each container offers enough stability during transit, especially if our partners work in regions where temperature and humidity swing wider than usual.
From our experience, requests for 2-chloro-4-iodo-6-(trifluoromethyl)pyridine come from teams scouring for a reliable framework to build more complex targets. The molecule’s three distinct substituents—chlorine, iodine, and trifluoromethyl—open up pathways unavailable if a client only has a monosubstituted pyridine or a less reactive analog.
Chemists pursuing cross-coupling or seeking to harness selective reactivity look to this scaffold because iodine offers a reactive handle, while trifluoromethyl influences both electronic properties and metabolic stability. Nearly every order we fulfill leads into Suzuki, Sonogashira, or Buchwald-Hartwig reactions on the client’s site. That matters not just for synthetic yield but for regulatory filings where trace impurities from an upstream supplier can pull an entire product off the path to clinical or commercial use.
We’ve seen more pharma groups develop kinase inhibitor pipelines with this backbone. Others, especially in crop science, use the molecule as a building block for actives demanding both potency and rainfastness. What works so well is the way the trifluoromethyl group resists metabolic breakdown, while the halogens give selective activation points for further coupling. This is not an all-purpose ingredient, but it is relied upon where selectivity in downstream chemistries gives a competitive edge.
With over a decade working inside this plant, I can line up dozens of pyridine derivatives, but this compound’s trifecta of functional groups sets it apart. Single-halogenated pyridines certainly find markets, but their reactivity limits the downstream chemistry. The combination of chlorine and iodine, each positioned around the ring, lets chemists sequence their reactions—iodine first for the more sensitive coupling, chlorine next for a more robust transformation. The order of these plays a major role in yield, purity, and, ultimately, project cost. Most other derivatives with just one handle don’t grant that flexibility.
Where trifluoromethyl is swapped for alkyl or alkoxy, downstream products display different metabolic and physical properties. Clients in pharma detect the differences in clearance rates and binding, while agrochemical developers notice shifts in volatility and soil binding. Such changes often become clear only after pilot production or field trials—by then, choosing the right starting material becomes a matter of cost containment, not just experimental convenience.
Many research groups once asked for 2-chloro-4-pyridine analogs with simpler substituents. After a few syntheses or scale-ups, the trend veers back to the tried-and-true combination that our product delivers, because the time and resource savings become evident on the order history.
Clients and partners often express concern about continuity of supply and quality drift. These issues aren’t abstract to a manufacturer—they haunt every production meeting and shipment we send out. External market forces, from global shipping disruptions to regulatory scrutiny, put pressure on batch release schedules. We manage risk by securing a reliable source of raw pyridine, and by sticking to validated synthesis steps that scale cleanly whether we’re running ten kilos or a hundred.
Each batch gets released only after internal review by teams who have run the same sample through routine and stress tests—forced degradation, accelerated thermal cycling, and moisture uptake. These aren’t steps for show; they catch issues before they reach the next link in the chain. Several years ago, one batch failed due to excessive iodine release. Recovery took over two weeks, and we fielded direct calls from project leads waiting on API intermediates. Our clients’ lost time and budget reflected back on our shop floor in new SOPs and better analytical oversight.
Transparency matters in specialty chemicals. We keep certificates of analysis detailed and accessible, not only for traceability but because the learning moves both ways—feedback from users often pushes us to improve specs or find workarounds for their process challenges. When questions roll in about possible metal content, particle size, or packaging, our technical team answers directly, drawing on past lot data and actual plant runs, never relying on generic guidance.
Working with pyridine derivatives generates hazards that paper checklists rarely capture in full. Chlorinated and iodinated intermediates build pressure in reactors, and even trace moisture turns a routine filtration sticky or hazardous. We engineered local exhaust and upgraded our PPE stock not because regulations changed, but because team members ran into real-world surprises during scale-up. Vent scrubbers and specialized waste handling limit accidental releases—a measure that both ensures compliance and protects the folks operating the lines. Our familiarity with fluorinated chemicals grew through sheer repetition; we keep the necessary neutralizing agents and monitoring equipment on hand because mishaps, if not quickly handled, escalate fast.
Training sessions walk all newcomers through these specifics, using close-call stories and results from post-shutdown reviews to ground lessons in reality. We find nothing cements safe practice like direct experience—a leaky flange or an odd pump vibration tells more than a line in a safety manual ever does. Visitors and clients taking plant tours quickly pick up that every workstation and exit path reflects lived-in knowledge far more than a polished poster ever could.
Many synthetic targets start with a research team calling for a few grams, often to try out a new coupling route. Other times, a project ramps to multi-kilogram quantities in weeks. Our approach adapts because the market rarely gives years of runway; a team sees promise in a pathway, funding follows, and supply must keep up. We retain small reactors for pilot work and keep modular setups for fast scale jumps. Every batch demands its own tight controls—a synthesis on a small scale might tolerate a variation that spells trouble at larger volumes. Having run both ends, we often help clients adjust solvent choices or reagent addition rates based on bottlenecks our crews have seen in practice.
Our technical liaisons share methods seasoned by repetition. For example, we noticed certain carbons in the trifluoromethyl group show inconsistent reaction rates during some coupling protocols. Sharing this, we helped a client solve a stalling step in a late-stage intermediate, moving from lab scale to pilot plant within days. No textbook outlines every pitfall; much of our advice comes from catalogued mishaps, small victories in purification, and the lost sleep that comes from getting promised samples ready for clinical candidate deadlines.
Doubt about batch integrity hurts a project more than any delay. Our own process engineers push for full NMR and LC-MS workups on every batch, not only to assure purity but to pin down the smallest side products. Comparing chromatograms to past batches or reference standards gives us early warning on raw material shifts. Any downstream process involving this pyridine derivative, especially those under GMP or tight regulatory review, leans heavily on this analytical rigor.
We learned the cost of neglecting this years ago. A minor unknown peak on an HPLC trace once seemed harmless. Months later, it showed up as a complication in a customer’s final product validation, costing both teams lost time. Reworking analytical protocols and setting tighter thresholds for unknowns became our new standard. Downstream chemists benefit as much as we do; every extra reference helps smooth the path toward registration or regulatory filings.
Specialty chemicals attract scrutiny not just for process yields but waste streams. Our first attempts at scaling trifluoromethylation brought heavy solvent loads and more halogenated byproducts than a basic waste stream could manage safely. Through process tweaks—solvent swaps, improved crystallization, and aggressive distillation cuts—we’ve dialed down both solvent use and the need for offsite waste disposal.
Working with local environmental officers, we take pride in transparency around emissions and effluents. Even as the regulatory landscape tightens, our in-house engineers model each process for fugitive releases and monitor the effluent for trace byproducts. These changes ripple into compliance certificates and lower insurance rates, but the practical impact is felt by our staff and their families—less exposure, safer work, and a steadier business that meets neighbors’ expectations for stewardship.
Many buyers have turned more attention toward the chain of custody and ESG metrics for their intermediates. We recognized this by building not only audit trails but also plans for process improvements tied to emission reductions—often driven just as much by operator feedback as by management edicts. Solutions that prove themselves on the shop floor stick much longer than any top-down directive.
Requests for this pyridine derivative keep evolving. Some projects demand less residual solvent, others ask for tighter particle size ranges, and a handful want unusual packaging to fit robotic feed systems. Our role isn’t to lecture but to meet chemists wherever their workflow heads next.
Production crews retool equipment, handlers learn new labeling, and technical experts troubleshoot process quirks—adaptable because of trust built through years of direct interaction. The most tangible mark of loyalty isn't an order form, but the repeat calls for last-minute batch changes or advice on a route modification. As manufacturers, this is the real proof: delivering consistent, traceable product that adapts to the needs of those shaping the next wave of chemical innovation.
No specialty chemical survives by standing still. The demand for 2-chloro-4-iodo-6-(trifluoromethyl)pyridine in pharmaceutical and agrochemical pipelines has shown us that robust process knowledge, transparent QA, and direct engagement make the real difference. Every scaling step, from small-volume to full-scale runs, carries with it lessons that reshape both our production and our policies.
Our crew has weathered shifts in global supply, sharpened analytical thresholds, and found new ways to cut waste—each time, moving closer to both the needs of innovative chemists and the growing expectation for responsible manufacturing. The collaborative spirit at the core of specialty chemical production is what keeps every kilogram leaving our plant relevant and reliable, batch after batch.