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HS Code |
112565 |
| Productname | 2,3,6-Trichloro-5-(trifluoromethyl)pyridine |
| Casnumber | 116083-39-1 |
| Molecularformula | C6HCl3F3N |
| Molecularweight | 266.44 g/mol |
| Appearance | Colorless to light yellow liquid |
| Boilingpoint | 195-197 °C |
| Density | 1.685 g/cm3 at 25°C |
| Solubility | Insoluble in water |
| Purity | Typically ≥98% |
| Refractiveindex | 1.518 - 1.523 |
| Flashpoint | 83 °C (closed cup) |
| Smiles | C1=C(C(=C(N=C1Cl)C(F)(F)F)Cl)Cl |
| Inchi | InChI=1S/C6HCl3F3N/c7-3-1-4(8)13-2-5(9)6(3)12-10-11 |
| Synonyms | 2,3,6-Trichloro-5-(trifluoromethyl)pyridine |
As an accredited 2,3,6-Trichloro-5-(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 100 grams of 2,3,6-Trichloro-5-(trifluoromethyl)pyridine, tightly sealed, with hazard and identification labels. |
| Container Loading (20′ FCL) | 20′ FCL: Loaded with securely sealed drums or bags, each labeled, ensuring safe, moisture-free transport of 2,3,6-Trichloro-5-(trifluoromethyl)pyridine. |
| Shipping | **Shipping Description:** 2,3,6-Trichloro-5-(trifluoromethyl)pyridine should be shipped in tightly sealed containers, protected from moisture and light. Ensure labels comply with hazardous chemical regulations. Transport according to local, national, and international guidelines for hazardous goods, keeping the package upright and secure to prevent leakage or accidental exposure during transit. |
| Storage | Store 2,3,6-Trichloro-5-(trifluoromethyl)pyridine in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Use secondary containment to avoid spills and keep away from heat sources. Ensure the storage area is clearly labeled, and access is restricted to trained personnel using appropriate personal protective equipment. |
| Shelf Life | Shelf life of 2,3,6-Trichloro-5-(trifluoromethyl)pyridine is typically two years when stored in a cool, dry, tightly sealed container. |
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Purity 99%: 2,3,6-Trichloro-5-(trifluoromethyl)pyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and product yield. Melting point 64°C: 2,3,6-Trichloro-5-(trifluoromethyl)pyridine of melting point 64°C is used in agrochemical manufacturing, where it provides thermal stability during formulation processes. Moisture content <0.5%: 2,3,6-Trichloro-5-(trifluoromethyl)pyridine with moisture content <0.5% is used in specialty chemical production, where it minimizes unwanted side reactions. Molecular weight 264.43 g/mol: 2,3,6-Trichloro-5-(trifluoromethyl)pyridine of molecular weight 264.43 g/mol is used in custom synthesis applications, where it enables precise formulation calculations. Stability temperature up to 120°C: 2,3,6-Trichloro-5-(trifluoromethyl)pyridine with stability temperature up to 120°C is used in high-temperature processing environments, where it maintains chemical integrity over prolonged periods. Particle size < 50 µm: 2,3,6-Trichloro-5-(trifluoromethyl)pyridine of particle size < 50 µm is used in catalyst production, where it improves dispersion and catalytic activity. Low impurity (<0.1%): 2,3,6-Trichloro-5-(trifluoromethyl)pyridine with low impurity (<0.1%) is used in laboratory reagent preparation, where it ensures reproducible analytical results. Flash point 89°C: 2,3,6-Trichloro-5-(trifluoromethyl)pyridine with flash point 89°C is used in industrial solvent formulations, where it enhances safety in handling and storage. |
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In the process industry, few molecules draw as much attention as 2,3,6-Trichloro-5-(trifluoromethyl)pyridine. Colleagues in both advanced materials and active ingredient development have pushed the limits of design, and in our manufacturing halls, every kilogram of this compound tells a story of engineering and quality. Making this pyridine derivative takes a blend of experience, well-controlled chlorination reactions, secure handling of trifluoromethyl sources, and clean separation steps. Every batch presents subtle adjustments: minor shifts in reaction temperature can mean the difference between a product that meets high-performance applications and setbacks that waste time and material. We do not rely on hope for these reactions to proceed as expected; they require vigilant monitoring throughout.
Operators at our plant have learned over the years that many challenges arise from the inherent reactivity of the intermediates. Improper handling results in nuisance byproducts like over-chlorinated pyridines or unreacted starting material. Early in our history, we found that simple measures like inerting the reactors and gradually feeding the trifluoromethyl reagents provided more control, but poor temperature regulation destroyed yields. Now, with robust monitoring and precise dosing, we handle scale-up and produce lots that meet our QC benchmarks every time.
Many end users overlook the importance of precise purity benchmarks until inconsistent results emerge in their own synthetic pipelines. What sets 2,3,6-Trichloro-5-(trifluoromethyl)pyridine apart in our catalog comes down to the crystalline finish and defined melting and boiling points. Typical specifications include purity above 98% by GC; small levels of mono- or dichloro analogs, if present, are tightly controlled because they hinder downstream reactivity and complicate purification for end uses. We maintain color control too—our experienced crew evaluates every batch for minimal coloration, since subtle hues might indicate contamination from trace byproducts.
Packing and storing this product is not routine. Moisture ingress poses a real risk not just for product stability, but for downstream chemistry. We’ve shifted to nitrogen-purged, sealed containers for all shipments and hold inventory in dedicated spaces where temperature and humidity stay within strict parameters. This focus on material handling ensures labs and production facilities receive 2,3,6-Trichloro-5-(trifluoromethyl)pyridine with no surprises when it arrives; no clumping, no off-odors, and no question about shelf life.
The reach of 2,3,6-Trichloro-5-(trifluoromethyl)pyridine spans several sectors—especially where researchers need a stable, electron-deficient pyridine nucleus ready for further elaboration. The largest volume leaves our gates bound for agrochemical intermediates. In these processes, the compound serves as a versatile backbone, delivering robust electron-withdrawing capability that enhances activity of herbicides and fungicides. The presence of the trifluoromethyl group and repeated chlorination provides chemical stability under tough field conditions. Fine-tuning that reactivity at the pyridine ring allows formulators to hook different functional groups in subsequent coupling reactions, which broadens the range of molecules producers can target.
Beyond agriculture, customers in pharmaceutical intermediate synthesis request this compound as a coupling partner for specialized heterocyclic frameworks. It tolerates strong conditions—acidic or basic—without decomposing, which means medicinal chemists can design lengthy reaction sequences knowing their central intermediate will survive intact. More recently, development teams at specialty coatings and electronic materials firms have asked about larger quantities, hoping to leverage the same high-performance properties for next-generation circuit materials and protective polymers.
Most of the time, the value appears only once the molecule becomes something else entirely, yet all the way through, researchers depend on that initial lot for consistent behavior batch to batch. We have seen ambitious startups struggle with supply bottlenecks when forced into a cycle of scouting for consistency; feedback reaches us that, given the time investments in high-value process development, reliable supply is worth a premium.
Chemists have several options for halogenated pyridines and trifluoromethyl-substituted aromatics. Why do so many keep coming back to 2,3,6-Trichloro-5-(trifluoromethyl)pyridine instead of choosing a dichloro or tetrachloro alternative? Much of the distinction lies in a balance between reactivity, stability, and price. Mono- or dichloro analogs jump too readily in downstream coupling or substitution, sometimes leading to excess reactivity and side products. Those with full halogen coverage, like pentachloro derivatives, stay too inert for practical modifications unless severe reaction conditions are used.
For those working via nucleophilic aromatic substitution or transition-metal-catalyzed couplings, this compound’s substitution pattern opens the door to functionalize the only free position on the ring—a feature not available in the more heavily chlorinated versions. The trifluoromethyl at the 5-position provides strong electron-withdrawing effects, but it sits far enough from the active sites to keep the ring reactive. That arrangement forms the sweet spot for downstream modifications: strong field effects but accessible chemistry.
Economics cannot be ignored. More elaborate pyridines fetch higher prices both for the extra chlorination and for the special handling and purification they require, but buyers often find little gain in performance compared to the jump in cost and complexity. We build our 2,3,6-Trichloro-5-(trifluoromethyl)pyridine on mature process technology and decades of yield improvement, passing a stability-cost advantage back to users.
Experienced operators know chemistry doesn’t stop at the flask. Workers on the plant floor can spot upstream solvent impurities that will cause headaches downstream, and logistics staff adapt to storage hiccups they didn’t write procedures for in school. The most persistent improvement came with addressing chloride build-up in the main reactors. Early runs often failed because subtle changes in chloride levels would skew the selectivity and foul up downstream purification. By reviewing mass balances for every run, the team pinpointed stages that required careful venting or neutralization for consistent results.
Process safety has taught us that strong exotherms demand respect. Misjudging reaction rates could lead to vapor evolution that jeopardizes not just yield but equipment and operator safety. To get around these, instrumented controls tied to pressure and temperature monitoring now govern reagent addition rates. These are not selling points so much as they are real-life requirements to keep people and property safe.
Many researchers seek greener routes for products like this, but trusted electropyridination and halogenation routes struggle to hit the mark for both yield and cost. We’ve experimented with new catalysts and solvent swaps but have yet to see stable, scalable improvements in this specific chemistry. Investment continues in this direction, though—all echo request for safer, more sustainable options. Feedback from buyers on environmental impact of solvents or effluents drives many of our priorities, influencing equipment upgrades and emission controls in ways that go beyond box-checking compliance.
Each run of 2,3,6-Trichloro-5-(trifluoromethyl)pyridine makes or breaks on tight specifications; small changes in upstream temperature or atmospheric conditions may escape detection in laboratory glassware but wreak havoc in multi-ton scale. We dedicate analytical resources to gas chromatography and NMR confirmation. No shipment leaves the plant without certification against customer-agreed specs for purity, moisture, color, and volatile content. Lab chemists alert production to any deviation, and if issues arise, we investigate clear back to raw material lots and operator notes.
More often than not, customer claims relate not to chemical composition but to subtle impurities that influence downstream reactivity—for example, adventitious iron or inorganic salts that may sneak in depending on metalware cleanliness. Our protocols include metal ion screens and residual solvent checks to preempt surprises. We have also responded to requests for finer particle sizing for those looking to use the compound in automated dispensing setups, shifting part of the operation to controlled milling and blending.
Packaging choices reflect both safety and the end user's need for simple, loss-free transfer. Some compounds become volatile or degrade quickly once exposed, so our team purges every vessel with inert gas and uses high-density containers proven to prevent both moisture and light ingress.
In R&D environments, every month counts. Laboratories and full-scale operations both count on on-time supply. Buyers inform us that intermittent deliveries can cause gaps in their multi-month workflows, forcing them to revalidate stocks or even reassign research staff. We meet these requirements with disciplined inventory management, safety stock, and trustworthy logistics partners. In the past, global disruptions from weather to border delays showed us that single-source dependencies put entire projects at risk; as a result, we built out redundant raw material contracts and keep dialogue open with customers about lead times and forecast needs.
Occasional surges in demand—driven by new launches in crop protection or emerging interest from electronics—can create tension in available supply, and our team adapts capacity on the fly to cover both spot needs and long-term agreements. Meanwhile, our quality and compliance specialists help maintain confidence for importers facing tough new standards or regulatory procedures in their own jurisdictions.
Over years of handling 2,3,6-Trichloro-5-(trifluoromethyl)pyridine, worker safety and environmental stewardship guide our choices. Training covers not just routine PPE, but strong emphasis on correct handling of chlorinated intermediates; spills or mishandling could generate not only wasted product, but put neighboring operations at risk. We install leak monitoring and ventilation in every workspace where the material is repackaged or transferred, and implement emergency drills based on real incident reviews, not just regulatory minimums.
Optimizing waste capture and destruction has seen the greatest evolution in recent years, with solvent recovery topping our list of improvements. We audit disposal streams to ensure low-impact discharge and invest in new destructors that minimize halogen release. Ongoing dialogue with regional authorities and neighbors keeps us tuned to how our activities affect our community.
A supply relationship for specialty chemicals evolves as research evolves. Feedback from process chemists, either on purification quirks or changes in regulatory status, shapes our next batch runs and procedure adjustments. Requests sometimes challenge our process norms: several biotech partners have called for audit trails that track every step, not just final testing. Others in electronics ask for even tighter specs on trace metals, requiring us to upgrade in-line purification.
We occasionally bring customers onsite for run-throughs of plant procedures, opening the floor for frank discussion about what works and what fails. These exchanges lead to co-development—such as adjusting product form for automated handling, or retooling equipment to handle larger campaign orders for one-off projects. Users appreciate not just continuity of supply, but an open door to address technical needs before they drift into crises.
The continued expansion of 2,3,6-Trichloro-5-(trifluoromethyl)pyridine into new markets creates both opportunities and pressure. Global chemical registration frameworks evolve rapidly, raising requirements for traceability and compliance. We stand ready to respond—not with hollow reassurances, but with documented procedures and proven audit trails. These requirements are not burdens; they drive us to refine every facet of our operation.
Meanwhile, the push for greener, low-impact synthesis techniques means ongoing R&D and investment. Academic and industrial partners reach out about routes to reduce waste or energy input. Many routine chlorination and trifluoromethylation technologies are over a half-century old. Translating new innovations—whether flow reactors, alternate catalysts, or new separation technologies—into reliable plant-scale improvements remains a hill to climb, not just for cost, but for scale and robustness. As regulations tighten on halogen management, continuous monitoring and rapid reporting form a new frontline in compliance and risk reduction.
2,3,6-Trichloro-5-(trifluoromethyl)pyridine may appear to be just another line item in a chemical catalog, but its journey from raw materials to reliable, high-purity shipments showcases the balance between process chemistry, operator experience, tight logistics, and product stewardship. By learning from every campaign and collaborating closely with users, we ensure consistent support for both routine applications and emerging breakthroughs that rely on these specialty intermediates. Long-term engagement with process improvements, ongoing investment in environmental responsibility, and real attention to researcher feedback shape a product experience that delivers more than molecules—it builds trust for the future of advanced synthesis.