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HS Code |
555370 |
| Iupac Name | 2,6-dichloro-4-methyl-3-(trifluoromethyl)pyridine |
| Cas Number | 86604-74-4 |
| Molecular Formula | C7H4Cl2F3N |
| Molecular Weight | 230.02 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 212-214 °C |
| Density | 1.49 g/cm3 (at 20 °C) |
| Solubility In Water | Insoluble |
| Flash Point | 93 °C |
| Smiles | CC1=NC(=C(C(=C1Cl)C(F)(F)F)Cl) |
| Inchi | InChI=1S/C7H4Cl2F3N/c1-3-5(7(10,11)12)6(9)13-4(2)8/h1-2H |
| Refractive Index | 1.495 (at 20 °C) |
As an accredited Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- is supplied in a sealed amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | 20′ FCL: Standard shipping container loads 12–14 MT of Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)-, securely packed in drums. |
| Shipping | 2,6-Dichloro-4-methyl-3-(trifluoromethyl)pyridine should be shipped in tightly sealed containers, clearly labeled, and protected from moisture, heat, and incompatible substances. Ship according to regulations for hazardous chemicals, using appropriate cushioning and secondary containment. Ensure packaging complies with DOT, IATA, or IMDG guidelines, as it may be classified as a dangerous good. |
| Storage | Store Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Protect from direct sunlight and incompatible substances such as strong oxidizers and acids. Use appropriate chemical safety cabinets if possible, and keep out of reach of unauthorized personnel. Store according to all applicable regulations. |
| Shelf Life | Shelf life of Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- is typically 2-3 years when stored in a cool, dry place. |
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Purity 98%: Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced by-product formation. Melting Point 58°C: Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- with melting point 58°C is used in agrochemical formulation, where it provides enhanced processability and uniform dispersion. Molecular Weight 264.04 g/mol: Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- with molecular weight 264.04 g/mol is used in fine chemical production, where it guarantees precise molar control and consistent batch results. Stability Temperature up to 120°C: Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- with stability temperature up to 120°C is used in catalyst manufacturing, where it delivers thermal robustness and sustained chemical activity. Particle Size <50 µm: Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- with particle size less than 50 micrometers is used in advanced material research, where it supports improved reactivity and homogenous mixing. |
Competitive Pyridine, 2,6-dichloro-4-methyl-3-(trifluoromethyl)- prices that fit your budget—flexible terms and customized quotes for every order.
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We first worked with 2,6-dichloro-4-methyl-3-(trifluoromethyl)pyridine years ago, long before it became a staple for research and development teams pursuing demanding synthesis routes. Most chemists who contact us know their raw material must do more than meet the right purity threshold; they need reliable consistency across every kilogram and container. Our perspective is rooted in the practical: every variant and impurity alters a synthetic pathway, and even minuscule deviations lead to later problems. The chemists here remember the days when each batch brought surprises, some pleasant, others much less so. We set about offering a product you can trust time after time, not one that simply looks good on paper.
2,6-dichloro-4-methyl-3-(trifluoromethyl)pyridine stands out not just for its multi-substituted skeleton but for the way its electron distribution tailors reactivity. Its two chlorines dramatically alter the nucleophilicity at the ring's remaining positions. The methyl group at position 4 opens new doors for sidechain functionalizations and downstream derivatization, while the trifluoromethyl at position 3 impacts the compound’s lipophilicity and boiling point. After years of manufacturing, we still field new questions from researchers looking to exploit unique reactivities introduced by this arrangement of groups. As a bridge molecule, it doesn’t behave the same as pyridine, nor as simple methyl- or chloro- derivatives. For each shipment, we run spectral analysis by NMR and GC-MS to confirm the chemical fingerprint matches both the literature references and your practical requirements.
The product you see from us isn’t born of generic mixing: our model began as a bespoke process. Modifying standard Vilsmeier and Sandmeyer reactions, we built a scale-up protocol around minimizing unwanted byproducts—especially chlorinated tars and unreacted precursors. While no two factories are identical, we settled on temperature controls, solvent recovery setups, and specialized glass-lined reactors to ensure predictability from gram-scale to multi-ton batches. Our chemists spend more time than many on post-synthesis purification: repeated column chromatography, fractional distillation under reduced pressure, and careful selection of drying techniques. It’s easier to make something “good enough” than something that genuinely meets demanding R&D or production standards every cycle.
This pyridine derivative plays a pivotal role in several sectors. In agricultural chemistry, it’s a favorite for researchers exploring new routes to herbicides and fungicides—those fluorinated and methyl-chlorinated motifs are prized for tuning biological activity. Pharmaceutical developers link this scaffold to aryl or heterocyclic groups, chasing activity in anti-infective or anti-cancer screens. Even specialty polymer manufacturers have started asking us for tailored variants to give their end materials halogenated bulk and volatile stability.
We’ve found the compound’s reliability especially critical for teams working on sensitive coupling chemistries, such as Suzuki and Buchwald–Hartwig reactions, where the halogen pattern dictates selectivity. Generation of ipso-intermediates, fluoroalkylation strategies, or even basic nucleophilic aromatic substitution—these all depend on starting materials that don’t introduce mystery contaminants or odd reactivities. Over the past decade, we’ve seen more requests for high-purity, low-residue batches to meet regulatory requirements in Europe and North America. Most clients don’t have time for batch-to-batch analysis; they rely on our own controls and transparency.
Experienced chemists working with ligands or building blocks sometimes ask us why this compound shows results that differ from 2,6-dichloropyridine or 4-methylpyridine. Our answer lies in the electron-withdrawing prowess of the trifluoromethyl group. This trifluoromethyl isn’t just another quirky substituent—it slashes the energy needed for some substitutions but can slow alkylation at others. Contrasting it with simple dichloro- or methylpyridines, it frequently offers increased metabolic stability, shifting the kinds of transformations possible in late-stage functionalizations. In our experience, attempts to substitute this molecule with similar analogues often end in unexpected yield drops, problematic side reactions, or issues during purification—costing precious time and resources for scale-up teams. The right material at this position saves headaches down the line.
Unlike some isomeric forms, the 2,6-dichloro- substitution pattern in this molecule shields the ring from overreaction at unwanted sites. Many customers who’ve run into trouble using less-hindered pyridine derivatives come to us, having struggled with mixtures or ring openings in harsh reaction conditions. We discuss their synthesis plans openly and adjust the batch specifications or purity levels as needed, sometimes even preparing custom lots to fit particular downstream steps. We’re familiar with the demands of chiral synthesis as well: avoiding trace enantiomeric starters, or working out ways to eliminate persistent chlorinated byproducts.
Many in the lab get frustrated jumping between brands, discovering that some batches of 2,6-dichloro-4-methyl-3-(trifluoromethyl)pyridine simply refuse to dissolve, react, or distill cleanly. We’ve spoken to several synthetic chemists who lost weeks to unforeseen impurities—minor things that only show up deep into a project. You won’t catch this compound in our lineup if we can’t guarantee tight limits on water content, residual solvents, or related substances. We’ve spent years refining our protocols, using Karl Fischer titration for moisture and calibrating chromatography standards against trace contaminants. It takes significant equipment and vigilance, but we see our reputation as inseparable from the trust our customers place in us.
From small trials to full production runs, we employ redundant checkpoints: real-time HPLC sampling, archive retention for cross-referencing, and chain-of-custody systems that track every drum and vial. Sometimes we’ll hold back a delivery if an anomaly pops up—no matter the rush. Our team reviews each abnormality, tracks it to its source, and logs adjustments for later batches. We treat knowledge sharing as an essential part of the business, openly discussing successful runs and honest exposures to potential process hazards. In a global market with complex supply chains, tight data helps avoid the all-too-common pitfalls of inconsistent or counterfeit material.
Our work teaching new staff about this molecule always starts with regulatory frameworks—those governing handling, environmental impact, and permitted impurity levels. We collaborate with regulatory compliance officers in Europe, Asia, and the Americas, furnishing purity and impurity profiles with each batch, always prepared for evolving guidelines. The halogenated structure of this compound means special consideration during production waste treatment. We run closed-loop recovery systems for both chlorinated and fluorinated byproducts, deploying advanced scrubbers and neutralization steps to minimize impact. Our technical and safety teams conduct regular environmental risk reviews, updating disposal and emissions protocols nearly every year.
We’re also seeing more manufacturers, especially in pharma and agrochemicals, facing stricter residual solvent and genotoxic impurity thresholds. Each regulatory tightening prompts a look at our plant, sometimes investments in better reactors or more stringent filtration. More requests come in for trace analysis reports—sometimes down to parts per million or billion. We answer with transparency, data-packed certificates, and full disclosure about production runs and analytical methods. Vendors hoping to cut corners rarely keep up when audit teams visit to verify compliance and traceability, especially with persistent organohalogens like those in this class of pyridines.
Some newcomers to this field overlook subtle storage hazards presented by multi-halogenated organics. The nature of 2,6-dichloro-4-methyl-3-(trifluoromethyl)pyridine demands cool, dry conditions—certain solvents or container types can encourage decomposition or off-flavors that later wreak havoc in sensitive syntheses. Our warehouses use monitored humidity controls and inert gas blankets for bulk material. We sidestep unnecessary risks by packing smaller quantities in chemically compatible bottles, never reusing containers or skimping on sealing. During transport, even brief exposure to sun or temperature fluctuations can alter the compound just enough to shift a reaction’s pathway in your lab. We document all storage and transit conditions, keep digital thermologs, and offer guidance to customers shipping the product across borders or storing it for long periods.
These details—often invisible during purchasing decisions—separate reliable results from failure in the lab. Our long experience handling this material has taught us to never treat logistics as an afterthought. Even solvents used for cleaning containers or moisture in shipping atmospheres can leave residues or initiate hydrolysis. Each member of our logistics and QC teams takes pride in preemptively minimizing risk, passing along lessons from past incidents to keep products uncompromised.
We don’t believe in hiding behind technical jargon or canned product blurbs when people call us with questions. Over the years, each batch of this pyridine derivative has sparked new ideas and troubleshooting—sometimes making all the difference to a crucial synthetic route or formulation. Our technical support staff, many of whom have spent years on the manufacturing side, field in-depth discussions about scale-up safety, alternate solvents, and custom purity targets.
Colleagues from research-driven companies have invited us to review their synthetic steps, sometimes resulting in subtle tweaks to our process or custom modifications—part of the give-and-take that drives real progress. If a customer reports a minor side reaction, we bring samples back to our analytical team, look for overlooked microimpurities, then adjust upstream steps or loading points. Most importantly, we view transparency and openness as key to building trust. Those who’ve worked with us see our willingness to troubleshoot and document every claim as proof of our commitment—not only to product but to the chemists counting on it.
Today’s chemical landscape moves fast. New regulatory requirements call for lower trace impurities, while novel applications stretch the expected limits of materials like 2,6-dichloro-4-methyl-3-(trifluoromethyl)pyridine. We continuously refine our processes, informed by feedback from a network of synthesis experts. If someone encounters an unexpected GC peak, we investigate upstream supply chains and production logs. Knowledge travels within our factory walls—sometimes the solution to a problem in fluorine recovery informs a later tweak for methylation rates or helps us select better analytical standards for future lots.
Many industry observers focus on price or delivery times. We try to shift the conversation to long-term value: robust processes, honest analytics, and willingness to answer tough questions. Our product’s demand comes from groups who’ve seen thinly controlled batches ruin weeks of work or who want a reliable partner for confidential project support. Chemists in pharma, agrochemicals, and advanced materials markets know consistency and expertise shape outcomes more than catalog numbers or spec sheets.
The reality of chemical manufacturing rarely matches the elegant simplicity of a textbook synthesis. Unplanned exotherms, equipment wear, labor shortages, and fluctuating raw material quality all shape each batch of 2,6-dichloro-4-methyl-3-(trifluoromethyl)pyridine. Inconsistent supply of high-purity starting materials, shifting safety requirements, and demand for ever-purer intermediates push us to adapt. Rather than fixate on silver-bullet solutions, we invest in ongoing training, flexible process controls, and open feedback loops with end users.
Digitalization helps—each run logs hundreds of variables, helping track and predict deviations. We extend support to customers scaling up from grams to kilograms, sharing both successes and problems experienced along the way. No system claims perfection, but a culture of openness and recorded learning minimizes repeat mistakes. When a customer identifies a bottleneck—say, solubility in a new solvent or a byproduct that later complicates purification—we pull in chemists seasoned in practical troubleshooting, not just theoretical fixes.
2,6-dichloro-4-methyl-3-(trifluoromethyl)pyridine has grown from a specialty reagent to a backbone for high-stakes, innovative chemistry. As downstream uses advance—whether pushing into bioconjugation or adaptive polymers—the price of inconsistency only rises. We see each batch as more than a product; it's a reflection of decades of sweat, technical creativity, and relentless refinement. Stable supply and proven quality save researchers and producers from costly surprises that delay launch or kill promising projects.
Most who reach out to us want more than a drum or bottle; they want answers, proactive solutions, and a reliable partner. We meet these requests by maintaining rigorous standards, documenting every aspect of the value chain, and collaborating openly with those pushing technological boundaries. The small decisions made each day in manufacturing—tightening a process, cross-training a technician, or catching a subtle impurity trend—ripple outward. These are lessons learned from real production floors, not just from theory or catalog descriptions. We’re committed to a future where precision and honesty define every shipment of 2,6-dichloro-4-methyl-3-(trifluoromethyl)pyridine sent out our doors.