2,6-Dichloro-4-(trifluoromethyl)pyridine

    • Product Name: 2,6-Dichloro-4-(trifluoromethyl)pyridine
    • Chemical Name (IUPAC): 2,6-dichloro-4-(trifluoromethyl)pyridine
    • CAS No.: 82761-12-2
    • Chemical Formula: C6H2Cl2F3N
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    Specifications

    HS Code

    670059

    Chemical Name 2,6-Dichloro-4-(trifluoromethyl)pyridine
    Molecular Formula C6H2Cl2F3N
    Cas Number 79055-62-2
    Appearance White to off-white crystalline solid
    Boiling Point 210-214°C
    Melting Point 40-42°C
    Density 1.59 g/cm³
    Smiles C1=CC(=NC(=C1C(F)(F)F)Cl)Cl
    Inchi InChI=1S/C6H2Cl2F3N/c7-4-1-3(6(9,10)11)2-12-5(4)8/h1-2H
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Refractive Index 1.534
    Storage Conditions Store in a cool, dry, well-ventilated area away from incompatible substances

    As an accredited 2,6-Dichloro-4-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g quantity of 2,6-Dichloro-4-(trifluoromethyl)pyridine is packaged in an amber glass bottle with a secure screw cap.
    Container Loading (20′ FCL) 20′ FCL container typically loads 10–12 MT of 2,6-Dichloro-4-(trifluoromethyl)pyridine, packed in 25 kg or 50 kg drums.
    Shipping 2,6-Dichloro-4-(trifluoromethyl)pyridine is shipped securely in tightly sealed, chemical-resistant containers, compliant with regulatory standards for hazardous materials. Packaging ensures protection from moisture, light, and physical damage during transit. Appropriate labeling, documentation, and handling instructions are included to ensure safety and compliance with international shipping regulations for chemicals.
    Storage Store **2,6-Dichloro-4-(trifluoromethyl)pyridine** in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Ensure proper labeling and avoid storage near heat sources. Follow all local regulations and consult the safety data sheet (SDS) for specific handling and storage guidelines.
    Shelf Life The shelf life of 2,6-Dichloro-4-(trifluoromethyl)pyridine is typically several years if stored in a cool, dry, and sealed container.
    Application of 2,6-Dichloro-4-(trifluoromethyl)pyridine

    Purity 98%: 2,6-Dichloro-4-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high assay ensures reproducible reaction yields.

    Melting point 43-46°C: 2,6-Dichloro-4-(trifluoromethyl)pyridine with a melting point of 43-46°C is used in agrochemical formulation, where solid-state processing stability is maintained.

    Molecular weight 232.99 g/mol: 2,6-Dichloro-4-(trifluoromethyl)pyridine with molecular weight 232.99 g/mol is used in heterocyclic compound development, where predictable stoichiometry supports precise formulation.

    Stability temperature up to 150°C: 2,6-Dichloro-4-(trifluoromethyl)pyridine with stability temperature up to 150°C is used in high-temperature reaction processes, where thermal integrity is critical for product quality.

    Low residual solvent (<0.5%): 2,6-Dichloro-4-(trifluoromethyl)pyridine with low residual solvent content (<0.5%) is used in custom synthesis projects, where minimized impurities facilitate downstream purification.

    Particle size D90 <100 µm: 2,6-Dichloro-4-(trifluoromethyl)pyridine with particle size D90 <100 µm is used in solid dispersion systems, where uniform granulometry enhances dissolution rates.

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    Certification & Compliance
    More Introduction

    Understanding 2,6-Dichloro-4-(trifluoromethyl)pyridine: Value, Application, and Differentiation

    Introduction to a Key Building Block

    Chemistry shapes nearly every aspect of modern industry, yet few outside of laboratories know the names of the compounds that enable a world of practical products. Among them, 2,6-Dichloro-4-(trifluoromethyl)pyridine stands out as both a quiet workhorse and a powerful enabler in complex organic synthesis. Each time a pharmaceutical gets crafted or an advanced agrochemical emerges, there’s a solid chance that this pyridine derivative helped set the foundation. The importance of reliable intermediate chemicals only grows as new innovations put heavier demands on purity, reactivity, and efficiency.

    What Sets This Molecule Apart

    What makes 2,6-Dichloro-4-(trifluoromethyl)pyridine more than just another name on a bottle? A careful look at its chemical structure tells a story of versatility and selective reactivity. The core features—a pyridine ring substituted with two chlorine atoms and a trifluoromethyl group—offer unique advantages in downstream reactions. Chemists see real value in its reactivity profile, especially in nucleophilic aromatic substitution, where the interplay between electron-withdrawing groups speeds up key steps. These traits play out in better selectivity, higher yields, and cleaner reactions. One learns quickly that synthetic shortcuts rarely lead to success in high-stakes applications. Products made with dependable intermediates, such as this one, carry the confidence born from robust, reproducible chemistry.

    Specifications That Matter

    People sometimes overlook how much difference the finer points make in high-grade chemicals. Laboratories put a lot of stock in consistency from batch to batch, and for good reason. Commercial 2,6-Dichloro-4-(trifluoromethyl)pyridine usually appears as a colorless to pale yellow liquid. Rigorous analysis, especially by NMR and GC methods, shows that the best supplies meet high standards for purity—often upwards of 98%—to cut down on downstream surprises. Solubility in most organic solvents adds another layer of convenience. It’s also worth noting the boiling point, usually between 180 and 200°C, which allows for practical handling at scale without runaway volatility.

    Some may wonder about the relevance of details like melting point or density. In my experience, these numbers are not trivia; they help guide handling, storage, and process control. For many operations, a stable compound at room temperature means fewer headaches and lower costs. Small gains in operational reliability, multiplied across tons of annual consumption, save time and resources—not to mention safety risks.

    Where the Value Shines: Applications

    The reach of 2,6-Dichloro-4-(trifluoromethyl)pyridine stretches far beyond a single field. Its most recognized use lands squarely in the middle of pharmaceutical and agrochemical synthesis. Drug discovery teams often search for a balance of potency, selectivity, and metabolic stability. The unique arrangement of the pyridine ring, with tough chlorine atoms and a trifluoromethyl group, helps tune the biological activity of target molecules. This subtle control over structure can make or break a whole drug development program.

    On the agricultural side, this pyridine derivative finds its way into the assembly of herbicides and fungicides that need rugged activity against pathogens. Chlorines anchor the molecule against premature degradation, while the trifluoromethyl group strengthens both the compound’s persistence and its activity spectrum. A few decades ago, crops relied on simpler formulations, but mounting challenges—resistance, regulatory oversight, and environmental scrutiny—demand better tools. Farmers, as well as consumers, feel the impact when chemists get these choices right.

    Personal Perspective: The Human Side of Specialty Chemistry

    Years ago, as I watched a pilot plant ramp up a new batch of this pyridine derivative, the room buzzed with the nervous energy that comes with scale-up. Any misstep could mean hours of cleaning, wasted raw materials, or even a riskier situation. But what struck me most was the attention paid to lot-to-lot consistency. Workers checked readings, matched samples to reference spectra, and tracked every detail for traceability. The lesson stuck with me: the unseen compounds, handled with precision, can make the visible products work as promised.

    Folks outside the chemical industry often don’t notice the safety measures and technical care behind these intermediates. Personal protective gear, air filtration, and robust spill plans are not just box-checking—they shield both workers and the broader community from potential harm. These realities remind us that the story of a chemical isn’t just what it does, but also the responsibility that comes with making and moving it around.

    Comparing to Other Pyridine Derivatives

    Many intermediates look similar at first glance, yet the differences can shape whether a chemical route succeeds or stalls. Some related compounds swap out chlorines for fluorines, or replace the trifluoromethyl group with other electron-hungry atoms. These changes seem small but can flip the switch in reactivity and selectivity. For example, 2,4-dichloro-3-(trifluoromethyl)pyridine may share the same backbone but behaves differently under typical synthetic conditions.

    This particular molecule strikes a balance between activation and stability. Take away one chlorine and you lose some charm in halogen-directed reactions. Remove the trifluoromethyl group and you often give up a lot of metabolic toughness. So, for companies running high-value campaigns in drug development or advanced crop protection, the smart bet stays with the version that consistently gets the job done.

    Market Expectations and Quality Assurance

    Today’s market asks for more than just technical specs. Pharmaceutical and agrochemical companies increasingly audit their suppliers for sustainable production, waste management practices, and long-term consistency. A trusted source of 2,6-Dichloro-4-(trifluoromethyl)pyridine does not just ship out bottles—it delivers trust, continuity, and peace of mind. This is especially critical in regulated sectors. Product recalls cost more than just money; they chip away at the credibility hard-earned over years.

    Traceability programs pop up as a sign of maturity in supply chains. Every batch gets logged, tested, and certified upstream, which helps downstream users maintain compliance with international quality norms. It matters greatly to see a lot number that matches a certificate and a shipment history that lines up with environmental reporting. Over the years, I have seen suppliers lose major clients over minor documentation slip-ups. Trust builds slowly but disappears quickly if gaps appear.

    Safety, Storage, and Responsible Practice

    Handling specialty chemicals always brings up the topic of safety, and rightly so. 2,6-Dichloro-4-(trifluoromethyl)pyridine, like many pyridine derivatives, has a distinct odor and can cause irritation if mishandled. Standard storage involves sealed, inert containers kept away from heat sources and incompatible materials. Facility managers balance required ventilation, temperature control, and access to emergency equipment. In regions with tight regulations, companies sometimes go further, adding secondary containment and regular training for every team member involved.

    I recall walking through a storage area and seeing not just labeled shelves but locked cabinets and regular inspection logs. The tangible sense of responsibility was clear in the neat, clearly marked aisles and the way workers cross-checked everything before shipment. As the industry moves toward tighter oversight and public interest grows in chemical risk, such visible diligence becomes part of any reputable operation’s DNA.

    Looking Ahead: Innovation, Supply, and the Drive for Better Chemistry

    Pressure never lets up in the markets for basic chemical intermediates. As new drugs and next-gen crop protection agents arise, the demand for high-purity, reliable starting materials follows close behind. Customers want products that check all the boxes—performance, reliability, sustainability, and traceability. Meeting ever-tougher quality audits becomes just as important as competitive pricing. The story of 2,6-Dichloro-4-(trifluoromethyl)pyridine’s role in the market mirrors the progress of the specialty chemicals field itself: a march towards higher standards, with no room for weak links.

    Unlike bulk commodity chemicals, where tonnage wins the day, specialty intermediates like this one focus on targeted performance. Quality takes priority over volume. This shift creates room for innovation—not just in new synthetic routes, but in packaging, logistics, and lifecycle management. Reduced hazardous waste, energy use, and streamlined paperwork lighten the load for producers and customers. I’ve spoken to chemists eager to experiment with greener synthesis methods, exploring alternative solvents or continuous production technologies to trim costs and environmental impact. Changes take time, but momentum is building.

    The Question of Sustainability and Responsibility

    More voices call for sustainable chemistry, and with good reason. The impact of synthesis routes on water use, atmospheric emissions, and waste disposal trickles downstream to every part of our daily lives. A molecule’s footprint does not end when it leaves the loading dock. Leading suppliers now monitor the environmental cost of each production run and report figures to both authorities and customers. It matters to buyers that their chosen intermediates don’t leave unnecessary scars on the planet.

    Some production routes for 2,6-Dichloro-4-(trifluoromethyl)pyridine rely on harsh reagents—strong acids, chlorinating agents, or specialized catalysts—which can strain both budgets and ecosystems. Teams that succeed in minimizing waste generation or switching to milder reaction conditions find an edge in a world growing less tolerant of legacy pollution. Government incentives add another dimension, rewarding suppliers who employ safer materials and closed-loop processes. Real improvement emerges through gradual, persistent effort rather than short-term fixes.

    Solutions and Pathways Forward

    There’s no single trick to improving the way specialty chemicals get made or used. Building a more sustainable foundation means blending technical innovation with a culture of transparency and learning. Greater collaboration between suppliers and end users creates feedback loops—what doesn’t work gets flagged early, and new approaches get the testing and validation needed for real adoption. Sharing best practices across companies and countries lifts the whole sector.

    Some promising steps include investing in process intensification. Switching from large, batch-based setups to smaller, continuous-flow systems can dial up both yield and safety, shrinking the footprint and slashing energy costs. Increased automation and digital monitoring catch process deviations before quality slips. This kind of investment pays off over time, shielding businesses from the cost of recalls and production hitches.

    Research also points to the value of cooperative risk assessment. Supply chains that encourage data sharing on safety incidents, environmental releases, and best handling methods learn faster and bounce back more quickly from setbacks. Regulatory bodies, for their part, can support this transparency by updating guidelines to keep pace with new evidence about environmental and occupational exposures.

    The Significance for Future Growth

    One could say that the road ahead for specialty intermediates like 2,6-Dichloro-4-(trifluoromethyl)pyridine depends as much on responsible business practice as it does on sheer technical know-how. The need for complex, high-purity compounds continues to rise with each new breakthrough in medicine or crop science. Competition among suppliers no longer hinges solely on who can make a product cheaper, but on who can deliver it with traceable quality and a lighter environmental shadow.

    Reflecting on the years spent working alongside chemists and plant managers, the lessons always circle back to basics: meet the spec, handle with care, document every step, and keep searching for safer, cleaner, smarter ways to get the job done. The markets will sort out winners and losers, but society expects the science and stewardship to work hand in hand.

    Conclusion: The Path Forward for 2,6-Dichloro-4-(trifluoromethyl)pyridine

    In the end, the true value of this pyridine derivative emerges from the intersection of performance, safety, and sustainability. Its place in the toolkit of modern synthesis is secure, shaped by years of research, careful process development, and relentless focus on reliability. As industries push toward cleaner chemistry and higher ethical standards, every stakeholder shares the burden and the benefit. Chemicals like 2,6-Dichloro-4-(trifluoromethyl)pyridine become more than intermediates; they represent the commitment to building a future where science and responsibility walk side by side.