2,6-bis(trifluoromethyl)pyridine

    • Product Name: 2,6-bis(trifluoromethyl)pyridine
    • Chemical Name (IUPAC): 2,6-bis(trifluoromethyl)pyridine
    • CAS No.: 461-78-3
    • Chemical Formula: C7H3F6N
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    146279

    Name 2,6-bis(trifluoromethyl)pyridine
    Cas Number 2404-40-8
    Molecular Formula C7H3F6N
    Molecular Weight 217.10
    Appearance Colorless to pale yellow liquid
    Boiling Point 156-158°C
    Melting Point -11°C
    Density 1.482 g/cm³
    Refractive Index 1.403
    Flash Point 50°C
    Smiles FC(F)(F)c1cccc(n1)C(F)(F)F
    Pubchem Cid 151147
    Solubility Slightly soluble in water; soluble in organic solvents
    Inchi InChI=1S/C7H3F6N/c8-6(9,10)4-2-1-3-5(13-4)7(11,12)14/h1-3H

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2,6-bis(trifluoromethyl)pyridine, sealed with a Teflon-lined cap and labeled for laboratory use.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2,6-bis(trifluoromethyl)pyridine: Typically loaded in sealed drums or IBCs, ~10-14 tons/net per container.
    Shipping 2,6-Bis(trifluoromethyl)pyridine is typically shipped in sealed, chemical-resistant containers to prevent moisture and air exposure. It should be packaged according to relevant regulations, labeled as a hazardous material, and transported with appropriate documentation. Storage and shipping conditions may require cool, dry environments, away from incompatible substances and sources of ignition.
    Storage 2,6-Bis(trifluoromethyl)pyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and prolonged exposure to light. Store under an inert atmosphere if possible, and clearly label the container. Ensure access is restricted to trained personnel.
    Shelf Life 2,6-Bis(trifluoromethyl)pyridine is stable under recommended storage conditions; shelf life is typically several years if kept tightly sealed.
    Application of 2,6-bis(trifluoromethyl)pyridine

    Purity 99%: 2,6-bis(trifluoromethyl)pyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and minimal side-product formation.

    Boiling Point 185°C: 2,6-bis(trifluoromethyl)pyridine with a boiling point of 185°C is used in high-temperature catalytic processes, where it enables solvent recovery without decomposition.

    Melting Point -5°C: 2,6-bis(trifluoromethyl)pyridine with a melting point of -5°C is used in low-temperature organic transformations, where it maintains compatibility with cryogenic conditions.

    Molecular Weight 215.11 g/mol: 2,6-bis(trifluoromethyl)pyridine having molecular weight 215.11 g/mol is used in agrochemical research, where its defined molecular profile aids in precise dosage formulation.

    Moisture Content <0.2%: 2,6-bis(trifluoromethyl)pyridine with moisture content below 0.2% is used in moisture-sensitive coupling reactions, where it prevents hydrolysis and maximizes product yield.

    Stability Temperature up to 120°C: 2,6-bis(trifluoromethyl)pyridine with stability up to 120°C is used in polymer modification processes, where it delivers consistent activity without thermal degradation.

    Particle Size <50 µm: 2,6-bis(trifluoromethyl)pyridine with particle size less than 50 µm is used in fine chemical formulations, where it facilitates homogeneous mixing and uniform distribution.

    Assay 98.5% minimum: 2,6-bis(trifluoromethyl)pyridine with an assay of at least 98.5% is used in electronics material synthesis, where it ensures high purity and minimal electrical interference.

    Water Solubility <0.01 g/L: 2,6-bis(trifluoromethyl)pyridine with water solubility below 0.01 g/L is used in hydrophobic coatings, where it imparts pronounced water-repellent properties.

    Residual Solvent <500 ppm: 2,6-bis(trifluoromethyl)pyridine with residual solvent content below 500 ppm is used in active pharmaceutical ingredient production, where it meets stringent regulatory requirements.

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    Certification & Compliance
    More Introduction

    Introducing 2,6-bis(trifluoromethyl)pyridine: Crafting Quality from the Source

    The Story Behind 2,6-bis(trifluoromethyl)pyridine

    Everytime we open a drum of freshly synthesized 2,6-bis(trifluoromethyl)pyridine, a distinct sense of accomplishment fills the production floor. Seeing that clear, slightly yellowish liquid with its unmistakable sharp aroma reminds us why this compound holds a special place for us—and for our customers. In our industry, people often overlook the craftsmanship and knowledge behind each batch of fine chemicals. Many see only the chemical structure and leave it at that, ignoring the journey from raw precursors to high-purity product. Here, that journey happens on site, under our care, backed by years of process reliability and constant scrutiny.

    The requisition for 2,6-bis(trifluoromethyl)pyridine stems from its practical advantages in organic synthesis, pharmaceutical intermediates, and advanced materials development. Chemists appreciate the robust electron-withdrawing effect of the trifluoromethyl groups, especially clearly positioned at the 2 and 6 spots on the pyridine ring. They know this substitution dramatically changes reactivity versus unsubstituted pyridine or even mono-trifluoromethyl analogs. It takes only one look at a reaction profile or a thermal decomposition chart to realize why labs and R&D teams order kilograms at a time—each experiment counting on the product’s stability and genuine consistency.

    Quality Rooted in Production

    Some talk about supply as if chemicals switch hands on paper and show up at your dock in pristine form. We know the difference comes long before it’s packed in a drum. At our plant, handling 2,6-bis(trifluoromethyl)pyridine isn’t just batch chemistry—it’s embedded in our safety protocols, monitored by trained eyes, and sampled with purpose. By keeping the entire process in-house, we control every variable we can. The starting materials need to be clean—impurities in the original trifluoromethylating agents or pyridine base will follow all the way to the final compound, sometimes in parts per million but still detectable by GC or NMR. After multiple distillation cycles, we check viscosity, color, and purity not once, but as many times as it takes. Every drum matches the specs we claim—near colorless, minimum 99% GC purity, moisture below thresholds that a pharma plant would accept.

    In each manufacturing run, we rely on our own experience with vacuum control and reflux temperature adjustment to prevent minor hydrolytic degradation. Traces of water can change everything, so we never skip monitoring Karl Fischer titration results. Our production team has learned the hard way that shortcuts in washing glassware or not drying columns properly only cost more in rejected product later. It’s the attention to dozens of details that keeps our output consistent—otherwise, the quality that a technically trained customer expects simply doesn’t emerge.

    Applications That Drive Innovation

    2,6-bis(trifluoromethyl)pyridine doesn’t just sit on a shelf. Its real role unfolds in the hands of process chemists, specialists in medicinal chemistry, and polymer researchers looking to push boundaries. The electron-withdrawing trifluoromethyl groups make this pyridine a unique ligand in catalytic systems. In Suzuki coupling reactions, we’ve heard directly from project leads that using our material often gives tighter yields on terphenyl targets, especially where other substituents hamper conversion rates. For those involved in agrochemical synthesis, the compound offers a key structural element for targeting persistent pests or modulating plant growth regulators, where traditional heterocycles underperform.

    Several of our longtime partners in contract research organizations favor 2,6-bis(trifluoromethyl)pyridine in route scouting when designing new active ingredients. The presence of two CF3 groups not only boosts metabolic stability but can guide selectivity in multi-step transformations. The isolation of analogs or related derivatives becomes much more predictable with a solvent-stable, non-hygroscopic starting material—qualities painstakingly checked batch after batch here. Some customers use it in specialty material research, doping it into advanced polymers to impart flame retardancy and increase dielectric constants for electronics. Others want it pure enough for analytical reference standards, going so far as to request direct certificates of analysis for every batch. We cater to both the grand-scale commercial synthesis and the microgram-precision analytical market.

    Key Differences: What Sets It Apart

    Comparisons between 2,6-bis(trifluoromethyl)pyridine and classic pyridine-based building blocks surface in technical meetings every month. The contrast jumps out: adding a single trifluoromethyl alters the acid-base balance of the ring, but introducing two at the 2 and 6 positions fundamentally transforms electron distribution. As a result, researchers gain fine-tuned reactivity. Some alternate materials—simple pyridine, 2-trifluoromethylpyridine, or 2,4-bis(trifluoromethyl)pyridine—don’t bring the same shift in basicity, volatility, or solvent compatibility. Our product boasts higher resistance to oxidation and stands up longer under strong base or acid conditions. That means fewer surprises mid-synthesis and greater reliability in biomolecule or materials work.

    Those who work with trifluoromethyl-substituted aromatics know the risks of trace byproducts leftover from rougher manufacturing approaches. Volatile acidic residues, split-off side chains, or incomplete substitution show up in poorly managed synthesis, but our facility runs with careful feedstock control and frequent in-process HPLC checks. We intentionally slow down certain reaction steps to maximize selectivity—if a batch takes longer but comes out with sharper purity, that’s how we run it. Experience taught us never to chase output rate over reliable analytics. That philosophy lets customers focus on research and scale-up, not re-purifying faulty intermediates.

    Physical Specifications We Stand Behind

    Our own standards draw a line at 99% minimum purity, as determined by gas chromatography. Impurity profiling gets cross-checked on both GC and NMR. Drums leave our warehouse with clear labels on water content, typically verified below 0.1% using Karl Fischer titration. Some users in drug development request explicit optical clarity requirements, so we regularly run UV-Vis assessment to weed out trace chromophores that might co-crystallize in complex reactions. Our experienced staff tracks odor changes and color shifts, too—sensory checks can sometimes flag problems before equipment does.

    We process requests by container size, ranging from research vials for pilot projects up to multi-kilogram drums for industrial manufacturing. Our logistics team packages and seals every shipment in clean-room conditions. By minimizing atmospheric exposure, we reduce the risk of moisture or contamination. We learned the hard way that summertime humidity can creep into unguarded drums during loading, so now every batch moves out under desiccation where needed.

    Meeting Tight Project Demands

    Every research group or production line takes 2,6-bis(trifluoromethyl)pyridine and tests it a bit differently. Some labs barrage it with aggressive oxidation states, others check its behaviour in low-temperature environments. Partners have called us to discuss exact cutoff points for trace organic byproducts because their applications can’t tolerate even fractions of a percent of contamination. Over years of meeting these specs, we’ve adapted our production schedule to allow reprocessing on rare occasions when a drum’s profile drifts out of range. No team on the floor ever shrinks away from calling for a new run if QC data isn’t up to our published marks.

    For one pharmaceutical partner, we engineered a customized crystallization protocol to drive down a persistent impurity seen with their in-house test method—something not visible with typical analytics, but flagged during formulation. After a few cycles of dialogue, feedback, and testing, both teams felt satisfied with results that supported their stringent filing requirements abroad.

    Pursuing Safety and Stewardship

    As much as purity marks matter, no production schedule can take shortcuts on safety. On the shop floor, we devote training time to handling potential hydrolytic and thermal decomposition byproducts, providing real-world guidance that comes from years of troubleshooting. Our operations crews know that protection from fluorinated vapors ranks high—fume extraction systems undergo quarterly checks and maintenance, not because an outside consultant told us but because prolonged exposure can irritate even the most seasoned chemist. Residual solvents and spent media get treated in our on-site waste neutralization plant, removing majority of halogenated residues before they leave our site.

    We build every shipping package to contain accidental leaks, and our support staff communicates batch identity, handling guidance, and reactivity pointers directly to customer teams. Working late or running the plant over weekends to meet a critical shipment happens often—lead scientists and floor supervisors pitch in together. Early in our production development, we studied thermal and storage stability at a range of temperatures to provide users with honest data about real-world shelf life, not just theoretical numbers. If a batch doesn’t meet its declared stability in field trials, the team investigates root causes and adapts.

    Adaptability and Customer Collaboration

    Many projects don’t follow textbook routes. Collaborations with research groups frequently lead to minor tweaks in 2,6-bis(trifluoromethyl)pyridine’s specifications. We listen to customer chemists, sometimes agreeing to narrow GC retention index windows or lengthen shelf-life guarantees to fit tough project timelines. Those requests teach us where our own production process can adapt—sometimes rerunning a fractionation stage, tightening nitrogen sparge during final drying, or setting aside a drum for additional moisture-treatment.

    Beyond the transactional, these exchanges let us gain insight into what end-users truly value. During a major contract, a client in the display materials industry provided a direct process feedback loop, flagging a subtle yellowing in some drums. Our analysis revealed trace iron from a condenser weld in a seldom-used reactor port. Fixing that at the source required temporary downtime, but it protected our reputation and kept every subsequent shipment clear and stable. Every batch since passes additional scrutiny for color impurities—especially vital in optical applications.

    Process Improvements Over Time

    The chemistry behind 2,6-bis(trifluoromethyl)pyridine has evolved since we first began making it. Early years saw only kilogram-scale output; subsequent investment in pilot reactors, improved distillation columns, and more sensitive analytical tools have brought our process to its current precision. Each advancement—new in-line NMR sampling, automated vacuum controllers, redesigns to condensers—came in response to real problems reported either internally or by a partner. Teams learned that close monitoring of the introduction rate for the trifluoromethyl source greatly reduced runaway exotherms, improving not only safety but also product purity. Managing reaction time windows now gets documented per lot, and any deviation triggers additional QC testing before release.

    Requests for even tighter impurity specifications grow every year. Our process chemists often respond with new cleanup steps, like additional passes through neutral alumina to catch hard-to-separate trace esters, or changing the point at which in-process sampling begins. These continual refinements allow our product to meet the shifting demands of an industry where tomorrow’s needs rarely match today’s.

    Sourcing Raw Inputs Responsibly

    As demand for fluorinated aromatics grows, responsible sourcing matters more than ever. The origins of our starting materials—both pyridine and the trifluoromethylating agents—impact final product reliability. Over the years, we’ve watched trends in supply shift, with major producers tightening controls and some lower-grade variants entering global markets. Our team maintains direct relationships with suppliers, scrutinizing every shipment with certificates, in-house testing, and random spot checks. We’ve had to reject entire lots occasionally, knowing a few cents saved on basics would cost us dearly in reputation and customer trust.

    We keep backup supplier contracts in place to buffer against unforeseen shortages or sharp price spikes. Each lot of raw material goes through identity confirmation—again using our own analytical infrastructure, not just relying on outside paperwork. This diligence keeps feedstock variability from sneaking into our process and helps ensure each customer's final test matches ours.

    Looking Toward Tomorrow’s Chemistry

    2,6-bis(trifluoromethyl)pyridine stands at the intersection of modern catalyst design, robust pharmaceutical research, and advanced materials development. Every order, whether destined for a multi-ton pharmaceutical intermediate or a single gram for analytical calibration, reflects teamwork, process science, and pride in outcome. Our focus remains steady: produce every batch at a quality level that supports the next breakthrough, troubleshoot with energy, and keep listening to the chemists who depend on our product.

    Continuous improvement in both process and product guides our work. The next generation of researchers will try new routes and applications that those before them never imagined. The team here wakes up to the challenge of making sure that our 2,6-bis(trifluoromethyl)pyridine performs as reliably in their hands as it does in ours—one batch at a time, year after year.