3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine

    • Product Name: 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine
    • Chemical Name (IUPAC): 3,2-difluoro-4-(trifluoromethyl)pyridine
    • CAS No.: 1427045-18-2
    • Chemical Formula: C6H2F5N
    • 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

    970332

    Chemical Name 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine
    Molecular Formula C6H2F5N
    Cas Number 163194-58-1
    Appearance Colorless to pale yellow liquid
    Boiling Point 145-147°C
    Density 1.43 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents
    Refractive Index 1.425
    Melting Point -21°C
    Flash Point 41°C
    Smiles FC1=NC=C(C(F)=C1C(F)(F)F)F

    As an accredited 3-fluoro-2-fluoro-4-(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 vial, 5g quantity, sealed with PTFE-lined cap; labeled with chemical name, formula, hazard pictograms, and batch information.
    Container Loading (20′ FCL) 20′ FCL loads 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine securely in sealed drums or containers, ensuring safe, compliant international chemical transport.
    Shipping **Shipping Description:** 3-Fluoro-2-fluoro-4-(trifluoromethyl)pyridine is shipped in tightly sealed, chemical-resistant containers to prevent leaks. It is transported under ambient conditions, away from heat or ignition sources, with clear hazardous labeling. Proper documentation in compliance with regulatory requirements ensures safe and legal transport. Handle with appropriate protective equipment during shipping and handling.
    Storage Store 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or acids. Avoid heat, moisture, and sources of ignition. Label clearly and protect from direct sunlight. Use appropriate chemical storage cabinets and ensure access is limited to trained personnel.
    Shelf Life **Shelf Life:** 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine is stable under recommended storage conditions; typical shelf life is 2-3 years when unopened.
    Application of 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine

    Purity 98%: 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal impurities.

    Molecular weight 185.06 g/mol: 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine with molecular weight 185.06 g/mol is used in agrochemical development, where it facilitates accurate dosing and formulation consistency.

    Boiling point 110°C: 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine with a boiling point of 110°C is used in fine chemical manufacturing, where it enables safe solvent recovery during distillation processes.

    Stability temperature 25°C: 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine exhibiting stability at 25°C is used in laboratory reagent storage, where it maintains chemical integrity under standard room conditions.

    Particle size ≤10 µm: 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine with particle size ≤10 µm is used in solid formulation processes, where it improves homogeneity and dispersibility in blends.

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    Certification & Compliance
    More Introduction

    3-Fluoro-2-fluoro-4-(trifluoromethyl)pyridine: A Reliable Building Block for Modern Chemistry

    Introduction to 3-Fluoro-2-fluoro-4-(trifluoromethyl)pyridine

    Working every day with 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine offers a front-row seat to how specialty organofluorine chemistry evolves to match the demands of precision-driven industries. Our manufacturing team knows the molecular quirks of this aromatic fluorinated pyridine from the inside out: the fine balance it strikes between reactivity and stability means chemists in pharmaceutical, agrochemical, and advanced materials research call on it frequently.

    Several fluorine atoms on the pyridine ring set this compound apart from more familiar pyridine building blocks. The electronic effects from these fluorine atoms and the trifluoromethyl group shift the electron density, altering how it participates in further synthesis. People often ask about differences between this material and the more common trifluoromethylpyridines or monofluorinated pyridines. Years of lab work and production scaleups confirm that introducing multiple fluorines transforms the whole reactivity pattern—not just for nucleophilic aromatic substitution, but also for transformations driven by catalysts, which often display enhanced selectivity and a broader range of successful outcomes.

    Producing 3-Fluoro-2-fluoro-4-(trifluoromethyl)pyridine: A Discipline in Attention

    Producing a molecule with two fluorine atoms and a trifluoromethyl group involves more than standard batch synthesis. It demands a methodical approach rooted in solid chemistry and careful process design. Not every manufacturer can offer rigorous purity standards for this specific model because minor isomeric impurities can stubbornly resist separation. We see these challenges up close, and years of tweaking reaction conditions, working closely with analytical teams, and recalibrating purification steps pay off in the end.

    Controlled reaction temperatures, careful selection of reagents, and precise timing form the backbone of our process. Getting any one of those wrong can mean lower yields or more difficult isolations. Plant experience shows that modest differences in solvent grades or reaction timing can tip the scales between a manageable batch and a serious headache. Our team developed internal monitoring and quality checks at several key stages, so product coming out the door consistently passes strict NMR and HPLC assessments. We don’t cut corners—fluctuations in purity or performance translate to project delays for partners relying on consistent results.

    Understanding Specifications and Quality Benchmarks

    Every batch passes through an array of analytical screens before we deliver it to customers. Besides standard identity checks such as NMR and GC-MS, focus lands squarely on ensuring the right isomeric makeup—ensuring no contamination with mono- or difluorinated congeners that would complicate downstream chemistry. Specifications do more than tick regulatory or paperwork boxes; they protect the reputation of our partners as well as our own.

    From personal experience, it’s clear that customers running critical synthetic steps in drug discovery or crop protection depend on batch-to-batch reproducibility. The presence of unwanted by-products can introduce variability in yields or lead to hard-to-trace failures in scale-up. We commit to a tight purity window, and lots that fall even slightly outside our target won’t leave our warehouse. Over the years we’ve found that even within global standards, raising our own bar for purity and traceability keeps development pipelines moving and builds trust along the chain.

    Uses: Real-World Impact in Diverse Industries

    3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine’s main appeal sits in its versatility as a building block. The high fluorine content does more than add a technical detail to its IUPAC name—it delivers valuable physicochemical traits. Fluorinated aromatics often underpin breakthrough candidates in pharmaceuticals. Their presence can sharpen metabolic stability or allow lead structures to pass through animal models with lower off-target effects. Chemists searching for new kinase inhibitors or next-generation analgesics frequently explore scaffolds containing this motif, knowing that substituted pyridines often serve as key intermediates or pharmacophores.

    In agrochemicals, crops benefit from the fine-tuned bioactivity that fluorinated heterocycles afford. As resistant pests and weeds continue to emerge, new active ingredients must combine potency against targets and resilience under field conditions. Trifluoromethylated, multi-fluorinated pyridines offer tighter binding and improved selectivity—traits that go hand in hand with environmental persistence, so comprehensive screening and stewardship must remain a priority. It’s rewarding to hear from customers in this sector who report more consistent field results or greater flexibility in designing crop input packages.

    Advanced materials researchers draw on these compounds for specialty coatings, electronic components, and niche energy storage applications. The influence of perfluoroalkyl groups on solubility, thermal resistance, and dielectric strength unlocks opportunities previously out of reach for proteins, polymers, and lubricant additives. Years of supply relationships show that material scientists often request small-lot batches or custom packaging to fit unique pilot lines or research facilities—our direct manufacturing background means we can pivot fast and supply to specification without extra layers of delay.

    How This Compound Stands Out

    Every time we consider the specifications of 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine against more established pyridine derivatives, the distinctive chemical footprint stands out. For one, the multifluorination directs reactivity, allowing for cross-coupling strategies or regioselective functionalization steps that fail or prove too slow with less fluorinated analogs. We’ve watched research partners cut out weeks of troubleshooting simply by pivoting to this variant—the correct substitution pattern opens doors for smooth Suzuki or Buchwald-Hartwig couplings at positions otherwise inaccessible.

    Compared to single-fluorine pyridines, this compound resists hydrolysis and oxidative degradation more effectively. Over long-term storage and repeated usage, that edge in stability adds up. Many labs don’t have dedicated nitrogen gloveboxes or inert-atmosphere handling, so minimizing product loss or decomposition in open air not only saves money, but reduces downtime and experimental variability. For companies integrating this compound into multi-step syntheses, that reliability shifts the economics of their entire process.

    Physical form and handling characteristics matter, too. We invest time in managing the drying and packaging conditions, so users encounter a manageable solid—not a sticky mass or partially liquefied product subject to caking. Flowability and dosing precision can make or break automated set-ups in larger production lines. Our manufacturing team keeps direct feedback loops with users—if a particular particle size or blending modality supports a running pilot plant more efficiently, we act on that feedback rather than waiting for complaints to pile up.

    Quality, Traceability, and Safety: More Than Compliance

    Production scale brings real safety challenges. Beyond meeting regulatory documentation, we focus hard on root-cause analysis and pre-emptive monitoring. Fluorine chemistry sometimes draws unwarranted skepticism, yet with disciplined procedures and clear lines of responsibility, risks remain manageable. Every team member receives hands-on training for fluorinated intermediates, and we routinely revisit our protocols to reflect the most current insights from incident reporting and global safety conferences.

    In our facility, traceability means every drum of product has a story. Batch numbers link back to detailed records of raw materials, operating conditions, and analytical data. This degree of precision supports not just recall scenarios but also continuous improvement. The people on our floor know the value of feedback from partners using these pyridine derivatives across the world: robust performance data and straightforward incident reporting help us refine our own processes and encourage open dialogue between supply chain links.

    From a manufacturing perspective, meeting the latest local and international regulatory requirements goes hand in hand with earning and keeping user trust. Document workflows and lot verification no longer serve just as legal shields — they function as daily operational tools that help catch subtle impurities or performance deviations early. Delivering to customers in critical pharmaceutical development, we've seen how even a trace miss in trace metals or water content triggers downtime that can cascade through an entire development schedule. Internalizing quality and traceability as core parts of product stewardship keeps us competitive without sacrificing throughput or reliability.

    Addressing Sustainability and Responsible Stewardship

    Organofluorine chemistry attracts attention for both its benefits and broader environmental impacts. We’ve felt that scrutiny firsthand from customers and regulatory agencies. Although this compound delivers efficiency and performance in diverse end-use scenarios, our responsibility does not end at the loading dock. Closed-loop recovery and rigorous emissions control—both in laboratory-scale and multi-ton production—form a non-negotiable part of our commitment to responsible stewardship.

    As a chemical manufacturer immersed daily in real lab-scale and plant-scale challenges, we push for incremental improvements—lowering solvent usage, exploring alternative fluorination strategies, and commissioning cutting-edge scrubber systems to capture downstream by-products. Collaboration with academic and industrial partners continues to generate imaginative solutions for safer, less resource-intensive production routes. Swapping legacy reagents for greener alternatives not only bolsters our environmental credentials but also frequently yields efficiency gains and cost savings that benefit all partners.

    End-of-life management receives just as much thought. Conversations with downstream users have led to more robust take-back programs for spent materials and packaging. No single producer can dictate circularity in organofluorine supply chains, but engaging transparently with customers, regulators, and independent researchers has advanced safer handling and disposal frameworks. By keeping channels open and supporting talent in green chemistry, we ensure this compound remains a responsible choice for those seeking high-value fluorinated intermediates.

    Collaborative Solutions for Real-World Challenges

    Manufacturing 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine encourages a direct, collaborative style with customers and technical partners. Facing scale-up bottlenecks? We offer insight honed from dozens of project launches, so customers sidestep routine pitfalls. Dealing with international shipping constraints or complex customs documentation for a fluorinated intermediate? Our team navigates those waters routinely, eliminating delays and helping projects stay on target.

    Every phone call from a process chemist or a line manager brings unique demands—sometimes rapid turnaround for a pilot batch, sometimes transparency about trace impurity profiles for regulatory submissions. Our structure means in-house chemists and engineers remain involved after sales—they continue to answer technical questions, troubleshoot batch processes, and participate in continuous improvement projects alongside R&D teams at customer sites. Over the years, that culture of accessibility strengthened not just our track record for product quality, but also the speed and reliability of customer problem-solving.

    Direct relationships cut both ways. We take complaints seriously and address them at source, whether improving product drying, accelerating analytical reports, or packing smaller aliquots for more manageable storage. These feedback loops don’t always generate accolades, but they do build a sense of shared ownership in the product’s ongoing evolution.

    Looking Ahead: The Place of 3-Fluoro-2-fluoro-4-(trifluoromethyl)pyridine in the Future of Synthetic Chemistry

    The past decade gave this compound a starring role in specialty chemistry. For researchers pushing into harder-to-access molecular territories—whether in pharmaceuticals, agrochemicals, or advanced functional materials—this multi-fluorinated pyridine unlocks possibilities standard starting materials cannot reach.

    Ongoing collaboration with academic centers and innovation hubs expands what we know about new reactivity patterns, scalable coupling partners, and alternative transformations. Input from synthetic chemists continues to shape our understanding; open dialogue about real-world hurdles encountered in using the product leads to meaningful innovation in manufacturing practices. Having open lines with both hands-on users and development chemists means we stay ahead of evolving needs, responding faster when process tweaks or alternative grades are needed.

    Scientific progress always involves testing limits. Our journey supplying 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine shows that sustainable innovation and responsible supply go hand in hand. Whether the end application is a groundbreaking medication or a new crop protection molecule, having reliable, direct access to this key building block supports breakthrough thinking and underpins measurable results.

    Every kilo produced in our facility carries the lessons of years dedicated to precision, safety, and improvement. In a market saturated with resellers and generic offerings, choosing a direct manufacturer who understands and values the product pays practical dividends—whether in purity, safety, sustainability, or simply speed in adapting to customer-driven needs. The chemistry behind 3-fluoro-2-fluoro-4-(trifluoromethyl)pyridine is sophisticated, but the underlying philosophy driving its production remains straightforward: build trust through quality, reliability, and open communication, letting the compound do the work in hands of innovators across the world.