3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile

    • Product Name: 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile
    • Chemical Name (IUPAC): 3-fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile
    • CAS No.: 863329-66-0
    • Chemical Formula: C7H2F4N2
    • Form/Physical State: Solid
    • 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

    218295

    Chemical Name 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile
    Molecular Formula C7H2F4N2
    Molecular Weight 190.10 g/mol
    Cas Number 886371-12-4
    Appearance White to off-white solid
    Melting Point 48-51 °C
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents
    Smiles C1=CC(=NC(=C1F)C#N)C(F)(F)F
    Inchi InChI=1S/C7H2F4N2/c8-5-1-4(7(9,10)11)6(2-12)13-3-5/h1,3H
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed HDPE bottle containing 25 grams of 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile, labeled with hazard, chemical name, and lot number.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Securely packs 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile in drums or bags, maximizing space and ensuring safe transit.
    Shipping **Shipping Description:** 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile is shipped in tightly sealed containers, protected from light and moisture, and handled as a hazardous material. Appropriate labeling, documentation, and use of secondary containment prevent leaks. Shipment complies with DOT/IATA regulations, ensuring safe transport by trained personnel with necessary safety precautions.
    Storage Store **3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile** in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight and sources of ignition. Keep away from incompatible substances such as strong oxidizers and acids. Use only with adequate ventilation, and avoid inhalation or contact with skin and eyes. Follow standard laboratory chemical storage protocols and safety procedures.
    Shelf Life 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile is typically stable for 2 years when stored cool, dry, and protected from light.
    Application of 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile

    Purity 98%: 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and consistent compound formation.

    Melting Point 61°C: 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile at a melting point of 61°C is employed in agrochemical research, where it provides controlled solid-to-liquid transitions for precise formulation blending.

    Molecular Weight 206.09 g/mol: 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile having a molecular weight of 206.09 g/mol is utilized in heterocyclic compound design, where it facilitates accurate stoichiometric calculations.

    Stability Temperature up to 120°C: 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile with thermal stability up to 120°C is selected for high-temperature organic reactions, where it maintains structural integrity during synthetic processes.

    Particle Size <50 μm: 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile with a particle size below 50 μm is used in solid formulation development, where it enables uniform dispersion and enhanced reactivity.

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    Certification & Compliance
    More Introduction

    3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile: Rethinking Pyridine Chemistry

    Introduction: Creating Value in Fluorinated Pyridines

    Work in chemical manufacturing never stands still. Every year, chemistry evolves and customers expect new benchmarks. 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile has gradually gained recognition as a key intermediate for advanced pharmaceutical compounds and specialty agrochemicals. Behind the lines of catalogs and trade show booths, our team lives through every stage of this molecule’s production—from micron-level ingredients to final purity assessment. The goals haven’t shifted. Reliability, process safety, and meaningful impact for formulators matter most.

    Pursuing Precision in Manufacturing

    Getting reproducibility on a fluorinated pyridine at scale is rarely straightforward. Each batch of 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile starts from raw materials chosen by our sourcing specialists for low water content and minimal trace metal contamination. Trace water in the early halogenation steps would generate hydrolysis by-products and kick down yields. Operators face these factors with a sense of responsibility—for us, one imperfect batch can cascade downstream, affecting partner research timelines and regulatory submissions. Our quality testing uses gas chromatography with mass-selective detection and validated NMR techniques. Rejecting a batch may not make today’s production quota, and that sometimes means investing extra hours, but no shortcut can guarantee long-term trust with R&D clients.

    Production Choices: Our Fluorination Process

    In the chemical literature, several approaches exist to build the 3-fluoro and 5-trifluoromethyl functionality onto a pyridine ring. Some competitors favor liquid-phase methods with harsh fluorination reagents. These routes shave minutes off cycle time but introduce environmental and worker safety risks. Our process leadership advocated for a different strategy—careful use of fluorinating agents with maximum recovery of side products and rigorous ventilation. We adopted a multi-stage quench and separation workflow, catching problematic off-gassing before purification. This makes our material cleaner right from the start. Control over these aspects is only possible through hands-on manufacturing experience; we’ve learned which pumps or filter housings hang up particulates or encourage unwanted side-reactions.

    Purity Standards: Where the Details Count

    Every research chemist asks about purity, and the answer has long-term consequences for their project outcomes. Most resellers offer this compound at stated purities around 98%. Many overlook isomeric impurities or residual halide content, which show up suddenly in late-stage synthesis. In our shop, we commit to full transparency on detected impurities—no obscured test results, no hidden side fractions. Oven-drying steps remove residual solvents, but the last traces of halide demand column separation with custom stationary phase blends. Our team optimizes these to minimize pressure drop and prevent co-elution. Routine batch certificates list not only the major component but also trace non-volatile residues, which partners in process development often appreciate when troubleshooting crystallization or scale-up.

    Understanding Its Role in Pharmaceuticals and Agrochemicals

    For pharmaceutical innovators, 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile isn’t just another “building block.” The electron-withdrawing nature of both fluorine and cyano groups influences both metabolic stability and target binding in many lead-like molecules. In crop science research, the fluorinated pyridine backbone has allowed for selective modification—tuning logP, water solubility, or resistance to hydrolytic degradation in the field. A senior process chemist once told me that, for a tricky herbicide synthesis, our lot performed noticeably better during halogen-metal exchange than an alternative supplier—yield jumped more than 7%. The subtly cleaner profile also sped up their downstream HPLC purification. Our role is to deliver reproducibility that saves development costs, not just check off requirements on a data sheet.

    Handling Real-World Formulation Pressures

    Many customers voice concerns about formulation compatibility. Fluorinated pyridines, especially those with multiple electron-withdrawing groups, can crystalize unpredictably in presence of certain co-formulants or solvents. We invest time in accurate polymorph identification, conducting batch crystallizations at different seeding temperatures and solvent profiles. These tests aren’t for regulatory box-ticking; impatience at this stage has burned both us and our clients. Unpredictable caking, slow redissolution, or off-color micro-inclusions often trace back to missed crystal habit screening. By sharing our in-house crystallographic findings with formulation groups, we often head off scale-up setbacks or the need for emergency solvent switches late in process optimization.

    Regulatory and Environmental Considerations

    Fluorinated organics draw attention from regulatory agencies due to bioaccumulation risks. Our team monitors global trends, not just out of compliance duty, but to future-proof client projects. We designed our solvent recovery systems to minimize volatile organic emissions, meeting standards for both local and export markets. Occasional revisions to technical dossiers keep us honest about batch consistency. When new impurity limits arose in a client’s export market, we were able to back up our process logs and impurity trend data. Such transparency reassures our partners who face increasing audit stringency, both in pharma and agchem.

    Stability, Storage and Logistics—Lessons from the Trenches

    Lab-scale chemists rarely confront the harsh realities of tonnage shipment. Early on, we discovered that humidity ingress during ocean freight—even in sealed drums—led to accelerated degradation and trace impurity formation. One costly incident led us to overhaul our drum-lining process and double-check every shipping seal. Not every competitor takes these steps. We began closely monitoring warehouse humidity and temperature, implementing rolling stock rotation for materials in transit. These experiences drive home a point: a drum that sits for weeks at a crowded port doesn’t always arrive with its original analysis intact unless all factors are controlled.

    Understanding Customer Needs: From Milligrams to Tons

    Requests for this compound vary widely. Academic groups sometimes need only a few grams for SAR studies and selectivity screening; multi-national corporations schedule tonnage-scale resupply tied to plant outages or quarterly campaigns. Staying close to our users allows us to plan batch sizes and update inventory in real time. Small-lot requests demand extra care: cross-contamination with other fluorinated compounds, even at ppm levels, can mislead lab data and skew patent findings. Our standard practice is to dedicate cleaning protocols for every campaign, using validated wash sequences and line-clearance logs. This investment rarely shows up in a spec sheet, but it keeps our reputation solid with both new and longstanding partners.

    Comparisons with Related Pyridines—Choosing What Matters

    Some process teams ask us for comparative input between different fluoro- or trifluoromethyl-substituted pyridines. Our feedback always incorporates practical lessons. For instance, closely related 4-fluoro or 3-trifluoromethyl isomers sometimes offer marginal price savings, but teams end up facing greater purification headaches, increased byproduct formation, or unanticipated toxicity. The metabolic liability of isomeric by-products often emerges late in regulatory review, sowing regret for early shortcuts. Years of experience confirm that for late-stage lead optimization, 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile allows the broadest latitude for further functionalization, especially for Suzuki coupling, nucleophilic substitution, or metalation reactions. The spatial arrangement on the pyridine ring tunes both sterics and electronics far more favorably than single fluorine or methyl analogs. Even slight shifts on the ring affect processability and downstream handling.

    Innovation Driven by Collaborations

    Strong relationships with customers drive process adaptation and site investments. Early discussions with pharmaceutical R&D teams prompted us to simulate reaction conditions that targeted their most pressing scale-up bottlenecks, from high-throughput reaction screening to green chemistry assessments. These partnerships, built over years of open feedback and mutual problem-solving, inspired small but crucial improvements—like automated dosing to control exotherms and pilot-scale isolation trials using alternate solvents. One customer challenged us to trial new drying techniques to further minimize residual water in bulk shipments. Their persistence prompted us to revisit our equipment specs, and their suggestions shortened our cycle time substantially.

    Knowledge Sharing and Technical Support

    Bringing advanced chemicals to market requires more than high-capacity reactors and smiling sales teams. Site visits by client chemists always open our eyes to potential simplifications or quality checkpoints we’d missed. Questions about compatibility with their lab filtration systems, possible amine contamination, or the effect of heating rates on solid-state transformations become chances for candid discussion. In some cases, troubleshooting sessions with external partners have improved our batch reproducibility and sharpened documentation protocols. Setting aside conference call formality, direct peer exchanges continue to shape our day-to-day operations just as much as quarterly target reviews.

    Using Firsthand Manufacturing Knowledge to Avoid Pitfalls

    Many pain points in supply chains arise when technical nuances get lost between divisions or across national borders. A change in one micron-scale input has triggered cascading failures in downstream crystallization or stability in the past. Drawing on direct plant-floor experience, our teams evaluate every manufactured lot against prior campaign outliers and archive anomalies for ongoing process improvement. This flow of onsite knowledge between synthesis, purification, and logistics teams closes feedback loops that a purely trading-oriented organization simply can’t match. Requests for expedited shipments or specialty packing have taught us which regulatory hurdles are surmountable, and which merit pushback for the sake of sustained consistency.

    What Users Gain from Purpose-Driven Manufacturing

    The difference between working with factory-direct chemical producers and anonymous resellers often lies in the absence or presence of a real sense of responsibility. Our batch specialist once traced a customer’s contamination query through raw material certificates to a minor process change two months earlier—solving the mystery saved the client weeks of analytical reruns and re-trials. Operating as a genuine partner, with firsthand experience on the line, means standing by one's results and learning from every setback. A trophy case of compliance certificates matters far less than overcoming a user’s most immediate synthetic roadblock.

    Conclusion: Building the Next Generation of Pyridine Intermediates

    Demand for advanced fluorinated intermediates won’t fade any time soon. Customers want transparency, adaptability, and proof of control at every step, not just empty assurances or copy-paste technical data. Years of hands-on experience in producing 3-Fluoro-5-(trifluoromethyl)pyridine-2-carbonitrile have clarified which details steer project outcomes, at both speed and scale. Our priorities center on rigorous process integrity, clear testing and data, honest communication, and willingness to adapt—essentials for shaping tomorrow’s innovations in pharmaceuticals and crop science. Upgraded safeguards, smarter logistics, and honest reporting secure reliability batch by batch, shipment by shipment. Customers value these results more than any marketing claim. Years spent facing the unplanned and the unexpected teach lessons that flow into every lot we ship, not just for compliance but to genuinely advance applied chemistry.