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2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile

    • Product Name 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile
    • Alias 2,6-Dichloro-5-fluoronicotinonitrile
    • Einecs 681-673-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    433939

    Product Name 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile
    Cas Number 121151-21-9
    Molecular Formula C6HCl2FN2
    Molecular Weight 191.99 g/mol
    Appearance White to off-white solid
    Melting Point 85-89°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, keep container tightly closed
    Smiles C1=C(C(=NC(=C1Cl)C#N)Cl)F

    As an accredited 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile is securely sealed in an amber glass bottle with safety labeling.
    Shipping 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile is shipped in tightly sealed containers to prevent moisture and air exposure. The packaging complies with chemical safety regulations, clearly labeled with hazard warnings. It should be transported under ambient conditions, away from incompatible substances, and handled by trained personnel following all applicable shipping and handling guidelines.
    Storage 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong acids and bases. Use dedicated chemical storage cabinets when possible. Avoid exposure to moisture and ignition sources. Always follow local regulations and the manufacturer’s safety data sheet for proper storage protocols.
    Application of 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile

    Applications of 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile in Industrial Manufacturing

    2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile serves as a critical intermediate in the synthesis of advanced agrochemicals, pharmaceuticals, specialty pesticides, and fine chemicals. As the original manufacturer, we support a range of high-value sectors by offering this compound with batch-specific documentation and technical guidance for precise downstream integration. The following sections present core application areas based on industry practice and validated production routes.

    1. Synthesis of Insecticidal Active Ingredients (Agrochemical Industry)

    Leading agrochemical producers utilize this compound as a pyridine ring building block in the multi-step synthesis of neonicotinoid and related systemic insecticides, where controlled halogenation and nitrile substitution are essential for target molecule bioactivity and field stability. Quality control and compliance with trace impurity thresholds are strictly managed throughout the process to achieve crop protection standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for agrochemical manufacturing
    • REACH Regulation (EC) No. 1907/2006
    • EUROPEAN GREEN DEAL and Sustainable Use Directive 2009/128/EC

    Typical usage ratio

    • Dosage ranges from 5% to 15% w/w in active intermediate reaction stage, optimized according to target molecule yield and process throughput

    Downstream process integration

    • Added directly to nucleophilic aromatic substitution stage using precision addition equipment and temperature-controlled reactors for subsequent cyclization/halogenation steps

    Final product types

    • Finished insecticidal active substances for formulation into suspension concentrates, wettable powders, or granules
    • Technical-grade bulk insecticide intermediates for export to custom blending plants

    2. Pharmaceutical Intermediate for Anti-Viral Drug Synthesis

    Pharmaceutical manufacturers adopt this fluorinated pyridinecarbonitrile as a key intermediate in the synthesis of complex heterocyclic drug candidates, especially within anti-viral and anti-inflammatory research pipelines. The material enters routes for active pharmaceutical ingredient (API) assembly where halogen and nitrile moieties are preserved or selectively transformed during sequential coupling and protection/deprotection operations.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP General Chapters <800> and <1116> for contamination control
    • 21 CFR Part 211 (US FDA) for finished pharmaceuticals
    • Ph. Eur. Monographs for API intermediates

    Typical usage ratio

    • Commonly 3%–10% by molarity in selected condensation, Suzuki coupling, or nucleophilic aromatic substitution reactions; the proportion varies with target drug structure and regulatory impurity limits

    Downstream process integration

    • Introduced at the core scaffold construction stage or late-stage diversification, often pre-purified by recrystallization or chromatography to meet strict QC parameters for downstream coupling partners

    Final product types

    • API intermediates for anti-infective and immunomodulatory drug candidates
    • Isolated pyridine-substituted scaffolds, further derivatized to produce final small molecule medicines

    3. Herbicide Intermediate for Pyridine-Type Weed Control Agents

    Major crop science companies incorporate this raw material in the synthesis of next-generation pyridinecarboxylic acid herbicides and related analogues, valued for their selectivity in broad-acre weed management. The chemical structure suits downstream conversion into carboxylic acids or amides, with careful control of reaction conditions to ensure conversion rates and minimize by-product formation.

    Industry compliance standards

    • EPA Regulations (USA) for Pesticide Manufacturing
    • ISO 14001 Environmental Management
    • Chinese GB 2763 Maximum Residue Limits for Pesticides in Foods
    • Chemical Facility Anti-Terrorism Standards (CFATS)

    Typical usage ratio

    • Usually 7%–12% w/w per batch during synthesis of the target pyridine intermediate; actual proportion adjusted for final herbicidal agent design

    Downstream process integration

    • Charged into high-pressure reactors during catalytic amination or hydrolysis steps, with in-line analytical monitoring to confirm purity and conversion completeness before formulation

    Final product types

    • Bulk herbicide intermediates for further esterification
    • Finished herbicidal technical concentrates for agricultural formulation houses

    4. Fine Chemical Intermediate for Specialty Coating Additives

    Producers of advanced surface coatings utilize this compound for manufacturing select pyridine-based additives that provide chemical resistance and durability to high-performance industrial paints and electronic-grade lacquers. Its incorporation influences surface energy and crosslinking density, supporting specialized end-use applications in sectors such as automotive, electronics, and high-spec flooring.

    Industry compliance standards

    • ISO 12944 for protective paints and coatings
    • REACH Annex XVII for chemical restrictions in coatings
    • RoHS Directive 2011/65/EU for electronics
    • VOC content limits per EPA 40 CFR Part 59

    Typical usage ratio

    • Concentration typically maintained between 2%–5% w/w depending on end-use performance targets and compatibility assessments with other resin components

    Downstream process integration

    • Blended into main binder manufacturing step or introduced during curing agent synthesis; followed by dispersion and in-line QC checks for homogeneity and end-point analysis

    Final product types

    • Crosslinked resin additives for industrial anti-corrosion coatings
    • Functionalized hardeners for electronics encapsulation materials

    5. Intermediate in Veterinary Pharmaceutical Synthesis

    Veterinary drug manufacturers deploy this molecule in the scalable synthesis of fluorinated pyridine-based agents with anthelmintic or antiparasitic functions. The compound's distinctive structure contributes to the required physicochemical profile for safe and stable veterinary APIs, especially where metabolic pathway resistance is targeted.

    Industry compliance standards

    • VICH GL35 for Good Manufacturing Practice (GMP) in veterinary products
    • US FDA Guidance for Industry #205
    • EU Regulation 2019/6 on veterinary medicinal products
    • Chinese Veterinary Pharmacopeia

    Typical usage ratio

    • Standardized between 4%–9% w/w in synthetic batch feeds based on pharmacokinetic endpoints and residue control studies

    Downstream process integration

    • Integrated at intermediate scaffold formation phase, with subsequent transformations and purification steps carried out under animal drug GMP protocols

    Final product types

    • Active pharmaceutical ingredients for veterinary oral, injectable, or topical dosage forms
    • Registered feed additive concentrates for animal health programs
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    Certification & Compliance
    More Introduction

    2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile: A Behind-the-Scenes Look from the Manufacturer

    Getting to Know the Chemistry Up Close

    Talking shop as a producer of 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile, I know firsthand how much care goes into every vessel and batch. This compound, also known in short as 2,6-DCFPyCN, stands out with a unique blend of chlorine and fluorine atoms anchored to a pyridine ring, plus that all-important cyano group. There's a reason we work up close with every detail of its structure—the arrangement opens up a toolbox of possibilities for high-value chemistry, especially when building blocks for next-level agrochemicals, pharmaceuticals, and specialty materials are in demand.

    How the Structure Shapes Its Role

    Years of synthesis work have shown us how not all halogenated pyridines are created equal. The pairing of 2,6-dichloro and a 5-fluoro substitution gives this molecule a specific set of reactivity options. The two chlorines, flanking the ring, create electronic effects that prime the molecule for some reactions and shield it from others, shaping downstream chemistry. Chemists searching for selective points of substitution, whether they're looking to introduce further groups or preserve existing ones, have told us time and again that this arrangement fills a gap other intermediates leave wide open.

    Most competing intermediates swap fluorine or chlorine to other positions, or drop the cyano group, but that tweaks both polarity and electronic properties. Take 2,3-dichloro or 2,6-difluoro variants: they might sound similar, but the subtle shift in positions puts some synthetic routes out of reach, or demands much harsher conditions. That might seem minor, but in a process where every cent counts, shaving time off a reaction or avoiding a side reaction can make the difference between pilot plant curiosity and commercial-scale success.

    Real-World Production: More Than Just Numbers

    On the factory floor, producing 2,6-DCFPyCN isn’t just about following a recipe. It calls for control at every stage—tight raw material management, careful temperature monitoring, and, most of all, patience for hard-won yields. We don’t cut corners, because introducing impurities or leaving behind unreacted starting material can throw off downstream users. Purity levels rarely take care of themselves. Every time we scale up, we spend days on analytics—HPLC, GC, NMR—to check for byproducts or isomeric contamination. What comes off our lines isn't just a number in a database; it's a promise to our partners that their syntheses can start with confidence.

    Physical characteristics matter, too. We know that a free-flowing, off-white solid saves a lot of hassle in both handling and measuring. Some manufacturers laugh off the headaches that come from clumping, static, or excessive dust, but when you're charging reactors at night while watching the humidity climb, you remember every design decision you made along the way.

    Why Specifications Stay Tight

    Years delivering to multinational crop protection labs and small fast-moving startups have taught us the same lesson: nobody wants to troubleshoot a process failure to find trace amounts of an unexpected impurity. We keep our purity benchmarks on the north side of 98%, with water content and residual solvents checked per batch. Sometimes, quality managers from the pharmaceutical sector ask for COAs with extended impurity profiles or for customized analysis packages—from inorganics to potential mutagenic residuals. We treat these requests as the normal course of business. Each new spec request helps us understand how a single kilogram of product can form the backbone of a multi-billion dollar market further down the line.

    The Market Context: Responding to Demanding Industries

    Applications drive change. In the agrochemical world, research chemists need that cyano group exactly where it sits on the ring if they're to block, trigger, or modulate biological action. Some of the top-selling herbicides and insecticides in the last twenty years have a pyridine core, tailored substitution patterns, or need a clean handoff from one intermediate to the next. A small slip in purity can cascade into trouble with downstream catalytic couplings or halogenation.

    In pharma, where regulatory hoops and downstream synthesis can take more than a decade to yield an approved drug, a single change in halogen position can break a patent strategy or render a candidate inactive. Early-stage researchers count on us not only for reliability but for the willingness to share our process data, help troubleshoot scale-up, and flag impurities that could carry through to final products. Being open about process history helps our customers pass FDA scrutiny and avoid batch rejections.

    Differences Compared to Other Halogenated Pyridines

    Fine differences in chemical structure produce big differences in both synthetic behavior and end-use. Bringing experience from multiple intermediates, we see the 2,6-dichloro, 5-fluoro substitution as a rare combination. Other chlorofluoropyridines often push the fluorine ortho or para, or stack all halogens together. This disrupts both resonance and inductive effects, locking chemists out from some coupling reactions entirely or saddling them with costly protecting group steps.

    What we've learned is that 2,6-DCFPyCN's substitution pattern enhances selective functionalization at the remaining unmodified positions. These options matter in medicinal chemistry when optimizing libraries or searching for a lead. In agrochem, they open routes to new analogs. The cyano group's location doesn't just tweak solubility or boiling point—it sends signals to the electronic system that can be exploited in cross-coupling or nucleophilic aromatic substitution. These are subtleties you only appreciate after handling hundreds of kilo-scale campaigns and seeing how each variant plays out in final product yields.

    Our Priorities in Serving End-Users

    Delivering what’s needed for demanding syntheses means running a lean operation with room for customization. We've rebuilt sections of our plant to provide campaign-based, dedicated lines for specialty intermediates like 2,6-DCFPyCN. Every campaign starts with raw material tracing. Our teams coordinate with suppliers to verify batch history of basic building blocks, making sure nothing gets in that doesn't belong. The plant PLCs record every parameter—temperatures, agitation speeds, pressure profiles—so any customer who asks to trace back a batch's process conditions can get the data they need. This is the level of transparency our partners have come to expect, and the only way we keep trust over repeated orders and long-term supply contracts.

    We keep raw material contracts close to home—selecting vendors that hold up to the same level of scrutiny we ask of ourselves. When either a phosgene-free policy or a fluorination step comes under new regulations, we adjust process flows and documentation, making sure compliance doesn't take a backseat. That focus extends to batch release, shipping documentation, and certificate of analysis routines, adjusted to match both local and export requirements.

    Adapting to Regulatory and Environmental Expectations

    Lately, conversation has shifted toward environmental impact. Producers like us face a challenge: meeting strict product specs while reducing emissions and solvent waste. We've invested in closed-system reactors and solvent recovery units. In most runs, over 90% of used solvents are reclaimed on site and redirected back into the process. Waste fractions get treated by licensed contractors, and regular audits keep everyone honest. Engineers have built in real-time monitors for scrubber performance, not because regulations say so, but because we've seen how unexpected vent streams can become headaches if ignored.

    We've also dropped certain problematic reagents from pilot plant protocols, even at the expense of yield, once we understood downstream risks. Working directly with EHS officers from our client companies, we've rewritten MSDS details to reflect both updated toxicology and process changes. Many of these tweaks slow cycle time or bump up costs, but we see them as the price of long-term trust with buyers who return every year.

    Usage Across Industries: Lessons Learned from the Field

    Feedback from our clients often shows just how versatile 2,6-DCFPyCN can be, even within the same field. A pharmaceutical lab may use it as a core for anti-infective leads, chasing SAR trends by swapping out different groups on the pyridine ring. Agrochemical research units pick it for the backbone in herbicide or pesticide candidates, taking advantage of the unique balance between electron-withdrawing and electron-donating effects introduced by the substituents.

    One story stands out: a mid-sized firm trying to adapt a process they ran for 2,6-dichloropyridine to 2,6-DCFPyCN to cut three steps from their route. Their initial try ran into trouble—yields stumbled because the added cyano group changed the reactivity profile enough to trigger a different impurity. Working together, we shared detailed batch results, helped them adjust base choice and phase ratios, and twenty kilos later they’d lifted yield from 35% up to 78%. These are the kind of deployments that show the material’s real-world worth, and why we stay involved beyond the loading dock.

    It’s not just big names who benefit. R&D startups use our product to chase new patents in the crop protection space. Some coatings and polymer research groups have tested our 2,6-DCFPyCN as a functional monomer, exploiting the cyano chemistry to impart resistance or adhesion in specialty resins. The bottom line is: once users understand the subtle differences this molecule brings to the table, they often find more uses than we ever predicted from the plant floor.

    A Manufacturer's Perspective on Process Improvements

    Continuous improvement isn't just a slogan for us; it’s required by the pace of innovation and regulatory shifts. Take filtration: Small changes in filtration media or temperature profile can bring big wins in cycle time and ease of downstream purification. On more than one occasion, swapping to a finer-grade filter lifted our lot rejection rate down by double digits, especially on large batch runs. Analytical upgrades—LC-MS aside GC—helped us catch minor byproducts before customers ever saw them.

    Process optimization comes down to more than chemistry. Worker safety, plant uptime, preventive maintenance, and process adaptability are what keep orders on track. Modifying glass lining spec or vent design isn’t glamorous work, but we learned the hard way that mineral build-up or tiny leaks can introduce trace impurities that no one wants to see on a COA. Tightening these details means smoother runs, tighter specs, and peace of mind for both sides of the supply chain.

    We've responded to requests for new particle sizes, adjusting crystallization parameters or milling protocols per campaign. One pharma client requested finer crystalline material for easier blending in solid formation steps; we ran process trials, validated each lot, and shipped fresh within forty-eight hours of final QA signoff. The feedback loop between our technical service team, QC lab, and production floor turns tight customer deadlines from stress points into opportunities for closer cooperation.

    Respect for Intellectual Property

    The research organizations and production companies we supply depend just as much on confidentiality as on technical excellence. It’s standard practice on our end to sign NDAs, restrict access to project specifics, and run batch documentation in isolated, password-protected networks. On several custom synthesis projects involving 2,6-DCFPyCN, our chemists work directly with client scientists, sometimes even side by side. Every step, from order confirmation to final delivery, runs through encrypted channels and closed files.

    If a project emerges involving a new application or a patentable route, we respect both the letter and spirit of intellectual property rules. We train all our teams—lab, plant, and logistics—in what's okay to discuss and what stays compartmentalized. The value our product brings is tied to our reputation for keeping customer projects secret, as much as to the molecule’s chemistry itself.

    Looking Ahead: Supporting Innovation and Production Growth

    The pace of demand for specialty intermediates like 2,6-DCFPyCN continues to increase. Customers push for faster delivery schedules, better batch-to-batch reproducibility, and more flexibility in supply formats—as drum, bag, or even solution. We're spending more on plant automation, batch traceability, and digital systems to stay ahead of these changes. We work closely with shipping partners to meet new transport regulations for both bulk and sample shipments, and are exploring modular setups to keep pace with demand spikes or expansion into new territory.

    Product-by-product customization demands a flexible mindset. Sometimes, new syntheses require a fine-tune of analytical specs or a one-off pilot batch, then a return to standard mode for the next campaign. We maintain a regular training cycle for our chemists and operators, making sure they stay on top of best practices for both process safety and analytical troubleshooting. There's no single right answer—each customer's needs steer us toward continual improvement.

    Why Commitment Matters In Every Batch

    Making 2,6-Dichloro-5-Fluoro-3-Pyridinecarbonitrile isn’t just about the molecules. From raw material sourcing to analytics, from environmental care to batch traceability, it's about meeting expectations for quality and reliability. Every drum shipping from our warehouse represents not just fine chemical inside, but the trust our partners place in our people and processes.

    Our experience shows that commitment to transparency, adaptability, and technical support creates wins for everyone involved. Each time we improve a purification step or help a customer scale up, we're reminded why close partnerships across the value chain are vital in the world of specialty chemicals. We believe 2,6-DCFPyCN exemplifies how the right combination of expertise—chemical, operational, regulatory—can keep innovation flowing into the fields, factories, and labs that rely on trusted building blocks.