3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro-

    • Product Name: 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro-
    • Chemical Name (IUPAC): 2,6-dichloro-5-fluoropyridine-3-carboxamide
    • CAS No.: 86393-34-2
    • Chemical Formula: C6H3Cl2FN2O
    • Form/Physical State: Powder
    • 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

    309331

    Iupac Name 2,6-dichloro-5-fluoropyridine-3-carboxamide
    Molecular Formula C6H3Cl2FN2O
    Cas Number 86393-34-2
    Appearance Solid
    Structure Pyridine ring with amide group at position 3, chlorines at 2 and 6, fluorine at 5
    Smiles C1=CC(=NC(=C1Cl)F)C(=O)NCl

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

    Packing & Storage
    Packing White plastic bottle, screw-cap sealed, amber label; contains 25 grams 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro-, with hazard and storage information.
    Container Loading (20′ FCL) Loaded in 20′ FCL with secure packaging, labeled as 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro-, compliant with chemical transport regulations.
    Shipping **Shipping Description:** 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- should be shipped in tightly sealed containers, protected from light and moisture. Handle as a potentially harmful substance, complying with relevant hazardous material regulations. Transport at ambient temperature unless otherwise specified, and include appropriate labeling and documentation for safe and legal handling during transit.
    Storage Store 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat, direct sunlight, and incompatible substances such as strong oxidizing agents. Protect from moisture. Keep in a designated chemical storage cabinet. Ensure proper labeling and handle using appropriate personal protective equipment to avoid contamination or accidental exposure.
    Shelf Life 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- typically has a shelf life of 2-3 years when stored in cool, dry conditions.
    Application of 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro-

    Purity 98%: 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- with purity of 98% is used in pharmaceutical intermediate synthesis, where high assay ensures consistent bioactive compound yield.

    Melting point 185°C: 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- having a melting point of 185°C is used in solid-formulation development for drug delivery systems, where thermal stability improves processing reliability.

    Particle size D90 <50 µm: 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- with particle size D90 less than 50 µm is utilized in fine chemical manufacturing, where reduced particle size allows for enhanced dissolution and mixing rates.

    Stability temperature 120°C: 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- stable up to 120°C is employed in high-temperature reaction processes, where thermal resilience maintains structural integrity.

    Moisture content <0.2%: 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- with moisture content below 0.2% is applied in sensitive polymer matrices, where minimal water content prevents hydrolytic degradation.

    Molecular weight 234.01 g/mol: 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- at molecular weight 234.01 g/mol is used in analytical reference standards, where precise mass aids in accurate quantification.

    Solubility in DMSO 50 mg/mL: 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- soluble in DMSO at 50 mg/mL is used in compound library preparations, where high solubility facilitates concentrated stock solutions.

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    Certification & Compliance
    More Introduction

    3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro-: Direct Insights from the Manufacturer

    Perspective on Advancing Pyridine Chemistry

    Our daily work in pyridine derivative production rarely stands still. 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- offers a true example of high-precision organic synthesis. Over years of hands-on process optimization, we have found that introducing both chlorine and fluorine atoms at the 2,6 and 5 positions of the pyridine ring unlocks distinct reactivity and selectivity. These halogen groups transform the molecule’s behavior, making it a sought-after building block in pharmaceutical and agrochemical research right at the bench and in pilot plants. Our strong grasp of halogenation chemistry allows us to produce this compound at high purity, and we’ve watched demand shift steadily toward these multifunctional heterocycles, particularly as stricter regulations push end users to seek more refined synthetic intermediates.

    Model Variants and Real Production Environments

    Our standard batch process for 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- centers around a model with tight specifications on impurity profiles and residual solvents. We control moisture content and assay using GC and HPLC, as even small variations can influence downstream reactivity in medicinal chemistry. In the early days of scale-up, we tackled issues of reproducibility. Combining solvent extraction with crystallization gave us a reproducible white to pale yellow crystalline solid, usually packed in protected containers with nitrogen overlays. This physical stability is essential for safe transfer and storage. Each lot reflects our practical learning about halogenated pyridines — you cannot cut corners with reagent quality or air-sensitive handling. Any lapses show up during pilot reactions, sometimes in the form of sluggish reactivity or trace hydrolysis. Our production teams learned early how such details affect the behavior in condensation or coupling steps on the client side.

    What Sets This Compound Apart from Other Pyridinecarboxamides

    Operators who regularly handle pyridinecarboxamides know that halogen patterns define how these molecules interact with nucleophiles, catalysts, and even environmental moisture. The 2,6-dichloro pattern blocks certain positions to many common transformations. The 5-fluoro substitution increases electron-withdrawing effects and shifts the compound’s solubility and reactivity. Unlike the parent nicotinamide or simple substituted analogues, this compound resists non-specific ring activations and holds up well under both acidic and mild basic conditions. We’ve traced these differences back to field feedback as well. Clients confirm that this derivative enables highly selective cross-couplings, especially Suzuki and Buchwald–Hartwig reactions, where steric and electronic tuning matter. Purification after these steps is significantly easier compared to less-substituted pyridinecarboxamides, as unreacted starting material and byproducts can be isolated cleanly, with fewer needs for chromatography. This reality lowers solvent use and reduces labor. Our process chemists have built solvent screening data alongside our clients, showing a clear drop in emulsification during workup. It’s the result of edge-to-edge process experience.

    Our Approach to Specification Consistency

    No synthetic batch walks through a factory without checks at each stage. We maintain a control chart of critical impurities, especially unhalogenated pyridinecarboxamide and mono-chloro/mono-fluoro contaminants. Gas-phase reactions always carry some risk of overhalogenation but by logging every pressure and temperature deviation, we catch small discrepancies before they create out-of-spec shipments. Our facilities treat each intermediate quench and final isolation as a learning point. Skilled operators have encountered and solved problems ranging from filter plug-ups to batch-to-batch color drift. The result is a product offering genuine batch integrity. The lot-to-lot consistency we now achieve is not just a claim but hard-won reliability over years at the plant level. Packages reach the warehouse with a full spectrum analysis and archived reference vials. Discovery teams working downstream have told us that these efforts translate to time saved and confidence in their high-throughput screenings.

    User Experience: Trends in Downstream Applications

    Our customer base cuts across biopharma, crop protection, and advanced material suppliers. In recent years, more clients have moved away from scattered, spot-purchased intermediates toward full lifecycle partnerships. We regularly hold technical exchanges with buyers to walk through their reaction schemes, looking for choke points where our 2,6-dichloro-5-fluoro-pyridinecarboxamide can play a role. Its use as a pharmaceutically relevant intermediate far outpaces older, less substituted variants — particularly in routes to kinase inhibitors, central nervous system drugs, and veterinary APIs. The addition of halogen and amide functionalities provides not only chemical resilience but helps molecular modeling predict lower off-target effects, supporting the push for cleaner clinical trial candidates.

    One striking point is how this compound performs in scale-up for process development. Many traditional pyridine derivatives present fouling or require multiple re-crystallizations. By contrast, our product provides reproducible yields with reduced batch failures due to its higher crystalline purity and improved stability profile. Direct users — process chemists, pilot-plant managers, QC analysts — regularly share how much less downtime they encounter for column regeneration and purification line cleaning. In our own facility, moving to this grade transformed our pilot-scale capacity, trimming solvent washes and material losses by more than a quarter compared to simpler analogues.

    Benefits Rooted in Direct Production Experience

    Some producers can only describe book-value properties. After making hundreds of metric tons, we understand real-life advantages that show up only during long production campaigns. The tightly controlled halogen distribution suppresses background reactivity. Users report cleaner reactions without ‘random’ substitution. As a manufacturer, we see fewer ‘rogue batches’ that require investigation or expensive rework. Instead, downstream users find they can push higher concentrations without generating troublesome side products, especially in automated vessels or high-pressure reactors.

    Handling and storage demands real-world vigilance. We lock down our warehouses to maintain low humidity and stable temperatures, minimizing hydrolysis or polymerization that can sneak up on an operator. Analytical data built up over years shows this compound resists caking, even with long-held stocks. This translates directly to smoother batch weighing and faster charge times. It’s not just surface-level convenience — in one case, an end-user avoided a three-day delay thanks to our product’s predictable, free-flowing character. That comes from hard-earned facility upgrades and daily care in packing lines.

    Quality Oversight Informed by Industry Demands

    Inspections by regulatory partners push manufacturers to move beyond minimum standards. Our quality control division is staffed by analysts who have spent years on the factory floor and picked up the instinctive ability to spot trends before they become problems. Blending rigorous documentation with on-site tests, our workflow captures impurity spikes quickly. We’ve integrated routine residual solvent testing (NMR, GC-MS), moisture titration, and halide analysis. The result is documentation robust enough for direct submission for DMFs and regulatory filings, with minimal back-and-forth or corrections.

    From grinding mills to bulk packers, everyone in the chain understands the responsibility of meeting international transportation and storage guidelines. This is not theory. Over the past years, we have upgraded our labeling, harmonized with GHS standards, and invested in operator training after several field incidents traced to shortfills or labeling discrepancies. Trust is built not by a document, but by error-proof processes and responsive technical support. Our team routinely fields calls and conducts on-site troubleshooting — not reading from manuals, but drawing on cycles of learning from incidents and customer feedback. The best compliment we receive comes from repeat customers who say the chain of custody and certificate transparency matches the top benchmarks in the industry.

    Response to Industry Shifts and User Needs

    Demand for specialty chemicals is moving fast, driven by biotech innovation and toughened environmental regulation. Traditional commodity pyridine derivatives can no longer meet the demands for cleaner, more efficient drug pathways. Our chemists keep close watch on emerging needs — we keep a list of client-requested modifications that guide future process development campaigns. For the 2,6-dichloro-5-fluoro compound, every year brings a new use case, sometimes from application fields we didn’t anticipate. Recently, organocatalytic and photochemical labs have found this scaffold useful for custom ligand design in transition metal complexes. These collaborations open up rare, direct exchange between synthetic manufacturers and discovery labs, shortening iteration times and feedback loops.

    For firms moving from small-molecule design to scale production, access to consistent, well-characterized intermediates can make or break project timelines. We work side-by-side in troubleshooting — from impurity migration to solvent crossover and on through to post-reaction workup. Our plant managers know that minor upstream tweaks in isolation protocols can translate to major simplification or headaches for downstream QC checks. By staying responsive and flexible, we help users keep programs moving, rather than sending out explanations of backorders. This agility is backed by investment in both traditional batch reactors and new continuous-flow lines, opening doors to custom batch sizes and shorter lead times for urgent formulations.

    Solutions to Industry Challenges: Lessons Learned and Shared

    Challenges never leave a production floor. Handling multi-halogenated pyridinecarboxamides tests every aspect of plant safety and regulatory building. Raw material purity is the biggest pain point. We learned the cost of cutting corners in early procurement. Pre-shipment vendor audits, batch tracking, and in-house qual checks caught several near-misses, keeping out trace polychlorinated biphenyls that could destroy a whole customer process. These lessons moved us to build a closed-loop supplier screening system, with every drum assigned a scannable reference linked to both quality audits and user feedback.

    Scaling up from lab to multi-ton lots, we faced an array of crystallization and drying hurdles. Fine-tuning our anti-solvent addition sequence and air sweep protocols reduced clumping, reduced batch cycle times, and improved overall yield. Experienced plant operators, not just textbooks, taught us to spot subtle color and odor changes that signal the need to pull a sample for GC testing. By listening to the hands-on experts, we protected entire production runs from unseen process upsets.

    Waste management never remains an afterthought. Halogenated process liquors bring special controls. We moved early to build an in-house destruction facility certified for halogen waste, routinely recycling solvent streams and minimizing landfill streams. These measures reduced regulatory headaches for our partners and led to recognition from regional environmental authorities for responsible stewardship. The knock-on effect frees up both our teams and customer support, reducing the slowdowns that come with compliance queries and audits.

    Supporting Future Innovation as a Manufacturer

    On the floor, every successful batch of 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- is the result of close coordination across research, operations, and logistics. Operators take pride in machines running clean and batches finishing to target, but these outcomes come only after cycles of dialing in, learning from missed specs, and investing in both people and hardware. Our daily meetings—where chemists swap notes with equipment techs—mean process tweaks go straight from idea to pilot to standard operating procedures in days, not quarters.

    We stay close to leading academic groups and industry consortia, trialing synthesis pathways and collecting reaction data on new routes and structures. Joint projects with pharmaceutical innovators open the door for fine-tuned derivatives: additional halogenation or deuterium substitutions. This close feedback loop provides insights into not just what is possible, but what works efficiently at manufacturing scale, sparing both developer and formulator months of troubleshooting.

    Ultimately, the way we bring 3-Pyridinecarboxamide, 2,6-dichloro-5-fluoro- to the market comes from deep-rooted pride in chemical manufacturing. Technical advances grow from respect for skilled hands and clear sight of production realities. By sharing lessons, supporting user challenges, and always seeking better process control, we aim to move this crucial pyridine derivative from a specialty item to a benchmark standard in the field.