pyridine, 3,5-dichloro-2,6-difluoro-

    • Product Name: pyridine, 3,5-dichloro-2,6-difluoro-
    • Chemical Name (IUPAC): 3,5-dichloro-2,6-difluoropyridine
    • CAS No.: 84194-35-8
    • Chemical Formula: C5HCl2F2N
    • 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

    637205

    Iupac Name 3,5-dichloro-2,6-difluoropyridine
    Molecular Formula C5HCl2F2N
    Molecular Weight 184.97 g/mol
    Cas Number 108639-99-8
    Appearance Colorless to pale yellow liquid
    Boiling Point 189-192 °C
    Density 1.51 g/cm3 (at 25 °C)
    Solubility In Water Slightly soluble
    Flash Point 75 °C
    Chemical Structure Smiles c1c(F)nc(c(F)c1Cl)Cl
    Pubchem Cid 176149

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

    Packing & Storage
    Packing 250g of 3,5-dichloro-2,6-difluoropyridine is supplied in a sealed amber glass bottle with a tamper-evident cap.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Ships in 200 kg HDPE drums, 80 drums per 20’ FCL, totaling 16 metric tons per container.
    Shipping Pyridine, 3,5-dichloro-2,6-difluoro-, should be shipped in tightly sealed, chemically resistant containers, clearly labeled, and in compliance with relevant regulations for hazardous materials. It must be protected from moisture, heat, and incompatible substances, with proper documentation and handling precautions to ensure safe transport. Refer to the SDS for detailed shipping requirements.
    Storage Store pyridine, 3,5-dichloro-2,6-difluoro- in a cool, dry, well-ventilated area, away from direct sunlight, heat, and incompatible substances such as strong oxidizers and acids. Keep tightly sealed in a chemically resistant container. Avoid exposure to moisture and ignition sources. Ensure appropriate labeling and access for authorized personnel only. Implement secondary containment to prevent leaks or spills.
    Shelf Life The shelf life of 3,5-dichloro-2,6-difluoropyridine is typically 2-3 years when stored in a cool, dry, airtight container.
    Application of pyridine, 3,5-dichloro-2,6-difluoro-

    Purity 99%: Pyridine, 3,5-dichloro-2,6-difluoro- with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures minimized side reactions and product quality.

    Melting point 56°C: Pyridine, 3,5-dichloro-2,6-difluoro- with melting point 56°C is used in agrochemical formulation processes, where optimized melting point allows for controlled solid-to-liquid transitions.

    Stability temperature 120°C: Pyridine, 3,5-dichloro-2,6-difluoro- with stability temperature 120°C is used in high-temperature organic synthesis, where enhanced thermal stability prevents decomposition.

    Molecular weight 201.99 g/mol: Pyridine, 3,5-dichloro-2,6-difluoro- with molecular weight 201.99 g/mol is used in medicinal chemistry screening, where precise molecular parameters support accurate compound identification.

    Particle size <10 microns: Pyridine, 3,5-dichloro-2,6-difluoro- with particle size less than 10 microns is used in advanced material manufacturing, where fine particle size improves dispersion and reactivity.

    Refractive index 1.56: Pyridine, 3,5-dichloro-2,6-difluoro- with refractive index 1.56 is used in optical coating development, where consistent refractive properties enhance light transmission control.

    Water content <0.1%: Pyridine, 3,5-dichloro-2,6-difluoro- with water content below 0.1% is used in anhydrous reaction systems, where low moisture levels prevent hydrolysis and maintain process integrity.

    Assay ≥98%: Pyridine, 3,5-dichloro-2,6-difluoro- with assay greater than or equal to 98% is used in catalyst design, where high assay delivers reliable reactivity and yield consistency.

    Density 1.52 g/cm³: Pyridine, 3,5-dichloro-2,6-difluoro- with density 1.52 g/cm³ is used in solvent blending for electronic applications, where controlled density provides stable phase compatibility.

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    Certification & Compliance
    More Introduction

    3,5-Dichloro-2,6-Difluoropyridine: Practical Insights from the Manufacturer’s Perspective

    Serious Chemistry, Focused Solutions

    Pyridine rings with multiple halogenations have long attracted the interest of both industrial and research labs for their intriguing electronic properties and reactivity. As a chemical manufacturer with decades devoted to the reliable production of halopyridines, our journey with 3,5-dichloro-2,6-difluoropyridine stands as an example of walking the fine line between consistency and innovation. We’ve seen engineers, chemists, and project managers weigh up dichloro-difluoropyridine against simpler analogues and walk away more convinced each year that its unique substitution pattern brings something special to the table.

    Our batch records—spanning thousands of kilograms—show that demand for this compound stays steady, despite shifts in the fine chemicals and pharmaceutical markets. The model we manufacture falls under CAS 58113-29-0, produced through a multi-stage halogenation and purification process perfected over several years. The product’s consistent structure (C5HCl2F2N) is checked for trace impurities down to low ppm levels. Chlorines at the 3 and 5 positions deliver a degree of chemical resistance not easily matched by mono- or tri-halogenated pyridines. At the same time, the two fluorines at the 2 and 6 positions tweak both acidity and electronic effects, fine-tuning the molecule’s suitability as a scaffold in crop protection and active pharmaceutical ingredient development.

    From Technical Details to Practical Workflows

    Many customers visit our site or send technical teams for a first-hand look at the process lines and the checks we use to keep impurities—like mono-halogenated by-products—out of the supply. Through these conversations, we’ve learned that real-world applications push the limits of purity and handling convenience further each year. The right melting point, solvent compatibility, and tight particle size distribution save endless time at downstream steps, especially in pilot plant or scale-up work. While it’s easy to copy a recipe from the literature, actually removing tetrahalogenated pyridine contaminants on a large scale gives many labs trouble; without the right distillation and crystallization equipment, product consistency suffers batch to batch. We built up our process step by step, often learning through costly setbacks before nailing the right cleaning and containment routines.

    Compared to the more widely known 3,5-dichloropyridine or 2,6-difluoropyridine, this di-chloro, di-fluoro variant resists hydrolysis and oxidative attack more strongly. In one collaboration with a European agrochemical partner, months went into evaluating whether less-substituted rings could serve as intermediate substrates. None matched the stress-test results of the difluoro-dichloro system: Aqueous exposure at elevated temperature and pressure still produced high recovery, and the pattern of decomposition stayed predictable—helping chemists design more robust synthesis pathways.

    Handling and Storage: Learning from Hard Experience

    We learned early on that the volatility of halopyridines demands strict attention to containment and workflow layout. 3,5-dichloro-2,6-difluoropyridine releases a pungent, sharp odor if exposed, even in small spills. Careless transfer procedures can lead to ambient air contamination, which fouls both person and instrument. Over years of moving from drums to tighter, inerted packaging, we’ve seen a significant reduction in complaints about odor and drift, which helps keep both internal teams and external inspectors happy.

    Moisture is an ever-present challenge, as the difluoro groups offer decent resistance but do not eliminate all risk. Early customers who stored this compound near open process water or in poorly climate-controlled storage reported clumping, altered melting points, and—in rare cases—off-color development signaling breakdown products. These headaches cost time and money, delaying the handoff to research or kilolab formulation. Our approach uses foil-lined drums, nitrogen backfilling, and dedicated storage areas. Results speak for themselves: over 99% retention of key quality indicators even in multi-month storage.

    Supporting Syntheses Large and Small

    Feedback from the production floor shows that customers working at the fine chemical, electronics, and pharma interface value repeatability above almost every other factor. The reactivity of pyridines with this substitution set allows for a smoother nucleophilic aromatic substitution, opening routes to more complex molecules without unwanted side-products, a feature especially prized in sensitive pharmaceutical pipelines. We learned, over many cycles of pilot plant and kilo lab work, that product consistency matters as much as the route’s overall yield. Small differences in impurity profiles or physical form have way outsized impacts on flow chemistry, continuous systems, and even manual syntheses.

    Direct substitution at the halogen positions is a top reason buyers specify this difluoro-dichloro ring over cheaper or more common starting points. Where projects need electron-deficient rings, this structure clamps down on side reactions, narrowing the process window for potentially explosive intermediates or hydrolysis-prone steps. In our own pilot demonstrations with contract partners, the higher cost per unit is more than offset by reduced downstream purification and fewer process shutdowns—a surprise, at first, but borne out batch after batch.

    Applications: From Bench to Market

    Many firms come to us because they need a precise building block that unlocks new routes for pharmaceuticals, crop protection, and specialty chemicals. The 3,5-dichloro substitution pattern, paired with 2,6-difluoro, evolves the standard pyridine ring into something different: it alters both electron density and reactivity, shifting ideal coupling partners and oxidation resistance in ways unsubstituted or singly-halogenated pyridines cannot.

    A prominent example: researchers working on new herbicides and insecticides turn to halopyridines as core fragments. At several conferences and private presentations, teams describe the extra fluorine atoms yielding activity profiles that tackle resistant pest populations. We dug deep into comparative studies, seeing first-hand that, in some series, adding just one more fluorine at the right spot radically improves metabolic stability against plant enzymes—a detail supported by both in-house and customer-run tests.

    In organic electronics, this structure’s electron-withdrawing character keeps device performance stable, especially under the high thermal and light stresses that sideline less robust analogues. Teams building OLEDs or solar cell prototypes watched their early materials degrade until they switched to better-substituted pyridines. Market feedback soon reached us: purity and substitution pattern in the starting material made a world of difference, saving entire development budgets from endless rework.

    Comparing to Other Pyridines: What Matters and What Falls Short

    We field hundreds of inquiries yearly about switching from 2,6-difluoropyridine, 3,5-dichloropyridine, or even simpler pyridine itself to this more complex tetra-halogenated version. The price per kilo runs high, but buyers doing side-by-sides spot the value beyond simple cost: higher recoveries, lower downstream purging requirements, and fewer product recalls or late-stage approval headaches. Working chemists see the difference fast, especially in reactions where unreacted starting materials, side reactions, or batch-to-batch drift plague more basic pyridine derivatives.

    While less-substituted compounds win on price and initial availability, large-scale process engineers and synthetic chemists know the deeper costs lie in failure modes. We’ve seen projects stall on scale-up because of unstable intermediates from using mono- or dihalogenated pyridines in place of more robust, electron-deficient alternatives. Where reactors clog or produce dangerous off-gassing, a more precisely tuned building block makes all the difference between smooth 24/7 operations and repeated shutdowns. Past trials taught us that ignoring these differences leads to missed deadlines and considerable overhead.

    Regulatory and Environmental Lessons Learned

    Running a manufacturing process for halogenated pyridines involves navigating a thicket of regulations across borders. The difluoro-dichloro combination doesn’t slip quietly past environmental and health scrutiny; it demands robust emissions controls, waste reduction strategies, and worker safety routines. Early process development work led us to invest in upgraded containment, advanced scrubbing systems, and solvent recovery lines that cut residual emissions below detection limits. Regulators who once eyed specialty halopyridines with suspicion now inspect our lines, often commending the extra investment in monitoring and real-time process data.

    The story often changes at a typical user’s site. Without appropriate local capture or waste protocols, halopyridines could escape to air or water, drawing regulatory attention and community concern. Many of our long-term customers recount early missteps, then revisit their own routines after benchmarking our containment and handling. Reinforcing best practices through technical data sheets and on-site training helped keep incidents low and approvals steady—even in the face of shifting local and international requirements.

    Building Trust through Transparency

    Many in the chemical supply chain chase the next trend, pivoting from one “blockbuster” intermediate to the next. Our practice has always started with supply stability and clear communication with users. Every lot of 3,5-dichloro-2,6-difluoropyridine leaves our gate accompanied by batch chromatograms, full impurity reporting, and a record of process changes—small or large—done over time. Several partners audit our production lines each year, walking through quality checkpoints, reviewing environmental logs, and inspecting training records for production staff.

    Open-door policies bring commercial benefits: projects using our material often spend less time troubleshooting failed syntheses, and much less on after-sale support. Teams move faster because they know what to expect from each drum or tote—no blended lots, unexpected color changes, or process-drift surprises. Across pharma and agrochemical verticals, this reliability means less downtime and fewer delays in registration or product launch.

    Innovation in Practice: Investing for the Next Stage

    Chemical manufacturing stays relevant only by moving forward. Our R&D group branches into greener halogenation methods, aiming for higher conversion and lower waste. Phase-transfer catalysis has netted some gains, as has improved solvent handling to cut environmental impact. Each technology upgrade started after close study of process bottlenecks—often flagged by customer audits or our own maintenance crews. Innovations take time to validate at scale, but the pursuit pays off with cleaner product, fewer by-products, and a smaller footprint per ton produced.

    New recycling streams for spent solvents and halide waste not only reduce disposal costs but change how our teams think about raw materials and recovery. Management regularly pushes for better process analytics, helping operators spot deviations or impurity spikes days earlier than before. Each investment ripples out to end users as more stable pricing and supply, a benefit felt deeply in long campaigns or life-of-project contracts.

    Facing the Future, One Batch at a Time

    The world for halogenated pyridines keeps evolving. Regional market instabilities, raw material disruptions, and sharp changes in regulatory frameworks test even the best-laid plans. Through these shifts, working with real feedback loops—between process engineers, customer technicians, and regulatory advisors—keeps us grounded. Our core philosophy: focus on what the molecule must deliver in process performance, shelf life, and safety, not just in theoretical properties or cost.

    Every so often, a customer’s project fails, sometimes spectacularly, when a cheaper or less substituted pyridine breaks down under heat, light, or chemical stress. Each case brings our team back to the basics: deep dives into structure-activity relationships, hands-on troubleshooting in the lab, and—occasionally—tweaking process parameters to fit a new partner’s way of working. Partnerships that grow out of these crises often last longest, as mutual understanding of risks and capabilities runs deep.

    Supporting Stakeholders, from Lab Bench to Full Scale Plants

    The best feedback sessions happen face-to-face, surrounded by samples, lab notes, and real-world vials showing what worked and what did not. We don’t sell a theoretical product to anonymous users; our reputation rides on every kilo delivered meeting the needs of the next synthetic pathway or production run. Across industries, from pharmaceuticals to advanced materials, the difference between success or failure often boils down to attention to detail at the source. Too many dismiss impurities, residual moisture, or suboptimal packaging as afterthoughts. Our experience contradicts this at every turn.

    Client projects regularly use our product to carve new ground: deeper into pest-resistant crops, cleaner electronics layers, or more stable pharma lead compounds. This ongoing feedback shapes not just minor tweaks, but core production design and quality assurance. Years ago, we responded to chronic particle size drift with new milling and sieving stages; yield, purity, and processability all improved overnight. These investments rarely get spotlighted in annual reports, but customers immediately see the frontline impact.

    Experienced Voices across the Process Chain

    Production workers—the hands guiding every step from raw material reception to finished goods—provide the first signs that something’s off. Whether from a change in upstream halogen supply or ambient humidity spikes, they catch deviations long before QC or management notices. We learned to listen, embedding regular communication channels and troubleshooting sessions that spot issues early and minimize unscheduled batch reprocessing. This hands-on culture grew from years of near-misses, not theoretical playbooks.

    Technical support carries this pragmatism forward. When end users call, they rarely need textbook answers; real-world troubleshooting always traces back to specifics: batch number, storage conditions, moisture history, and actual process flows. Only chemical manufacturers, who live with the full arc from synthesis to long-term storage, gain this perspective. Our support teams bring practical, evidence-driven guidance, using internal case studies to help users skip the costly errors of first-time runs.

    Toward Cleaner, Safer, and More Reliable Chemistry

    Many users narrow their sights to a product spec sheet, missing the wider process realities behind the line items. Years of process optimization tell us that only the full, lived-in experience with a compound—its quirks, hidden vulnerabilities, and real performance—builds knowledge that lasts beyond a single contract. We bring this to every partner conversation, not because it makes for glossy copy, but because it anchors real project success.

    3,5-dichloro-2,6-difluoropyridine, from our process lines, stands as a material refined by experience, not guesswork. All claims—from purity to reactivity to storage regime—started with facts gathered through repeated, sometimes painful, cycles of learning. Our goal remains clear: ensure every batch delivers on the promise of higher process reliability, improved safety, and new opportunity for chemistry that matters.