pyridine, 2,6-dichloro-4-methyl-3-nitro-

    • Product Name: pyridine, 2,6-dichloro-4-methyl-3-nitro-
    • Chemical Name (IUPAC): 2,6-dichloro-4-methyl-3-nitropyridine
    • CAS No.: 156099-26-4
    • Chemical Formula: C6H3Cl2N2O2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    796644

    Common Name 2,6-Dichloro-4-methyl-3-nitropyridine
    Iupac Name 2,6-dichloro-4-methyl-3-nitropyridine
    Cas Number 32728-54-8
    Molecular Formula C6H4Cl2N2O2
    Molecular Weight 207.02
    Appearance Yellow solid
    Melting Point 50-54°C
    Boiling Point No data available
    Density No data available
    Structure Pyridine ring substituted with chlorine at positions 2 and 6, methyl at 4, nitro at 3
    Smiles CC1=CC(=NC(=C1[N+](=O)[O-])Cl)Cl
    Inchi InChI=1S/C6H4Cl2N2O2/c1-3-2-4(7)10-6(8)5(3)9(11)12/h2H,1H3
    Solubility No data available
    Refractive Index No data available

    As an accredited pyridine, 2,6-dichloro-4-methyl-3-nitro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, labeled “2,6-Dichloro-4-methyl-3-nitropyridine”, hazard pictograms, tamper-evident seal, tightly closed cap.
    Container Loading (20′ FCL) 20′ FCL loaded with securely sealed drums of pyridine, 2,6-dichloro-4-methyl-3-nitro-, ensuring safe, efficient chemical transport.
    Shipping Pyridine, 2,6-dichloro-4-methyl-3-nitro- should be shipped in tightly sealed containers, away from heat, sparks, and incompatible substances. Ensure compliance with hazardous chemical transport regulations. Label the package clearly, and use appropriate protective packaging to prevent leaks or spills. Consult the SDS and local guidelines for specific shipping and handling requirements.
    Storage Pyridine, 2,6-dichloro-4-methyl-3-nitro- should be stored in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and clearly labeled. Use chemical-resistant storage cabinets and secondary containment to prevent leaks. Handle and store using appropriate personal protective equipment to avoid exposure.
    Shelf Life Shelf life of pyridine, 2,6-dichloro-4-methyl-3-nitro-: Stable for 2–3 years if stored in a cool, dry, airtight container.
    Application of pyridine, 2,6-dichloro-4-methyl-3-nitro-

    Purity 98%: pyridine, 2,6-dichloro-4-methyl-3-nitro- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield conversion and minimal by-product formation.

    Melting point 95°C: pyridine, 2,6-dichloro-4-methyl-3-nitro- with a melting point of 95°C is used in agrochemical formulation, where it allows precise solid-phase processing and formulation stability.

    Molecular weight 221.04 g/mol: pyridine, 2,6-dichloro-4-methyl-3-nitro- with a molecular weight of 221.04 g/mol is used in fine chemical development, where it facilitates accurate stoichiometric calculations in complex synthesis.

    Particle size <50 µm: pyridine, 2,6-dichloro-4-methyl-3-nitro- with particle size below 50 µm is used in catalyst support preparation, where it ensures homogeneous dispersion and optimal catalytic activity.

    Stability temperature up to 120°C: pyridine, 2,6-dichloro-4-methyl-3-nitro- stable up to 120°C is used in high-temperature polymerization reactions, where it provides consistent reactivity and prevents decomposition during processing.

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    Certification & Compliance
    More Introduction

    Introducing Pyridine, 2,6-Dichloro-4-Methyl-3-Nitro-: Our Experience Behind Its Development

    Meet the Product Shaped by Years of Direct Manufacturing

    Pyridine, 2,6-dichloro-4-methyl-3-nitro- has grown from an idea on the drawing board to a staple in the hands of chemists across pharmaceuticals, agrochemical vetting, and specialty research. Long years in production have taught us not to judge a compound simply by its IUPAC string or CAS profile. Trends in heterocyclic chemistry produce a constant appetite for functionalized pyridines, but careful choice in substitution patterns changes everything—from physicochemical behavior to reactivity and downstream application. Our technical team doesn't rely on generic roadmaps for this compound; every figure—melting point, solubility, chlorination depth—eventually traces back to a reaction decision made at kiloliter scale. Choices in solvents, purification pressures, and raw input grades must prove themselves batch after batch. That is the practical side of making a dependable pyridine derivative, and generations of chemists have tuned the process under active plant conditions rather than at the pilot stage alone.

    Model Highlights and Purity Benchmarks

    This compound’s main draw comes from its precisely controlled dichloro and nitro substitution pattern. Introducing a bulky methyl group at position 4 acts as both an electronic lever and a process handle; it channels reactivity along predictable lines when used as a coupling partner, and its crystalline form means that material handling in large containers no longer carries the losses or static issues we’ve seen in more volatile analogs. Our typical product arrives as a distinctly yellow crystalline powder, where color consistency itself provides quick feedback to anyone familiar with batch manufacturing. Years ago, batches with browner or uneven hues flagged unwanted byproducts and signal us about mother liquor composition or incomplete chlorination. Now, our processing discipline, from fluorinated solvent recovery to staged washing and flexible drying protocols, pushes purity levels comfortably above 98 percent in routine runs. Sub-percent residuals—such as monochloro or trichloro variants—demand continuous monitoring. Every incoming raw load faces analytical cross-checks: NMR, GC-MS, and routine HPLC all in-house. Variability scares chemists in downstream labs, so we chase it out at the source, and we’ve learned from every failed batch how to prevent repeat issues on the next run.

    Hands-On Differences from Other Pyridine Derivatives

    Many ask where this molecule fits among the jungle of pyridine derivatives. Years working at the reactor tell a story that technical sheets rarely show. Simple pyridines behave differently; more symmetrical substitution patterns tend to boost stability but can block further functionalization. You might see a 2,6-dichloro ring in pesticides or pharmaceutical intermediates, but without that methyl at 4 and nitro at 3, the reactivity profile shifts. The nitro group pulls electron density away, which opens the molecule up to more nuanced nucleophilic attacks—a feature sought by medicinal chemists developing libraries for structure-activity relationships. We see customers struggle with other dichloro-pyridines whose solubility or dusting characteristics make scale handling a battle; after enough caked bags and uneven pours, plant operators develop strong opinions on these subtleties.

    Other manufacturers sometimes take shortcuts that risk excess moisture or residual solvent. Our facility is built for high-throughput drying and inert packaging. Any water activity above low single digits immediately shows up during remote storage or transport; a clumpy mass means trouble for automated tablet lines or even straightforward reactors. Year-round moisture monitoring isn’t some distant lab task—it’s plant floor routine, and stubborn wet patches have forced us to reengineer drying protocols just to keep product flow steady between seasons. For researchers used to hunting down impurity peaks in LC-MS traces, real-world differences come down to how consistent the core chemical signature remains. Our own QC records track deviations, and we constantly refine our craft by scrutinizing side-product drift, not just in-house but through customer feedback—especially when new applications push this molecule into previously untested territory.

    Applications That Show Its Unique Traits—and Limitations

    Synthetic chemistry teams often call us for insight beyond the data sheet. This compound often plays a starring role as a key intermediate in specialty active ingredient synthesis: insecticides, herbicides, and select anti-infective scaffolds. It enters the stage where robust electrophilic aromatic substitution is required. That nitro at 3, nestled beside twin chlorines, makes the ring a fine target for amine introduction or oxygenation, depending on catalyst and protocol. Those chlorines don’t just dangle—they define the reactivity, acting as the launchpads for nucleophilic aromatic substitution, often under mild enough conditions that heat damage stays minimal. Whether working with metal catalysts or basic amine nucleophiles, experienced process chemists have learned to exploit the arrangement, as methyl branching can steer both yield and selectivity.

    Agrochemical projects frequently demand this type of intermediate for the development of new pyridine-based actives—often as a staged functionalization point, adding tailored substituents at positions most open to further chemistry. The dichloro configuration handles electron management, making this molecule a versatile building block. Generic dichloro-pyridines often struggle with poor downstream coupling yields; our own experience has shown the methyl-nitro arrangement preserves more reliable reactivity. Pharmaceutical chemists turn to it for early-phase library generation, where downstream transformations such as reductions, cross-couplings, or amide insertions ride on both the stability of the intermediate and the predictability of each substitution.

    Production Nuances from Factory Floor to Dispatch

    Not all chemistry happens in the theoretical vacuum of the R&D lab. Batch-to-batch consistency separates a manufacturer from a catalogue reseller. We built our synthesis from the ground up, starting with carefully sourced chlorinated pyridine feedstock. At this scale, purity in the starting material decides the headache levels further down the chain. Over years, we’ve fought these battles—reactivity swings, out-of-range melting points, and the occasional off-gas scare. It takes real hands-on experience to judge whether a batch that reads “in spec” on a meter will deliver in a customer process—or whether it will jam a feeder or clump below freezing.

    During scale-up, we learned solvents choose you, not the other way around. Early runs using standard chlorinated solvents produced batches that left too much residual on drying. A switch to fluorinated and sometimes greener alternatives, along with continuous recovery systems, has kept contaminants strictly in check. Our drying regime forced us to invest in staged airflow control: too much and the fines fly everywhere, clogging collectors and wasting material; too little, and moisture or solvent residues persist. These aren’t theoretical process notes—they are real-world fixes based on trial, error, and a few hard lessons in cost and consistency.

    Transportation brings its trials. Pyridine derivatives show striking sensitivity to stacking pressure, long-range temperature changes, and static from container surfaces. Experience says that even the smallest lapse in drum sealing lets in enough moisture during overland travel to undermine had-fought stability. We worked with packaging partners to design double-liner bags with robust outer shells, and our logistics team keeps a running log of batch condition reports from every significant route. In a world where lost weight, cross-contamination, or sluggish discharge means lost value, insisting on standards isn’t theoretical—it’s the result of fixing every mistake we’ve seen or inherited.

    Working with End Users: Honest Feedback Loops and Process Support

    Unlike a faceless distributor, our lab and plant teams frequently communicate directly with end-use chemists. Sometimes this contact starts as a complaint—“this batch pours differently from the last,” or “a new impurity shows up under our high-res HPLC.” Rather than hiding behind email replies, we invite customers to visit our plant, share their process parameters, and show them our cleaning and drying routines. Candid conversations between end users and manufacturing chemists fast-track tweaks nobody would discover by swapping purchase orders or reading spec sheets alone.

    Our R&D team doesn’t sit on the sidelines. We often help troubleshoot problematic downstream reactions, especially where the batch-to-batch variability of a substituted pyridine compound creates drifts in yield or impurity profiles. Whether it means running small-scale side-reactions in our auxiliary labs or adjusting trace moisture readings, support comes with a real commitment to fixing field issues. For every change in analytical standard or emerging end-use, there’s a lesson added to our internal library, and adjustments made so that future production closes the loop.

    Solution-Oriented Manufacturing: Meeting Regulatory and Inspection Realities

    Manufacturing substituted pyridines never stands still. Regulations change—sometimes slowly, sometimes overnight. Each update brings stricter controls on emissions, trace metal content, and safe-handling procedures. We maintain active dialogue with inspectors—to the benefit of our customers as much as our own operations. For example, strict adherence to local and global safety standards shapes everything, from drum labeling to the air-handling in the final packaging building. Auditors and client visitors frequently tour our plant to view records—real-time, not staged for inspection—and their observations often spark process upgrades, not just compliance routines. Nothing in the chemical business stays finished for long. Instead, it’s a constant improvement cycle: one batch teaches lessons for the next.

    Market shifts and new applications for 2,6-dichloro-4-methyl-3-nitro-pyridine bring new regulatory hoops, particularly in the move toward greener chemistry. Solvent recovery, waste minimization, and ever-tightening limits on volatile organic components force us to design each part of the process with end-of-life in mind. We track not only product purity but also cradle-to-grave environmental impact. Collaborating with responsible disposal partners and revisiting every upstream step, we focus on full-cycle stewardship. Our technical teams feed this grounding back into everything, from process planning to talking shop with end chemists looking to certify products under tougher environmental regimes.

    Reliability in Global Supply: The Manufacturer’s Perspective

    No one understands supply chain volatility better than the team that churns out the final product, week in and week out. We have weathered everything from raw material shortages to shipping disruptions that ripple through every level of the market. Over time, this builds in muscle memory—holding buffer stocks, qualifying secondary sources, and building flexibility into production schedules. Each batch serves as a testimony to the discipline and work put in by teams committed to the product being more than an entry in a database.

    Market feedback steers process tweaks over and above monthly reviews. During years of global logistics squeezes, every extra day in transit risked quality and added to customer anxiety. We’ve taken this seriously, investing in packing upgrades, real-time tracking, and responsive documentation—not for shelf appeal, but because those gaps cost all of us time and resources. Surviving in the space of substituted pyridines means rolling with every process, materials, and regulatory change, always listening to feedback from our partners up and down the supply line.

    Looking Beyond: Future-Proofing Through Chemical Experience

    The business of manufacturing 2,6-dichloro-4-methyl-3-nitro-pyridine never coasts on autopilot. To drive stability and adapt to changing market or technical needs, we continue investing in laboratory upgrades, adoption of process analytic technology, and opening labs for rapid feedback runs. Inspiration doesn’t always come from isolated research, but more often from the workshop floor: process engineers, plant workers, and field chemists all bring their day-to-day lessons to every team discussion.

    When the market asks for new levels of trace impurity control or reduced batch-to-batch variability, direct input from veteran plant chemists often points to unexpected solutions—tweaks in temperature ramp rates, milling blade angles, or timer settings. We take pride in making improvements visible not just as numbers on a cert but in the lived experience of product users. Customer needs evolve and so do production challenges—no amount of textbook chemistry replaces tweaks born of hands-on run-throughs in real settings.

    Conclusion: Why the Manufacturer’s Journey Matters

    Working directly with this compound over the years, our team has witnessed not just the technical intrigue of its unique substitution, but the unglamorous work it takes to deliver reliability at industrial scale. People who work in chemistry expect the material in their container to behave as the last one did—not to surprise them with strange dusting, off-odors, or drifting reactivity. Delivering this confidence requires more than meeting a spec; it’s built on every person in the chain caring about their piece of the production puzzle.

    To the manufacturing team, each lot teaches a lesson in chemistry, process control, and collaboration. With active listening to both regulatory expectation and customer feedback guiding every tweak, our process for producing pyridine, 2,6-dichloro-4-methyl-3-nitro- stands as a reflection of experience, adaptation, and the commitment to quality that only a direct manufacturer can truly cultivate. Our door is always open to those looking for more than just another bottle—those looking for chemistry backed by the conviction of those who made it.