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HS Code |
163817 |
| Product Name | Methyl 2,6-Dichloroisonicotinate |
| Cas Number | 41859-41-0 |
| Molecular Formula | C7H5Cl2NO2 |
| Molecular Weight | 206.03 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 69-72°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | COC(=O)C1=NC(=CC(=C1)Cl)Cl |
| Inchi | InChI=1S/C7H5Cl2NO2/c1-12-7(11)4-2-5(8)10-6(9)3-4/h2-3H,1H3 |
| Density | 1.48 g/cm³ (approximate) |
| Storage Temperature | Store at 2-8°C |
| Synonyms | Methyl 2,6-dichloropyridine-4-carboxylate |
As an accredited Methyl 2,6-Dichloroisonicotinate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of Methyl 2,6-Dichloroisonicotinate is packaged in a sealed amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | Methyl 2,6-Dichloroisonicotinate should be shipped in tightly sealed containers, away from incompatible materials, under cool and dry conditions. Ensure compliance with local regulations regarding hazardous chemicals. Proper labeling and documentation are required. Handle with care to prevent leaks or spills during transit. Use appropriate protective packaging for safe transportation. |
| Storage | Methyl 2,6-Dichloroisonicotinate should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizers. Properly label the container and store it in a designated chemical storage cabinet to prevent accidental exposure or contamination. |
Applications of Methyl 2,6-Dichloroisonicotinate in Industrial ManufacturingMethyl 2,6-Dichloroisonicotinate serves as a specialized intermediate in several highly-regulated chemical manufacturing processes. Its unique substitution pattern and chemical reactivity support a spectrum of advanced downstream synthesis routes, each governed by stringent industry protocols. Below, we detail its principal industrial application scenarios for direct business clients in the sector. 1. Agrochemical Active Ingredient SynthesisThis compound acts as a key building block in the synthesis of pyridine-derived agrochemical actives, particularly herbicides and fungicides. Manufacturers introduce it during early-stage heterocyclic nitrogen ring construction. The precise dichloro-functionalization supports specific substitution reactions, which feed into substitution or coupling steps with various functional groups to build target molecules in multi-step batch or continuous production lines. Downstream processors must conform to strict environmental and operator safety protocols due to the compound’s reactivity and the toxicity of some subsequent intermediates. Industry compliance standards
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2. Pharmaceutical Intermediate ManufacturingThe material supports the production of select nicotinic acid derivatives for subsequent use in active pharmaceutical ingredient (API) synthesis. Its electron-withdrawing dichloro substituents enable regioselective reactions, supporting functional group transformations crucial to the preparation of specialty intermediates for CNS drug candidates and antivirals. Tight raw material traceability and solvent control are required throughout, complying with good manufacturing practice systems to meet downstream customer regulatory submissions. Industry compliance standards
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3. Fine Chemical Building Block in Dye ManufacturingMethyl 2,6-Dichloroisonicotinate is converted into specialty intermediates for the synthesis of chromogenic and azo compounds used in high-performance dyes. Its substitution pattern favors regioselective substitution and easy functionalization, enabling tailored chromophore assembly for demanding textile and industrial coloration products. Downstream processors rely on strict elemental impurity profiling and batch-to-batch consistency for color performance, adhering to sector-specific emission and effluent control legislation during production. Industry compliance standards
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4. Electronic Chemical Intermediate for Liquid Crystal MaterialsThe compound is utilized in the production of tailored heterocyclic intermediates for liquid crystal (LC) monomer synthesis. The dichloro substituents confer desired electronic and steric properties for mesogen construction, crucial for high-performance display and electronic component manufacturing. Downstream processes demand ultra-high purity and trace contaminant monitoring, involving careful solvent management, intermediate filtration, and multi-stage purification. Compliance with electronic-grade standards minimizes interference in subsequent LC formulation and device filling stages. Industry compliance standards
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Chemists in our plant walk familiar halls, pass large reactor tanks lined with corrosion-resistant steel, and glance at batch cards marked “Methyl 2,6-Dichloroisonicotinate” with a sense of continuity. We don’t see this compound as a catalogue item, but as a project woven into the patterns of daily work. Plenty of researchers dialing in new crop protection molecules and pharma intermediates turn toward it because—based on our own hands-on production—it lands at a rare intersection of reliability and practical reactivity.
Looking at the structure of methyl 2,6-dichloroisonicotinate, you’ll notice it falls within the isonicotinate family, yet those two chlorines at positions 2 and 6 give it key differences from typical isonicotinates or even the mono-chlorinated versions. Each batch here aims for a purity above 99%, checked by GC against an in-house reference standard made on the same line. Our colorless crystalline material holds tight to its melting point through repeat heating and cooling, signaling a stable synthetic route and solid compound integrity.
Most requests arrive in the 25 kg or 200 kg drum sizes, and we usually send out technical grade or lab grade, according to who plans to use it in downstream syntheses or application development. Routine HPLC scans on outgoing drums catch even small-scale side products, keeping our delivered stock as consistent as we expect ourselves, regardless of what’s going on in the market.
Our earliest industrial partnerships grew from this compound’s simple promise: “give the same predictable reaction, over and over.” It’s hard to overstate how much that means in scale-up chemistry. From what we’ve seen, methyl 2,6-dichloroisonicotinate suits two jobs better than related compounds. First, it acts as a precision intermediate for pyridine-based fungicides and herbicides. The electron-withdrawing chlorines tune the pyridine ring, making staff in our own lab coax out clean, selective substitutions without running into persistent side-products common to other isonicotinates. Second, it serves as a scaffold for pharmaceutical research—attracting R&D teams exploring anti-infective scaffolds and CNS actives, where ring-chlorination is crucial for tuning reactivity and metabolic resilience.
If you compare this compound to its single-chlorine analogs, side-chain substitutions on other isonicotinates run into trouble in selectivity. The extra chlorine at position 6 brings down the likelihood of double adducts or unwanted condensation on the ring. That means downstream transformation—think etherification, amidation, or Suzuki cross-coupling—shows cleaner conversion. Our own analysts keep logs of impurity profiles to track yearly trends and can back up these claims with long-term historical QA data.
The demands of production mean balancing several things at once: speed, consistent output, and safe handling. Raw material purity, drying, and the exact catalyst ratios used in our reactors don’t always show up on a certificate of analysis, but they decide a lot about how methyl 2,6-dichloroisonicotinate will behave for the end user. There is in-house discussion over just how much to fine-tune these steps to give our regular partners the most hassle-free experience.
Anyone making a stepwise synthesis knows that ringing purity out during the intermediate stages saves more pain in the final workup than almost any late-stage purification. For this reason, we’ve invested in enhanced solvent recovery and high-vacuum filtration across synthesis stages. Our route for methyl 2,6-dichloroisonicotinate doesn’t cut corners: we use a proprietary chlorination route on the isonicotinate backbone, followed by careful methylation, and then multiple finishes including recrystallization and drying under reduced pressure. The end result—batch after batch—matches published standards but tends to outperform commercial lots from aggregators who don’t have vertical integration.
Unlike more volatile chloro-derivatives, this compound’s methyl ester makes it amenable to handling in both open and closed systems, with no notable hydrolysis under typical factory conditions. Colleagues at client sites have contacted us about using our compound in both glass-lined and PTFE reactors, observing stable output even when moving between lab and bulk manufacturing.
We field a lot of questions every year from customers evaluating whether methyl 2,6-dichloroisonicotinate will solve a specific route bottleneck. The answer isn’t always yes, but in our direct experience, the consistency and selective performance have stood time’s test in real-world projects. Researchers have bent it toward exploratory molecules for active pharmaceutical ingredient (API) screening. Agricultural manufacturers figured out early that its stability in organic solvents and resistance to acidic and basic hydrolysis simplifies cleanup and reduces production downtime when shifting between campaigns.
Tracing its journey through our supply chain, we see it start as fine, pale crystals in our isolated intermediate storage, then move by airlift to drum filling after in-process checks. QA teams—many of whom have handled this same molecule for years—recognize the key spectroscopic peaks and impurity patterns immediately. The culture we build around this compound reflects how much stock we put in repeat experience. Our longest rug ratings and customer survey scores came off the back of this approach: not from overnight changes, but from steady hands on every part of the process.
Colleagues sometimes ask about using methyl 2-chloroisonicotinate or methyl 4-chloroisonicotinate as alternatives. We’ve trialed them both. While all share the pyridine backbone, their single chlorination sites don’t always direct substitutions with the kind of precision most modern reactions require. With only one chlorine, substitution patterns broaden, and you risk a more complex mixture of products, necessitating more intensive purification downstream. By contrast, the 2,6-dichloro analog narrows the reactive window, making it viable on both pilot and plant scale without climbing separation costs or chasing after elusive minor isomers.
In comparison to unsubstituted methyl isonicotinate, the dichloro form increases overall ring electron deficiency, streamlining oxidative addition and Suzuki-type couplings. As a result, absolute yield jumps and colored byproducts decline in our monitored production runs. Some of our clients in advanced pharma synthesis leverage this reactivity to install more challenging groups, which would otherwise demand protecting group strategies. Our feedback loop with these teams—which includes regular exchange of synthetic conditions and impurity data—has shown that working with the dichloro variant cuts down the need for post-reaction purification steps, directly dropping both labor and solvent spend. Stories from our partner sites often highlight that change in their annual treatment costs for downstream purification media.
As a manufacturer who’s handled this material for years, I can say its stability in transit and storage has given it a reputation for dependability at scale. We’ve tracked it over month-long shipping routes to high-humidity Asian ports and arid North American sites, with little change in crystalline appearance or GC profile. Our distributors come back with low incidence of shipping damage or degradation. More importantly, clients using the compound for downstream reactions say it tolerates a range of working conditions—both rigorous batch protocols and continuous feed systems.
This isn't an all-purpose chemical. Its primary value emerges in specialized roles—delivering a clean starting point for stepwise transformations or acting as a late-stage scaffold-building block. Bulk customers in crop protection have noted that compared to some cheaper monochloro alternatives, our product reduces plant shut-down periods and messier workups, giving production teams more uptime. In pharmaceutical pilot plants, researchers have managed high-throughput runs with less binder, lower catalyst loading, and fewer failed lots because of robust starting purity—something we take pride in measuring and maintaining.
Manufacturing methyl 2,6-dichloroisonicotinate at scale presents its own safety and compliance challenges. The chlorination steps use regulated precursors and create an on-site responsibility for waste minimization and careful halogen management. Over the past years, we’ve invested in secondary containment, multi-step neutralization systems, and advanced fume scrubbers to stay aligned with local and global guidelines. Regular monitoring means we keep solvent emissions and process losses well below regulatory triggers—verified through annual third-party audits.
We also work with our industrial users on responsible packing and shipping protocols. Overpacking, leak tests, and tamper-evidence remain a fact of life in our logistics preparation. For end users, our technical team provides detailed handling protocols and consultation for inert atmosphere storage or safe transfer, reducing the risk of cross-contamination in busy factories. While we handle most of our technical correspondence directly, we also maintain ties with academic users to improve safety data and gather fresh observations about degradation or reactivity limits.
The value of our methyl 2,6-dichloroisonicotinate has a lot to do with how it performs in real-world syntheses. On the line, process chemists turn over more logs to this compound than almost any other isonicotinate derivative because it saves time at several steps—raw material handling, intermediate isolation, final purification. Every shipment is linked to a tracked QC chain, with data spanning back several years to reveal any deviations or trends. When issues arise—like an uptick in moisture content after a particularly wet season—we adapt drying protocols and run another set of analysis to protect downstream results.
What doesn’t show up on paper: the kind of behind-the-scenes troubleshooting that has built our knowledge about this product. Experienced staff take one look at a slightly yellowed crystal batch and can suggest a tweak in the drying oven or an extra hour on the stir line. This hands-on cycle between lab, plant, and shipping floor leaves us with practical confidence in every outgoing drum.
Chemicals like methyl 2,6-dichloroisonicotinate don’t move on hype or generic spec sheets alone. Users in the field trust it for the daily, unglamorous business of getting chemistry done, which is the backbone of dozens of active projects worldwide. Over time, the trust we’ve built by consistently delivering high-quality material translates to stronger partnerships, less firefighting for customers, and continued process optimization on our end.
When feedback leads us somewhere new, we adapt processes—the introduction of high performance resins for finer filtration, or the real-time logging of downstream complaint rates. Sometimes even a minor tweak in solvent grade makes a detectable difference for our demanding pharma users. Staying close to the reality of everyday synthesis, we’re always searching for small gains in both yield and purity, because that’s what keeps our partners returning year after year.
Inside our facility, years of knowledge and teamwork walk alongside every product drum. Making methyl 2,6-dichloroisonicotinate from scratch means knowing the ins and outs of every step—choosing the right grade of chlorinating agent, nailing the exotherm controls, troubleshooting the methylation stage, and watching each batch pass the same rigorous analytical check that’s run since the beginning. Long-serving staff talk about the compound with pride, swapping notes on subtle process changes and minor fixes that preserve its benchmark reliability.
Other companies offer similar products, but our experience tells a different story. We handle each production run not as a singular task, but as a chance to reaffirm the quality we stake our name on. Each drum we send contains not just material, but years of process knowledge and a commitment to the best outcome for every client’s project.
We don’t rest easy just because a product has stood the test of time or found its way into a hundred supply chains. Innovation here tends to be quiet and incremental—another improved filter, a slight change in process temperature, or fine-tuning a GC calibration. These details make their mark over hundreds of shifts, ensuring methyl 2,6-dichloroisonicotinate’s consistent performance in the many finished products and intermediates made by our clients.
One lesson we return to: it’s one thing to meet a spec, another to shape a product through dozens of choices at all steps. The more track record we build, the easier we find it to offer tangible guarantees about outcome and quality. That’s how we maintain our promise, not just in writing but in every shipment that leaves our floor.
Most industrial producers court large-volume buyers, but our history with methyl 2,6-dichloroisonicotinate includes supporting smaller teams—those pioneering new synthetic routes or troubleshooting process bottlenecks on tight budgets. Plenty of times we’ve guided young researchers or small innovation labs, helping them navigate the practical issues of scaling up from gram to multi-kilogram syntheses. This kind of technical support, underpinned by hands-on manufacturing experience, keeps our product relevant and trusted in both major and niche applications.
Whether in fungicide synthesis, pharma intermediates, or other custom molecules, the stories that come back to us focus on performance and trust. That sense of partnership, built on open communication and consistent follow-through, is the real backbone beneath all the claims on paper. Methyl 2,6-dichloroisonicotinate stands out because it reflects that tradition—one batch, one conversation, and one long-term result at a time.