2,6-Dichloro-3-Cyano-4-Methyl.pyridine

    • Product Name: 2,6-Dichloro-3-Cyano-4-Methyl.pyridine
    • Chemical Name (IUPAC): 2,6-dichloro-3-cyano-4-methylpyridine
    • CAS No.: 32737-34-5
    • Chemical Formula: C7H3Cl2N2
    • Form/Physical State: Solid
    • 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

    361983

    Product Name 2,6-Dichloro-3-Cyano-4-Methylpyridine
    Cas Number 864064-58-2
    Molecular Formula C7H3Cl2N2
    Molecular Weight 187.02 g/mol
    Appearance White to pale yellow solid
    Melting Point 76-80°C
    Purity Typically >98%
    Solubility Soluble in organic solvents such as dichloromethane and acetone
    Density Approximately 1.5 g/cm³
    Smiles CC1=NC(=C(C(=C1Cl)C#N)Cl)
    Inchi InChI=1S/C7H3Cl2N2/c1-4-2-6(8)7(10-3-11)5(9)12-4/h2H,1H3

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

    Packing & Storage
    Packing A 100g amber glass bottle with a secure screw cap, labeled "2,6-Dichloro-3-Cyano-4-Methylpyridine," featuring hazard and safety information.
    Container Loading (20′ FCL) 20′ FCL can load about 11 MT of 2,6-Dichloro-3-Cyano-4-Methylpyridine, packed in 25 kg fiber drums or bags.
    Shipping 2,6-Dichloro-3-Cyano-4-Methylpyridine is shipped in sealed, chemical-resistant containers to prevent leakage and contamination. It is labeled according to UN regulations as a potentially hazardous material. Shipping complies with local and international guidelines, ensuring the package is protected from moisture, extreme temperatures, and physical damage during transit.
    Storage Store 2,6-Dichloro-3-Cyano-4-Methylpyridine in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Keep away from moisture. Ensure proper labeling and secure storage to prevent unauthorized access. Follow standard chemical hygiene practices and wear appropriate personal protective equipment when handling.
    Shelf Life 2,6-Dichloro-3-cyano-4-methylpyridine has a typical shelf life of 2-3 years when stored in cool, dry conditions.
    Application of 2,6-Dichloro-3-Cyano-4-Methyl.pyridine

    Purity 99%: 2,6-Dichloro-3-Cyano-4-Methyl.pyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high-purity ensures consistent active ingredient yield.

    Melting Point 120°C: 2,6-Dichloro-3-Cyano-4-Methyl.pyridine with melting point 120°C is used in agrochemical formulation, where controlled melting behavior improves processability.

    Particle Size <10 μm: 2,6-Dichloro-3-Cyano-4-Methyl.pyridine at particle size <10 μm is used in high-performance catalyst manufacturing, where fine particle distribution enhances reaction rates.

    Moisture Content <0.5%: 2,6-Dichloro-3-Cyano-4-Methyl.pyridine with moisture content <0.5% is used in specialty chemical production, where reduced moisture prevents unwanted side-reactions.

    Stability Temperature 50°C: 2,6-Dichloro-3-Cyano-4-Methyl.pyridine with stability temperature 50°C is used in polymer additive development, where thermal stability maintains additive integrity during processing.

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    Certification & Compliance
    More Introduction

    2,6-Dichloro-3-Cyano-4-Methylpyridine: Experience from the Production Floor

    Introduction Through Practice

    At our facility, success starts with diligence in synthesis and a dedication to consistent, real-world feedback from downstream users. Over the past two decades, producing 2,6-Dichloro-3-Cyano-4-Methylpyridine (2,6-DC-3-C-4-MP) has challenged our ingenuity and taught us the value of hands-on manufacturing. This compound, recognized widely for its unique substitution pattern on the pyridine ring, continues to prove itself across several fields, with crop protection often topping the list. Every batch that leaves our plant blends reliability, chemistry know-how, and a responsive approach to the quirks of pyridine-base intermediates.

    From Sourcing to Finished Product: Real Lessons Learned

    Raw material quality stands at the foundation of product integrity. We select chlorinated and nitrile-bearing intermediates whose origins are verified through supplier visits and bonafide audit trails. With this foundation, every step in production — from halogenation to cyano group introduction and methylation — receives strict scrutiny. Experts at each station remain accountable for yields, color, and trace contaminant profiles. Over time, this vigilance cut impurity spikes and trimmed production downtime, allowing us to fine-tune the final output’s purity to exceed 98% by HPLC.

    Unlike broad-label manufacturers, we avoid mixing sources or shifting specifications based on market swings. The expertise flows from cumulative feedback. Early batches taught us major by-products often stem from temperature instability in the halogenation stage. Once we implemented in-line sensors and rapid-response controls, not only did batch-to-batch consistency rise, but off-color product — previously a customer concern — nearly disappeared.

    Packaging evolved as well. By switching from basic double-walled bags to lined fiber drums with anti-static liners, we prevented moisture ingress and static charge buildup, issues that can affect product handling and stability. Customers working in specialized formulation plants noticed fewer caking incidents and reduced waste, feedback we take seriously each time we design packaging formats.

    What Makes 2,6-DC-3-C-4-MP Stand Out?

    2,6-Dichloro-3-Cyano-4-Methylpyridine earns its keep precisely because of its structure. The dual chlorines and cyano group push the electron density of the pyridine ring in a way that traditional di- or tri-chlorinated analogues simply don’t. This subtlety, as reported by formulation chemists and pesticide developers, translates to a better platform for downstream transformations. Our clients in crop science consistently report that this skeletal arrangement improves the selectivity and durability of active ingredients.

    Compared with 3-chloropyridine or more heavily substituted pyridines, 2,6-DC-3-C-4-MP maintains a balance between reactivity and stability during manufacturing of next-step compounds. For example, many manufacturers in the agricultural sector highlighted that the cyano group position provides a predictable point for further functionalization, which leads to higher synthetic yields and less waste. As a manufacturer who’s processed thousands of kilos, the subtle differences show up not just in lab assays, but in how smoothly reactors run and filters hold up batch after batch.

    The Value of Purity and Repeatability

    Technical-grade material with even tiny side product contamination causes plug-ups in continuous reactors or reduces desired yields down the line. Over the years, we’ve encountered situations where a 0.5% increase in residual chlorinated side products led to entire runs being scrapped at partner sites. Mistakes like these cost money and erode trust. That’s why our team invests in in-process checks and post-filtration sampling, using up-to-date analytical techniques. By focusing on HPLC and GC-MS at critical points, not only do we achieve 98%+ purity, but we also maintain consistent impurity profiles. This detail makes all the difference to downstream process engineers and chemists, who rely on the absence of variable side products for their own process control.

    Through relentless troubleshooting and honest reporting with our users, we’ve found even small tweaks — better pH control during final washes, switching to argon overlays during crystallization — reduce process upsets. These aren’t changes we made to pad marketing claims; they came directly from working with stakeholders who told us what damages their process flow and what saves time in their QC labs.

    Applications: Insights Gained from Field and Industry

    Most inquiries about 2,6-DC-3-C-4-MP spotlight its critical use as a building block for herbicides, particularly those belonging to the pyridinecarboxylic acid class. Major innovation in this field came about because this compound enables efficient aldol condensation and cross-coupling routes otherwise difficult with traditional pyridine derivatives. Over repeated seasons, formulators at major agrochemical firms told us that switching to our material curbed their catalyst consumption and curbed batch reworks. The positive feedback loop we’ve built with these firms keeps us grounded in the real benefits our compound brings.

    Pharmaceutical inquiries follow a separate trajectory. The compound doesn’t serve as an API itself very often, but its substitution pattern makes it invaluable for custom synthesis projects seeking specific electron-withdrawing patterns. Each year, our technical support scientists are pulled into more projects involving medicinal chemistry tweaks. Lessons learned show that, unlike less-functionalized pyridines, our compound lends itself to more precise halogen-metal exchange or Sandmeyer transformations, so custom synthesis partners stay on track without expensive purification setbacks.

    The pigment and specialty dye markets represent a smaller but persistent base. For these clients, consistency in hue and lack of side product chromophores mean less disturbance in their color matching routines. Open feedback led us to include tailored compendial testing and stability guarantees, which reduced rejections on their end and saved costs for both parties.

    What We’ve Learned by Listening to End Users

    Dialogues with multinational formulators and large contract manufacturers shaped many of the changes in our plant. For example, a repeated request came from Asian formulation plants about dusting during handling. We began milling to a slightly larger average particle size and adopted a granulation step, directly responding to worker safety concerns (without changing solubility or reactivity). This adaptability fostered stronger partnerships and repeat business.

    Some of our earliest shipments arrived at customer docks with subtle differences in batch color, which flagged quality doubts. Taking these remarks seriously, we improved our drying and recrystallization protocol, then sent improvement reports directly to our customers. Transparency about the fixes we made encouraged more straightforward communication — clients became more willing to tip us off regarding issues before they escalated.

    We’ve received technical reports, for instance, about the impact of residual base compounds affecting downstream Tolman’s reagent coupling. The solution was not obvious; only close tracking of upstream process steps and real chromatography data settled how to adjust base washes and final filtration. Every issue like this, reported openly, keeps us nimble and prevents repeating costly errors. Mutual respect and information exchange shift the manufacturer-client relationship away from adversarial posturing toward a truly productive partnership.

    Global Standards and Regulatory Considerations: A Practitioner’s View

    Meeting international standards remains a challenge, largely because regulatory demands don’t always align across borders. REACH in Europe, FIFRA in the United States, and emerging playbooks in India or Brazil set different impurity limits and reporting needs. Drawing on our experience, we create detailed impurity maps so each region receives shipments pre-qualified for local compliance. In instances when certain standards restrict a secondary aromatic amine or trace isomer, we separate and warehouse batches accordingly. Our technical regulatory team holds frequent internal reviews, staying ahead of changing limits and alerting production in advance.

    Confidence in compliance stems from real paperwork and genuine data, not marketing gloss or unsubstantiated claims. Our customers frequently request batch-specific certificates that include not just purity, but full analytic spectra and manufacturing history. Fulfilling such requests requires a strong record-keeping ethos, a company-wide understanding of the regulatory landscape, and an ingrained respect for documentation. These efforts, while resource-intensive, have a long-term payoff: smooth customs clearance, low audit risk, and — most importantly — credibility.

    Scale-Up Experience: From Kilograms to Tons

    Moving from bench-scale synthesis to multi-ton manufacture of 2,6-DC-3-C-4-MP taught us more about real-world chemistry than any textbook. On small scale, certain impurity profiles stay hidden, but at volume, temperature gradients and solvent vapor retention give rise to new issues. Our engineers spent hundreds of person-hours mapping reactor wall temperatures and optimizing agitator speeds to prevent hot spots, which not only increased yields but also sharply reduced polymer byproduct formation.

    Filtration efficiency and cake washing developed into another area of practical knowledge. Early on, water washes were inadequate for complete sodium ion removal, leading to slow-forming precipitates in partner reactions downstream. Adapting washing cycles with mixed solvents eliminated this headache, cutting the problem by more than 95% as verified by customer reports and our own analytic logs.

    As our scale grew, waste management practices became more critical. With a focus on reducing hazardous effluent, we built an in-house solvent recovery loop and began on-site treatment of acidic and chlorinated side streams. Not only does this uphold our environmental commitments, but it has become a point of reassurance for sustainability-minded clients. They value seeing quantifiable reductions in our annual emissions statistics, which we’re happy to share as part of ongoing partnership reporting.

    Comparison to Similar Compounds: Insights from Product Development

    We routinely field technical queries asking why not opt for similar pyridine derivatives, such as 2,3,6-trichloropyridine or 3,5-dichloro-2-cyanopyridine. Drawing from our years of plant operation and field feedback, 2,6-DC-3-C-4-MP occupies a unique sweet spot. Its methyl group, in tandem with the two chlorines and a cyano moiety, confers both selectivity in key reactions and industrial process robustness.

    Other derivatives can match its reactivity in theory, but process engineers tell us that harder-to-control boiling points and less forgiving impurity profiles make them riskier for continuous operation. The methyl substituent also brings subtle advantages for volatility and crystallization, which have real consequences in large-scale manufacturing. In practice, this means shorter cycle times, fewer filtration headaches, and easier downstream separation.

    One of the less-discussed benefits of 2,6-DC-3-C-4-MP reveals itself in formulation stability. Comparable dichloropyridines occasionally break down faster under UV or alkaline storage, shortening shelf life for downstream products. Over years of stability studies and actual customer shelf life testing, our compound held up better, reducing batch recalls and repackaging costs for partners. Technical teams appreciate documentation from long-term storage trials, highlighting the trust that grows from open data sharing.

    Continuous Improvement: Where We Go from Here

    Each new production campaign becomes a source of data and feedback. Newer reactor designs and automated in-line monitoring give us more control and let us run predictive analytics on potential process upsets before they materialize. As more clients demand lower impurity thresholds, especially for pharmaceutical or fine chemical use, we stay ready to upgrade purification steps or invest in new process controls when feedback points to emerging needs.

    Ongoing partnerships with academic researchers keep us grounded in the latest chemistry and offer opportunities to test new synthetic strategies. Our technical support team remains an open resource, always inviting honest feedback. Experience shows us that the strongest working relationships root themselves in reliable communication and in taking responsibility when adjustments are needed.

    Conclusion: Experience That Makes the Difference

    Manufacturing 2,6-Dichloro-3-Cyano-4-Methylpyridine teaches lessons that extend well beyond synthetic steps and purity figures. At its core, it’s about responding to feedback, anticipating industry needs, and adjusting our practices in real time. The distinctive design of this compound gives our customers — in crop science, specialty chemicals, and beyond — both short-term success and long-term reliability. Real progress comes not from chasing the lowest cost or fastest production, but from standing behind quality and process transparency, and from drawing daily lessons from our users and partners.