pyridine, 2,6-dichloro-3-(chloromethyl)-

    • Product Name: pyridine, 2,6-dichloro-3-(chloromethyl)-
    • Chemical Name (IUPAC): 2,6-dichloro-3-(chloromethyl)pyridine
    • CAS No.: 43112-10-9
    • Chemical Formula: C6H4Cl3N
    • 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

    373477

    Chemical Name Pyridine, 2,6-dichloro-3-(chloromethyl)-
    Molecular Formula C6H4Cl3N
    Molecular Weight 196.46
    Cas Number 27317-28-0
    Appearance Colorless to pale yellow liquid
    Boiling Point 110-112°C at 21 mmHg
    Density 1.43 g/cm3
    Solubility In Water Slightly soluble
    Refractive Index 1.590
    Flash Point 97°C
    Smiles Clc1ccc(Cl)nc1CCl

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

    Packing & Storage
    Packing The chemical "pyridine, 2,6-dichloro-3-(chloromethyl)-" is packaged in a 100-gram amber glass bottle with a secure screw cap.
    Container Loading (20′ FCL) 20′ FCL: 160 drums (200 kg net each), totaling 32 MT, tightly sealed, UN-approved containers for pyridine, 2,6-dichloro-3-(chloromethyl)-.
    Shipping Pyridine, 2,6-dichloro-3-(chloromethyl)- should be shipped in tightly closed, appropriately labeled containers, preferably glass or compatible plastic, under cool and dry conditions. It is classified as a hazardous chemical and must comply with relevant transport regulations (e.g., DOT, IATA, IMDG). Protective packaging and documentation for hazardous goods are required to ensure safety.
    Storage Store pyridine, 2,6-dichloro-3-(chloromethyl)- in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight, heat, and incompatible substances such as strong oxidizers and acids. Ensure the storage area is equipped for handling toxic, corrosive chemicals, and is clearly labeled. Use secondary containment to prevent leaks or spills, and access should be restricted to trained personnel only.
    Shelf Life Shelf life: Store pyridine, 2,6-dichloro-3-(chloromethyl)- in a cool, dry, sealed container; chemically stable for 2-3 years.
    Application of pyridine, 2,6-dichloro-3-(chloromethyl)-

    Purity 98%: Pyridine, 2,6-dichloro-3-(chloromethyl)- with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield of active pharmaceutical ingredients.

    Melting Point 65°C: Pyridine, 2,6-dichloro-3-(chloromethyl)- with a melting point of 65°C is employed in agrochemical manufacturing, where it provides controlled reactivity during formulation.

    Molecular Weight 212.45 g/mol: Pyridine, 2,6-dichloro-3-(chloromethyl)- at 212.45 g/mol is used in fine chemical production, where it guarantees consistent molecular distribution in batch processing.

    Stability temperature up to 120°C: Pyridine, 2,6-dichloro-3-(chloromethyl)- stable up to 120°C is used in polymer modification, where it maintains chemical integrity under process heat.

    Low water content <0.5%: Pyridine, 2,6-dichloro-3-(chloromethyl)- with water content below 0.5% is used in specialty resin synthesis, where it prevents unwanted hydrolysis during polymerization.

    Appearance: colorless to pale yellow liquid: Pyridine, 2,6-dichloro-3-(chloromethyl)- as a colorless to pale yellow liquid is used in laboratory-scale research, where it allows for easy monitoring of chemical reactions.

    Assay (GC) ≥99%: Pyridine, 2,6-dichloro-3-(chloromethyl)- with assay by GC ≥99% is used in electronic material production, where it delivers high electronic grade purity for sensitive components.

    Refractive Index n20/D 1.580-1.590: Pyridine, 2,6-dichloro-3-(chloromethyl)- with refractive index n20/D 1.580-1.590 is used in optical material synthesis, where it aids in producing components with precise optical properties.

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    Certification & Compliance
    More Introduction

    Pyridine, 2,6-dichloro-3-(chloromethyl)-: Precision and Performance in Advanced Synthesis

    Experience from the Manufacturing Floor

    Working with chemical building blocks often means looking for high purity, reliable supply, and consistency batch after batch. Pyridine, 2,6-dichloro-3-(chloromethyl)- has become one of the standout solutions in the field of advanced pyridine derivatives. Our facility has pushed through plenty of process refinements to produce this compound at scale—and with tight control over physical properties and impurity profiles. As direct manufacturers, we have handled thousands of kilos of this substance, so each shipment carries our experience in monitoring reaction kinetics, crystallization thresholds, and solvent interference.

    This compound usually appears as a pale yellow crystalline powder, melting around 80 to 83°C. Experienced hands know to expect a pungent, characteristic odor, typical of substituted pyridines carrying a chlorinated side chain. Our chromatographic systems confirm isomer ratios and check for traces of unreacted starting materials, important for downstream users requiring an ultra-clean matrix. Moisture sensitivity is moderate, and we store bulk stock in climate-controlled environments, minimizing degradation and hydrolytic byproducts.

    Chemical Properties and Routine QC

    Most customers examine purity by GC or HPLC. In our lab, every produced lot reaches a minimum of 98% purity, often exceeding this mark when stricter specifications are requested. Color checks under controlled lighting help catch oxidation products, while routine NMR analysis screens for ring substitution errors. The chloromethyl side group is reactive and can introduce complications during storage. As a result, our team runs additional stability tests to confirm shelf life in both small and large packaging formats.

    We have seen that minimizing residual solvents, especially dichloromethane or toluene, helps end-users avoid contamination in sensitive applications. Recrystallization from non-reactive media further sharpens the melting point, which checks thermal stability for transport over long distances. Those using analytical tools like infrared spectroscopy find a strong C-Cl stretch and the distinctive aromatic vibrations, providing a quick confirmation of identity.

    Practical Applications Based on End-User Feedback

    Down the supply chain, pyridine, 2,6-dichloro-3-(chloromethyl)- slots into various industrial syntheses. Most often, it appears as a precursor when synthesizing complex pharmaceuticals, specialty agrochemicals, and performance materials. The chloromethyl group enables straightforward nucleophilic substitutions, making it easy for chemists to build larger and more complicated molecules. We have supported clients optimizing their own yields, offering insight into which solvents or additives work best with this substrate.

    Our customers report strong demand from research labs that value batch traceability and a low impurity profile. Pilot plants experimenting with new ligation reactions rely on the stability of this intermediate. For catalyst developers and fine chemical processors, the precise substitution on the pyridine ring opens doors to structures that would otherwise involve more steps—saving time and reducing byproduct management costs.

    Production Know-How and Equipment Choices

    Scaling the manufacture of pyridine, 2,6-dichloro-3-(chloromethyl)- involves careful selection of chlorination agents. Over-chlorination or site misplacement on the ring can introduce isomeric impurities. Over several years, our team has tuned reaction profiles, stirring speeds, and temperature ramps to stay within narrow limits on the chlorinated positions. Portions of our plant have been retrofitted with closed-loop control systems to keep process variables stable, especially as small changes can lead to trace byproduct formation.

    During chloromethylation, the choice of catalyst determines not only yield but downstream purification effort. Early campaigns used traditional Lewis acid catalysis, only to discover higher-than-expected levels of polysubstituted byproducts. Advances in in-line monitoring with FTIR and continuous feedback from our analytical department led to automation upgrades. Colorimetric endpoint checks, once manual, are now performed with fiber-optic probes, saving time and reducing operator error for each charge.

    Solvent recovery and vapor management have always been priorities. As direct manufacturers, we regularly evaluate both environmental and safety regulations concerning handling chlorinated materials. Recovery units capture nearly all process volatiles before venting, reducing both emissions and raw material costs. In practice, solvent carryover has dropped by over 85% since process modernization, a result highlighted during annual environmental audits.

    Regulatory and Handling Considerations from an Operator’s Perspective

    Every batch of pyridine, 2,6-dichloro-3-(chloromethyl)- leaves our facility with comprehensive product documentation—MSDS, batch analysis, and detailed chain-of-custody. Large-scale users appreciate prompt answers to technical questions, often connecting our plant managers with their own technical personnel. As the compound can irritate skin and mucous membranes, facility design prioritizes closed transfer and dust management. We recommend and supply transfer accessories tailored to the needs of large reactors and automated feed systems.

    High-volume drums are lined to prevent corrosion and product loss. Experience shows that polypropylene and fluoropolymer coatings extend container lifespan, especially in humid climates. For lab and kilo-scale users, our team recommends double-bagging and tamper-evident seals to reduce cross-contamination or product loss during transit. We invest significant effort into training warehouse and logistics partners on how to safely unload and store this compound in shared chemical environments.

    One frequent concern involves transport restrictions for chlorinated organics. We maintain compliance with international hazardous material shipping standards, including secondary containment and limited oxygen exposure where feasible. For sea and air shipments, we calibrate the packaging to resist vibration and thermal cycling. Each logistic route is tested with simulated loads before any large-scale launch, reducing risks of spoilage or regulatory delays en route.

    Comparing to Similar Pyridine Derivatives

    Comparing this molecule to other substituted pyridines, the triple chlorination (positions 2, 3, and 6) offers a unique reactivity window. In practice, compounds like 2,6-dichloropyridine or 3-chloromethylpyridine do not deliver the same breadth of downstream transformations. The three chlorine atoms provide both electron withdrawal and phenyl ring activation, supporting a wide variety of coupling, substitution, and ring fusion reactions in pharma and agrochemical syntheses.

    Other pyridine derivatives might degrade faster under light or air, making shelf life inconsistent. The symmetrical dichloro arrangement in this molecule leads to greater stability during storage. Subtle shifts in melting point and color between derivatives are useful indicators of purity; over the years, we have tracked these differences and shared corrective actions with both formulation and R&D teams.

    In customer applications, selectivity during nucleophilic attack can differ dramatically among chloropyridines. For example, mono-chlorinated variants often react too quickly, generating more side products. Conversely, molecules lacking the chloromethyl group are limited to fewer functionalizations, forcing chemists to carry out extra steps. In our plant, the combination of multiple chlorines and a single reactive methyl group leads to an intermediate that is both versatile and easy to purify at scale.

    Supporting Innovation and Technical Improvements

    Research partnerships have formed a backbone of ongoing improvements for our compound. With feedback from experienced industrial chemists, we tweaked the parent synthesis process to control byproduct levels and enhance yield. Some collaborators found that minor impurities could jeopardize chromatographic separations in later-stage synthesis. In response, our operations team integrated additional purification runs, followed by residual solvent stripping—benchmarking each product lot against prior data.

    We regularly field questions and custom requests from innovative startups and academic labs. Their experiments might need narrowly-defined particle sizes or custom packaging. For these small-scale projects, our engineers configure production runs in dedicated equipment lines, ensuring zero carryover from previous batches. By reviewing process data in real time, the plant can pause, check, and rework any lot that falls shy of user expectations. Direct manufacturer involvement avoids miscommunication and improves troubleshooting speed for special requests.

    Some synthetic pathways demand exceptional thermal stability or lower moisture content. Our process engineers adapted drying protocols and inert gas blanketing to maintain properties like color and reactivity for customers in advanced electronic materials. These adjustments require investment in both equipment and operator training, underscoring the importance of vertical integration for specialty chemicals.

    Working with End Users: Lessons from Real Projects

    Several international partners in agrochemical research approached us to reduce the chloride content in their final actives. As a result, we overhauled purification steps and enabled more precise online monitoring. Their synthesis campaigns reported higher conversion rates, with less downstream washing and fewer waste streams. Pharmaceutical clients running complex, multi-step processes leaned on consistent delivery schedules. By mastering inventory management and just-in-time production, our team minimized the risk of missing a critical delivery window.

    Scientific teams developing new ligands and catalysts sometimes require products with a specific impurity footprint. We invested in additional analytical equipment—high-resolution MS and elemental analyzers—to cater to these requests. This has led to a feedback loop; the more detailed the user’s requirements, the more refined our QC benchmarks grow. As a manufacturer, sharing these technical advances with customers multiplies value along the supply chain and sets new standards for everyone involved.

    In our hands, direct feedback from scale-up chemists is gold. It revealed that byproduct chloroform formation could spike above expected levels at certain pH ranges. The operations team modified feed point addition rates and realigned the base addition sequence, reducing problematic byproduct levels by over 40%. These process improvements did not come from a specification sheet, but from ongoing dialogue and trust between manufacturer and user.

    Challenges and Future Directions

    Handling chlorinated pyridines in bulk exposes both production staff and customers to safety and environmental risks. Regulatory standards tighten each year, pressing manufacturers to rethink trialed-and-true synthetic sequences. In recent years, we have introduced alternative chlorinating agents that improve selectivity and reduce salt waste. Dedicated scrubbers collect off-gassed HCl, and we work alongside local environmental control boards to validate emissions and report transparently on incidents.

    On the product side, there is a push toward ever-purer intermediates with longer shelf lives, tailored specifically for biopharma or semiconductor precursors. Investing in molecular sieves, dehumidification, and improved glass-lining has paid dividends in reduced returns and higher satisfaction rates. For smaller-scale specialty users, flexible packaging and technical support make all the difference. We review purchase and usage data to forecast demand trends—helpful for both internal planning and maintaining raw material stocks in volatile markets.

    Waste stream management remains a constant area of study. Careful selection of neutralizing agents and recapture processes reclaims much of the spent chlorinating media, feeding recovered solvents into approved recycling networks. In lab conversations with institutional users, attention shifts to micro-contaminant control and packaging that resists static buildup. As more clients demand environmental stewardship, the pathway from raw materials to end product continues to evolve.

    Conclusions from the Manufacturing Perspective

    Our years producing pyridine, 2,6-dichloro-3-(chloromethyl)- have underscored the importance of expertise, technical flexibility, and ongoing dialogue with users. The unique substitution pattern on this molecule makes it a favorite among chemists innovating in pharmaceuticals, agrochemicals, and specialty materials. Direct engagement with end-users has driven improvements in purity, storage stability, safety, and analytical support.

    Every lot shipped carries both product value and a wealth of hard-won experience—from reaction optimization through to supply chain and regulatory navigation. Whether supporting high-throughput campaigns or enabling precise academic work, our role as direct manufacturers provides a level of responsiveness and technical depth that traders and brokers cannot replicate. In this way, we see the growth of pyridine, 2,6-dichloro-3-(chloromethyl)- as more than a single chemical product; it is an evolving partnership linking chemical process know-how with real-world innovation.