2-(chloromethyl)-3,4-dimethoxypyridine HCl

    • Product Name: 2-(chloromethyl)-3,4-dimethoxypyridine HCl
    • Chemical Name (IUPAC): 2-(chloromethyl)-3,4-dimethoxypyridine hydrochloride
    • CAS No.: 866156-36-1
    • Chemical Formula: C8H11Cl2NO2
    • 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

    397397

    Product Name 2-(chloromethyl)-3,4-dimethoxypyridine HCl
    Chemical Formula C8H11Cl2NO2
    Molecular Weight 224.09 g/mol
    Cas Number 146137-55-5
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in water and polar organic solvents
    Storage Temperature 2-8°C (refrigerated)
    Sensitivity Moisture sensitive
    Smiles COC1=C(N=CC(Cl)C1)OC

    As an accredited 2-(chloromethyl)-3,4-dimethoxypyridine HCl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5g sample of **2-(chloromethyl)-3,4-dimethoxypyridine HCl** is provided in a sealed amber glass bottle with labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 10MT packed in 25kg fiber drums, lined with double polyethylene bags, safely secured for chemical transport.
    Shipping 2-(Chloromethyl)-3,4-dimethoxypyridine HCl is shipped securely in airtight, chemical-resistant containers to prevent moisture and contamination. Packaging adheres to regulatory guidelines for hazardous materials. Clearly labeled for identification and hazard information, it is transported under controlled conditions to ensure safety and chemical stability during transit.
    Storage 2-(Chloromethyl)-3,4-dimethoxypyridine HCl should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong oxidizing agents. Protect from light and avoid exposure to heat. Use appropriate gloves and safety goggles when handling, and ensure that storage complies with all relevant chemical safety regulations.
    Shelf Life The shelf life of 2-(chloromethyl)-3,4-dimethoxypyridine HCl is typically 2 years when stored in a cool, dry place.
    Application of 2-(chloromethyl)-3,4-dimethoxypyridine HCl

    Purity 98%: 2-(chloromethyl)-3,4-dimethoxypyridine HCl with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal yield and minimized by-product formation.

    Melting Point 193–196°C: 2-(chloromethyl)-3,4-dimethoxypyridine HCl featuring a melting point of 193–196°C is used in custom organic synthesis, where precise thermal properties lead to controlled reaction conditions.

    Moisture Content <0.5%: 2-(chloromethyl)-3,4-dimethoxypyridine HCl with moisture content less than 0.5% is used in medicinal chemistry research, where low water content prevents unwanted hydrolysis and degradation.

    Particle Size <50 µm: 2-(chloromethyl)-3,4-dimethoxypyridine HCl with particle size below 50 micrometers is used in catalyst development, where fine particle distribution promotes improved reactivity.

    Stability Temperature up to 60°C: 2-(chloromethyl)-3,4-dimethoxypyridine HCl stable up to 60°C is used in high-throughput screening, where thermal stability allows consistent sample handling.

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    Certification & Compliance
    More Introduction

    2-(chloromethyl)-3,4-dimethoxypyridine HCl: A Reliable Choice for Modern Chemistry

    Understanding What We Make

    Every day on the production floor, 2-(chloromethyl)-3,4-dimethoxypyridine hydrochloride stands out as more than a mouthful to pronounce—it's a specialized building block for researchers and process chemists who care about high-value synthesis. This isn’t a simple raw material. The compound steps into the hands of our partners, finding a place in the foundation of pharmaceutical development, agrochemical efforts, and advanced organic synthesis. People working in these fields count on the product’s reliability, which reflects months of hands-on research and disciplined process refinement.

    What Sets this Compound Apart

    Competition among intermediates in the pyridine family is intense. Many times, engineers seek modifications on the pyridine nucleus because of its versatility for functionalization. Our 2-(chloromethyl)-3,4-dimethoxypyridine HCl brings a chloromethyl group at the 2-position plus two methoxy groups at the 3 and 4 positions. By offering this exact substitution, it carves out pathways that more generic pyridine derivatives can’t fill. In more familiar chemistry, the methoxy groups influence electronic effects, helping improve selectivity and reactivity in coupling reactions. Meanwhile, the hydrochloride form increases shelf stability compared to the neutral base, helping with storage over longer project timelines.

    Many similar products wind up hampered by inconsistent reactivity or instability, especially outside controlled environments. Our years of experience dealing with the quirks of pyridine reagents taught us where impurities lurk and which process steps are most vulnerable to small errors. Lab-scale batches rarely tell the whole story. Each run at production scale means checking, not just for purity, but for batch-to-batch consistency and manageable handling—success here means fewer surprises for users downstream. Engineers and chemists striking at complex syntheses relying on this intermediate expect every bottle to work like the last. Achieving this outcome has pushed us to refine handling and purification setups that suit this molecule’s nature, especially during solid isolation and drying.

    Serving Real-World Applications

    Process chemists in drug discovery recognize the impact a reliable supply of reactive intermediates brings to the table. The chloromethyl group on this molecule provides a ready handle for substitution reactions—alkylation, nucleophilic attacks, and more. Such routes help construct more complicated heterocyclic frameworks in new drug candidates. Hundreds of benchtop routes can be traced back to a dependable source of this compound. Run-of-the-mill substitutes can’t always match its performance. Under pressure to save time, chemists fall back on options they know will behave as published, so confidence in the source matters.

    Some researchers working on crop protection have found the unique structure of this pyridine derivative lets them build more complex molecules with less risk of side reactions. Not all competitors provide material that stands up to demanding process screens. Unwanted isomer formation, contamination, or moisture uptake during storage can sideline months of effort. Here, a tight grip on particle control, water content, and residual solvents complements analytical data. Our crew found, by monitoring production and keeping a close eye on reaction profiles, tighter control gave us a consistent edge.

    Downstream Chemistry and Structural Merits

    From a synthetic standpoint, the dual methoxy substitution offers an electron-donating punch that tunes reactivity for both nucleophilic and electrophilic chemistry. Many researchers focusing on structure-activity relationships seek out derivatives like this precisely for the subtle—but significant—influence on the final activity profile of drug or material candidates. Years ago, we received feedback on the headaches caused by batch variability from generic suppliers. Once we recognized how minor shifts in process conditions could change impurity profiles, our team doubled down on analytical control and in-process monitoring.

    Our approach to 2-(chloromethyl)-3,4-dimethoxypyridine HCl does not depend on shortcuts. There’s no substitute for a clean, sharp batch at the start of a multistep campaign. We designed our operation so finished lots show high purity as measured by HPLC, controlled water content, and rugged packaging to protect against light and moisture. Feedback loops between lab and production let us tackle anomaly batches fast—trace byproducts stem entirely from raw material shifts or changes in filtration sequence. Fixes are built on data, not guesswork, with every gram supporting a project in motion.

    The Role of Analytical Data and Traceability

    Our entire line leans on traceable records and robust batch data. Customers ask about reproducibility, and we ground every shipment in clear chromatography, mass spec data, and moisture analysis. It’s tempting to overlook the unglamorous tracking work behind the scenes. In reality, robust documentation helps rapid troubleshooting when challenges arise—even years after the batch ships out. The value of this information system becomes clear when a unique use case crops up or supply chains stretch over continents. Consistency begins at raw material intake and stretches all the way to the bottle in the customer’s hands.

    The hydrochloride salt form also improves handling: compared to its free base, users see less clumping, more predictable solubility, and reduced volatility. This practical difference has proved important for partners scaling up—especially those who need reproducible dosing for long campaigns. Material flow, storage, and shelf-life feed directly into project risk calculations. Engineers here have spent the time studying how the salt responds to open air, ambient moisture, and mild heating. Our difficulties with earlier generations of packaging—losses from caking, or partial deliquescence under humid warehouse conditions—forced new investments in vacuum-sealed packaging and humidity indicators. Lessons stick when every investment directly impacts a customer’s project timeline.

    Methods Developed from Hands-On Experience

    Time on the production line, with all the real-life wrinkles it brings, has shaped the current process for this product. In the early years, we ran into regular roadblocks—batch scale-ups failed, minor changes in stirrer speed or temperature caused purity to slip. Clean-up steps after synthesis left tiny residues that spoiled downstream chemistry for clients, and solvent choice for crystallization changed recovery rates by more than a little. We started aggressive root-cause tracking, comparing every successful batch to less successful ones. Eventually, the most reliable route leaned on slightly lower cooling rates post-reaction and double recrystallization from ethanol and ether when purity standards demanded it.

    Maintaining high chemical yield and purity relies on more than standard operating procedures. A seasoned crew paying attention to daily reports matters just as much. Our operators put in the sweat and vigilance, catching shifts in viscosity or reaction color early. Over time, this hands-on vigilance has become a habit that echoes through the finished product line. Ultimately, we found direct communication with end users drew the clearest picture of what counts in daily applications—and what problems feel like under a tight timeline.

    Comparing with Other Pyridine Intermediates

    Not every pyridine-based intermediate delivers the distinct profile offered here. Simple 2-chloromethylpyridine hydrochloride, lacking the twin methoxy groups, cannot provide the same electron-rich environment. Alternative substitutions may stabilize or destabilize other molecular regions, but only this particular structure creates a balance between reactivity and stability sought by many medicinal and agrochemical chemists. We’ve spent years comparing our results against similar products from global markets, tracking both yield and selectivity in complex end-stage synthesis.

    Some commercial alternatives aim for broader utility, offering more generic substitution. That approach widens the field but sacrifices process specificity—side reactions, reduced selectivity, or even awkward shelf life. Our years of supply show that a tighter target, with high purity and limited side-products, benefits scale-up partners who value time over one-size-fits-all versatility. We regularly see customers return after failed runs with off-the-shelf intermediates, seeking out this exact product because it solves real-world scale-up pain points.

    Reliability Born from Real-World Stress Testing

    Decades of feedback and long-term trends drive us to revise and strengthen our manufacturing standards. We once supplied a large volume batch to a high-throughput screening group that ran into precipitation issues during dissolution. Digging into retained samples, we tied the cause to a minor impurity buildup not visible by routine thin-layer chromatography. This experience led directly to process adjustments—new column protocols, stricter solvent cutoffs, and more frequent in-process checks. Documentation backed every fix, laying down a record that still supports quality audits today.

    Trace elements, packing density, and chloride content now face tight monitoring, and the team meets frequently to review complaints, near-misses, and off-spec queries. This control culture has cemented trust. Partners know what reaches them is not only certified by lab data but backed by the daily discipline of skilled workers—people who measure progress by real impact, not just completed checklists. Several colleagues here have been at it for decades; their know-how gets passed on to new hires, building resilience against both familiar and new manufacturing risks.

    Addressing Customer Pain Points

    Chemical manufacturers sometimes lose sight of customers’ day-to-day battles—unexpected quality drops, hard-to-handle product forms, or obscure documentation breakdowns. Our clients often describe how a single mishap in intermediate quality can threaten timelines and budgets. Close feedback channels have pointed us toward faster documentation, standardized packing options, and straightforward shipping preparation. If something goes wrong, rapid traceability lets us provide replacement material or answer auditors’ questions without stalling the end-user’s work.

    Practical details—like keeping residual moisture in check, ensuring crystalline flow, or simply providing clear lot traceability—depend on steady investment in process and people. Years ago, some teams approached us frustrated with other batches that absorbed moisture so quickly they became difficult to weigh. After dedicating repeated runs to optimizing drying conditions and moisture barrier packaging, we heard concerns vanish. Every lesson like this reinforces the value of attention to basics; shortcuts with intermediates catch everyone out, sooner or later.

    Building Better Solutions for Tomorrow

    This compound’s development tells a story of adaptation, practical learning, and ongoing problem-solving. Every improvement evolved out of direct partnership with users—bench chemists, scale-up engineers, and procurement leaders. The ongoing challenge rests in raising purity, reducing batch-to-batch drift, and anticipating new requirements as downstream chemistry advances. Occasionally, a partner proposes unique application conditions or more stringent environmental controls; our willingness to trial these ideas and adopt new procedures helps set our team apart.

    Continuous investment in analytical equipment lets us tackle new impurities as soon as they crop up, and our team regularly reviews emerging literature to keep production standards a step ahead. As demands shift—whether for higher reaction selectivity, greener solvents, or tougher shelf life—we adapt equipment, rewrite batch records, and, when useful, adjust raw material procurement. The result: a production ecosystem built to meet today’s expected outcomes and tomorrow’s surprises.

    Supporting Advanced Synthesis and Research Progress

    The progress made possible by this intermediate reflects the larger ambitions of the research sectors we serve. Scientists and engineers need to trust the materials they handle so that their own results stand up to scrutiny. Many of our partners pursue tight timelines, rigorous development pathways, and the need for regulatory precision. Our approach is practical, shaped by decades of shared lessons. We understand that no two campaigns are exactly alike, and each order could support anything from a speculative new target in oncology to the next generation of sustainable crop protection agents.

    By putting effort into batch reliability, documentation integrity, and customer support systems, we provide more than a molecule—we enable the smooth progress of research and process development that advances both health and industrial progress. Our workers take pride in the role, knowing each shift contributes to a larger purpose in the scientific community. By cultivating a deep understanding of what works, and why it matters, we build partnerships that last beyond a single project or campaign.

    Driving Standards, Not Just Making Molecules

    We thrive at the intersection where process reliability meets the high standards of our customers. Years of practical learning shaped the 2-(chloromethyl)-3,4-dimethoxypyridine HCl we make today. There’s always room to push further—tighter margins on purity, improved packaging for longer-distance shipments, better adaptability for new forms of synthesis. The process never truly finishes, and every shipment reflects ongoing dedication to scientific progress, safe handling, and predictable results.

    Advances in analytical technology and tighter feedback cycles from clients mean we catch problems earlier, adapt production strategies faster, and set higher standards for every incoming lot. The path forward runs through continued collaboration with users and a close reading of what researchers demand from their most critical intermediates. The legacy of reliable chemistry builds not from grand pronouncements, but through a thousand practical improvements. That’s what keeps this product relevant in a continually advancing field, and what shapes our future work every day.