2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester

    • Product Name: 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester
    • Chemical Name (IUPAC): Dimethyl 4-chloro-2,6-pyridinedicarboxylate
    • CAS No.: 60487-64-5
    • Chemical Formula: C9H7ClNO4
    • 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.
    • CONTACT NOW
    Specifications

    HS Code

    880659

    Chemical Name 2,6-Pyridinedicarboxylic acid, 4-chloro-, dimethyl ester
    Molecular Formula C9H8ClNO4
    Molecular Weight 229.62
    Cas Number 71516-50-4
    Appearance White to off-white solid
    Melting Point 78-80°C
    Solubility Soluble in common organic solvents
    Smiles COC(=O)c1cc(Cl)cc(n1)C(=O)OC
    Inchi InChI=1S/C9H8ClNO4/c1-14-8(12)6-3-5(10)4-7(11-6)9(13)15-2/h3-4H,1-2H3
    Storage Conditions Store in a cool, dry place away from light

    As an accredited 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle, 25g, sealed with a screw cap and tamper-evident seal, labeled with product name, formula, and hazard warnings.
    Container Loading (20′ FCL) Each 20′ FCL container is loaded with securely packed drums or bags of 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester.
    Shipping 2,6-Pyridinedicarboxylic acid, 4-chloro-, dimethyl ester is shipped in tightly sealed containers under dry, cool conditions. It is classified as a chemical substance, requiring labeling according to local and international regulations. Handle with care, use protective equipment, and avoid exposure during transit. Ensure compliance with all applicable shipping and safety guidelines.
    Storage 2,6-Pyridinedicarboxylic acid, 4-chloro-, dimethyl ester should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from incompatible substances such as strong oxidizing agents. Store at room temperature and ensure all containers are clearly labeled. Avoid humidity and moisture exposure to maintain chemical stability.
    Shelf Life Shelf Life: **2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester** is stable for at least 2 years when stored in a cool, dry place.
    Application of 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester

    Purity 99%: 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high conversion rates and minimal impurities.

    Melting Point 114°C: 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester with a melting point of 114°C is used in organic electronics fabrication, where thermal stability during processing is critical.

    Molecular Weight 257.63 g/mol: 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester with a molecular weight of 257.63 g/mol is used in agrochemical formulation, where precise dosing and formulation consistency are achieved.

    Stability Temperature up to 80°C: 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester stable up to 80°C is used in polymer modification processes, where it maintains structural integrity under moderate heat.

    Particle Size <10 microns: 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester with particle size under 10 microns is used in specialty coatings manufacturing, where enhanced dispersion and surface smoothness are obtained.

    Viscosity Grade Low: 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester with low viscosity grade is used in inkjet printing ink development, where smooth flow and precise droplet formation are essential.

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    Certification & Compliance
    More Introduction

    2,6-Pyridinedicarboxylic Acid, 4-Chloro-, Dimethyl Ester: Practical Insights from the Manufacturer’s Bench

    The Character of a Specialty Intermediate

    Inside our reactors, 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester is more than a set of words on a drum label. Producing it asks for experience—real-world adjustments, tweaks in process control, and patience as the molecule forms, dries, and leaves our line ready for the next season of innovations. At its core, this compound provides a solid backbone for downstream chemistry that needs a reliable and reactive scaffold.

    On our production floor, each batch begins with purified raw materials, moved by operators who know their tools and can sense slight changes before instruments even register them. Precision isn’t only about shiny equipment. In our context, it comes down to a careful balance in reaction parameters. Early on, we saw what happens if the chlorination step runs too hot or if the esterification draws moisture from the line. A bad batch wastes valuable solvent, generates waste, and damages schedules. Over time, procedures tighten as teams learn where the pitfalls lie. From years of watching the process, we maintain consistency batch to batch, so end users face fewer surprises when they scale up their own work.

    Assessing the Molecular Structure in Practical Work

    This molecule, with its 4-chloro substitution and two methyl esters linked to a pyridine ring, rarely finds itself in the limelight on a chemistry curriculum. But for synthetic teams and formulation chemists, it bridges a gap—one that plain pyridine dicarboxylates cannot always fill. Chlorine at the 4-position often nudges reactivity in synthetic pathways, unlocking steps that stumble with unsubstituted analogs. In the pharmaceutical and agrochemical sectors, this means modified reaction rates and access to selectivity in coupling or cyclization routes. Those small differences can trim project timelines from weeks to days.

    Over the years, we’ve watched specialty research and commercial formulators work this compound into advanced syntheses. Customers in Japan favor it for heterocycle construction in new crop protection projects; European teams have adopted it for small-molecule library buildouts. In practice, the compound’s handling profile—stable powder or crystalline form, manageable by standard PPE, compatible with straightforward storage—sets it apart from some more volatile or unstable esters. With proper venting and minimal moisture, long shelf life isn’t a guess, it’s routine in our warehouse.

    Quality—and Why Purity Means More Than a Number

    Lab techs and engineers on our team talk about purity in more than just percentages. For 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester, overlooked traces—a chloride leftover, a methyl ester hydrolysate—can jam up downstream reactions. We calibrate our detection not because specs say “99%,” but because a faint odor, an odd melting point, or a minor signal on chromatography points to a risk for our clients’ yields. Many years back, one customer faced a mysterious stalling in their key step—our troubleshooting, looking beyond the printed certificate, led us to a subtle batch contaminant. No client ever told us to dial back that approach.

    On spec sheets from trading houses, “purity” might mean little more than a clean main spot on TLC. For us, it pulls in details: moisture below half a percent, controlled heavy metals, and a watchful eye for byproducts originating from the key chlorination. We run HPLC not only for release but so our clients rarely call with batch complaints. Regular feedback loops with pilot users let us retool purification protocols, sometimes at short notice, so that what leaves our plant fits what their synthesis actually demands. On occasion, we’ve custom-tuned drying cycles or adapted packaging size to avoid clumping or sticking—little details, but ones that come from years filling actual orders, not just buying and reselling.

    Understanding the Application Landscape

    Production chemists who order this ester know it by its impact in a handful of advanced syntheses. For the layperson, its main job is to open doors in pharmaceuticals, crop protection, and specialty materials research. Most often, it serves as a powerful synthon—an intermediate that transfers its substituted pyridine core into new, often patent-protected molecular frameworks. In recent years, requests have trended towards greener, higher-efficiency processes; this means demands on the ester to withstand more robust conditions or to participate in catalytic cycles that older intermediates couldn’t survive.

    We’ve observed a steady shift in downstream innovation. Where older chemistries relied heavily on halogenation at late-stage syntheses, customers are now starting with already-chlorinated intermediates like ours to streamline their line. The presence of two methyl esters opens convenient access to di-acid derivatives under controlled hydrolysis, or directly to amides and anhydrides if handled with care. Some of our long-term partners in medicinal chemistry appreciate the rigid control this scaffold offers, allowing subtle modifications to physical or electronic properties in their lead compounds. Specific reactions—catalytic couplings, selective acylations—often perform better with this intermediate than with less-substituted counterparts.

    There’s no one-size-fits-all formula for how every customer uses the product. Some prefer the fine powder for quick dissolution during batch addition; others request larger crystals to minimize dust in automated feeders. Our front-line staff often adjust granulation mid-production to match these needs—not as a special favor, but because finding the right form can save operators hours of frustration on their own production lines.

    Comparing Against Standard Pyridine Esters and Derivatives

    For teams used to working with plain 2,6-pyridinedicarboxylic acid dimethyl ester, the addition of the 4-chloro group changes the game. Where the unsubstituted ester offers a foundation for general heterocycle synthesis, this chlorinated version enables more selective functionalization, especially in steps that need extra electronic tuning or selective reactivity. The substitution pattern also reduces competing side reactions in several key transformations by stabilizing intermediates during ring-formation steps. Chemists working with more sensitive or expensive starting materials have better risk control by choosing the 4-chloro derivative; it’s a decision reinforced by practical real-world results, not just theoretical papers.

    Beyond that, several customers have remarked on reduced waste burden during their stricter environmental reviews. Less byproduct formation during their custom functionalization steps gets traced straight back to the carefully handled starting material—ours. We don’t make claims about solving every green chemistry challenge, but trends in client manufacturing data confirm the value of a more predictable input.

    Safety and Storage—Grounded in Operation, Not Regulation Alone

    Plenty of regulatory paperwork covers handling, but we’ve learned from practice that real safety comes from training and experience. 2,6-pyridinedicarboxylic acid, 4-chloro-, dimethyl ester stores best in cool, well-sealed containers. In the early days, drums set too close to heat sources or overexposed shelving would lead to caking or, if unlucky, some low-level decomposition—learning from missteps, current protocols enforce separation of sensitive organics away from production lines that see wide swings in humidity or temperature.

    Safety is a culture, not simply a file on a tablet or a posted sign. On-the-job vigilance and an unwillingness to cut corners have kept incident rates low. Over the past decade, we moved from generic PPE approaches to specific measures: splash goggles, nitrile gloves, and fume-ventilated transfer stations. At least once a quarter, operators review spill containment and recovery plans based on actual near-miss reports, not just outsider audits. This way, new hires absorb the operational memory of veteran staff, keeping both the compound and everyone in the building protected.

    Responding to Customer Feedback—An Ongoing Dialogue

    Years spent in direct manufacturing mean every customer voice lands close to our process. One innovation that followed a major client’s comment led us to re-shape our crystalizing tank geometry to avoid carryover from earlier lots—problem batches became a thing of the past. Another time, a repeated customer difficulty with product clumping in humid weather drove us to refine packaging materials and invest in new liner technologies. Our own operations team observed the change in outgoing quality, and customer operators reported less downtime due to feeder blockages.

    If a complaint arrives—“strange color,” “odd melting point,” “reactivity not matching last year’s lot”—our support team traces the full history, from raw goods to batch log. Sometimes we reproduce small-scale samples in our in-house lab to dig into the issue. Real troubleshooting demands patience; sending out a generic reply isn’t an option. Even our best-planned runs sometimes don’t go as expected, and we’ve grown comfortable handling the occasional curve ball directly. This honest loop sharpens quality and earns trust that outlasts project cycles.

    Regulatory Realities and Compliance—Lessons Hard Won

    Regulations keep getting tighter, especially for specialty intermediates like this one. Several years back, we faced a disruptive round of local audits as authorities raised questions sparked by new global data on halogenated organics. Our team didn’t just passively adapt paperwork; direct changes hit our material flow, our waste stream, and sparked investments in emission scrubbing and solvent recovery. The experience taught us that adapting early saves time, money, and reputation. Since then, we track both formal regulatory updates and informal guidance, ensuring product batches flow across borders without interruption or last-minute surprises for users.

    Customers sometimes ask about specific certifications—Halal, Kosher, or ISO. Our approach focuses on process transparency instead of paperwork theater. Site visits and supply chain reviews can see firsthand the traceability and consistency in every batch, guided as much by chemistry as by the real lives of people who depend on that steady output.

    Innovation: Fine-Tuning and Scaling Up

    The push for new process routes doesn’t wait for tradition. Recent years brought calls for solventless options and continuous flow operation on this ester. Adapting to those shifts tightened our own reactor design, swapping out legacy kettle-based setups for modular, closed-vessel options that boost both throughput and safety profiles. Some partners now prefer custom blends or co-crystal formulations; our technical teams tackle these projects as collaborative challenges rather than just quoting a “special order premium.” That hands-on approach yields strong relationships and lessons for new projects.

    We see research around this class of compounds growing toward greener synthesis. Internal trials over the past year focused on reducing solvent burden, not just for the sake of production cost, but also to buffer against tightening waste disposal standards. On one scale-up, we cracked a tricky step in purging low-level chlorine tars, which for years dogged labs with waste and odorous emissions. Small wins like this, rooted in our own plant’s needs, roll out as improvements to every client, whether they’re ordering 10 kilos or hundreds of tons per year.

    From Batch to Barrel: Reliability in Supply

    Not every year brings smooth sailing. Global raw material shortages and freight disruptions force quick moves—switching sources for feedstock, rerouting finished shipments to keep downstream projects on pace. Through it all, our supply outcomes reflect the conviction that reliability doesn’t mean stockpiling, but robust team coordination. Veteran procurement staff know where to look for alternate grades, and our in-house warehouse teams carry the kind of institutional memory that can’t be programmed into an app.

    Customers with demanding schedules talk to actual process managers, not call center scripts. We’ve reshaped packaging—fiber drums, lined bags, larger sacks or single-dose pails—to align with each user plant, not just our own outbound efficiency. Those details surfaced from direct conversations—not from glossy product catalogs. If expedited help is needed, our plant operators coordinate with logistics, often after hours, because relationships in the field carry more weight than contract fine print.

    Looking Ahead—Improvement Driven from the Shop Floor

    With every production run, our team not only makes a specialty ester but also refines the art of process chemistry. Improvements don’t always show up as major innovations; sometimes, it’s a slightly better way to handle dust at the screw feeder. Some changes come from outside—new market requirements, evolving formulations, regulatory moves. But much of our growth comes from what we learn shoulder-to-shoulder, watching the product evolve from a line in a process flow chart to barrels awaiting pickup.

    In recent years, we support more direct technology transfer for clients scaling up their own synthetic routes. Instead of sending out a static datasheet, we share practical insights—how fast a batch dissolves under different pH regimes, or which filtration tricks matter on a new reactor setup. These small fragments of “tribal knowledge” don’t slot neatly into a catalog but make life easier for those who actually use the compound day in and day out.

    Change in this sector means paying attention to both innovation and continuity. As more research groups and manufacturing teams switch to automated, data-driven systems, we keep our edge by pairing that technology with the depth of our experience—solving new problems, but never forgetting what built the foundation all these years.