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HS Code |
512511 |
| Chemical Name | 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester |
| Cas Number | 18947-43-2 |
| Molecular Formula | C7H5Br2NO2 |
| Molecular Weight | 310.93 |
| Appearance | White to off-white solid |
| Smiles | COC(=O)C1=CC(Br)=NC(Br)=C1 |
| Inchi | InChI=1S/C7H5Br2NO2/c1-12-7(11)4-2-6(9)10-5(8)3-4/h2-3H,1H3 |
| Purity | Typically >97% |
| Synonyms | Methyl 2,6-dibromoisonicotinate |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle with a secure cap and labeled with product details and hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL holds 10–12 MT of 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester, packed in 25 kg fiber drums. |
| Shipping | **Shipping Description:** 4-Pyridinecarboxylic acid, 2,6-dibromo-, methyl ester should be shipped in tightly sealed containers, protected from light and moisture. It must comply with applicable hazardous material regulations. Ensure appropriate labeling and documentation. Handle with care, using temperature control if required, and avoid contact with incompatible substances during transport. |
| Storage | 4-Pyridinecarboxylic acid, 2,6-dibromo-, methyl ester should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. Protect from moisture, direct sunlight, and sources of ignition. Store away from incompatible substances, such as strong oxidizers and bases. Label containers clearly, and keep storage area organized to avoid accidental spills or contamination. |
| Shelf Life | Shelf life: Store 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester in a cool, dry place; typically stable for 2 years. |
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Purity 98%: 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester with a purity of 98% is used in pharmaceutical intermediate synthesis, where it enables high yield and consistent product quality. Molecular weight 307.97 g/mol: 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester with a molecular weight of 307.97 g/mol is used in organic synthesis applications, where it provides precise stoichiometric control. Melting point 104-106°C: 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester with a melting point of 104-106°C is used in high-temperature reaction protocols, where it offers thermal stability and improved processing safety. Stability temperature up to 80°C: 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester with stability temperature up to 80°C is used in controlled-temperature manufacturing processes, where it ensures minimal decomposition and reliable performance. Particle size <50 microns: 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester with particle size below 50 microns is used in fine chemical formulation, where it allows for enhanced dispersion and uniform reactivity. |
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Direct experience with the synthesis and handling of 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester reveals its role in advanced chemical research and manufacturing. Chemists and engineers often search for robust building blocks that bring both selectivity and reactivity. Our production team navigates every step in the synthesis of this ester to ensure consistency and purity—a critical factor in the tightly regulated settings where this molecule often sees use.
At the plant-level, the process starts with bromination under monitored conditions to achieve dibromination at the 2- and 6-positions of the pyridine ring. The next stage carefully introduces the methyl ester group through esterification. Each batch comes under strict scrutiny for impurities, such as monobrominated or unreacted starting materials, which could interfere with downstream applications. Our reactors and synthesis lines use glass-lined vessels and corrosion-resistant equipment to prevent contamination, keeping trace metals and unwanted ions at bay.
Unlike simple pyridine carboxylate esters, this molecule incorporates two bromine atoms that expand its utility. Halogenation increases the molecule’s function in cross-coupling reactions—something not possible with unsubstituted methyl esters. Academic and industrial chemists point to the 2,6-dibromo motif as a favored activation point for Suzuki or Stille couplings, paving the way for more complex heterocyclic structures or pharmaceutical targets. In bulk pharmaceutical manufacturing, the combined presence of both the pyridine and brominated carbons means fewer steps in synthesis, reducing reaction times and waste. Fewer steps upstream mean cost savings downstream, especially when scaling up for high-volume production.
Our own analytical lab tests every batch using HPLC and NMR to confirm that methyl 2,6-dibromonicotinate consistently meets purity thresholds above 98%. Moisture content and residual solvents fall below industry tolerances. This sort of attention minimizes unwanted side products in catalytic couplings and downstream transformations. Years of experience confirm that color, melting point, and solubility serve as quick indicators of batch performance—a pale solid, free from yellowing, signals the absence of oxidation side products. Solubility both in polar and weakly nonpolar solvents simplifies purification for end-users, who may require re-crystallization or remove byproducts before further elaboration.
Over years in storage and shipping, we have seen how environmental control influences quality. Secure, sealed containers prevent uptake of moisture and air, which could degrade the ester bond or impact bromine stability. On the production floor, operators handle the material in low humidity zones, keeping caking and hydrolysis at bay. We favor solid crystalline storage over liquid dispersion because the compound travels better, resists hydrolysis, and holds up to seasonal temperature changes in global transit. Once opened, this ester holds its integrity best when tightly resealed and stored below room temperature, reducing hydrolysis that can occur in exposed, high-humidity conditions.
Some manufacturers offer mono-brominated or unsubstituted pyridinecarboxylate esters. Our plant engineers see the drawbacks firsthand when clients pursue syntheses requiring further bromination—the risk of regioisomeric mixtures or unintended dibromination climbs sharply and wastes precious production hours in downstream purification. The direct route to the dibromo-methyl ester outpaces competing approaches in yield and reproducibility.
Certain clients in agrochemical discovery once sourced similar esters with fewer bromines, only to request our dibromo derivative after finding the mono-variant too unreactive in key palladium-catalyzed steps. Others point to methyl esters of unrelated acids with similar molecular weights but lacking the electron-deficient pyridine ring. Those products often fail to match the same breadth of reactivity or versatility in ligand design.
Buyers approach with wide-ranging objectives. The most frequent projects use this ester as a substrate or precursor in the synthesis of multi-ring scaffolds, active pharmaceutical ingredients, or specialty chemicals for advanced materials. Medicinal chemists leverage its selective reactivity to build libraries of heterocycles; it offers a gateway into new molecular territories by providing not just a handle for metal-catalyzed cross-coupling, but also an avenue for further functionalization at strategic points on the ring.
On our end, knowledge of downstream goals allows us to tailor production in subtle ways—batch size, solvent system, and particle size distribution respond to the needs of high-purity research or bulk synthesis operations. For example, certain large buyers developing kinase inhibitors value the clean, narrow melting point range and homogeneous crystal habit. This means fewer complications during upscaling or integration into automated reaction platforms.
Chemists sometimes theorize about perfect yields or ideal reactant conversions, but plant operators face real-world constraints. Not every run proceeds as planned; controlling the bromination step requires close monitoring to avoid excessive oxidation or over-bromination. Over the years, we’ve invested in real-time spectroscopic monitoring and process automation to respond quickly if a batch deviates from target specs. That vigilance helps maintain long-term supply agreements with clients, especially those in regulated industries where consistency matters more than speed.
Batch records confirm the tightest control occurs at the final recrystallization. This stage removes colored impurities and small molecule by-products not always caught by routine tests. Technicians who work hands-on with the product every day recognize differences in crystal size and color that a robotic system might overlook—an important touchpoint for safeguarding product quality before it leaves the plant.
Feedback from clients in Europe and North America shaped our traceability protocols. Each production lot carries not just batch records, but analytical data tied directly to the manufacturing date and exact source of raw materials. Regulatory auditors, especially those from pharmaceutical firms, ask tough questions about cross-contamination controls or process validation. Answering those questions starts with rigorous vendor evaluation and raw material inspection—by the time our 2,6-dibromo-methyl ester ships, there’s a clear line of sight from production to shipping container. Customers operating under GMP requirements have found value in both the documentation and the reliability found in our outbound shipments.
Over time, increased scrutiny surrounds use and disposal of halogenated intermediates. We manage waste streams at source, separate residual organics from aqueous effluents, and employ on-site neutralization before discharge. These routines prevent brominated by-products from contaminating groundwater or soil—an essential practice in any region with strict environmental oversight. Plant operators receive regular training on safe handling and emergency protocols. Making these investments lowers risk not just for staff working hands-on, but for the communities around our production site.
Stakeholders further up the chain sometimes overlook the hazards of pyridine derivatives or organobromine compounds. From the manufacturer's viewpoint, continuous staff education covers both accidental exposure and emergency containment, tailored to the unique volatility and toxicity profile of this ester. Our safety audits occasionally lead to adjustments in production layout or improved PPE standards, always reflecting lessons learned directly on the plant floor rather than distant office policy.
A few years ago, increased demand for custom derivatives triggered a significant shift toward continuous flow synthesis. Small-scale batch models struggled to keep up; bottlenecks appeared wherever process cooling or transfer rates failed to meet rising needs. By reconfiguring part of the synthesis to a flow setup, the team reduced heat build-up, improved reactant mixing, and shrank the production timelines for kilo-scale and multi-ton orders alike. Clients running rapid exploratory chemistry, particularly in biotech, noted the resulting drop in lead times.
This flow approach allows incremental adjustments. Technicians can dial in temperature and pressure with more precision, responding to shifts in feedstock quality or targeted end-use specs. Instead of lengthy scale-up delays, new production campaigns build directly off established flow modules, keeping client project timelines on track. These upgrades put our intermediates ahead of competitors using legacy batch models prone to re-work or inconsistent batch properties.
Research teams sometimes request related esters or alternate halogenation patterns. Drawing on our manufacturing experience, we recognize the real chemical limits—some positions on the pyridine ring resist substitution, or certain esters hydrolyze faster than methyl derivatives, reducing shelf life or raising storage costs. By sharing actual stability data, including rates of hydrolysis under varying pH and temperature, we help clients make informed decisions before committing to new derivatives.
On occasion, a buyer weighs using ethyl or tert-butyl esters, hoping for tuned reactivity or improved volatilization properties. Experience shows methyl esters hit the sweet spot for most processes: they dissolve readily in both polar aprotic solvents and organic phases, and saponify predictably under mild alkaline conditions. The dibromo variant preserves the ring’s reactivity, and methylation avoids the steric hindrance larger esters sometimes create in cross-coupling or amidation reactions. Sharing this comparative data saves time and project funds for research teams that otherwise might pursue impractical syntheses.
On the other side of our shipping dock, customers often cite the effect of intermediate purity on final API or agrochemical yield. Small differences in residual bromine or unintended isomers ripple through later synthetic steps, affecting crystallization behavior or biological assay results. By prioritizing consistent control at the esterification and bromination steps, we support higher throughput and more reliable outcomes for the next users in the value chain. Clients scaling up to pilot or full production report smoother workflow integration, with fewer surprises at QA or stability testing.
Greater predictability in the behavior of our 2,6-dibromo methyl ester also supports automated reaction optimization—reliable physical and analytical properties mean fewer re-tests or failed reactions when employed in high-throughput screening or combinatorial synthesis. For project engineers setting up automated lines, small details in how the intermediate dissolves, handles temperature, or resists oxidation make all the difference in keeping timelines and budgets on track.
Recent years brought supply shocks and price swings across the brominated intermediates market. Slowdowns in upstream bromine production or changes in export policy ripple through supply chains, putting just-in-time inventory strategies under stress. Plant managers see the effects firsthand—secure access to bromination agents, reliable transport, and proactive procurement all play a role in insulating production from global volatility.
Keeping open channels with trusted suppliers supports just-in-time flexibility, avoiding excessive inventory that can lead to unwanted degradation or out-of-spec material. At the plant, we track shipment timelines, weather patterns, and geopolitical developments that could delay critical inputs. These precautions ensure customers find available, high-quality intermediates even when the global landscape shifts quickly. Plant teams anticipate demand spikes, pre-qualify backup raw material suppliers, and build up buffer stock ahead of forecasted market tightness. The result: fewer disruptions and sustained product quality through turbulent periods.
Ongoing training and process optimization drive each improvement in our offering. Staff at the line level get involved in lean process reviews, suggesting refinements from the perspective of daily use. Adoption of real-time data monitoring feeds back into the system, catching minor abnormalities early before they become costly quality deviations. Maintenance schedules integrate operator input, and equipment purchases reflect firsthand knowledge about what keeps the synthesis and purification lines running.
Using new instrumentation, our lab can now detect minor impurities as soon as they appear, long before they could compromise a batch. Integrated data management simplifies sharing certification and traceability with clients, reassures regulators, and supports quick response should a recall ever become necessary. These efforts reflect not remote policy but the cumulative wisdom of the people who work every day with 4-pyridinecarboxylic acid, 2,6-dibromo-, methyl ester.
Working directly with this molecule for years, we see every batch, every challenge, every customer outcome. By controlling quality, investing in people and technology, and staying transparent with the market, we build more than just an intermediate. This hands-on commitment gives our partners assurance they’re sourcing a reliable, high-performing ester, supported not by paperwork alone, but by real-world experience from synthesis to shipment. Every improvement our team makes flows directly to the buyer, supporting successful outcomes in advanced chemical manufacturing, research, and beyond.