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HS Code |
603453 |
| Chemical Name | methyl 3-bromopyridine-4-carboxylate |
| Cas Number | 142137-99-5 |
| Molecular Formula | C7H6BrNO2 |
| Molecular Weight | 216.03 |
| Appearance | light yellow to brown solid |
| Melting Point | 57-61°C |
| Boiling Point | 325.6°C at 760 mmHg |
| Density | 1.6 g/cm3 |
| Solubility | soluble in organic solvents (e.g., DMSO, ethanol) |
| Smiles | COC(=O)C1=CN=CC(=C1)Br |
| Inchi | InChI=1S/C7H6BrNO2/c1-11-7(10)5-2-3-9-4-6(5)8/h2-4H,1H3 |
| Refractive Index | 1.596 |
| Storage Conditions | store in a cool, dry place, tightly sealed |
| Flash Point | 151.6°C |
As an accredited methyl 3-bromopyridine-4-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Methyl 3-bromopyridine-4-carboxylate, 5g: Supplied in a sealed, amber glass bottle with tamper-evident cap and safety labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed 20-foot full container load of methyl 3-bromopyridine-4-carboxylate, compliant with chemical shipping regulations. |
| Shipping | Methyl 3-bromopyridine-4-carboxylate is shipped in accordance with applicable chemical safety regulations. It is securely packed in sealed containers to prevent leaks and contamination. The packaging includes appropriate labeling with hazard information. Shipment is typically made via ground or air transport, accompanied by safety data sheets and documentation for safe handling and delivery. |
| Storage | Store methyl 3-bromopyridine-4-carboxylate in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep it separate from incompatible substances such as strong oxidizing agents. Recommended storage temperature is typically room temperature (15–25°C). Ensure proper labeling, and avoid exposure to moisture. Handle under an inert atmosphere if the compound is moisture-sensitive. |
| Shelf Life | Shelf life of methyl 3-bromopyridine-4-carboxylate is typically 2 years, if stored tightly sealed, cool, and protected from light. |
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Purity 98%: Methyl 3-bromopyridine-4-carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and minimal byproduct formation. Molecular weight 230.02 g/mol: Methyl 3-bromopyridine-4-carboxylate with molecular weight 230.02 g/mol is used in agrochemical research, where it enables precise formulation and compound consistency. Melting point 55–58°C: Methyl 3-bromopyridine-4-carboxylate with a melting point of 55–58°C is used in solid-phase synthesis, where it facilitates controlled processing and storage stability. Stability temperature up to 120°C: Methyl 3-bromopyridine-4-carboxylate with stability temperature up to 120°C is used in chemical process development, where it allows thermally robust reaction conditions. Particle size < 50 microns: Methyl 3-bromopyridine-4-carboxylate with particle size below 50 microns is used in formulation science, where it improves dispersion and uniformity in reaction mixtures. Viscosity grade standard: Methyl 3-bromopyridine-4-carboxylate with standard viscosity grade is used in fine chemical manufacturing, where it enables uniform mixing and enhanced process control. |
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In the dynamic world of specialty chemicals, methyl 3-bromopyridine-4-carboxylate carves out its own important place. As a chemical manufacturer with a history of producing pyridine derivatives, seeing patterns and shifts in demand offers valuable insight into what matters to chemists and production managers downstream. This compound bridges lab innovation with actual, scalable results in pharmaceutical, agrochemical, and fine chemical research and synthesis.
Model numbers and grades are much more than catalog entries here. For methyl 3-bromopyridine-4-carboxylate, purity and trace impurity control shape each batch’s success. We track every lot as it moves from raw pyridine stocks to the methyl ester end-product. Assays above 99% are standard, but getting residual solvents—especially polar traces—below the detection limit can push production timelines or force rework. These are real-world pressures, not just claims. In practical handling, this compound emerges as an off-white to pale yellow crystalline powder, boiling between 150-160°C at reduced pressures. Moisture sensitivity requires regular monitoring. Packaging in sealed drums lined with poly bags preserves material from ambient humidity and possible air oxidation, which is critical over long-haul shipping or storage in fluctuating climates.
Each specification sheet we provide gets corroborated by in-house NMR, GC-MS, and HPLC, not just spot-checked but scrutinized for evidence of process efficiency or drift. Customers working in scale-up appreciate seeing chromatographic clarity, because it hints at fewer downstream headaches. Even at small scales, trace impurities alter NMR interpretation or lead to lower overall yields. Chemical buyers have learned to look for more than a simple purity guarantee—a comprehensive production record supports every drum.
In the field, methyl 3-bromopyridine-4-carboxylate lives up to its reputation for versatility. Medicinal chemists rely on the electron-deficient bromine at the 3-position and the ester group at the 4-position to unlock a toolbox of transformations. Suzuki and Buchwald-type couplings work with this structure, supporting the synthesis of more elaborate heterocycles or pharmaceutical intermediates. Nucleophilic aromatic substitution opens doors for libraries of analogs, which medicinal chemistry teams need for SAR studies.
Pharmaceutical manufacturers look beyond the lab demonstration. Robustness counts: how does the product perform in kilo-scale batches, not just during single test reactions? The methyl ester resists saponification under mild handling, but aggressive bases can hydrolyze it readily for carboxylic acid production. The bromine’s reactivity allows for palladium-catalyzed cross-couplings both in batch and in flow chemistry settings—a feature process engineers evaluate during pilot runs. Quick dissolution and non-clumping properties—factors manufacturers can control through drying and screening—save time at charging steps.
Intermediate scale buyers, such as contract research organizations, find the clean profile valuable for direct application. Preparing libraries of pyridine derivatives for biological screening, researchers avoid losses from challenging purification steps. For agricultural innovation teams developing new crop protection molecules, the electron-withdrawing bromine center provides functional diversity when designing lead optimizations. Reaction sequence planning becomes more efficient when the precursor performs predictably, without reveal of unexpected byproducts.
In competitive chemical spaces, there’s no substitute for first-hand experience with how a product behaves under real factory or lab conditions. Over years of feedback from both R&D teams and full-scale production users, several practical differences stand out when comparing methyl 3-bromopyridine-4-carboxylate to related compounds such as methyl 2-bromopyridine-4-carboxylate, 2-chloro-4-pyridinecarboxylic acid methyl ester, or simple pyridine esters.
Reactivity profile sits at the forefront. The 3-position bromine directs regioselective coupling possibilities that aren't available with 2-substituted pyridines. Most practical chemical documentation will show that the reactivity window for the 3-bromo compound enables milder conditions in some palladium-catalyzed cross-couplings. Side reactions, such as unwanted homocoupling or oligomerization, occur less frequently due to improved substrate control. For industrial process chemists, predictable reactivity reduces both troubleshooting and raw material costs, especially when scaling up from gram benchwork to hundreds of kilograms.
Handling properties form another, subtler point of differentiation. Some analogs, particularly those with ortho-substitution or free acids rather than esters, bring issues like deliquescence or dusting during transfer. Our team’s own experience running long multi-step syntheses tells us that the combination of methyl ester and 3-bromo configuration fixes most of the micro-scale handling headaches. The powder holds together well during pneumatic transport or bag dumping, and doesn’t cake after weeks in unconditioned storage. These points, while not apparent on a datasheet, regularly show up in customer feedback and site audits.
From a sustainability point of view, more selective downstream coupling yields equate to less chemical waste and easier solvent recovery. This can take a load off effluent treatment and align better with tightening environmental controls in regions moving toward green chemistry frameworks. This particular bromopyridine ester fits high-throughput digital planning as well: the NMR clarity and LC profile support machine learning-driven synthesis planning, which matters to teams working at the leading edge of automated chemistry today.
From a manufacturer’s perspective, the journey to high-quality methyl 3-bromopyridine-4-carboxylate rarely follows a perfectly linear workflow. The raw material sourcing for building the pyridine core matters deeply—contaminated or aged pyridine starting material leads to color-forming side reactions, which create downstream purification bottlenecks. Direct bromination instead of indirect pathways streamlines our batch cycle, especially when tuning the process for maximum selectivity at the 3-position. Bromine handling on an industrial scale always brings strict safety and containment protocols to the forefront. Maintaining process integrity, even at high loadings, builds more consistent output.
Solvent selection and drying sequences also shape the everyday realities in plant operations. A poorly selected extraction solvent traps impurities, making downstream flash chromatography uneconomical at production quantities. The methylation step, if uncontrolled, risks generating di- or tri-substituted byproducts that lower overall yield and challenge product isolation. Our plant has learned from early runs that post-reaction filtration and low-temperature crystallization pull much cleaner product than direct distillation. These refinements don’t just help us—they create value for customers who stake timelines on reliable supply without drifting batch quality.
For every large batch, extensive in-process monitoring confirms that bromination runs to completion and forwards only the 3-substituted isomer. Purity and physical form audits before release prevent any excess fines, oversized crystals, or bulk solidification that could create dosing problems for high-precision metering. Feedback loops with trusted users regularly reveal subtle improvements—granule size tweaks that speed up dissolution, or pelletized forms that work better in automated weighing systems for research departments. Even small gains in process efficiency or product usability compound over multiple production cycles.
Laboratory testing for stability stands as standard protocol, but walking the actual warehouse aisles and seeing stored drums tells the real story. Methyl 3-bromopyridine-4-carboxylate remains stable for over twelve months in our controlled inventory, but even short exposures to moist air can change appearance or trick lead chemists into worrying about batch integrity. Prompt transfer into sealed packaging under inert atmospheres, along with fast shipping, helps maintain the unadulterated powder state required for most sensitive synthesis applications.
Regular retesting cycles catch any edge-case degradation or contamination before dispatch. This is more than a ‘tick the box’ compliance — returned or slow-moving stock always cycles through retesting before reapproval. Mirroring end-user storage conditions at our own facility leads to confidence in field performance, especially for global buyers seeing seasonally-induced warehouse temperature swings. Few things can disrupt a production run like a powder that won’t dissolve or reacts unexpectedly due to trace contaminant pickup in transit.
Real stories from formulation specialists echo these concerns: missed stability data translates to lost time, wasted resources, and unwanted solvent washes at scale. Expiry dates on outgoing lots aren’t just cosmetic; they reflect genuine, observed shelf-life under warehouse, sea transit, and operational conditions.
From high-throughput drug discovery campaigns to pilot plant validations, methyl 3-bromopyridine-4-carboxylate connects concept with reality. Its chemical stability under typical bench conditions and amenability to a broad range of coupling and substitution reactions mean both exploratory researchers and full-scale plant chemists use it with confidence. Our own process chemists have put it through continuous flow platforms, high-speed batch runs, and even microwave-assisted reactions; in each context, the compound remains manageable and predictable.
Medicinal chemistry teams embrace its versatility. Lead discovery efforts often depend on introducing fine-tuned substituents to the pyridine core, and the 3-bromo, 4-carboxylate motif provides reliable access to a diverse set of functionalized analogs. Either direct functionalization or stepwise transformations through the ester or bromo positions expand the available chemical space. Fine chemical R&D benefits from ease of introducing further elaborations—amide couplings, ester hydrolysis, nitrogen displacement—without complex protection/deprotection sequences.
Process development engineers analyze scalability, separating compounds based on isolation efficiency and downstream compatibility. Handling behavior during bulk packaging relates directly to time wasted on unplanned dissolving or cleaning steps. For those supporting continuous manufacturing—an emerging industry requirement—predictable melting point and absence of low-boiling impurities minimize fouling of process lines or crystallizer blocks.
Real-world chemical manufacturing faces unexpected hurdles, and methyl 3-bromopyridine-4-carboxylate production teaches hard lessons alongside breakthroughs. Impurity control sometimes heads off course with changes in precursor lots; calibrating bromine delivery so that substitution occurs cleanly at the 3-position demands regular process reevaluation. Several initial pilot runs gave lower-than-target yields until adjustments in temperature control and agitation routines established reproducible outcomes.
Handling and worker safety are never abstractions. Bromine chemistry requires protective gear and containment standards. Our process engineering teams have spent years automating hazardous steps to protect operators without sacrificing throughput. Even seemingly small changes—like switching drum liners to higher-integrity barrier films—came directly from feedback after a batch transit mishap resulted in off-color powder at arrival.
Sustainability pressures from regulators and end-users alike press manufacturers for leaner, less wasteful syntheses. Improving bromination selectivity and recycling process water are regular projects for plant managers, who balance compliance with rising input costs and customer sustainability audits. This product, due to its consistent conversion and low off-cuts, already outperforms many legacy pyridine intermediates on several green metrics, but there’s no finish line in process optimization.
On occasion, sudden swings in demand for specialty pharmaceuticals create supply chain strain. Lead times stretch, and robust relationships between manufacturer and customer matter more than published stock lists. Over years, it's been clear: open channels, clear technical disclosure, and honest feedback about what’s possible—and what isn’t—protect production schedules for both sides. In specialty chemicals, no amount of templated guarantee replaces daily QA checks or the simple experience of walking the production floor.
Looking back on years of supplying methyl 3-bromopyridine-4-carboxylate, practical lessons shape our confidence in the product and its applications. Chemical buyers and sourcing teams rely on more than just documentation—they expect actual performance and clear technical support. The compound’s reactivity, physical stability, and proven track record across global markets continues to make it a preferred option for chemistries ranging from exploratory synthesis to full production.
Continuous improvement—incremental or step-change—remains part of the manufacturer’s routine. Customer feedback, whether from pharmaceutical developers, agrochemical researchers, or contract manufacturers, underlines where the product delivers and where it surprises. Each batch reflects collective operational know-how, years of iterative tweaking, and deep listening to partners across the chemical industry. Manufacturing methyl 3-bromopyridine-4-carboxylate isn’t just a matter of following a recipe. It stands as a demonstration of attention to detail, direct experience, and the tangible benefits of reliable, well-characterized chemical inputs in a world that demands ever greater precision and results.