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HS Code |
512142 |
| Iupac Name | methyl 5-bromo-2-fluoropyridine-3-carboxylate |
| Cas Number | 153034-99-0 |
| Molecular Formula | C7H5BrFNO2 |
| Molecular Weight | 234.02 |
| Appearance | White to off-white solid |
| Solubility | Soluble in organic solvents such as DMSO and DMF |
| Smiles | COC(=O)C1=CN=C(C=C1Br)F |
| Inchi | InChI=1S/C7H5BrFNO2/c1-12-7(11)4-2-6(9)10-3-5(4)8/h2-3H,1H3 |
| Synonyms | 5-Bromo-2-fluoro-3-pyridinecarboxylic acid methyl ester |
| Pubchem Cid | 12464650 |
As an accredited 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 50-gram amber glass bottle with a tightly sealed cap, labeled with the chemical name, CAS number, and safety information. |
| Container Loading (20′ FCL) | 20′ FCL loads 10MT of 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester, packed in 25kg fiber drums. |
| Shipping | **Shipping Description:** 3-Pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester is shipped in tightly sealed, chemical-resistant containers, protected from moisture and light. The package is clearly labeled with hazard information and handled following applicable regulations for potentially hazardous chemicals. Ensure appropriate documentation accompanies international or domestic shipments in compliance with local and international transport laws. |
| Storage | Store 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from light and moisture. Store under inert atmosphere if necessary. Clearly label the container and ensure access is restricted to qualified personnel. Use appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life: Stable for at least 2 years if stored in a cool, dry place, protected from light and moisture. |
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Purity 98%: 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity levels. Molecular weight 246.01 g/mol: 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester with molecular weight 246.01 g/mol is used in agrochemical research applications, where it enables precise compound formulation control. Melting point 55-58°C: 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester with melting point 55-58°C is used in crystal engineering studies, where it facilitates reproducible crystallization and material handling. Stability temperature up to 120°C: 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester with stability temperature up to 120°C is used in high-temperature reaction protocols, where it provides consistent chemical stability during thermal processes. Particle size <50 microns: 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester with particle size <50 microns is used in formulation of fine chemical blends, where it enhances dispersion and homogeneity. Solubility in DMSO: 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester with high solubility in DMSO is used in medicinal chemistry assays, where it ensures efficient compound delivery and bioavailability. |
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Every day in the plant, the production team works with intermediates like 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester, which highlight the fine-tuned detail driving innovation in pharmaceutical and agrochemical synthesis. Years of process development and scale-up give us more than a chemical formula; this methyl ester represents the continual improvement that makes downstream transformations cleaner and more reliable. The compound models as C7H5BrFNO2, and as a halogenated pyridine carboxylate, it features a distinct profile with the bromine and fluorine positioned to support advanced coupling chemistry.
Labs worldwide rely on compounds with accurate halogenation patterns for selective cross-coupling, nucleophilic substitutions, or ring-modification reactions. Here, the 5-bromo and 2-fluoro substituents sit on the pyridine nucleus, creating precise reactivity unmatched by less complex isomers. Our on-site quality control confirms structure and purity with HPLC and NMR at every batch release. Physical appearance is a pale crystalline solid, often with a faint odor, reflecting both the esterification and aromatic core.
Application steers every step of how we manufacture 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester. It stands out as an intermediate designed for performance under the pressures of research deadlines and regulatory compliance. Medicinal chemists choose this molecule because the electron-donating and withdrawing effects on the pyridine ring set up valuable points for further functionalization. These features make the methyl ester a favorite for selective Suzuki, Buchwald–Hartwig, or Stille couplings where bromo or fluoro groups react as unique handles. Compared to unsubstituted esters, reactions here proceed with higher site-selectivity and reduced side-products, streamlining the purification stages that often slow scale-up.
Day-to-day, we see customers demand not just chemical reactivity, but also purity and batch-to-batch consistency. Each operation from raw material qualification through recrystallization and packaging responds to customer audits and feedback. In the facility, operators monitor the methyl esterification step closely, tuning temperature profiles and reagent ratios to minimize alcoholysis byproducts and drive full conversion. This level of production focus yields a material that builds trust with repeat users.
Not all pyridine esters behave alike in multi-step synthesis. The addition of a bromine at the 5-position and fluorine at the 2-position introduces significant electronic and steric features. Bromine offers high utility in palladium-catalyzed cross-coupling reactions, opening access to substituted pyridines not available from other starting materials. Fluorine, on the other hand, influences both the reactivity and the metabolic stability of finished pharmaceutical molecules. Chemists aiming for selective functionalization or altering the pharmacokinetic profile of drug leads find value in these specific substituents.
By contrast, the methyl ester of 3-pyridinecarboxylic acid without these halogens lacks the nuanced reactivity seen here. Mono-substituted variants do not support the same breadth of downstream manipulations, especially in heterocyclic synthesis. Our compound offers a unique window to install bulkier, more complex groups, supporting discovery in oncology, anti-viral, or crop protection projects. In-house feedback highlights how the dual halogen pattern saves months during route exploration, shrinking the trial-and-error phase that persists with less sophisticated intermediates.
In the manufacturing area, reliability always takes center stage. Operators log temperatures, monitor solvent recoveries, and maintain close communication with quality assurance. Production staff frequently point out that conventional esters can introduce byproducts during transesterification, leading to unexpected color changes or residue formation. In contrast, our 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester exhibits less tendency toward hydrolysis or transesterification under routine handling. This limits waste and simplifies post-reaction workups—two practical advantages that play a significant role in development timelines.
The investment in reaction parameters—stirring, control of exotherms, and staged addition of reagents—translates to higher overall yields. Fewer impurities at this stage mean easier purification and more reliable analytical data downstream. The team routinely documents conversions upwards of 95 percent, driven by persistent refinement rather than luck or one-off procedures. Not every production run goes to plan, but accumulated expertise helps the team anticipate and solve challenges before they reach the customer.
The product line has steadily grown to accommodate research labs looking for gram quantities as well as commercial clients moving into multi-kilo campaigns. Scaling up from initial batches brought distinct hurdles—solubility, mixing, and crystallization all required process adaptation. Early scale-up trials highlighted the importance of controlling solvent composition and temperature, as minor deviations could cause oiling-out or off-spec material. Now, standardized batch records and SOPs capture each detail, locking in performance even as projects move from pilot to full-scale manufacture.
Clients trust the repeatability gained from rigorous manufacturing practices. With each batch, materials are drawn for in-process control, confirmed by analytical specialists inside the plant. Full spectral libraries help track any unexpected shifts in structure or purity, and out-of-spec batches are flagged immediately before they reach the packaging area. This disciplined approach wins repeat business from discovery teams that value seamless supply chains, especially when synthetic plans need to move from bench to production scale without costly revalidation.
Through years of experience, the team understands that attention to detail keeps workers and communities safe. Halogenated pyridines require thoughtful handling; staff follow strict SOPs for ventilation, glove choices, and containment. Methyl esters may pose inhalation or contact hazards, so production managers enforce up-to-date training for all crew members. Waste solvents undergo recycling and incineration on-site, ensuring compliance with local and international environmental standards. These steps come from a commitment to responsible industry practice, not just regulatory checklists.
Continuous improvement programs in the plant invite technician feedback on equipment upgrades, fume hood performance, and emergency drills. Operators who handle the product day in and day out notice the subtle changes in batch behavior or handling risks long before management. Open reporting gives voice to these observations, leading to changes in labeling, packaging design, or process fume mitigation. This real-world insight makes every new batch safer not just for users inside the plant, but also for research chemists working halfway across the world.
Direct lines of communication set our approach apart. Commercial staff routinely answer questions from synthetic chemists who push reactions to the limit. Insight from the lab bench often leads to shared process changes—a tweak in drying protocols for better storage stability, or a shift in particle sizing to improve handling during robotic dispensing. The supply chain adapts with every customer call, sharing lessons that only arise from actually running reactions, not just skimming academic papers.
Scientific support means more than sending out certificates of analysis. The technical team reviews each inquiry for solubility, compatibility with standard cross-coupling conditions, and batch preparation as specifications shift. Raw material qualification includes impurity profiles that anticipate the downstream fate of minor constituents. Instead of simply shipping drums and turning away, technical support works alongside users to troubleshoot solubility, color variation, or compatibility questions. This level of hands-on partnership closes the gap between manufacturer and final application.
Shifts in the global chemical supply chain bring new demands. As halogenated building blocks become more regulated and precursor tracking more intense, sourcing high-purity raw materials calls for constant vigilance. Our procurement team manages long-term supplier relationships and keeps watch for shifts in regulatory status for starting materials like 5-bromo-2-fluoropyridine. Audit trails document origin and chain of custody for every kilogram moved into the plant. In a landscape where regulations evolve year to year, flexibility in sourcing and transparent record keeping matter to every link in the chain.
Environmental rules for effluent halogens and volatile organics continue to tighten. Plant management stays ahead of regulations by optimizing solvent use, recycling streams, and capturing emissions before they leave the stack. Staff work closely with regional agencies to measure and reduce impact well before compliance dates demand action. This proactive stance stems less from marketing than genuine pride in running a modern, responsible production site.
Behind sterile drums and analytic reports, the real difference lies in the accumulated knowledge from each day at the plant. Operating experience builds a subtle judgment for how this compound behaves at scale, how it supports synthetic creativity, and how it enables new discoveries. Competitive industries chase faster cycle times and new intellectual property; the users who return year after year cite not just product quality, but manufacturer flexibility in responding to project pivots, new regulatory demands, or sudden jumps in required scale.
The methyl ester of 3-pyridinecarboxylic acid, 5-bromo-2-fluoro—so simple on paper—emerges as a complex tool shaped by feedback, production control, and evolving client need. Researchers building libraries or moving lead compounds into production do so with greater certainty when every step, from procurement of raw materials to final shipment, runs inside a system built for transparency and support. The story behind every drum or bottle connects innovation in the lab to the daily practice of chemical manufacturing.
Partnership with clients focuses development targets in real time. Extension of this compound’s halogenation or ester group offers new directions, especially as demand for unique heterocyclic scaffolds grows. Engagement with clients who push downstream chemistry leads to refined grades, custom packaging, or adapted supply schedules. These collaborations spark new methods for direct amination, alkylation, or fluorine displacement, as synthetic teams leverage the methyl ester’s full potential.
The evolution of this product echoes industry trends toward higher selectivity, greener chemistry, and smarter use of labor and capital. While no chemical solution covers every scenario, the methyl ester continues to outperform less functionalized alternatives for teams charting new routes in drug and agrochemical discovery. New ideas come from academic partners, process engineers, and operators on the floor who see the subtle signs of change or opportunity. The practical lesson is clear: knowledge built on direct handling and continued process improvement surpasses specification sheets or off-the-shelf descriptions.
Years in the field show that reliability matters most in building supply confidence. Projects with high stakes in drug or crop protection research depend on tight lead times and validated batches. By investing in plant upgrades, in-house staff development, and open dialogue with clients, the production team delivers more than chemical raw material. Each time a new use or reaction succeeds, that success reflects hundreds of decisions on the manufacturing floor, in the lab, and across logistics.
Many intermediates pass through labs unnoticed, but 3-pyridinecarboxylic acid, 5-bromo-2-fluoro-, methyl ester stands apart through purposeful synthesis, rigorous testing, and open learning from every stakeholder. With shifting global needs and more demanding expectations from industry and regulators, experience rooted in manufacturing guides improvements that competitors chasing speed or price alone cannot match. In this way, each batch made earns not just approval but also the trust that comes from direct, transparent production and long-term partnership.