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HS Code |
120919 |
| Iupac Name | 2-Bromo-5-fluoro-3-methylpyridine |
| Synonyms | 2-Bromo-5-fluoro-3-picoline |
| Cas Number | 635317-41-6 |
| Molecular Formula | C6H5BrFN |
| Molecular Weight | 206.017 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC1=C(N=CC(=C1Br)F) |
| Inchi | InChI=1S/C6H5BrFN/c1-4-2-6(8)5(7)9-3-4/h2-3H,1H3 |
As an accredited Pyridine, 2-bromo-5-fluoro-3-methyl-2-Bromo-5-Fluoro-3-Picoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, tightly sealed with a screw cap, labeled with chemical name, hazard pictograms, and batch information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 160 drums x 200 kg HDPE drums, total net weight 32 MT, packed securely for safe transport. |
| Shipping | Shipping of Pyridine, 2-bromo-5-fluoro-3-methyl (2-Bromo-5-fluoro-3-picoline) requires secure, leak-proof packaging, compliance with local hazardous materials regulations, and proper labeling. The chemical should be shipped under ventilation, away from incompatible substances, and protected from extreme temperatures. Safety data sheets (SDS) must accompany the shipment for handling and emergency instructions. |
| Storage | Store 2-Bromo-5-fluoro-3-methylpyridine in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep in a cool, dry, well-ventilated area, segregated from incompatible substances such as strong oxidizers and bases. Use appropriate chemical storage cabinets and clearly label containers. Maintain storage at room temperature or as specified by the manufacturer’s safety guidelines. |
| Shelf Life | Shelf life of Pyridine, 2-bromo-5-fluoro-3-methyl is typically 2 years when stored in a cool, dry, airtight container. |
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Purity 98%: Pyridine, 2-bromo-5-fluoro-3-methyl-2-Bromo-5-Fluoro-3-Picoline with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield conversion and minimal side product formation. Melting point 45°C: Pyridine, 2-bromo-5-fluoro-3-methyl-2-Bromo-5-Fluoro-3-Picoline with a melting point of 45°C is used in agrochemical research, where it enables controlled processing and stable formulation blending. Molecular weight 208.98 g/mol: Pyridine, 2-bromo-5-fluoro-3-methyl-2-Bromo-5-Fluoro-3-Picoline at molecular weight 208.98 g/mol is used in custom catalyst design, where predictable reactivity patterns optimize reaction efficiency. Stability temperature up to 120°C: Pyridine, 2-bromo-5-fluoro-3-methyl-2-Bromo-5-Fluoro-3-Picoline with stability temperature up to 120°C is used in high-temperature organic synthesis, where it maintains chemical integrity and reproducibility. Particle size <5 μm: Pyridine, 2-bromo-5-fluoro-3-methyl-2-Bromo-5-Fluoro-3-Picoline with particle size less than 5 μm is used in formulation of fine chemical reagents, where it promotes rapid dissolution and homogeneity. |
Competitive Pyridine, 2-bromo-5-fluoro-3-methyl-2-Bromo-5-Fluoro-3-Picoline prices that fit your budget—flexible terms and customized quotes for every order.
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From years of manufacturing specialty pyridines, a compound like 2-bromo-5-fluoro-3-methylpyridine (2-Bromo-5-Fluoro-3-Picoline) stands out for good reasons. The chemical structure—one that carries both bromine and fluorine substituents along with a methyl group on the pyridine ring—may look unassuming to some, but its reactivity profile creates swift benefits in both research and industrial-scale synthesis. Over the last decade, demand for this molecule has shown steady growth, especially as the pharmaceutical and agrochemical sectors search for reliable, well-reproducible heterocyclic intermediates.
This pyridine derivative draws seasoned attention, not only for its role in synthetic chemistry but for the technical challenges it presents. The process starts with carefully selected raw materials. Brominating an already fluorinated picoline, for example, means recognizing how both halogens impact site-selective reactivity and stability throughout the process. Our years refining these steps play out in small details: strict control over reaction temperature, fine-tuned agitation profiles, and solvent management that reduces risk of side product formation. We have seen these practical challenges reflected in customers’ R&D results—slight deviations in impurity profiles often amplify downstream. This offers real assurance for formularies relying on tight batch-to-batch replicate performance.
Each improvement learned from production feedback or analytical results feeds back into plant practices. Early on, we discovered how certain glass-lined reactors caused slight trace-metal contamination where stainless steel did not. Incremental improvement, genuine trial and error, shapes tighter chemical purity. Through repeated campaigns we have reached routes that not only improve yields but also minimize byproduct contamination, which ultimately grows confidence for chemists who trust the supplied product as a key intermediate—especially in regulated end-use syntheses.
Users rarely want surprises during scale-up or downstream coupling reactions. This is where tight specifications prove their value. Over years, customers pointed to color, moisture content, and halide purity as frustration points from competitive offerings. In response, process adjustments improved color by reducing certain early-stage impurities; custom packaging blocks moisture ingress that otherwise threatens halogen functionality during prolonged storage.
We catalog specifications that matter in actual applications: measurable purity (typically exceeding 98% GC or HPLC), water content managed to low ppm by Karl Fischer titration, and direct halogen assay to confirm both bromine and fluorine content meet stated values. These numbers did not drop from the sky—they stemmed from collaboration with synthetic teams translating bench-scale findings to commercial batch runs. Lab-to-plant communication stands behind these decisions, not just abstract standards or empty marketing words.
Chemists keep coming back to 2-bromo-5-fluoro-3-methylpyridine for very practical reasons. The positioning of the bromine on the pyridine ring lends itself well to Suzuki, Stille, and other palladium-catalyzed cross-coupling reactions quite familiar to many. That isn’t just textbook knowledge—actual users demonstrate, for instance, how the methyl group in the 3-position restricts certain unwanted side reactions, stabilizing the adjacent functional sites during heated or prolonged reactions.
On several occasions, client partners in pharmaceutical development needed to elaborate specific scaffolds with site-selective modifications. Observing our product in their hands showed that the combined electron-withdrawing effect of the fluorine and methyl steadied subsequent substitutions, lending higher selectivity in constructing heterocyclic libraries. The implications seemed clear: not all halogenated pyridines are created equal, even from an analogous starting point. Our team saw many projects where switching from a vendor offering standard 2-bromopyridine to our bromo-fluoro-methyl variant gave strikingly improved yields, fewer byproducts, and more robust product isolation.
Years making a variety of pyridine derivatives clarify small but significant ways this compound outruns others. Regular pyridine, even methyl-substituted versions, miss the electronic finesse provided by both the bromine and the fluorine in these specific ring positions. Chlorinated or iodinated analogues offer different reactivity, often less predictable. Using 2-bromo-5-fluoro-3-methylpyridine, our clients experience greater predictability in reactions. The ortho-fluorine not only modulates the electronic environment but also lends subtle steric influence, which, for advanced medicinal chemistry, impacts both synthetic routes and, later, the properties in lead candidates.
Direct feedback from pharmaceutical processors highlighted differences that spring from seemingly small structural changes. Flipping the location of the methyl from the 3- to the 4-position, or using a 2-chloro instead of a 2-bromo, produces shifts in reaction selectivity and sometimes leads to instability under palladium catalysis. For some, those differences spell the boundary between a scalable process and a promising route that stalls during regulatory compliance batches. Continued dialogue with drug discovery partners taught our teams repeatedly that, in the real world, such differences are not trivial details; they dictate the pace at which discoveries move from analysis to manufacturing.
Pharmaceutical innovation has drawn on halogenated heterocycles for decades. 2-bromo-5-fluoro-3-methylpyridine figures prominently as a launch pad for library synthesis and lead expansion. In the past, our materials helped speed up several pre-clinical programs, enabling teams to quickly test new SAR (structure-activity relationships). The clean reaction profiles made possible by this product allowed fewer purification steps, a claim substantiated over projects where time crunches limited opportunities for repeated chromatographic runs. Our manufacturing history taught us that even a 1% reduction in impurity content can tangibly ease regulatory documentation and overall process risk.
Agrochemical applications benefit in similar fashion. Over the years, field chemists told us about the importance of reliable stock for quick modifications in active ingredient formulations—sometimes to counter mounting resistance in pest populations, sometimes to improve environmental persistence in different crop climates. With dual halogen substitution and a methylated backbone, this compound offers versatility seldom matched by either mono-halogenated or unsubstituted pyridines. Its controlled reactivity ensures both innovation and safety in handling at industrial scale.
Producing this compound on a regular basis sharpened our grasp on a range of process variables. For example, halogen management turns out to be more than simply adding reagents. Overbromination remains a lurking pitfall; we devote concerted attention to reagent addition rates and reaction cooling. Batch records, spanning years, capture lessons in keeping byproduct halopyridines below detectable limits. Analytical labs provide feedback loops: retention times drifting on HPLC profiles can indicate new traces or the need to recalibrate purification steps. It takes time and practical discipline to keep quality metrics locked in place over annual production cycles.
Packaging also became a talking point. In earlier years, we received complaints about product degradation linked to unsuitable container materials. Nowadays, more robust drums and fresh desiccant systems block exposure to ambient moisture, preserving both appearance and chemical integrity all the way to the user’s bench or plant line. Attention to shipping details—especially for export-bound lots—reduced latent issues like caking or sub-visible particulates that result from minor transit vibrations.
Decades in manufacturing halogenated organics impart a sense of responsibility about stewardship, both for the environment and for people working with these compounds day in and day out. We routinely assess all waste streams to keep brominated and fluorinated byproducts from entering the water system. Manufacturing process revisions, including in situ neutralization steps, have lowered hazardous effluent loads year over year. Regular audits keep the team focused on keeping emissions low and demonstrating compliance not because of regulation, but because it keeps our plant and community safer.
Worker health also guides decisions, starting at the design of closed systems to minimize operator exposure. By strictly managing pressure, temperature, and emissions, job safety reaches beyond simply issuing PPE—our practical efforts reduce the risk of accidental exposure or acute reactivity, which, with halogenated organics, always deserves attention. An ongoing dialogue with staff, shaped by decades of experience in scale-up chemistry, helps spot and solve problems before they reach criticality.
Analytical know-how represents the backbone of our product consistency. Chromatography and mass spectrometry have moved from occasional spot checks to full-release controls. Purity profiles, already tight under regular GC and HPLC, gain further insight from nuclear magnetic resonance analyses. These aren’t abstract tests—they detect cross-contamination from other halogen sources, impurities from solvents, and shifts after extended transit times. Our data archive—spanning hundreds of batches—lets us track drifts, investigate outliers, and improve future campaign planning.
Clients, especially those scaling from gram to multi-kilo lots, appreciate detailed certificates of analysis and trend data. Tracing micro-level impurities over months or years helps recipients trust not just this product, but the broader supply chain reliability. There’s no shortcut here: investment in analytical capability, including method development and ongoing calibration, pays off in field performance where exploratory chemistry cannot tolerate uncertainty.
Pyridine derivatives like 2-bromo-5-fluoro-3-methylpyridine keep evolving alongside advances in medicinal and agrochemical research. Client collaborations repeatedly highlight the need for not just purity, but also specific isomer ratios, controlled halogen speciation, and minimized residual solvents. Over time, we have tailored parts of our production route to satisfy the most stringent user-defined tolerances. For example, specialty projects in new drug discovery sometimes called for high-purity lots with critical moisture exclusion—extra investments in cleaning, drying, and container testing grew from these direct requests.
We do not work in isolation. Regular conversations with research chemists, plant engineers, and process safety experts across leading sectors keep our processes adaptive. As companies seek to build new molecular frameworks with improved biological properties or resistance profiles, the demand for predictably reactive, highly characterized starting materials will grow. Connecting decades of feedback, from gram-scale academic labs to commercial manufacturing plants, we see our task as not just molecule production but enabling discovery, with the foundation of controlled, reproducible chemistry.
Experienced process developers know the difference that right building blocks make. Many off-the-shelf pyridines come from third-party networks with less oversight. We receive regular inquiries from project leads who struggled with off-spec material sourced from volume suppliers, reporting problems like unpredictable color, solvent residues, or variable coupling efficiencies that trace back to inconsistent halogen content.
Our experience producing at source, not through distribution networks, proves its value here. With control from raw material choice through to the fill-and-pack stage, results align with project-specific requirements, whether the customer is advancing a new drug program, preparing seed chemistry for agrochemical rollout, or testing material in academic innovation. We welcome requests for custom analytical data because our processes already include archived method validation files.
Ongoing investment in plant infrastructure sets the stage for even more reliable output. Over recent years, we upgraded reactor automation, improved filtration systems, and implemented smart in-line monitoring. These changes, inspired by on-the-ground input from both plant operators and customer teams, keep output quality aligned with evolving expectations.
We listen when formulation scientists request larger lots, longer shelf-life, or tailored solvent mixes for immediate downstream use. Such adaptation means more than compliance, it means reducing process bottlenecks for users who depend on flawless starting points for time-sensitive research and production.
Supplying 2-bromo-5-fluoro-3-methylpyridine reflects more than commodity chemical production. This is a process honed by direct lessons from end users—pharmaceutical teams scaling new scaffolds, agrochemical developers responding to environmental demands, and researchers needing surety as they push scientific boundaries. Experience proves the necessity of consistent, clean, and clearly characterized intermediates; every improvement in our process maps back to reduced risk and accelerated success for users.
Our company culture rarely favors easy claims or template language. Daily effort goes into sustaining a supply chain based on transparency, feedback-driven modification, and a sense of shared responsibility that covers safe production, environmental protection, and enabling the next wave of chemical innovation. At the end of each batch, after the reactors cool and analyses complete, the measure of our work is the success our users gain from consistently reliable chemical building blocks—2-bromo-5-fluoro-3-methylpyridine stands as a case in point.