|
HS Code |
629042 |
| Chemical Name | Pyridine, 3,5-dibromo-2-fluoro-4-methyl- |
| Molecular Formula | C6H4Br2FN |
| Molecular Weight | 285.915 g/mol |
| Cas Number | 214872-55-0 |
| Appearance | Pale yellow to brown solid |
| Smiles | Cc1c(Br)nc(F)c(Br)cc1 |
| Inchi | InChI=1S/C6H4Br2FN/c1-3-4(7)2-5(8)10-6(3)9/h2H,1H3 |
| Synonyms | 3,5-Dibromo-2-fluoro-4-methylpyridine |
| Storage Temperature | Store at room temperature, away from light |
As an accredited Pyridine, 3,5-dibromo-2-fluoro-4-methyl- 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 25-gram amber glass bottle with a screw cap and a clear label displaying hazard and handling information. |
| Container Loading (20′ FCL) | 20′ FCL (Full Container Load) for Pyridine, 3,5-dibromo-2-fluoro-4-methyl- typically holds securely packed drums or bags, maximizing shipping efficiency. |
| Shipping | **Shipping Description:** Pyridine, 3,5-dibromo-2-fluoro-4-methyl- should be shipped in tightly sealed containers, protected from moisture and incompatible materials. It should be classified and labeled as a hazardous chemical, handled according to applicable regulations (such as DOT or IATA), and transported in compliance with all safety and environmental guidelines for brominated and fluorinated organics. |
| Storage | Store 3,5-dibromo-2-fluoro-4-methylpyridine in a cool, dry, well-ventilated area away from heat, sparks, open flame, and incompatible substances such as oxidizers. Keep container tightly closed when not in use. Protect from moisture and direct sunlight. Use appropriate containers made of compatible materials, and ensure proper labeling. Store in a chemical storage cabinet if possible, and follow all relevant safety regulations. |
| Shelf Life | Shelf life of Pyridine, 3,5-dibromo-2-fluoro-4-methyl- is typically 2-3 years when stored in a cool, dry place. |
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Purity 98%: Pyridine, 3,5-dibromo-2-fluoro-4-methyl- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal impurities. Melting point 70–72°C: Pyridine, 3,5-dibromo-2-fluoro-4-methyl- with melting point 70–72°C is used in agrochemical formulation processes, where it provides ease of handling and consistent recrystallization. Molecular weight 285.92 g/mol: Pyridine, 3,5-dibromo-2-fluoro-4-methyl- with molecular weight 285.92 g/mol is used in medicinal chemistry research, where it enables precise stoichiometric calculations for reaction optimization. Stability temperature up to 120°C: Pyridine, 3,5-dibromo-2-fluoro-4-methyl- with stability temperature up to 120°C is used in industrial scale-up reactions, where it maintains chemical integrity under thermal processing conditions. Particle size ≤10 µm: Pyridine, 3,5-dibromo-2-fluoro-4-methyl- with particle size ≤10 µm is used in advanced formulation of specialty coatings, where it allows uniform dispersion and optimal surface coverage. |
Competitive Pyridine, 3,5-dibromo-2-fluoro-4-methyl- prices that fit your budget—flexible terms and customized quotes for every order.
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Every batch of Pyridine, 3,5-dibromo-2-fluoro-4-methyl- brings its own challenges and opportunities for those of us working hands-on in chemical manufacturing. From the very start—handling the raw materials, calibrating reactors, cleaning glassware—this compound’s identity takes shape through hard work and constant attention to detail. We rely on a specific synthesis route, one refined over years to limit unnecessary side-products and allow precise control of every substitution on the pyridine ring. Adding bromo, fluoro, and methyl substituents in exact locations is a test of technique, not luck. Our line runs on tight temperature profiles and well-chosen flow rates to avoid degradation or the formation of unwanted regioisomers.
Metrics matter in this line of work. For this model of pyridine derivative, purity does not just boost downstream performance, it also keeps processes running smoothly for users who may base entire syntheses on our intermediate. Our analytical team uses methods like NMR, HPLC, and mass spectrometry daily to double-check outcomes. The goal remains the same: a reliable, repeatable product matching or exceeding specification. In this business, one faulty batch can set back weeks of research or delay an entire manufacturing campaign. Any time we see a droplet of discoloration or a shift in melting point, we trace the issue right back to its point of origin and adjust our technique.
Compared to a basic pyridine or a singly substituted analog, this compound carves out its own niche. Researchers and process chemists have made clear they need structures with precisely placed electron-withdrawing and electron-donating groups. The two bromo atoms at the 3 and 5 positions are more than decorative—they modulate reactivity, especially for stepwise cross-coupling, halogen exchange, or nucleophilic substitution. The fluorine at position 2 presents its own effect, tightening the ring and changing polarity. The methyl group at position 4 offers a balance, supplying a small amount of electron density and subtle steric bulk. Where plain pyridine might fall short in applications like pharmasynthesis or advanced materials, this compound meets the demand for more selective reactivity and specialized electronic properties.
No product survives long on its name alone; users judge it by what it helps them create. For example, in pharmaceutical R&D, selectivity often means fewer unwanted byproducts when building out a target molecule. Medicinal chemists have told our technical team that well-made, multi-substituted pyridines can decide whether a synthesis moves forward or stalls. One reason lies in the way these functional groups offer specific anchors for Suzuki, Stille, or Buchwald–Hartwig couplings. Academic researchers often want small, predictable variations along a heterocyclic scaffold to track SAR (structure-activity relationships). Our manufacturing experience shows that even 1% byproduct from mispositioned halogens can complicate purification down the line, so we keep a tight rein on substitution patterns throughout.
Compared to 2,6-dibromopyridines or fluoromethylpyridines with different substitution, this 3,5-dibromo-2-fluoro-4-methyl model provides a unique balance of reactivity and steric effect. The difference becomes clear in the lab: reactivity toward palladium-catalyzed cross-coupling, solubility, and melting point all shift with changes in the substitution pattern. These impacts aren’t theoretical. Our customers relay feedback where switching from a mono-brominated to our dibromofluoromethyl version shortened synthesis time or improved the selectivity for a new ligand candidate in catalysis screening.
Pyridines serve as backbone structures in both fine chemical synthesis and new materials development. Buying a simple pyridine is no trick; getting hold of a rare, multi-functionalized ring, on the other hand, still requires practical skill in selective halogenation, methylation, and fluorination. Through years of process improvement and troubleshooting, our team has learned the quirks of handling reactive intermediates at scale. Bromination, for instance, sometimes threatens to run away if the temperature spikes. Excess methylation can lead to over-alkylation and unwanted side products. Careful planning in sequence and stoichiometry pays off. The lessons we’ve learned running these reactions repeatedly, scaling from flasks to reactors, have filtered back into our SOPs and training programs.
Each shipment we produce comes backed by process history—our own, not just something picked off a database. We stand behind each lot because our technicians, engineers, and analysts have spent hours hands-on with every batch, tuning the method to squeeze out impurities and tuning chromatography to catch small drifts in composition.
Interest in highly adorned pyridines has grown alongside the rise in demand for new pharmaceuticals, crop protection agents, and performance materials. Regulatory agencies now focus on data transparency, traceability, and hazard minimization. For us, this means doubling back to optimize not only yield but also minimize waste and solvent use. In practice, that involves continuous review of our process streams, recycling compatible solvents, and capturing off-gases to meet or beat environmental targets. Customers now expect more than purity: they want information on process history and data supporting regulatory submissions. Analytical transparency is now a minimum, not an add-on.
Supplying a multi-substituted pyridine involves regular conversations with both end-users and R&D labs. Process documentation once meant handwritten records and scattered spreadsheets. Now, digital logs and standardized QC reports give our partners confidence in traceability and repeatability. Supply chain disruption years have made clear to many buyers that purchasing directly from manufacturers with in-house synthesis is not just about cost—it is about reliability, quality, and a clear answer on where things originated. Our plant, run with onsite chemists and operators, allows real-time control over quality and flexibility in scheduling new runs for specialty orders.
Each process step in synthesizing this compound, from bromination to methylation to final purification, has its own risks. Temperature control, reagent purity, and even tiny changes in mixing protocol show up in the outcome. Early in the scale-up phase, we observed batches with higher background impurities; by tracking every variable, we adjusted stirring speed and order of addition, raising reproducibility. In the drying and crystallization step, too rapid cooling sometimes trapped solvent, introducing unseen hazards in packaging. Our operators learned from each deviation, and improvements were logged back into our digital process system, supporting both on-the-fly troubleshooting and long-term process improvement.
Once, a run of coils on a heat exchanger threatened to break down, driving up batch temperatures during the halogenation step. Because our team maintains a culture of quick observation and action, we caught the spike before it could cause a runaway. Since then, we have installed backup systems, and key process parameters are logged minute-to-minute for better early warning. This type of learning—from real incidents, not textbook cases—now guides the way we design safeguards and checklists, making it less likely for slip-ups to recur.
Our relationship with users does not end at the loading dock. Research chemists, process scientists, and engineers bring back reports from their pilot plants and laboratories. Some reach out looking for tweaks to physical form—maybe a finer crystal for better dissolution, a slurry for safer handling, or specific solvents with higher flash points. We work alongside these customers to modify protocols or adapt particle size as production changes from the lab scale to commercial output. The unexpected challenges, such as pressure buildup on redissolution or partial decomposition in storage, push us to refine stabilization protocols and tweak our quenching and isolation steps.
Through this continuous feedback cycle, we have identified where improvements mean least work for the user—such as tighter melting range or improved filtration characteristics. Our plant infrastructure, built to flex between different heterocycle projects, means we do not juggle long setup times or unplanned stops. If a customer trial reveals unique needs for handling or storage, our technical team works with them directly to redesign packaging or adjust our drying process—a level of responsiveness that rarely comes from intermediaries or trading houses.
Applications span several sectors. In pharmaceutical synthesis, our 3,5-dibromo-2-fluoro-4-methyl-pyridine gives medicinal chemists the building blocks for scaffolds in kinase inhibitors, antibacterial agents, or heterocyclic drug leads. Each substituent plays a role in forming the necessary binding interactions or boosting metabolic stability. The selectivity engineered into the molecule allows precise downstream coupling, reducing side reactions and drag on purification workflows.
Chemists in agrochemical development look for efficient introduction of functional motifs that can withstand tough environments—crop formulations cannot afford variable yield or trace contaminants. The structure of this compound, specifically its electron-poor and electron-rich zones, makes it especially suitable for building into pest control agents, herbicide cores, or intermediates for fine-chemical libraries. The reliability of each batch has become a selling point in global agrochemical registration dossiers, where product provenance and consistency reduce the workload of compliance and cut down on regulatory retesting.
Material scientists report using our product as a stepping stone into ligands or monomers for organic electronics, advanced polymers, or specialty coatings. A seemingly simple modification at one position of the ring can give dramatically different charge transport or binding properties in final coatings. Based on real conversations with application chemists, new uses continue to emerge as the community becomes more aware of the difference high-control manufacturing quality can make.
Years of manufacturing this compound have made clear that every step—from incoming raw materials, through each layer of process refinement, up to finished product—becomes a record of skill and attention. Each time a challenge appears, instead of just patching problems, we chase the root cause and build the solution back into our process. Examples pile up over time: an unexpected impurity profile gets traced to a subtle solvent-grade difference; solubility drift leads us to retune drying cycles and crystallization rates. We learn what makes a difference not from protocols alone, but from facing the unexpected and seeing what it takes to hit consistent, tight specifications run after run.
Bringing a compound like 3,5-dibromo-2-fluoro-4-methyl-pyridine to market at scale is not just a technical achievement—it's the outcome of hundreds of small choices made on the ground. There are no silver bullet solutions. Even automation, while crucial for batch safety and record-keeping, cannot replace a well-trained process team or the tacit skills learned through years at the bench and in the plant. As chemists retire and new generations join, our training now includes everything from trend-spotting in analytics to rapid-response drills on plant safety and routine troubleshooting. Every member of our team contributes to the overall reliability of delivered product.
Across dozens of industries, demand trends keep moving. The push for greener, safer, and more sustainable chemistry means even in established products, we keep retooling the synthesis. Recent investments in process intensification let us cut reaction time, use fewer process solvents, and reduce total waste output. Customers ask hard questions—about shelf-life, about hazardous byproducts, about compliance with regulatory frameworks like REACH or TSCA. Our team collects and supplies documentation with every shipment, drawn directly from our plant records—not provided by a third-party or overseas vendor with no manufacturing stake in the details. This lets partners downstream spend less time on compliance and more on their core research or product launch.
Some industries—such as the development of photonic materials or custom specialty chemicals—have growing needs for design flexibility. Here again, our manufacturing plant’s combination of flexibility and control means we can scale from grams to multi-kilogram lots without long downtimes or switching lines. This flexibility matters most to innovators who may need only a few kilos for a pilot project, expanding to commercial production as programs succeed. Instead of relying on static warehouse stock or hoping a distributor tracks down the lot number, partners in these sectors value the working relationship as much as the product: fast feedback, transparent records, and the knowledge that those supplying the compound actually made it, watched it, and refined it to meet a real-world use case.
Changing customer needs, new regulatory frameworks, and the unpredictable challenges of the global supply chain keep us sharp. Our investment in in-house analytical labs, real-time batch monitoring, and digital traceability reflects an ongoing commitment to reliability and improvement. Steric and electronic effects that might seem subtle on paper can decisively shape a downstream synthesis or formulation; this drives our team’s insistence on tight controls at every process step. Queries about restart time, impurity carry-over, or exact process signature do not catch us off guard—we invite these audits, because detailed records and staff experience stand behind every run.
Part of manufacturing is developing a collective memory. Over time, analysis of past failures—batch deviation reports, customer complaints, process upsets—builds a resource for future improvements. Bringing together data from these cases, we train new operators not just in the basics of synthesis, but in proactive risk detection and process optimization. We learn more from what goes wrong than from a hundred smooth runs.
Direct relationships with users, from the bench scientist to the process engineer, let us adjust proactively. Whether a customer report points to a new regulatory concern in Japan or an unexpected shift in reaction kinetics in a biopharma trial, we factor these lessons back into development. This keeps our offering relevant and tuned to the scientific world outside the plant gates. Regular visits to research campuses, industry conferences, and technical working groups allow our manufacturing and technical support team to stay current and anticipate shifts in demand or regulatory outlook. This helps us redesign process parameters, tweak QC endpoints, or develop new analogs as market needs evolve.
Reliability runs deeper than hitting a certificate of analysis for one shipment. We view our part in the chemical industry as a joint project alongside our partners—forming the foundation for new medicines, advanced materials, and innovations still in the earliest research pipeline. By holding fast to hands-on, detail-driven process improvement and supporting every request with direct institutional know-how, we help keep projects moving and minimize the obstacles between an idea and execution.
Our focus extends beyond the pyridine ring. We apply what we have learned on one compound to improve outcomes on the next: how to identify reaction runaways before they form, how to tweak a quenching step for higher safety, how to minimize solvent loss and maximize reuse. The very act of manufacturing teaches all involved to value rigor, adaptability, and straightforward communication with end users. With each new campaign, we continue not just to supply a product, but to deepen the level of support, transparency, and reliability we bring to the chemical landscape.