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HS Code |
907127 |
| Product Name | 6-Bromo-3-fluoropyridine-2-carboxaldehyde |
| Molecular Formula | C6H3BrFNO |
| Molecular Weight | 204.00 g/mol |
| Cas Number | 942162-97-2 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and DMF |
| Storage Temperature | Store at 2-8°C |
| Smiles | C1=CC(=NC=C1C=O)BrF |
| Inchi | InChI=1S/C6H3BrFNO/c7-5-1-4(3-10)6(8)9-2-5/h1-3H |
As an accredited 6-BroMo-3-fluoropyridine-2-carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 10 grams, tightly sealed with tamper-evident cap, labeled with chemical name, purity, CAS number, and hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL (Full Container Load) safely stores and ships 6-Bromo-3-fluoropyridine-2-carboxaldehyde in sealed, secure chemical drums or containers. |
| Shipping | 6-Bromo-3-fluoropyridine-2-carboxaldehyde is shipped in secure, airtight containers, clearly labeled with hazard and handling information. The chemical is transported according to local and international regulations for hazardous materials, typically under controlled temperature and away from incompatible substances to ensure safety and product integrity throughout transit. |
| Storage | 6-Bromo-3-fluoropyridine-2-carboxaldehyde should be stored in a tightly sealed container under a dry, inert atmosphere (such as nitrogen) at room temperature or lower. Protect from moisture and direct sunlight. Store in a cool, well-ventilated area away from incompatible materials such as strong oxidizers and acids. Ensure appropriate chemical labeling and limit exposure to air to maintain stability. |
| Shelf Life | 6-Bromo-3-fluoropyridine-2-carboxaldehyde typically has a shelf life of 2 years when stored tightly sealed, cool, and protected from light. |
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Purity 98%: 6-BroMo-3-fluoropyridine-2-carboxaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures reliable downstream product formation. Melting Point 45°C: 6-BroMo-3-fluoropyridine-2-carboxaldehyde featuring a melting point of 45°C is applied in organic electronic material development, where controlled phase transition enables consistent film processing. Molecular Weight 220.97 g/mol: 6-BroMo-3-fluoropyridine-2-carboxaldehyde at molecular weight 220.97 g/mol is utilized in agrochemical research, where the defined mass supports precise stoichiometric calculations. Stability Temperature 80°C: 6-BroMo-3-fluoropyridine-2-carboxaldehyde stable at 80°C is used in high-temperature catalytic reactions, where thermal resilience maintains chemical integrity throughout processing. Particle Size <50 µm: 6-BroMo-3-fluoropyridine-2-carboxaldehyde with particle size below 50 µm is employed in fine chemical formulation, where improved dispersion accelerates reaction kinetics. Assay 99%: 6-BroMo-3-fluoropyridine-2-carboxaldehyde with an assay of 99% is used in medicinal chemistry research, where maximum analyte concentration enhances experimental accuracy. Moisture Content <0.5%: 6-BroMo-3-fluoropyridine-2-carboxaldehyde featuring moisture content less than 0.5% is applied in peptide coupling processes, where low water content prevents unwanted hydrolysis. |
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Manufacturing specialty chemicals brings a set of challenges that industry outsiders rarely imagine. From raw material sourcing through the final QC check, every step demands discipline — this is especially true for heterocyclic aromatic compounds where purity, trace impurity control, and batch-to-batch consistency make the difference between a promising new compound and a shelf full of useless by-products. Our team has seen these challenges up close with 6-BroMo-3-fluoropyridine-2-carboxaldehyde, a core intermediate we have produced at commercial scale for several years. Unlike more common benzene-based intermediates, this compound is tailored for pharmaceutical and crop protection research, thanks to its fused halogen and carbonyl functionalities.
In our labs, halogenated pyridine aldehydes like this molecule call for specific handling. The fluorine atom at the 3-position creates distinct reactivity—and that single atom can change both physical properties and reactivity compared to its non-fluorinated cousins. Incorporating both bromo and fluoro substituents in the pyridine ring isn’t just about increasing molecular weight. Bromine gives synthetic chemists a reliable point for subsequent cross-coupling, while the para aldehyde opens the door for the formation of imines, hydrazones, or more advanced building blocks. This dual reactivity supports a much wider library of downstream compounds compared to single-halogen products.
Our manufacturing batches for 6-BroMo-3-fluoropyridine-2-carboxaldehyde see regular orders from med-chem teams and process R&D groups who have learned the hard way that off-grade starting materials lead to scale-up failures. Impurities seem minor in milligram test reactions, but they become nightmares in scale-up or regulatory submissions. Isolation of this compound is sensitive to both atmospheric moisture and temperature swings, especially during the final work-up. Our teams learned to manage reactor conditions to lock in consistent yields and color. Careful solvent choices during purification have reduced trace residuals, meaning researchers avoid unwanted side-products in the following steps—especially important for regulatory-compliant APIs.
General product descriptions mean little unless they’re backed up with real process documentation. Over dozens of batches, we have seen that the melting point, spectral fingerprints (NMR and LC-MS), and chemical assay must align across the lot—not just on a single sample but in every drum. Because the aldehyde group is sensitive to air and light, operators receive training to minimize handling losses. Our QC managers insist on full chromatographic purity, as fluorinated pyridine impurities tend to show up as unexpected spots on TLC. Experience has taught us that even minor side-products can poison catalytic hydrogenation or Suzuki couplings. For 6-BroMo-3-fluoropyridine-2-carboxaldehyde, we run each batch through headspace GC to ensure no residual solvent, and keep moisture levels below 0.2% by Karl Fischer. These steps come from real failures we’ve had to troubleshoot, not from a textbook or stock spec sheet.
Ask any scientist who has tried to reproduce a published synthetic route and they’ll confirm the difficulty of finding precisely the right intermediates. The success of fragment-based drug discovery and next-generation fungicides depends on access to building blocks that deliver predictable outcomes. We have partnerships with pharma and agrochemical firms who rely on this product for rapid analog synthesis during early medicinal chemistry campaigns. With both a bromo and a fluoro substituent, this molecule enables unique regioselective coupling, often unlocking new SAR (structure activity relationship) possibilities unavailable from single-halogen or non-fluorinated aldehydes. Its use goes beyond just core skeleton construction—it also finds application in modifying electron density of heterocycles, producing fine-tuned activity profiles that give our client’s candidates an edge in crowded IP landscapes.
Handling active halogenated aldehydes is more than just labeling a drum “hazardous.” The chemical’s volatility and its tendency to react with atmospheric water mean storage conditions must remain controlled. Our engineering team routinely audits every batch for possible pressure buildup, especially during summer months or in warehouses with outdated HVAC. We replaced open-top drums with nitrogen-purged containers years ago, after a single leaky shipment cost us an expensive customer and taught us to introduce better moisture barriers. Drum management procedures shaped by day-to-day experience—not dictated from above—help keep workers and end-users safer. Spent process solvents from the synthesis contain both fluorinated and brominated organics, pushing us to invest in on-site solvent reclamation and halogen stripping, so downstream waste loads meet environmental targets.
Aldehydes on pyridine rings have become common in custom synthesis, but this one stands out for its rigid control over substituent positions. Some lesser products in the market use non-regioselective halogenation, which leads to mixtures of positional isomers. Those mixtures cost client time untangling analytical puzzles. Our route locks in the bromo at the 6-position and fluorine at the 3-position, with the aldehyde at position 2, eliminating positional ambiguity. This kind of control stems from repeated route optimization—multiple rounds of vendor selection, pilot reactions, and down-the-line feedback loops from customers who compared our materials to competitors side-by-side. There isn’t a shortcut: controlling reactivity at each introduction and quench step took us nearly a year of production trials. Our learning was simple: for complex building blocks, the synthetic route is only valuable if every step can be controlled at scale.
During the early years, customers would call in frustrated about micro-scale workups that failed during scale-up. In response, we invited process chemists to walk our floor and discuss their next steps. We learned that even trace amounts of unreacted 3-fluoropyridine or dibromides could suppress yields downstream—issues not revealed in TLC, but noted during kilo-lab or pilot scale. Fixing those issues informed how we ran each distillation, the grade of inert gas for transfers, the brand of filter aids used, and even the glassware cleaning routines. Our customers expect us to anticipate downstream failures and share best practices—and it paid off. Several partners today openly credit our batch records for reducing regulatory review times, because auditors flagged fewer ambiguous peaks or unknowns on their submission data.
Being a manufacturer, the pressure to chase quick margins often stares us in the face. We see requests for cut-rate, off-spec material—especially in industries that tolerate lower purity, but we’ve had to turn down rushed projects for the sake of our own reputation. The most memorable project failures happened on orders we should have declined—reactor fouling, lost product in isolation, customer rejections that bit into margins and trust. Maintaining robust batch records, transparent impurity profiles, and process documentation drives up costs, but skipping those steps guarantees headaches for everyone involved. We welcome researchers to inquire about upstream and downstream traceability, because those conversations keep us sharp and drive new mini-improvements every season.
We have watched the global supply chain shift, expand, choke, and reorganize, especially in the last decade. More than a few pharmaceutical customers have learned that overseas materials bought from resellers don’t always match specs or certificates. With a haloaromatic building block like 6-BroMo-3-fluoropyridine-2-carboxaldehyde, a slight difference in moisture can make the difference between a successful and a failed API campaign. Having direct communication with the actual producer means feedback flows both ways: requests for even tighter impurity specs, custom packaging for cold-chain, or last-minute rush orders when research pivots midstream. Our own sales and production staff work side-by-side. We share data on complaint rates, delivery times, and batch retests across functions, so technical issues become a shared challenge instead of siloed blame. Our culture relies on mutual trust with clients—we know sloppy work costs us, and even a minor deviation can snowball during scale-up.
No technical sheet can substitute for experience, so we share what we’ve learned: keep 6-BroMo-3-fluoropyridine-2-carboxaldehyde tightly closed, preferably in amber glass or lined steel drums under inert gas. Short periods at room temperature do not degrade it rapidly, but long-term exposure to open air or sunlight leads to gradual hydrolysis and darkening—compromising both assay and downstream yield. Most common mishandling involves transferring material with damp scoopulas or non-dedicated spatulas, leading to spot contamination. Using PTFE-lined caps and molecular sieves in desiccators really stretches the shelf life, especially in high-humidity climates. Customers who follow these simple routines see batch-to-batch reproducibility hold steady, and NMR spectra match reference material with no surprises.
Making high-quality intermediates brings pride and stress. We have chosen to invest in high-performance reactors, frequent process audits, and resilience in raw materials procurement so clients don’t need to worry about surprises mid-trial. Decades spent troubleshooting our own processes taught us that reliable product doesn’t emerge from luck or shortcuts; it comes from a culture of improvement and feedback from hands-on chemists. When researchers request data beyond the certificate of analysis, we welcome it—knowing someone will spot trends that help us refine both process and product. The real difference between a commodity chemical and a specialty intermediate comes from the relationships built around it: upstream learning passed forward, downstream problems taken as lessons, not errors.
The chemical value chain is rarely linear. From regulatory shifts in halogenated waste disposal, to supply tensions on fluorinated reagents, we have felt pressure from many sides. By investing in local supply partnerships and keeping our own waste treatment facilities in top order, we navigate tighter export rules and evolving trace impurity standards. Our regulatory team keeps an eye on global harmonization so that one batch can serve customers in several countries without custom rework. For large orders, we schedule regular reviews with client QA teams—sharing insights on transportation, long-term stability, and even packaging improvements learned from field failures. This sort of attention helps both sides avoid expensive surprises, especially in time-sensitive R&D campaigns.
Few products highlight the collaboration between chemists, engineers, and end-users like 6-BroMo-3-fluoropyridine-2-carboxaldehyde. Internally, we share case studies about scale-up lessons, unexpected NMR shifts, and creative solutions for waste abatement with our peers. Newer team members spend time shadowing operators who remember early production headaches, passing down hard-won tricks. Our openness to outside input creates a pipeline for improvement. Responding to surface-level complaints is easy—true advancement comes from caring about downstream chemistry, demonstrating a willingness to revisit routes, tweak process variables, and share both wins and stumbles. Customers gain not just a raw material, but a link in a community that takes responsibility for every drum that leaves our gate.
Across the industry, the best results follow reliable partnerships. Synthetic chemists, process engineers, and QC analysts know the difference between top-tier and commodity-grade building blocks. 6-BroMo-3-fluoropyridine-2-carboxaldehyde requires the kind of real-world knowledge that comes from sustained production, direct feedback, and a willingness to solve—not sidestep—challenges. Our story isn’t just about selling a molecule; it’s about supporting discovery, reducing waste, and making each project run just a bit smoother, because the work doesn’t end at the drum’s barcode. We invite researchers, project leaders, and new partners to connect, share their next synthesis target, and experience how hands-on manufacturing support can unlock new potential with every order.