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HS Code |
608593 |
| Product Name | 2-Bromo-3-Formylpyridine |
| Cas Number | 14247-12-6 |
| Molecular Formula | C6H4BrNO |
| Molecular Weight | 186.01 g/mol |
| Appearance | Light yellow to yellow solid |
| Melting Point | 61-64 °C |
| Density | 1.703 g/cm³ |
| Purity | Typically ≥ 97% |
| Solubility | Soluble in organic solvents like DMSO, dichloromethane |
| Synonyms | 2-Bromo-3-pyridinecarboxaldehyde |
| Smiles | C1=CC(=C(N=C1)Br)C=O |
| Inchi | InChI=1S/C6H4BrNO/c7-6-4-5(3-9)1-2-8-6/h1-4H |
As an accredited 2-Bromo-3-Formylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g sample of 2-Bromo-3-Formylpyridine is sealed in an amber glass bottle, labeled with chemical details and hazard warnings. |
| Shipping | 2-Bromo-3-formylpyridine is shipped in tightly sealed containers, protected from light and moisture, under standard chemical shipping regulations. The package is clearly labeled with hazard information. It is shipped via approved carriers, ensuring compliance with local and international transport regulations for hazardous materials. Handling instructions and safety data sheets are included. |
| Storage | 2-Bromo-3-formylpyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep away from strong oxidizing agents and moisture. Store under an inert atmosphere if possible. Ensure appropriate labeling and access controls to prevent unauthorized handling. Always follow standard chemical storage and safety procedures. |
Applications of 2-Bromo-3-Formylpyridine in Industrial Manufacturing2-Bromo-3-Formylpyridine is a specialized chemical intermediate widely used in demanding synthesis routes across the pharmaceutical and agrochemical industries. Its unique structure provides specific reactivity that enables downstream manufacturers to construct advanced molecular frameworks not easily accessible with other pyridine analogs. Below are detailed industrial application scenarios focusing on the actual integration points, compliance standards, formulation usage, and end-product types for this material. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) Building BlockMany leading pharmaceutical manufacturers employ this material as a key intermediate in the synthesis of pyridine-based APIs, especially where brominated and formyl functionalities are central to biological activity. Its role in targeted condensation and cross-coupling steps allows precise modification in the late-stage assembly of complex molecules, with strict adherence to regulatory requirements in every batch. Purity and traceability remain critical as this intermediate frequently appears in patent-protected synthetic pathways for CNS and oncology drug substances. Industry compliance standards
Typical usage ratio
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2. Agrochemical Intermediate for Fungicide SynthesisThis material serves as an essential heterocyclic synthon in the industrial manufacturing of modern pyridine-based fungicides, particularly those requiring site-specific bromination patterns to achieve target crop protection profiles. Its inclusion enables precision design in multi-step agrochemical production, supporting high conversion rates and selective functionalization favored by agrochemical regulatory agencies. Industry compliance standards
Typical usage ratio
Downstream process integration
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3. Key Intermediate for Custom Chemical Contract Manufacturing (CDMO)Custom chemical development and contract manufacturing often require unique heterocyclic fragments for rapid medicinal chemistry and fine chemical projects. 2-Bromo-3-Formylpyridine is implemented as a privileged scaffold in high-value, custom syntheses where no direct analogs can substitute its reactivity. Its traceability and batch-level documentation meet the stringent requirements of contract customers in regulated markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Starting Material for Electronic Chemical SynthesisThis pyridine derivative finds utilization in the development of specialized functional materials for thin-film electronics and optoelectronic manufacturing, where precise substitution patterns matter for tuning electronic and optical behavior. R&D operations in electronic materials value unique brominated compounds to achieve required charge transport or emission properties in downstream device applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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For chemists and process engineers pushing into specialized syntheses, the demand for reliable building blocks never lets up. 2-Bromo-3-Formylpyridine, molecular formula C6H4BrNO, has carved out a spot as a dependable intermediate for pharmaceutical, agrochemical, and functional material fields. Our production focuses on the direct needs of people who spend their days in labs and on process lines, not in offices.
In the facility, careful batch records track each run of 2-Bromo-3-Formylpyridine from start to finish. The material rolls off the line as a pale yellow-to-beige crystalline solid. This appearance comes from a tight grip on impurity control during both reaction and workup. For most uses, we supply it in 98.0% minimum purity, checked by HPLC and confirmed for identity by 1H NMR. Moisture stays below 0.5% KF. Residual solvents, particularly DMF and toluene, fall well under stricter EU and US pharma guidelines, and our filtration steps weed out insolubles that could derail a small coupling run.
Typical particle size sits between 100 and 500 microns. If a formulary chemist needs a special grind or microcrystalline cut for rapid dissolution, our team can tweak the isolation protocol. We do not rotate lots between distributors, so every container sold — whether one kilogram or a drum — comes direct from our own workshop. That kind of supply chain discipline has cut down on damaged product, mismatched labels, and substitute deliveries that used to frustrate our earlier years.
We watched the appetite for 2-Bromo-3-Formylpyridine pick up momentum as patent filings for kinase inhibitors and anti-infective leads spread. In the hands of a pharmaceutical process chemist, this molecule often becomes a prized synthon for Suzuki-Miyaura couplings after reduction to the corresponding alcohol or further transformation of the aldehyde group. It bridges a tough gap — robust enough to withstand air and shipping, but reactive enough to slot into the modern benchtop’s toolkit.
Crop protection chemists make a different kind of use. Their teams value the strong selectivity the aldehyde brings, along with the reliability of the bromo functionality for quick cross-coupling. The tight melting range we offer (65-69°C) lets screeners predict reactivity with a range of coupling partners. When a new herbicide scaffold needs quick gram-to-kilo scale-up, little quirks in crystallinity or trace heavy metals can creep in and slow progress down. By keeping each step transparent, we help speed up that race from milligram library to multikilogram seed batch.
Our R&D crew has hammered out a scalable and reproducible synthesis, side-stepping many headaches of legacy chemistries. Early batches would sometimes bring along colored impurities or traces of unreacted starting material, leading to sticky residues upon isolation. Through repeated cycles of root-cause analysis, we dialed in the reaction temperature and distillation parameters — knocking out side reactions and driving down waste.
Choosing to control raw material quality was not a popular move at first; some in purchasing thought commercial feedstock should be “close enough.” That attitude changed when low-purity 3-formylpyridine repeatedly poisoned our bromo-introduction step, filling up the scrubbers and setting off alarms over nitrogen levels. Today, every drum of starting pyridine gets fingerprinted before use, protecting every downstream reaction from batch-to-batch swings. This push toward full traceability comes from necessity, not slogans.
Once isolated, the product runs through cold-room storage before packing. No amount of packaging science can substitute for real environmental control. We train warehouse staff to catch off-odors, clumping, or dust contamination. More than once, their vigilance caught a leaking valve or a batch with residual moisture before it left the floor. These small details make the difference between a smooth high-throughput synthesis and a run that stalls halfway through.
The world of substituted pyridines is crowded, but details set each molecule apart. Some users compare 2-Bromo-3-Formylpyridine to the isomeric 2-Bromo-4-Formylpyridine or the more reactive 3-Bromopyridine as electrophilic partners. Our technical team works through the options with customers almost weekly. The formyl group at the 3-position tunes the electronic distribution — affecting coupling, nucleophilic attack, and side-chain modification rates. That’s critical during lead optimization or fragment growing, because it cuts the number of purification steps downstream.
While the 2-bromo, 4-formyl isomer might look similar by name, our own test runs show it drags in more side reactions under the same coupling conditions, likely due to different resonance forms destabilizing the intermediate. Many case studies reflect back our own experience: higher-yielding reactions, tighter chromatography, and fewer byproducts when starting with the 3-formyl variant. For teams chasing purity, that translates to smoother process validation and lower operating costs, well beyond the cost of a single intermediate.
Product substitution sometimes flares up in sourcing cycles or tender bidding. Some groups try to substitute 3-bromopyridine or 2-bromopyridine and tack on an aldehyde after the core coupling step. Every time, final step yield takes a hit, and rarer, more stubborn impurities show up in column fractions. We’ve spoken with contract manufacturers who wished they hadn’t chased price over process fit. Sticking with 2-Bromo-3-Formylpyridine shortens route length, helps avoid build-ups of unsightly byproducts, and lowers the number of gram-scale sulfonation or reduction steps.
Conversations with end-users directly shape our manufacturing decisions. A few years ago, a European team flagged persistent off-color product — their HPLC showed a peak at 0.4% at 240 nm, right where they couldn't tolerate it. We overhauled the recrystallization protocol, shifted to a new type of solvent (screened for both cost and ecological safety), and invited them for a site visit. Now, not only did the color spec fall under 20 APHA units batch after batch, but overall yield-to-purity increased by 4%. Discrepancies rarely begin and end with paperwork. We still bring in customer lots for off-test analysis, closing the loop through real-world data, never assumptions.
With regulatory changes rolling out ever more frequently, documentation and batch-to-batch reporting take up much of the conversation today. No one wants to be the one holding delivery when an audit lands unexpectedly. In our factory, certificate of analysis generation happens in real-time, not as an afterthought once all drums are stacked. Every employee in QC knows who runs which test and why. This mentality ensures that documentation parallels the product, not lagging behind it. Our partners have seen faster audits and smoother tech transfer as a direct result.
Bringing fine chemicals to market at scale brings its share of headaches. Handling pyridine derivatives tests both patience and infrastructure. Early attempts at ramping output above 100 kg made crystal formation unpredictable — products occasionally oiled out, trapping trace solvents and chopping up scalability. We invested in jacketed filtration and vacuum drying setups that minimize thermal lag throughout the batch, ensuring slow, even cooling. By keeping the process transparent to operators and visitors alike, rework costs stayed low and rejections became rare.
The most persistent stumbling block has always been controlling unwanted side-product formation. In particular, brominated byproducts at the 5-position or double formylation threatened to derail both analytical testing and downstream performance. Our technical crew built a library of failed processes over the years, marking each run, every deviation, and all raw data traces. No database alone will teach how to smell an off-batch or notice subtle changes in filter cake color; that insight comes from hands-on training and walk-downs by senior staff. By putting experienced chemists on the production floor and giving them authority, we dodge issues before they leave the facility — what should be the standard everywhere, but often is not.
Waste treatment regulations push site teams to find new solutions for spent solvent and pyridine waste. Years ago, we learned hard lessons after an inspection found above-limit emissions. Since then, closed loops and inline monitoring became built into every new process change. The focus shifted from just meeting the spec to giving neighbors less reason to file complaints. Solvent recovery, previously an afterthought, now increases overall efficiency and gives the plant a smaller environmental footprint — something people in the community actually notice.
Buyers discover real value in working with manufacturing teams who own every step from raw material selection to final drum sealing. Many common frustrations — trace impurities, mismatched specs, uncertain lead time — tie back to long, layered supply chains and lack of transparency. Teams who depend on reliable 2-Bromo-3-Formylpyridine often need more than a shipping notice or a standard COA; they need to be certain about what’s coming through the door, right down to the last ppm.
Research and innovation depend on predictability, whether the product ends up in a pilot run for a novel therapy or a multi-ton campaign backing up a mainline pesticide. Direct dialog with process chemists and QC managers, not just with account reps, shapes product improvements. Last year, we worked closely with a pharmaceutical partner ramping up a new candidate. They flagged a tendency for certain lots to cake during storage, risking uneven reactivity during later coupling steps. Back at the plant, we mapped storage conditions and adjusted drying curves. The lessons fed into the next cycle, and by mid-year, returns for caking dropped off the complaint lists. Not everyone wants to share process quirks, but those who do wind up with better product consistency and happier development teams.
Every kilo matters. Smaller research teams order 2-Bromo-3-Formylpyridine five or ten kilos at a time to test new synthetic hypotheses. The university teams usually face strict budget controls and long procurement cycles. A surprising number still request test lots — even after multiple purchases — just to confirm nothing has shifted. We never penalize these requests; anyone serious about their results should demand the same from suppliers as they demand from themselves.
Moving up, contract research organizations frequently need parallel runs of closely related molecules. Contamination or cross-mixups between products like 2-Bromo-3-Formylpyridine and 2-Bromopyridine can ruin whole downstream screens. By sealing product lines and keeping labeling audit trails tight, we reduce the risk of error from packing to shipment. Automation helps, but dedicated people — with years on the floor — make the true difference.
The scale-up to industrial production puts even more pressure on supply reliability, cost stability, and regulatory compliance. Multikilogram orders require early scheduling and real-time project tracking to avoid plant bottlenecks. We prioritize transparency at every stage, feeding real-time analytics into availability projections. No last-minute surprises; no disconnected warehouses. If one batch falls outside spec, it won’t ship, no matter the pressures.
Years ago, 2-Bromo-3-Formylpyridine played a specialized role in a few high-end projects. Current demand reflects a shift toward broader, more aggressive development goals in pharmaceutical and agricultural chemistry. As international regulations shift, our teams adapt, not by making claims for market share, but by listening to the stories of people at the bench. Early adopter programs and collaborative synthesis experiments bring valuable feedback. Product improvements rarely come from the desk — they come from what goes right and wrong during real synthesis.
Customers sometimes ask about green chemistry options, whether our process can incorporate cheaper or safer halide sources, or if direct air oxidation paths could cut down on energy spend. While each alternative pathway brings its own risks and developmental hurdles, we keep them on the table and invest in small-scale pilot runs. Changes don’t come quickly in fine chemical synthesis. Rushing a new process to production can compromise both safety and yield. Our investments always follow real needs — lower hazard profiles, reduced solvent load, leaner product isolation. Future improvements will likely center around process intensification and molecular recycling, giving users more confidence in both safety and supply.
We take responsibility for the process as much as for the product. Auditors ask hard questions about waste handling, emissions, storage conditions, and safety protocols, and a manufacturer who can answer with real data — not just spreadsheets — earns trust. Our process documentation contains every anomaly, every deviation, every fix. Rarely does a dramatic breakthrough solve production headaches; relentless small-scale adjustment does the heavy lifting.
Direct access to process records and analytical data wins over regulatory bodies and longtime customers alike. It clears up miscommunications and stops problems before they develop into larger ones. By handing over chromatography traces, batch run data, and even failed batches, we support open discussion and quicker troubleshooting. Customers often point out the difference in maximum allowable impurity levels or off-cut fractions between manufacturers; ours bear the weight of real process control, not just marketing promises. We take it personally when standards slip — pride in the work has no substitute.
2-Bromo-3-Formylpyridine often represents an inflection point in a synthesis pathway: a molecule that, done properly, removes barriers for downstream construction of ever-more-complex targets. Researchers who commit their time, funding, and creativity to a project deserve a supply partnership anchored in experience, openness, and hands-on problem solving. In a world where too many chemicals come with generic documentation and little recourse when something fails, we put our name and reputation behind each kilogram shipped out.
The chemistry community’s expectations keep rising. Whether chasing sharper pharmacophores, greener process routes, or tighter regulatory control, every stakeholder raises the bar for intermediate quality. As a manufacturer, we see that clear path: remaining rooted in everyday process discipline, never passing the buck, and always favoring long-haul partnerships over one-off sales. Continuous efforts go into refining 2-Bromo-3-Formylpyridine for next-generation challenges. The molecules from our plant aren’t just line items on a spreadsheet — they’re decades of practical know-how, trusted relationships, and direct manufacturing commitment distilled into every batch.