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HS Code |
577889 |
| Chemical Name | 6-bromo-3-fluoro-pyridine-2-carbaldehyde |
| Molecular Formula | C6H3BrFNO |
| Cas Number | 1178778-90-1 |
| Appearance | Pale yellow to brown liquid |
| Purity | Typically ≥97% |
| Storage Temperature | 2-8°C |
| Solubility | Soluble in common organic solvents |
| Synonyms | 2-Formyl-6-bromo-3-fluoropyridine |
| Smiles | C1=CN=C(C(=C1Br)F)C=O |
| Inchi | InChI=1S/C6H3BrFNO/c7-5-1-4(3-10)9-2-6(5)8/h1-3H |
| Hazard Statements | Irritant; handle with care |
As an accredited 6-bromo-3-fluoro-pyridine-2-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 10 grams; white screw cap, tamper-evident seal, labeled with chemical name, formula, hazard pictograms, and lot number. |
| Container Loading (20′ FCL) | 20′ FCL loaded with securely packed drums of 6-bromo-3-fluoro-pyridine-2-carbaldehyde, compliant with chemical transport safety regulations. |
| Shipping | **Shipping:** 6-Bromo-3-fluoro-pyridine-2-carbaldehyde is shipped in tightly sealed containers under inert atmosphere to prevent degradation. The package is labeled according to chemical safety regulations, and compliant with UN, IATA, and DOT guidelines. Temperature control may be used if required, and all shipments include material safety data sheets (MSDS) for handling and emergency measures. |
| Storage | 6-bromo-3-fluoro-pyridine-2-carbaldehyde should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances like strong oxidizing agents. Keep the container tightly closed and properly labeled. Store at 2–8°C (refrigerator) is recommended. Handle under inert atmosphere if sensitive to moisture or air. Use appropriate chemical storage cabinet and follow standard laboratory safety practices. |
| Shelf Life | 6-bromo-3-fluoro-pyridine-2-carbaldehyde typically has a shelf life of 12-24 months when stored cool, dry, and protected from light. |
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Purity 98%: 6-bromo-3-fluoro-pyridine-2-carbaldehyde with a purity of 98% is used in medicinal chemistry synthesis, where it ensures high yield and target compound fidelity. Melting Point 68-70°C: 6-bromo-3-fluoro-pyridine-2-carbaldehyde with a melting point of 68-70°C is utilized in pharmaceutical intermediate manufacturing, where controlled solidification improves process reproducibility. Stability Temperature up to 50°C: 6-bromo-3-fluoro-pyridine-2-carbaldehyde stable up to 50°C is applied in fine chemical production, where thermal stability enhances storage and handling safety. Molecular Weight 220.01 g/mol: 6-bromo-3-fluoro-pyridine-2-carbaldehyde with a molecular weight of 220.01 g/mol is used in heterocyclic building block formation, where accurate stoichiometry supports precise reaction design. Color Slightly Yellow: 6-bromo-3-fluoro-pyridine-2-carbaldehyde with a slightly yellow color is used in chemical research, where color uniformity aids in visual quality assessment. Solubility in DMSO: 6-bromo-3-fluoro-pyridine-2-carbaldehyde soluble in DMSO is applied in lead compound discovery, where enhanced solubility accelerates screening workflows. |
Competitive 6-bromo-3-fluoro-pyridine-2-carbaldehyde prices that fit your budget—flexible terms and customized quotes for every order.
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We have spent years refining our approach to producing specialty pyridine derivatives. In our shop, nothing leaves the facility without meeting stringent purity protocols, and 6-bromo-3-fluoro-pyridine-2-carbaldehyde is no exception. Chemists working in active pharmaceutical ingredient (API) research or in fine chemicals manufacture understand the headaches that come with batch-to-batch variability, trace contamination, or inconsistent reactivity. Our team runs every batch through rigid quality control, including HPLC, NMR, and mass spectrometry, because we know the downstream impact when something doesn’t match up. Some of our peer manufacturers attempt to speed up production or cut costs at the purification stage, often leading to residual byproducts that complicate further chemistry. We invest in additional purification—not just to hit a target number but to create a reliable standard for demanding applications.
6-Bromo-3-fluoro-pyridine-2-carbaldehyde sits in a sweet spot between structural complexity and synthetic utility. The compound features a bromine atom at the 6-position, a fluorine at the 3-position, and a reactive formyl group at the 2-position of the pyridine ring. For chemists, that means three orthogonal handles: bromine offers a route for cross-coupling (Suzuki-Miyaura, Buchwald-Hartwig, or Stille), fluorine alters both electronic properties and metabolic stability, and the aldehyde group opens up access to imines, oximes, and more. This combination isn’t just decorative. Each group serves a purpose, and only a handful of suppliers globally bring the material with the tight control that ensures all three positions are correctly substituted without unintended isomers or over-halogenated byproducts.
We emphasize running the synthesis under conditions that limit side reactions. Many researchers have told us about difficulties handling pyridine-based aldehydes from other sources—issues like partial oxidation to the acid, or poor storage stability because of residual moisture and decomposition products. Our facility maintains a dry, inert atmosphere during both production and packaging stages, using nitrogen and vacuum-sealed bottles, to help chemists get consistent results during their own synthetic work.
Our typical lot of 6-bromo-3-fluoro-pyridine-2-carbaldehyde exceeds 98% purity, confirmed by multiple orthogonal methods. Water content is kept below 0.2%, something we pay close attention to since excess moisture speeds up hydrolysis and can wreck high-throughput screening campaigns in pharma labs. We've had several partners from medicinal chemistry teams tell us that lower-grade material, often bought based on price alone, stalled reactions or introduced visible impurities in downstream NMR. Those headaches are avoidable by using batches produced with experience, patience, and a practical understanding of how this compound fits into multi-step synthesis.
The physical appearance of our material is a pale yellow crystalline solid or, in some circumstances, a low-melting solid depending on storage and handling, packed in amber glass to reduce photodegradation. We avoid the temptation to send out material that hasn’t had sufficient drying time or purification, as we have learned from long experience how quickly a poor batch can ruin customer trust and publication efforts.
The core application for 6-bromo-3-fluoro-pyridine-2-carbaldehyde is in the creation of pharmaceutical intermediates and advanced agrochemical scaffolds. When our clients design kinase inhibitors, antifungal agents, or crop protection molecules, small modifications to the pyridine core can radically alter their compound’s activity and selectivity. The presence of both bromine and fluorine allows for subsequent coupling and substitution steps that would not be possible—at least not efficiently—if only a single halogen were present.
In our internal research, we have seen how switching from simple pyridine-2-carbaldehyde to the 6-bromo-3-fluoro variant gives a different polarity profile, and the steric bulk at the 6-position can control regiochemistry in further transformations. Fluorine is more than just a medicinal chemistry “fashion statement”—it blocks certain metabolic pathways, prolongs compound half-life, and can quiet ferocious reactivity at adjacent positions on the ring. By offering a starting point with this nuanced balance of electronic effects, we give chemists more latitude in their synthesis planning.
Many labs still use unsubstituted pyridine-2-carbaldehyde or the simple mono-bromo versions because they appear cheaper and more widely listed. We routinely field calls from researchers who have wasted months trying to build molecular complexity onto those less-functionalized cores, only to realize the extra steps introduce cost, lower yields, or unwanted byproducts. Starting from 6-bromo-3-fluoro-pyridine-2-carbaldehyde, teams sidestep several hazardous or tedious halogenation steps—and don’t need to gamble with inconsistent reactivity.
Another point of difference comes in handling. Lesser aldehydes, especially in pyridine systems, tend to oxidize in ambient storage, especially if shipped long distances or exposed to humidity. We seal our product under anhydrous, inert atmosphere to maintain the true aldehyde functionality, preserving the sharp NMR and high GC purity that researchers demand. The feedback we receive—after years of handling other manufacturers’ unstable or malodorous pyridine aldehydes—is that our packaging and attention to post-synthesis stability saves whole research timelines from unexpected setbacks.
We regularly survey chemists working in both large discovery groups and startup biotech labs about problems in scale-up, isolation, and downstream purification involving pyridine-2-carbaldehyde derivatives. The weight of experience points to one central frustration: the lack of predictability with off-the-shelf intermediates. Many have told us about the domino effect created by microvariability in impurity profile, which can turn a straightforward coupling step into a string of failed or low-yield reactions.
We take that feedback seriously. Our facility incorporates a feedback loop between NMR, MS, and GC data collected from each lot and the spot-testing done at client sites. We care less about checking boxes and more about hearing how the material translates into real chemistry—how quickly it dissolves, whether strange peaks show up in crude NMR, and whether coupling partners react as expected. Over the last several years, no other product has prompted as much two-way communication between our shop and research labs as this aldehyde scaffold. The dialogue has driven us to push for cleaner product, improved packaging, and shorter lead times, all grounded in actual bench intuition.
As producers, we often see our role stopping at the drum or bottle, but the story for a material like 6-bromo-3-fluoro-pyridine-2-carbaldehyde continues long after it leaves our shelves. Our team tracks how the compound fares under a variety of shipping conditions—hot, cold, humid, and arid environments. With some intermediates, companies face customs delays or warehouse shelf time that rarely factored into original planning. We have redesigned storage protocols to keep the aldehyde protected from trace moisture and light, and we have updated outer packaging to withstand both overland and air transport.
We see the effect in repeat orders for larger scale as pilot reactions succeed and enter production, but also in the quiet reduction in troubleshooting queries we receive. We do not stop at purity data in a certificate; we think about what a scientist will face six months after buying, as they reach to replicate or scale up an old process. That mindset means we constantly review degradation profiles and keep active batch samples stored under stress conditions—to catch any new issues before customers run into them.
While the synthetic route to 6-bromo-3-fluoro-pyridine-2-carbaldehyde has matured over years of development, certain challenges remain. Handling highly active brominating reagents, managing exotherms, and controlling regioselectivity all require discipline and vigilance—no batch is truly routine. Our chemists encounter occasional bottlenecks when raw material availability dips or when we need to adjust batch sizes for fluctuating demand in medicinal research.
We respond by maintaining a buffer stock, pre-qualifying alternate vendors for starting materials, and keeping all process changes documented down to the lot level. Changes in regulatory frameworks around hazardous shipments can catch manufacturers flat-footed, and we stay engaged with new rules affecting export controls or labeling. From firsthand experience, ignoring these changes costs valuable time and invites compliance risk.
Some clients diverge from the classic reactivity pathways and push for use in heterocyclic synthesis or in novel organometallic frameworks. We support those exploratory projects, lending samples and analytical support, because their success broadens both our technical portfolio and the future versatility of the compound for the rest of the community. Over time, these conversations help us tailor the physical packaging, suggested conditions, and technical bulletins to match reality instead of textbook assumptions.
Choosing a high-purity 6-bromo-3-fluoro-pyridine-2-carbaldehyde might seem like a small decision in the context of an entire multi-step synthesis. From our vantage point, that decision becomes pivotal during troubleshooting or scale-up. Unforeseen impurities, altered melting points, or inconsistent color can send chemists down time-consuming false trails. Every extra hour spent hunting for impurity sources or repeating purification procedures adds cost, frustrates staff, and pushes key milestones further away.
By investing early in a rigorously controlled intermediate, project leaders find more predictable progress. We have seen clients in pharmaceutical research unlock SAR (structure-activity relationship) data more quickly with fewer dead-end synthetic routes. Agrochemical developers report cleaner yields of final actives using our material, saving both labor and costly post-synthesis remediation. We do not claim our compound solves every research challenge, but we stand by the fact that starting with a high-grade, well-characterized intermediate shrinks risk across the process.
Every batch of 6-bromo-3-fluoro-pyridine-2-carbaldehyde we send out reflects not only our technical standards, but our broader commitment to supporting scientific innovation. We see ourselves as more than manufacturers—our business is rooted in partnership with people at the bench, facing real-world constraints and expectations. We listen to their feedback on solubility, reactivity, and storage behavior, and integrate those lessons into the next manufacturing cycle.
Production of high-value pyridine scaffolds continues to evolve alongside advances in organic synthesis and the demands of regulators. As environmental and safety guidelines tighten, we proactively assess waste streams, solvent choices, and energy consumption without compromising purity targets. The expectation is not just to deliver material that works today, but to ensure we can serve the next wave of challenging synthetic problems as the field grows.
Our stake in the chemical industry is not just economic. There is a concrete sense of fulfillment in seeing a time-tested process yield material that empowers others to do breakthrough research. Each successful batch represents countless iterations, tweaks, and the wisdom of chemists who know what questions to ask, when to slow down, and when to innovate.
To those who are redefining boundaries in medicinal chemistry or materials science using 6-bromo-3-fluoro-pyridine-2-carbaldehyde, we offer both our product and our expertise. We provide technical details not as a formality, but as part of an ongoing dialog with peers who hold high standards and expect consistent results. Every bottle that leaves our facility is a handshake, a promise, and an invitation to collaborate in the ongoing advancement of chemical science.