|
HS Code |
190968 |
| Chemical Name | 6-fluoro-2-methyl-pyridine-3-carbaldehyde |
| Molecular Formula | C7H6FNO |
| Cas Number | 79678-49-2 |
| Appearance | Pale yellow to yellow liquid |
| Boiling Point | 215-217°C |
| Density | 1.21 g/cm3 |
| Purity | Typically >97% |
| Solubility | Soluble in organic solvents (e.g., DMSO, methanol) |
| Refractive Index | 1.545-1.555 |
| Flash Point | 93°C |
| Smiles | CC1=NC=C(C=O)C(F)=C1 |
As an accredited 6-fluoro-2-methyl-pyridine-3-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25g of 6-fluoro-2-methyl-pyridine-3-carbaldehyde, labeled with hazard symbols and chemical information. |
| Container Loading (20′ FCL) | Loaded in 20′ FCL with secure, sealed drums; stored under cool, dry conditions to prevent degradation of 6-fluoro-2-methyl-pyridine-3-carbaldehyde. |
| Shipping | 6-Fluoro-2-methyl-pyridine-3-carbaldehyde is shipped in tightly sealed containers, typically made of glass or compatible materials, to prevent leaks and contamination. It is transported under ambient or controlled temperatures, away from direct sunlight and incompatible substances. Appropriate labeling and documentation, including hazard identification, are provided in accordance with chemical safety regulations. |
| Storage | 6-Fluoro-2-methyl-pyridine-3-carbaldehyde should be stored in a tightly sealed container, under an inert atmosphere, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep separate from oxidizing agents, acids, and bases. Store at room temperature or as recommended by the supplier. Use appropriate personal protective equipment when handling. |
| Shelf Life | 6-Fluoro-2-methyl-pyridine-3-carbaldehyde should be stored in a cool, dry place; shelf life is typically 12-24 months. |
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Purity 98%: 6-fluoro-2-methyl-pyridine-3-carbaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product quality. Melting point 54°C: 6-fluoro-2-methyl-pyridine-3-carbaldehyde with a melting point of 54°C is used in fine chemical manufacturing, where controlled phase behavior supports efficient processing. Molecular weight 139.12 g/mol: 6-fluoro-2-methyl-pyridine-3-carbaldehyde at a molecular weight of 139.12 g/mol is used in agrochemical discovery, where precise molecular integration enhances target specificity. Stability temperature up to 120°C: 6-fluoro-2-methyl-pyridine-3-carbaldehyde with stability up to 120°C is used in high-temperature condensation reactions, where thermal robustness maintains compound integrity. Particle size <50 microns: 6-fluoro-2-methyl-pyridine-3-carbaldehyde with particle size below 50 microns is used in catalyst preparation, where fine dispersion optimizes catalytic efficiency. Water content <0.5%: 6-fluoro-2-methyl-pyridine-3-carbaldehyde with water content less than 0.5% is used in moisture-sensitive syntheses, where dryness prevents side reactions and impurities. |
Competitive 6-fluoro-2-methyl-pyridine-3-carbaldehyde prices that fit your budget—flexible terms and customized quotes for every order.
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Working day in and day out manufacturing specialty pyridine derivatives, I see firsthand what sets a truly high-grade batch apart. 6-fluoro-2-methyl-pyridine-3-carbaldehyde isn’t the sort of compound you stumble across in every fine-chemicals portfolio. Its synthesis draws on a precise blend of fluorination and methylation techniques that challenge even experienced operators. Our team has refined temperature control, solvent selection, and isolation conditions right on the production floor – no two runs behave exactly the same. Even tiny variations in pressure or the nature of starting materials force hands-on adjustments, tuned by years of collective expertise. While other derivatives might ride more predictable process flows, this molecule expects you to stay alert at every step.
The presence of both the fluorine atom on the 6-position and the methyl on the 2-position significantly alters the electronic character of the pyridine ring. Chemically, this means the aldehyde group reacts more selectively than a non-fluorinated or non-methylated analog would. Over the years, our in-process QC teams have cataloged subtle drifts in reactivity that stem from even fractional impurities, especially isomers. It's not only a matter of chemical curiosity. Downstream developers—especially those in agrochemicals and pharmaceuticals—require a consistently pure material. Minor isomer contamination or trace metal content changes final product yields and safety profiles in real synthesis work. Our experience on the factory floor connects directly to these concerns, from the operator adjusting the reactor jacket to the analyst running the final purity check.
Every lot of 6-fluoro-2-methyl-pyridine-3-carbaldehyde comes off our lines with a close eye on the properties demanded by real research and commercial applications. Targeted GC purity runs above 98% w/w, measured against freshly calibrated standards, not just once but at several critical stages in production. Moisture content never escapes our vigilance: water can disrupt subsequent transformations like oxidations or conjugations. Proudly, we've driven residual solvent levels below most published thresholds, so our clients never encounter issues during crystallization or scale-up. We record melting points, refractive index readings, and spectral data, forming an operational baseline that feeds back into process optimization and customer support. There is no “good enough”—feedback from end-users has pushed us to cut process variation to consistently low single-digit ppm for most common impurities.
Demand signals rarely rise by surprise. Research teams in life sciences and crop protection value the unique reactivity profile that our product offers. The electron-withdrawing effect of the fluorine shifts how nucleophiles and electrophiles attack the pyridine. Medicinal chemists prefer this scaffold in various lead-optimization programs. They report improved bioavailability and metabolic stability compared with non-fluorinated versions. Our records show repeat orders most often from advanced R&D labs seeking to build fluorinated heterocycles or explore structure-activity relationships.
Importantly, when we field requests for pilot-scale or multi-ton lots, the pattern is clear—users don’t want the unpredictability of mixed-supplier or repackaged stock. They need direct verification of composition, batch records, and support for audits. Direct manufacturer access to analytical archives and process histories saves time and skips third-party errors. We've shaped our internal logistics to keep this commitment strong, running regular retests and storing reserve samples for every shipment.
Seasoned manufacturers know that shortcuts in chemical sourcing or process steps backfire. Starting from substandard fluorinating agents may yield byproducts that resist downstream removal. We control entry materials tightly, running spot tests before transfer into main kettles. The methylation and subsequent formylation must be sequenced and timed precisely to minimize isomer drift. Operators are trained to read reaction “personality”—watching color shifts, exotherms, and even skillfully interpreting the behavior of stirring paddles as indirect markers of good process health.
Smaller lab suppliers, not directly involved in industrial-scale production, sometimes struggle here. Their small-batch experience doesn’t reliably scale. This plays out when customers report batch-to-batch inconsistencies—color variation, trace residue, or off-odors that only emerge at scale or under extended storage. We’ve responded to these differences by automating certain dosing steps but kept other operations under direct operator judgement. Skilled staff catch subtle shifts that machines miss, and this blend of careful mechanization with human oversight sets our facility apart from automated-only or lab-only producers.
How this fluoro-methyl carbaldehyde performs under reaction conditions guides users more than any technical data sheet. From conversations with chemists at scale-up stage, we've seen its value shine in acylation reactions and selective reductive aminations, especially where steric control is key. The electron-withdrawing fluorine helps stabilize intermediates that otherwise decompose using a simple pyridine-3-carbaldehyde. For those working to synthesize heterocyclic seed molecules, these differences mean fewer purification headaches and improved overall yields.
In contrast, non-fluorinated or single-substituted analogs don’t provide the same combination of reactivity and resistance to over-reduction. We’ve heard feedback from pilot plants in pharma research—switching to our compound saved hours in downstream column purification, reducing waste and costs. More than once, a customer knocked on our door after cheaper alternatives failed in scale-up. Their process required the distinctive behavior that only the fully substituted fluoro-methyl aldehyde brings.
On the bench and in reactors, nuanced differences in pyridine carbaldehydes come alive. The addition of a 6-fluoro group coupled with 2-methyl substitution reshapes nucleophilic attack rates and guides selectivity. For example, 2-methyl-pyridine-3-carbaldehyde, lacking the fluorine, produces a noticeably higher rate of side-chain oxidation and doesn’t stand up as well in oxidative cross-coupling conditions. In-process analytics at our plant show cleaner conversion rates and fewer heavy-metal residues in final product than we see with non-fluorinated intermediates.
We have manufacturers’ perspective on this. Every time we push a process, we compare analytical traces and practical yields. We don’t just read the literature benchmarks—we create our own, working from kilogram samples up through production scale. Typical downstream users need confidence that the aldehyde function retains its reactivity for their specific transformation. Our material demonstrates consistent endpoint specification, where lower-grade variants fall short due to trace decomposition or hydrolysis.
Flow chemistry sometimes improves yields for simpler compounds, but our molecule resists such automation. The aldehyde group shows a tendency to oligomerize under certain conditions, particularly if the solvent loses water control. Early on, we faced unexpected batch failures around atmospheric humidity swings—a problem absent in lab-bench scale. We built drying steps upstream, added moisture-tracking sensors, and adopted shorter hold times at elevated temperature. It wasn’t a theoretical solution; operators and managers spent late nights walking the line, grabbing spot samples, running real-time NMR checks.
This is not an inert off-the-shelf building block; it demands real vigilance. Safety procedures reflect this reality, as aldehydes can volatilize at lower thresholds or form peroxides if left exposed. Training pairs hands-on apprenticeship with ongoing formal instruction in process safety. By building our own expertise, we pass confidence downstream. If our teams can’t master each problem, we can’t reasonably expect customers to do so further down the chain.
Many of our major clients had tried multiple distributors or lab-scale suppliers before seeking manufacturer-direct sourcing. They shared similar frustrations—unclear origins, variable storage histories, and limited support for root-cause investigations when their own processes faltered. By maintaining traceable batch logs, reserve samples, and rapid communication with end-user technical teams, we close these gaps. We're able to offer not just certificates of analysis, but interpretive support—spotting why a reaction underperforms, or how to better store material at user sites.
This degree of transparency and back-and-forth feedback loop only works when there is a hands-on, open relationship. All levels of our operations, from bench chemists to logistics planners, contribute to these solutions. Every suggestion or complaint from a user feeds back into process improvement. If a customer flags instability under certain conditions, we take it to pilot scale, verify root causes, and—where feasible—adjust internal processes to improve the next batch. These aren’t theoretical improvements, but results visible cycle to cycle across our entire operation.
Direct production means we’re not only aware of, but also control, the storage, packaging, and shipment processes. From our experience shipping temperature-sensitive aldehydes internationally, changes in transit environment can impact product quality and usability. For this compound, rapid temperature swings or pressure fluctuations could prompt condensation or slow polymerization. Our warehouse and shipping teams routinely double-wrap containers, use certified secondary seals, and document every handoff, logging times and conditions at each stage. By controlling these critical links, we prevent quality drift, and our clients have come to expect this level of diligence.
Pyridine derivatives with active aldehyde groups don’t tolerate neglect. If third parties or unknown handlers step into the chain, minor mishandling amplifies into product degradation or even safety incidents. By shouldering the responsibility from synthesis through final delivery, we sidestep these pitfalls and take accountability for every lot that leaves our gates.
Chemical manufacturing faces relentless cost pressures. In the specialty realm, the temptation rises to cut corners—simpler solvents, unpurified reagents, relaxed storage. Direct experience tells us that any apparent savings slip away in the face of performance failures or costly plant shutdowns caused by compromised raw material. Running high-purity reactions efficiently does not just protect yields; it protects reputations. Our facility invests in real-time monitoring and closed waste loops, not to “tick boxes,” but because we find fewer incidents, cleaner air, and an engaged workforce when safety and sustainability remain core priorities.
As regulations tighten, especially on halogenated intermediates, our early investment in scrubbers and closed-system fluorination gives peace of mind. Geographically, not every site can operate this technology safely or economically. Our longtime commitment to vertical integration—sourcing, reaction, analytics, and final shipment under one roof—has insulated us from many recent supply chain disruptions.
We owe many of our improvements to critical feedback from seasoned users in both research and manufacturing. Some need higher purity for key reactions; others face regulatory hurdles on trace impurities or documentation. If an emerging customer in a novel area—say OLED intermediates or experimental pharmaceuticals—encounters bottlenecks not seen by existing users, we don’t treat it as an outside concern. Instead, their challenges fuel further process tweaks. Our staff frequently revisits earlier production stages or tests new protocols derived from customer discovery work. This approach shapes both the process and the product, and places adaptability at the core of what we do.
We have established pilot facilities within our campus where scale-up and process changes can be safely trialed side-by-side with current production. Feedback flows from user to chemist and back again, never filtered through multiple third-parties. Material that proves itself at pilot scale finds its way rapidly into mainline production, and improvements in waste handling, energy use, or throughput translate directly into value for those relying on this building block.
From an operational point of view, this compound’s utility doesn’t rest solely on structure or published reactivity charts. Real value emerges from its reliability—down to the last vial in a multi-ton shipment. The unique arrangement of substituents allows chemists to explore reaction pathways blocked to more basic pyridines. Its well-documented performance history, as much as any technical property, stands as a testament to the care invested in its manufacture.
Manufacturing this aldehyde has driven us to a deeper understanding of both process and product—each new batch adds to that body of experience. We learn from users pursuing next-generation targets, as much as from colleagues working on the production line. Success comes from this shared knowledge—translating the challenges of the plant floor into value for each scientist, engineer, and production manager at the user end.
As demands evolve—more sustainable chemistry, tighter impurity profiles, new downstream applications—the expectations placed on specialty intermediates like 6-fluoro-2-methyl-pyridine-3-carbaldehyde continue to rise. Our experience tells us that the future will belong to those who bring not only technical know-how, but also flexibility and responsiveness to changing needs. We’re already trialing continuous flow variants, exploring greener synthesis alternatives, and partnering with research teams to benchmark new reaction types. These aren’t distant aspirations, but ongoing projects tackled regularly by our full in-house crew.
Every day spent manufacturing and refining this compound renews our commitment—to safety, quality, and real-world problem solving. We see this as the foundation of strong relationships with our users, and the key to translating chemical precision from tank to test tube and back again.