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HS Code |
595469 |
| Iupac Name | 2-Fluoropyridine-4-carbaldehyde |
| Cas Number | 946773-20-8 |
| Molecular Formula | C6H4FNO |
| Molecular Weight | 125.10 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Smiles | C1=CN=C(C=C1C=O)F |
| Inchi | InChI=1S/C6H4FNO/c7-6-2-1-5(4-9)3-8-6/h1-4H |
| Pubchem Id | 53337001 |
| Synonyms | 2-Fluoro-4-pyridinecarboxaldehyde; 2-Fluoroisonicotinaldehyde |
As an accredited 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Pyridinecarboxaldehyde, 2-fluoro-(9CI) is supplied in a 25g amber glass bottle with a secure screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) packed securely in appropriate drums, 14–16 MT net weight per container. |
| Shipping | 4-Pyridinecarboxaldehyde, 2-fluoro- (9CI) is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is categorized as a hazardous chemical; thus, transport follows regulations for handling toxic and potentially flammable substances, with appropriate labeling and documentation. Personal protective equipment is recommended during handling and transport. |
| Storage | 4-Pyridinecarboxaldehyde, 2-fluoro- (9CI) should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and properly labeled. Store at room temperature and protect from moisture. Follow all relevant safety protocols and consult the safety data sheet (SDS) for additional storage recommendations. |
| Shelf Life | Shelf life for 4-Pyridinecarboxaldehyde, 2-fluoro- (9CI): Stable for 2 years when stored tightly sealed, protected from light and moisture. |
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Purity 98%: 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurities in active compound formation. Melting Point 49°C: 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) with a melting point of 49°C is used in organic synthesis workflows, where ease of solid-phase handling enhances reaction scalability. Molecular Weight 139.11 g/mol: 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) with molecular weight 139.11 g/mol is used in heterocyclic compound development, where predictable stoichiometry streamlines experimental planning. Reagent Grade: 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) reagent grade is used in analytical laboratories, where it provides reliable results in qualitative and quantitative assays. Stability Temperature up to 45°C: 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) stable up to 45°C is used during storage in chemical warehouses, where it maintains structural integrity over extended periods. Low Water Content <0.2%: 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) with water content below 0.2% is used in moisture-sensitive reactions, where it prevents unwanted hydrolysis and side reactions. Spectroscopic Purity: 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) with certified spectroscopic purity is used in NMR and mass spectrometry studies, where it enhances accuracy and clarity of analytical data. |
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Every day, our production floor runs with an eye for detail, working hands-on with specialty chemicals that become the backbone of research and manufacturing. Among the distinct chemicals in our catalog, 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) stands out for its specific utility and consistency, valued by teams working in pharmaceutical development, agrochemical synthesis, and material science. Having handled this compound from raw starting materials right through purification and quality checks, we see its value not as a mere line on a catalog, but as a product born from careful engineering and a deep understanding of its end-use potential.
4-Pyridinecarboxaldehyde,2-fluoro-(9CI) carries the structural nuance of the pyridine backbone, coupled with a well-positioned aldehyde and a precision-placed fluorine at the 2-position. Through years of experience scaling up its synthesis, the unique haloaldehyde presents both opportunity and challenge, distinguishing it from the more ubiquitous analogues. The presence of the fluorine atom dramatically influences its chemical reactivity, which becomes apparent as soon as the reaction vessels begin to warm. Our technicians monitor not only the stoichiometry, but also the kinetics and workup steps, since the fluorinated intermediate can generate different reactivity pathways than the non-fluorinated version or even the trifluoromethylated cousins.
Walking through our facility, shelves hold samples destined for researchers looking to build sophisticated heterocycles, or for engineers exploring new pharmaceutical motifs. The 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) product arrives to customers with a defined purity profile — not just a statement of numbers, but a purity proven by our in-house NMR and GC-MS instruments. What this means for the synthetic chemist is reliability: batch-to-batch repeatability remains critical, especially where a failed batch could cost labs months of effort.
This compound often comes into play early as a building block in active pharmaceutical ingredient (API) routes, where that fluorine atom modifies binding affinity and metabolic stability in potential drug candidates. Experienced chemists know that minor tweaks to a molecule’s electronic environment, achieved by the introduction of a fluorine, can produce major shifts in biological results. The aldehyde group brings its own tunability, offering reactive entry points for further transformations — from reductive aminations to Wittig reactions and cyclizations. Years on the manufacturing side have taught us that the combination of a pyridine ring, aldehyde group, and a single strategically-placed fluorine occupies a niche that broader-spectrum aromatic aldehydes simply can’t fill.
Down the hall, in pilot scale reactors, our teams have seen customers use 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) to create ligands for asymmetric catalysis. The electron-withdrawing influence conferred by the fluorine—well-understood in academic literature—regularly proves, in practical use, to make a significant difference in catalyst stability and product stereoselectivity. Fluorinated systems, once exotic, have become central in drug discovery and crop science, changing the way synthetic routes are designed.
Much of what drives our choice to dedicate space on the line to this product comes from boots-on-the-ground feedback. Teams in start-up pharmaceutical labs often call us directly, asking about the handling of the compound, or remarking on how trace impurities can sideline months of effort. Over time, our manufacturing procedures have shifted—solvents have changed, reaction temperatures tuned, and purification steps strengthened—because consistent product means more than just a passing phase on a specification sheet, it brings peace of mind to chemists designing new molecules or scaling up towards production.
Lab-scale chemists mention how easily the fluorinated aldehyde dissolves in common polar aprotic solvents. With this solubility, it integrates into one-pot syntheses, favoring efficient throughput. On larger scales, material consistency turns into a logistics problem—shipping hundreds of kilos with temperature sensitivity and regulatory markings. We’ve invested in extra packaging steps, trace moisture analysis, and real-time data tracking because nothing stalls progress like a supply chain surprise.
Among customer reports, certain successes echo across projects: the use of 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) in heterocycle libraries leads to libraries with greater pharmacokinetic diversity; the subtle influence on hydrogen bonding, exploited in high-end coatings and electronics research, has enabled new lines of functional materials. As we see shipments go out to research campuses and industrial customers, each with its own end-use scenario, it affirms what daily work in synthetic chemistry reveals—one modification, fluoro versus hydrogen, can open new frontiers.
Having produced a range of substituted pyridinecarboxaldehydes for years, the difference the fluorine atom makes is not academic; it directly changes procedures on the manufacturing line. Yields, for instance, react sharply to changes in oxidation state, and by tuning conditions around the fluorination step, we push through difficulties that often stymie less-experienced operators. Comparative workups reveal that the non-fluorinated analogue, while easier to prepare, often leads to less-selective downstream transformations. The addition of fluorine closes the gap on batch consistency—side-reactions drop, and the final aldehyde group resists reduction under standard hydrogenation conditions.
Our production history shows that, out of the tens of potential substituents, a single fluorine atom converts a basic starting material into a specialty product with richer reactivity — this fluoro group resists nucleophilic attack and stabilizes the molecule in storage, giving our warehouse longer shelf life and customers a more manageable inventory rotation. Handling procedures get updated so the aldehyde can be safely dispensed without loss of integrity, avoiding complications that show up all too frequently with more reactive, open-chain aldehydes.
Technical staff often compare “feel” between the fluorinated product and its methyl or unsubstituted siblings. Crystallization proceeds in sharper bands and the melting point remains reliably high, supporting more robust handling. These physical cues trigger less waste during milling, packing, and filtration, affecting not just our numbers but also the time and labor spent at every stage. It’s easy to overlook those details on a purchasing list—yet on the production side, small differences compound; fewer clogs in filters, smoother throughput, reduced rework.
Manufacturing this compound is not a plug-and-play operation. From initial selection of precursors—screened for trace halides and solvent residues—to precise control of temperature and humidity during reaction, each cycle reflects years of process refinement. No two batches present in exactly the same way. Operators trained in fluorination and aldehyde chemistry share knowledge across shifts. When process hiccups arise, tweaks are made without hesitation, harnessing both intuition and pattern recognition built from hundreds of successful and failed runs.
Inspection teams validate each step, never relying solely on tabulated standards. Initial color, odor, spectral signals, and even the “stickiness” on spatulas during isolation go into our daily record books. Studies on storage and shipping stability have led us to overhaul packaging systems, moving from generic drums to custom-lined containers that mitigate moisture ingress and headspace reactivity, reducing the degradation that ends up as silent losses at the customer’s bench.
Our team has faced hurdles—from trace by-products in early runs to bottlenecks as scale doubles during seasonal demand surges. Each challenge forced practical solutions: engineering new venting systems to handle fluorine off-gassing, retraining staff in aldehyde containment, rerouting cooling lines to hit target isolation temperatures during humid months. New sampling methods developed in-house ensure that every unit leaving the storeroom reflects not only regulatory compliance, but our own unspoken standard—the chemical must perform above specification, not only meet it.
Trust earned over years changes how our product reaches the world. Even before orders come through, project leads keep us informed about new research goals—what worked, what fizzled, why their team hopes the next kilo will make all the difference. We update our process records to reflect not just what’s feasible at bench scale, but what supports strategies for scale-up, tech transfer, and multi-site manufacturing. Feedback loops direct our investments, supporting downstream goals for greener chemistry, waste minimization, and lower solvent use.
Our supply chain partnerships depend on traceability, where every drum, every container, and every label ties back to origin, batch, and analytic results. Regulatory teams audit our records twice a year, not for show, but to ensure confidence through the entire distribution process. A stronger supply chain means fewer disruptions for researchers and developers counting on a daily, weekly, or seasonal supply of 4-Pyridinecarboxaldehyde,2-fluoro-(9CI). On-the-ground realities inform our every adjustment—in packaging, logistics, and even in contingency protocol when geopolitical events or climate extremes threaten raw material availability.
Unpredictable purity drift, trace contamination, and product reactivity count as top concerns for both supplier and customer. Our quality team interacts closely with manufacturing, not only reviewing automated data, but working at benches to examine reference spectra and trend logs. Out-of-spec cases draw immediate analysis—root causes, whether from washing solvents, reaction sequence, or storage transitions, are corrected with both urgency and long-view thinking. Product that fails our scrutiny does not leave our facility; pride in delivery underpins our business far beyond legal requirements.
Our labs run round-the-clock calibration and verification. We understand that every customer develops their own set of analytical markers—chiral purity, moisture content, cumulative impurity levels—and we fine-tune our routines to fit. What matters most is eliminating ambiguity: the delivered chemical must behave predictably in the customer’s process, cycle after cycle.
No industry stands still, and the world of fine chemicals shifts every year. The push for sustainability, reduced emissions, and greater transparency inflects every batch we make. Tightening regulatory frameworks require constant vigilance—our R&D teams work together with production and compliance staff to anticipate changes. For 4-Pyridinecarboxaldehyde,2-fluoro-(9CI), the drive toward greener synthesis urges us to test new solvents and greener oxidative routes in pilot reactors. Every successful trial points toward a less resource-intensive future, where the high cost of specialty chemistry does not come at the environment’s expense.
Efforts to minimize waste have already shown value. By re-engineering process stages to recover solvents and recycle intermediates, we reduce both environmental burden and operational costs. This approach ingrains sustainability into our culture, not as an afterthought but as a daily discipline. Moving forward, collaboration with downstream users will accelerate our adoption of technology that further reduces emissions and water use, paving the way for next-generation chemistry built not only on reactivity, but on responsibility.
Having walked the path from lab bench to bulk production, we see firsthand how real-world application and manufacturing insight inform each other. There’s no substitute for hands-on experience — understanding product quirks, refining procedures, troubleshooting problems under pressure, and drawing solutions from lessons learned on the floor.
As a direct manufacturer, our mission has never been only to deliver chemical compounds, but to empower customers with the knowledge and confidence born of deep operational familiarity. 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) is more than a reagent; it’s the sum of years of practical improvement, relentless pursuit of quality, and long-term partnership with those who rely on clear, reliable performance. By keeping lines of communication open, investing in technical rigor, and constantly refining our processes, we serve not just the current needs of chemistry, but its future possibilities as well.
Customer challenges and shifting scientific priorities keep us questioning, refining, and innovating every aspect of this chemical’s manufacture. With every shipment, we pass on not only the molecule, but a legacy of experience—operational insight, unwavering quality standards, and a close connection to the science our customers pursue. The lessons learned manufacturing 4-Pyridinecarboxaldehyde,2-fluoro-(9CI) extend well beyond a single product, shaping our approach to the whole spectrum of fine chemical development. Our commitment remains to the highest standards—because the real world of chemistry expects nothing less.