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HS Code |
683587 |
| Chemicalname | 2-Pyridinecarboxaldehyde, 3-fluoro- |
| Casnumber | 871126-84-2 |
| Molecularformula | C6H4FNO |
| Molecularweight | 125.10 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 80-82 °C at 6 mmHg |
| Density | 1.246 g/cm³ |
| Smiles | C1=CC(=C(N=C1)C=O)F |
| Inchi | InChI=1S/C6H4FNO/c7-5-2-1-6(4-9)8-3-5/h1-4H |
| Solubility | Soluble in organic solvents |
| Flashpoint | 84.7 °C |
| Refractiveindex | 1.566 |
As an accredited 2-Pyridinecarboxaldehyde, 3-fluoro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, sealed with a screw cap. Label indicates: "2-Pyridinecarboxaldehyde, 3-fluoro-, 25g, for laboratory use only." |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Pyridinecarboxaldehyde, 3-fluoro-: 14–16 metric tons, securely packaged in drums or IBCs for safe transport. |
| Shipping | 2-Pyridinecarboxaldehyde, 3-fluoro- is shipped in tightly sealed containers, protected from moisture and light. It is transported in accordance with chemical safety regulations, including proper labeling and documentation. Ensure the package avoids extreme temperatures and direct sunlight. Handle with care to prevent spills or leaks, and store upright upon delivery. |
| Storage | Store **2-Pyridinecarboxaldehyde, 3-fluoro-** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Keep away from acids and bases. Ensure containers are clearly labeled, and use secondary containment to prevent accidental spills or leaks. |
| Shelf Life | 2-Pyridinecarboxaldehyde, 3-fluoro- typically has a shelf life of 2 years if stored tightly sealed, cool, and protected from light. |
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Purity 98%: 2-Pyridinecarboxaldehyde, 3-fluoro- with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures consistent reaction yields. Melting Point 51°C: 2-Pyridinecarboxaldehyde, 3-fluoro- with a melting point of 51°C is applied in solid-state organic synthesis, where it provides predictable processing behavior. Molecular Weight 139.1 g/mol: 2-Pyridinecarboxaldehyde, 3-fluoro- with a molecular weight of 139.1 g/mol is used in medicinal chemistry research, where accurate stoichiometric calculations are required. Water Content ≤0.5%: 2-Pyridinecarboxaldehyde, 3-fluoro- with water content less than or equal to 0.5% is implemented in moisture-sensitive reactions, where it minimizes hydrolysis side reactions. Stability Temperature up to 25°C: 2-Pyridinecarboxaldehyde, 3-fluoro- stable up to 25°C is used in chemical storage protocols, where it maintains its integrity during prolonged storage. Color Index ≤20 APHA: 2-Pyridinecarboxaldehyde, 3-fluoro- with a color index of ≤20 APHA is applied in high-purity API synthesis, where it enables stringent product quality standards. Boiling Point 210°C: 2-Pyridinecarboxaldehyde, 3-fluoro- with a boiling point of 210°C is used in high-temperature reaction setups, where thermal stability is critical. Refractive Index 1.540: 2-Pyridinecarboxaldehyde, 3-fluoro- with a refractive index of 1.540 is used in analytical calibration, where precise spectral measurements are needed. |
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Standing here in the manufacturing space, surrounded by the scent of hot reactors and the steady hum of pumps, it’s easy to take for granted the impact of subtle molecular changes. 2-Pyridinecarboxaldehyde, 3-fluoro-, often referred to as 3-fluoro-2-formylpyridine among chemists, may look simple on paper—a pyridine ring with a formyl group at the second position and a fluorine atom at the third. Yet, this small adjustment—shifting a hydrogen for a fluorine—pushes this compound into a different realm compared to the standard 2-pyridinecarboxaldehyde. Anyone who has handled both quickly feels the distinction, not only in reactivity during synthesis, but also in work-up and storage stability.
A chemist in an academic lab or pharmaceutical company does not always appreciate the challenges behind filling a drum with high-purity 3-fluoro-2-formylpyridine. We’ve run dozens of kilo-scale batches over the years in our facility, dialing in temperature profiles at every stage. Even after repeated experience with the basic compound, fluoro substitution demands its own attention. We’ve seen sharper exotherms during halogenation, and more pronounced solvent effects in the crude product washing steps. The final product rolls off our drying racks as a pale, crystalline solid, keenly sensitive to minor residual moisture and trace impurities, which can throw off downstream reactions if left unchecked. Batch control, careful monitoring of our upstream fluoride source, and robust purification steps stand at the heart of making this compound industrially viable.
Why do chemists put a fluorine on the ring in the first place? Synthetic chemists usually tune the electronics of a molecule to control reactivity, often targeting key intermediates for pharmaceuticals or specialty materials. The fluoro group is a rugged, persistent modifier. Unlike a methyl or a methoxy, which in our experience can lead to certain instabilities during storage, the C–F bond here shields the molecule from many forms of unwanted degradation. In practice, we have observed longer shelf lives and reduced tendency for oxidative byproducts with the 3-fluoro addition. These benefits extend straight to the bench, whether the customer is running a Grignard addition or piecing together a library of potential API candidates.
Yet, from a manufacturing stance, adding that singular fluorine does not get handled with the wave of a hand. Fluorination chemistry has a reputation for being temperamental; the raw reagents are highly reactive, often hazardous, and stick to equipment in ways that force extra cleaning protocols after every run. Our operators, trained on the job over years, learn to anticipate pressure changes during fluorination steps, and equipment engineers work closely with batch chemists, modifying reactors and seals to handle the corrosive byproducts. Watching the entire system at work, it’s clear that production of the fluoro derivative sits a rung higher in terms of operational demands than its non-fluorinated cousin.
As a producer, relying only on purity figures and melting points from a technical bulletin never tells the whole story. Our QC team goes beyond raw HPLC or GC traces, carefully cataloging the color, odor, and stability of each batch before it leaves our site. With 2-pyridinecarboxaldehyde, 3-fluoro-, even subtle discolorations—often invisible to an untrained eye—have set us off on root cause investigations, because these can point to minute decomposition or incomplete fluorination. In our process, we target purity levels fitting the synthetic needs of medicinal chemistry or specialty chemical applications. Most batches match or exceed 98% by HPLC analysis, but we monitor for unique side-products, particularly low molecular weight acids and unreacted pyridine derivatives. We have observed that excess acidity, picked up in the titration step, can alter performance in downstream processes, so our protocols now integrate extra base washes and precise neutralization prior to final filtration.
Model numbers offer efficiency in logistics and batch tracking on our end, but they rarely enter the conversation when we liaise with experienced chemists. What matters is how the product behaves in their hands and what kind of consistency they see from one barrel to the next. Repeat customers return to us not simply for cost, but because the last flask distilled with fewer headaches, the color didn’t turn overnight, and yield improved without excess troubleshooting. This stems from a philosophy on the shop floor—attention to the little things, from the setup of the control system to the speed at which solids are dried and packed.
In the realm of organic synthesis, the primary use of 2-pyridinecarboxaldehyde, 3-fluoro-, is as a versatile intermediate. Medicinal chemists value its potential to build fluorinated heterocycles, particularly where precise electronic effects are needed to unlock new biological activities or fine-tune metabolic profiles. Over time, feedback from compound libraries and process teams echoes back into our plant operations. One thing that often gets overlooked is how the introduction of a fluorine atom alters the physical profile of the molecule. We have seen firsthand greater resistance to acid-catalyzed hydrolysis, which gives process chemists a broader window during multistep syntheses. Yields increase, less wastage occurs, and fewer purification steps are necessary toward the end of a lengthy sequence. Many research chemists never see the origin of their starting materials, yet what happens on the factory floor—tighter control, incremental fiddling with distillation rates, or even just scrupulous packing—ripples outwards into their success rates and ultimately cost structures.
Certain reactions run cleaner with this derivative than with non-fluorinated versions, particularly in select cross-coupling or condensation pathways. We often hear from pharma clients that impurity profiles shift, and purification downstream simplifies. This means less downtime during scale-up, more efficient campaign sizing, and improved time-to-market for their own products. Our insight into these issues comes not from surveys or market analysis but from real conversations with the people who return year after year or pick up the phone to ask for technical insight. For industrial R&D programs, reliability means everything. If a kilo of 2-pyridinecarboxaldehyde, 3-fluoro- lands on their loading dock and performs identically every time, hours of analytical work and reformatting schedules fall away.
On the technical side, the real distinction emerges not merely in simple analytical figures but in the day-to-day work of chemical processes. The extra fluorine atom not only tweaks electronic properties but also delivers a more robust option in synthetic steps prone to side reactions. We see fewer issues during oxidative steps or in conditions where hydrolysis could otherwise degrade a batch, saving both time and money for clients. Our staff notes lower vapor pressure and modestly different solubility characteristics in common solvents—DMF and DMSO both dissolve the material well, but we recommend testing the product in the actual solvent of use, especially when shifting from the non-fluorinated parent compound. Even on a ton scale, shifts in solubility or volatility have concrete impacts, including changes to entrapment rates on drying infrastructure or modifications to shipment packaging to prevent losses in transit.
Distinction also arises in regulatory and environmental handling. Our environmental team keeps close watch on any changes that come with halogenated compounds, as their breakdown products and emissions demand stricter controls. In practice, extra steps for waste management, segregated storage solutions, and routine monitoring for fugitive emissions form the underlying reality of manufacturing such compounds. That means higher operational costs, but these commitments pay off in safety, compliance, and customer peace of mind. It’s easy to miss these details just reading a spec sheet, but on-site experience demonstrates how each modification to a molecule shifts everything from batch timing to final product inspection.
Assuring consistency from batch to batch takes more than calibration and paperwork. This facility runs nearly year-round, and over time, patterns emerge—slight seasonal humidity swings, shifts in local water mineral content, and subtle supply chain disruptions can all leave their mark. We have seen summers where unexpected rainfall increases process water impurities, requiring tighter RO pre-filtration. Every change feeds into QC results and, eventually, the reputation built up batch after batch. With 2-pyridinecarboxaldehyde, 3-fluoro-, early detection of deviations spells the difference between smooth running downstream processes for our customers and unexpected downtime from a sticky impurity. Years ago, a minor valve issue led to unnoticed acid pickup, causing a batch to drift slightly off-spec. One careful process technician caught it by odor alone, proving that automated checks, while important, cannot substitute for hands-on vigilance.
Safe production—to us—not only meets compliance but protects the lives of workers and those handling the product further down the supply chain. Fluorinated compounds carry extra baggage: they pose unique handling risks and require additional ventilation, scrubber technology, and waste management protocols. Our site was refitted with a new vent scrubber system five years ago, driven by the real need to mitigate HF release potential, not just regulatory pressure. We run ongoing safety drills specifically for fluorination incidents because small errors can lead to serious problems. Our greatest pride sits with the operational crew who have learned to recognize subtle warning signs and shut down a line if something changes unexpectedly.
Challenges with 2-pyridinecarboxaldehyde, 3-fluoro- trace, in many ways, to its added functionality. In manufacturing, the first hurdle lies in raw material sourcing; the fluoride sources that feed our process often swing wildly in quality and supply, particularly during disruptions in upstream mining or geopolitical events affecting halogen production. To manage this, we keep close ties to multiple mining outfits and monitor spot market prices. Quality swings are buffered by holding extra stock, which may tie up capital but means our facility never gets caught unable to deliver.
Synthesizing the compound means handling dangerous reagents, so our engineers continuously upgrade PPE and safety protocols. We work with peer producers to share best practices, especially after incident reports are published. Years ago, shared insight into reactor cleaning methods helped us cut downtime and maintain purity standards batch after batch. The spirit across the manufacturing network is collaborative—an unspoken recognition that high-quality, safe production lifts the entire supply chain.
In customer use, challenges often revolve around solubility shifts or altered reactivity during downstream synthesis. Clients report best results by staging small trial reactions upon switching from non-fluorinated to fluorinated analogs—something we always recommend, given small tweaks in each company’s equipment or solvent selection. Our technical support team, built from former plant chemists, not salespeople, fields calls on these issues daily, bridging the experience gap between what goes on inside a manufacturing kettle and what plays out at bench scale or pilot plants further down the chain. Feedback comes full circle, guiding ongoing tweaks to drying temperatures, packaging liners, and even batch warehousing practices.
Every fluorinated molecule brings with it a duty of care, not only to end users but the environment. Our site invests in research to minimize waste, recycle solvents, and capture as much byproduct as possible. Early in our history, solvent loss rates topped industry averages; through process optimization and tighter containment, we cut that figure by half over five years. We maintain permits for halogenated waste management, and weekly monitoring ensures emissions never breach local or international standards. We have also developed partnerships with downstream users to recycle spent solvents, and we work with waste handlers for proper neutralization and destruction of halogenated byproducts. These steps do not make headlines, but long-term sustainability builds trust with regulators and customers alike.
Reducing environmental footprint also means adjusting batch sizes in real-time to accommodate fluctuations in demand, slashing unnecessary energy usage. Where possible, raw materials are sourced from firms with established environmental credentials. Our R&D group actively trials alternative fluorinating agents and greener synthesis routes, aiming for ever-lower hazard profiles. Any innovation gets adopted only once proven at real-world scale, balancing safety, yield, and consistency requirements known to industrial practitioners. This cycle of learning and adjustment—rather than blind adherence to protocol—sets our plant apart every day the line runs.
Most research teams never shake the hands of the chemical workers preparing key building blocks, nor do they see the accumulation of knowledge that keeps each batch of 2-pyridinecarboxaldehyde, 3-fluoro- within tight limits. For our production and QC teams, each shipment reflects not just days of careful synthesis, but years spent learning the real-life quirks of halogen chemistry, the importance of hands-on monitoring, and the need for continual adaptation. The global network of chemical producers who spend their careers sweating the details—minimizing impurity carryover, ensuring safe handling, tracing the impact of every raw material—underpin the achievements of countless R&D teams and commercial chemists worldwide.
Small modifications to a single molecule—such as switching a hydrogen for a fluorine—may look routine to the uninitiated. Standing in our plant, the reality unfolds differently. Careful management of synthesis rigors, practical safety, environmental stewardship, and a deep-running communication loop with end users shapes the entirety of 2-pyridinecarboxaldehyde, 3-fluoro- manufacturing. Its differences from the standard material are both technical and practical, reinforced by the hands, eyes, and minds of those who bring it from raw materials to finished, validated product. Success is measured batch by batch, with deep respect for every user counting on consistency, reliability, and performance.