|
HS Code |
185095 |
| Chemical Name | 2-Fluoro-5-nitropyridine |
| Cas Number | 4487-72-3 |
| Molecular Formula | C5H3FN2O2 |
| Molecular Weight | 142.09 g/mol |
| Appearance | Yellow to light brown solid |
| Melting Point | 48-51°C |
| Boiling Point | 234-236°C |
| Density | 1.46 g/cm³ |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like DMSO and methanol |
| Smiles | C1=CC(=NC=C1[F])[N+](=O)[O-] |
| Inchi | InChI=1S/C5H3FN2O2/c6-4-1-2-5(8-3-4)7(9)10/h1-3H |
| Refractive Index | 1.564 (predicted) |
| Storage Conditions | Store at room temperature, in a dry and well-ventilated place |
As an accredited 2-Fluoro-5-nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Fluoro-5-nitropyridine (Sigma Aldrich, 5g): Supplied in a sealed amber glass bottle with tamper-evident cap and hazard labeling. |
| Shipping | 2-Fluoro-5-nitropyridine is typically shipped in tightly sealed containers under ambient conditions. During transport, it is protected from moisture, heat, and direct sunlight. The package includes appropriate hazard labeling and documentation, as the chemical is classified as harmful. Shipping complies with relevant safety and regulatory standards for laboratory-grade chemicals. |
| Storage | 2-Fluoro-5-nitropyridine should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight in a cool, dry, well-ventilated area. Keep separate from oxidizing and reducing agents. Store at room temperature unless otherwise specified by the manufacturer (Sigma-Aldrich/Merck/TCI). Use secondary containment to prevent spills and ensure proper chemical labeling at all times. |
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On the production floor, chemists and technicians rely on reliable materials that behave predictably in every batch. Here, our focus is on 2-Fluoro-5-nitropyridine, an intermediate that’s grown in demand across pharmaceutical synthesis, agrochemical discovery, and custom contract manufacturing. With each kilogram passing through our reactors, we see not just data points but a solid track record of real-world applications that depend on its purity, performance, and consistency. Our background in multi-step syntheses began decades ago, at a time when fluorinated pyridines were considered difficult to scale. Now, with purpose-built facilities and refined methods, we manage such molecules with the same hands-on approach that has guided our operations through industrial evolution.
Chemists looking for 2-Fluoro-5-nitropyridine expect genuine quality. This particular compound, with formula C5H3FN2O2 and CAS number 4487-59-6, stands out due to its electron-withdrawing nitro group and unique fluorine substitution pattern. These features matter because they unlock transformations in Suzuki couplings, nucleophilic aromatic substitutions, and serve as building blocks in creating biologically active heterocycles. Over the years, we have paid attention to the practical issues that arise—off-odors, instability on storage, inconsistent melting ranges—and adjusted our process controls to target stable, free-flowing crystals and high assay with low impurities. In synthesis, there’s no room for unwelcome side products or sluggish reactivity, so our quality assurance highlights not just purity, but also reactivity profiles batch to batch.
Production at scale means more than filling drums. Maintaining batch traceability and reproducibility in 2-Fluoro-5-nitropyridine manufacture starts with raw material selection and extends to the last stage of vacuum drying and packaging. Our technicians measure each lot for attributes like appearance—usually pale yellow or off-white fine crystals—alongside critical values such as purity, typically 98% and above by HPLC. Moisture control is no afterthought, since even a hint of water can hamper reactivity for processes like nucleophilic substitution. Particle size matters for certain downstream uses, so sieving and process choices reflect that feedback. Customers in both pilot and full-scale projects ask about solubility, so our technical service team can share practical tips—soluble in common polar aprotic solvents, modestly soluble in alcohols, minimal solubility in water. This data helps researchers avoid problems when translating reactions from milligram to kilogram scale.
After years of project support, we’ve seen 2-Fluoro-5-nitropyridine used for everything from lead optimization in medicinal chemistry to as a starting point for library synthesis. Some partners go on to build kinase inhibitors and other bioactive pyridines, while others transform it into advanced intermediates for crop protection compounds. Our customers share one concern: the compound’s reactivity can be both a benefit and a liability. For example, the ortho relationship between the fluorine and nitro groups increases reactivity for displacement, but it also means extra care must go into handling, storage, and even waste disposal. Projects run most smoothly when chemists use well-characterized material that doesn’t carry over synthesis-side impurities. We encourage open feedback, and use it to improve how we dry, package, and ship these sensitive building blocks, especially for clients working in regulated environments.
Sometimes the market introduces pressure for lower-cost alternatives, but shortcuts in process design rarely pay off in fine chemicals. With this compound, controlling process safety has always come first. During nitration and fluorination, careful monitoring reduces formation of hazardous by-products, which would complicate downstream waste streams. In routine surveys of customer satisfaction, consistency in performance and reliable documentation matter more than shaving off pennies per gram. As a manufacturer, we step in to troubleshoot reactions, offering insight drawn from hundreds of runs spanning pilot to ton scale.
Every manufacturer develops their own “signature” in how they make specialty pyridines. In the market, one can find chlorinated pyridines, alternative nitro substitutions, or fluoro isomers—each with unique manufacturability, cost, and stability profiles. Among these, 2-Fluoro-5-nitropyridine commands steady demand because it strikes a sweet spot: the balance of electron density and activation due to its substitution pattern makes it a versatile intermediate. For example, switching the nitro group to another position alters reactivity, sometimes rendering the product too stable or not reactive enough for further derivatization. Fluorine’s location on the ring changes not just reactivity but how it interacts with catalysts and nucleophiles. In practical terms, we see customers trial several isomers for parallel syntheses before settling on the one that hits the sweet spot for yield, ease of purification, and step economy.
From our experience, this compound’s relatively straightforward purification—through crystallization and not simply chromatography—sets it apart from more troublesome pyridines that tend toward stubborn residual oils. Many researchers come back to 2-Fluoro-5-nitropyridine after running into solubility or caking problems with other halogenated intermediates. Its manageable toxicity profile—while demanding responsible handling and PPE, as with all aromatic nitro compounds—makes it approachable for both experienced process chemists and smaller research outfits. That blend of reactivity and practicality has led to broad uptake in both specialist contract labs and large-scale production facilities looking to streamline their route to target molecules.
Over years of production, we learned that the devil lies in the details. Handling 2-Fluoro-5-nitropyridine means planning around its air and moisture sensitivity. Evaporation of low molecular weight fluorinated by-products, absorption of atmospheric water, and even minor photodegradation can all contribute to the appearance of high baselines on HPLC or drifting assays. Regular retesting, tightly sealed packaging under inert gas, and light-resistant bags have all evolved from direct customer needs, not abstract industry best practices. Larger lots sometimes require custom packaging, not just because of logistics but to preserve the compound’s integrity during extended transit.
Part of our job is explaining why meticulous storage matters. If a customer leaves an open drum on a warm dock, esterification or hydrolysis by ambient moisture nudges impurity levels up. In such cases, technical support becomes as important as supply. We often recommend transferring the compound into smaller amber bottles kept in dry, cool rooms. This advice stems from our own headache when dealing with reclaimed returns which have turned sticky or discolored due to mishandling.
In the world of chemical manufacturing, making an intermediate isn’t just about filling orders. Many of our customers come to us early in their R&D process, sometimes while developing new routes or scaling up a bench-scale protocol. The technical conversations can range from simple supply forecasting to deep dives into kinetic profiles and by-product controls. We run application tests in actual reaction media that customers are likely to use, so the data we share reflects real-world behavior, not just idealized lab numbers. Application support includes sharing tips on reaction conditions, likely side reactions, and ways to sharpen yields through tweaks in temperature or solvent. These practical exchanges drive the compound’s popularity among chemists working on tight timelines.
Each new project brings up challenges. Sometimes a client switches from a smaller supplier only to find the profile or reactivity doesn’t match what their team expects. In these cases, we offer on-site or virtual technical troubleshooting, comparing process data and digging into minute details like moisture pickup or the source of unexpected signals in spectral data. Years of making this intermediate from multiple starting materials have given us experience to quickly isolate the root of such issues—often traced back to overlooked trace-level contaminants or slight pH shifts in the final washes.
Attention to sustainable chemistry keeps growing every year. 2-Fluoro-5-nitropyridine, like many fluorinated intermediates, posed challenges for greener synthesis decades ago. In response, we’ve worked with process chemists to improve yield, minimize hazardous reagent consumption, and make waste streams more manageable. By redesigning reaction sequences and upgrading distillation equipment, we cut solvent losses and reduced high-temperature degradation. These refinements, while behind the scenes, have meaning: less environmental burden and improved safety in the plant.
Advances in recovery and recycling help, but not every approach fits fluorinated compounds. In practice, we partner with downstream users to map out end-of-life disposal or recovery for spent reagents and solvents. Customers are increasingly aware of green chemistry metrics, so our process transparency—showing mass balance, energy usage, and potential points of loss—serves both compliance and innovation. Industry moves in this direction have made it easier for our team to adopt safer alternatives, including less hazardous fluorine sources or milder oxidants when possible.
The jump from gram-scale research to production-scale synthesis draws on a manufacturer’s ability to tweak, adapt, and respond fast. Early in our adoption of 2-Fluoro-5-nitropyridine production, challenges appeared at every step—yield drops at scale, variation in crystallization, and delays due to inconsistent supply of raw materials. Having pilot reactors and analytical control within walking distance from the main plant floors gives us room to solve problems directly. There’s no substitute for hands-on troubleshooting: adjusting agitation, optimizing crystallization temperature windows, or running small-scale mock-ups before committing to larger batches. These practices have become part of our operating culture.
Communication bridges gaps between R&D and production. Chemists on the plant floor give feedback right to synthesis teams or QA staff, so we’re able to close the loop on specification variance and evolve our testing standards. Manufacturing is never static; each run of 2-Fluoro-5-nitropyridine carries insight from last quarter’s customer feedback, new regulatory fact sheets, and evolving application notes from advanced research labs.
Compliance grows more complex each year, with rising demand for purity documentation, traceable batch records, and third-party verification. As a producer, investing in data integrity pays off: every lot comes with detailed certificates not because regulations demand it, but to give researchers and process engineers reassurance during audits or submissions. Some partners seek material for preclinical development, others for registration batches, and both require unambiguous evidence for chain-of-custody and impurity profiles.
Experience shows that audits don’t simply check boxes—they teach us new ways to tighten process controls, refine documentation, and anticipate customer questions. The need to support filings or custom regulatory packages means giving direct access to formulation chemists or regulatory professionals. Over time, this specialist support helps downstream users launch new projects faster, with fewer surprises in QC or later syntheses. A careful record of every batch, every calibration, every test result stands behind each shipment. As regulations evolve to cover new health and environmental concerns, we adjust protocols, strengthen documentation practices, and keep data accessible for ongoing compliance.
From the inside, making 2-Fluoro-5-nitropyridine is about more than filling orders. Each project, each delivery, connects us to people at every stage of the discovery and development pipeline. The partnerships that last bring open conversations about process challenges, feedback on material performance, and requests for improved documentation or batch sizes. Our team responds not through formulaic emails but by walking back through production logs, retracing analytical steps, or even redesigning parts of a process to meet sudden demand spikes. In our experience, real trust builds with transparency—letting the customer know how we approach each problem and what steps we take to fix it.
Looking out across years of production, we trace the growth in demand for this intermediate to creative work by customers—not marketing brochures or search rankings. Research groups and production engineers alike continue to revisit 2-Fluoro-5-nitropyridine because they can count on the performance, clarity of documentation, and responsive troubleshooting that our reputation has been built upon. This approach drives sustained improvements in manufacturing, technical support, and product quality.
Science does not stand still, and neither does chemical production. Each shipment of 2-Fluoro-5-nitropyridine represents more than the sum of its specifications; it encapsulates a living dialogue between manufacturer and end-user. New projects, quickly shifting timelines, and emergent technical challenges all feed back into how we plan, produce, and support this product. By keeping lines of communication open, by watching changing needs in pharmaceutical and agrochemical R&D, and by putting technical expertise right behind each batch, we contribute not just a chemical— but a source of real value to discovery pipelines around the world.