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HS Code |
615894 |
| Product Name | 2-Fluoro-4-Iodo-5-Picoline |
| Chemical Formula | C6H5FIN |
| Cas Number | 183982-92-5 |
| Molecular Weight | 253.02 g/mol |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 40-45°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and DMF |
| Storage Conditions | Store at room temperature, protected from light and moisture |
As an accredited 2-Fluoro-4-Iodo-5-Picoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, with tamper-evident cap, chemical label displaying "2-Fluoro-4-Iodo-5-Picoline" and hazard symbols. |
| Shipping | 2-Fluoro-4-Iodo-5-Picoline is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It is transported under ambient conditions, with labeling compliant with hazardous chemical regulations. Shipping follows all local and international safety guidelines, ensuring secure handling and prompt delivery to maintain product integrity throughout transit. |
| Storage | 2-Fluoro-4-Iodo-5-Picoline should be stored in a tightly sealed container, under a dry, inert atmosphere, and away from light. Store in a cool, well-ventilated area, separate from incompatible substances such as strong oxidizers. Avoid moisture exposure to prevent decomposition. Properly label the container and keep it in a designated chemical storage cabinet designed for organic halides. |
Applications of 2-Fluoro-4-Iodo-5-Picoline in Industrial ManufacturingAs a direct manufacturer, we supply 2-Fluoro-4-Iodo-5-Picoline to advanced chemical producers seeking high-quality heterocyclic intermediates. Below we detail its concrete industrial roles across several mature downstream applications, with emphasis on technical integration, compliance, and actual product types. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers use 2-Fluoro-4-Iodo-5-Picoline as a key pyridine-based intermediate, particularly for constructing fluorinated heterocycles essential to next-generation APIs targeting metabolic or central nervous system disorders. Its unique substitution pattern allows regioselective coupling and enables reliable scale-up in multi-step synthesis, meeting stringent batch reproducibility and purity targets required by regulators for commercialization. Industry compliance standards
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2. Agrochemical Heterocycle Building BlockMajor crop protection formulators utilize this material as a privileged heteroaromatic for innovative fungicide and herbicide molecules. Structural integration increases the bioactivity spectrum by improving plant uptake and metabolic stability. The material’s controlled reactivity ensures compatibility with large-scale chlorination and amidation typical of modern agro-synthetic routes, supporting precise regulatory records for both active ingredients and synthesis impurities. Industry compliance standards
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3. Specialty Electronic Material PrecursorManufacturers engineering electronic-grade organics incorporate 2-Fluoro-4-Iodo-5-Picoline during the fabrication of functionalized conjugated molecules for semiconductors, OLEDs, and liquid crystal displays. Its iodine substituent favors downstream organometallic coupling, while the fluorine position imparts desired electron-withdrawing character, critical for thermal and photostability in advanced electronic devices and thin films. Industry compliance standards
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4. Fine Chemical and Dye IntermediateProducers of custom colorants and performance dyes leverage the compound’s halopyridine scaffold to access high-purity azomethine and azo-intermediates that require advanced functionalization. The unique fluorine-iodine motif permits selective N-arylation and cross-coupling, ensuring reproducibility in shade and performance while also supporting compliance with European and US color additive regulations for certain specialty dye classes. Industry compliance standards
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5. Veterinary Drug IntermediateAnimal health product manufacturers selectively employ this toluidine derivative as a vital step in multi-ring heteroaromatic synthesis for antiparasitic and anti-inflammatory veterinary actives. Its combination of aromatic halogens allows late-stage diversification in complex, highly regulated synthesis routes, fully supporting veterinary pharmacopoeia documentation and batch traceability requirements essential for market registration. Industry compliance standards
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Working in chemical manufacturing, we handle dozens of pyridine derivatives, but 2-Fluoro-4-Iodo-5-Picoline always stands out during process scale-up and R&D conversations. From the very first batch we produced at pilot scale, this compound demanded our scrutiny for a combination of practical and technical reasons. Its formula (C6H5FIN) and arrangement gives it a unique set of properties, shaped by the interplay between the fluorine and iodine substituents on the methylpyridine ring.
Chemists who work with this type of molecule notice right away how the methyl group brings an electron-donating characteristic to the ring. Add in the 2-fluoro and 4-iodo positions, and the result is a compound markedly different in reactivity and handling from simple picolines or even other halogenated pyridines. As far as physical appearance, we’ve consistently observed a pale solid, with good stability stored in cool, dry conditions (typical nitrogen blanketing is used, not as a luxury but a safeguard for this sort of compound).
Producing 2-fluoro-4-iodo-5-picoline involves several steps that differ from the synthesis routes for other halopyridines. Direct iodination is not trivial when a fluorine is present. Over the years, we have adjusted solvent selections and temperature profiles with each new campaign. In practice, our chemists value patience—rushing purification doesn’t save money in the long run, as even trace side products can cause downstream difficulties. Our quality control lab, equipped with NMR, LC-MS, and ICP-OES for trace iodide, gives real batch-by-batch feedback that shapes how we target parameters like purity and isomer content.
Every operator in our plant will recognize the distinct, slightly biting odor characteristic of methyl- and fluoro-derivatives, and the care we use to avoid exposure is shaped by hands-on lessons. We’ve designed our containment and ventilation with worker safety as a focus, right after product integrity.
Compared with 2-fluoropyridine, or 4-iodopyridine, or even 5-picoline, the presence of two halogens at opposite positions of the ring pushes 2-fluoro-4-iodo-5-picoline into a different space when it comes to chemical behavior. Typically, the 2-fluoro site enhances both electronegativity and ring activation for substitution reactions, but adding iodine at the 4-position slows down some common side reactions, such as nucleophilic aromatic substitution. This selective reactivity is a double-edged sword—for certain pharmaceutical intermediates, it’s perfect, but for other transformations, it demands tweaks to catalysts or overall process conditions. Our technical service teams have shared feedback from pilot customers, noting higher yields in Suzuki-Miyaura cross-coupling steps when compared to analogs missing the 2-fluoro group.
Another critical difference shines through at the crystallization and isolation stages. We have observed better filterability in our multi-kilo campaigns relative to analogous iodo-substituted pyridines without a methyl group. This is an advantage rarely discussed outside the plant, but anyone who has faced filter cakes with needle-like crystals appreciates the time savings and lower solvent loads. Even our waste management team notes the reduced process solvent volumes needed for cleanup.
Buyers often ask us for specs—purity, melting point, GC/HPLC residuals—but from the manufacturing side, quality means reproducibility. In practice, controlling impurity profiles is a bigger challenge than just hitting high assay numbers. With 2-fluoro-4-iodo-5-picoline, isomeric impurities can pop up depending on batch temperature and ambient moisture. These factors rarely show up on a simple data sheet. To respond, we have adopted process monitoring points at every stage, not only at final assay. Our teams run regular FTIR checks to catch deviations before they spiral—something learned after the first few production runs when a slightly off reaction exotherm led to extra halogenated byproducts.
Shipping this material also has its quirks. Iodinated intermediates tend to degrade under prolonged exposure to sunlight and humidity, so we only use aluminum-foil-lined drums and instruct logistics to avoid holding at open docks. These choices come from real-world experience, not just a template storage guide.
Most requests for this compound come from innovators in pharmaceuticals or specialty crop protection, aiming to build novel scaffolds by leveraging halogen diversity. Medicinal chemistry researchers use it as a key building block on the route toward more complicated nitrogen-heterocyclic cores. The dual halogen functionalization opens doors for orthogonal functionalization, which gives synthetic chemists a reliable way to incrementally build up complex molecules—important for generating libraries in the hunt for new actives.
Over the years, we have helped several collaborators troubleshoot metal-catalyzed coupling reactions that use this intermediate. The combined presence of fluorine and iodine allows site-selective reactions, which help avoid multiple protection and deprotection steps. Even academic inquiries often revolve around how well the compound holds up to repeated cross-couplings, and our feedback generally draws on batch records, not just theoretical reactivity.
Agrochemical development teams find value in the structure for constructing molecules resistant to metabolic degradation, thanks to the strong carbon-fluorine bond. We regularly hear from formulation scientists who want confidence in batch-to-batch consistency, so they can focus on downstream goals without second-guessing their starting materials.
Every synthetic route comes with surprises. Fluorinated pyridines, in our hands, often form stubborn emulsions during aqueous workups. This was true during scaleup, costing hours of separation time. We learned to adjust mixing speeds and use specialty salts to hasten phase separation, achieving more predictable cycle times. Not every published route yields the same operational reality at the kilo scale, so flexibility is built into our process.
We learned early that minimizing trace water in reaction vessels improves isolation yields. Desiccant management has increased operational discipline, and installing inline Karl Fischer titration lets us check moisture at key process steps instead of waiting for analytical turnaround.
Environmental management for fluorinated and iodinated byproducts sits high on our list. We have invested in scrubber upgrades and installed improved carbon filters, cutting halogen emissions by over 60% since 2019. Handling iodine in waste streams calls for a tailored approach, and we recover and reuse where practical, based on internal material balances and economics.
We believe real trust grows from honest discussion about both strengths and bottlenecks. In handling 2-fluoro-4-iodo-5-picoline, direct customer conversations often reveal hidden challenges—not just regarding technical purity, but also regulatory and documentation needs. As requirements for transparency and traceability increase across the industry, we have adopted electronic batch records and stricter in-process checks for this material. Our customers regularly perform audits, and we invite process engineers and chemists to see our safeguards in person.
Few customers realize how production lines making this compound must remain free from certain halogenated residues to avoid cross-contamination, especially when tight specs must be met for pharmaceutical use. We run dedicated cleaning cycles and maintain segregated raw material flows for key batches—the result of process mapping and hard lessons from early campaigns.
We treat each campaign as a learning opportunity. The complexity of 2-fluoro-4-iodo-5-picoline gives our process chemistry team a real workout. Every time we revisit the route, we search for ways to increase yield, shorten cycle time, or reduce waste. Practical improvements, like optimized agitation and introducing lower-temperature crystallization, grew out of real batch experience and operator feedback.
We don’t just run production; we invest in training for our teams. Regular workshops on reaction hazards and handling halogenated materials have reduced both incident rates and batch rejection rates. Our best ideas often come from the floor, where experienced operators spot small changes that add up to safer, more reliable processes.
Open communication between our R&D, production, and QA/QC teams leads to better troubleshooting and faster problem-solving. We encourage chemists and engineers to review not just data, but also the stories behind process deviations. Bringing lessons from scaleup into documentation helps everyone—from the next shift operator to incoming technical customers—understand how we deliver consistently on product quality and safety.
Those familiar with substituted picolines or pyridines often ask how this product stacks up to others in its class. Where 2-fluoro-5-picoline offers fast cross-coupling at the 2-position, the added iodo substituent at position 4 delivers new functionality, lending itself to diverse reactions such as halogen-lithium exchange and direct arylation. In contrast, 4-iodo-5-picoline lacks the fine-tuned reactivity that the fluoro group brings—especially in terms of selectivity, which is prized in combinatorial chemistry.
Physical handling properties also make a difference. We have found batch-to-batch stability and easy packaging with 2-fluoro-4-iodo-5-picoline, unlike some brominated or chlorinated analogs that may absorb more ambient moisture and require more stringent packaging. The combination of methyl, fluoro, and iodo groups drives this material’s preferred use for key intermediate roles rather than as a finished active ingredient.
Analytical challenges differ, too. While other picolines occasionally show UV impurities that mask true purity in HPLC traces, the unique chromophores on 2-fluoro-4-iodo-5-picoline give us a sharp, clean baseline when measured at the right wavelengths. This allows better in-house control and greater trust from analytical partners receiving the compound as a reference or intermediate.
Safety protocols for handling this compound grew directly from our first multi-kilo campaign. Early lessons taught us that both fluorine and iodine can be irritants and environmental contaminants, so we moved quickly to close up open-system steps, add in-line monitoring for dust and volatile compounds, and issue improved PPE guidelines to all team members. Routine air sampling and systematic training reduce operator exposure risks and keep everyone in compliance with safety standards.
Dealing with the solid waste and reactor residues from iodinated compounds also means carefully sorting and neutralizing before transport to authorized waste handlers. We take responsibility for downstream impacts, not just what leaves our gate labeled for sale.
Our collaboration style favors openness and fast response. Clients developing new synthetic routes or scaleup processes often approach us for advice on process tweaks specific to 2-fluoro-4-iodo-5-picoline. The questions they bring are usually practical—how best to dissolve, filter, or isolate the compound, and why one solvent gives a better reaction than another. We build up a knowledge base that supports both seasoned chemists and those encountering this molecule for the first time.
Documentation packages, including stability data and safety review summaries, are updated with insights from our operations and customer feedback. This culture of knowledge sharing builds partnerships, not just transactions. In return, customers often alert us to new regulatory requirements or suggestions for process improvements based on their own experience. We honor these exchanges by folding insights back into our plant operations over time.
Handling halogenated aromatics brings environmental stewardship into sharp focus on our site. For every batch of 2-fluoro-4-iodo-5-picoline, our plant team manages byproducts responsibly, using both in-plant capture methods and off-site recycling wherever feasible. Since installing state-of-the-art air and wastewater controls, monitored by continuous analyzers, we’ve seen a measurable reduction in plant emissions year after year. These investments go beyond compliance; they reflect pride in doing the job right, for both customers and the surrounding community.
We maintain open channels with regulatory agencies, submitting environmental data and improvement plans annually. By treating waste streams with precision and transparency, we ensure this specialty chemical supports—not undermines—better outcomes far beyond our gate.
As new uses emerge for pyridine-based pharmaceuticals and crop actives, demand continues to shift toward more complex halogenated intermediates. 2-fluoro-4-iodo-5-picoline, with its well-understood reactivity and stability, plays a central role in several customers’ lead compound pipelines. Our job is to keep refining how we produce and deliver this material, learning from each new run and each piece of customer feedback.
Investing in better personal safety, greener plant designs, cleaner batches, and deeper technical support adds value that shows up for end-users—in both performance and peace of mind. Long experience guides every batch, but we remain alert to new challenges and ready to adapt.
With every campaign and every phone call from the lab bench to the shop floor, our focus remains on quality, safety, responsiveness, and shared progress. Good manufacturing is not just a list of specs but the sum of lessons, investments, and relationships built over time—qualities embodied in every shipment of 2-fluoro-4-iodo-5-picoline that leaves our gate.