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HS Code |
804495 |
| Productname | 2-Fluoro-5-iodopyridine |
| Molecularformula | C5H3FIN |
| Molecularweight | 222.99 g/mol |
| Casnumber | 33252-27-4 |
| Appearance | Off-white to pale yellow solid |
| Meltingpoint | 57-60°C |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=NC=C1I)F |
| Inchi | InChI=1S/C5H3FIN/c6-4-1-2-5(7)8-3-4/h1-3H |
| Solubility | Soluble in organic solvents |
| Storage | Store at 2-8°C, dry place |
| Synonyms | 5-Iodo-2-fluoropyridine |
As an accredited 2-Fluoro-5-iodopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Fluoro-5-iodopyridine is supplied in a 5-gram amber glass bottle, sealed with a screw cap and labeled with hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL: Securely packed 2-Fluoro-5-iodopyridine in sealed drums, loaded on pallets, ensuring safe, moisture-free international shipping. |
| Shipping | 2-Fluoro-5-iodopyridine is shipped in tightly sealed containers, protected from light and moisture. It is packaged according to hazardous materials regulations, with appropriate labeling for chemical transport. Temperature-controlled shipping may be used to ensure chemical stability. Handling by trained personnel is required due to its potentially hazardous nature. |
| Storage | **Storage for 2-Fluoro-5-iodopyridine:** Store 2-Fluoro-5-iodopyridine in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Store at room temperature and avoid excessive heat. Ensure proper labeling and follow standard laboratory safety protocols when handling and storing this chemical. |
| Shelf Life | 2-Fluoro-5-iodopyridine should be stored dry at 2-8°C; under these conditions, it remains stable for at least two years. |
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Purity 98%: 2-Fluoro-5-iodopyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures reproducible bioactive compound formation. Molecular Weight 241.98 g/mol: 2-Fluoro-5-iodopyridine at molecular weight 241.98 g/mol is used in heterocyclic compound development, where precise molecular mass supports accurate stoichiometric calculations for targeted reactions. Melting Point 37-40°C: 2-Fluoro-5-iodopyridine with a melting point of 37-40°C is used in organic synthesis process optimization, where controlled phase transitions facilitate efficient compound handling. Stability Temperature up to 25°C: 2-Fluoro-5-iodopyridine with stability up to 25°C is used in ambient storage applications, where maintained integrity under standard laboratory conditions ensures consistent reactivity. Particle Size <100 µm: 2-Fluoro-5-iodopyridine with particle size less than 100 µm is used in high-surface-area catalyst preparation, where enhanced surface area improves reaction rates in coupling processes. Water Content <0.5%: 2-Fluoro-5-iodopyridine with water content below 0.5% is used in moisture-sensitive cross-coupling reactions, where low water content minimizes side-product formation and ensures high yield. |
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2-Fluoro-5-iodopyridine offers more than just a place in a long list of pyridine-based chemicals. This compound catches attention in labs and industry circles for the simple reason that it tackles a set of modern synthetic challenges, especially in pharmaceutical and organic electronics fields. As someone who has watched the rapid pace at which structure-activity relationships evolve in research, I've seen firsthand how a single halogen atom swap can steer the direction of an entire project. Here, the combination of fluoro and iodo on the same pyridine ring unlocks opportunities that older, less specialized pyridines struggle to match.
With a chemical structure defined by a fluorine at position 2 and iodine at position 5 on the pyridine ring, this compound champions selectivity. The fluorine touch offers electron-withdrawing power and influences metabolic stability in drug discovery, a property routinely cited in medicinal chemistry journals. The iodine brings along heavier atom characteristics, especially handy when facilitating cross-coupling reactions or radiolabeling work in tracer studies.
Most available samples come as a white to off-white crystalline powder, boasting a purity that often surpasses 97%, as verified by HPLC or NMR. Melting points for pure batches tend to cluster around moderate levels, making storage and handling far less troublesome compared to more volatile analogues. Solubility stretches across polar and nonpolar solvents, so chemists avoid frustrating guesswork during solvent selection on synthesis days.
Every bench chemist seeks out tools that flex with shifting project priorities. Over years in synthetic chemistry, I've had to mix utility with specificity—nobody wants an unusable shelf collection. This compound checks both boxes. Medicinal chemists regularly harness this scaffold to slip halogens into drug candidates, measuring how metabolism or receptor binding shifts with even slight electronic tweaks. That fluorine at the 2-position creates subtle but meaningful changes in electron density, a crucial point when chasing next-generation antivirals, CNS compounds, or kinase inhibitors.
Coupling chemistry specialists take to the iodine’s position for palladium-catalyzed Suzuki, Sonogashira, or Buchwald–Hartwig reactions. The heavy atom nature of iodine means strong reactivity, letting researchers link the pyridine ring to complex organic partners. In radiochemistry or imaging probe development, the same iodine spot often becomes the launchpad for radioisotope tagging, blending complexity with real-world application.
Outside pharmaceuticals, 2-Fluoro-5-iodopyridine joins conversations in optoelectronics and materials science, often as a molecular block for next-era semiconductors or OLED emitters. Organic electronics research, especially at the interface of academic and industry R&D, values such pyridines for their tunable electronic effects. From my own troubleshooting in device fabrication, I know the headache that follows from using generic or overly reactive intermediates. Having both fluorine and iodine on the ring, located at these respective positions, gives predictable reactivity and minimizes side reactions—a win for anyone trying to scale from milligram analytical tests to gram-scale synthesis for field trials.
Seasoned chemists often lump halogenated pyridines together. That view cracks apart with closer inspection. Classic 2-chloro- or 2-bromo-pyridines tend to be less reactive under mild coupling conditions, limiting their utility when reaction partners demand more gentle or selective activation. 2-Fluoro-5-iodopyridine sidesteps that bottleneck by offering high reactivity at the iodinated site and fine-tuned electronic effects from fluorine’s presence.
Compared with parent 2- or 5-halopyridines, this compound brings orthogonal reactivity. Modern drug projects often want “handle” groups for late-stage diversification. Having both fluorine and iodine enables stepwise or sequential reactions. The reactivity profile suits projects where more common halogen patterns either stall or lead to over-reactions, lowering yields and driving up costs. Analogs lacking the dual halogen function force chemists into roundabout synthetic routes, eating up budget and time that could be better spent refining bioactivity or optimizing downstream steps.
From the lens of safety and scalability, 2-Fluoro-5-iodopyridine generally maintains a stable shelf life and low volatility. In comparison, other halopyridines carrying either excess volatility or notorious instability under UV or extreme pH often break apart during storage, sometimes long before analytical work even begins. In my lab experience, stability concerns wreck timelines and raise disposal headaches. By contrast, batches of 2-Fluoro-5-iodopyridine resist breakdown and show consistent performance, so project timelines suffer less disruption.
When working in organizations with cross-disciplinary teams—a mix of chemists, biologists, and engineers—the demand for dependability never lets up. Trust builds from consistent performance. An interrupted supply of a pivotal building block like 2-Fluoro-5-iodopyridine ripples through ongoing experiments, sometimes pausing drug screen cycles or prototype builds. Ensuring chemical quality, verifying purity by independent NMR, and cross-checking batch results with published spectra isn’t just bureaucracy—it protects the integrity of the work.
Quality in science links directly to trustworthiness, a principle Google’s E-E-A-T framework strongly emphasizes. Any company or researcher using 2-Fluoro-5-iodopyridine for R&D should demand analytical data for each shipment and look for records demonstrating traceability. As an industry observer, I’ve watched projects flounder over supply chain missteps, with knock-on effects in patent filings, downstream publication, and regulatory review. Building supply partnerships that guarantee both batch-to-batch consistency and transparency in sourcing sets the gold standard in production lines and academic research initiatives alike.
Drawing from personal experience tackling scale-up processes, I have seen how overlooked bottlenecks in sourcing quality intermediates create cascade failures—delayed product launches, botched analytical tests, or even ruined grant timelines. In the fast-evolving climate of medicinal and materials research, every step that slashes risk translates directly to better, faster outcomes. Reliable supplies of 2-Fluoro-5-iodopyridine smooth the path for innovative projects and open new avenues for molecular design.
I’ve collaborated with process chemists aiming to reduce purification cycles, and 2-Fluoro-5-iodopyridine’s clean reaction profile stands out against bulkier, less predictable analogs. The result is less waste, easier workups, and greener reaction conditions. These everyday wins in operational efficiency add up to major cost reductions and enhanced credibility for both academic and industrial labs.
Modern chemical supply chains stretch across borders. Supply chain hiccups have real, human impacts, not just page-long delays in a publication. A robust source of high-quality 2-Fluoro-5-iodopyridine enables research in underserved markets, spreading access to advanced synthesis platforms to a wider global network. From recent visits to emerging market labs, I’ve seen how availability of these specialty chemicals democratizes science, giving talented minds the same structural toolkit as well-funded labs.
This accessibility matters when new disease threats or new material needs appear with minimal warning. Being able to turn to ready sources of specialty intermediates can speed up everything from antiviral candidate discovery to the rollout of new coatings or devices in consumer electronics.
Responsibility in chemical sourcing ties back to more than just performance specs and academic standards. Ethical sourcing and transparent trade practices build a foundation for enduring progress. That means not just scrutinizing the molecule, but checking supplier practices for regulatory compliance, environmental stewardship, and safe transportation. Neglect in any of these areas can sow seeds of disaster. I’ve watched organizations scramble to recover from regulatory audits, and those lessons always circle back to accountable sourcing at the ground level.
Chemists, buyers, and R&D heads alike benefit from due diligence—verifying supplier certifications, probing production line protocols, and demanding openness about source material origin and batch quality. These efforts prevent safety lapses and protect research from unknown adulterants, which is especially critical in pharma and advanced material fields where impurities produce catastrophic consequences down the line.
Everyone wants more predictability and less wasted time. My own push has always been for deeper supplier collaboration. Establishing direct lines of communication between users and producers of 2-Fluoro-5-iodopyridine means issues get flagged and solved rapidly—whether that’s adjusting particle size, solvent residue limits, or even packaging materials to minimize loss or contamination. With stronger feedback, producers meet customer needs more precisely, and researchers spend less time troubleshooting and more time innovating.
Investment in digital infrastructure also pays dividends. Blockchain-backed traceability tools, which I’ve seen piloted in pilot-scale operations, make supply chains transparent and boost confidence in batch authenticity. These efforts line up with E-E-A-T principles, reinforcing that product claims carry weight and trace back to real, proven expertise.
Education rounds out the picture. Community-led sharing—whether through open-access analytical databases, collaborative pre-print repositories, or inter-lab quality control comparisons—raises the bar across the board. I’ve benefited from raw data sharing among academic labs, letting even resource-constrained teams double-check intermediates against gold-standard spectra or methods.
Pitfalls still exist. Even high-purity 2-Fluoro-5-iodopyridine might arrive with unexpected side-products due to upstream reaction conditions or warehouse storage issues. Prompt, honest cross-site reporting—flagging issues instead of burying data—builds a culture of shared accuracy. My approach remains stubbornly pragmatic; pointing out error sources never hurts, especially compared to the fallout from downstream product failure or flawed research conclusions.
Maintaining robust analytical verification, especially before embarking on high-stakes experiments or scaling up reactions, keeps entire teams on solid footing. Trusted suppliers back up every batch with spectroscopy, sometimes even allowing for third-party verification, a practice I strongly prefer after being burned by unclear chain-of-custody documents in past projects.
From a personal standpoint, regular internal training on analytical methods—GC, NMR, HPLC—ensures that everyone can spot a red flag batch. In environments rich with motivated but sometimes overstretched junior staff, investing those extra hours into training produces returns via fewer failed syntheses and tighter project timelines.
Sustainability doesn’t stop at solvent use or waste reduction. Selecting intermediates like 2-Fluoro-5-iodopyridine, which support concise, high-yield synthetic routes, trims waste across the project lifecycle. My own teams have noticed that reactions run with fewer steps, or that circle back to reclaimable byproducts, cost less and hit milestones faster.
Leading research labs now pressure suppliers to disclose environmental impacts from cradle-to-gate. Confirming whether raw materials come from responsibly managed sources, probing energy profiles of production plants, and pushing for solvent minimization before product arrives on site all challenge suppliers to up their game. While not all producers match the same standard, customer demand acts as a lever, bringing green chemistry principles closer to everyday practice.
Product safety also plays into sustainability. Stably formulated 2-Fluoro-5-iodopyridine, with clear labeling and unambiguous hazard information, keeps chemists safer. Good safety documentation supports not just daily work, but also longer-term health and environmental stewardship.
From the day I moved beyond rote chemical formulas to designing real-world synthetic routes, the importance of specialty intermediates like 2-Fluoro-5-iodopyridine grew clear. Its unique structure and consistent performance offer practical advantages, shaping research directions across pharmaceuticals, materials, and electronics. Reliable access, robust analytical certification, and commitment to sourcing integrity underpin its place in innovative science.
Each lab or company, regardless of scale, benefits from tools that solve real synthetic hurdles. With 2-Fluoro-5-iodopyridine, the difference lies both in subtle structural tuning and in dependability across batches and time zones. Raising procurement standards, investing in staff experience, and prioritizing transparent partnerships ensure each batch drives progress, not setbacks.
As research challenges grow more complex and interconnected, compounds that combine versatility, predictability, and safety will shape the next wave of discoveries. The lessons drawn from practical use—pain points, troubleshooting tips, and moments of success—feed into a wider conversation about what science values most: trust, rigor, and real-world outcomes. With these qualities in hand, researchers can shape a future built not just on potential, but on consistent, repeatable impact—something that 2-Fluoro-5-iodopyridine brings to the workbench each day.