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HS Code |
815325 |
| Product Name | 3-Fluoro-2-Iodopyridine |
| Cas Number | 261953-36-6 |
| Molecular Formula | C5H3FIN |
| Molecular Weight | 238.99 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 208-210°C |
| Density | 2.11 g/cm3 |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=NC=C1F)I |
| Inchi | InChI=1S/C5H3FIN/c6-4-2-1-3-8-5(4)7/h1-3H |
| Solubility | Soluble in organic solvents (e.g., DMSO, dichloromethane) |
| Storage Conditions | Store in a cool, dry, and well-ventilated place, away from light |
As an accredited 3-Fluoro-2-Iodopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams, with a tamper-evident seal, labeled "3-Fluoro-2-Iodopyridine" and hazard warnings clearly displayed. |
| Shipping | 3-Fluoro-2-Iodopyridine is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous chemical, requiring compliance with applicable transportation regulations. Packaging ensures minimal risk of leakage or contamination, and the material is typically shipped via specialized courier services approved for hazardous materials. |
| Storage | 3-Fluoro-2-Iodopyridine should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. It should be kept away from incompatible substances such as strong oxidizers. Store at room temperature or as recommended by the manufacturer, and ensure proper labeling and handling to avoid contamination or accidental exposure. |
Applications of 3-Fluoro-2-Iodopyridine in Industrial ManufacturingAs a specialized manufacturer of 3-Fluoro-2-Iodopyridine, we provide this intermediate to global industrial customers for advanced synthesis in regulated and innovative sectors. Detailed below are the major downstream applications recognized in current industrial practice, with key technical and regulatory aspects addressed for each use scenario. 1. Pharmaceutical Active Ingredient SynthesisPharmaceutical manufacturers utilize 3-Fluoro-2-Iodopyridine as an essential halogenated building block for constructing pyridine-containing APIs, especially in oncology and CNS therapies. Its defined substitution pattern supports regioselective coupling and efficient introduction of fluorine atoms, facilitating downstream modification under GMP-compliant conditions. Facilities using this intermediate must validate each batch for residual iodine and fluoroaromatic by-products as part of the active pharma ingredient (API) registration files. Industry compliance standards
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2. Agrochemical Intermediate Production3-Fluoro-2-Iodopyridine serves as a strategic precursor in the manufacture of modern crop protection agents, especially pyridine-derived herbicide and fungicide families. It enables precise fluorine introduction to enhance bioactivity and metabolic stability. Agrochemical formulation sites implement documented control over batch identity, trace fluorinated impurities, and raw material provenance, following international regulatory requirements for food safety and environmental protection. Industry compliance standards
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3. Electronic Chemicals and OLED MaterialsProducers of advanced electronic chemicals employ this pyridine derivative in the synthesis of electron-deficient heterocyclic scaffolds, which are key for organic light-emitting diodes (OLEDs), thin film transistors, and organic photovoltaic materials. It is precisely dosed to achieve controlled doping and high-purity layer uniformity, with stringent review of trace halogen content, metal contaminants, and batch reproducibility under electronic grade QC protocols. Industry compliance standards
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4. Custom Fine Chemical Synthesis ServicesCDMO (Contract Development and Manufacturing Organization) and fine chemical companies source 3-Fluoro-2-Iodopyridine for exclusive molecule production, specialty ligands, and advanced research reagents. Custom projects demand validated traceability, analytical reporting of residual solvents and halogenated by-products, and adherence to strict customer-specific synthesis protocols. End-users require a well-defined impurity profile and consistent lot-to-lot quality, with documented batch records and specification alignment. Industry compliance standards
Typical usage ratio
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3-Fluoro-2-Iodopyridine has earned respect among synthetic chemists for its unique structure and utility in building complex molecules. We have devoted years to mastering its production, drawing on accumulated experience in halogenated pyridine chemistry. Unlike many common building blocks, this compound features both a fluorine and an iodine atom on the pyridine ring, specifically at the 3 and 2 positions. This pattern leads to marked differences in reactivity, selectivity, and downstream synthetic options. Our daily operations bear out the reality that small changes in a molecule’s substitution pattern can overhaul a synthetic route.
As a manufacturer involved at every stage from raw material sourcing to quality inspection, we recognize the fine balance required to generate 3-Fluoro-2-Iodopyridine at scale. Not every plant can safely and reproducibly handle the highly reactive intermediates or manage the waste generated in halogen exchange. We have had to optimize each parameter, not just for yield but for reliability, worker safety, and supply continuity. By prioritizing continuous flow systems and in-line monitoring, our teams limit batch-to-batch variation, keeping both process engineers and end users confident in each delivery.
This compound shows its value in medicinal chemistry, agrochemical development, and material science. The presence of fluorine on a molecule often improves metabolic stability and modulates biological properties without adding excessive bulk. The iodine atom offers a highly reactive site for further transformations via palladium-catalyzed cross-coupling, including Suzuki, Sonogashira, and Buchwald–Hartwig reactions. Unlike more traditional dichloro- or dibromo- pyridines, the fluoro-iodo combination encourages selectivity—a trait proven valuable when constructing libraries of analogs or focusing on rapid structure-activity relationship explorations.
We routinely field requests for both standard and custom-packaged 3-Fluoro-2-Iodopyridine. The compound supports rapid diversification in drug discovery projects, enabling introduction of aryl, alkynyl, amine, or other functional groups under mild conditions. This flexibility streamlines SAR studies, lets researchers test new ideas without redesigning entire routes, and accelerates timelines for lead optimization. Our own interactions with clients have underlined the importance of consistent purity, especially for organometallic coupling work where metal traces or non-volatile residues can block a reaction or contaminate downstream products.
Years ago, growth in fluorinated intermediates was driven mostly by demand from large pharma companies. More recently, we’ve helped emerging biotech and academic groups bypass the headaches of handling halogen-laden molecules in-house. Sourcing this intermediate from a manufacturer with deep infrastructure and validated handling procedures can eliminate bottlenecks and free up researchers to focus on synthesis rather than safety protocols. Our technical team works closely with chemists confronting new cross-coupling challenges, offering advice not just on physical property data but on actual lab experience gained through thousands of pilot and production runs.
Several factors set 3-Fluoro-2-Iodopyridine apart from related compounds such as 2-bromo-3-fluoropyridine or 2-chloro-5-fluoropyridine. The fluorine atom alters the electron density of the ring, changing its reactivity profile and making certain positions more or less prone to further substitution. The iodine atom, thanks to its size and weak C–I bond, opens a window for carbon–carbon or carbon–heteroatom couplings that less reactive bromides or chlorides simply don’t match.
Our experience with different halogen combinations has shown clear differences in solubility, melting point, and chemical handling. For example, 2,3-difluoropyridine might suit certain nucleophilic aromatic substitution reactions but falls short for Suzuki or Sonogashira work, where the iodine site in 3-Fluoro-2-Iodopyridine performs cleanly under typical conditions. Purification of the iodo analog, while sometimes more demanding due to its higher molecular weight, results in a product with well-controlled impurity profile—ideal for demanding pharmaceutical or agricultural research applications.
From a manufacturing standpoint, iodinated pyridines call for specialized containment, due to both the cost of iodine and the need to manage off-gassing or trace contamination. We invested in dedicated halogen handling lines to prevent cross-contamination between different materials and to achieve high-purity batches. This discipline reflects not just regulatory compliance, but mutual respect for the end users who trust our products in mission-critical research.
Sourcing precise raw materials makes a noticeable difference in yield and product quality. Our operation maintains regular audits of supply chains for fluorinated and iodinated reagents. Any drift in feedstock purity or physical properties can set back an entire production run. We rely on trusted suppliers, using in-house analytical methods to confirm each lot before it enters our reactors.
Handling and storing hydroiodic acids, bases, and fluorinating agents require not just technical knowledge but everyday vigilance. Specialized ventilated zones, sealed transfer systems, and real-time environmental monitoring all play a part in keeping our teams safe and production lines running. These investments, honed over years of chemist-driven feedback, directly translate into reliability for our partners. Accidents in this field are most often traced to complacency or corner-cutting; we maintain a culture of continuous education, rewarding team members for flagging risks and improving our protocols.
Yields for halogenated pyridines can vary wildly depending on the reaction sequence and exact conditions. From catalyst choice to stirring speed and solvent profile, every detail matters. We keep extensive records of each run, noting not just headline yield but underlying parameters like crystallization point, color, and analytical spectra. Regular collaboration with equipment manufacturers helps refine our set-ups and troubleshoot recurring variations—nobody can afford waste or downtime in today’s just-in-time R&D landscape.
Our internal analytics lab uses quantitative NMR and GC-MS to verify not only final purity but residual solvents and trace catalyst content. Many customers use the compound in sensitive cross-coupling or pharmacological screens, where impurities or trace metal residues can obscure results. By maintaining a direct path from raw material intake to end-product packaging and shipment, our team can rapidly trace and correct any deviation.
Batch consistency has often posed difficulties across the industry. A few years back, unacceptable variability between lots from one supplier reminded us that repeatability lies at the core of chemical manufacturing. We responded by rebuilding much of our batch-tracking and documentation systems, allowing any customer complaint or question to be rapidly investigated and data to be shared transparently. These systems, including barcoded traceability and digital logbooks, have tightened our feedback loop between plant, quality assurance, and clients.
Storage and shipping conditions for iodo-fluoropyridines also deserve attention. We package 3-Fluoro-2-Iodopyridine under an inert atmosphere in high-integrity containers, minimizing both hydrolysis and oxidation during transit. Over the years, we have seen colleagues underestimate the sensitivity of this material—led to avoidable degradation and customer returns. By systematically monitoring storage and transport stability, we keep product loss to a minimum and ensure researchers receive consistent, high-quality starting materials.
Halogenated intermediates raise important questions about responsible waste management and environmental stewardship. Our own experience has revealed the complexities involved in recovering and recycling spent solvents or halogen byproducts. While not every facility devotes resources to solvent recovery or responsible disposal, we believe that responsible handling is not just about compliance but about standing behind your final product.
Our facility uses solvent distillation and halogen neutralization systems developed in collaboration with environmental engineers. These measures recover significant fractions of process solvents and reduce the carbon footprint compared to decades-old incineration methods. The adoption of closed-loop systems in our plant has improved efficiency and provided reassurance for clients mindful of expanding regulatory frameworks in the US, EU, and China.
Our chemists work continuously to improve atom economy and selectivity within our production process. Small increases in step yield or reduction in unwanted byproduct lessen the need for reprocessing and decrease our waste profile, while offering fair and consistent pricing for end users. Challenges in halogenated intermediates are ongoing, but few efforts repay as much as targeted process optimization and proactive engagement with the latest sustainable chemistry advances.
Customers regularly approach us with questions about unusual reactivity or potential impurities. We willingly share not only summary analytical data but deeper insights into physicochemical behavior under different storage or reaction conditions. Years of feedback from medicinal chemistry labs and pilot plant technicians have shaped our approach. For example, our support chemists often highlight common problems related to crystallization solvent choice, which can either concentrate or obscure trace impurities invisible to HPLC.
Research moves too quickly to tolerate unclear answers or missing technical support. Our internal knowledge management systems log not only batch data but recurring troubleshooting tips, solvent behavior, and cross-coupling compatibility. This open, documented flow of information helps chemists build efficient, robust synthetic routes while avoiding pitfalls seen by others across the industry.
Handling iodo- and fluoro-substituted aromatics brings additional regulatory scrutiny. Regional authorities ask for detailed documentation not only of chemical composition but for safety data ranging from volatility to inhalation risk. Our documentation is backed by in-house testing and provides actionable safety protocols suited for bench-top or pilot-plant settings.
We offer clear guidelines for handling spills, managing accidental contact, and proper disposal methods. Technical data is supported by real-life procedural knowledge, shared from our teams to client labs. This way, buyers receive not just a dry data sheet but practical ideas for handling, storage, and emergency procedures, born from hard-won experience in day-to-day plant operations.
Interest in fluorinated intermediates continues to expand. The unique space occupied by 3-Fluoro-2-Iodopyridine comes down to its role as a convergence point in modern medicinal and agricultural chemistry. We have seen projects leverage its reactivity to access new heterocyclic scaffolds or fine-tune physical properties in crop protection agents. Our product has landed in some surprising places: specialty materials, fluorescent dyes, and advanced battery electrolytes.
Precise, reliable access to this intermediate lets research move quickly from hypothesis to experiment. As an upstream partner, we value ongoing conversations with our customers. Every year brings new synthetic challenges, new regulatory guidance, and new expectations for quality. Meeting these with real expertise—that’s what manufacturing at scale truly means, and what our clients expect when they reach for 3-Fluoro-2-Iodopyridine built on proven process control, thoughtful engineering, and a shared commitment to chemical progress.
We see ourselves as more than a supplier. Our technical team regularly joins discussions on reaction optimization, new coupling methodologies, or emerging analytical techniques. By working directly with innovators in medicinal and process chemistry, we gain feedback that steers our future investments. The demand for pure, traceable halogenated intermediates will only grow as targets become more complex and timelines shrink.
3-Fluoro-2-Iodopyridine represents a fusion of specialized knowledge, informed risk management, and continuous improvement. We commit to transparent practices, supporting successful research outcomes and efficient industrial processes. Our door remains open to technical questions, project-specific requests, and problem-solving partnerships in this ever-changing landscape.