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HS Code |
645390 |
| Chemical Name | 2-Fluoro-5-Iodobenzonitrile |
| Cas Number | 369-93-9 |
| Molecular Formula | C7H3FIN |
| Molecular Weight | 263.01 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 44-48°C |
| Density | 1.92 g/cm³ (estimated) |
| Purity | Typically >98% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1I)F)C#N |
| Inchi | InChI=1S/C7H3FIN/c8-6-2-1-5(4-10)3-7(6)9/h1-3H |
As an accredited 2-Fluoro-5-Iodobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5-gram amber glass bottle labeled "2-Fluoro-5-Iodobenzonitrile," sealed with a screw cap, and featuring standard chemical hazard warnings. |
| Shipping | 2-Fluoro-5-iodobenzonitrile is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packages are clearly labeled with hazard information per regulatory standards. It is typically shipped as a hazardous material, requiring appropriate documentation and compliance with DOT, IATA, and IMDG regulations to ensure safe transport. |
| Storage | 2-Fluoro-5-iodobenzonitrile should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep separate from incompatible substances, particularly strong oxidizers. Properly label the storage container and ensure access is restricted to trained personnel. Use appropriate secondary containment to prevent leaks or spills. |
Applications of 2-Fluoro-5-Iodobenzonitrile in Industrial Manufacturing2-Fluoro-5-Iodobenzonitrile serves as a precision-engineered intermediate for advanced chemical synthesis in regulated pharmaceutical and fine chemical sectors. We supply this material strictly for downstream segments with established manufacturing processes and verifiable regulatory requirements. On this page, we present its principal industrial applications, including downstream industry standards, practical formulation ratios, critical process entry-points, and the end products manufactured by sector specialists. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) SynthesisThis aromatic halogenated nitrile acts as a key building block in the multi-step synthesis of several small molecule APIs, particularly in anti-inflammatory and oncological development pipelines. Its chemical structure enables regioselective transformations, which downstream processors apply during late-stage functionalization steps for API core modification. Our clients integrate this intermediate under tightly controlled cGMP environments with full traceability requirements. Industry compliance standards
Typical usage ratio
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2. Agrochemical Synthesis for Crop Protection AgentsThis compound enables modular synthesis of advanced agrochemical actives, such as selective herbicides and fungicide intermediates. Its dual halogenated and nitrile functionality provides synthetic leverage for structural diversification, offering downstream formulators access to key scaffolds used in modern crop protection chemistry. Manufacturer partnerships focus on scalability and process validation according to agricultural chemical control frameworks. Industry compliance standards
Typical usage ratio
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Final product types
3. Advanced Material Science: Liquid Crystal Monomer ManufactureDownstream processors in the liquid crystal and display sector employ this material for the synthesis of fluoro- and iodo-functionalized monomers essential for high-purity nematic and smectic liquid crystals. Precision in halogen content and trace impurity control is crucial, as final materials must deliver precise dielectric and alignment behavior in application-specific LC devices. Manufacturers implement stringent batch release certification with real-time analytical verification. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Synthesis: Specialty Dye IntermediatesManufacturers utilize this molecule as a core intermediate in the elaboration of functionalized aromatic systems leading to high-performance dyes for textiles, electronics, and imaging applications. Its substitution pattern enables tailored electronic effects in chromophore synthesis, with critical control at the nitrile and halogen sites for lightfastness and solubility modification. Downstream users emphasize traceability and sustained lot-to-lot quality through formalized QC documentation. Industry compliance standards
Typical usage ratio
Downstream process integration
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Years of hands-on chemical synthesis have taught us that small changes in molecular structure can create big differences in value for downstream users. In the case of 2-Fluoro-5-Iodobenzonitrile, every batch reflects both experience and direct engagement with the quirks of aromatic halogenation. We’ve learned not from manuals, but by reacting, analyzing, testing, and repeating the process until we reached consistency. Through this close work, we’ve realized the real demands customers place on intermediates like this one—not just in theory, but in their labs, on their production lines, and ultimately in their scale-up projects.
Every chemist working at the production line knows that combining fluorine and iodine atoms on a benzonitrile framework produces a substance with a distinct personality. 2-Fluoro-5-Iodobenzonitrile serves as more than a reagent; it represents the intersection of reactivity, selectivity, and product design shaped by years of feedback from pharmaceutical and material science partners. This molecule’s practical advantages emerge from the way it handles, the routes it opens, and the reliability batch after batch. It doesn’t just fill a spec sheet detail—it brings unique chemistry to the table.
Let’s talk about what makes this compound, with the structural formula C7H3FIN, stand out in actual practice. We manufacture it mainly as a pale, off-white crystalline solid under strict temperature and moisture controls. The melting point arrives within a well-defined range, and the product maintains stability when kept away from light and air. Over the years, our focus has always been on repeatable purity—ensuring each kilogram falls within narrow HPLC and GC analysis results, because we know inconsistent material can throw off multi-step syntheses downstream.
Producing this compound requires precision, especially during the installation of iodine at the 5-position. We learned early on that iodine placement affects not only the reactivity but also how other groups can be introduced later—no shortcut gets around the side-reactions when protocols are rushed. Our engineers refine these procedures to cut back undesired byproducts, and that translates directly to higher yields for partners running Suzuki or Sonogashira couplings. Balancing the fluorine and iodine substituents creates a reactive site at the 5-position, with fluorine at 2-position bringing a twist in electron density that opens doors for aromatic substitution or further functionalization.
Batch size depends on our reactor schedule, but quality controls never drop. NMR, mass spec, and elemental analysis remain standard, because quite a few clients validate every drum before moving into the next step. What they want from us isn’t just a chemical—they rely on batch-to-batch reproducibility, fast filtration, and reliable solubility in common organic solvents.
Our business partners use 2-Fluoro-5-Iodobenzonitrile as a key building block, mostly in pharmaceutical R&D, specialty chemicals, and agrochemical intermediates. One of the common threads in their feedback is how it enables direct access to complex molecular frameworks. The combination of cyano and halo groups turns this molecule into a switchboard, ready for further transformations through palladium-catalyzed cross-coupling, nucleophilic substitutions, or directed ortho-metalations.
Real production stories highlight the advantages. Take the process development teams racing to build new kinase inhibitors. They pick 2-Fluoro-5-Iodobenzonitrile for selective C-C or C-N bond formation rather than designing longer, multi-step routes. Time and again, research data shows that the halogen dance on this ring makes the difference—it saves synthetic steps, reduces overall waste, and cuts purification headaches.
Organic materials researchers have highlighted the value when tailoring new fluorinated aromatic scaffolds for advanced polymers, OLEDs, or liquid crystal materials. The distinct ortho-fluoro effect and strong leaving group at 5-iodo ensure clean, high-yield substitution chemistry, reducing the risk of impurity carryover downstream. Most users return because they see that careful selection of raw material quality shows up in final product performance, whether they’re working at bench or pilot scale.
Decades of experience in aromatic halide chemistry taught us the subtle difference between meeting spec and meeting real-world requirements. Handling 2-Fluoro-5-Iodobenzonitrile introduces challenges rarely covered in textbooks—particle size control, filtration speed, and safe storage practices. Years in the field revealed the need to refine crystallization techniques, limit residual solvents, and keep strict eye on trace metal analysis, because even small deviations can derail sensitive downstream reactions.
Not all benzonitrile derivatives behave alike in process environments. Some similar molecules react sluggishly or generate unwanted side products under coupling conditions. The unique substitution pattern of 2-Fluoro-5-Iodobenzonitrile eliminates many of these headaches, letting chemists reach target molecules using milder catalysts or lower temperatures. Our benchmarks show shorter reaction times and cleaner profiles compared to either non-fluorinated or non-iodinated isomers, and the difference becomes stark as processes scale beyond the lab.
Having spent years optimizing purification, our teams pay attention to practical concerns. Dust control, moisture prevention, and packaging design all make a tangible difference. Once, a customer called to say the ease of dissolving our product—and its lack of clumping—cut an hour off every prep run in their kilo lab. These kinds of details only emerge after hundreds of orders and plenty of direct feedback, and they keep us invested in incremental improvements.
Day-to-day, users judge us not only by nominal purity but also by invisible details: low residual solvent, absence of heavy metals, absence of uncommon isomers. Each batch report comes from our own QA/QC lab, staffed by technicians who trace, identify, and challenge any outlier well before shipment.
Market demand asks for technical transparency. Over the years, we chose to routinely disclose spectral data (NMR, IR, MS) and impurity profiles as standard, not special-request paperwork. Customers in pharma and electronics rely on these reports to validate performance and safeguard their own downstream processes—not just to tick off a regulatory box, but to keep operations smooth and safe.
Consistency from batch to batch encourages trust. Fine-tuning milling and drying parameters, enhancing inert gas packaging, and preventing sample cross-contamination become routine inside our facility. We insist on storing 2-Fluoro-5-Iodobenzonitrile in properly lined drums, always under nitrogen, never exposed to open air—all practiced from years of learning which protocols hold up best under all seasons and shipping routes.
Not every day in the plant goes smoothly. Fluorinated aromatics pose unique hurdles during isolation and work-up. Solvents bind, purities drift, yields fall. Sometimes the smallest change—switching a filter aid, tweaking the cooling rate—can make or break a campaign. Long ago, we overestimated the stability at ambient humidity, only to learn from a spoiled drum and an urgent customer call. That hard lesson cemented why real-world controls matter more than nice-sounding protocols.
In our experience, scaling up from gram to ton means more than just bumping numbers on the equipment spec sheet. Some intermediates demand extra care during transfer, dissolve-up, and crystallization steps. Our practice of continuous small-batch monitoring—rather than infrequent big-batch sampling—caught process drifts early, avoiding bigger losses. Years of improving this cycle-by-cycle taught us how to spot instability before it grows out of hand.
For any manufacturer, speed and predictability shape the rhythm on the floor. Teams plan shifts around known drying times, solvent recovery, and downtime for cleaning. By tuning raw material logistics and practicing just-in-time production, we keep delivery schedules in sync with partners who rely on punctuality. We believe the discipline shown in daily quality checks outweighs the cost of any missed shipment or off-spec drum, especially as partners scale their own production.
Longstanding relationships with R&D groups and pilot plant specialists deepen our appreciation for feedback. One specialty pharma group once flagged microcontaminants that, while present below regulatory thresholds, interfered with their late-stage coupling step. Our chemists reached out, ran side-by-side tests, and tweaked quenching and filtration to cut background signals on their end-product NMR—a fix that stuck across subsequent years and many kilos. This back-and-forth, built on trust and shared troubleshooting, matters far more than dry certificates. Real quality emerges through dialogue, not only inspection.
We’ve seen innovative material science groups push 2-Fluoro-5-Iodobenzonitrile into territory we hadn’t envisioned—tailoring their own ligands for metal-organic frameworks, modifying the benzonitrile for novel dye applications, even building up advanced lighting materials. These lessons trickle back into our own synthesis lines, encouraging us to keep reactant and impurity levels within even tighter bands. Open communication about tricky side-reactions or unexpected coloration during processing helps everyone evolve, from our plant managers to the scientists doing the final application testing.
Our laboratory keeps improving standards not just to meet spec, but to set benchmarks that invite these next-stage collaborations. The best ideas about improving shelf-life, batch homogeneity, and handling safety come from user stories, not only our internal meetings. We absorb and act on these stories, knowing that every improvement unlocks greater freedom for customers in developing new drugs, advanced polymers, and functional materials.
Anyone who’s worked with halogen-substituted aromatics knows that not all benzonitriles react the same in cross-coupling or substitution reactions. Take 2-Fluoro-5-Chlorobenzonitrile or 2-Fluoro-5-Bromobenzonitrile, for example. In field trials, the iodo variant consistently showed superior yields in Suzuki-Miyaura reactions and in routes requiring cleaner conversion with less recourse to harsh conditions. This comes down to iodine’s higher reactivity as a leaving group, particularly relevant in forming biaryls or attaching alkynes. Fluorine’s role further differentiates reactivity, channeling electronic effects that chemists value for specific transformation patterns.
Using a fluoro-chloro or fluoro-bromo version sometimes meant tougher reaction conditions or slower rates, leading to more side-products and complicated separations. In multistep syntheses, those downstream headaches can double the challenge. Years back, a customer switched from brominated to iodinated material and saw batch success rates jump, alongside fewer purification cycles and lower solvent consumption. Our own isolation steps, developed for the iodo derivative, help keep final product purities high, reducing the need for extensive scrubbing in customer labs.
Not all benzonitrile isomers provide the same flexibility in functional group incorporation. With the iodo group at 5 and fluro at 2, downstream users unlock pathways closed to other substitution patterns. This flexibility enables faster prototyping and shorter cycle times for innovative projects—an advantage we see reflected in reorder patterns from both pharma and advanced materials sectors.
Direct hands-on work with this product keeps sparking new ideas for reliability and efficiency. We’ve shifted from generic drums to lined, airtight containers that keep moisture out better during long transportation. Positive feedback from users about easy weighing and transfer motivates our operators to maintain that standard. We keep reviewing small details—like tweaking batch drying to keep particle flow loose and prevent clumping—which has cut down on dust during handling and sped up dissolving times for customers.
Site engineers rotate between plants and spend days at packaging stations to see how hands-on workers manage drum opening and resealing. Incorporating these observations, we’ve introduced safety and workflow refinements based on real-world use, far removed from abstract notions of “ease of use.” Small things—like print clarity on labels and grip texture on containers—come from honest feedback loops, which carry as much weight as input from synthetic chemists.
We also keep an eye on energy use, water handling, and greener reagents when improving our own process steps. Efforts focus on reducing chemical waste in the halogen exchange stage and capturing solvents for recycling. These moves matter for cost, plant safety, and regulatory compliance alike. Our team realizes this work never finishes, as each production run offers another chance for smarter, more efficient operations.
Reliability grows through error correction, not just smooth days. We log and review every customer’s feedback about off-odors, color shifts, delayed dissolution, or unexpected residue. Every problem report leads to a lab check, process review, and—if needed—a full trace back through synthesis steps. Years of practice make it clear that trust comes not from perfect stats, but from fast, honest, and thorough problem resolution.
Direct dialogue with end-users keeps process data fresh. We share root-cause analyses, corrective actions, and insights from pilot or scale-up setbacks, so that all partners know we aim for accountability as much as technical excellence. Sometimes our toughest critics end up our best collaborators, helping us rework bottlenecks that could have gone unnoticed by internal teams alone.
Experience remains our teacher. A generation back, aromatic halogenation felt like alchemy, with plant operators learning by feel as much as by notepad. Today, analytical instrumentation guides us, but human oversight fills the gaps. Changes in raw material supply or new analytical thresholds don’t catch us unprepared—regular reviews and stubborn attention to incremental improvement keep us positioned as a preferred supplier for those who rely on 2-Fluoro-5-Iodobenzonitrile for both their everyday routines and boldest innovations.
We keep looking for better routes, safer work-ups, and cleaner product delivery methods built on two decades of hands-on manufacturing. From small pilot drum experiments to full-scale tanker runs, each step builds on insights gathered from inside our doors and from direct customer conversations. Our chemists, engineers, and logistics teams see every order as a fresh challenge—a chance to show that commitment to real-world results remains as strong as ever.
Ultimately, 2-Fluoro-5-Iodobenzonitrile tells a story about how direct manufacturing experience, honest troubleshooting, and active dialogue can shape outcomes in labs, on plant floors, and across growing markets. As chemical makers and everyday process stewards, we know what it takes to meet the rigors of both the bench scientist and the scale-up manager. Trust, built batch by batch, drives every improvement. The cycle continues: feedback leads to tweaks, and tweaks lead to better results for everyone working with this uniquely versatile intermediate.