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HS Code |
578373 |
| Chemical Name | 1-Fluoro-4-Iodobenzene |
| Molecular Formula | C6H4FI |
| Molecular Weight | 237.00 g/mol |
| Cas Number | 352-22-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 196-198°C |
| Melting Point | 10-12°C |
| Density | 1.916 g/cm3 |
| Refractive Index | 1.607 |
| Synonyms | p-Fluoroiodobenzene; 4-Fluoroiodobenzene |
| Flash Point | 81°C |
| Solubility | Insoluble in water |
| Smiles | Ic1ccc(cc1)F |
| Inchi | InChI=1S/C6H4FI/c7-5-1-3-6(8)4-2-5/h1-4H |
As an accredited 1-Fluoro-4-Iodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 1-Fluoro-4-Iodobenzene; labeled with chemical name, CAS number, hazard pictograms, and safety warnings. |
| Shipping | 1-Fluoro-4-iodobenzene is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous material, following all relevant chemical regulations. The package is clearly labeled with hazard warnings, and transportation is arranged via approved carriers specializing in chemical substances to ensure safe, compliant delivery. |
| Storage | Store **1-Fluoro-4-iodobenzene** in a tightly sealed container under a dry, inert atmosphere (such as nitrogen or argon) away from moisture, heat, and light. Keep it in a cool, well-ventilated area, separated from incompatible substances like strong oxidizers. Use secondary containment to prevent leaks or spills, and label the storage area clearly for hazardous organic chemicals. |
Applications of 1-Fluoro-4-Iodobenzene in Industrial Manufacturing1-Fluoro-4-Iodobenzene acts as a key building block for multiple industries operating across fine chemistry, pharmaceuticals, agricultural science, and specialty polymers. The following industrial segments integrate this raw material for specific downstream synthesis, process optimization, and end-product manufacture. All details below reflect real production use-cases and compliance environments as encountered by major global producers. 1. Pharmaceutical Intermediate SynthesisMajor pharmaceutical manufacturers use 1-Fluoro-4-Iodobenzene for cross-coupling reactions such as Suzuki, Buchwald-Hartwig, and other metal-catalyzed routes in active pharmaceutical ingredient (API) development. As a halogenated benzene, it provides a functional aromatic scaffold for targeted modifications in the synthesis of novel anti-cancer agents and CNS modulators. Its high reactivity and selectivity enable late-stage diversification needed for complex molecule assembly. Our plant batches meet strict batch-to-batch reproducibility and impurity thresholds as specified by international regulatory filings. Industry compliance standards
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2. Agrochemical Active ProductionLeading agrochemical companies deploy 1-Fluoro-4-Iodobenzene in the synthesis of advanced herbicides, fungicides, and insecticides targeting resistant species. The intermediate introduces controlled fluorine and iodine substitution patterns that improve target binding affinity and metabolic stability. Our plant ensures high-purity lots, supporting applications where even trace impurities can alter agrochemical toxicity or degrade field performance. Quality tracking aligns to downstream tox batch records and EPA registration protocols. Industry compliance standards
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3. Electronic Chemical PrecursorsManufacturers in the electronic and display materials sector employ 1-Fluoro-4-Iodobenzene to build high-purity aryl intermediates for OLED and advanced liquid crystal displays. The raw material's unique halogenated substitution supports desired charge-transport and stability properties in custom aromatic monomers, which are further polymerized for thin-film electronic applications. Material consistency meets strict trace-metal and ionic contaminant limits as required by device-grade specifications. Industry compliance standards
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4. Specialty Dye and Pigment IntermediatesProducers of high-end dyes and electronic pigments integrate 1-Fluoro-4-Iodobenzene into arylamine and azide-based coupling schemes for the fabrication of colorants with tailored optical and chemical resistance profiles. The dual halogen structure allows developers to precisely control chromophore substitution patterns, improving fastness and compatibility with polymer matrices in specialty applications such as security inks, photoresistors, and fiber coloration. Our output conforms to sectoral purity and traceability standards required for regulatory disclosure and user safety. Industry compliance standards
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5. Chemical Research and Custom Synthesis LabsContract development and innovation labs routinely select 1-Fluoro-4-Iodobenzene as a precursor for small-scale custom syntheses supporting med-chem pipelines and fine-chemical exploration. The compound’s structural attributes assist in the structural-activity relationship (SAR) studies, providing predictable reactivity in exploratory arylation and halide-exchange protocols. Rigorous small-lot QC is performed for accurate analytical referencing and repeat research output. Industry compliance standards
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In the fields of pharmaceutical research, agrochemical development, and advanced material science, 1-Fluoro-4-Iodobenzene stands out as a highly sought-after halogenated aromatic compound. As manufacturers, we’ve produced this molecule at industrial scale for over a decade, refining our processes to meet the rigorous benchmarks that custom synthesis labs demand. Chemists worldwide have increased their demand for 1-Fluoro-4-Iodobenzene due to its role as a key intermediate where both fluorine and iodine substitution provide powerful handles for further transformations. The molecule’s structural formula, C6H4FI, consists of a fluorine atom and an iodine atom bound to the para positions of a benzene ring, making it a versatile substrate for a variety of downstream reactions.
Our production leverages batch synthesis with careful temperature and pressure controls, resulting in a product that consistently exceeds 99% purity, confirmed by GC and NMR. Quality control checks each batch for residual starting materials, moisture content, and trace impurities like dibromobenzene or difluorobenzene, which can alter reactivity in sensitive coupling reactions. Over many years, our technical staff has learned the nuances in distillation and crystallization steps that help minimize side-products and yield a crystalline product with excellent handling properties.
In organic synthesis, the para arrangement of fluorine and iodine on the ring is not just a point of curiosity but the driving force behind the compound’s popularity. The iodine atom, with its large size and reactive bond, enables direct installation of new functional groups using well-known methods like Suzuki, Sonogashira, and Heck couplings. At the same time, the fluorine atom imparts electron-withdrawing character, tuning the ring for selectivity in electrophilic aromatic substitution and cross-coupling chemistry. Chemists often need a molecule that offers both a reactive iodine for palladium catalysis and a resilient fluorine that can survive harsh conditions for subsequent transformations. Few compounds deliver both these features in such a concise package.
Our partners in pharmaceutical R&D have explained just how much a consistent, reliable batch of 1-Fluoro-4-Iodobenzene saves them wasted time. A small impurity profile or unexpected isomer content can derail months of research during route optimization. Sourcing from the original manufacturer means avoiding the pitfalls sometimes encountered with repackaged or relabeled material, where contamination or residual solvent content can fluctuate. Several academic teams reported that some off-spec batches from resellers changed their yields by 20% or more compared to our direct shipments. We routinely provide COAs with every lot, including actual HPLC and GC traces, to give process chemists peace of mind during their scale-up work.
1-Fluoro-4-Iodobenzene fills a unique spot in the toolbox of synthetic chemists, fueling the development of drug candidates, crop protection agents, and organic electronic materials. Medicinal chemists use it as a critical intermediate while designing potential anticancer agents, kinase inhibitors, and CNS-active molecules. The fluorine atom modifies metabolic stability and pharmacokinetics, while the iodine atom enables rapid diversification via cross-coupling with boronic acids or alkynes. Our direct customers have published structures containing this building block in patent applications for new APIs and high-performance OLED materials.
Fluorinated aromatics also turn up in active agrochemicals due to their environmentally favorable degradation profiles and powerful pest resistance properties. Researchers in crop protection appreciate that precise substitution reduces off-target activity. While fluorination generally brings metabolic stability, para-iodination allows for strategic late-stage modification, letting teams create libraries of compounds for biological testing. In the specialty polymer field, 1-Fluoro-4-Iodobenzene can serve as a monomer precursor for advanced polymers with tuned dielectric and thermal properties, responding to industry demand for lighter, more robust electronics.
Experience has taught our team that handling conditions can play a defining role in the long-term storage and reactivity of halogenated aromatics. To guard against trace hydrolysis and to prevent gradual decomposition, we use moisture-tight, amber glass bottles with PTFE-lined caps, and offer custom kilo-scale packaging in stainless drums for pilot plant or commercial runs. Our protocol includes nitrogen blanket purging and cold storage where needed; thorough documentation prevents mishaps that cost time and money in a high-throughput laboratory or production plant. Our support doesn’t stop at the point of sale—chemists can call us directly to troubleshoot storage or process questions, saving valuable time as challenges arise. No batch leaves our facility without a fresh QA run and an updated analysis report.
In our daily work, we hear comparisons between 1-Fluoro-4-Iodobenzene and other halogenated benzenes—namely 4-Fluorobromobenzene and 4-Fluorochlorobenzene. The difference between these molecules ties back to both their reactivity and their suitability for specific coupling reactions. The iodine substituent in 1-Fluoro-4-Iodobenzene reacts most rapidly in Pd-catalyzed coupling, outpacing bromide and chloride analogs thanks to its lower bond dissociation energy. This is invaluable for researchers aiming to append a broad range of aryl or alkynyl units without harsh reaction conditions.
Bromo- and chloro-derivatives often respond sluggishly or require additional ligands or catalysts, raising both cost and complexity. The selectivity profile is also enhanced with the fluoro/iodo combination, since some methods risk overreacting less-selective bromo- or chloro-derivatives. As a result, using 1-Fluoro-4-Iodobenzene can cut down on byproducts, lower catalyst usage, and provide access to substitution patterns not affordable through single-halide routes. We’ve seen multinational pharmaceuticals switch to our iodofluorobenzene even for existing projects to simplify their process chemistry.
The preparation of 1-Fluoro-4-Iodobenzene isn’t without its hurdles. Sourcing high-purity fluorinated benzene and ensuring regioselectivity in subsequent iodination takes careful process control. Over the years, our team developed a proprietary route that skips over the typical tin-mediated halogen exchange, avoiding heavy metal residues that slow the downstream work-up and create persistent waste. Selecting the right catalyst and optimizing the anhydrous conditions have increased our yields while making waste treatment more straightforward for our site’s environmental engineers.
Our experience also covers the logistics of hazardous goods transport, including temperature-controlled shipping and regulatory compliance for both air and sea freight. We invest in continuous staff training on UN packaging codes and track each shipment to prevent exposure to sunlight or accidental contamination. Working closely with customs and import teams across multiple jurisdictions provides consistent delivery times and reduces customer delays. Hundreds of tons of halogenated aromatics cross borders every year, and keeping that flow steady calls not just for paperwork but for reliable communication from plant to loading dock to lab bench.
Organic halides often face scrutiny for environmental impact and safety. Our plant holds certifications for emissions management, with scrubbers and solvent recovery units tailored to the chemistries of aromatic halogenation. Every production cycle is closely monitored; waste streams go directly for reclamation or, where needed, incineration under conditions that meet or exceed national guidelines. We track safety incidents meticulously, working with local authorities and industry groups to share best practices and enhance worker protection. Years without lost-time incidents speak to this commitment.
The pathway to greener chemistry isn’t always simple in industrial halides. We continue to refine our catalysts, aiming for further reductions in metal load and improved atom economy. Internal R&D collaborates directly with academic partners to pilot electrochemical methods and photochemical halogenation as alternatives to legacy syntheses. Responsible sourcing policies exclude suppliers with poor environmental track records; robust supplier audits drive both compliance and transparency through our supply chain.
Learning directly from customer problems has shaped our troubleshooting support and product design. A process chemist in Boston once faced low yields due to trace potassium still present from a previous synthetic step—our technical advisor diagnosed the impurity by LC-MS and provided handling guidelines for improved washing and solvent swap. Over the years, custom packaging based on feedback has cut losses from perished material. Interactions with end-users guide us to supply the size, packaging type, and documentation needed for seamless project onboarding and regulatory submission.
Our laboratories remain accessible for contract analytical services: teams can request NMR, purity analysis, and impurity identification, especially for validation runs or method transfer projects. Engineer-to-engineer conversations speed up method development, reducing time to market or regulatory approval. Beyond simply shipping a product, we provide real, ongoing partnership for every downstream project.
As markets shift and regulatory standards evolve, demand rises for specialty grades and customized derivatives. Our site now regularly responds to requests for isotopically labeled or high-stability versions of 1-Fluoro-4-Iodobenzene, including deuterated and 13C-labeled forms for advanced metabolic studies. Flexible production in smaller reactors lets us deliver these tailored compounds on short notice without tying up major batch capacity reserved for multi-ton orders.
Continuous feedback sparks innovation. It’s not unusual for process chemists to call asking for help in selecting an optimal halogen pattern for late-stage diversification. Our in-house synthetic experts walk through published literature, discuss reaction profiles, and recommend the best building block. It’s rewarding to see a one-off suggestion turn into the foundation for an improved, patentable pharmaceutical or a next-generation electronics material.
Serving a global customer base calls for flexibility and responsiveness. We have learned to manage both bulk orders for multinational companies and packed shipments for small research labs, all of which benefit from direct sourcing. We frequently work with shipping partners to pre-clear product through customs, anticipate regional compliance regulations, and provide the supporting technical data sets specific to market requirements. Our years-long relationships with customers allow us to problem-solve side-by-side, reducing their risk and optimizing their return on investment.
Supplying 1-Fluoro-4-Iodobenzene places us at the intersection of chemistry, safety, and industrial logistics. Familiarity with every production variable—whether it’s starting material quality, iodination parameters, or packaging integrity—helps us guarantee a product that not only meets published specifications but truly streamlines process chemistry at scale. Our role extends beyond simple manufacturing; it means taking full responsibility for consistency, documentation, and technical support, so that researchers can focus on innovation, not remediation.
Continuous improvement keeps us agile as new scientific challenges emerge. By investing in process upgrades, environmental compliance, and technical support, we reinforce our commitment to reliability and partnership in chemical manufacturing. Direct experience with every detail of 1-Fluoro-4-Iodobenzene means we can achieve the rare combination of flexibility, quality, and supply chain security—all of which matter daily to those at the front lines of discovery.