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HS Code |
308134 |
| Productname | 2-Fluoro-4-Iodoaniline |
| Casnumber | 29632-70-8 |
| Molecularformula | C6H5FIN |
| Molecularweight | 237.02 g/mol |
| Appearance | Light brown to beige solid |
| Meltingpoint | 46-49 °C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | Nc1ccc(I)cc1F |
| Inchi | InChI=1S/C6H5FIN/c7-4-1-2-5(9)6(8)3-4/h1-3H,9H2 |
As an accredited 2-Fluoro-4-Iodoaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with a screw cap, chemical hazard labeling, and printed product details including “2-Fluoro-4-Iodoaniline”. |
| Shipping | 2-Fluoro-4-Iodoaniline is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous chemical, following all safety and regulatory guidelines. Transport complies with local, national, and international regulations for hazardous materials to ensure safe delivery and prevent leaks, spills, or environmental contamination. |
| Storage | 2-Fluoro-4-iodoaniline should be stored 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 and acids. Use appropriate safety measures, including personal protective equipment, when handling. Label the container clearly and store in accordance with relevant chemical safety regulations. |
Applications of 2-Fluoro-4-Iodoaniline in Industrial Manufacturing2-Fluoro-4-Iodoaniline serves as a key halogenated aromatic intermediate for several demanding production sectors, offering precise reactivity in fine chemical synthesis. As a direct manufacturer, we support down-the-line producers with material that meets stringent benchmarks in each downstream environment. 1. Pharmaceutical Intermediate SynthesisAPI manufacturers select 2-Fluoro-4-Iodoaniline for advanced heterocyclic and aromatic amine coupling reactions during route development for kinase inhibitors, CNS actives, and certain targeted oncologics. The compound’s unique substitution pattern delivers regioselectivity vital for halogen-exchange or Suzuki–Miyaura cross-couplings under GMP-controlled environments. Material integration occurs at intermediate formation, especially for molecules where both fluorine and iodine substitution are strategic to enhance potency or metabolic stability. Developed batches undergo full traceability from input to in-process controls till the isolated crystalline intermediate stage. Industry compliance standards
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2. Agrochemical Building Block ManufacturingProducers in the crop protection sector utilize this raw material as a key halogen donor during the construction of fluorinated and iodinated phenylamine intermediates. Downstream synthesis leverages its dual halide activation for precision-stage introduction into specific herbicidal or fungicidal precursor molecules, predominantly in high-yield batch or continuous flow set-ups. Processing steps involve nucleophilic substitution and amide bond formation, supporting SAR (structure–activity relationship) optimization for new-generation agrochemicals. Industry compliance standards
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3. Dye and Pigment Precursor ProductionThe dyes and colorants industry adopts 2-Fluoro-4-Iodoaniline as an essential aromatic amine for the diazotization and coupling stages in specialty pigment synthesis, especially where high-purity halogenated substituents influence chromophore stability or shade. The material acts as a key starting block during azo-coupling for disperse and reactive dyes, as well as in direct sulfonation processes utilized for ionic organic pigments. Integration includes closed-system reactions under solvent and pH-controlled batch environments, monitored for residual byproducts and unreacted amines. Industry compliance standards
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4. Electronic Chemicals and OLED Material SynthesisProducers in advanced electronics leverage this compound for its reactive halogen profile in the construction of arylamine building blocks used in OLED emissive and hole transport layers. The unique positioning of fluorine and iodine enables stepwise integration into custom molecular platforms for fine-tuning device energy levels and thermal stability. Entry typically occurs at the aryl amination or direct C–N bond formation stage, using cross-coupling catalysis. Material quality must meet electronics-grade standards, with intensive QC for trace metals, anion contaminants, and batch reproducibility. Industry compliance standards
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5. Custom Fine Chemical Synthesis for Research and DevelopmentContract research and custom synthesis organizations use 2-Fluoro-4-Iodoaniline as a structural motif for building complex molecules during medicinal chemistry campaigns, materials development, and analytical method standards. Material enters at strategic bond-formation steps, supporting both library expansion and scale-up pilot studies. Documentation follows full batch genealogy, including CoA and residual solvent analysis. Use spans across gram-to-multikilogram scale depending on development stage and downstream analytic requirements. Industry compliance standards
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In our sites, the batch vessels see a steady demand for precision compounds, and 2-Fluoro-4-Iodoaniline regularly comes up in requests from R&D labs and production chemists looking to push new frontiers in pharmaceuticals, agrochemicals, and specialty materials. The molecular formula, C6H5FIN, and CAS number 29632-74-4, sit on many synthesis routes, opening doors to complex molecules that straight-line analogues simply can’t. Over the years, we’ve witnessed shifts in what chemists are after—subtle changes in functional groups keep advancing the field, and this compound’s fluoro and iodo substitution offers advantages hard to get from more conventional anilines.
Chemists often compare the performance, reactivity, and final yield imparted by ring-substituted anilines for cross-coupling reactions. The 2-fluoro and 4-iodo substitution pattern offers a unique profile: the electron-withdrawing fluorine at the ortho position nudges reactivity on the aromatic ring, while the para iodine provides a versatile handle for Suzuki, Buchwald-Hartwig, and Sonogashira couplings. Instead of stepping through risky multi-step halogenation in-lab, our clients seek this product to shorten development cycles and cut sources of error. In fact, several teams come back with the same observation: using this intermediate streamlines their workups and shores up process robustness—with the added benefit of cleaner analytical purity downstream.
We deliver 2-Fluoro-4-Iodoaniline to >98% GC purity as standard. This wasn’t arrived at by market consensus or data sheet recommendations but distilled over years collaborating with process chemists, regulatory consultants, and analytical heads. Material with visible off-colors, extra residual base, or broad melting ranges usually signals trouble. A clear, nearly-white crystalline product means less doubt at each process stage and easier isolation of final targets. Our tests monitor impurity profiles: we watch for difluoro, diiodo, and other cross-contamination, as well as low-level moisture and volatile organics, because we know how a bad impurity profile can blow up a well-thought-out route. Each run gets analyzed by NMR, HPLC, GC-MS, and titration to ensure that what lands on our customers’ benches won’t derail their workups.
We started producing substituted anilines a decade ago with a small batch reactor and have since scaled up through pilot reactors to full production vats. Each step of that scale-up process taught us about thermal management, fine control of halogenation, and thorough purification. Not every lot yields the same—temperature spikes or distillation hiccups show up in the final numbers. We rely on stable supply chains for high-purity starting materials, tracing each drum of raw aniline and reagent. Cross-contamination in valves or residue from previous campaigns can introduce wildcards into purity, so our operators run dedicated lines or intensive cleaning cycles. By handling each shipment ourselves and keeping lines direct from our reactors to our customers, we have seen fewer customer complaints, less uncertainty in repeat orders, and a reputation for reliability that stacks up against anybody in the field.
Aromatic halides follow predictable patterns, but adding a fluorine at the ortho and an iodine at the para makes this aniline sparkle for cross-coupling reactions. Medicinal chemistry teams have told us about their frustration with meta- or ortho-substituted analogs that failed in late-stage route design due to unpredictable reactivity. The electron-withdrawing pull from the 2-fluoro improves selectivity, especially in palladium-catalyzed reactions when aiming for mono-functionalization. The para-iodo group stands apart as the most reactive handle for oxidative addition, giving higher yields in coupling chemistry without resorting to harsh conditions seen with bromo or less reactive chloro anilines. Researchers use this molecule in creating heterocyclic frameworks, protected amine intermediates, and even as a basis for radiolabeling probes.
Many customers arrive at our doorstep after toying with monofluoro- or monoiodoanilines, or even bromine-substituted structures, and hoping to access similar reactivity cheaply. Experience shows that simple ring substitutions cannot always substitute for the specific performance offered by the 2-fluoro-4-iodo arrangement. The ortho fluorine acts not only as an electronic modulator but can influence sterics in neighboring reactions, guiding selectivity in ways neither a second iodine nor a meta or para-halogen could. The iodine, comfortable for palladium to access in catalysis, outperforms bromine or chlorine, which often stall or cause harsh reaction mixtures. As a result, efficiency climbs and waste drops off—a point that always lands with cost-minded or scale-up-focused process engineers.
For every batch, we sample at the end of synthesis, after purification, and again before packaging. Unlike high-turnover traders or contract packagers, we keep accountability at every stage—records trace from reagent intake to finished kilogram drums sent for filling. Small impurities like residual phosphorus or trace heavy metals, if allowed to accumulate, have caused serious headaches in downstream hydrogenations and oxidations, as our customers freely report. Our in-house analysts prioritize customer-reported pain points, scrutinizing not only total halide counts and melting point ranges but also spectral fingerprinting for early warning signs of isomerization or unintended cross-coupling products. Every deviation gets logged for process adjustments, rather than being written off as a “market tolerance.”
2-Fluoro-4-Iodoaniline is much more stable than some of its nitro- or polyhalogenated relatives, but careful packaging matters. This compound holds up best in amber glass or lined steel, protected from light and humidity, particularly for long storage or international transit. We’ve encountered occasional challenges with glass etching or condensation if packaging is neglected, so we monitor microclimate indicators in our warehouses and have shifted to vacuum-sealed liners for larger shipments. Waste reduction hits the bottom line: customers who get consistently dry, free-flowing product don’t need to run it through drying ovens or additional purification, which not only saves time but minimizes product loss.
Shortcuts in sourcing either base aniline or key halogenating agents can upend an entire production campaign, not just by lowering yield but by introducing trace contaminants that linger through all purification steps. Our approach stays rooted in relationships with vetted, regularly audited suppliers—from the producer of fluoro intermediates in East Asia, to the iodine supply out of Chile—which reduces batch-to-batch risk. With direct oversight, we avoid the speculative sourcing that plagues non-manufacturer traders and deliver on schedule with documentation tracking every chain of custody.
Having worked through countless scale-up consultations, pilot plant trials, and custom concentration requests, we offer more than bulk delivery. Technical support is driven by the real-life challenges our partners report: need to hit a tighter melting point, lower trace halides, or push for a solution that avoids certain solvents, we troubleshoot directly with researchers and process development chemists. Experience growing from gram-scale lots into multi-ton campaigns means we can spot scale-up bottlenecks before they hit larger budgets and timelines. Our records on solvent recovery, batch yields by temperature profile, and risk flags from previous runs help customers accelerate their process validation and tech transfer.
New product introductions often bring up questions on residue, hazardous waste, and REACH or TSCA status. We prepare 2-Fluoro-4-Iodoaniline in compliance with all relevant national and international environmental regulations, and our internal waste handling keeps discharge and exposure risks low. Years of experience have shaped our systems for effluent filtration, halogen recovery, and off-gas scrubbing, keeping us ahead of regulatory changes and community expectations. By working with chemists and environmental officers, we continually improve capture rates and reduce lifecycle footprint—a smart approach for customers aiming for green chemistry targets or who need RoHS- or SVHC-compliant materials.
Consistent customers, especially in Europe and North America, point to avoided rework and reject rates as a key cost saving. Each kg produced with tight purity, stable melting point, and no off-odor translates to smoother downstream campaigns. Comparing marginal cost with higher-priced specialty intermediates reveals that up-front investment in direct-from-source product brings return through labor, solvent, and waste reduction, especially at semi-bulk scale. We remain mindful of fluctuating raw material pricing, and plan production to smooth out volatility for end-users.
It’s common for chemists in pharmaceutical R&D to report how hard it is to source stable, clean, and responsive aromatic amines for their screening panels. The first-run discovery work often grinds to a halt when impure intermediates clog up columns or introduce new, poorly-characterized byproducts. By keeping purity high and batches consistent, we support end-users in prepping discovery lots quickly, with less risk of project delays or lengthy troubleshooting. Our operators and technical support hear weekly about project milestones accelerated by effective building block supply. Supporting these successes, rather than mere sales volume, has built lasting partnerships.
Anilines, especially those with heavy halogenation, have earned a reputation for requiring care in storage and handling. We provide user guidance drawn from decades of incident reporting, not generic data sheet precautions. Operators running pilot campaigns in enclosed or low-ventilation areas need to avoid inhaling dust; contact with bare skin can lead to irritation. Most of our long-term users already have established PPE and ventilation protocols, but early-stage labs sometimes neglect these basics—so our instructions highlight real-field pitfalls, such as static buildup or drip leaks, that come with bulk transfers or intensive use. Taking care at the user end prevents lost batches, extended clean-up, and safety incidents.
Our quality system benefits directly from user feedback across markets and application areas. Synthetic chemists, formulation heads, and process engineers routinely share observations on ease of handling, reaction profile, and any red flags that emerge at scale. This feedback stream feeds into annual improvement projects, enhancing yield, process safety, and packaging design. Every revised batch protocol addresses at least one field-raised concern—often even borrowed by other teams across our facilities. We attend industry workshops and user group forums, moving beyond laboratory theory to focus on actionable best practices shared between real production operators, not just sales or marketing staff.
Outsourced re-packagers and commodity traders have no direct lens into real production realities. As direct manufacturers, we know every vessel, each filtration step, and the ins-and-outs of our analytical signatures. This connection to process builds flexibility: custom lots, new packaging, or client-compliant material can be handled quickly—no waiting for third-party approvals or slipping lead times. Because we see the full journey from plan to shipment, every customer order receives the same level of control, and repeat customers develop confidence in future-facing partnerships. Word-of-mouth carries more weight than flashy brochures or catalog promises, and our greatest marketing is the error-free shipments partners rely on.
Emerging demands in medicinal chemistry, specialty polymers, and novel catalysts are pulling forward a new generation of fluorinated and iodinated intermediates. Our experience with 2-Fluoro-4-Iodoaniline production sets the foundation for rapid adaptation to next-generation derivatives and compositions. Customers’ ambition to move from milligram-scale test reactions to long-running multi-ton campaigns gives us clear guidance on where to optimize next—be that in process safety, in raw material availability or in distribution reliability. Open lines to our customer base keep us nimble and rooted in practical chemistry, not just theoretical aspirations.
Those who depend on high-quality intermediates find reassurance in the direct relationship a manufacturer provides. We keep operations transparent, prioritize constant improvement, and follow every lot from its raw material origins through to final shipment. 2-Fluoro-4-Iodoaniline stands as a signature product in this approach, allowing advanced chemistry teams to innovate rapidly and confidently, without distraction or surprises from unreliable source material. Our mission remains to keep every batch as good or better than the last, supporting the growth and achievement of our partners across synthesis, scale-up, and final product launch.