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4-Iodoaniline

    • Product Name 4-Iodoaniline
    • Alias para-Iodoaniline
    • Einecs 219-028-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    391021

    Name 4-Iodoaniline
    Cas Number 106-47-8
    Molecular Formula C6H6IN
    Molecular Weight 219.03 g/mol
    Appearance Light tan to brown crystalline powder
    Melting Point 154-158 °C
    Boiling Point 283 °C
    Density 2.045 g/cm³
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Synonyms p-Iodoaniline, 1-Amino-4-iodobenzene
    Storage Temperature Room temperature
    Smiles Ic1ccc(cc1)N
    Inchi InChI=1S/C6H6IN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2

    As an accredited 4-Iodoaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Iodoaniline is packaged in a sealed amber glass bottle, labeled clearly, containing 25 grams of fine, off-white powder.
    Shipping 4-Iodoaniline is shipped in tightly sealed containers, protected from moisture and light, and labeled according to hazardous material regulations. It is transported as a hazardous chemical, requiring appropriate safety documentation and compliance with international shipping standards to ensure safe handling and prevent exposure during transit.
    Storage 4-Iodoaniline should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, strong oxidizing agents, and direct sunlight. It should be clearly labeled and kept away from incompatible chemicals. Storage areas must be equipped with spill containment and appropriate safety equipment. Use only in a fume hood to avoid inhalation exposure.
    Application of 4-Iodoaniline

    Applications of 4-Iodoaniline in Industrial Manufacturing

    We provide 4-Iodoaniline to high-precision industries that require strict control over impurity profiles and batch consistency. Our product supports advanced manufacturing in pharmaceuticals, agrochemical synthesis, dye intermediates, and specialty polymers, meeting rigorous downstream specifications and compliance requirements across each sector.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Esteemed pharmaceutical manufacturers frequently employ 4-Iodoaniline in the synthesis of targeted heterocyclic and aromatic compounds. It serves as a reliable halogenated aniline precursor in coupling reactions during small-molecule API development, where trace-level impurities and isomeric purity directly impact downstream pharmacological attributes. Its critical role spans the preparation of antithyroid, anticancer, and certain psychiatric drug intermediates, wherein strict regulatory compliance and cGMP process control dictate all stages of procurement and handling.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <921> for Reagents
    • European Pharmacopoeia (Ph. Eur.) guidance for pharmaceutical intermediates
    • FDA 21 CFR Part 210/211

    Typical usage ratio

    • Usually 0.2–2.5 molar equivalents relative to key cyclization or coupling reactants; the molar ratio depends on the specific synthetic route, with tighter ranges (0.8–1.1 eq.) used in direct arylation protocols

    Downstream process integration

    • Introduced after initial ring substrate pre-modification as the primary nucleophilic coupling agent in Buchwald–Hartwig and Ullmann-type amination processes under inert, contamination-controlled synthesis vessels with QC traceability

    Final product types

    • Active pharmaceutical ingredients for generic and innovator drugs, including benzothiazole-based antithyroid APIs (e.g., methimazole derivatives), select antipsychotics, and oncology intermediates

    2. Agrochemical Synthesis for Herbicide and Pesticide Development

    Commercial agrochemical producers utilize 4-Iodoaniline as a core building block to construct selective aromatic and heterocyclic rings, especially in triazine and benzimidazole-based pesticide actives. Its halogen functionality enables the introduction of performance-enhancing substituents, which directly modulate field stability and biological selectivity. Stringent trace impurity thresholds during upstream and downstream processing assure that no residual byproducts compromise environmental safety or crop residue tolerances.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • ISO 9001:2015 Quality Management System for agrochemical active production
    • OECD Guidelines for Testing of Chemicals
    • REACH Regulation (EC) No 1907/2006 (European Union)

    Typical usage ratio

    • Applied at 0.5–1.5 molar equivalents as a nucleophile or electrophile, depending on substitution stage within multi-step herbicide or fungicide synthesis

    Downstream process integration

    • Added post-chlorination or nitration of aromatic ring substrates in closed-loop synthesis lines, performing as a selective precursor for site-specific iodination or further amine-functionalization within reaction cascades

    Final product types

    • Benzimidazole and triazine herbicide actives, systemic fungicides, and active pesticide ingredients for crop protection formulations

    3. Dye and Pigment Intermediate for Specialty Colorant Manufacture

    Producers supplying high-performance dyes and pigment dispersions incorporate 4-Iodoaniline into their synthetic routes to achieve precise molecular modifications for the electronics, textile, and specialty ink industries. Its introduction of an iodine functional group into aromatic systems facilitates formation of aza dyes, metal complexation dyes, and advanced colorfast pigments. Accurate feed ratio and strict handling mitigate off-tone byproducts, essential for reproducibility in colour-critical applications.

    Industry compliance standards

    • OEKO-TEX® STANDARD 100
    • EN 71-3:2019 Safety of Toys—Migration of certain elements
    • ISO 9001:2015 for pigment and dye chemical processing
    • EU REACH Annex XVII—restrictions on azo colorants

    Typical usage ratio

    • Used at 1.0–1.3 molar equivalents versus polyaromatic precursor substrates in key colorant-forming steps; fine-tuned by the chromophore target and depth of shade required

    Downstream process integration

    • Incorporated during the diazotization or oxidative coupling stages where halogenation of aniline units determines final pigment structure; performed in batch or continuous stirred reactor systems with monitored effluent control

    Final product types

    • High-purity azo dyes, metal-complex dyes for inkjet printers, photoreactive pigments for photographic films, and durable textile dispersions

    4. Specialty Polymer Synthesis for Advanced Material Applications

    Producers of advanced specialty polymers select 4-Iodoaniline to introduce targeted amino and halogen functionalities into polymerizable units, facilitating the production of high-performance resins and engineering plastics. Its role in step-growth polymerization and cross-coupling chemistry supports the development of materials with elevated thermal stability, flame-retardancy, or electronic properties, serving industries such as aerospace, electronics, and high-performance coatings where monomer purity critically controls polymer attributes.

    Industry compliance standards

    • ISO 14001 for Environmental Management in polymer manufacture
    • UL 94 Flammability Standard for plastic materials
    • RoHS Directive 2011/65/EU for restricted substances in electrical/electronic polymers
    • REACH Regulation Annex VII for polymeric precursors

    Typical usage ratio

    • Typically 0.3–0.8 molar equivalents per core monomer unit, depending on the crosslinking and target molecular weight of the end-use resin

    Downstream process integration

    • Introduced in early oligomerization stages for step-growth polymerization or as a co-monomer in Suzuki or Sonogashira coupling during the backbone assembly in solvent-intensive reactor systems; attention given to halogen retention and end-group purity

    Final product types

    • Flame-retardant engineering plastics, specialty polyamides, functionalized polyarylenes for electronics, and advanced coating resins used in aerospace and microelectronics
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    Certification & Compliance
    More Introduction

    Understanding 4-Iodoaniline: From Synthesis to Industrial Value

    From Chemical Bench to Industrial Scale: Our Perspective on 4-Iodoaniline

    Producing 4-iodoaniline at scale has taught our team the value of precision and consistency. Behind every kilogram lies a string of exacting standards, thorough isolation, and relentless quality checks. The molecule itself, C6H6IN, stands apart in its niche, joining the ranks of iodo-substituted aromatics that serve as critical building blocks in many industries. Our process starts with aniline as the core, followed by highly controlled iodination steps to ensure the para-isomer dominates the final product. Over years of refinement, we have fine-tuned yield and purity by optimizing reagents, temperature controls, and isolation techniques.

    Every lot of 4-iodoaniline that leaves our facility targets a minimum purity of 99%, with melting points in the range of 155–158°C. We routinely check for residual metals, halogens, and unreacted aniline through both HPLC and GC analysis, striving for levels well below industry tolerances. Particle size matters little for most downstream uses, given the compound's main function as a precursor, not an end-use product. Moisture levels are kept low to prevent aggregation and degradation, something our synthesis team monitors closely in both storage and shipping environments.

    Why 4-Iodoaniline Matters for Progress

    At its core, 4-iodoaniline serves an enabling role in the world of chemical synthesis. Research labs and manufacturing lines use this compound as a springboard for structural transformations. Human health infrastructure depends on its reliable availability, as the compound sites itself at the junction where basic chemical feedstocks become tailored pharmaceuticals and agrochemicals.

    Synthetic chemists have long turned to 4-iodoaniline for the construction of more complex molecules through palladium-catalyzed couplings such as Suzuki-Miyaura and Buchwald-Hartwig aminations. These methods breathe new life into aromatic chemistry, letting users bolt on everything from simple alkyl chains to intricate heterocycles. Because iodine's leaving group properties far exceed those of bromine, and even more so compared to chlorine, those working with 4-iodoaniline often report faster reaction rates and cleaner conversions.

    We have supplied this compound to research teams developing candidate anti-cancer compounds, as well as agricultural chemists designing herbicide scaffolds. The para orientation of the amino group on the aromatic ring reduces side reactions compared to ortho or meta substituted analogs, making downstream transformations more predictable. In certain diagnostic imaging protocols, 4-iodoaniline derivatives play a supporting role, attaching radiolabels via the available iodine for PET scans or related analytical tools.

    Practical Differences Between 4-Iodoaniline and Other Haloanilines

    Not all aniline derivatives behave the same way, despite similar names. Substituting chlorine or bromine for iodine in the para position makes a striking difference in reactivity and in the cost structure. Iodine's ability to leave the aromatic system under mild conditions makes 4-iodoaniline a versatile partner in cross-coupling reactions. Coupling steps proceed under lower activation energies—something we confirm in our clients’ feedback, where switchovers from p-bromoaniline to p-iodoaniline often halve reaction times or raise isolated yields.

    On the price side, raw iodine runs higher than bromine or chlorine, so the initial product cost sits above those analogs. Yet, improved conversion rates and selectivity end up saving time and reducing the complexity of downstream purification. Certain clients with high-volume processes still pick bromo- or chloro- derivatives for bulk intermediates, but those looking for maximum reactivity shift to 4-iodoaniline even at a premium. We regularly discuss these tradeoffs with customers who need cuts in cycle time or want new chemistries beyond what standard halides allow.

    On the safety end, 4-iodoaniline requires careful handling, as with other aromatic amines. Its higher molecular weight lets it pack less vapor tension compared to lighter halo-anilines, but the fundamental risks of exposure—skin absorption and inhalation—still demand gloves, masks, and containment protocols throughout handling and formulation. We maintain stringent air quality in our production suites, and our operators have medical check-ups tailored to the aromatic amine hazard profile.

    Building Trust with Transparency and Field Experience

    Customers from biotechnology, fine chemical, and pharmaceutical sectors want more than a certificate of analysis. They visit our site, ask how we store raw iodine, inquire about the life cycle of our reaction workup solvents. Fielding these questions keeps us sharp, but also drives us to invest in improved plant air filtration, digital temperature logs, and solvent reclamation systems.

    It took years to understand the subtleties of crystal growth for crystallization and recrystallization of iodoanilines. Batch consistency hinges on both the reactor setup and the quality of upstream feedstocks. We regularly evaluate alternative iodinating agents, both for environmental impact and cost. Some attempts to bypass traditional methods with "greener" oxidants or milder conditions work well in the lab but do not scale. Our view—born of repeated trials and failures—is that batch reproducibility carries more weight than breakthrough yields with unstable exotics.

    For clients who require material at metric ton scale, we give particular attention to packaging and impurity tracking. We learned early on that shipment delays often stem not from the synthesis itself, but from leaching or degradation during transit. Our packaging crew adopted new drum liners and multi-layer bags after a single batch lost its marketability in a damp spring. Keeping field logs of each shipment helped uncover trends that led to these packaging updates. Over time, small operational shifts like these set the foundation for more reliable global deliveries.

    Supporting Innovation Upstream and Downstream

    As new industrial fields emerge—OLED lighting, specialty polymers, targeted radiotherapy—the demand for advanced chemical building blocks grows. Innovation stems from available tools, and 4-iodoaniline stands as one such tool in the hands of enterprising chemists. By working closely with partners pushing the frontiers of organic electronics and pharmaceuticals, we’ve tailored production runs to stricter specs or shifted focus toward custom derivatives.

    A recurring request from advanced materials customers centers on trace metal content. Cross-coupling catalysts work at ppm or even ppb levels, so impurities—especially palladium, copper, or nickel—must stay as low as possible. After feedback from these users, we invested in better purification columns and switched to high-purity iodine grades, even at higher sourcing costs. We now offer 4-iodoaniline with metal impurities quantified by ICP-MS, and we can align specs with the requirements of each partnership.

    Looking downstream, many of our customers run into regulatory or environmental questions tied to aromatic amines. We believe transparent collaboration between manufacturers and buyers sets the right standard. We routinely share synthetic route details under non-disclosure agreements when regulatory bodies ask for impurity profiles or environmental impact statements. Many of our longtime clients reference these disclosures in their filings, reducing time to registration and smoothing out the route to market.

    From Lab Curiosity to Industrial Mainstay: The Path of 4-Iodoaniline

    Decades ago, 4-iodoaniline was something chemists produced in multi-gram lots, used mostly for small-scale test reactions or as a reference compound. Now, demand grows each year, with pharmaceutical APIs and specialty monomers as primary destinations. Our own journey mirrored this evolution: with each plant upgrade, we moved from hand-stirred reactors to automated systems with in-line spectroscopy, capable of tighter process controls and faster troubleshooting.

    Not everything runs smoothly in the world of specialty chemical production. Raw material shortages—especially iodine—have tested our grit. Surges in global demand or temporary mining bottlenecks forced us to expand supplier networks and qualify alternative sources. We keep transparent stock reports and update customers regularly, never inflating yield forecasts. In our view, sustainable partnerships last longer on real numbers and straightforward communication than on rosy projections.

    Listening to feedback from research scientists improved our own understanding of 4-iodoaniline’s potential. Several groups reported unexpected side-products when using third-party material; further discussion pointed to trace DMSO from solvent swaps in the supplier’s process. We took these findings back to our own team and updated our cleanup protocols, verifying each step by NMR and mass spectrometry to make sure these off-flavors no longer occurred on our end. Small changes accumulate: a single impurity eliminated here, a faster filtration method there.

    Quality Control: More Than Just a Final Step

    Quality touches every layer of our operation. Our team documents raw material checks, sets critical process parameters, and relies on regular instrument calibration. On busy production weeks, cross-disciplinary teams check chromatograms, discuss batch deviations, and adjust as soon as a line drifts from baseline. Our philosophy: no single analytical technique tells the whole story, so we run orthogonal tests on each batch where possible, confirming both main peaks and background fragments.

    Every kilogram of 4-iodoaniline ties many people together—operators, analysts, packaging teams, logistics. Each team brings specialized knowledge, from safe iodine handling to crystal packing. We encourage internal reporting of issues, incentivizing candor when something goes off-track. This brings to light complications early, from instrument drift to unexpected solvent interactions.

    Final packaging includes tamper-evident closures and careful sealing procedures. For high-sensitivity applications, we layer additional barrier materials to block humidity ingress. All labeling includes batch numbers encoded for traceability down the supply chain; if a complaint arises, we can trace a drum back to the day, operator, and instrument set. No system prevents every problem, but a tight paper trail narrows the window for error and speeds corrective action.

    Navigating Environmental and Safety Pressures

    Producing aromatic amines brings regulatory scrutiny. Worker exposure to amines and halogens sits near the top of safety briefings, and we run exhaust systems at higher negative pressures to keep airborne concentrations low. Teams undergo bespoke safety training—emphasizing both practical steps and the reasoning behind them. Each accident avoided or exposure kept under limits stands as a daily proof of progress.

    Waste generated during synthesis—spent iodine, reaction solvent, filtration cake—goes through in-plant treatment or is sent to accredited disposal partners. In recent years, new solvent recovery systems started to pay dividends, capturing high-boiling materials for re-use and cutting our waste volumes. Our regional authorities monitor releases closely, so each plant modification gets logged, tested, and sometimes re-tested by outside assessors. Whistleblower channels ensure anyone can flag a concern without friction.

    As legislative frameworks tighten, particularly in the EU and North America, our documentation has grown more detailed. Product stewardship is no longer a slogan, but a compliance requirement built on records, sample archiving, and safety audits. Buyers in strict jurisdictions often visit in person, confirming our storage, documentation, and containment practices meet their own codes of conduct. This relentless focus keeps us pushing toward safer and lower-impact operations, a win for our people as well as the industry.

    Working Hand in Hand with Customers

    Beyond the batch, the value we provide rests in our shared journey with each customer. Technical service representatives field questions that stretch beyond formal specifications. Whether troubleshooting solubility issues in large-scale reactors or helping customers retrofit their equipment for higher throughput, our advice is rooted in field experience. We maintain a library of case reports gained from years of collaboration, and adapt as our clients innovate or regulations shift.

    Some customers want ultra-high purity for early-stage clinical research, while others prefer steady, reliable volumes for steady-state production. rather than force a single approach, we build tailored supply plans—timing output runs to global shipping constraints, staging inventory near end-users, and updating process documentation as new compliance demands arise. Our logistical support team can expedite certification paperwork, regulatory letters, or bespoke packaging on tight timelines.

    We never pretend that 4-iodoaniline is the right solution in every scenario. Complicated projects may still favor other aromatic building blocks, for legal, practical, or chemical reasons. By sharing what works, owning up to failures, and keeping communications open, we support customers in making the best choice for their project, not just our bottom line.

    Staying Ahead Through Community, Not Just Chemistry

    Chemistry production rarely exists in a vacuum; we take the industry’s pulse through trade associations, technical forums, and joint research initiatives. Each year, new green chemistry goals emerge, along with updated toxicity and hazard data. Our staff attends symposia and participates in standards committees. Better industry practices follow as a result: new extraction solvents, emission controls, or product stewardship codes become common ground, allowing even direct competitors to benchmark progress.

    Several of our staff contribute to peer-reviewed literature, drawing on our daily work and feedback cycles. These articles do not just boost reputation—they bring outside critique, which leads to further improvements. Young chemists rotating through our internship programs inject fresh ideas and challenge inherited wisdom. Experience counts, but fresh eyes catch overlooked risks or growth opportunities.

    Our experience producing 4-iodoaniline affirms key lessons. Industrial chemistry depends on small refinements, honest audits, and close partnership with the wider ecosystem of researchers, manufacturers, regulators, and users. Continuous improvement shapes all aspects of our work, from quality assurance to logistics and sustainability planning. As the world’s needs evolve, so too must our approach, never settling for “just good enough.”

    Conclusion: The Value of Trusted 4-Iodoaniline Supply

    4-Iodoaniline continues to anchor important industrial processes, research breakthroughs, and specialized applications. Its difference from other haloanilines stems not just from chemical properties, but from the experience and care that goes into each batch. Our commitment to quality, safety, and partnership informs every decision, from raw material buying to final delivery. Trust grows over consistent practice, transparent responses, and a shared drive toward innovation and safety. Every conversation with a partner—every technical challenge met—enriches both our company and the broader field that relies on these molecules of progress.