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HS Code |
188273 |
| Chemical Name | 4-Chloro-2-Iodoaniline |
| Cas Number | 6231-57-4 |
| Molecular Formula | C6H5ClIN |
| Molecular Weight | 253.47 g/mol |
| Appearance | Light brown to off-white solid |
| Melting Point | 107-110°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥ 97% |
| Synonyms | 2-Iodo-4-chlorobenzenamine |
| Smiles | Nc1cc(I)ccc1Cl |
| Inchi | InChI=1S/C6H5ClIN/c7-4-1-2-5(8)6(9)3-4/h1-3H,9H2 |
As an accredited 4-Chloro-2-Iodoaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a white screw cap, labeled as 4-Chloro-2-Iodoaniline, includes hazard warnings and lot number. |
| Shipping | 4-Chloro-2-Iodoaniline is shipped in tightly sealed, chemical-resistant containers, typically under ambient conditions but protected from moisture and light. Labeling includes hazard identification, and transport complies with local, national, and international regulations for hazardous chemicals, ensuring safe handling and delivery. Shipments are carried out by certified carriers specializing in chemical logistics. |
| Storage | 4-Chloro-2-Iodoaniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep it away from direct sunlight and moisture. Clearly label the container and avoid exposure to heat and ignition sources. Store under conditions recommended in the safety data sheet (SDS). |
Applications of 4-Chloro-2-Iodoaniline in Industrial ManufacturingAs an established manufacturer of 4-Chloro-2-Iodoaniline, we serve global partners operating in specialized chemical synthesis sectors. The following sections detail how this intermediate integrates into actual production environments, focusing on high-value downstream applications where it contributes critical performance, compliance, and economic benefits. 1. Pharmaceutical API Synthesis (Azelastine and Related Intermediates)Within pharmaceutical production, 4-Chloro-2-Iodoaniline forms a building block for specific antihistamine active ingredients, with particular use in second- and third-step intermediates for azelastine synthesis. Its precise halogen substitution enables control over molecular reactivity and selectivity, reducing byproduct formation in final coupling reactions. Large-volume batch reactors and GMP-validated lines incorporate this compound at conversion-critical steps to minimize impurity carryover in the API crystallization stage. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)In agrochemical manufacturing, 4-Chloro-2-Iodoaniline enters as a core intermediate for phenylurea and other heterocyclic herbicides, underpinning targeted crop protection products. Its dual halide profile allows for stepwise N-alkylation and diazotization in continuous-flow synthesis, supporting fine-tuned structure–activity relationships for selective weed or fungal inhibition. Downstream producers rely on its reactivity to ensure environmental metabolite profiles remain within portfolio-specific regulatory thresholds. Industry compliance standards
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3. Dye and Pigment Synthesis (Azo and Triarylmethane Colorants)Specialty colorant companies employ 4-Chloro-2-Iodoaniline for synthesizing high-performance dyes, especially where specific chromophore modifications demand unique electron-withdrawing functionality. It is most commonly diazotized and coupled in multi-stage batch processes to create custom azo and triarylmethane dyes. The presence of both halogen groups supports tuning of bathofugal absorption peaks, critical for textile and ink industries targeting niche spectral performance and wash-fastness requirements. Industry compliance standards
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4. Electronic Chemical Synthesis (Organic Semiconductor Intermediates)In electronic material manufacturing, this compound supports the synthesis of halogenated aniline-based semiconductor building blocks. The iodo and chloro substituents contribute to solution processability and fine energy level modulation within certain OLED emitter and hole-transport material syntheses. Integration occurs in inert-atmosphere reactors with strict moisture controls, as downstream performance hinges on trace purity and precise stoichiometric input during oligomerization or Suzuki coupling for optoelectronic thin films. Industry compliance standards
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5. Fine Chemical Synthesis (Custom Halogenated Building Blocks)Custom synthesis providers depend on 4-Chloro-2-Iodoaniline as a halogen-rich amine scaffold, ideal for iterative functionalization in contract manufacturing of specialty intermediates. Its structure facilitates targeted Suzuki, Ullmann, or Sandmeyer reactions, supporting development of customer-specified molecules for research or niche regulatory inquiry chemicals. Precise batch tracking and full analytical traceability are central in these projects, with compound purity and defined substitution critical for successful customer qualification. Industry compliance standards
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Among aromatic intermediates, 4-Chloro-2-Iodoaniline stands out for its precise balance of halogen substitution and amine functionality. In our production lines, we deal with an array of aniline derivatives, and this compound consistently brings chemists and engineers back due to its reliable delivery in advanced syntheses. The specific placement of chlorine and iodine atoms directly influences the reactivity and directability that our downstream partners look for in complex molecule construction. Over the years, repeated requests and feedback from our customers have solidified its position in our catalog—not because of aspirational marketing, but because of proven, hands-on results in the lab and factory alike.
Every batch of 4-Chloro-2-Iodoaniline leaves our site after stringent quality control. We always measure purity using HPLC and NMR, aiming for at least 98% purity as a baseline; in many runs, it exceeds that mark, passing 99%. Trace metals from our iodination and chlorination processes are held to strict limits, since experience taught us that even minor contamination influences yields and downstream reactions. Moisture levels remain low, well below 0.5%, due to our controlled drying protocols. The chemical arrives as a pale to faintly yellow crystalline powder. Each internal lot is labeled for traceability, as we value both regulatory compliance and the comfort that comes from knowing every gram matches customer expectations. The melting point typically falls between 72°C and 78°C, and this range is checked against expected standards with each production run.
Colleagues in process R&D repeatedly tell us that placement of halogens in an aniline core changes everything about the synthetic route. Swapping the positions can mean the difference between a selective coupling and a cascade of side reactions. 4-Chloro-2-Iodoaniline’s chlorination at the para position makes the ring markedly more electron-deficient than meta- or ortho-substituted variants. This property drives selectivity in Suzuki and Sonogashira couplings, while the iodine on the ortho position opens the door to high-yielding cross-coupling reactions. There’s nothing academic about it—when a medicinal chemist asks us specifically for the 4-chloro-2-iodo isomer, it’s because previous candidates failed on the bench, or because only this pattern delivers the right intermediate to move a synthesis forward.
We don’t offer other isomers in this series unless asked for a custom run. Over the years, we’ve handled requests for the 3-chloro-2-iodo variant, but without the same demand or feedback on success rates in applied chemistry. The interaction between halogen orientation and amine position consistently affects catalytic cycles, especially in iterative aromatic functionalizations. Our direct experience collaborating with kilo-lab and pilot plant operators has shown this pattern over and over.
Most of the 4-Chloro-2-Iodoaniline shipped from our facility ends up in pharmaceutical research labs, agrochemical studies, and material science incubators. In medicinal chemistry, groups count on the selective iodine for robust metal-catalyzed couplings, while the chlorine often survives downstream functionalizations. Over the past decade, we have directly supported several published syntheses of kinase inhibitors and heterocyclic building blocks, where the route runs more efficiently thanks to the aniline’s particular substitution pattern. Customer feedback tells us that impure or ill-positioned starting materials spell disaster: chromatography headaches, dropped yields, and wasted time. By keeping contaminants and byproducts minimal, we find our partners return—an endorsement more persuasive than any promotional line.
Agrochemical developers use the compound as a springboard for diverse crop protection agents. Material chemists explore its potential in optoelectronic and dye applications, though many projects remain proprietary. In every case, the unique interplay of halogen atoms with the basic amine has opened doors for scaffold elaboration that would otherwise require multiple steps—often outside the tolerance of advanced molecules or sensitive catalysts.
One common question from buyers new to this intermediate involves its difference from, say, 4-Chloroaniline or 2-Iodoaniline. In our production facilities, we’re well aware of their unique identities—the purity controls, crystallization profiles, and even the waste management strategies change based on substitution. Pure 4-Chloroaniline won’t deliver the same reactivity pattern under palladium catalysis; it lacks the strategic iodine, which acts as a more reactive leaving group than the chlorine. Without iodine, transformation options narrow, and the overall efficiency drops.
The same holds true in reverse: pure 2-Iodoaniline reacts faster under oxidative addition, but the missing chlorine robs chemists of orthogonal functionalization pathways. 4-Chloro-2-Iodoaniline bridges both, offering two distinct reactive handles—indispensable when multi-step synthetic complexity needs to be managed without introducing fresh starting materials at every stage. Colleagues who have run direct comparisons find the differences anything but trivial, especially as projects scale and reproducibility becomes king.
Real reliability comes not just from the name on the drum, but from every subtle process control we enforce at the plant. Chlorine and iodine incorporation are handled using time-tested procedures our team refined across dozens of campaigns. We don’t chase every trend, but rather adapt our workflow only when new evidence supports better outcomes—whether it’s a gentler oxidant, a faster crystallization cycle, or more efficient waste stream recycling.
Packing matters, too. Years of spill and degradation incidents have convinced us that tight-sealing HDPE drums or aluminum foil bags are worth the investment, even at smaller scales, to combat both photodegradation and trace moisture uptake. Customers often compare our batches, finding lower levels of breakdown products—because imperceptible contamination in storage can be a project-ender months later. We listen, and we change our line configurations accordingly.
Our earliest campaigns demanded careful management of heat and gas evolution during iodination, especially since inconsistent temperature control leads to over-iodinated byproducts. Experience shaped a protocol where reaction exotherms are never left to automatic damping; operators track the endpoint reaction by both analytical monitor and visual cue. By maintaining a steady line of communication between plant chemists and Q.C. lab, we solved lingering problems with color impurities—no small matter for sensitive final applications.
We place real trust in our production crew’s years on the floor. The experienced shift lead knows the scent, texture, and even the way a fresh batch settles in a scoop; those instincts keep mistakes from creeping in where no instrument would catch them. Over time, we’ve invested in both continuous improvement and operator training, favoring stability over relentless upscaling. Sustainable growth matches long-term supply confidence with employee expertise—a combination our returning partners value as much as a consistent specification sheet.
Hazard control doesn’t end with the safety datasheet. We’ve learned the hard way that even mild UV or high humidity will kick-start degradation, with lingering impact on both physical quality and assay performance. Our warehouses run filtered ventilation with tight access logs; only those cleared to handle aromatics access inventory, cutting accidental contamination rates. We’ve replaced urea-formaldehyde shelving that sometimes reacted with trace amine offgassing—a lesson from lost product that only comes after high-impact reviews.
Every shipment leaves with a pack date, but our advice to the customer always reflects our own storage audits. Reducing temperature fluctuations in storage rooms, eliminating trace organics in the air, and logging every opening event—these steps keep the product stable in the box as in our bulk tank. Several kilo-labs and pilot plants have thanked us for this attention, noting that lots received from less rigorous sources force them to filter before use, sapping time and introducing avoidable risk. Clean handling paired with airtight records delivers trust, not just compliance.
Our waste treatment lines integrate both pre- and post-reaction halogen recovery. Chlorinated and iodinated waste, if dumped or poorly managed, risks regulatory action and real harm to workers and communities. Our plant shifted years ago to closed-loop solvent handling and off-gas capture, based not just on compliance targets but hard-learned lessons from rework and environmental monitoring results. Today, all byproducts move to licensed destruction or are recycled when purity allows; plant audits reflect that.
Several years back, a surge in demand for 4-Chloro-2-Iodoaniline forced us to review not just our batch processes, but supply chain inputs. We partner directly with certified raw material suppliers, some local, others global, each audited for compliance and ethical sourcing. Disruption in iodine supply has occurred, but by maintaining a varied supplier base and strategic inventory, we keep production flowing so our commitments never break. True supply chain stability comes from transparency and relationships—qualities that can only grow through years of shared challenges and mutual respect.
As more research teams turn to cross-coupling and halogenated anilines, feedback on desired specs continues to pour in. Larger particle size or higher surface area for select reactions, ultra-high purity for advanced workups, supporting documentation for each lot—requests like these shape every incremental process adjustment. We test new purification media, invest in real-time monitoring, and trial greener oxidants not because regulations force our hand, but because actual outcomes in the field push our team forward. The right tweaks are never decided in boardrooms or executive circles, but by direct input from those running the chemistry.
Previous years have taught us that sudden changes—whether in regulatory standards or global logistics—require nimble response and steady commitment. By staying close to end-users, both in technical support and ongoing dialogue, we keep improving the final product in line with actual need, not hypothetical trends. Each technical inquiry or complaint pushes both us and our partners ahead, and those insights inform every batch and update.
4-Chloro-2-Iodoaniline, in our hands, moves from line item to essential chemical because we treat every kilo as a collaboration with end users—whether in new drug discovery or manufacturing scale-up. There’s only so much literature or marketing spin can explain about the distance between reliable intermediates and those that repeatedly fail to deliver. What keeps users coming back is less about spec sheets and more about lived process wisdom coupled with documented consistency. Every request, every improvement, every challenge met on our production line feeds directly into the reliability and effectiveness of each batch delivered.
By matching production with real user insight, adapting to changing regulatory and technical demands, and placing credibility and transparency at the center of every operation, 4-Chloro-2-Iodoaniline from our manufacturing floor remains a mainstay in innovative chemical applications. We look forward to every new synthesis this essential intermediate helps to unlock, knowing that behind every gram lies not just process, but shared understanding between maker and user.