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HS Code |
192020 |
| Chemical Name | 4-Iodo-2,6-Dimethylaniline |
| Cas Number | 698-74-0 |
| Molecular Formula | C8H10IN |
| Molecular Weight | 247.08 g/mol |
| Appearance | Pale yellow to light brown solid |
| Melting Point | 72-74 °C |
| Density | 1.66 g/cm³ (estimated) |
| Solubility | Slightly soluble in water |
| Smiles | CC1=CC(=C(C=C1N)I)C |
| Synonyms | 2,6-Dimethyl-4-iodoaniline |
| Pubchem Cid | 132719 |
As an accredited 4-Iodo-2,6-Dimethylaniline 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 4-Iodo-2,6-Dimethylaniline, sealed with a screw cap, labeled with hazard and product details. |
| Shipping | 4-Iodo-2,6-Dimethylaniline should be shipped in tightly sealed containers, protected from light and moisture, and clearly labeled. It must comply with all relevant hazardous material transport regulations, including the use of appropriate cushioning and secondary containment, to prevent leaks or spills during transit. Transport only with authorized, trained carriers. |
| Storage | 4-Iodo-2,6-dimethylaniline should be stored in a tightly sealed container, away from light, heat, and moisture. Keep it in a cool, dry, and well-ventilated area, separate from incompatible substances like strong oxidizers and acids. Proper labeling and secondary containment are recommended to prevent leaks or spills. Handle under an inert atmosphere such as nitrogen, if possible. |
Applications of 4-Iodo-2,6-Dimethylaniline in Industrial Manufacturing4-Iodo-2,6-Dimethylaniline serves as a high-purity intermediate in several specialty chemical production chains. Our manufacturing process delivers consistent material quality for demanding downstream integrations. This section details its specific roles and regulatory needs in modern industries. 1. Pharmaceutical Intermediate for Antihypertensive Sartan APIsMajor pharmaceutical manufacturers source 4-Iodo-2,6-Dimethylaniline as a crucial building block when synthesizing biphenyl-based sartan antihypertensives. This aniline derivative undergoes nucleophilic aromatic substitution to construct tetrazole and biphenyl frameworks for API assembly, particularly in downstream active pharmaceutical ingredient plants. Consistent iodine placement and methyl substitution deliver precise reactivity profiles required by GMP-compliant production lines, optimizing both reaction selectivity and downstream yields during multi-step organic synthesis. Industry compliance standards
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2. Synthesis of High-Performance Pigment PrecursorsIn the pigment manufacturing sector, 4-Iodo-2,6-Dimethylaniline enables precise diazotization and coupling to yield complex azo and triarylmethane pigment intermediates. Formulators in ink, coating, and specialty colorant factories utilize its unique iodo functionality for advanced halogen-exchange reactions, leading to improved purity and brightness in downstream pigment dispersions. This route ensures excellent thermal and photostability demanded by premium inkjet and coating applications. Industry compliance standards
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3. Agrochemical Intermediate for Crop Protection SynthesisLeading agrochemical formulators incorporate 4-Iodo-2,6-Dimethylaniline as a key intermediate to build selective heterocyclic ring systems in modern herbicide and fungicide APIs. The electron-rich aniline ring is essential in integrating iodo and methyl substituents to increase biological selectivity and reduce off-target effects. It enters synthetic sequences via halogen-metal exchange or direct amination, supporting scalable production that meets strict international agrochemical safety and traceability standards. Industry compliance standards
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4. Specialty Monomer for Functional Polymer SynthesisPolymer chemists select 4-Iodo-2,6-Dimethylaniline as a specialty monomer to introduce steric hindrance and electronic modulation in advanced engineering resins. Through nucleophilic aromatic substitution and subsequent polymerization, the material imparts enhanced chemical resistance and thermal stability to electronics-grade and high-performance plastics. Downstream plants implement tightly regulated blending to meet stringent tensile and dielectric property requirements in electrical and automotive markets. Industry compliance standards
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5. Fine Chemical Intermediate for Liquid Crystal SynthesisLeading display and electronic material suppliers specify 4-Iodo-2,6-Dimethylaniline for its role in producing advanced biphenyl and azomethine core structures used in high-performance liquid crystal formulations. Its defined substitution pattern supports precise electronic properties and phase transition temperatures, which are critical for liquid crystal display (LCD) applications. Process control engineers integrate this intermediate at etherification or aryl coupling stages under high-purity, closed-system conditions to maintain defect-free crystal performance. Industry compliance standards
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6. API Intermediate for Veterinary MedicinesVeterinary pharmaceutical producers employ 4-Iodo-2,6-Dimethylaniline in the synthesis of aromatic amine derivatives that form functional groups in modern anti-infective and anti-inflammatory treatments for livestock. The intermediate supports rapid construction of activatable rings and side chains, used further in amide or ether formation steps as required by regulatory and pharmacopoeia standards. Downstream production mandates analytical traceability and batch retention consistent with animal health regulations worldwide. Industry compliance standards
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In the world of specialty chemicals, 4-Iodo-2,6-dimethylaniline earns its place in complex syntheses, fine-tuned intermediates, and innovative material applications. At our plant, years refining aromatic amination and halogenation build up real insight into what customers expect from this class of aniline derivatives. Countless small improvements shape what leaves the reactor: purity, consistency, freedom from common byproducts. Self-respect as a producer hinges on reliable quality, not just hitting assays on a spec sheet.
Producing 4-Iodo-2,6-dimethylaniline takes more than ordering the right raw materials and plugging values into a batch record. The methyl groups on the ring come from targeted alkylation, with conditions that keep ortho selectivity locked. Halogenation, especially with iodine, has a mind of its own—ring activation, incomplete substitution, and deiodination battle for control. Controlling every stage, we protect against partially iodinated byproducts and over-alkylated impurities. Anything less chews up downstream yield and clouds the reliability of analytical data.
Compared to standard anilines, the paired methyl groups at 2 and 6 have one job: they shield the amino group, altering both reactivity and selectivity. In dye manufacture, crop protection development, and fluorescent probe synthesis, this modulation can change the entire process design. Bringing the iodo substituent into the ring introduces a heavy atom, unlocking direct routes to aryl iodides that aren’t easy from chlorinated or brominated analogs. Clients who tried simpler anilines often report sluggish coupling reactions or messy isolations. Substituent pattern, like this one, makes all the difference.
End-users know that minor changes in starting materials ripple through an entire synthetic route. Take a developer building biaryl molecules for pharmaceutical research—they trust each batch for symmetry, reactivity, and scale-up consistency. With 4-Iodo-2,6-dimethylaniline, Suzuki and Ullmann coupling reactions often run cleaner and faster compared to using less functionalized anilines. Our customers share data showing sharper TLCs, higher isolated yields, and straightforward workups. In pigment manufacture, the added methyl groups tune hue and shade without lability issues found in unsubstituted analogs.
Research teams in electronics material synthesis tell us the iodo position opens selective cross-coupling, giving them flexibility building up dendrimers, OLED scaffolds, and advanced sensors. The difference our process achieves—minimal metal contamination, absence of residual alkyl halide, and stable shelf profile—saves valuable validation time. Over the years, we’ve learned it pays to use a resin-filtration cleanup and high-vacuum drying, pushing micro-contaminant levels even lower than industry averages.
Quality with this compound isn’t just purity on paper. Moisture sensitivity, air handling, and physical consistency (no clumps, caking, or brittleness) have real-world impacts. Chemists here still remember the first time a known batch clumped after shipment—nobody likes a ruined kilo crumbling out of a drum. So, we built in strict drying steps, switched to double-liners, and standardized pack-out at an inerted nitrogen deck. Each scoop comes the same way, batch after batch. QA pulls real samples for spectral and elemental analysis, never just reviewing indirect logs.
The story of this product relies on feedback. Clients in Asia reported slight off-odors with an earlier lot; turns out, trace carryover from minor byproducts mattered. Since then, we tuned oxidative quenching parameters and improved the final wash. North American partners pushed for even higher iodo content, seeking to avoid downstream vacuum distillation. Small tweaks, made repeatedly, show in glowing testimonials: “Our reactions run twice as fast,” or “Recovery improved by 10 points.”
Supplying this specific aniline derivative isn’t just a one-size-fits-all job. Some customers require full bulk deliveries in sealed drums, others need 10g bottles for project launches. We track every batch from synthesis to warehouse, tying analytical results directly to the customer file, so traceability is complete. Few things matter more than real chain-of-custody. When temperature spikes threatened stability in a cross-country shipment, we responded by switching to validated refrigerated logistics, sparing the client weeks of downtime.
The key for us isn’t only about the molecule. It’s building trust both ways. Chemists on our production lines know every shipment’s purpose, whether for clinical research, polymer innovation, or pigment formulation. When a batch doesn’t meet our own internal criteria—by color, by NMR—no one hesitates to rerun purification or reschedule delivery. That discipline forms the backbone of our product’s reputation.
Over the years, we watched the field evolve. Early requests mostly came from dye makers, searching for strong colorfastness and consistent shade. Today, molecular imaging scientists, electronics engineers, and agrochemical developers drive demand for structural specificity and extreme batch-to-batch reliability. This shift isn’t just a paper trend—clients now ask about GC-MS trace impurities, storage stability at subzero conditions, and compatibility with sensitive catalysts.
With every conversation, we adapt our approach. Adding real-time monitoring in the final stage, introducing extra in-line filtration, seeking out greener solvent choices—these are hard-won lessons. We see environmental pressure shaping how complex aromatics like 4-Iodo-2,6-dimethylaniline are perceived. No one wants runaway emissions or waste streams that draw unwanted attention. By recycling filter cakes and pushing for next-generation deiodination methods, we cut footprint and costs together.
Manufacturing 4-Iodo-2,6-dimethylaniline brings hurdles that don’t appear with monocyclic or less-substituted anilines. Standard anilines lack both steric hindrance and halogen reactivity, often forcing users into multi-stage syntheses if they need customized aryl donors or higher selectivity. The dual ortho methyl groups here not only block unwanted side reactions but also change how the amine behaves in both nucleophilic and electrophilic attacks. This subtle detail reshapes entire product lines.
Many prospective buyers feel drawn to bulk commodity anilines for cost reasons. Our philosophy: cutting corners at the start means problems multiply in the next step. The iodo group, the heavy hitter of the halogens, beats its bromine and chlorine cousins for reactivity in couplings—cleaving cleaner, leaving less metal residue, and supporting lighter reaction conditions. Where others settle for 99% purity, we monitor for multiple byproducts at trace levels, knowing each can have outsized impact on depending downstream needs.
Demand for data and traceability keeps rising, and for good reason. Raw materials, especially those heading for regulated sectors, must come with ironclad supporting documentation. We deliver HPLC, NMR, and elemental assay profiles, including detailed impurity tables and full spectral overlays. Life sciences firms appreciate these extra steps, since regulatory submissions hinge on proof of unambiguous identity and absence of problematic contaminants. Our strict batch control—ready records at every step—gives partners peace of mind if inspectors ever start asking questions.
We have never waited for customer complaints to shape our documentation standards. Knowing that one lost COA can stall an entire project, we maintain digital copies aligned with each batch number and client account. If a downstream researcher in Europe needs a rapid audit, they get a direct line to one of our technical chemists, not a generic support queue. Over time, these connections break the stereotype that specialty chemicals must come with risk or hassle.
Every advanced aromatic brings unique manufacturing and logistical obstacles. Iodinated compounds, including 4-Iodo-2,6-dimethylaniline, raise both safety profiles and waste management questions. Iodine byproducts resist conventional trapping, so we keep investing in upgraded filter media and improved neutralization. Years ago, a persistent problem appeared: small pockets of unconverted starting material, almost invisible by crude melting point, sabotaged one batch’s shelf life. Following a trusted partner’s suggestion, we installed FTIR inline detection and cut out the issue for good.
Supply chain volatility also shapes our routines. Bulk iodine can spike in price, and shipping restrictions never make things easier. Still, our procurement and planning teams work cross-functionally with operations to lock in sources and raw material buffers. Experience proves that run-to-order doesn't satisfy fast-moving labs. Keeping safety stock and proven logistics partners means customers don’t wait weeks for replenishment, even if market surprises hit.
Good chemistry grows stronger when producers and formulators pull together. In developing new uses for 4-Iodo-2,6-dimethylaniline, we partner directly with end-users to dial in reactivity, optimize scale, and troubleshoot bottlenecks. A pigment maker sought brighter, more stable colors for outdoor inks—a series of bench trials with our technical team produced a new grade, with both finer particle control and a tighter melting range.
Recently, a pharma startup faced clogging during scale-up. Our troubleshooting pointed to sub-micron particulate, invisible in small-scale NMR. By examining their filters and running parallel mill tests, we helped them transition to cleaner continuous processing. The lesson: real partnership and knowledge beat an anonymous supplier relationship every time.
Industry-wide, expectations around chemical stewardship keep rising. Handled the old way, aromatic halides risk legacy contamination—heavy metals, persistent organics, and excessive water use. Over several cycles, we moved towards water-recycling bicycles, mercury-free catalysis, and comprehensive spent-solvent reclamation. Our waste partner audits our operations, flagging anything that could put either reputation or process continuity at risk.
We keep records, not just for compliance, but to motivate ongoing improvement. Less waste, lower energy, smaller carbon footprint—these become selling points, not burdens. When setting up a new process line for 4-Iodo-2,6-dimethylaniline, installing solvent capture equipment shaved several percent off total emissions and improved lab air quality as an unexpected bonus. Taking these extra steps pays off: regulators see real action, and customers benefit from cleaner, more predictable products.
Being a manufacturer means living with every outcome—good, bad, or unexpected. 4-Iodo-2,6-dimethylaniline challenged us to rethink even basic protocols. Is nitrogen blanketing enough on humid days? Is a glass liner or PTFE reactor better at scale? Do we sample at the right frequency, or risk missing late-emerging side products? Every successful campaign answers some questions and raises new ones. True refinement calls for patient iteration and shared lessons.
We’re never quick to claim perfection. But by tightening up SOPs, adopting new analytics, and listening closely to partners, we build up hard-fought confidence in every gram produced. From pilot trials to ton-scale contracts, our journey with this compound mirrors the larger chemical landscape—a mix of innovation, collaboration, and grounding in reliable science.
We come to work knowing that every order of 4-Iodo-2,6-dimethylaniline stands for a leap forward in someone's project—a pharmaceutical campaign, a materials science breakthrough, a creative pigment. Decades spent refining both product and process, learning from wins and mistakes, drive us to keep delivering better, safer, and more consistent results.
By keeping integrity at every step, listening to changing needs, and investing in people and equipment, we serve as more than just a source of supply. We work as genuine partners in discovery. For all who rely on this compound's unique features—chemical stability, functional selectivity, and smooth integration into advanced routes—our commitment is both simple and enduring: dependable quality, personally backed, batch after batch.