|
HS Code |
255843 |
| Cas Number | 13291-25-5 |
| Molecular Formula | C10H13I |
| Molecular Weight | 260.12 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 66-68 °C |
| Boiling Point | Unknown |
| Density | 1.6 g/cm3 (estimated) |
| Purity | Typically ≥98% |
| Solubility In Water | Insoluble |
| Smiles | Cc1c(C)c(I)c(C)c(C)c1 |
| Inchi | InChI=1S/C10H13I/c1-5-6(2)8(4)10(11)9(3)7(5)12 |
| Synonyms | 1-Iodo-2,3,5,6-tetramethylbenzene |
As an accredited 2,3,5,6-Tetramethyliodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25-gram bottle of 2,3,5,6-tetramethyliodobenzene comes in a sealed amber glass container with a secure screw cap. |
| Shipping | 2,3,5,6-Tetramethyliodobenzene is shipped in tightly sealed containers to prevent moisture and light exposure. It should be stored in a cool, dry place, away from incompatible materials such as strong oxidizers. Shipping follows all relevant hazardous material regulations, typically classified under UN 3077 (Environmentally Hazardous Substance, Solid, N.O.S.). |
| Storage | 2,3,5,6-Tetramethyliodobenzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from moisture and light. Ensure the storage area is chemical-resistant and properly labeled, and follow all relevant regulations for handling and storing hazardous chemicals. |
Applications of 2,3,5,6-Tetramethyliodobenzene in Industrial Manufacturing2,3,5,6-Tetramethyliodobenzene plays a specialized role in multiple advanced chemical production chains as a Halogenated Aromatic building block. Due to its unique reactivity profile and strict compliance with downstream regulatory requirements, it serves important functions in the synthesis of high-value performance materials, specialty electronic chemicals, and advanced agrochemical intermediates. Below we present verified industrial scenarios where this raw material is integrated, with clear details for technical customers. 1. OLED Material SynthesisThis aromatic iodide serves as a key halogenated intermediate for custom-tailored organic electroluminescent compounds in OLED (Organic Light Emitting Diode) device manufacturing. Its methyl-masked structure enables precision Suzuki-Miyaura or Stille coupling during the late stages of small molecule and polymer-based emitter synthesis, providing advanced fine-tuning of electronic and packing properties essential for high-brightness and high-lifetime display applications. Industry compliance standards
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2. Specialty Agrochemical Intermediate ManufacturingIn crop protection synthesis, this compound acts as a controlled-activity aromatic building block in the creation of complex pre-emergence herbicide and fungicide intermediates. It offers a methyl-protected iodinated ring, enabling precise downstream substitutions for selective activity optimization, especially in new-generation phenyl-substituted agrochemicals. Industry compliance standards
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3. Advanced Liquid Crystal Material SynthesisThe compound’s structural features enable its use as a mesogenic precursor or rigid core unit in the production of specialized liquid crystals for flat panel displays and photonic devices. Its high purity and defined substitution are required to meet precision optical requirements, facilitating the creation of custom aryl-functionalized liquid crystal molecules for improved thermal stability and switching response. Industry compliance standards
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4. Pharmaceutical API Intermediate SynthesisThis aromatic iodide supports late-stage diversification in the production chains of advanced active pharmaceutical ingredient (API) intermediates, particularly for drug candidates requiring methylated phenyl scaffolds. It is critical for introducing defined aryl frameworks in complex organic syntheses, enabling fine-tuning of pharmacokinetic properties and patent-specific structures within GMP controlled facilities. Industry compliance standards
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5. High-Temperature Polymer Additive SynthesisAs an aromatic iodine source featuring four methyl groups, this compound acts as a highly specific functionalizing agent for the synthesis of specialty additives in high-performance polymers. Its incorporation via aryl coupling chemistry allows for precise control over polymer branching and thermal behavior, which is exploited in engineering resins used in electronics and specialty coatings. Industry compliance standards
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Competitive 2,3,5,6-Tetramethyliodobenzene prices that fit your budget—flexible terms and customized quotes for every order.
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For over twenty years, our chemists have worked with 2,3,5,6-Tetramethyliodobenzene, a specialty aromatic compound known by its CAS number 73558-68-8. Bringing this material from raw input to packaged product requires not just skill in halogenation and aromatic substitution but practical, hands-on understanding of each step. In daily practice, we evaluate, adjust, and optimize every batch ourselves. Our approach always puts purity and consistency up front. We rely on our own reactors, not third-party equipment, so we set the controls and watch the parameters continuously. Any slight shift in proportion or temperature gets caught and corrected right on the work floor.
By developing each manufacturing run in-house, from raw xylene selection all the way through to iodination and final isolation, we keep a close grip on variables that affect quality. In contrast, generic or redistributed lots often reveal unpredictable impurity spikes—sometimes seen as stubborn off-colors or excess halogen residues after shipment. Customers who depend on exacting syntheses, such as those in pharmaceutical or advanced electronic applications, can’t afford surprises in reactivity or contamination. We’ve seen how batches with uncontrolled byproducts slow down catalyst reactions or introduce instability into polymerizations.
Our 2,3,5,6-Tetramethyliodobenzene stands out for its high, verifiable purity. We routinely achieve 99% or higher based on GC/MS and NMR verification, performed here on freshly isolated product, not just on pooled or theoretical values. Our facility’s controlled environment means particulate matter and moisture uptake remain minimal; each production cycle is rapidly dried, milled, and sealed to avoid degradation. Over the years, we’ve tested our processes by submitting samples for external analytics—consistently, results confirm the tight match between our in-house certificates and third-party findings. This approach gives customers more confidence in active iodo-aryl content and lower batch-to-batch swings.
Crystalline quality varies among sources in the market. We take special care during the crystallization and drying steps to ensure tight particle size distribution. This yields better solubility profiles and fewer issues with solid handling, especially once customers move to pilot or manufacturing scale-up. Documentation alone cannot tell the full story—a quick inspection under the microscope, which we perform routinely, quickly reveals whether a lot formed uniform, clear crystals or if issues from poor cooling control led to occluded material or sticky solids.
This compound’s unique arrangement—four methyl groups and a single iodine substituent—offers more than structural intrigue. Many customers who approach us are targeting uses in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to build up substituted aromatic frameworks. The para relationship between the methyls influences electron density at the iodine site, which shifts reactivity compared to other iodo-methylbenzenes. Years of joint development work with downstream API makers, OLED material houses, and university research labs give us a first-hand look at what small adjustments to substitution patterns mean in real chemistry. Unmet challenges, such as slow reactivity or competing side reactions, often turn out to be linked to subtle differences in starting material composition.
We’ve supported projects from the screening of new catalysts to the optimization of polymer precursors. Contract labs share their findings with us: lots showing even a hint of chlorinated or brominated analog entries can confuse their reaction analysis or produce misleading catalytic screening data. It’s not just the headline purity that matters but background levels—halides, heavy metals, oddball xylene isomers—that throw off advanced programs. Through regular feedback and round-table collaboration, we’ve changed synthetic protocols on our side to reduce cross-contamination and meet the reality of demanding custom syntheses.
With hundreds of halogenated aromatics out there, selection gets confusing. What sets this product apart is the impact of its methyl shielding on the benzene ring, combined with high iodine content. If customers have tried 2,3,5,6-tetramethylbromobenzene or the chloro analog for coupling chemistry, they’ve seen less efficient oxidative addition or faced more reluctant cross-coupling. The atomic weight and polarizability of iodine dramatically amp up reactivity at that position, which can either unlock challenging bond-making or, if the upstream material’s purity is off, lead to tar formation or degraded yields.
In the last five years, as aryl iodides became more important in advanced medicinal chemistry and display technology, we noticed buyers growing more sophisticated in how they judge different versions. Our own experience handling and purifying these compounds lets us comment directly: brominated aromatics can be a little easier to transport, but their lower reactivity limits their usefulness in dense functionalization. Iodinated aromatics like 2,3,5,6-Tetramethyliodobenzene demand tighter handling protocols but open doors to clean, high-conversion couplings and less waste generation downstream. We have also seen chemical suppliers offering similar-sounding products—sometimes using ambiguous naming conventions—but few can guarantee matched impurity profiles or physical homogeneity from lot to lot because they are trading, not making.
Making this compound at industrial scale presents distinct challenges compared to bench synthesis. Our early years were full of trial and error—solvent selection, iodine source quality, phase transfer catalysts, and temperature ramps all played a role. With thousands of kilograms through our reactors, we learned firsthand how changes in condenser efficiency or raw xylene lot variations affect downstream conversion. Many producers chasing fast turnaround overlook these factors and wind up with inconsistent end product. Facilities that don’t thoroughly wash equipment between runs or rely on low-quality iodine risk contaminant carryover and batch variability.
Modern chemical industries now push for more mindful handling of iodine waste, and this affects the economics and sustainability profile of everything from reagent procurement to final disposal. By implementing closed-loop iodine recovery, we reduce environmental footprint and help stabilize procurement costs over time. Our on-site recycling setup catches valuable material after each reaction step and allows reprocessing back into future lots. This not only benefits the environment but also shields users from volatility in elemental iodine supply or price shock. Years ago, while collaborating with process chemists at a specialty API firm, we responded to their sustainability targets by boosting recoverable iodine content and lowering outgoing effluent. Achieving this required investment in equipment and labor but paid dividends for everyone in the supply chain.
One customer, working on scale-up for a next-generation OLED material, noticed erratic results with other sources of 2,3,5,6-Tetramethyliodobenzene. They traced issues back to hidden contaminants—microscale fluoride or bromide impurities that complicated their Pd-catalyzed couplings. After switching to our in-house made product, their yields stabilized, and the physical properties of their target compound hit analytical targets repeatedly. This wasn’t luck. Each shipment passed a double round of QC here, and we provided batch-level NMR spectra and mass balance tracking.
Another customer in the agrochemical sector highlighted a different issue. Long-term storage of other suppliers’ material led to caking and difficult weighing, causing bottlenecks in their formulation line. We offered tightly sieved lots with immediate vacuum packing, reflecting what we saw in our own usage trials. Their workflow improved, and they shared productivity gains with us—feedback that helped us further refine packaging for all future lots. This example shows why direct engagement with customers, instead of arms-length distribution, feeds practical improvements into the process.
Customers face relentless scrutiny regarding traceability in advanced chemical industries. Regulations require more than specifications on paper; every step from input selection to packaging leaves a fingerprint. Our own internal audits follow the same path as external inspections. Each worker receives hands-on training, not just written SOPs, in identifying off-spec product, responding to trace impurity alerts, and documenting each handoff on the production line. Every drum receives labeling matched to master control records, which we maintain for years after the lot leaves our storage.
Keeping detailed, verifiable batch histories allows us to answer customer questions about source material, reaction conditions, or post-production analytics directly, without guesswork or delay. Armed with firsthand process knowledge, our team can help customers quickly trace any out-of-spec event back to root cause and propose real adjustments.
As a company investing heavily in hands-on synthetic chemistry, we’ve seen first-hand that risk often comes from unchecked variables. Whether it’s humidity creeping into storage drums in the summer, or supply chain hiccups with halogen inputs, we developed our own mitigation strategies out of hard experience. Our main storage is tightly climate-controlled, and our procurement process includes pre-shipment inspection and real content analysis, so expectations set match what gets delivered. Physical inspections, not just paperwork, form the backbone of every acceptance and outgoing shipment.
Unexpected reactivity or incompatibility seen at the customer’s site nearly always ties back to small, overlooked differences in manufacturing practice—or in some cases, outright mislabeling or substitution by third parties. Our technical staff actively reviews feedback and, in some cases, visits client sites to observe or troubleshoot real-world challenges. Sometimes customers discover new problems we never faced in-house, such as gel formation during reactor charging or unexpected residue under certain drying conditions. We see these as learning opportunities and collaborate with end-users to test minor formulation tweaks, reactor parameter shifts, or storage protocol updates. Solutions emerge from real, ground-up experimentation, not abstract theorizing.
Innovative sectors like pharmaceuticals, OLED development, and precision agrochemicals often rely on specialty halogenated aromatics for foundational synthetic steps. 2,3,5,6-Tetramethyliodobenzene stands out for its unique profile—elevated reactivity, manageable physical handling, and minimal background interference. Over the years, we’ve worked with innovators developing new organocatalysts, bioconjugates, and polymer backbones. They’ve told us how switching raw material sources can sideline R&D projects overnight due to reactivity swings or unknown contaminants. By rooting production in our own facility, not off-shore outsourcing or speculative buying, we anchor reproducibility and reliability at the very start of the value chain.
We also run regular pilot projects exploring next-generation applications—these stress-tests expose hidden weaknesses in process or packaging early on, long before commercial shipping. Our ongoing partnerships with university researchers and contract manufacturers keep us sharp; they push us for more information, deeper analysis, and tested assurances on new use cases. If a project needs a subtle adjustment—such as crystalline form, particle size, or hydration—our team can actually make it, not just source it elsewhere.
Our commitment extends beyond filling orders. Workshops, on-site visits, and technical bulletins keep users informed about best practice in storage, transfer, and handling. Sharing what we’ve learned through years of direct experience shortens the learning curve for customers ramping up new processes. Customers who join our collaborative webinars or request on-site demonstrations often walk away with practical pointers that get applied right away at the bench or plant level.
Direct feedback loops between manufacturing and user mean that small wins—such as tighter sieve cuts, lower solvent carryover, or faster reaction onset—move from one sector to another. This culture fosters straightforward, evidence-backed improvements that benefit buyers, researchers, and downstream innovators. By maintaining a focus on fact-driven, shared knowledge, we keep quality high and problem-solving sharp, making 2,3,5,6-Tetramethyliodobenzene not just another catalog chemical, but a partner in advanced synthesis.
Great chemistry relies less on glossy brochures and more on everyday habits—testing, observing, fixing, and repeating. Every lot of 2,3,5,6-Tetramethyliodobenzene brought through our plant is a direct result of this mindset. We invest in process controls, personnel training, and ongoing analytics, knowing full well that users stake their own success on our material’s performance. Small differences in input often echo through every downstream step, and we aim to keep those differences positive. Standing as a hands-on manufacturer, we see both the science and the reality on the floor: progress comes from steady refinement, honest reporting, and shared commitment to better results. For those searching for a dependable, high-purity iodoarene—on scale or in the lab—we’re ready to support your next step.