|
HS Code |
598452 |
| Productname | 3-Methyl-4-Iodophenol |
| Casnumber | 183416-41-1 |
| Molecularformula | C7H7IO |
| Molecularweight | 234.04 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 95-99°C |
| Boilingpoint | 340.2°C at 760 mmHg |
| Density | 1.899 g/cm3 |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥ 98% |
| Smiles | CC1=C(C=CC(=C1)I)O |
As an accredited 3-Methyl-4-Iodophenol 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 3-Methyl-4-Iodophenol, securely sealed, with hazard warnings and chemical identification label. |
| Shipping | **Shipping for 3-Methyl-4-Iodophenol:** This chemical is shipped in sealed, inert containers to prevent contamination and degradation. It is packaged according to hazardous materials regulations, with appropriate labeling for safe handling. During transit, temperature and humidity controls are maintained, and all shipping complies with local and international chemical transport guidelines. |
| Storage | 3-Methyl-4-Iodophenol 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 materials such as strong oxidizers and bases. Ensure the storage area is clearly labeled and accessible only to trained personnel. Use secondary containment to prevent accidental spillage or environmental release. |
Competitive 3-Methyl-4-Iodophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Speaking as a manufacturer, not only from a position of technical know-how but with the reality of day-in, day-out hands-on production, I can say that 3-Methyl-4-Iodophenol stands out in the world of specialty chemical intermediates. Unlike its simpler cousins in the phenol family, this compound brings together both a methyl and an iodine substituent on a phenolic core—a detail that makes all the difference for researchers and process chemists working at the cutting edge.
Demand for this chemical comes from a mix of pharmaceutical developers, crop protection innovators, and vendors in the advanced materials field. There are good reasons for this, and these come down to the chemistry, the performance in synthesis, and the reliability we’ve built into the manufacturing workflow.
Our 3-Methyl-4-Iodophenol comes in a high-purity crystalline form. Most batches exceed the standard 98% threshold by HPLC, targeting impurities well below the limits required by downstream applications. Over the years, we’ve received feedback from analytical chemists who count on the product’s clarity in their assays as a critical factor for reproducibility. During the scale-up of any innovative drug or agrochemical, dirty or inconsistent intermediates add months to development timelines. We recognized this problem early, so our production and QC teams run materials through multiple purification stages—a step not every company is willing to do because it affects throughput and cost. This process delivers material that behaves consistently, no matter if a client orders 100 grams or several kilograms.
Melting point and texture matter just as much as chemical analysis when clients move to pilot or production scale. Variations in particle-size and grind can slow reactions or complicate dissolution. In our experience, controlling these factors helps avoid surprises in flow chemistry setups or chromatography runs. We package the compound under inert atmosphere for reliable shelf-life and ease of handling, addressing concerns about iodine loss or phenolic discoloration, especially for international shipments.
Many might ask, why combine both methyl and iodo groups at those precise positions? It’s not just academic. The methyl group, sitting adjacent to the oxygen atom, introduces electronic and steric effects that can steer subsequent substitution chemistry in useful directions. The iodine atom—one of the most useful leaving groups in aromatic chemistry—opens the door for a whole toolkit of transition metal-catalyzed couplings, including Suzuki, Sonogashira, and Buchwald-Hartwig reactions. These are not theoretical advantages: our clients routinely report that this intermediate increases hit rates in compound library generation, especially where selective and high-yielding transformations are key.
Comparing with 4-iodophenol, a close but less tailored relative, the methylated variant displays better solubility profiles in non-polar solvents and a tendency toward superior handling characteristics. Some have mentioned fewer issues with caking or clumping in the lab stockroom. The subtle shift from 2-position to 3-position on the methyl group also delivers less interference in typical coupling chemistry, based on our internal data from pilot projects and partners' feedback.
Our team has seen requests for this intermediate grow alongside the surge of structure-activity relationship studies and high-throughput synthetic efforts. Over years—sometimes after discussions with process chemists at the bench—we have adapted our methodologies to eliminate batch-to-batch variability. The most common bottleneck occurs due to residual inorganic iodide or hydroquinone isomers, both notorious for ruining reaction selectivity down the line. We faced tough lessons scaling from 1-gram to multi-kilo lots, so today, our reactors, distillation trains, and isolation suites follow protocols that reflect those hard-won lessons.
In the rare event of a product complaint, most issues come from storage or atypical use conditions rather than from process errors. We rarely see returns, and when they do occur, we treat each instance as an opportunity for improvement. The materials science behind iodinated aromatics carries inherent risk for degradation or color shifts if exposed to light, heat, or trace moisture. Despite aggressive packaging, clear storage guidance on the label, and temperature-controlled shipping, a few surprises pop up in real-world environments. It has spurred us to create a support process that does not push problems back onto the customer; instead, we help troubleshoot methods, and frequently, design custom batch sublots if needed.
Pharmaceutical research teams put this intermediate to work as a key scaffold for synthesizing kinase inhibitors, hormone analogs, and several other targeted small molecules. In-house studies and customer reports have shown solid yields in palladium-catalyzed functionalizations, particularly during late-stage diversification where high selectivity matters. The phenol group helps anchor protecting groups or linkers for combinatorial synthesis, and further derivatization at the iodine site enables a broad range of drug-like molecules.
Agricultural chemistry represents another growing application. Many crop-protection libraries now build on platforms derived directly from this phenolic structure. The methyl group improves lipophilicity and, in our experience, often enhances field performance of the final product. Especially where precise structure-activity discrimination is needed, this molecule’s unique substitution pattern offers real advantages.
Some clients in polymers and advanced materials use this compound as a monomer precursor, particularly where custom linkers or aromatic spacers are required. The reactivity of the iodide allows them to build backbone connectivity with high precision—something more difficult to achieve with chlorinated or brominated analogs that often lag in reaction efficiency.
Experience has shown that halogenated aromatics aren’t all equal in lab or plant settings. Our production lines once handled comparable quantities of bromo or chloro derivatives before the market shifted toward iodides, drawn by faster kinetics and less harsh conditions in coupling reactions. The heavy atom effect of the iodine also opens up routes in radio-labeling, especially for rapid PET tracer synthesis in diagnostic research. This methyl-iodo combination has proved resistant to side-reactions common to the family, providing a cleaner reaction profile and less byproduct contamination.
Users who are accustomed to 4-iodophenol or 3,5-dimethylphenol will spot both structural and handling differences. The interplay between the ortho-methyl and para-iodo locants delivers greater regioselectivity in directed ortho metalation and palladium catalysis. We have also tracked improved crystallization behavior during process scale-up, which makes the downstream handling—from filtration to drying—far less fraught with loss or operator error. These sorts of manufacturing minutiae form the core value-add, though you rarely see them listed in data sheets or sales literature.
Problems do crop up in this chemistry space, usually traceable to the iodine’s lability under harsh base or extended exposure to sunlight. Chemists running scale-up batches at remote sites have sometimes reported drop-off in yields or unexplained off-colors. Our technical support often consults on process tweaks: replacing open-glass transfers with amber flasks, dropping batch temperatures, or adding scavenger resins. A lot of progress comes through old-fashioned dialogue between manufacturer and lab—finding the middle ground between pure theoretical optimization and practical daily routines.
Not every manufacturing plant is equipped to produce iodinated intermediates safely and at scale. Our facilities underwent upgrades to dedicated containment and waste handling units after an uptick in volume requests. Iodine recovery, a significant cost and compliance issue, receives substantial attention: spent process streams now route through iodine-specific traps and regeneration cycles, cutting raw iodine replenishment by more than half over several years. These upgrades required significant capital investment, but made a measurable difference—not just for operating cost, but for sustainable practices. Expensive halogenated intermediates draw regulatory scrutiny, and as producers, we bear the responsibility for safe, legal, and traceable outputs.
Disposal of waste water or solvent extractions once carried higher risk of trace halide residue. Now, in-plant monitoring addresses issues before outfalls ever approach contract limits, and feedback from community audits has reinforced the importance of transparency. One of the often-overlooked challenges faced in manufacturing isn’t technical but public: every operational step draws on community trust, regulatory insight, and a dedication to continual process audit. The chemical itself might be the focus, but the process reliability surrounding it—waste management, energy management, raw material sourcing—differentiates specialists from commodity suppliers.
A recurring question from scale-up clients centers on batch reliability from gram to multiple kilogram quantities. Many have run headlong into changes in impurity profile, particle morphology, or bulk handling as they cross these boundaries with compounds from other vendors. Our experience—built up from repeated multi-step campaigns—shows that each stage, from raw iodine metal purchase to final purification, alters the outcome in large and sometimes unexpected ways. Process transfer from laboratory glassware to full-scale reactors means furnace temperatures, agitation profiles, and solvent substitution must be empirically validated, not just extrapolated from small-scale experiments.
We often encounter requests for custom pack sizes, alternative solvents, or different packaging types. Sometimes it’s to fit unique automation lines; sometimes, the goal is to reduce re-packaging and potential contamination. For some clients, product arrives in pre-weighed PTFE vials with nitrogen overlay to preserve integrity over long-term storage. Others prefer standard amber glass, triple-bagged for extra moisture control. We tailor these steps not as novelty but based on specific failure modes observed in the field—an example of how close listening to actual lab and plant concerns shapes the manufacturing approach.
Every innovation brings challenges, and 3-Methyl-4-Iodophenol sits squarely in the sights of both technical and logistical roadblocks. Price volatility for elemental iodine in the global market brings uncertainty, so supply chain continuity goes hand-in-hand with quality. Material once sourced from unreliable brokers now comes straight from rigorously vetted suppliers, with full traceability to source, as lessons from past disruptions taught us that even the smallest contamination or substitution can ripple through production runs.
Another common hazard in iodinated chemistries comes from thermal and oxidative degradation—not just during storage, but during synthetic transformations. The thermal mass and batch cycling in jacketed vessels or rotating evaporators must be checked and recalibrated frequently, as small differences in equipment can mean big swings in batch reproducibility. The wisest approach has always been to build in test runs, re-validate specifications, and welcome on-site technical audits from our largest clients. This level of engagement often solves problems before they reach the customer.
Within the plant, cross-contamination with other halogenated lines has been a key focus. Switching reactor trains between chlorinated and iodinated runs can introduce unwanted side products unless cleaning protocols go above ordinary standards. Our approach now separates these workflows entirely, reinforced by real-time analytics and stepwise cleaning validation—choices shaped not by checklists but by experience with costly failed runs. Documentation and open communication among operations, quality, and logistics teams have become standard, providing transparency and accountability at every stage.
Sometimes the value of a product comes down not to what it is, but how it is made and who stands behind it. We’ve learned that customers rarely care just about purity numbers—they want reliability, technical backup, problem-solving, and the confidence that a partner can adapt to new needs. Many staff in our technical support hold decades of hands-on chemistry experience. This isn’t just marketing speak; it translates into real support when a process goes sideways, when a delivery is needed fast, or when a large-scale experiment uncovers new handling realities. We believe in accountability and quality that lives up to what’s promised—not what can be glossed over in a data sheet.
At its core, the difference between 3-Methyl-4-Iodophenol and related products from general traders is the control over the process and outcome. As actual makers, we insist on traceability back to the kilogram, batch-level analytics, and customer-directed process tweaks based on honest feedback. The capacity to adapt—whether it is shipping a new solvent system, meeting a last-minute purity upgrade, or resolving an off-nominal storage event—has been earned at the cost of many late nights and hands-on troubleshooting, not just theoretical expertise.
Our roadmap remains rooted in listening closely to the chemistry community and evolving our practices as new demands arise. Whether the challenge is scale, regulatory scrutiny, novel applications, or extreme handling requirements, the feedback loop with customers across research and industry keeps the standard high. 3-Methyl-4-Iodophenol continues to play a unique part for those on the frontier of synthesis—and for our part, we take pride in delivering a product that isn’t just another reagent, but a carefully engineered building block, trusted and proven in real-world chemical applications.