|
HS Code |
772677 |
| Chemical Name | 4-Iodo-2,6-Xylenol |
| Cas Number | 2970-96-1 |
| Molecular Formula | C8H9IO |
| Molecular Weight | 248.06 g/mol |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 109-112°C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Synonyms | 4-Iodo-2,6-dimethylphenol |
| Structural Formula | IC6H2(CH3)2OH |
| Smiles | CC1=CC(=C(C=C1I)C)O |
As an accredited 4-Iodo-2,6-Xylenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, tightly sealed with tamper-evident cap, hazard labeling, product name, and lot number clearly displayed. |
| Shipping | Shipping for 4-Iodo-2,6-Xylenol requires secure, leak-proof containers, labeled according to hazardous material regulations. Store and transport in cool, dry conditions, away from incompatible substances and ignition sources. Ensure all documentation complies with local, national, and international regulations, including correct UN number and hazard class. Trained personnel should handle transport. |
| Storage | 4-Iodo-2,6-xylenol 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. Protect from light and moisture. Ensure appropriate labeling and store away from heat sources and ignition. Use secondary containment if possible to prevent spills or leaks. |
Competitive 4-Iodo-2,6-Xylenol prices that fit your budget—flexible terms and customized quotes for every order.
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In the world of specialized chemical building blocks, 4-Iodo-2,6-Xylenol stands out for its versatility and reliability. On our manufacturing floor, batches of this compound take shape each week under rigorous conditions. Anyone who has handled halogenated phenols knows that they’re not created equal. Our teams invest in the careful orchestration of each production step, working from years of real-world experience and taking hundreds of small variables into account. A molecule like 4-Iodo-2,6-Xylenol demands that kind of hands-on approach if it’s going to serve the demanding needs of its users.
Our commercially available 4-Iodo-2,6-Xylenol keeps to a model based on a tightly regulated purity threshold, usually 99% minimum by gas chromatography. Each lot we produce is traceable, batch-coded, and cross-referenced with its spectra—typically NMR and mass spec validated. Physical details can sometimes distract from what users really need to know, so let’s focus on the aspects that impact daily work in synthesis and applied research.
This compound forms needlelike crystals under ambient conditions and, like other aromatic iodides, its iodine substitution adds a degree of chemical tunability. Compared with multinuclear substituted xylenol derivatives, the single-position iodination on the para ring creates predictable reactivity. We’ve found that a melting point in the range of 127–130°C reflects good process control. Color and odor are easily monitored, but ultimately, it’s the confirmed structure and absence of contaminants—particularly residual solvents and byproducts—that let this product perform reliably at the bench.
What defines this compound isn’t just its molecular identity but how it behaves in the hands of chemists, engineers, and technicians. Many customers turn to 4-Iodo-2,6-Xylenol as a core intermediate when they want to introduce iodine into more complex structures. Our direct conversations with downstream users—especially those synthesizing active pharmaceutical ingredients or specialized catalysts—show us where strengths and pain points exist.
Unlike generic xylenols, this product resists oxidation under typical storage and transport because the bulky iodine atom blocks reactive sites. That makes shelf stability less of a worry for production teams under pressure. Iodinated aromatics sometimes trigger concerns about trace metal or halide contamination, but strict raw material screening and facility design mean our analysts keep such issues under tight control. On the flip side, customers often ask about how this iodinated xylenol compares to more commonly used bromo- or chloro-analogues.
The heavier iodine atom offers a smoother route to certain palladium- or copper-catalyzed cross-couplings. You need less forcing conditions compared to chloro-xylenol, which keeps downstream byproduct generation lower and improves yield. For phenol functionalization, the reactivity shift can make or break a synthesis. In practical terms, the aryl-iodide bond can cleave efficiently under mild conditions, and in our hands this has trimmed cycle times for sp2–sp2 bond formations. Researchers needing to avoid harsh bases or temperatures, perhaps to accommodate sensitive ligands or sidechains, have flagged this as a key reason for making the switch.
Here in our plant, practical decisions impact how 4-Iodo-2,6-Xylenol reaches the user. We’ve seen that even subtle shifts in packaging can affect workability: our customers in fine chemicals and pharma want dust-free dispensing and packaging inerted under nitrogen. The compound can discolor if exposed to strong light or open oxygen, so opaque liners and secure seals matter. Centrifuge-dried material rather than standard oven-drying gives a product with reproducible handling characteristics whether you're weighing milligrams or setting up a 50-liter batch.
Feedback loops with end users have led to adjustments in our crystallization protocols. For example, certain solvent combinations keep clumping at bay, allowing easier transfer without loss. Small details such as anti-static steps get mentioned too seldom in generic write-ups but make a concrete difference for those at the production line or lab bench. Our QA team maintains strict cross-checks with every lot; if a shipment runs outside established performance norms, we’ll spot it before you do.
Direct experience with closely related products teaches plenty about fit-for-purpose selection. Take 4-Chloro-2,6-Xylenol and 4-Bromo-2,6-Xylenol—in-house, we run head-to-head reactivity trials and side-by-side yield studies. Chlorinated versions bring cost advantages and sometimes better solubility in weaker polar solvents, but users pay a price in reactivity. The aryl chloride bond holds up to much tougher conditions, which is fine for some industrial settings but wastes time and materials when higher turnover is possible with the iodo analog. Bromo-xylenol evens out the cost-reactivity curve but doesn’t reach the same cross-coupling performance.
Another point of difference: iodinated compounds like this draw regulatory scrutiny, particularly in pharma and crop protection sectors. Our decades of audit experience reflect the fact that you need clear provenance for iodine sources and must track possible radioisotope contamination, even if not immediately relevant for routine synthesis. 4-Iodo-2,6-Xylenol produced at our facilities clears these hurdles each time, backed by full documentation to keep compliance managers at ease.
Every batch signed off by our technical team passes through not just routine purity checks, but also specialized analysis for trace impurities and byproducts. Anyone who has seen the headache caused by even a fraction of a percent of ortho- or meta-isomers in a reaction will know that such details matter. We routinely dig deeper than just HPLC and GC—our QC labs cross-check with FTIR and elemental analysis, pooling experience from years of support for high-temperature, high-pressure, and scale-up settings.
It’s worth sharing that the iodine handled in this environment—volatile by nature—demands strict stage separation and air handling. Neglecting such details can impact product quality or run the risk of unwanted residuals that can poison downstream catalysts. The care we take on the manufacturing side directly shields users from these headaches.
Many of our regular buyers are synthetic chemists and scale-up engineers—people who want to shave hours from projects and cut down on rework. Over years of regular supply to these labs, we hear directly what works and what slows things down. The opportunity with 4-Iodo-2,6-Xylenol is the combination of high reactivity with robust storage and transport properties. Users bring up yield improvement in many classic Suzuki and Buchwald–Hartwig coupling reactions. The more accessible leaving group makes a real difference for catalyst turnover frequency and overall throughput.
Feedback sometimes brings up solubility in certain nonpolar solvents—here, our teams have tested modifications in particle size distribution to support smoother dissolution and dispersion. The best results often come with a trade-off between flowability and dusting, so adjustments happen batch by batch, ultimately based on user preference and end-use requirements. No “off the shelf” standard ever truly matches the demands of complex process schemes, so we keep that line of communication open.
Iodinated aromatics draw price pressure from both raw material swings and regulation. Over the years, we’ve invested in upstream supply security, qualifying multiple iodine sources and locking in contingency protocols for production interruptions. Scale matters too; although lab quantities can sometimes be packed off in a single shift, custom projects or multi-metric ton lots demand a different approach. Our plant scheduling team balances engineering constraints against customer timing—rush orders for 4-Iodo-2,6-Xylenol aren’t rare, especially as end-users scale up pilot processes.
Questions about supply risk aren’t just academic either. Freight security, packaging stability under extreme climates, and rapid analytical turnaround for lot acceptance keep the links in a lean and secure supply chain. We cross-train shipping staff on both chemical handling and basic analytical procedures. This doesn’t just prevent mix-ups; it means exceptions or anomalies get flagged and addressed fast, even outside the QA office. Projects succeed or fail at the margin, so even seemingly minor shipping bugs receive full attention.
Experience handling halogenated phenols like 4-Iodo-2,6-Xylenol sets a certain standard for health and safety. Our operators and product handlers work in local exhaust systems with dedicated PPE routines, not as an afterthought but as the only way to keep exposure low and avoid cumulative skin or respiratory contact. Packaging reflects this too, with robust outer drums, tamper-evidence, and spill-mitigation features.
On the environmental side, iodine can pose legacy challenges if waste handling shortcuts occur. Our solvent recovery and recycling teams manage mother liquors with strict segregation, using both in-house and third-party audit paths. Product residues are tracked so downstream users receive clear waste coding and advice for compliant disposal—another practical, and not just theoretical, responsibility. The plant teams understand that end-of-life stewardship starts with the choices made at the primary production step.
Most of what we’ve learned about 4-Iodo-2,6-Xylenol has come from engagement with colleagues and customers in labs, factories, and sometimes at the point of a production bottleneck. Each time a partner reaches out with a process snag, our technical and production groups circle around the problem—sometimes leading to new crystallization tweaks, sometimes they spark a rethink on packaging or QA hold-points.
Because this compound serves both as a starting material and, occasionally, as a reference standard, the feedback loop is active and ongoing. Project needs keep shifting. A customer one week might want solvent-free micronized grades; the next, they ask for raw spectra to confirm identity on their own instruments. We approach every order as a direct collaboration, not just a transaction. This day-to-day partnership keeps both our products and our thinking sharp.
Selection often comes down to understanding the final target and the capabilities of available intermediates. Chemists eyeing an efficient route to biaryl motifs often find 4-Iodo-2,6-Xylenol gives them a strategic edge. The iodine’s increased leaving ability saves both time and auxiliary additives in cross-coupling protocols, and the lower byproduct levels translate to easier downstream purification.
Compared with less reactive derivatives, this compound lets users condense multi-pot transformations and streamline batch-to-batch reproducibility. For those scaling up, the differential in energy consumption between iodo- and chloro-couplings becomes significant over many runs. Anecdotes from manufacturing teams confirm that even a modest boost in conversion rate compounds benefits across hundreds of liters of throughput.
Our business faces new questions every year: shifting regulatory requirements, sustainability mandates, evolving synthetic routes. The appetite for high-purity aryl iodides is rising, driven by demands in both advanced materials and pharmaceutical research. Our R&D and process engineering units keep testing greener and safer synthetic approaches. Already, newer oxidation systems and solvent cycles have trimmed energy use and waste, though without the glossy claims sometimes seen elsewhere.
We’re always in search of more efficient and sustainable pathways, not only for compliance, but also for cost control that we can pass on to customers. Staff training and process safety investments will always be non-negotiable, based on the hard lessons learned over many years. If product developments point the way to safer, cleaner, or more robust handling, we’re ready to adapt—because the trust our partners place in us depends on it.
Third-party commentary can sometimes gloss over the realities of specialized compound manufacture. For 4-Iodo-2,6-Xylenol, practical wisdom accumulates on the plant floor and in the QA lab, not just behind a desk. Every parameter, from sourcing to storage, enters into the equation that ultimately impacts a customer’s bottom line. Our experience shows that no two applications or process schemes are really alike; the detailed feedback we gather from direct users keeps us ahead of inefficiencies and close to where innovation happens.
At the end of the day, the value in this high-purity iodo-xylenol flows from constant improvement, active listening, and solutions built on both scientific diligence and hands-on experience. We look forward to supporting our partners—old and new—as they take on the next generation of synthetic and process challenges.