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HS Code |
332532 |
| Chemical Name | 2,4,6-Triiodophenol |
| Cas Number | 609-23-4 |
| Molecular Formula | C6H3I3O |
| Molecular Weight | 499.80 g/mol |
| Appearance | Light yellow to brown solid |
| Melting Point | 155-160 °C |
| Solubility In Water | Slightly soluble |
| Density | 3.13 g/cm³ |
| Pka | 7.3 (for the phenolic hydrogen) |
| Synonyms | Phenol, 2,4,6-triiodo- |
| Storage Conditions | Store in a cool, dry, well-ventilated place |
As an accredited 2,4,6-Triiodophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 10 grams of 2,4,6-Triiodophenol, labeled with safety warnings, chemical name, CAS number, and hazard pictograms. |
| Shipping | 2,4,6-Triiodophenol should be shipped in tightly sealed, chemically resistant containers, protected from light, moisture, and physical damage. Package should comply with local and international regulations for hazardous chemicals. Ensure correct labeling, include safety data sheets, and handle with proper protective equipment to prevent exposure or contamination during transportation. |
| Storage | 2,4,6-Triiodophenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from light. Avoid exposure to moisture and incompatible substances such as strong oxidizers. Store at room temperature and ensure containers are properly labeled. Handle with appropriate personal protective equipment, and prevent release into the environment. Keep out of reach of unauthorized personnel. |
Applications of 2,4,6-Triiodophenol in Industrial ManufacturingAs a direct manufacturer of 2,4,6-Triiodophenol, we supply this specialty compound to critical sectors requiring precision halogenation for advanced formulations. The following scenarios reflect established, large-volume downstream uses, each segment governed by industry-specific compliance systems and processing practices to ensure quality and functional outcomes. 1. X-Ray Contrast Agent Intermediate SynthesisProducers of iodine-based X-ray contrast media rely on 2,4,6-Triiodophenol as a high-purity halogenated phenol source for constructing core molecular structures of non-ionic and ionic contrast agents. Accurate addition and monitoring through GMP-compliant lines supports stringent batch quality and impurity control during multi-stage pharmaceutical synthesis, ensuring safe diagnostics for end users in medical imaging. Industry compliance standards
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2. Radiopaque Polymer ManufacturingCompounders using engineering plastics for medical and dental devices incorporate 2,4,6-Triiodophenol to achieve precise radiopacity. This additive introduces high atomic number elements during melt blending or reactive extrusion, enhancing device visibility under X-ray while maintaining polymer matrix performance. Strict documentation ensures traceability through device registration processes across regulated markets. Industry compliance standards
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3. Chemical Research Reagent Production2,4,6-Triiodophenol serves as an anchor material for specialized research reagents, including radioiodinated tracers, halogenated reference standards, and analytical calibration compounds. Research chemical manufacturers control incoming purity and batch-to-batch consistency per laboratory standard requirements, supplying certified material to pharmaceutical R&D and analytical labs worldwide. Industry compliance standards
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4. Reactive Building Block for Halogenated Agrochemical SynthesisProducers of select herbicide and fungicide actives employ 2,4,6-Triiodophenol as a controlled iodine donor and aromatic substrate, facilitating the construction of high-performance halogenated crop protection molecules. This enables efficient downstream formation of target ring systems and active ingredients subjected to agrochemical regulatory review, supporting modern, regulated agriculture. Industry compliance standards
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Starting with raw phenol under meticulous conditions, our facility controls every step of the triiodination reaction to bring out pure 2,4,6-Triiodophenol with minimal impurities. We set batch consistency as a principle, never cutting corners with temperature regulation, reaction timing, or post-synthesis purification. Over the years we’ve seen how small fluctuations in process variables—not just feedstocks, but the smallest details of catalyst handling—translate to significant changes in analytical purity and yield. Achieving a steady high content of the desired isomer pays dividends for repeatability in downstream chemical syntheses and reduces waste at the purification stage.
A defining feature from our plant is our ongoing commitment to traceability. With each lot, our lab provides a comprehensive test report for iodine content, melting point, moisture, and residual organic impurities. A decade ago, analytical results ranged more widely across production sites. Today, the margin seldom tips beyond established reference values. From an industry standpoint, this shift reflects broader improvements in manufacturing, but for us it’s a testament to the checks and sharpshooting we deploy inside the process.
Through direct collaboration with researchers and industry partners, we’ve learned how crucial specification integrity has become, especially for advanced material R&D or radiolabeling chemistry where side-products may compromise the entire process. Other triiodinated phenols may show up as minor by-products, but our build targets low isomeric impurity, because that consistency means reproducibility in downstream reactions.
Quality matters to project outcomes, so every technical grade of 2,4,6-Triiodophenol we offer achieves a strict target of >99% purity by HPLC or GC, depending on client requirements. Final melting point hovers in the expected range for the crystalline solid, and we confirm final product matches spectral profiles based on NMR and mass spectrometry, not solely on titration data. Our physical product is always a free-flowing powder or crystalline solid, dependent on storage humidity. Long discussions with academic and industrial users taught us that even a small variability in free iodine content or presence of dibromo impurities can cause analytical headaches. So we double down on endpoints, like Karl Fischer moisture and loss on drying, because details like these turn up later in solubility and formulation steps.
Specifications run deeper than laboratory numbers. We pursue consistency from drum to drum, pallet to pallet. Our QC sampling runs across multiple points of each batch rather than just a surface scoop. We found early on that uneven cooling in large batch reactors can leave “hot spots” of impurity—so we worked directly with our engineering lead to redesign reactor geometry and add dynamic mixing. Post-synthesis, our washing and drying lines focus on removing trace halides, because such residues can easily introduce unwanted side reactions or color instability in analytical-grade downstream work. With every cycle, the process gains another notch of reliability.
2,4,6-Triiodophenol stands apart in the halogenated phenol family because the three large iodine atoms alter both steric and electronic properties in ways small lab-bench changes can’t mimic. Many processes that can substitute chloro or bromo derivatives find themselves at roadblocks when they try to swap in triiodinated alternatives. Our clients report that substitution patterns make or break coupling yields. Iodine atoms not only serve as excellent leaving groups, but their electron-withdrawing nature also modulates the phenol reactivity for directed ortho-metalation or cross-coupling strategies—a tactic common in designing radio-iodinated tracers or pharmaceuticals with high target specificity.
Over years of close contact with the fine chemical sector and academic teams, we’ve noticed requests for triiodinated compounds growing steadily, largely because alternative halogenations—chlorine and bromine—lack the same mass or radiopacity. Medical diagnostics, especially X-ray imaging and radiotracer fields, lean heavily on the high atomic number of iodine and its effect on electron density. With 2,4,6-Triiodophenol, researchers can build scaffolds where they use the phenolic ring both as a handle for further functionalization and as a mass booster in radiology applications. Our team keeps detailed feedback loops with these users so the purity and appearance standards anticipate their fine tuning at the synthesis and formulation level.
Our time working with partners in diagnostics and contrast agent synthesis showed how much product color, flow, and cleanliness matter upstream of an actual experiment. We’ve seen orders rejected elsewhere for tiny traces of tar or sticky residues, even when papers report “visual purity.” On our end, the plant team focuses on removing not just visible contaminants but trace moisture, because excess water or dissolving byproducts can haze the final product or degrade long-term stability. By rotating stock, vacuum-sealing drums, and tracking shipment conditions, we keep actual shelf performance in line with lab results—not just at day of packaging, but months down the line.
Batch after batch, we work with teams synthesizing labeled radiotracers by introducing 125I or 131I onto the phenol. Here, even a small amount of the non-iodinated or partially brominated phenols impacts radiochemical yield, requiring extra purification. By adjusting feedstock ratios and refining iodination time, we reduced these by-products often overlooked in standard protocols. This experience—gained from both customer reports and in-plant troubleshooting—shapes the procedural updates we make to keep the triiodo content high and the off-target halides below reporting limits. Researchers, in turn, avoid headaches downstream in their separation and activity measurement steps.
Development in specialty polymers leans on our triiodinated phenol, too. The tri-iodine backbone tunes refractive index and mass loading—factors critical in advanced optics and high-density plastics. Whether the user case is a dye precursor, a pharmaceutical intermediate, or a reference compound in mass spectrometry, clean 2,4,6-Triiodophenol underpins successful outcomes. Over the years, project feedback circled back to us, highlighting unexpected performance boosts just from the higher lot-to-lot consistency. The manufacturing team takes these outcomes as benchmarks, adjusting in-line monitors and batch timing to lock repeatability at scale.
We know how easily halogenated phenols absorb moisture or discolor if left in contact with air. Each drum is filled at strictly controlled humidity, packed under nitrogen, and sealed not just for aesthetics but to prevent product shifts that affect long-term reliability. Plant safety protocols—archived, reviewed, and updated—came from direct experiences: once a minor leak produced delays, we overhauled everything from packing floor layout to venting arrangements. That learning curve now underwrites a robust, safe workflow that delivers clean product and minimizes nuisance dust or residue that could cause batch contamination.
Sustainability sits at the heart of all process changes we make. By optimizing recycle loops for iodine recovery, we cut chemical consumption in half compared to historical bench protocols. Every effort goes into reducing raw material waste and decreasing treatment requirements for secondary effluent. We see waste-handing not just as a compliance measure but as a direct performance metric for the plant. Fewer off-spec batches mean less landfill waste. Our solvent recovery rate has increased, leading to cleaner process water output and lower overall environmental footprint. We invest heavily in these cycles, knowing that as our feedstock sourcing tightens upstream, efficient resource use will define our long-term competitiveness.
Over the past decade, we formed dialogue with academic partners across chemistry, biology, and materials science. This process led to iterative changes in our analyte reporting, packaging sizes, and supply chain logistics. Many projects fail in late-stage development due to a lack of reliable raw material. By supporting round-robin testing and joint lab trials, we ensure our product helps projects reach the finish line instead of becoming a variable in troubleshooting sessions.
Several international projects exploring novel contrast agents or new catalysis strategies chose our 2,4,6-Triiodophenol because the documentation package includes actual chromatograms from finished lots, not only batch-level averages that mask outliers. This transparency sets a clear bar for other fine chemical suppliers but also holds us accountable internally each production cycle. We encourage labs to match these details against their own reference standards, spot differences, and feedback so we can close any gaps quickly and precisely.
Procurement leaders reiterate, time and again, the importance of transparent origin and chain-of-custody data. Our site tracks every shipment from raw phenol intake through every mixing, heating, and QA sampling point. In the digital age, blockchain-enabled record keeping or simply tightly-monitored logbooks make the difference between delayed shipments and real competitive edge. By keeping processes open and learnings shareable, we help the industry as a whole raise its bar—while still leading from inside our own plant’s practice.
Direct contact with labs using our triiodinated phenol opens up new perspectives on process design. Sometime ago, a user reported unexpected discoloration during phenol activation; together we traced it to an exotic stabilizer that interacted with residue from our drying phase. This led us to adjust our DPPS (dry product protection scheme) in-house. It’s these lessons—scattered throughout regular orders, troubleshooting calls, and site visits—that let us stay ahead of field needs. Our formula shifts with real-world user requirements, not just our own plant’s schedule.
We work closely with major pharmaceutical innovators who use 2,4,6-Triiodophenol as a starting material for targeted iodination of active drug candidates. Human or veterinary, these products demand the absence of trace transition metals or oxidative residues. Several trials forced us to rethink filtration media mid-production, shifting from common organic filters to specialized ceramic beds that trap even trace colloidal contaminants. Every so often we overhaul a portion of the plant process in response to results shared by user QC labs. This push-pull working style builds trust and drives shared improvement, rather than one-sided delivery.
Lithium-ion battery research groups also flagged the potential of iodine-dense phenolics to enhance charge carrier transport within certain electrolyte formulations. Their feedback pointed out residue issues not in textbooks—so we coordinated a separate production campaign with altered wash cycles and air-exclusion procedures. Meeting niche application needs only comes from a flexible blend of process size, QA rigor, and collaborative feedback, something our team commits to with each client order.
The landscape for 2,4,6-Triiodophenol continues to evolve. As pharmaceutical and materials manufacturers reach for heavier halogenated phenols to create new molecules, higher standards for purity, traceability, and documentation follow. We’ve moved beyond thinking of our product merely as a batch output. It’s now part laboratory tool, part competitive edge. New uses for triiodinated phenols, like smart polymers or next-gen radiolabeled compounds, require not just purity, but proven absence of interfering background chemistries. Where decades ago the market treated such fine chemicals as commodity goods, today the buyers demand documented, batch-level quality control across every shipment.
Our future focus stays tied to feedback from the field. Each client and project brings a new challenge. From requests to tune the hue of a final product, to new analytical techniques that reveal previously hidden process drifts, the lessons we gather drive continuous improvement. We track not just analytical data, but packaging performance and handling ease, listening to logistical partners and laboratory users alike. As the regulatory bar rises and industry consolidates around trusted supply partners, we set our course by the real needs of those who deploy our material at the sharp end of research, commercialization, and innovation.
As a chemical manufacturer rooted in decades of hands-on synthesis and QA, we see 2,4,6-Triiodophenol as both a challenge and an opportunity. Every batch is a reflection of the relentless pursuit of purity and practical usability. From targeted molecule construction to specialty polymer development, the demands never stand still. Our approach blends technical rigor with real-world adaptability, bringing together in-plant expertise, close customer partnerships, and a willingness to rethink core steps. By keeping relationships transparent and supply chains accountable, we help build both confidence in the research bench and reliability in commercial use. The story of every drum we ship is really the story of learning, feedback, and shared industry progress—a story we keep writing daily, side by side with those shaping tomorrow’s breakthroughs.