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HS Code |
488937 |
| Iupac Name | 2,6-Diiodo-4-nitrophenol |
| Molecular Formula | C6H3I2NO3 |
| Molecular Weight | 420.90 g/mol |
| Cas Number | 700-72-7 |
| Appearance | Yellow solid |
| Melting Point | 198-202°C |
| Solubility In Water | Slightly soluble |
| Smiles | c1c(I)cc([N+](=O)[O-])c(I)c1O |
| Pubchem Cid | 230437 |
| Synonyms | 4-Nitro-2,6-diiodophenol |
| Ec Number | 615-313-0 |
As an accredited 2,6-Diiodo-4-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g quantity, white screw cap, hazard labels, clear chemical name, and CAS number, securely shrink-wrapped. |
| Shipping | 2,6-Diiodo-4-Nitrophenol is shipped in tightly sealed, chemically resistant containers to prevent moisture and light exposure. It is labeled according to hazardous materials regulations due to its toxic and environmental risks. Shipping complies with local and international guidelines for dangerous goods, ensuring safe handling, storage, and transportation at controlled temperatures. |
| Storage | 2,6-Diiodo-4-nitrophenol should be stored in a tightly sealed container, protected from light, moisture, and incompatible materials such as strong reducing agents. Store at room temperature in a cool, dry, and well-ventilated area, away from heat and ignition sources. Properly label the container and ensure access is limited to trained personnel, complying with all applicable chemical storage guidelines. |
Applications of 2,6-Diiodo-4-Nitrophenol in Industrial ManufacturingAs a direct manufacturer, we supply 2,6-Diiodo-4-Nitrophenol to select industrial sectors where its chemical structure and reactivity meet precise downstream technical needs. Below, we outline its practical use cases across regulated specialty applications, detailing compliance prerequisites, typical formulation levels, how the material incorporates into production, and the main categories of finished goods produced by our clients. 1. X-ray Contrast Media Intermediate ManufacturingThis material serves a defined role as a halogenated building block during the synthesis of non-ionic iodinated X-ray contrast agents. Manufacturers incorporate it at a controlled stage to precisely introduce diiodophenol structures—essential for fine-tuning radiopacity and pharmacokinetics of the final contrast medium. Industry compliance standards
Typical usage ratio
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2. Specialty Antimicrobial Coating AdditiveSpecialty coatings producers add this compound to engineering polymers or resin matrices to impart stable, broad-spectrum antimicrobial surfaces. Its halogenated nitrophenol motif enhances activity against biofilm-forming microorganisms when embedded in high-contact surfaces for medical or food industry use. Industry compliance standards
Typical usage ratio
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3. Reference Substance in Analytical Reagent FormulationLaboratory reagent manufacturers use this material as a primary standard or reference spike for developing and validating detection protocols in trace halogenated phenol analysis. It provides a benchmark for method sensitivity and selectivity, specifically in industrial water and food contact material testing labs. Industry compliance standards
Typical usage ratio
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4. Intermediate for Organic Electronic Material SynthesisWithin the specialty electronics sector, integrators deploy this diiodo-nitrophenol derivative in the controlled synthesis of high-dielectric organic compounds, contributing to material precursors for photoresist and thin-film transistor (TFT) applications. Its halogen-rich structure supports the design of organoiodine compounds that tailor charge mobility or light absorption in finished electronic layers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Crafting 2,6-Diiodo-4-Nitrophenol is less about routine and more about control. Everything starts with the heart of its molecular structure, which demands meticulous handling throughout iodination and nitration. Each stage brings a series of checks, not only for purity but also for consistency in pale yellow to faint orange crystalline form. You can run thousands of grams, and the difference from earlier runs still jumps at you if you let the smallest variable slide. That is the lesson chemical manufacturing keeps teaching us. At our facility, the journey from precursor phenol to the finished product always revolves around controlling temperature, properly introducing iodine sources, and precisely timing the nitrating step. It’s never just about yield; it’s about crafting 2,6-Diiodo-4-Nitrophenol that holds up to analytical scrutiny every time we pile a batch on the drying rack.
What marks this compound out isn’t simply the two iodine atoms or the nitro group fixed on the ring. Synthetic chemists in research, pharmaceutical development, or specialty material labs like it because they know what to expect batch after batch—tight melting point, clean appearance, and strong assay results. Those benchmarks don’t come from reading catalogues or copying textbook procedures. They come after years of adjusting vacuum oven settings, checking crystal granularity, and checking what impurities seem to “ride along” during scale-up.
Anyone who walks the production floor knows some products head straight for high-importance projects. It’s not just another specialty phenol. The substitution pattern on 2,6-Diiodo-4-Nitrophenol unlocks precise coupling reactions and positions it as a preferred intermediate for certain agrochemical candidates and active pharmaceutical ingredients (APIs). Synthetic versatility, stemming from the iodine atoms, lets downstream processes forge new C-C and C-N bonds with more confidence in regioselectivity. Projects that target iodinated aromatic scaffolds—whether for contrast agents, dyes, or as molecular markers—see improved reliability when starting from a consistent supply.
Sourcing for this material often starts with one question: Will the physical and chemical specs hold up across procurement cycles? Chemists get frustrated working with off-color crystals, broad melting ranges, or ambiguous assay numbers. Manufacturing this molecule, we have learned to push for narrow melting points, clear, uniform granulation, and strict control over iodide, nitrite, and metal residuals. We’ve seen what happens to reaction kinetics and downstream product isolation when batch impurities slip through, so close monitoring of side-product profiles isn’t optional. Quality-driven output isn’t about chasing perfection but about removing surprises for anyone making those next-step intermediates or final products.
Our standard lot model covers production scales ranging from small multi-kilo R&D batches to larger custom orders. Purity by HPLC runs over 98% in every outgoing supply; results are anchored by NMR and GC-MS backing. Sometimes clients need tighter specs, down to trace-ion quantification, and we can deliver with proper lead time so that nothing in the lot profile interferes with analytical development. The crystalline material flows well in bench-top handling or mechanical feeding—something less obvious until you’ve upscaled and see clumping in the blender or vacuum transfer. Year after year, we have tweaked the washing and drying, moving away from archaic batch draining and pushing toward continuous filtration and vacuum-dried discharge. Every step cuts down on trace solvents and maximizes lot-to-lot reproducibility.
Shipping isn’t a mere afterthought; robust packaging resists moisture, shields from UV exposure, and ensures steady properties from our warehouse to yours. Storing the batches in the dark and under cool, dry atmospheric control, we cut down on oxidation risk and color shift. Our plant doesn’t tolerate the shortcuts that push other products toward quick spoilage or unexplained impurity spikes. We know that rerunning a synthesis, especially with expensive iodinated reagents, costs time and budget. Avoiding the trap of “good enough” material, our team focuses instead on shipping dependable, data-backed lots, even if it means a little more time in quality control.
2,6-Diiodo-4-Nitrophenol highlights how niche molecules serve as the backbone for more than just one industrial application. Unlike related compounds—say, the tetraiodinated analogs or the parent 4-nitrophenol—this one threads the needle between high iodine content for reactivity and selectivity, along with manageable safety and handling. We have produced its non-nitro and differently positioned analogs, and every one reacts with a slightly different set of handling issues—particle size, static buildup, labile byproducts, filtration headaches. This 2,6-disubstituted nitro version avoids some notorious caking seen with the para-iodo alternatives, yet flows better than alkoxy-capped or denser halogenated derivatives. Our process leans heavily into minimizing dust and inhalation risk without sacrificing ease of weighing or accurate portioning.
Where many catalog vendors simply buy and repack, our in-house production grants real control at every node—reaction, purification, packing. We test more than the big three specs. Moisture, particle size distribution, trace organic residues, and packaging integrity pass multiple checkpoints before leaving our facility. Colleagues in fine chemicals share stories where low-batch purity or shortcut purification spells disaster, particularly in reactions requiring tightly tuned reagents or sensitive catalysts. From experience, the job does not end at “above 98%”; it embraces the analytics that signal trouble long before a client pulls out a problem chromatogram.
You see 2,6-Diiodo-4-Nitrophenol headed to three main uses: synthesis of complex heterocycles, as a stepping stone for targeted iodination sequences, and in some advanced photochemical processes. Take heterocycle synthesis—medicinal chemists demand gram-to-kilo lots that match earlier samples. If an intermediate fails a purity screen, an entire project can stall. Nailing batch uniformity here isn’t just convenient; it saves weeks chasing down performance deviations. Some clients design radiolabelled markers, using the iodine atoms for radioactive isotope introduction. For those users, any stray heavy metals or sodium content in our product shows up harshly in radiochemical purity, so our control over non-volatile residues becomes critical.
Physical stability often gets overlooked in product specs, but we’ve seen pronounced differences in degradation between crystalline forms and dense amorphous batches produced by some overseas suppliers. The crystalline product, as we make it, keeps its shelf life and puts less pressure on facility storage planning. In photochemical R&D, material clarity and control over trace contaminants dramatically influence reaction outcomes and colorfastness. Years ago, we fielded requests to supply this compound for unique dye applications. Only after switching our oxidation and quenching steps did customer yield rise above the old ceiling. Those improvements came from painstaking data collection, not just chasing greener numbers on a purity report.
Every specialty chemical producer boasts “high purity,” yet many just scrape by. The practical difference is noticeable at the bench. We don’t rely on excess chromatography to rescue a poor batch; we optimize reaction variables, monitor all byproducts, and enact corrective tweaks before isolation. Our team has seen firsthand how different water content, trace acid, or solvent residues show up in final user applications, and we respond with plant-level tweaks, not stopgap label claims. We share lot-specific full analytical certificates, not photocopies from production runs six months earlier.
No one understands user frustration more than those who have faced batch failures due to overlooked impurities, ambiguous physical form, or cut corners on packaging. Manufacturing every single drum in-house, we avoid the risks of altered supply chains or untraceable quality lapses. On request, we can tailor crystalline grit size, special solvent washing, or ultra-low metal content—these adjustments move beyond the standard and never come off a template. The tangible result is product you can trust, not just at the start of a run but through the last scoop from the drum.
Decades in chemical synthesis have taught us one truth: raw material consistency determines efficiency, cost, and downstream confidence. Every kilogram of 2,6-Diiodo-4-Nitrophenol we deliver carries the same analytical rigor, whether headed to the lead chemist at a pharmaceutical innovator or to a scale-up team running reactor loads for an agrochemical trial. We document each handling step, run repeat analytics across stages, and send retention samples to long-term storage for cross-checks as needed. Our solvent recovery, byproduct management, and environmental compliance standards match or beat national regulations. On average, process upgrades over the past five years have cut energy use by over 12%, waste solvent by a third, and improved product particle uniformity by a measurable margin. Through direct communication with users and batch feedback, continuous improvement remains a staple of our operational philosophy.
Unlike some alternatives with broad batch specifications, our product’s footprint in the analytical data file rarely deviates: melting point within one degree, HPLC retention scans stable, and impurity profiles checked for problematic iodinated byproducts. Whether researchers are designing new ligand scaffolds, plastics, radiotracers, or medical imaging agents, starting off with subpar technical grade means added time running columns, lower total yields, and headaches over unpredictable reactivity. We stake our work on avoiding those scenarios.
R&D never sits still. Lab teams want confidence at every technical step, and process engineers seek material that won’t humble a pilot plant with unexpected sticky residues or odd kinetics. Our on-site technical team keeps batch reproducibility at the center of every workflow. Our analytical support goes beyond simple lot tracking; we can support troubleshooting, novel purification strategies, and custom modification work. The feedback loops we maintain with long-term partners—especially those developing novel APIs or functional materials—inform every process tweak we make. It takes more than a spreadsheet; it takes operational memory and a lab team who’s seen the pitfalls of “nearly good enough.”
2,6-Diiodo-4-Nitrophenol remains a critical piece for chemists looking to create the next wave of bioactive candidates and specialty materials. Our product, produced on-site from raw material refinement through finished lot packaging, isn’t some off-the-shelf convenience but a deliberate answer to unmet needs for purity, stability, and fully transparent data. Whether clients need support on regulatory registration, new application development, or deeper supply attestation, they find a partner in our team right here. The margin for error shrinks when the next step in your synthesis depends on strict lot standards. We embrace the responsibility as actual producers, shaping projects and research efforts from foundation to finish.
We often say chemical manufacturing lives and dies by small details. With 2,6-Diiodo-4-Nitrophenol, small shifts in process variables lead to big changes in output quality, so we invest in skilled operators, well-maintained equipment, and constant process review. Our batches tell the story: consistent color, physical form, reactivity, and analysis every time the seal breaks on a container in your lab. This standard doesn’t come from wishful thinking, but from a deep bench of technical know-how, patience, and a willingness to fix problems before they happen.
We hold ourselves responsible not to cut corners—every batch should work as hard for you as we do to create it. Partnering with our manufacturing team means less stress about raw materials, more time pushing breakthroughs in your research environment. With each shipment, we share more than a compound; we supply a safeguard for your projects, built on direct experience delivering reliable specialty chemicals in the most demanding applications across continents and disciplines.