|
HS Code |
494880 |
| Productname | 2,3-Difluoro-4-Iodophenol |
| Molecularformula | C6H3F2IO |
| Molecularweight | 255.99 g/mol |
| Casnumber | 885277-55-0 |
| Appearance | White to off-white solid |
| Meltingpoint | 74-78°C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(C=C1F)I)F)O |
| Inchi | InChI=1S/C6H3F2IO/c7-3-1-2-4(9)6(10)5(3)8/h1-2,10H |
| Storagetemperature | 2-8°C |
As an accredited 2,3-Difluoro-4-Iodophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 5 grams, sealed with a PTFE-lined cap, labeled with chemical name, CAS number, hazard pictograms, and supplier details. |
| Shipping | 2,3-Difluoro-4-Iodophenol is shipped in a tightly sealed, chemical-resistant container under ambient conditions. The packaging ensures protection from light, moisture, and physical damage. All shipments comply with relevant hazardous material regulations, including clear labeling and documentation, to ensure safe handling and transport during domestic or international shipping. |
| Storage | 2,3-Difluoro-4-iodophenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and incompatible materials such as strong oxidizing agents. Protect from moisture and ignition sources. Proper chemical safety labeling is essential, and storage in a dedicated corrosives or organohalide cabinet is recommended to ensure safe handling and containment. |
Competitive 2,3-Difluoro-4-Iodophenol prices that fit your budget—flexible terms and customized quotes for every order.
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As a chemical producer with decades immersed in fluorinated intermediates and substituted phenols, we know the difference quality and process control make. Many fine chemical applications rely on precision at the gram and kilogram level, and 2,3-Difluoro-4-Iodophenol brings unique value to researchers and production chemists seeking a platform for advanced chemistry. Years of hands-on production have proven to us that materials aren’t just commodities—they’re the backbone of every project that runs on a tight timeline, or every scale-up that needs fewer surprises along the way.
2,3-Difluoro-4-Iodophenol, bearing the molecular formula C6H3F2IO, delivers a phenolic scaffold equipped with two fluorine atoms at the ortho and meta positions, along with an iodine at the para site. In our factories, the technical team pays close attention to these halogenation patterns. The positioning isn’t just semantics: many downstream couplings, further derivatizations, or pharmaceutical explorations depend on targeted reactivity. A single misplaced atom often translates to lost batches or dead routes. Over the years, we've heard from labs hitting bottlenecks with unreliable lots or contaminated sources. To address this, our standard batches reach purity values above 98% by GC and HPLC, and our QC group routinely screens for halide contaminants, water content, and residual solvents.
Producing halogenated phenols means managing sensitive chemistry. Most commercially available 2,3-difluoro-4-iodophenol originates from multi-stage reactions, typically starting with difluorophenol precursors and following through with selective iodination approaches. Efficiency isn’t just about higher yields—it’s also reducing byproducts that can poison later steps. Factory troubleshooting sessions often revolve around purifying batches from over-iodinated or under-fluorinated outliers. We've put resources behind monitoring trace elements and optimizing crystallization conditions. Each drum of material leaves with a batch record detailing temperature ramps, cleaning logs, and analytics. It’s this transparency that sets reputable producers apart from opportunistic traders.
Process teams in API synthesis, agrochemical discovery, and material science often approach us with demanding questions: What trace species are present? Can fluorescence be controlled? Will the iodine handle withstand Pd catalysis or copper coupling? These are practical concerns familiar from our own process scale-ups. The difluoro motif injects electron-withdrawing properties, often influencing reactivity on aromatic rings—chemically, this matters in regioselective cross-coupling, nucleophilic aromatic substitution, and the construction of fluorinated scaffolds used in pharma candidates and imaging agents. Other isomers, such as 2,4-difluoro-3-iodophenol, show different reactivity patterns and sometimes produce inconsistent outcomes in the same reactions. Our expert team is ready to discuss these distinctions, so your synthesis does not veer off path due to overlooked differences in substitution.
Not all halogenated phenols function alike. Competing products bear similarities at first glance, but the devil is in the details. In our own optimization work, we’ve charted how even subtle changes—such as the position of fluorines relative to the hydroxyl—affect solubility in key organic solvents, temperature stability, and organometallic coupling yields. For instance, some phenols precipitate or discolor during routine storage, indicating side reactions. Our longtime clients include lab managers who recall setbacks with off-specifications materials from unknown sources, or reagents delivered with vague certificates. We take this personally, supplying robust technical data—spectral fingerprints, impurity breakdowns, and custom particle size distributions—so that the material that lands on your bench matches what your process expects.
Customers often start with exploratory grams of 2,3-difluoro-4-iodophenol, running pilot routes or validating new coupling chemistries. As programs advance, the demand quickly moves to multi-kilogram lots. Transitioning from walks across the lab floor to drives around industrial plants, we've had to rethink containment, safe handling, and logistics. The crystalline form we produce stores well under dry inert atmosphere; QA tracks moisture pickup, with routine Karl Fischer titrations and weight checks. Bulk packaging options fit standard drum and custom container requests, with all documentation preserved from the smallest R&D vessel to the warehouse drum.
For projects sinking substantial investments into new leads or clinical probes, regulatory documentation and traceability turn critical. As a certified manufacturer, we supply full supporting documents: certificates of analysis, in-house analytical records, and process change notifications for every batch. Since regulations update often, our compliance team stays in close touch with customers working under cGMP or similar standards. Chemical production brings tick-the-box paperwork—material safety data, REACH information, and possibly custom impurity profiles. Our direct experience with pharmaceutical and agrochemical registration means you don’t wait weeks for answers if a regulator needs more detail. Solid documentation saves time and avoids drama in audits.
On the pharma side, 2,3-difluoro-4-iodophenol serves as a flexible intermediate in the synthesis of fluorinated building blocks, often heading toward more complex heterocycles or elaborated phenol ethers. Medicinal chemists tell us this combination—two fluoro and one iodo on a phenolic core—opens up access to libraries where both size and hydrogen-bonding play roles. The ortho-fluorine creates steric shielding, sometimes reducing metabolic oxidation, while the para-iodo group feeds directly into metal-catalyzed arylations. As researchers look to increase the fluorine content of drug candidates—often chasing improved bioavailability or longer metabolic half-life—having reliable supply of this phenol becomes critical. A single off-lot shipment can interrupt an entire SAR campaign or delay the scale-up of a preclinical lead.
Beyond drug discovery, our partners in the specialty materials sector look for halogenated phenols to build up blocks for advanced polymers, functional resins, and new electronic materials. The ring activation by two fluorines, paired with iodine as a versatile leaving group, helps form functionalized monomers or cross-linkers where durability, chemical resistance, or unique electronic properties matter. Our collaboration with R&D teams often begins at the bench, dialing in reaction details and accelerating transitions to pilot scale. At every stage, we stand ready to troubleshoot and provide feedback. Our experience includes tracking side reactions, stabilizing upon storage, and ensuring the material supports not just the synthetic route, but also bulk properties in application.
Unlike traders or repackagers, who typically source based on price lists, our experience stems from years spent over reaction vessels and filtration stations. We’ve faced the real-world setbacks—filter plug-ups, unexpected exotherms, or waste stream headaches. Our feedback to clients comes from actual pilot data, not just supplier brochures. Favorite troubleshooting topics include how to handle heat-sensitive iodophenols, managing solvent compatibility with fluorinated aromatics, and achieving optimal conversion rates in catalytic couplings. This background gives us the practical know-how to advise clients whether the aromatic substitution pattern matches what their protocol targets. Our years of observation reveal that off-the-shelf substitutes rarely perform the same, especially once scale and regulatory constraints enter the mix.
As pharmaceutical, agricultural, and electronics labs increase demands for specialty aromatics, back-end supply logistics become less forgiving. Being a primary manufacturer means direct management of production schedules, strict control over raw material sourcing, and the ability to issue timely updates as international conditions shift. From raw fluoro building blocks to final shipment, our team logs every process stage. Whether it’s a sudden spike in demand, supply chain disruption, or client-driven modification, we act—not wait for instructions from a third party. We've positioned our bottleneck reagents closer to daily production lines, and bulk safety stock is calculated based on customer forecasts, not wishful thinking. These measures translate into reliability, especially as materials like 2,3-difluoro-4-iodophenol drift from niche to mainstream use.
We regularly field requests for ultra-pure grades. This isn’t because clients are picky: new catalytic reactions, advanced NMR quantitation, or trace impurity studies demand it. Our QC system supports tight cutoffs for heavy metals, residual halides, and volatile species, not just the main assay value. Repeatable performance from batch to batch matters more than any glossy catalog photo. Dedicated investment in column purification and advanced crystallization methods minimize lot variations. We believe transparency builds trust, so spectral data, chromatograms, and impurity mapping form part of every release sheet.
Difference from more commonly available halogenated phenols, such as 2,4-difluoro-5-iodophenol or mono-fluorinated isomers, lies in both substitution pattern and reactivity. In our labs, we have explored this molecule’s reactivity: the combination of ortho–meta fluorines changes both acidity and leaving group properties, compared to ortho–para or meta–para variants. Benchwork shows the impact in coupling selectivity and downstream step yields. Knowing these subtleties matters when building a reliable route to target molecules. Less informed sourcing often leads to missteps—a costly lesson evidenced by returns and troubleshooting calls for underperforming intermediates.
Our support doesn’t end at shipment. We openly share the outcomes of our own route optimizations and analytical troubleshooting. Problem-solving sits at the core of manufacturing, where clients rely on our collective memory for answers to solubility, handling, or unwanted color changes during storage. Over the years, close technical partnerships have helped both sides avoid expensive misdirection in route scouting or yield improvement. Many process chemists recall times when an off-spec reagent stalled a whole campaign—a frustration we understand deeply. We step in with answer-driven conversations and follow-up documentation, not canned responses.
Producing and handling halogenated aromatics brings a real focus on environmental responsibility. As societal and regulatory attention sharpens on chemical waste, our operations invest in closed-system reactions, efficient halide recovery, and safe vent handling. This work isn’t easy or cheap, but we view it as foundational to responsible manufacturing. Waste stream audits, air and water monitoring, and solvent recycling are enforced by regular internal reviews. Mitigating chemical exposure risk—both for our own teams and downstream handlers—drives our continuous training and workflow adjustments. We choose to lead on these issues, not simply react to changing legislation.
Drawing from years of experience, our goal stays the same: empower clients to innovate without guessing whether their reagents will cooperate. We’ve seen enough changes in global supply over the past decade to appreciate why buyers demand more than basic purity and price checks. Providing a steady hand—from project inception to regulatory filing—turns out to matter as much as any single batch metric. Our daily work involves adapting production to support new applications or tweaking processes to limit waste, always with an eye toward delivering consistent, trustworthy product.
Every drum of 2,3-difluoro-4-iodophenol that leaves production carries the experiences of dozens of chemists, process engineers, and logistics pros. As manufacturers, we measure our reputation batch by batch, conversation by conversation. No shortcut replaces firsthand technical support, transparent analytics, or a listening ear for hard-to-solve challenges. Our clients’ breakthroughs shouldn’t stall because of unreliable reagents. From synthesis design to scale-up, from pilot vessel to multi-ton shipment, our collective efforts support your work at every step. That’s the standard we expect from ourselves and the one we bring to the benches around the world.