|
HS Code |
684860 |
| Chemical Name | 4-Fluoro-2-Iodo-Phenol |
| Cas Number | 252260-00-5 |
| Molecular Formula | C6H4FIO |
| Molecular Weight | 238.00 g/mol |
| Appearance | Light brown to tan solid |
| Melting Point | 70-74°C |
| Purity | Typically ≥97% |
| Smiles | C1=CC(=C(C=C1F)O)I |
| Inchi | InChI=1S/C6H4FIO/c7-4-1-2-6(9)5(8)3-4/h1-3,9H |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 2-Iodo-4-fluorophenol |
As an accredited 4-Fluoro-2-Iodo-Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 4-Fluoro-2-Iodo-Phenol; labeled with hazard symbols, product name, and CAS number. |
| Shipping | 4-Fluoro-2-Iodo-Phenol is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture ingress. Packages are labeled with appropriate hazard symbols and handled according to international regulations for hazardous chemicals. Temperature and light sensitivity are considered, and documentation includes Safety Data Sheets (SDS) to ensure safe and compliant transportation. |
| Storage | 4-Fluoro-2-iodo-phenol should be stored in a cool, dry, well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and stored in compatible, chemically-resistant containers. Segregate from strong oxidizing agents and bases. Properly label the storage vessel, and ensure access is restricted to trained personnel to minimize exposure and contamination risks. |
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At our facility, 4-Fluoro-2-Iodo-Phenol represents one of those clever molecular tools that pushes synthetic work into new territory. The team refers to its structure by heart: a phenol ring sporting both fluorine at the fourth position and iodine at the second. Nothing beats the crisp, pale appearance of a fresh batch, its fine crystals poured from the filter funnel. The smell is sharp—typical of halogenated phenols—a sure sign the reaction worked well. Each batch emerges under strict control, guided by a rigorous walk through every purification step.
Years producing this compound taught us that small changes in a molecule’s design unlock big leaps in how you can use it. This substance stands out as a multi-purpose building block. The presence of both a fluorine and an iodine on the aromatic ring isn’t accidental or decorative—it means the molecule delivers distinct reactivity during coupling reactions, useful in making pharmaceuticals, agrochemicals, and specialty materials. We chose each precursor ourselves, checked the reagents twice, and refined the process so each lot brings consistent performance to those who demand reliability in research or manufacturing.
This compound has unique chemistry built in. The iodine atom on the aromatic ring transforms Suzuki or Sonogashira couplings into direct, clean reactions. The fluorine helps with downstream metabolic resistance in drug design or adds matchless stability in material science. Both groups together open a toolkit of further substitution strategies for medicinal chemists and advanced polymer designers.
A point often overlooked: you won’t get the same flexibility from its close cousins. If you reach for 2-iodophenol or 4-fluorophenol alone, you’ll miss the synergy of two reactive positions. The dual-substitution pattern grants more control in stepwise synthesis. We designed, for ourselves and our partners, a workflow where this isn’t just a matter of yield—it makes new structures possible that single-halogen compounds cannot give.
Our technical crew stands over years of process improvement. Producing 4-Fluoro-2-Iodo-Phenol doesn’t just happen at the turn of a dial. Sourcing high-purity 2-iodophenol and bringing in reagents for selective para-fluorination takes juggling suppliers, scheduling maintenance on our vacuum lines, and checking every flask and column by hand. Our supervisors hate surprises, so we built in QA at every junction: purity checked by NMR and GC, moisture tracked to the trace level.
The organic chemist’s experience counts most when scaling up. Reproducibility never comes cheaply. Moisture in the solvents? Cross-contamination from lines? It all gets spotted and fixed before a single drum leaves the site. Each release batch is documented, with spectra on file for our own sanity as much as for compliance. We know that failures in scale-up rarely trace to the chemistry—they trace to attention, the kind you only get from running the same reaction hundreds of times.
Academic teams, scale-up groups in pharma discovery, and material scientists come to us with tough questions. They face bottlenecks because the bench-scale supply doesn’t match pilot batches, or impurities creep in. Our job is to fix those points. To them, 4-Fluoro-2-Iodo-Phenol is a path to functional molecules—a template for aryl ether formation, key intermediate for benzofuran scaffolds, or precursor in preparing complex heterocycles.
Manufacturing teams often puzzle over the stability of halophenols during storage or transport. We learned the hard way: temperature swings and humidity spikes cause decomposition or rearrangement. So we invest in robust containers, inert-atmosphere packaging, and overnight logistics—facts learned from past headaches, not just advice from technical brochures. We track lots. We recall past errors. Only then supply builds a reputation for dependability, not just availability.
Medicinal chemists require scaffolds that are both adaptive and predictable. They appreciate how the ortho-iodo group enables cross-coupling with boronates, alkynes, or amines—without side reactions that shrink yields. The para-fluoro resists metabolic breakdown in biological systems. That’s the molecular rationale, but from a manufacturer’s view, the reward lies in seeing hard-won batches underpin the synthesis of truly novel compounds—an anti-cancer lead, a new imaging agent, or a smart material.
Material science researchers interested in OLED technologies or high-performance polymers sometimes rely on this molecule to introduce halogenated phenol units into macromolecular structures. Here, the combination of iodine and fluorine can both adjust electronic properties and enable downstream functionalization. Real products—flexible display prototypes, specialty coatings for aerospace—owe a part of their story to compounds like 4-Fluoro-2-Iodo-Phenol.
Not every source brings the same analytical rigor to halogenated phenols. We emphasize batch-to-batch consistency, verified by side-by-side spectral analysis. Color, melting point, NMR peak positions—each gets checked, with documentation kept on file. Requests sometimes require custom handling: special particle sizes for automated dosing, or blending to a specific purity grade for ultra-sensitive applications. We listen, then deliver on those particulars instead of pushing tired one-size-fits-all stock.
Our pilot plant isn’t designed for just one molecule, but we configured lines and trained staff to handle sensitive iodo-fluoro aromatics. It’s not just a technical feat: years of refining washing procedures, holding times, and extraction protocols pay off in each drum we ship. We learned from cases where a customer flagged residual halide or volatile impurities, and we tweaked our process—see the learning in every kilo that runs through the final filter.
Safety matters at each step. Halogenated compounds demand respect, and every worker knows the protocol—protective gear, well-ventilated hoods, and secondary containment always in place. Bulk shipments mean attention isn’t optional. In the plant, each spill protocol has been tested, and every label tells the clear story of the hazards and precautions. We store the product away from heat or light, away from base-sensitive chemicals, and validate shelf stability with periodic checks.
Our experience with regulatory requirements keeps shipments moving across borders without setbacks. We never shortcut documentation. Each certificate points to the analysis we carry out in our own labs, signed by the analyst, not by a distant affiliate or anonymous third party. That’s a habit fostered by long experience—not just for peace of mind, but because customers build projects on reliable, traceable products.
We know few projects follow a simple path. New users often ask about solubility in their solvents, compatibility with planned catalysts, or shelf-life under various conditions. We answer from direct testing—and share what we see when our chemists tried it, not just what textbooks state. Whether a team faces separation issues, color changes during storage, or losses during distillation, someone in our group has already hit that wall and sketched out ways through.
Some customers prefer technical support by documents, others reach out for in-person advice. Either way, we respond with specifics, not by copying generic disclaimers. We share tips on how to avoid colored by-products in sensitive reactions or how to optimize purification steps for a particular downstream transformation. Collaboration means learning from both successes and setbacks, and we value reports from the field as much as feedback from our own lab work.
Demand for dual-halogenated phenols grows as chemical manufacturing leans toward smarter, more versatile building blocks. Increasingly, our customers in pharma, polymers, and specialty chemicals need intermediates that streamline their own synthesis pipelines. By focusing our process development on this compound, we meet the evolving demands for reactivity, selectivity, and purity—every lesson rooted in daily operations, not just read off a chart.
Each year the feedback loop tightens. A pilot synthesis in a research customer’s lab highlights a new requirement: higher purity to avoid catalyst poisoning, or batch-specific spectral documentation for regulatory filings. We adapt, reinforcing our own procedures and upgrading lab instruments to meet those calls. The experience on the floor isn’t just about making the target product, but about aligning what leaves our site with what’s truly needed in the real world.
Single-halogen phenols lack the strategic versatility of combination products. Substituting 2-iodophenol or 4-fluorophenol in target syntheses misses opportunities: either you lose functional handles for downstream coupling, or you introduce extra synthetic steps. Chemists appreciate 4-Fluoro-2-Iodo-Phenol for its two orthogonally reactive sites—a fact evident in both patent literature and academic publications featuring next-generation drugs, dyes, and molecular probes.
As manufacturers, we’ve worked with all the analogs. We can say from direct experience: dual substitution not only saves time and raw materials, but minimizes by-products and boosts throughput. The result isn’t confined to the bench—it translates into better batch safety, more predictable performance, and a cleaner footprint in both trial and scale production.
We treat each feedback report as material for process learning. One year, recurring color issues prompted our team to revisit all storage protocols, improve drum liners, and recalibrate detection for trace contaminants. In another case, we adjusted our purification steps after a handful of researchers needed a higher grade for a photolabile coupling. These aren’t just upgrades—they become part of our standard operating framework.
Customer-driven evolution pushes us to keep inventory tailored, analytical reports transparent, and technical conversations honest. We publish test results with every shipment, and keep a direct line open between our lab staff and user group leaders. Problems aren’t avoided—they’re solved upfront, and the solution gets rolled into every future lot.
Producing 4-Fluoro-2-Iodo-Phenol isn’t about filling catalogs—it’s about contributing a material that directly feeds scientific discovery. Each batch echoes the hands-on realities of gathering inputs, fine-tuning reactions, and meeting both regulatory and technical expectations. We build and sustain quality by constant oversight and investment, so each drum, every ampoule, paves the way for progress in research and industry.
Our links with global innovation are true to our roots. We started with basic halophenols decades ago, watching the requirements of our customers shift as technologies evolved. Dual-halogen products like this grew from incremental learning—a response to teams who needed more than just a single function per molecule.
Sourcing 4-Fluoro-2-Iodo-Phenol from the producer—rather than indirect channels—means confidence in what arrives at your lab dock. Every shipment connects to a real process, real oversight, and real answers if hurdles arise during synthesis. We don’t just supply: we back each lot with expertise, collaboration, and a record of performance that isn’t outsourced or second-hand.
For chemists on the clock, getting reliable, thoroughly-checked material outpaces any lab-saving shortcut. Our manufacturing experience flows right into each project we support—an investment visible in yield, reproducibility, and the kind of scientific certainty that drives innovation forward.
4-Fluoro-2-Iodo-Phenol stands for more than just another reagent on the shelf. It embodies decades of learning about what makes a functional, adaptable chemical building block. The dual-substitution design offers both immediate synthetic value and long-term opportunity for advancing research and industry. Our deep experience as the actual producer, plus lessons from each challenge along the way, means those who select this compound can count on more than a guaranteed supply—they gain a committed partnership in pursuit of progress.