Anhui Liwei Chemical Co., Limited
Products

4-Chloro-2-Iodophenol


    • Product Name 4-Chloro-2-Iodophenol
    • Alias 4-Chloro-2-iodo-1-hydroxybenzene
    • Einecs 682-027-7
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    271581

    Product Name 4-Chloro-2-Iodophenol
    Cas Number 637-92-7
    Molecular Formula C6H4ClIO
    Molecular Weight 254.45 g/mol
    Appearance Light yellow crystalline solid
    Purity Typically ≥98%
    Melting Point 82-86°C
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol and acetone
    Density 1.96 g/cm³ (at 20°C)
    Smiles C1=CC(=C(C=C1Cl)O)I
    Inchi InChI=1S/C6H4ClIO/c7-4-1-2-6(9)5(8)3-4/h1-3,9H

    As an accredited 4-Chloro-2-Iodophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Chloro-2-Iodophenol, tightly sealed, labeled with hazard warnings and chemical information.
    Shipping 4-Chloro-2-Iodophenol should be shipped in tightly sealed containers, protected from light and moisture. Package according to all relevant hazardous material regulations, using cushioned, leak-proof materials. Label as a chemical substance and handle with care to prevent breakage or spillage during transit. Avoid exposure to extreme temperatures and store upright.
    Storage **4-Chloro-2-iodophenol** should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and bases. Store at room temperature and clearly label the container. Follow all relevant safety procedures and local regulations for hazardous chemicals.
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    Certification & Compliance
    More Introduction

    Introducing 4-Chloro-2-Iodophenol: Thoughtful Sourcing and Real-World Performance

    Every new batch of 4-Chloro-2-Iodophenol marks the result of dozens of real-world adjustments on our production floor. Over years in phenol derivatives, we have refined this process into something precise, yet always under review. Chemists order this compound by its real-world profile: a pale, tannish solid that lands consistently within tight purity tolerances. Production never goes by the book alone—humidity on the line, subtle color shifts, or a supplier’s variable lot can all demand hands-on intervention. This is a benzenoid intermediate that many pharmaceutical and agrochemical labs prize not just for reactivity, but for ease of work-up and reproducibility during scale-up.

    Where 4-Chloro-2-Iodophenol Fits—And Where It Doesn’t

    We see the best use for this material in projects that need site-specific halogenation. The molecular structure—chlorine at the fourth carbon and iodine at the second—explains a lot about its utility. The electron density changes, opening new approaches to couplings and substitutions that aren’t possible with plain phenol or even single-halogen analogs. For teams building biaryl scaffolds or looking for a jump-off point for Suzuki or Stille cross-coupling, this intermediate provides both reactivity and control. Chemists working in heterocyclic synthesis rely on it to achieve precision in downstream steps, with both leaving groups amenable to selective transformation.

    Routine jobs such as toy chemical syntheses or projects focusing only on low-complexity structures often pass this one by—other, less costly substitutes are available for situations that don’t call for both a chlorine and an iodine in defined positions. But if selectivity, orthogonal reactivity, or novel halogen-handling matter, this one’s a workhorse.

    Direct Experience: Crafting Batch After Batch

    Production runs of this compound illustrate the tension between theoretical synthesis and practical realities. Raw iodine and chlorinated phenols don’t always behave as expected. Control over ortho-para ratios, byproduct minimization, and crystal formation keep us on our toes. The technicians here track not just reaction progress, but visual clues: a glimmer of unexpected color, a persistent emulsion in extraction. Many fine chemicals can bleach their way to purity through repeated washes; 4-Chloro-2-Iodophenol resists that shortcut. Real, hands-on purification steps set apart each lot, clarifying it for chromatography and bench work by others.

    Why Tinker With This Structure?

    The interplay of electron-withdrawing chlorine and electron-rich iodine on the benzene ring lets partners control downstream pathways. Modifying the routine conditions—shifting from basic to acidic media, using polar aprotic solvents or moving to metal-catalyzed reactions—shows the difference between this product and others. Mono-chlorinated or mono-iodinated phenols often lack this flexibility. With both groups present, the synthetic window broadens.

    Routine use covers fields far beyond lab-scale curiosity. In pharmaceutical R&D, we know project teams running parallel route screens count on this compound for both traditional and novel transformations. Agrochemical developers also draw on the dual reactivity profile as a basis for herbicide or fungicide lead design. Across both groups, feedback highlights that starting with genuine, high-quality material trumps obscure theoretical advantages—actual purity, consistent melting point, and measured water content build trust batch after batch.

    Specification: Achievable Details From Daily Work

    We have learned that providing only broad specs—say, “purity >98%”—never cuts it for serious users. Chromatograms from our in-house QC lab accompany every outgoing drum or bottle, detailing both primary content and trace impurity profile. Since some users need absence of residual metals or specific contaminants, we pull reference samples for extended testing. Water, handled poorly in synthesis, causes headaches in cross-coupling and crystallization. That’s why we never simply quote Karl Fischer results from a bulk batch: each lot’s actual test accompanies the material.

    Most of our customers request delivery between 100 grams and multi-kilo lots, aimed at either pilot studies or bench-to-plant campaigns. Keeping contamination low along the packaging line comes down to disciplined procedure. Every time an operator suits up for weighing, we recheck the balance calibration and review recent environmental controls. Pushing for extra precision doesn’t show up on certificates of analysis, but we know where shortcuts lead—a spike in complaints, wasted material, or, worst of all, years-old material creeping its way back for disposal.

    Why Source From a Direct Manufacturer?

    Years ago, we saw recurring problems in the market for high-end phenol derivatives. Traders and repackers commonly mixed lots from multiple sources, blending material to smooth out inconsistencies. End-users saw uneven melting points, faint color in solutions, and irregular byproduct peaks in HPLC traces. To avoid these headaches, teams increasingly reach out for direct sourcing and batch transparency. From our side, that means keeping traceability on every raw material shipment. It also means welcoming audits—chemists with real purchasing power increasingly want to see reactors, meet operators, and trace the paperwork for every batch. Direct lines from production to bench deliver confidence that doesn’t come from PDFs or unverified “spec sheets.”

    When talking about 4-Chloro-2-Iodophenol, it’s easy to get lost in technical terms. For us, the focus stays on providing actual utility and reliability. Chemists tackling longer syntheses depend on rapid, clear documentation for lot identity and handling conditions. Anyone handling scale-up receives details on solubility, storage, and hazard management based on firsthand incidents—deviations in storage temperature or lighting all come from actual experiments, not guesswork.

    Distinguishing Features: Not Just Another Halophenol

    Halophenols crowd any supplier’s catalog. Look close, and performance often reveals subtle but vital differences. Mono-halogenated phenols, for instance, generally offer lower cost and greater availability, but they lack the controlled, differentiated reactivity of our dual-substituted product. 4-Chloro-2-Iodophenol remains unique for applications where alternating activation and deactivation positions on the aromatic ring matter for selectivity or yield. The iodine atom, heavier and more electropositive, makes connections to cross-coupling chemistry straightforward. The chlorine position, less reactive yet vital for further derivatization, broadens downstream flexibility.

    One of our pharma clients, working on a heterocyclization pathway, struggled with unpredictable side products using commercially available mono-iodo compounds. Shifting their protocol to our 4-Chloro-2-Iodophenol cut byproduct peaks and lifted the main yield. Direct feedback like this keeps our R&D team tuning both analytical and isolation steps, always aiming for the purest, most stable product we can ship.

    Application Knowledge: What Works and What Fails

    Most chemical suppliers focus on standardized data, but production reality brings practical lessons. In storage, we have seen missteps with moisture pickup causing slow decomposition—a warning for users planning long-term inventories. On the bench, too much exposure to sunlight initiates slow side reactions. Smaller bottles or inert-atmosphere packaging can solve many issues if discussed in advance. The technical support line—staffed by our own plant chemists—fields repeat questions about residue formation, work-up simplification, or yield optimization for specific cross-coupling protocols. In every case, advice flows from direct experience with the batches at hand, not from generic safety sheets.

    In terms of usage, most requests stem from advanced intermediates for API synthesis, molecular fragments for lead optimization, and functional group templates for further arylation or acylation efforts. Researchers tackling Suzuki-Miyaura or Ullmann reactions report consistent conversion rates when starting from our material. Even outside pharmaceuticals, custom material developers ask for assurances on halide purity and minimal peroxide content for electronic applications. This exchange of real concerns keeps us grounded—the outcome always traces back to reliable batch history and careful sample retention.

    Scale-Up Lessons: From Flask to Reactor

    Many disappointments in chemical scale-up come not from failures in theory, but from inconsistencies in raw inputs. We have supported multiple clients as they transfer flask-based protocols up to pilot or commercial scale. The lesson repeats: poorly controlled intermediates magnify losses, slow purification steps, or force costly re-optimizations further down the chain. Steady supply of 4-Chloro-2-Iodophenol, matched to current and historical QC data, lets development teams focus on real process issues rather than box-to-box variability.

    Even so, surprises happen. We keep open channels with clients to troubleshoot every stage, passing along tips—whether it’s managing packed-bed reactor feeding or minimizing photolytic side reactions during long storage. Only a manufacturer involved day-to-day with this product can field and solve these sorts of troubleshooting calls in real time, pulling from retained batch samples if needed.

    Continuous Improvement: What We Change (And Why)

    The work doesn’t stop at repeatable synthesis. Every operator here files incident notes, whether tracking environmental variables or spotting early signs of off-target reaction. Some details seem trivial—fine dusting patterns on the filter, or the faint smell during handling—but they often predict downstream stability problems. Batch review meetings, at which everyone from QC techs to reactor operators weighs in, lead to procedure tweaks. We update our in-house manufacturing procedures as soon as credible evidence emerges, often after missed yields or tamper-evident packaging failures.

    Our internal lab routinely pushes for lower detection limits on trace contaminants, since persistent palladium, copper, or iron residues have real effects during sensitive catalysis steps. Customer-driven improvements have pushed us to explore new drying protocols, increase sampling rates during final blenddown, and shift packaging choices to suit end uses. These kinds of changes, grounded in ongoing collaboration between production and application, help us meet higher standards season after season.

    Quality, Traceability, and Real-World Trust

    Most customers ask early-on about certificates of analysis and regulatory documentation. Actual needs go further. Every time someone calls us about a puzzling HPLC peak or a faint off-odor, we reach into our retained archive for the actual lot sample, not just the paperwork. This level of traceability means there’s never any hedging or hiding mistakes—if something goes wrong, we admit it, name the source, and work on corrective action. Trust builds less from advertising than from addressing real-world hiccups openly and without delay.

    The regulatory environment may shift, or boil down to customer-imposed specs. We spend time reviewing every compliance bulletin, but keep the main focus on outcome—if a batch doesn’t match the user’s need, paperwork won’t hide it. By communicating directly with users at every stage, from inquiry to delivery, we maintain a cycle of feedback and adaptation tough for middlemen to match.

    Comparing To Similar Products—Honest Appraisal Over Hype

    Some buyers start with basic chlorophenols or iodophenols, thinking that swapping in a dual-substituted version will cover every need. Years of customer feedback and field trials show it’s not so simple. 4-Chloro-2-Iodophenol functions as more than a hybrid of its mono-halogen siblings. Its real value comes out where selectivity and ease of leaving group manipulation shape yield and purity. In Suzuki cross-coupling, for example, the iodide offers rapid turnover, while the chloro-site remains untouched for later derivatization. Mono-halogen phenols often force complex protection-deprotection steps or limit synthetic flexibility.

    We have shipped samples to groups convinced mono-halogen materials would suffice, only for the data to show missed targets or flagging selectivity. Time after time, a dual-substituted intermediate proves its worth at process or scale-up stage, cutting rework and clarifying chromatograms. Yet this isn’t a magic bullet—projects without these selectivity demands should use more readily available and cheaper options. Focused use, not hype, drives real value.

    Moving Forward: Production As a Collaborative Process

    Looking back at the past decade, production of 4-Chloro-2-Iodophenol handed us none of the quick wins sometimes promised by catalog entries. Each year brings supplier disruptions or subtle changes in regulatory climate—no batch goes out the door without personal sign-off from the team that ran, isolated, and packaged it. As new application notes roll in from our customers, each success and setback feeds back into our work, prompting refinements in both process and documentation.

    Working as a direct manufacturer grounds us in every aspect of the compound’s real-world journey. Whether your concern centers on ensuring no side reactions with heavy metals, optimizing a catalyst for new cross-couplings, or simply keeping shelf-life predictable, direct technical exchange with a producer—rather than a trader—remains a sound choice. Our approach never rests on checklists alone. The ongoing relationship with the chemists and technical teams further downstream shapes every improvement line by line.

    Summary: Pragmatic Excellence For Real Chemistry

    Producing 4-Chloro-2-Iodophenol means more than delivering a specification or a purity number. It requires daily scrutiny of raw materials, tight process control, and continuous communication with the scientists using it in critical work. Comparison with other halophenols only matters so far; what separates this compound is hands-on experience from plant floor to finished bench science. For projects demanding both selectivity and scalable, reliable quality, sourcing straight from a manufacturer who stands behind every lot offers genuine advantage.