Anhui Liwei Chemical Co., Limited
Products

Phenol, 4-Chloro-2-Iodo-


    • Product Name Phenol, 4-Chloro-2-Iodo-
    • Alias 4-Chloro-2-iodophenol
    • Einecs 401-090-5
    • 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

    661415

    Chemical Name Phenol, 4-Chloro-2-Iodo-
    Cas Number 63757-91-9
    Molecular Formula C6H4ClIO
    Molecular Weight 254.45 g/mol
    Appearance Light brown solid
    Melting Point 96-99°C
    Boiling Point No data available
    Density No data available
    Purity Typically ≥97%
    Solubility Slightly soluble in water
    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
    Synonyms 4-Chloro-2-iodophenol
    Storage Conditions Store at 2-8°C
    Hazard Statements Irritant; handle with care

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

    Packing & Storage
    Packing The 100g package of Phenol, 4-Chloro-2-Iodo-, comes in a sealed amber glass bottle with a clear hazard label.
    Shipping **Shipping Description:** Phenol, 4-Chloro-2-Iodo- should be shipped as a hazardous chemical, packed in airtight, chemically resistant containers. It must be labeled with appropriate hazard warnings and handled according to relevant regulations (such as DOT, IATA, or IMDG). Store and transport in a cool, dry place, away from incompatible materials and direct sunlight.
    Storage Phenol, 4-Chloro-2-Iodo- should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep away from heat and sources of ignition. Protect from light and moisture. Ensure proper labeling and prevent container damage; store in a corrosive-proof location compliant with local chemical storage regulations.
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    For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.

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    Tel: +8615380400285

    Email: sales2@liwei-chem.com

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    Certification & Compliance
    More Introduction

    Phenol, 4-Chloro-2-Iodo-: Our Experience at the Source

    The Chemistry Behind the Molecule

    We approach each batch of Phenol, 4-Chloro-2-Iodo- with a craftsman’s intent and a chemist’s precision. The structure combines the fundamental phenolic backbone with both chlorination and iodination, stacking two halogens at specific positions on the aromatic ring. At the plant, we see firsthand how the addition of the chlorine atom at the para position and the iodine at ortho truly shift the behavior of phenol derivatives. The chemistry may sound simple on paper, but every step matters. Even during purification, traces of positional isomers can creep in if reaction conditions slip, and we’ve learned that vigilance at every step preserves reproducibility batch after batch. The end compound offers a unique blend of reactivity—one we’ve seen requested time and again in research and synthesis labs.

    Where Skill and Attentiveness Matter Most

    Anyone can read a reaction protocol, but handling Phenol, 4-Chloro-2-Iodo- safely and efficiently requires hands-on training. Iodination can proceed with several reagents, but our process relies on carefully balancing reaction temperature and concentrations to minimize over-iodination and side reactions. I remember early scale-ups when simple things like incomplete stirring created hotspots, leading to product degradation or copper contamination. As direct manufacturers, adjustments to agitation speed, vessel geometry, and even the timing of acid addition emerged as the difference between acceptable and exceptional product. With each run, we reinforce controls that minimize byproducts, including dehalogenated or di-substituted variants.

    Purity Tells the Full Story

    We routinely see how high-purity Phenol, 4-Chloro-2-Iodo- changes customers’ outcomes. Trace impurities in similar products—whether mono-chlorinated, mono-iodinated, or alternate positional isomers—often result from process shortcuts taken outside the source manufacturing stream. Our own samples undergo multiple crystallizations and TLC verifications, not just instrument-based purity checks. In our lab, the final melting point and behavior in polar solvents often reveal subtleties that certificates of analysis cannot. Over years of production, we’ve seen time and again that additional purification rounds yield fewer complications downstream, especially during scale-up of pharmaceuticals, agrochemical actives, or intermediates for advanced material science.

    Applications Beyond the Usual Catalog

    Through discussions with research partners, we’ve watched this molecule find life outside obvious directed ortho-metalation or coupling reactions. Some customers have explored its use as a building block for selective fluorescent tagging, taking advantage of the heavy iodine atom for downstream imaging studies. We’ve also supported teams using it as an intermediate in Suzuki–Miyaura and Buchwald–Hartwig protocols. The combined electronic effects of chlorine and iodine shift both acidity and nucleophilicity, and skilled chemists can use these quirks to steer regioselectivity in subsequent steps. Over the years, phenol derivatives bearing a single halogen have proven too simple for certain applications, either lacking sufficient handle for further elaboration or producing less selective downstream activity. Phenol, 4-Chloro-2-Iodo- offers multiple points for strategic modification.

    Specifications as a Reflection of Process Care

    At the manufacturing level, our lot-to-lot consistency stems from real-time HPLC monitoring and batch-level NMR verification, not only batch averages or pooled analyses. We have found that regular checks through GC-MS on trace residual solvents such as dichloromethane or diisopropyl ether prevent surprises late in production, cutting down on complaints about background peaks in high-sensitivity applications. It’s tempting to write off these final sweeps as bureaucratic, but decades of direct customer feedback have made their importance self-evident. Even with suppliers advertising identical nominal specifications—melting point, assay, or appearance—minute differences emerge when scaling a reaction or using the molecule as a scaffold for rare target molecules.

    Differences from Other Phenols and Halides

    Compared with 4-chlorophenol or 2-iodophenol, this product’s dual substitution pattern delivers a unique chemical footprint. Not only do the two halogen atoms alter reactivity, but their specific positions matter for subsequent synthetic modification. Chlorine at the 4-position brings something different to aromatic substitution reactions compared with its placement at 2 or 3, especially when paired with an iodine atom at 2. The electron-withdrawing character of chlorine at the para position changes the acidity of the phenolic hydrogen, while the bulk and polarizability of iodine at ortho allow for selective halogen-metal exchange. In hands-on terms, this means a chemist working with our product gains access to differentiated sites for lithiation and cross-coupling.

    Batches we’ve compared from downstream distributors or resellers sometimes show unexpected side product peaks, owing to less controlled halogenation protocols. Without tight control, the lattice includes diiodo or dichloro byproducts, which complicate both yields and continuing reactions. Having direct command over synthesis, we adapt conditions in-house in real time and can trace unexpected outcomes back to their roots, optimizing continuously. The learning curve includes plenty of long nights and trial-and-error, but direct accountability lets us maintain a tighter standard than possible through only reselling or repackaging.

    A Manufacturer’s Perspective on Research-Grade Chemicals

    From a bench chemist’s view, every added level of structural complexity is both a tool and a complication. I’ve fielded dozens of calls from researchers asking after minute changes in batch purity or melt behavior across bottle sizes. Because we handle the entire production chain, we discuss their concerns directly with the operators, not through agents. Based on those conversations, we occasionally adjust drying conditions or extend quality checks for the next run. While the user interacts with a white crystalline solid in a glass bottle, we’re mindful of the entire process history: from coupling agent used to the drying cycle performed immediately before packaging.

    Research moves quickly. We’ve supplied Phenol, 4-Chloro-2-Iodo- under tight deadlines, charting production slots around customer needs without losing stringency on controls. Chemists in pharmaceuticals look for lots with minimal halogen scrambling to ensure their next substitution doesn’t throw a curveball. Material scientists watch for any trace metal content that might mess up conductivity or bonding downstream. Synthesizing this compound in-house allows us to take requests for custom scales, higher purity, alternate solvents for recrystallization, or special packaging with greater agility. Volume flexibility grants us better oversight, reduces wait times for our partners, and builds trust in every shipment.

    Safety, Sustainability, and Traceability

    Having hands-on experience with halogenation processes developed a deep appreciation for safety and environmental care. The route to Phenol, 4-Chloro-2-Iodo- includes handling iodine reagents, chlorinating agents, and acidic workups; even small leaks or waste mishandling can pose outsized risks. On our line, all waste is neutralized before discharge, and air extraction points have been designed based on incident logs from early production cycles. By sourcing iodine and chlorine responsibly and monitoring potential fugitive emissions, we make a real difference in both worker safety and wider environmental impact. Some of our toughest lessons came from scaling up processes that seemed trivial at small scale but brought unforeseen hazards with larger volumes.

    Traceability runs in tandem with safety. Each drum leaving our plant carries not just batch numbers, but a tested certificate that includes key synthesis parameters and analytical data. Internal audits check these claims at multiple points, allowing full backward traceability if an issue arises. When collaborating with regulatory-driven industries, this approach gives confidence that unseen problems don’t hide between the lines. Many in the field neglect this level of detail, but direct control over origin and verification keeps mistakes from snowballing down customer lines.

    Continuous Learning and Improvements

    As the actual producer, we receive direct feedback that often shapes future improvements. Sometimes it means revisiting the synthetic route to lower byproduct formation, or tweaking purification steps to push purity even higher for specialized uses. At other times, it requires adapting our documentation or labeling to keep up with evolving transport and compliance regulations in partner countries. It’s not just about making a molecule and shipping it out; it’s a back-and-forth process built through relationships with working chemists who let us know, in real terms, what helps or hinders their work.

    Batch scale and process variability arise year in and year out. From solvent availability disruptions to seasonal humidity changes impacting drying, every batch presents some new twist. Our team meets regularly to review both our results and the issues chemists report back. These meetings drive practical changes, like adding extra washing steps, holding temperatures longer, or switching to a different drying filter—steps that make a marked difference to the next run’s quality. A chemical isn’t defined only by its structure, but by the all the experience built into its manufacture.

    An Eye Toward the Future

    Even as new derivatives and synthetic approaches emerge, Phenol, 4-Chloro-2-Iodo- maintains distinct value due to the flexibility its dual halogens bring and the reliability our process adds. We continue exploring greener synthesis routes and alternatives to high-impact reagents. More laboratories seek out halogenated intermediates for next-generation drug scaffolds, specialty polymers, or molecular sensors. Each application brings a fresh perspective to our production routines, challenging us to balance consistency with evolving demands.

    With direct manufacturer control, we continue to invest in process improvements, data transparency, and open channels with researchers. The lessons of the past—failed batches, customer complaints, unexpected wins—shape a resilient approach that remains far more adaptable than what comes through layered distribution. Each shipment of Phenol, 4-Chloro-2-Iodo- reflects this hard-won expertise, connection to the end-user, and commitment to making chemical breakthroughs real.