Anhui Liwei Chemical Co., Limited
Products

Phenol, 3-Chloro-5-Fluoro-


    • Product Name Phenol, 3-Chloro-5-Fluoro-
    • Alias 3-Chloro-5-fluorophenol
    • Einecs (EINECS) 412-100-0
    • 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

    578070

    Cas Number 348-63-2
    Molecular Formula C6H4ClFO
    Molecular Weight 146.55 g/mol
    Iupac Name 3-chloro-5-fluorophenol
    Appearance White to off-white solid
    Melting Point 58-62 °C
    Boiling Point 222-224 °C
    Density 1.42 g/cm3
    Solubility In Water Slightly soluble
    Smiles C1=C(C=C(C=C1Cl)O)F
    Inchi InChI=1S/C6H4ClFO/c7-4-1-5(8)3-6(9)2-4/h1-3,9H
    Refractive Index 1.570 (Predicted)
    Flash Point 108 °C (Predicted)
    Synonyms 3-Chloro-5-fluorophenol; m-Chloro-p-fluorophenol
    Pubchem Cid 109918

    As an accredited Phenol, 3-Chloro-5-Fluoro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 100g amber glass bottle with a secure screw cap, labeled "Phenol, 3-Chloro-5-Fluoro-, 100g, for laboratory use."
    Shipping Phenol, 3-Chloro-5-Fluoro- should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Shipping must comply with local and international regulations for hazardous chemicals, commonly under the category of toxic solids. Proper labeling, documentation, and handling instructions are essential to ensure safety during transport and storage.
    Storage Store Phenol, 3-Chloro-5-Fluoro- in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and bases. Ensure proper labeling and secure storage to prevent leaks. Avoid moisture and sources of ignition. Use secondary containment and follow all relevant chemical safety regulations for hazardous substances.
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    Tel: +8615380400285

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    Certification & Compliance
    More Introduction

    Introducing Phenol, 3-Chloro-5-Fluoro-: Bridging Experience With Quality Manufacturing

    Understanding the Chemical Itself

    Experience in producing aromatic halogenated compounds, especially those in the phenol family, has taught us the significance of paying attention to subtle structural modifications. 3-Chloro-5-Fluoro-Phenol, often called simply 3-chloro-5-fluorophenol in day-to-day plant operations, represents a niche but steadily growing demand across both research and commercial synthesis. The formula, C6H4ClFO, conveys just part of the story—chemical properties and utility stem not only from the atoms themselves but from the selectivity brought by the fluorine on position five and chlorine at position three.

    Our manufacturing runs balance purity, reliability, and scalability. In routine batches, we target a minimum assay above 98%, achieved through established distillation and purification lines developed over years of practice. Quality monitoring starts with raw material inspection and is confirmed in every barrel or drum before sealing. The white to pale beige crystalline form appears familiar to those who have worked with halogenated phenols, but the difference here shows in both reactivity and downstream compatibility, a result of the specific halogen pattern.

    Why Users Seek This Structure

    Customers approach us with requests for 3-chloro-5-fluorophenol for one main reason: the dual halogen substitution opens reaction channels that mono-halogenated phenols or chloro- and fluoro-phenol isomers cannot. The presence of both groups changes not just the reactivity with nucleophiles and electrophiles, but also the predictability in further modifications.

    This molecule sees regular use as an intermediate in fields as distinct as agricultural chemistry, pharmaceuticals, and material science. For example, experienced process chemists exploit the activating and deactivating properties of the halogens to steer electrophilic substitution and nucleophilic aromatic substitution, depending on downstream needs. Placement at the 3 and 5 positions is critical—para-substituted analogs often frustrate certain routes due to steric hindrance or altered electronic effects, while other isomers may not provide the needed chemical selectivity.

    A typical request might come from a pharmaceutical developer aiming to build library compounds for screening. Here, the dual halogen effect serves not just as a synthetic handle, but as a building block in SAR (structure-activity relationship) studies, guiding further functionalization. Our customers have commented on the clear advantage: by using 3-chloro-5-fluorophenol, they can achieve higher yields or access scaffolds that are hard to synthesize from more common mono-halogenated phenols.

    Our Production Insights: Control, Safety, and Handling

    Few people outside production realize the challenges posed by halogenated phenol synthesis. The introduction of fluorine, whether by selective halogen exchange or direct fluorination, involves stringent control over moisture and residual acid—trace impurities can sabotage reactivity or trigger side reactions in later steps. In our facility, engineers put emphasis on both reaction containment and real-time analytics. Chromatographic fingerprinting and mass spectrometric confirmation—applied to every lot—reduce variability before the product moves toward formulation or further conversion.

    Worker safety and environmental responsibility become central when operating with compounds at this intersection of aromatic chemistry and halogenation. Chlorinated and fluorinated aromatics demand proper fume extraction, reactor coatings resistant to aggressive byproducts, and waste collection systems capable of isolating and neutralizing both acidic and organofluorine residues. Training spans both chemical engineering and practical hands-on operation—a philosophy that pays off in uptime as well as regulatory compliance.

    Comparisons That Matter: Not All Phenols Are Created Equal

    It helps to look at family resemblances and crucial differences. Standard phenol, while a staple in resin and disinfectant production, lacks both the altered electron density and the unique reactivity of the 3-chloro-5-fluorinated version. Chloro-phenols and fluoro-phenols alone do not give quite the same profile, especially in medicinal chemistry applications.

    Mono-chlorinated phenols, such as 2-chlorophenol or 4-chlorophenol, carry strong antimicrobial properties but rarely enter the same synthetic pathways as their di-substituted relatives. When only fluorine is present, as with 4-fluorophenol, the compound displays different hydrogen-bonding behavior and aromatic reactivity. In many synthesis tasks, mono-halogen derivatives serve as intermediates for dyes, brighteners, or herbicides but don’t unlock the same downstream complexity.

    By contrast, the dual-chlorine and fluorine setup in 3-chloro-5-fluorophenol shifts the balance of electron density not just around the ring, but at specific positions—unlocking new options for substitution and coupling. For example, cross-coupling reactions (Suzuki, Heck, Buchwald–Hartwig) can become smoother or more selective with this molecule compared to more basic phenolic substrates. The difference stems not only from theory but also from everyday feedback as customers report improved reaction yields or cleaner workups.

    Usage Patterns From the Production Line

    After years of supplying 3-chloro-5-fluorophenol, usage clusters have become clear. In pharmaceuticals, the compound regularly serves in producing building blocks for antiviral or anti-inflammatory candidates. Chemists want both rapid halogen exchange and minimal byproduct formation, which the dual-substituted phenol helps enable. This pattern repeats in agricultural chemical development—herbicide and insecticide R&D often reaches for the 3-chloro-5-fluoro motif because the electron-withdrawing nature at two points in the ring can impact both biological targets and metabolic stability.

    Material researchers—developing polymers or performance coatings—sometimes use 3-chloro-5-fluorophenol to fine-tune surface energy or introduce specific dipole interactions in specialty films. In these circles, the combination of halogens modifies not only the physical but also the optical and electronic properties, expanding the options for film formulation beyond what’s available through simpler phenols.

    Processes and Practical Considerations

    Every production run comes with learning. Tight control over reaction conditions gives us both yield and reproducibility. Multiple purification passes—often a mix of distillation under reduced pressure and preparative chromatography—become necessary to reach the purity levels demanded by API (active pharmaceutical ingredient) manufacturers or top-tier research labs. We place heavy reliance on GC-MS and HPLC for confirming the absence of isomeric impurities or residual halogenation byproducts, as even trace contamination affects downstream syntheses.

    Our packaging team treats stability as a priority. Phenol derivatives can discolor or degrade through light or moisture exposure, so sealed drums and amber containers have become standard across our shipments. Storage guidance extends to customers; based on our own stability monitoring, temperature and humidity recommendations are not boilerplate but reflect what preserves material over multi-month periods.

    Supporting the Customer Through Direct Manufacturing Experience

    Being closely involved in every stage—from weighing precursors to loading transport trucks—lets us pinpoint where users see the most value. Requests for documentation are met with records from our own analytical labs, built around long-standing familiarity with phenol halogenation. Traceability stretches back to incoming raw materials and solvent batches. Customers often request tailored advice—not just on ordering, but on optimizing reaction set-up with our product; here, practical synthesis notes, based on scaling-up and pilot runs, guide their process improvement.

    Close engagement reveals patterns in return orders or product feedback. Early batches launched years ago showed room for improvement in reducing volatile byproducts. Prompted by direct customer conversations, our R&D shifted process conditions, tightened fraction collection, and improved in-line analytics. The result: not only better purity but enhanced confidence among repeated buyers, many of whom share their insights on yield improvement or process robustness after switching to our 3-chloro-5-fluorophenol.

    Real-World Application Examples

    The compound’s versatility plays out in multiple industries. In one pharma example, a customer used our 3-chloro-5-fluorophenol as a precursor to an aryl ether that passed preclinical testing, thanks to the specific substitution pattern. In agrochemical formulation, ongoing projects use this compound as a core part of selective fungicide development. We’ve seen similar scenarios in specialty monomer synthesis for advanced electronics.

    Unlike commodity phenols, which often have multiple sources globally, 3-chloro-5-fluorophenol rewards supplier consistency and purity. Subtle changes in process affect melting point, color, and ultimately, the success of end-use applications. Regular collaborative troubleshooting between our technical staff and end users hones not just our product but also their synthetic outcomes. This two-way knowledge stream—rooted in our direct manufacturing involvement—brings efficiency and reliability far beyond catalog offerings.

    Difference Through Quality Control and Responsiveness

    Competitive advantage in this sector means more than meeting specifications. Repeatable quality, batch-to-batch, grows out of real investment in analytical hardware and training. NMR, FTIR, and HRMS reports rely on instruments run in-house and interpreted by chemists familiar with both routine and edge-case spectra. Our QC team knows the quirks of halogenated impurities and tracks them with a conservative margin, protecting customer projects from late-stage surprises.

    We monitor international regulatory changes concerning halogenated aromatics—especially those flags raised about persistence or environmental mobility—to ensure both compliance and customer guidance stays current. Shipping documentation, SDS files, and CONEG/RoHS status updates reflect what actually happens on the shop floor and in the analytical suites, based on the specific material batch, rather than generic boilerplate language. This manufacturer-to-client transparency, anchored in hands-on experience, minimizes unexpected disruptions for critical supply chains.

    Continuous Learning, Process Optimization, and Problem-Solving

    Consumer demand does not stay static; neither do the challenges in keeping material lead times short while costs remain competitive. We adjust reactor loadings, solvent choices, and purification cycles based on feedback, both internal and from trusted partners. When a production run drifts in crystallization yield, we re-examine both batch logs and real-time sensor readings to isolate the bottleneck—be it raw material grade, temperature profile, or transfer lines.

    Customer challenges feed directly into our process improvement. For example, concerns about off-odors or slight yellowing in samples triggered an investigation into trace oxidant sources, leading to equipment upgrades and more rigorous atmospheric control. These incremental improvements build a reputation for dependability and anticipate the needs of increasingly sophisticated users, whether in pharma, agchem, or advanced materials.

    Trends and Outlook: Meeting Tomorrow’s Demands

    Interest in halogenated phenols, especially those bearing both chlorine and fluorine, shows no signs of fading. Formulators and synthesis chemists look toward new targets with demanding selectivity or biological profiles, and our team answers with technical resourcefulness honed on small and large scales alike. As regulatory attention intensifies around aromatic halogenation byproducts and lifecycle, our commitment is to anticipate both safety and sustainability mandates through cleaner, lower-residual processes and careful material tracking.

    Investments in process safety, analytical depth, and operator training all reflect the daily reality of working hands-on with specialty chemicals. Our approach—shaped by actual production experience and open-ended technical dialogue—aims to provide our customers the confidence they need to pursue challenging research and efficient commercial scale-up. Phenol, 3-chloro-5-fluoro-, as we manufacture and supply it, stands both as a practical answer to targeted synthesis needs and as a bridge to new molecular possibilities.

    Closing the Gap Between Producer and User

    Direct experience turns formulas and purity numbers into reliable performance. Bottle-to-bottle, drum-to-drum, we see the impact of careful process management on customer outcomes—and respond by refining every stage, from synthesis to sampling. As markets shift and research ambitions grow, our specialty lines such as 3-chloro-5-fluorophenol evolve in quality and consistency.

    We openly share what we know, track new regulatory and industry trends, and accept project feedback as central to our role. Chemical manufacturing, at its best, links hands-on know-how with modern analytical rigor—ensuring both our partners and their projects benefit from true direct-supplier experience.