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4-Chloro-3-Fluorophenol

    • Product Name 4-Chloro-3-Fluorophenol
    • Alias 4-Chloro-3-fluoro-1-hydroxybenzene
    • Einecs 609-440-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    128145

    Chemicalname 4-Chloro-3-Fluorophenol
    Casnumber 88511-62-2
    Molecularformula C6H4ClFO
    Molecularweight 146.55
    Appearance White to light yellow solid
    Meltingpoint 63-67°C
    Boilingpoint 210-212°C
    Density 1.44 g/cm3
    Purity ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=CC(=C(C=C1O)Cl)F
    Inchi InChI=1S/C6H4ClFO/c7-5-2-1-4(9)3-6(5)8
    Refractiveindex 1.570
    Storagetemperature Store at 2-8°C
    Ecnumber 402-320-0

    As an accredited 4-Chloro-3-Fluorophenol 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 100 grams of 4-Chloro-3-Fluorophenol, sealed with a tamper-evident cap and labeled with safety information.
    Shipping 4-Chloro-3-Fluorophenol is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material and must comply with relevant transport regulations. Proper labeling, documentation, and safety measures are required to ensure safe transit and handling during shipping. Store in a cool, dry place upon arrival.
    Storage 4-Chloro-3-Fluorophenol should be stored in a tightly closed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect from light and moisture. Use appropriate personal protective equipment when handling. Clearly label the storage container and keep away from food and drink. Store at room temperature and follow all relevant chemical safety guidelines.
    Application of 4-Chloro-3-Fluorophenol

    Applications of 4-Chloro-3-Fluorophenol in Industrial Manufacturing

    Our 4-Chloro-3-Fluorophenol is manufactured for high-reliability integration into advanced chemical synthesis routes. The following application scenarios highlight its effective utilization in real-life industrial downstream fields, detailing compliance benchmarks, formulation ratios, process input points, and resulting end products per industry segment.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)

    Leading pharmaceutical manufacturers employ 4-Chloro-3-Fluorophenol as a key intermediate for producing specific fluorinated aromatic compounds, widely used in non-steroidal anti-inflammatory drugs (NSAIDs), anti-infectives, and certain oncology agents. Its unique substitution pattern delivers regioselective reactivity during etherification and acylation reactions, critical for the construction of bioactive molecules conforming to global regulatory expectations on traceability and quality. Our material supports multi-step reaction schemes with minimal batch-to-batch variance, ensuring predictable yields and specification adherence throughout GMP-regulated syntheses.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • European Pharmacopoeia (Ph. Eur.) Intermediate specifications
    • US FDA cGMP 21 CFR Part 211 and 210
    • Chinese Pharmacopoeia (ChP) standards for intermediates

    Typical usage ratio

    • 0.6 – 3.0 molar equivalents per target molecule, adjusted by synthetic pathway complexity and yield optimization; routine for step 2–3 in multi-step pharmaceutical synthesis.

    Downstream process integration

    • Introduced post-halogenation in aromatic substitution sequences
    • Used in Suzuki or Buchwald–Hartwig coupling reactions
    • Enters amidation steps to form fluorinated amides and ethers
    • Applied before protection/deprotection cycles in process R&D and scale-up

    Final product types

    • Fluorinated NSAID intermediates
    • Target API precursor materials
    • Oncology drug intermediates
    • Aromatic ether-based pharmaceutical intermediates

    2. Agrochemical Active Ingredient Manufacturing

    Major agrochemical process operators employ 4-Chloro-3-Fluorophenol in the synthesis of advanced phenolic scaffolds for selective herbicides and fungicides. The electron-withdrawing halogen atoms contribute to plant uptake efficiency and environmental stability in the final active molecule. Inside multi-hectare synthesis plants, our material supports downstream bromination and subsequent etherification stages, with precise stoichiometry management to constrain by-product formation. The raw material’s provenance and analytical traceability align with major multinational procurement protocols emphasizing worker safety and environmental compliance.

    Industry compliance standards

    • EPA FIFRA (US) production and reporting compliance for pesticide ingredients
    • REACH regulation (EC) No 1907/2006 registration and tonnage tracking
    • GB/T 31272-2014: Chinese technical requirements for pesticide intermediates
    • ISO 9001:2015 certified quality management systems in active ingredient supply

    Typical usage ratio

    • 5–18% by weight of total phenolic reactant mass in multi-component synthesis; precise ratio varies with desired halogen density and downstream molecule structure.

    Downstream process integration

    • Input after initial aromatic ring functionalization
    • Continuity to condensation/polycondensation for herbicide scaffolds
    • Use in chlorination/fluorination work-ups to improve stability
    • Bried reactions to yield specific fungicide precursors

    Final product types

    • Phenoxy herbicides (selective for cereal crops)
    • Triazole fungicide intermediates
    • Precursor compounds for seed treatment actives
    • Stabilized aromatic additives for crop protection

    3. Specialty Dye Intermediate Preparation for Electronics and Photonics

    Manufacturers supplying advanced dye and pigment components to OLED panel, photographic, and laser technology markets utilize 4-Chloro-3-Fluorophenol to achieve precise halogenation patterns for enhanced charge mobility and oxidative stability in aromatic chromophores. Integration into condensation and diazotization routes improves spectral absorption ranges and longevity, meeting strict standards for semiconductor wafer inspection and advanced imaging technologies. The use of high-purity grades simplifies downstream purification and enables batch reproducibility crucial for photonics supply chains.

    Industry compliance standards

    • EN 62471:2008 (Exposure limits for optical radiation for LEDs, ensuring dye safety)
    • RoHS Directive (EU) 2011/65/EU for electronic device components
    • IEC 61249-2-21 (Halogen-free materials requirements for electronics)
    • ISO 14001 Environmental Management (waste minimization, emissions control)

    Typical usage ratio

    • 3–8 mol% with respect to total aromatic moieties; adjusted per chromophore target wavelength and final dye performance criteria.

    Downstream process integration

    • Incorporated post-diazo coupling for extended conjugation
    • Used in halogen exchange and further cyclization steps for dye stabilization
    • Enter into C–O bond formation prior to dye-metal complexation
    • Processed in high-temperature reactors for fine control of color point

    Final product types

    • Blue and green emitter dyes for OLED displays
    • High-stability photographic colorants
    • Near-infrared (NIR) absorbing dyes for laser and medical imaging
    • Halogen-modified pigments for microelectronics patterning

    4. Fluorinated Polymer Additive and Intermediate Production

    Producers in the engineered polymer value chain adopt 4-Chloro-3-Fluorophenol to introduce halogenated functional moieties into specialty co-polymers. This enables improved hydrophobicity, thermal resistance, and controlled reactivity in polymers applied to electronics insulation or custom fluoropolymer blends. During co-polymerization or chain extension, our raw material activates as a functional handle, reacting consistently under bulk or solution phase techniques, while supporting downstream conformance to demanding purity and byproduct-limitation specifications demanded by high-technology converters.

    Industry compliance standards

    • UL 94 flammability rating (testing of polymer samples with halogen content)
    • IEC 60695-2-10 (electrical insulation material safety requirements)
    • ASTM D6288 (purity and migration checks for fluorinated plastics)
    • REACH SVHC compliance for fluorinated substances

    Typical usage ratio

    • 0.5–4.5 weight percent as a polymer feedstock modifier; dependent on required final polymer fluorine content and mechanical property targets.

    Downstream process integration

    • Added at the resin pre-polymerization blending stage
    • Used in chain extension to insert halogenated aromatic units
    • Engaged in solution polymerization for specialty coatings
    • Applied during bulk melt processing for film and fiber production

    Final product types

    • Fluoropolymer-modified insulation films
    • High-durability engineering plastics for automotive wiring
    • Functional resins for flexible printed circuit boards
    • Halogenated polymeric additives for specialty cable sheaths
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    Certification & Compliance
    More Introduction

    4-Chloro-3-Fluorophenol: A Vital Building Block in Modern Chemistry

    Understanding 4-Chloro-3-Fluorophenol from the Manufacturer’s Lens

    Over the years of hands-on manufacturing in the field of halogenated aromatic compounds, we have come to recognize the valuable role 4-Chloro-3-Fluorophenol (CAS: 700-31-8) plays in chemical synthesis. This compound features a benzene ring with one chlorine atom at the fourth position and a fluorine atom at the third, giving it a unique reactivity profile that chemists across various fields continue to count on.

    We produce 4-Chloro-3-Fluorophenol in our facility using controlled chlorination and fluorination sequences, followed by purification steps designed for high purity—usually not less than 98%. Quality control is critical. We use gas chromatography and spectroscopic analysis to track purity and ensure contaminants stay well below actionable thresholds, keeping batch-to-batch consistency tight so customers don’t run into issues mid-process.

    Over time, we’ve learned that subtle changes in halogen arrangement can mean the difference between a compound that works and one that doesn’t. Our process ensures precise substitution, avoiding overhalogenation or isomeric impurities that frustrate downstream use. It’s tempting to take such accuracy for granted until a reaction fails or a side product appears unexpectedly. This attention has made a difference in the trust we’ve built with customers, especially in sectors where even minor deviations can mean days of lost work or unusable product.

    What Sets 4-Chloro-3-Fluorophenol Apart?

    4-Chloro-3-Fluorophenol isn’t just another halogenated phenol stacked on a laboratory shelf. The interplay between the electron-withdrawing chlorine and fluorine atoms grants it markedly different chemical behavior from simpler analogs. In pharmaceuticals, agrochemicals, and advanced materials, this matters at the very root of product development. Our technical team often discusses the distinct reactivity: selectivity in substitution, the ease of forming reactive intermediates, and its flexibility in coupling reactions due to the dual influence from both halogens.

    Compared to phenol, mono-chlorophenol, or mono-fluorophenol, this particular arrangement tunes acidity, impacts solubility, and shifts nucleophilic aromatic substitution patterns. 4-Chloro-3-Fluorophenol enables fine-tuned synthesis, especially when downstream steps demand tight control over position-specific replacement or when forming diaryl ethers or carbon–carbon bonds. We’ve seen customers face setbacks using structural isomers or less substituted analogs that fail to deliver on reaction speed or yield. In contract manufacturing settings, predictability from the starting material drives both project timelines and final product quality.

    Specifications: Purity, Form, and Handling Experience

    Our experience shows that minor batch-to-batch variability in halogenated intermediates can throw off whole processes. So we keep our focus sharp on critical attributes like purity, moisture content, and controlled particulate sizing. 4-Chloro-3-Fluorophenol leaves our plant as a crystalline solid, with a pale off-white appearance, rarely deviating due to stringent environmental management. Packaging runs in airtight containers with inside liners, minimizing risk of hydrolysis or volatilization, a lesson learned after an early shipment years ago arrived at a client’s lab with moisture-induced clumping. Since updating packaging protocols, we regularly receive feedback about improved handling and storage.

    Routine production volume varies with market needs. More frequent orders from pharmaceutical and agrochemical developers over the past decade have let us streamline our process and keep raw material lead times short. Where projects demand special grades—for instance, in electronic intermediates—we can tailor purification and offer supporting data packages. We do not shrug off requests for smaller or larger scale batches. In earlier days, custom-scale manufacturing created workflow headaches; now, refinements in procedure and equipment let us transition between order sizes efficiently, which eases pressure for both our team and customers working on tight schedules.

    Why Industries Look Beyond Standard Phenols

    The market increasingly calls for building blocks that deliver more than basic reactivity. In medicinal chemistry, regulators look closely at byproduct profiles. Researchers use 4-Chloro-3-Fluorophenol to avoid problematic side reactions and access functionalized targets otherwise tough to build. Bioactive molecules containing both chlorine and fluorine atoms often show higher metabolic stability or altered receptor affinity, a trend well documented in primary literature and patent filings.

    In agrochemicals, having both halogens tunes activity against pests or weeds without hiking toxicity to non-target species. A basic phenol or simple halogenated variant doesn’t get the same results. Formulators aiming for potent yet environmentally mindful products need these subtleties. Over many collaborations with R&D teams worldwide, we’ve seen how this compound fills gaps that single-halogen phenols can’t address.

    Advanced material scientists turn to this compound when they need ring-substituted phenols for specialty polymers or functionalized monomers that offer precise control over the thermal and electrical properties of the resulting materials. We’ve learned that purity and precise isomer control are especially critical in this sector, as even trace contaminants can throw off catalyst behavior or material performance down the line.

    Comparative Benefits in Synthesis

    Looking across the product spectrum, 4-Chloro-3-Fluorophenol stands out when comparing synthetic accessibility, reaction pathway flexibility, and the physicochemical properties it imparts to target molecules. For example, in Suzuki, Buchwald–Hartwig, or nucleophilic aromatic substitution chemistry, the dual halogen pattern favors selectivity that mono-substituted phenols lack.

    Many chemists we work with point to cleaner reaction profiles, more predictable yields, and reduced unwanted byproduct formation. By contrast, phenolic substrates without the dual halogen atom framework may require additional protection/deprotection steps or generate more byproducts that stress purification columns. Over years of scale-up, we’ve taught ourselves to scrutinize key metrics: waste generation, conversion rates, and downstream compatibility.

    While every application brings its own requirements, our experience leads us to recommend 4-Chloro-3-Fluorophenol when a synthesis needs a halogen pattern that activates precise positions on the ring. This can make later steps—like constructing biaryl, aryl ether, or complex heterocyclic frameworks—drastically easier. By listening to customer experiences and actively troubleshooting alongside them, we’ve learned how little room there is for compromise on input quality, especially under commercial time constraints.

    Product Integrity, Storage, and Transportation

    Reliability in every drum of 4-Chloro-3-Fluorophenol matters as much to us as it does to the final user. Problems with trace metals, solvent residues, or thermal sensitivity usually stem from upstream laxness. To avoid these, we invest in routine equipment maintenance and environmental controls—a lesson we don’t forget after fielding calls about off-spec material, especially with tighter regulatory thresholds improving safety expectations worldwide.

    On our shop floor, we rely on moisture meters and nitrogen-blanketed tanks, especially in humid climates. We label every shipment with lot-specific data and stability guidance, and always encourage feedback from customers to identify points we can do better—sometimes an improvement comes just from boosting the seal on an inner bag or running another round of drying. Logistics arrangements emphasize temperature control, short dwell times, and clear chain-of-custody, based on experiences where a minor misstep caused big headaches at high-value labs on the receiving end.

    Ethics, Safety, and Regulatory Stewardship

    Chemicals like 4-Chloro-3-Fluorophenol demand a responsible attitude at every stage. From a manufacturer’s perspective, safe handling starts before raw materials ever enter the reactor. We run regular hazard and operability analyses, maintain on-site occupational training, and focus closely on environment and safety compliance. Our team is trained to spot and address health risks, such as skin and respiratory hazards presented by halogenated phenols.

    Regulations evolve and grow stricter over time. Jurisdictions demand more documentation and transparency, especially in the pharmaceutical and agricultural supply chains. Reach, TSCA, and other frameworks push us to keep product stewardship front and center. Over the years, we have invested in both product testing and supplier audits, cutting down on the risk of batch rejection due to uncontrolled variables. Each time we upgrade a facility or bring on a new synthesis route, the regulatory process shapes our choices of reactants, waste treatment, and shipping arrangements. Many of our clients express relief when a certificate of analysis, impurity profile, or safety data sheet comes back with no surprises—a result of careful planning at every manufacturing stage.

    Ethical manufacturing requires looking beyond just regulatory paperwork. We consult regularly with process engineers and health officers, taking seriously both local and global environmental impacts. Waste solvents and mother liquors undergo strict separation and treatment, and we've redesigned some process streams to recover or recycle halogen derivatives, reducing total impact over time. This approach makes our site safer and meets the growing expectations among industry partners for responsible manufacturing.

    Innovation Rooted in Practical Experience

    Every chemical plant operator develops a sense for what works over thousands of batches run and new methods tested. For 4-Chloro-3-Fluorophenol, our biggest innovations have come not only from new catalysts or reactors, but also from countless practical tweaks—modifying cooling profiles, adjusting feed rates, or investing in smarter analytics. Feedback from on-the-ground chemists and plant operators helps us spot where issues like slow filtration, unexpected volatility, or stubborn color bodies can be addressed before they ever reach your bench or production line.

    Open dialogue with customers, both large and small, gives us access to emerging needs—like microelectronic applications where trace ionic contamination wrecks device yields, or specialty pharmaceutical syntheses where even a small change in melting profile can set off alarms at QA. We have responded by testing new grades, expanding QC reporting, and supporting direct application trials. By maintaining a close relationship with everyone from purchasing agents to R&D chemists, we generate knowledge that formal specs or data sheets just don’t deliver.

    Solving Application Bottlenecks Together

    Projects sometimes stall when upstream intermediates don’t arrive as expected or introduce variability midstream. The reality on both sides of chemistry is about problem-solving, not just logistics. Once, a pharmaceutical client reported variable reaction times during a late-stage coupling using our 4-Chloro-3-Fluorophenol. Collaborative root-cause analysis uncovered a minor impurity from an unoptimized drying cycle. We modified that process, retested, and restored both customer and internal confidence.

    Another challenge cropped up for an agrochemical formulator needing very tight control over particle size for automated handling. Standard grind sizes led to clumping in feeders and inconsistent dispensing. After several process tests on our end—adjusting milling time, sifting, and environmental humidity—we established a targeted protocol and improved downstream reliability. These successes and failures have prompted us to keep close technical support open to end-users so that actionable data and support flow in both directions.

    Companies making waterborne coatings or resin intermediates rely on moisture-free input with tight color specs, often to meet regulator scrutiny or secure product approvals. Even a hint of color drift can set production back by days. To head off issues, we invested in new laboratory colorimeters and batch-testing infrastructure, pushing specification limits tighter year after year. These upgrades have directly improved approval speed for downstream products.

    Sometimes, uniqueness of 4-Chloro-3-Fluorophenol creates its own learning curve for chemists used to simpler analogs. Direct communication on solvent compatibility, optimal dissolution, or storage temperature often stops a minor hitch from growing into a major disruption—a philosophy we invest in daily, both because it keeps projects on track and because knowledge built on lived experience beats expectation every time.

    The Future of Halogenated Building Blocks

    Sustained demand for reliable, multi-functional starting materials drives ongoing improvement on the manufacturing floor. For 4-Chloro-3-Fluorophenol, we continue to monitor new regulatory guidance and emerging end-uses. As more industries push for cleaner, greener synthesis, we review and recalibrate our own processes to minimize energy use, cut hazardous byproducts, and recover more value from side streams. Investment in automation, smarter analytics, and digital batch tracking keeps our output both reliable and transparent.

    Many next-generation pharmaceuticals and fine chemicals are being designed to include precisely placed halogens for metabolic or environmental stability. Each shift in research priorities puts a premium on well-characterized, high-purity intermediates. Our experience leads us to anticipate that customizations—like isotopic labeling, ultra-high purity levels, or new environmental certifications—will soon be less “premium options” and more baseline expectations. As with every upgrade on the plant floor, we approach these emerging needs through steady trial, feedback, and knowledge-sharing rather than marketing hype. This long-term approach grows both our technology base and our trust with partners within and beyond the traditional chemical sector.

    Manufacturing 4-Chloro-3-Fluorophenol has never been just about technical accomplishment. The countless stories from R&D teams, formulators, and production chemists have shown us that even minute improvements upstream ripple outwards—smoothing launches, unlocking discoveries, or supporting safer, more effective products in medicine, agriculture, and advanced materials. Our pride as a manufacturer comes not from commodity output, but from the satisfaction of seeing real solutions materialize from genuine collaboration and the knowledge built day by day with every batch, every shipment, and every conversation.