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2,3,5,6-Tetrafluoroanisole

    • Product Name 2,3,5,6-Tetrafluoroanisole
    • Alias 1,2,4,5-Tetrafluoroanisole
    • Einecs 697-426-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    902058

    Chemical Name 2,3,5,6-Tetrafluoroanisole
    Molecular Formula C7H4F4O
    Molecular Weight 180.10
    Cas Number 2438-79-5
    Appearance Colorless liquid
    Boiling Point 116-118 °C
    Melting Point -27 °C
    Density 1.419 g/cm3
    Refractive Index 1.428
    Flash Point 38 °C
    Smiles COC1=CC(F)=C(F)C(F)=C1F
    Solubility Insoluble in water
    Purity Typically ≥97%
    Storage Conditions Store in a cool, dry place

    As an accredited 2,3,5,6-Tetrafluoroanisole 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 2,3,5,6-Tetrafluoroanisole; tightly sealed, labeled with hazard information and chemical details.
    Shipping 2,3,5,6-Tetrafluoroanisole should be shipped in tightly sealed containers under cool, dry conditions. Clearly label the package with hazardous material warnings, as applicable. Protect from physical damage, heat, and incompatible substances. Comply with local and international transportation regulations for chemicals. Use secondary containment to prevent accidental leaks or spills during transit.
    Storage 2,3,5,6-Tetrafluoroanisole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers and acids. Ensure the storage area is equipped with proper chemical safety signage and spill containment measures. Follow all relevant safety and regulatory guidelines for handling and storage.
    Application of 2,3,5,6-Tetrafluoroanisole

    Applications of 2,3,5,6-Tetrafluoroanisole in Industrial Manufacturing

    2,3,5,6-Tetrafluoroanisole forms a key building block in advanced chemical synthesis, especially in sectors emphasizing fluorinated aromatic compounds. As an original manufacturer, we supply this specialty intermediate to customers operating in tightly regulated fields where consistent quality, reliable reactivity, and high purity are essential for downstream production efficiency. Below we detail its principal industrial applications based on proven, audited manufacturing experience and customer process integration.

    1. Agrochemical Intermediate Synthesis

    Agrochemical formulators use this material to introduce fluorine patterns into selective herbicide and fungicide actives, capitalizing on its electron-withdrawing capacity to fine-tune bioactivity and field stability. It serves as a nucleophilic aromatic substrate during the construction of high-value active substances such as fluorinated phenoxyacetic acids and pyridine derivatives, often through oxidative or transition-metal catalyzed couplings.

    Industry compliance standards

    • REACH (EC) No. 1907/2006 for raw material purity control
    • ISO 9001:2015-certified production for agro-intermediates
    • EU Regulation (EC) No 1107/2009 concerning plant protection products
    • Chinese Ministry of Agriculture GB/T 1600 series for pesticide ingredients

    Typical usage ratio

    • 1-5% by weight in aromatic ether coupling steps; adjusted based on target fluorine incorporation and downstream yield requirements

    Downstream process integration

    • Added at the initial stage of the synthetic route, often serving as a limiting reagent in Friedel-Crafts alkylation, Ullmann coupling, or nucleophilic aromatic substitution, then proceeded by multi-step reactions to yield the target agrochemical active

    Final product types

    • Selective herbicides (e.g. fluorinated 2,4-D analogues)
    • Aromatic fungicides
    • Pyridine-based pesticide actives
    • Custom fluorinated crop-protection intermediates

    2. Pharmaceutical Research Intermediate

    Pharmaceutical manufacturers utilize 2,3,5,6-tetrafluoroanisole on pilot and scale-up lines for the synthesis of advanced intermediates, especially where fluorinated motifs confer metabolic stability in API leads. This material enables the regioselective introduction of fluoroaromatic ethers in heterocyclic and aromatic scaffolds, facilitating late-stage diversification via C–O or C–F bond transformations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • USP General Chapter <823> for quality assurance in synthesis
    • Ph. Eur. monographs regarding intermediates, where applicable
    • ISO 9001:2015 for process documentation and traceability

    Typical usage ratio

    • Ranges from 2% to 15% by molarity in the initial ring functionalization, depending on scale (gram to multi-kilo) and the complexity of the synthesis pathway

    Downstream process integration

    • Involved during aromatic O-methylation and fluorination reactions, often as a precursor for generating more complex fluoroaromatic side chains or as a functional group transfer agent at Stage 2–3 of total API synthesis

    Final product types

    • Experimental anti-cancer and CNS molecule intermediates
    • Fluorinated phenol derivatives for research compounds
    • Advanced small-molecule leads for clinical research
    • Structural fragments for preclinical drug candidates

    3. Specialty Polymer Monomer Feedstock

    Manufacturers in specialty polymers and fluoropolymers employ this compound as a reactive comonomer precursor, leveraging its multiple fluorine atoms to tune polymer backbone polarity and enhance surface properties. During polycondensation or radical polymerization, it imparts desirable characteristics such as increased hydrophobicity and chemical inertness to niche coatings and engineered plastics.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in fluoropolymer synthesis
    • ASTM D3132 for polymer monomer purity assessment
    • EU Regulation (EC) No. 1935/2004 on materials intended for food contact (if applicable for specific end uses)
    • RoHS Directive 2011/65/EU for restricted substances in electrical/electronic components

    Typical usage ratio

    • Commonly 0.5–3 mol% as a functional comonomer in stable radical or condensation polymerization recipes; proportioning varies to achieve target fluoropolymer characteristics

    Downstream process integration

    • Charged with principal monomers (such as styrene, acrylates, or vinyl ethers) into the reactor during pre-polymer solution preparation to introduce site-specific fluorine content within the final polymer backbone

    Final product types

    • High-performance coating additives
    • Low-surface-energy fluorinated resins
    • Specialty anti-graffiti or anti-corrosion films
    • Custom-engineered thermoplastic blends

    4. Electronic Chemicals and OLED Intermediates

    Within the electronics industry, this compound supports the precision synthesis of functionalized aryl building blocks for organic semiconductors and OLED (organic light-emitting diode) intermediates. The high fluorine density augments carrier transport properties and enhances environmental stability during the downstream fabrication of light-emitting and charge-transporting layers.

    Industry compliance standards

    • JIS C 5052 standards for chemicals in electronic device manufacturing
    • ISO 14644-1 for cleanroom process control during material handling
    • IEC 61249-2-21 for halogen-free materials in electronics (specialty applications)
    • Customer-specific purity standards for photoelectronic grade chemicals

    Typical usage ratio

    • 0.3–2% by weight in precursor mix formulations for OLED sublayer synthesis; adjusted to match luminous efficiency and charge injection requirements

    Downstream process integration

    • Introduced in the synthesis of fluorinated aromatic ligands or ether-forming condensation steps before coupling into larger π-conjugated structures for organic light-emitting or transport layers

    Final product types

    • Small-molecule OLED intermediates
    • Advanced aryl fluorides for display electronics
    • Photoresist additives
    • Organic semiconducting layer materials

    5. Fine Fragrance and Flavor Intermediate Synthesis

    The fine chemicals sector incorporates this raw material to introduce unique fluorinated aromatic segments into high-value fragrance and flavor intermediates. The ether group and fluorine configuration influence both volatility and olfactory profiles, especially in the synthesis of rare aromatic ethers and modulators for luxury perfumery or specialty food flavorants.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • FAO/WHO JECFA Food Additive Specifications for raw materials
    • ISO 9001:2015 for quality traceability in flavor/fragrance manufacturing
    • EU Regulation (EC) No. 1334/2008 on flavorings and certain food ingredients

    Typical usage ratio

    • Typically 0.1–1% by mass in key step reactions for specialty aroma compounds; scale and concentration defined by target note intensity and downstream processing yield

    Downstream process integration

    • Used during the methylation or fluorination of aromatic skeletons, often in the primary or secondary modification stages before esterification or etherification to fine-tune aromatic properties

    Final product types

    • Specialty aromatic ether components for perfumery
    • Trace fluorinated flavor molecules for premium food formulations
    • Custom manufactured aroma chemicals for fine fragrance brands
    Free Quote

    Competitive 2,3,5,6-Tetrafluoroanisole prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,3,5,6-Tetrafluoroanisole: A Closer Look from the Manufacturer’s Bench

    About Our Product

    2,3,5,6-Tetrafluoroanisole occupies a distinctive place in our production line. Decades in fluorinated chemistry have taught us to appreciate both the subtleties and the hard technical differences among fluorinated aromatic ethers. This compound delivers a unique molecular footprint: four fluorine atoms at key positions on the aromatic ring, together with a methoxy group, present opportunities for demanding synthetic applications. The specifications most requested—99.5% minimum purity (GC), moisture below 0.15%, color below 20 (APHA)—aren’t just technical targets, but results from repeated dialogue with pharmaceutical, agrochemical, and material science development groups. Because we handle each step of the process, from fluorination through final distillation, we’re in a position to guarantee reproducibility batch after batch—consistently clear liquid, no extraneous byproducts, and a clean GC trace.

    Practical Differences in Refinement and Utility

    Colleagues in research often ask about the practical significance between 2,3,5,6-Tetrafluoroanisole and less substituted analogs like 2,4-difluoroanisole or 2,3,6-trifluoroanisole. In our reactors and purification trains, tetrafluorination ramps up both the demands and the results. The electron-withdrawing nature of four fluorine atoms (versus one to three) dramatically lowers electron density on the aromatic ring, shifts boiling point, and tunes the reactivity. Our customers in the API field often draw on these properties to introduce downstream selectivity using milder reagents than would be required with less fluorinated starting materials. For example, the specific substitution pattern of 2,3,5,6-tetra influences both regioselectivity and overall yield when constructing biaryl linkages typical in active molecule frameworks.

    Handling practices differ frankly from less fluorinated relatives. Tetrafluorinated anisoles demonstrate greater hydrolytic stability in the laboratory environment. We’ve run comparative hydrolysis and found our product remains remarkably intact versus less fluorinated variants when exposed to trace moisture under ambient conditions. Operators appreciate the predictable evaporation rate and the absence of aggressive off-odors that can linger when an impure batch passes through QC. Scale-up teams report lower byproduct loading in subsequent halogenations, which ultimately means less column time and smoother cleanups.

    From Synthesis to Application—Direct Experience

    Years of process feedback tell us the route to 2,3,5,6-Tetrafluoroanisole is never a “one size fits all” operation. We’ve settled on selective nucleophilic aromatic substitution (SNAr) routes, making use of ortho/para directing effects. Upstream, our supply of fluoride sources must be tightly controlled—impurities or trace water create batch variability. We distill under vacuum and use custom-wrapped vessels to suppress static charges, since the fluorinated ethers can build up surprising static on scale. After repeated distillations, we store in specially treated containers to avoid leaching from closures, since even a small ingress of environmental contaminants can trigger color shifts unacceptable to advanced material users.

    End users value the thermal and oxidative stability offered by this structure. Our formulation customers, especially those in OLED material development, lean on tetrafluorinated anisoles for fine-tuning emission wavelengths. The altered electron density affects the transport and recombination behavior of charge carriers in the target polymer matrix. Product developers in the crop protection arena have told us the precise substitution pattern gives them consistent metabolic pathway prediction. Their synthetic chemists conduct stepwise halogenations and substitutions, relying on our detailed batch analysis to predict downstream compatibility.

    Specifying for Process and Regulatory Context

    Production isn’t just about hitting numbers. Every stage—reagents, batch records, tests—feeds into compliance. Since 2,3,5,6-Tetrafluoroanisole travels into regulated pharmaceutical and agrochemical supply chains, we maintain extensive documentation for each batch. It’s critical: most of our partners request CoAs reflecting residual solvents down to ppm. Internal records document fluoride and methoxy source materials right through to final release. Where regulatory authorities demand it, we provide full impurity profiling because even sub-0.1% levels can complicate approval for formulated end products.

    On-site, QC samples pull hourly during production runs. We sample from both head and tail ends of the tank and validate for both high-volatility and late-eluting impurities. Organic trace analysis follows each lot—if even faint, extraneous aromatic signals appear, the distillation schedule gets revised. Container integrity checks reduce the risk of contamination during storage and transit. Over the years, customer audits have shaped not only data retention times, but actual process improvements—from switching valves to more robust closure systems, to installing positive-pressure storage for shipment periods extending beyond one month.

    Field Outcomes and Technical Challenges

    Our technical staff routinely supports customers through pilot-stage observations. Once, a specialty pharmaceutical partner surfaced an issue with an unexpected impurity spike. Knowing the synthesis steps and sensitivities, our internal team traced this to an overlooked fluoride scavenger interaction, rather than a shipping or storage error. By tweaking the scavenger protocol, we eliminated the concern the very next batch—an onsite problem-solving story that long-term partnerships value.

    We’ve faced challenges scaling from pilot to full production. Maintaining a narrow distillation range gets harder as reactor volumes climb. Higher throughputs can amplify trace heating errors, so senior team members supervise every major scale-up, monitoring for drift in both boiling point and color index. We keep pilot-scale glassware and analytical gear ready to troubleshoot issues—one reason we can move nimbly between R&D batch support and commercial production needs. Customers appreciate direct disclosure of differences across years and batches—not just numbers on a sheet, but informed interpretation from chemists who work up close.

    Real-World Customer Requirements Shape Our Processes

    Client conversations drive changes in how we interpret specifications. Pharmaceutical programs demand clarity on the source and lot traceability of precursor materials. We respond by barcoding both drum and aliquot stages—matching each final liter of 2,3,5,6-Tetrafluoroanisole with a comprehensive genealogy. Researchers developing fluorinated building blocks for agricultural actives highlight the need for predictable reactivity profiles, so each batch undergoes selective bioassay screening for contaminants that might interfere downstream.

    Because advanced materials scientists continually push demands—especially for high-purity applications in polymer and optoelectronic development—we built in unplanned, hands-on steps. For instance, even once a batch meets HPLC and GC targets, we subject the final distillate to ultraviolet exposure checks, screening for photo-instability or subtle shifts in color that some users spot long before traditional analysis would.

    Molecular Design—Why Four Fluorines Matter

    Fluorination patterns don’t just “decorate” a molecule. Multiple fluorines on the anisole ring shape which synthetic routes work smoothly. Two, three, or four fluorine atoms can decide whether a downstream coupling requires a palladium catalyst or manages with milder bases. Four positions—2,3,5,6—shield the aromatic core from unwanted side reactions, making further substitutions more selective. We’ve followed up with users who explore alternative substitution patterns, and their reaction data confirms the differences. Even minor substitutions can dramatically affect yield and byproduct profiles. Four-fold fluorination frequently suppresses unwanted side-chain oxidations, which means fewer purification headaches.

    Direct Insights from Manufacturing Experience

    On our production floor, straightforward operational steps often carry outsized importance. For years, we’ve observed how operator skill directly shapes impurity profiles. Automated controls help, but real-world batch-to-batch consistency requires on-the-spot adjustment—altering reflux times or heads-and-tails cuts, sampling just a bit further down the column when raw material batches shift slightly in water content.

    Supply chain security remains a constant watch point. Raw material incidents, like delayed shipments of anhydrous fluoride sources or sudden market-driven price shocks, demand flexible sourcing plans. Our contracts include secondary source clauses, and we pre-qualify all backup sources for both precursor quality and contaminant content—experiences from the past guide these policies. A past supply crisis, where an unexpected transport holdup threatened several lots, drove our shift to greater onsite reagent storage, ensuring downstream projects don’t miss timelines.

    Environmental and Safety Considerations

    Experience teaches caution with fluorinated ethers production: specialized ventilation, antistatic precautions, and disciplined waste handling profile every operation. We’ve seen teams across the industry caught off-guard by what appears to be a benign, clear liquid—some overlook just how reactive fluorinated byproducts grow during distillation. Our staff train on both exposure and containment protocols. Residual waste management integrates modern scrubber systems to neutralize volatile remnants before they leave the plant, addressing both environmental standards and community responsibility. Working hands-on with these materials, we’ve learned the fine margins distinguishing safe handling from trouble.

    We deliberately maintain a small buffer between regulatory minimums and our in-house safety specs. Field audits and external process safety reviews reveal new risks at full-scale runs—such as subtle thermal runaway thresholds when scaling up heating. After a near-miss with thermal imbalance, strict interlocks now pause any batch where measured delta-T exceeds set limits.

    Long-Term Value and Process Control

    Customers in pharma and advanced materials value not just high-purity product, but clear, continuous quality records spanning years. Feedback from regulatory submissions flows regularly back to our technical and batch teams. We keep archived samples in temperature- and light-controlled rooms, allowing us to review and compare quality shifts year over year—an advantage in a market where documentation can be the difference between rapid approval and costly delays.

    As a manufacturer, we see “margin” not just in price but in process flexibility and speed. On more than one occasion, urgent customer requests triggered after-hours batch runs. Flexible scheduling is part of the real commitment. Years of developing skill with this specific tetrafluoroanisole lets us pivot rapidly between kilo-lab support and metric ton runs, keeping pace as research scales into production. Process know-how, alongside straightforward communication with both customers and internal staff, keeps projects moving forward.

    Adapting to Changing Application Demands

    Major industry changes drive evolution in what tetrafluorinated anisole variants can offer. New catalysts, developed by research partners, open reaction windows previously closed by traditional substituents. As more users work at the edge of electronics, pharmaceutical, and crop science, our product serves as both starting block and performance enhancer. Some customers want ultra-tight impurity controls, others prioritize specific reactivity patterns. Our internal R&D teams run pilot reactions mirroring client applications, spotting early any trend shifts—a practice honed over years of field collaboration.

    What Sets Our Tetrafluoroanisole Apart

    After years focused on this space, differences stand out. In practical use, our 2,3,5,6-Tetrafluoroanisole exhibits low color, minimal residual solvents, exceptional purity, and robust supply traceability. Having refined our packaging based on user feedback, we avoid common stability pitfalls—no off-odors, no leaky seals, and no photodegradation before the product gets into the customer’s hands. Purification workflows keep ion content and acid number reliably below detection limits, critical for sensitive downstream applications.

    Regular dialogue with customers leads to continuous refinement. A case comes to mind where an OLED developer required strips free from even sub-ppm metal contamination—an uncommon demand in the broader market. We adjusted both upstream cleaning protocols and downstream sample handling, not just to win a contract, but because these steps advanced our process control. That level of engagement keeps our chemistry sharp and our service relevant.

    Conclusion: A Long-Term View from the Manufacturer

    Making 2,3,5,6-Tetrafluoroanisole to a high standard means focusing on the hands-on realities—how the batch looks on the glass, how it behaves during transfer, how it interacts with partners’ chemistry. We don’t just sell chemical specs; we build direct relationships between our production, testing, and users. Each insight gleaned from production experience and customer feedback blends into a product that continues to earn its place in challenging syntheses and advanced materials.

    Over the years, our learning keeps evolving. Reliability springs not so much from a technical sheet, but from the accumulated experience of what works and what fails, what purity truly means in practice, and how chemistry moves from bench to industrial relevance. For partners relying on precision, predictability, and performance, our 2,3,5,6-Tetrafluoroanisole offers confidence built on real expertise.