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3,5-Difluoroanisole

    • Product Name 3,5-Difluoroanisole
    • Alias MFCD00001073
    • Einecs 629-031-1
    • 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
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    Specifications

    HS Code

    225278

    Name 3,5-Difluoroanisole
    Cas Number 372-42-7
    Molecular Formula C7H6F2O
    Molecular Weight 144.12
    Appearance Colorless liquid
    Boiling Point 167-169 °C
    Melting Point -26 °C
    Density 1.224 g/cm3
    Refractive Index 1.488
    Flash Point 58 °C
    Smiles COC1=CC(F)=CC(F)=C1
    Solubility Insoluble in water; soluble in organic solvents

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

    Packing & Storage
    Packing 3,5-Difluoroanisole is packaged in an amber glass bottle, 100 mL, with secure screw cap and clear hazard labeling.
    Shipping 3,5-Difluoroanisole is typically shipped in sealed, chemical-resistant containers to prevent leakage and contamination. It should be transported in accordance with local, national, and international regulations for hazardous chemicals, ensuring proper labeling. The shipping environment must be cool, dry, and well-ventilated, while avoiding exposure to heat, sparks, or open flame.
    Storage 3,5-Difluoroanisole should be stored in a tightly sealed container, away from heat, sparks, and open flames. Keep it in a cool, dry, and well-ventilated area, protected from moisture, direct sunlight, and incompatible substances such as strong oxidizers and acids. Ensure storage in a designated chemical storage cabinet and properly label the container to prevent accidental misuse.
    Application of 3,5-Difluoroanisole

    Applications of 3,5-Difluoroanisole in Industrial Manufacturing

    3,5-Difluoroanisole serves as a crucial intermediate for specialized synthesis in the fine chemicals sector. Its unique difluoro substitution pattern enables precise structural modifications required for advanced agrochemicals, pharmaceuticals, liquid crystal materials, and performance polymers. Our manufacturing process supports strict compliance and integration demands set by downstream producers in these application areas.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical companies employ 3,5-difluoroanisole as a key building block for the development of next-generation herbicides and fungicides. Its electron-rich aromatic system and selective methoxy and fluoro substituents enable rapid nucleophilic substitution and coupling reactions during active ingredient synthesis. Process chemists utilize it for constructing fluorinated phenyl rings in pre-emergent and post-emergent crop protection actives, demanding high purity and traceability throughout production.

    Industry compliance standards

    • ISO 9001:2015 certified quality management for intermediates
    • REACH (EC No 1907/2006) preregistration (if imported to EU)
    • Global Crop Protection Chemistry (FAO/WHO specifications)
    • US EPA 40 CFR Part 158 requirements for new active ingredients

    Typical usage ratio

    • 5–20% of total aromatic intermediates in active ingredient routes, adjusted based on desired fluorine content and target compound structure

    Downstream process integration

    • Introduced in the initial synthesis step for ring construction, often via halogen-metal exchange or direct coupling with haloaryl units

    Final product types

    • Selective post-emergent herbicides (e.g., difluoro-substituted phenoxyacetates)
    • Systemic and contact fungicides requiring fluoroaromatic moieties
    • Insect growth regulators derived from fluorinated benzene cores
    • Registration trial samples for EPA and OECD review

    2. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical manufacturers use 3,5-difluoroanisole in the synthesis of advanced pharmaceutical intermediates, especially for APIs incorporating difluorinated aromatic segments. The compound enables efficient C-H activation, transition metal-catalyzed cross-coupling, and subsequent transformation into biologically active scaffolds. Its consistent supply and ultra-low impurity profile address stringent GMP quality and regulatory expectations in medicinal chemistry and commercial API production.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredient intermediates
    • USP, Ph. Eur, or JP monographs (as relevant to intermediates)
    • 21 CFR Part 211 for quality control of starting materials
    • Traceability requirements for Drug Master File (DMF) submission

    Typical usage ratio

    • 10–40 mol% per synthesis batch, calculated to balance cost and target difluorophenyl incorporation in the final API

    Downstream process integration

    • Charged to the reactor during Stage I intermediate formation; participates in Suzuki, Buchwald-Hartwig, or SNAr pathways, followed by substitution or ring closure reactions

    Final product types

    • Small molecule APIs in oncology and CNS segments
    • Difluoroaromatic scaffolds for anti-viral drugs
    • Lead optimization compound libraries for pharmaceutical R&D
    • Phase II and III clinical trial pharmaceutical ingredients

    3. Liquid Crystal Display (LCD) Material Synthesis

    Producers of advanced display materials leverage 3,5-difluoroanisole as a core intermediate for crafting difluorinated liquid crystal compounds. The compound supports the design of anisotropic molecules with controlled dipole moments, essential for high-contrast, fast-switching LCD panels. Process customization and accurate compositional analysis support reliable integration in high-rank mixtures for TFT and IPS display manufacturing.

    Industry compliance standards

    • IEC 61249-2-41: Halogen-free material guidelines for displays
    • RoHS Directive 2011/65/EU for hazardous substances
    • International Electrotechnical Commission (IEC) display material purity standards
    • ISO 14001:2015 environmental management in downstream production

    Typical usage ratio

    • 3–10% within mixed liquid crystal material batches, ratio tailored for blend viscosity, dielectric anisotropy, and response time optimization

    Downstream process integration

    • Incorporated as a starting monomer or intermediate during Friedel-Crafts alkylation or etherification prior to final compound blending

    Final product types

    • TFT-LCD mixtures for high-resolution panels
    • IPS and VA-mode liquid crystal compounds
    • OLED alignment layers (where applicable)
    • Integrated circuit-compatible display modules

    4. High-Performance Polymer Monomer Synthesis

    Specialty polymer manufacturers use our compound in the design and synthesis of custom-engineered, fluorinated polyarylene ethers and polyimides. The molecule ensures high glass transition temperatures and chemical resistance in final polymers, crucial for electronic encapsulation, fuel cell membranes, and solvent-resistant coatings. Strict in-process monitoring maintains quality at every step of polymer monomer scale-up and final polycondensation.

    Industry compliance standards

    • UL 94 flame retardancy certification for polymer applications
    • ISO 9001:2015 for specialty polymer production systems
    • ASTM D638 and D790 for mechanical and thermal properties qualification
    • REACH compliance for new monomer substances

    Typical usage ratio

    • 5–25% of total di-/trifluoromonomer content per polymerization batch, selected to achieve required thermal/chemical resistance parameters

    Downstream process integration

    • Introduced after prepolymer formation step, usually via nucleophilic aromatic substitution reactions, then advanced to high-molecular-weight polymerization

    Final product types

    • High-temperature thermoplastics for electronics and aerospace
    • Fuel cell membrane materials (fluoropolymer blends)
    • Chemical-resistant industrial coatings
    • Low dielectric constant films for advanced circuit boards
    Free Quote

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

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    Certification & Compliance
    More Introduction

    3,5-Difluoroanisole: Experience from the Source

    A Closer Look at 3,5-Difluoroanisole

    Working every day at the intersection of chemistry and manufacturing, we get to see materials like 3,5-Difluoroanisole move from raw feedstock to refined, high-purity product. Chemistry is rarely about flashy innovation. Real progress rests in producing consistently clean intermediates that help drive a wide spectrum of chemical syntheses forward without drama. For organic chemists and makers of fine chemicals, this molecule isn’t the showstopper, but it seldom fails to prove its worth.

    The product we offer under our own process control, 3,5-Difluoroanisole, is often requested by teams working either in pharmaceutical R&D or materials science. It’s clear and nearly colorless, which points to purity, but physical appearance tells only half the story. Our crews rely on tight distillation curves and close HPLC readings to ensure we're delivering a material with minimal by-products and a fluorine pattern just as the molecule demands.

    How the Choice of 3,5-Difluoroanisole Impacts Synthesis

    There’s a reason the 3,5-difluoro pattern gets singled out in aromatic syntheses. Fluorination at these positions changes reactivity, not just for show, but in how the ring resists unwanted side reactions or moves through cross-coupling. It’s subtle until you see side-by-side comparisons in a real production run. Each substitution pattern acts differently: 2,4- or 2,5-difluoroanisoles, for example, behave much less predictably in some palladium-catalyzed routes. Working with the 3,5-variant brings an edge for many modern coupling or substitution chemistries.

    We’ve watched teams switch from lower-purity, multi-component blends to the cleaner, more consistent 3,5-Difluoroanisole we build in-house. The result is less batch-to-batch variation, which means less time spent troubleshooting and more spent pushing new chemistry forward. When a process reproducibility investigation comes across our desk, nine times out of ten the answer comes back to material traceability and actual physical purity – never the structural formula on a datasheet.

    Building Confidence from Batch to Batch

    Real-world manufacturing means finding not only the correct substance but also one that behaves the same each time it arrives. We run on site GC and NMR to catch even the low-level isomers, and it’s not rare for a customer to share a feedback story about one of their previous syntheses falling apart from impurities they couldn’t see until they sourced a more reliable supply. Whether 3,5-Difluoroanisole is used as a pharma building block, electronic intermediate, or specialty agrochemical component, batches call for not just the right isomer but tight purity specifications and traceable, controlled manufacture.

    Technical chemists often stress about batch repeatability. Drawing from our own process data, every distillation counts. The process we use for producing 3,5-Difluoroanisole doesn’t just stop at the usual column fractions; we conduct impurity mapping and stability checks to rule out the degradation that can come from long shipment or prolonged storage. Having wrestled with scale-up failures in our own history, we know that small changes in production conditions – temperature stability, reactor material changes, condenser cleanliness – can spell the difference between a predictable product and a headache, all revealed in downstream reactions.

    What Sets 3,5-Difluoroanisole Apart in Chemical Building Blocks

    In a world full of nearly identical fluorinated aromatics, the challenge is in how tightly the finished product matches project needs. People new to this family of compounds might assume little difference between 3,5-Difluoroanisole and alternatives like 2,4-difluoroanisole or even 3-fluoroanisole, but anyone deep in synthetic chemistry knows better. The fluorine substitutions at the three and five positions on the anisole ring interpret to different directing effects in lithiation, metal catalysis, and nucleophilic substitution, which impacts yields and selectivity for key drug intermediates and custom materials.

    Chemistry doesn’t unfold in an ideal world. We work with teams where impurities at even one percent can deactivate catalysts or slow down reactions leading to months of delays on an industrial scale. Because of this, we’ve built and constantly refined a synthesis and purification protocol designed to minimize typical aromatic and aliphatic byproducts, keeping our profile tight and ensuring downstream reliability. Stories from other suppliers’ batches with unexpected ortho- or para-fluorinated side products show how crucial this attention to detail can be.

    Specification Details That Matter on the Factory Floor

    It’s easy to focus on catalog numbers, but the actual game is in how closely a sample matches both chemical and physical specs over time. For our 3,5-Difluoroanisole, core parameters like GC purity, water content, and residual solvents consistently land inside narrow limits, not because it looks good on paper, but because troubleshooting real synthesis is tedious and expensive for everyone involved. Extended stability testing and impurity trending help isolate whether storage containers, transport temperature swings, or trace metals could shift product quality over six months or a year. These quiet steps keep production lines running — and failure investigations at bay.

    Certain users in R&D or production scale-up need flexibility with packaging and logistics. Over the years we've adapted to provide our material in a range of drum sizes, plastic or steel, as long as the chosen container can safeguard against contamination and moisture pick-up. These aren’t supermarket preferences but answers to practical needs: a four-liter glass bottle might work for bench chemistry, but plant operations want drum-scale without cutting purity corners. Our shipping team works closely with technical staff to make sure each type of container receives the right inerting and handling based on the planned use.

    Challenges Seen and Tackled in Real Production

    Making 3,5-Difluoroanisole isn’t a shortcut process. Upstream, precursor selection impacts not only cost but the profile of potential impurities, many of which aren’t removed by basic distillation steps. Downstream, traces of water or polar organics from work-up steps can wreak havoc in sensitive downstream reactions, particularly palladium-catalyzed or lithium-halogen exchange chemistries. We use in-line monitoring and regular batch reviews to head off problems before they hit the drum.

    Logistics bring their own hurdles. Most people picture chemical delivery as straightforward, but a single missed step in temperature control or container seal integrity sometimes leads to degradation or contamination that only shows up after material has been charged to a reactor. We invest in packaging reviews and shipment tracking, which often means erring on the side of redundant QA checks for critical orders shipped internationally. The feedback loop from users helps us tighten these practices — real mistakes in the field translate directly into changes on our production line.

    The Human Side of Producing Chemicals

    Chemistry is often thought of as precise and robotic, but our floor crews and chemists shape the product as much as our reactors do. A good run of 3,5-Difluoroanisole comes from small choices: confirming that every valve is tight, that process samples are pulled at the right stages, and that analytical instruments get their calibrations on time. Many teams discover after years of sourcing that a human touch translates into fewer unexplained plant incidents. When a customer asks for help troubleshooting, we’re able to retrace not just equipment settings but who ran which shift, who did the maintenance, and how shipping records line up. This level of transparency comes from having real people accountable across the manufacturing line.

    One phrase gets repeated often on our floor: clean in, clean out. That attitude influences not only the purification steps, but the way documentation is handled, from lot-tracking down to notes on any anomalies — even odd weather that might have caused micro-variations in temperature control. Our site managers work side by side with the technical team to follow up on anomalies, closing gaps between lab and plant so nothing gets lost in translation. This careful handling is what delivers a material chemists don’t have to fuss over and lets project managers stay focused on process, not procurement headaches.

    Applications and the Value Chain

    Labs and production facilities continue to uncover new uses for 3,5-Difluoroanisole. Working with both startups and major chemical players, we hear regular stories about this compound featuring in more than just classic pharmaceutical intermediates. Specialty material scientists use it in test batches to build fluorinated polymers with unique properties, and advanced agrochemical teams value its predictable reactivity profile for designing next-generation crop protection agents. The focus is never just on having any difluoroanisole, but specifically leveraging the 3,5-pattern when reaction predictability is on the line.

    For some customers, the bottom line is purity and documentation. A miss at this level means painstaking re-qualification and lost time. For others, scale counts more, as certain processes start at the gram and quickly accelerate to the ton. Our role sits at the intersection — constantly scaling production and refining purification as demand swings, all while keeping traceability intact. This push-pull drives continuous investment in both plant infrastructure and staff skills.

    Choosing the Right Chemical, Every Time

    A seasoned process development chemist can list a dozen places where poor material leads to lost time: stopped runs, unplanned shutdowns, or debugging hidden contamination. This is where the subtle distinctions among difluoroanisole isomers make or break plant economics. Many teams have learned hard lessons from unreliable sources and come to value reliability over rock-bottom cost. Over our years of manufacturing, we’ve seen how choosing a source with owning-site knowledge, detailed analytical backup, and hands-on operational transparency cuts short the pattern of headaches.

    The technical calls that reach us rarely ask for literature values — instead, we hear about melting points that don't match, subtle NMR shifts, or unexplained slow-downs in advanced reactions. Each of these issues finds a root cause in material profile or process drift upstream. By building credibility in our controls and sharing as much root-cause analysis as possible, we turn each problem encountered into an adjustment, making the product a little more practical for everyone in the value chain.

    Differences that Matter between 3,5-Difluoroanisole and Other Variants

    On paper, swapping in a similar-looking difluoroanisole isomer might seem easy, but the subtle chemistry creates real downstream consequences. The 3,5-fluorines affect both electronic and steric factors on the ring, meaning drug and materials chemists can realize higher yield, smoother purification, or cleaner analytical profiles with this isomer. We’ve talked with teams working on complex heterocycle precursors who saw product isolation improve markedly by switching from less defined difluorinated aromatics to the 3,5-pattern. These stories bear out the value of narrowing impurity windows and getting isomer composition right the first time.

    Our own experiences confirm that, in cross-coupling and substitution, the non-symmetrical isomers frequently introduce unpredictability. For those scaling reactions to the multi-kilo range, process bottlenecks often originate in uncontrolled impurities or mixed isomer content. By operating continuous improvement cycles around real-world feedback, we provide a variant that’s ready for heavy-lifting work, not only bench trials.

    Continuous Learning and Future Directions

    Supplying 3,5-Difluoroanisole over many years, we stay alert to the challenges that crop up both in our own process and at customer sites. Ongoing process validation, deeper analytical testing, and responsiveness to field challenges aren’t add-ons — they define whether the material sits on a shelf or translates to measurable value for our partners. We keep lines of communication open, inviting feedback and field data that strengthens not only our quality systems but everyone’s outcomes.

    Chemistry’s story often centers on reaction outcomes, patents, and discovery. In practice, it’s repeated attention to the basics – reliable sourcing, transparent production, tight analytical follow-up – that shapes whether a new material earns its keep. Our work with 3,5-Difluoroanisole, from initial drumming to kilogram and ton scale, is a result of thousands of small decisions by maker and user alike. Each improvement, adjustment, and lesson, marked by our batch records and real-world troubleshooting, sets the foundation for the next breakthrough in chemical manufacturing, research, and beyond.