Anhui Liwei Chemical Co., Limited
Products

2,6-Difluorophenol


    • Product Name 2,6-Difluorophenol
    • Alias 2,6-DFP
    • Einecs 221-170-1
    • 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

    113391

    Name 2,6-Difluorophenol
    Cas Number 1515-67-7
    Molecular Formula C6H4F2O
    Molar Mass 130.09 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.304 g/cm³
    Boiling Point 175-177 °C
    Melting Point −6 °C
    Refractive Index 1.512
    Solubility In Water Slightly soluble
    Flash Point 68 °C
    Smiles c1c(F)cccc1F
    Pubchem Cid 13861

    As an accredited 2,6-Difluorophenol 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 2,6-Difluorophenol, tightly sealed with a screw cap and hazard labeling for safety.
    Shipping 2,6-Difluorophenol is shipped in tightly sealed containers made of compatible materials, ensuring protection from moisture, heat, and direct sunlight. Packages are clearly labeled with hazard information, as the chemical is classified as hazardous. Transport complies with relevant regulations (such as DOT, IATA), and material safety data accompanies each shipment.
    Storage 2,6-Difluorophenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible substances such as strong oxidizing agents. Protect from light and avoid exposure to air for prolonged periods. Store in a chemical storage cabinet designed for flammable or toxic chemicals, following all relevant safety protocols and regulations.
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    Tel: +8615380400285

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    Certification & Compliance
    More Introduction

    2,6-Difluorophenol: Practical Value in Chemical Synthesis

    Direct Insights from a Manufacturer’s Bench

    We have spent years perfecting the production process for 2,6-difluorophenol, CAS number 395-38-8. In today’s market, serious chemists and industrial teams look for products that cut down troubleshooting and long waiting times. That’s not just a feature—it’s an expectation based on years of improvement and technical adjustment. Every batch that leaves our plant reflects incremental refinements we’ve implemented to control moisture, limit impurities, and maintain lot-to-lot consistency. From the early days of glass reactors and labor-intensive distillation, we’ve moved to closed systems, real-time monitoring, and online quality checks. This isn’t about hype, it’s about following through where others may cut corners.

    Understanding the Product: Structure, Form, and Delivery

    2,6-Difluorophenol stands out by the specific placement of fluorine atoms on the aromatic ring. That subtle modification, compared to phenol or single-fluorinated phenols, results in a compound with different reactivity, acidity, and volatility. Our product usually comes as a clear, colorless-to-pale liquid, with characteristic sharpness that separates it from non-halogenated phenols. Moisture content, residual solvents, and trace metals receive close attention, because even parts per million of contamination affect downstream work—whether running a Suzuki coupling or manufacturing complex pharmaceuticals.

    We found through hundreds of productions that glass packaging, nitrogen blanket, and careful handling during loading and shipping make a significant impact on shelf life. In some markets, local storage conditions can force a product to break down, so we designed our packaging to handle temperature swings and reduce light exposure. These aren’t abstract promises: they come from years of feedback from technical teams frustrated by out-of-spec shipments from less rigorous sources.

    Key Specifications: What Matters

    Chemists tend to worry about purity first. Our 2,6-difluorophenol achieves minimum 99% purity by GC, and LC methods spot possible aromatic or halogenated byproducts. We won’t pretend that 100% is attainable, but trace presence of related fluorophenols stays tightly controlled. Typical water content falls below 0.1% by Karl Fischer method. Acidity, as measured by titration, matches the values listed in literature for this compound. Boiling point sits comfortably around 150–156°C at atmospheric pressure, which helps in purification and process control. The density, near 1.3 g/cm³, lines up with accepted reference values and supports reliable metering in automated plant dosing systems.

    Volume offerings vary from multi-kilogram drums for large-scale projects down to 500g bottles for R&D and custom synthesis. Bulk users appreciate that our larger containers feature tamper-proof seals and vented closures, which help avoid pressurization if the product sits in a hot warehouse. These adjustments stem from real shipping incidents later resolved through changed practice. Investing in proper packaging is not about branding—it’s about ensuring chemists receive what they ordered and can focus on their transformations instead of product salvage work.

    Peculiarities and Advantages of 2,6-Difluorophenol

    The ortho arrangement of the fluorine atoms compared to monofluorophenols or para analogues changes electronic effects on the phenol ring. This property gives 2,6-difluorophenol reactive behavior useful in complex syntheses, such as stepwise halogen exchange, selective displacement, and transition metal catalysis. For instance, in our direct experience supporting pharmaceutical intermediates, the unique acidity of this molecule improves selectivity during etherification and cross-coupling, reducing side product formation and waste.

    We don’t see these gains with unsubstituted phenol or simple monofluorophenols. They might cost less, but their behavior in fine chemical synthesis often leads to more expensive purification or process adjustments. Knowing this difference means a chemist saves time and raw material by choosing the right reagent up front, not scrambling after a failed reaction. Our technical application team has collaborated directly with contract manufacturers to solve bottlenecks stemming from incorrect reagent selection—often by replacing generic phenol with 2,6-difluorophenol where the electronics mattered most.

    Market Trends and Shifts in Demand

    Global demand for fluorinated aromatics never stays the same for long. As we’ve seen in our two decades in the industry, pharmaceutical innovators and agrochemical developers keep shifting their requirements as regulations tighten and patent lifespans end. What keeps 2,6-difluorophenol relevant is its combination of manufacturability and functional versatility. In pesticide R&D and active ingredient scale-up, for example, this molecule often serves as a critical early-stage intermediate. Larger parties in custom synthesis often request specialty lots refined for palladium-catalyzed reactions, or process validation to meet regulatory expectations. These requests demand not just bulk supply, but batch reproducibility, impurity profiling, and flexibility to meet variable scale-up schedules.

    Traders may treat every liter as a commodity, but our reality involves regular adjustments and tight customer dialogue. During pandemic supply chain disruptions, we kept lines open with buyers planning quarterly orders, providing stability despite shifting import restrictions and delayed deliveries. Keeping integrity in both manufacturing and communication remains a core value because developers rely on our predictability for their operational planning.

    Applications: Real-World Use Cases

    The most common request for this material from our clients involves pharmaceutical intermediate synthesis. Whether in preclinical labs or scaled GMP facilities, 2,6-difluorophenol is often involved in forming diaryl ethers and constructing heterocyclic scaffolds. Its electron-deficient aromatic ring supports nucleophilic aromatic substitution, while the phenolic OH group opens doors for alkylation and acylation. Production teams favor our batches because robust control of byproducts cuts down on time spent in chromatography or solvent recovery.

    Veterinary compounds, herbicides, and specialty polymers all draw from the reactivity of 2,6-difluorophenol. Over the last decade, we've supported customer projects ranging from small diagnostic reagent kits to multi-tonne polymer additive campaigns. In advanced materials, the two fluorine atoms contribute to enhanced thermal and chemical stability, a point that’s come up repeatedly during technical visits with automotive coatings and electronics suppliers. A recurring story involves shifting from mono-fluoro to di-fluoro analogues to meet durability thresholds under harsh testing cycles.

    Every application brings its own complexities. R&D chemists in major life science firms might focus on modified ether linkages, demanding samples on short notice with full HPLC, NMR, and GC-MS data. For plant-scale projects, engineers request full quality documentation, audit trails, and long-term stability guarantees. We have had to adapt packaging, documentation, and technical support to these different user bases. Open, detail-oriented communication between our plant and client chemists has shortened troubleshooting cycles and helped avoid costly delays due to off-spec material.

    Quality Control: Lessons Learned on the Line

    Bad batches happen; ignoring feedback doesn’t solve them. Early on, we ran into bottlenecks with incomplete drying, leading to moisture issues in customer reactions. Field chemists flagged this fast. Adjustments in our process—moving from standard drying ovens to vacuum line dehydration—cut residual water dramatically. We continue to monitor each batch by both Karl Fischer titration and modern spectroscopic tools.

    We’ve also seen that downstream processes can be sensitive to even trace impurities, especially when clients use catalytic or highly selective transformations. Our in-house analytical team regularly checks for halogenated biphenyls, non-volatile acids, and residual solvents. Practical feedback from customers who encountered difficulties—stopped couplings, loss in yield—has forced real change. We broadened analytical checkpoints, moved to tighter column separation thresholds, and now supply additional COAs covering more than seventy impurity markers, not just the standards listed in monographs.

    Product recalls create headaches everyone wants to avoid. A key realization we gained is that batch auditing works better as an ongoing process than as a post-mortem report. It costs more, in both time and overhead, but that upfront investment replaced late-night crisis calls with smooth, predictable shipments. Our team prefers dialogue with chemists in advance—whether through online portals, video calls, or emails—instead of scrambling after things have gone wrong further down the pipeline.

    Comparing to Alternatives: What Real Differences Mean

    Some customers ask why they shouldn’t just use generic phenol or a less expensive monofluorinated derivative for their work. We point to actual case studies from the lab bench. In nucleophilic substitution or metal-catalyzed coupling reactions, the acidity and electronic profile of 2,6-difluorophenol can drop reaction times by hours or increase yields by double digits. Peers working with our product pulled full conversion in shorter times versus the closest analogues, reducing both waste and cost at scale.

    Experience in pilot-scale campaigns makes it obvious: using an inappropriate grade or insufficiently fluorinated phenol creates more complications than the initial savings justify. Every hour spent reprocessing, purifying, or explaining delays adds up. Not every project requires this level of specificity, but competitive synthesis markets reward those who work with the chemistry, not against it.

    There are specialty sources for mono-, tri-, and tetrafluorophenols geared toward specific segments. We offer those as well, but each structure change alters reactivity. In certain cross-coupling applications, only the ortho-difluoro substitution reduces unwanted side reactions. In medicinal chemistry, altered bioisosteric properties and metabolic stability dictate which reagent fits best. Our application support team walks through these choices with clients, drawing from both literature and our own production data.

    Environmental and Regulatory Considerations

    Environmental controls occupy more and more of our daily operation. 2,6-Difluorophenol is not free of handling risks—like other halogenated aromatics, careful management is essential. Over the years, we invested in on-site wastewater separation systems and closed-loop solvent recycling. Regulations in key markets like the European Union and North America drive the need for complete traceability, full safety documentation, and pre-clearance of supply chains.

    Clients increasingly seek compliance guarantees, especially as new medical and agricultural products face lengthy registration processes. We keep finished product samples in retained libraries for up to five years to support product recalls or adverse event investigations. Raw material and intermediate traceability is more than a paperwork burden; it’s a vital defense against accidental contamination, counterfeit, or non-compliance. As manufacturers, we experienced firsthand the shift away from “tick-box” compliance to real, auditable processes covering every stage from raw material verification to end-user shipment.

    We’ve partnered with transporters trained for hazardous deliveries, using proper UN-certified packaging options for air, sea, and ground. This focus keeps shipments secure even during international handovers. Our support documentation aligns with global chemical inventory listings, supported by regular reviews from trusted authorities. These commitments do not exist in a vacuum—they come from direct client requests, regulator visits, and firsthand experience with tightening supply chain protocols.

    Continuous Improvement: Commitment Rooted in Experience

    Learning from past mistakes and customer feedback has shaped our approach, from R&D through to bulk manufacture and global shipment. Every change to drying equipment, analytical procedures, and batch documentation emerged from concrete needs, not just internal brainstorming.

    Our open-door policy means technical experts, from junior synthesis chemists up to plant managers, can raise issues without bureaucratic hurdles. This spirit of operational transparency has led directly to improvements, such as optimizing temperature ramp protocols in distillation to cut impurity formation, or broadening impurity analyses after specific client feedback in the agrochemical sector.

    The chemical manufacturing landscape keeps moving. We keep improving our manufacturing and support processes out of necessity, not just compliance. Serving long-term clients in pharmaceuticals, agrochemicals, and specialty materials demands more than meeting specs. It takes open lines of communication, a critical eye on batch-to-batch quality, and a willingness to adapt quickly to new requirements and feedback.

    Practical Solutions to Common Challenges

    Product crystallization, especially in cold climates, has challenged transport and storage before final processing. We switched to improved insulation and phase-compatible secondary packaging for winter shipments. Customers in northern zones reported fewer incidents, saving costly delays and reshipments.

    Another persistent concern is odor dispersion in poorly ventilated storage rooms. We’ve experimented with lined drum seals and low-permeability barriers, cutting down fugitive vapor levels significantly. Facility managers in smaller plants have praised these changes, especially during seasonal high humidity.

    Downstream reactivity issues sometimes trace back to overlooked material incompatibilities—such as use of leachable seals or containers not rated for low-molecular-weight aromatics. We’ve collaborated with our packaging partners to identify and eliminate these issues, switching entirely to fluoropolymer-lined closures for our largest drums.

    Every time we field a complaint or satisfy a troubleshooting request, that experience feeds into next month’s lot reviews and supplier briefings. Our focus remains rooted in what customers face in real-world labs and reactor suites, not just theoretical purity or process optimization.

    Knowledge Sharing and Technical Support

    We have learned that providing transparent, data-rich support at every project stage minimizes confusion and builds trust. Chemists and plant engineers often approach us before or during project kickoffs with requests for spectral data, stability profiles, or impurity maps. Rather than gating this information behind rigid NDAs or red tape, we provide open access to technical sheets, method protocols, and historical batch data. It speeds up their own compliance work, shortens project timelines, and decreases onboarding friction.

    Our technical support staff speak from direct process experience. Many team members have rotated through production and QC laboratories before joining the customer-facing side. This hands-on perspective aids troubleshooting and avoids generic “refer to MSDS” answers. Everyone knows the stakes—projects hinge on timely and predictable chemical delivery, not just boxes on a shipping manifest.

    Collaborative development, both with large corporate clients and fast-moving start-ups, requires more than filling purchase orders. We participate in joint process review sessions, suggest troubleshooting steps based on shared datasets, and offer lot reservation services during extended development cycles. By acting as a true technical partner, we help clients push their own chemistry programs further, faster, and with fewer unexpected setbacks.

    Why It Matters: The Manufacturer’s Perspective

    For us, 2,6-difluorophenol isn’t simply an entry on a price list. It represents a body of practical experience—hard-won improvements, failed and successful scale-ups, and countless hours supporting chemists in the field. Our commitment to quality, documentation, and customer partnership grows from years of firsthand observation: reliable reagents drive project success, while shortcuts and poor transparency multiply delays and costs.

    Every new batch stands as a testament to lessons learned, feedback received, and the daily drive to make each lot better than the last. As applications expand and regulations evolve, we continue investing in our people, our production lines, and our technical support. For partners searching for more than just a vendor, but rather a manufacturer invested in their success, our door remains open—both in the lab and on the production floor.