Anhui Liwei Chemical Co., Limited
Products

Phenol, 5-Ethyl-2-Fluoro-


    • Product Name Phenol, 5-Ethyl-2-Fluoro-
    • Alias 5-Ethyl-2-fluorophenol
    • Einecs 'EINECS 401-230-3'
    • 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

    191995

    Chemical Name Phenol, 5-Ethyl-2-Fluoro-
    Cas Number 31456-36-1
    Molecular Formula C8H9FO
    Molecular Weight 140.16 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 226-228 °C
    Density 1.117 g/cm³ (approximate)
    Solubility In Water Slightly soluble
    Flash Point 107 °C (closed cup)
    Refractive Index 1.528 (approximate)
    Pubchem Cid 495892

    As an accredited Phenol, 5-Ethyl-2-Fluoro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g amber glass bottle with secure screw cap, labeled "Phenol, 5-Ethyl-2-Fluoro-," includes hazard warnings and batch details.
    Shipping Phenol, 5-Ethyl-2-Fluoro- should be shipped in tightly sealed containers, away from incompatible substances such as oxidizers. It must be transported using appropriate labeling and documentation, conforming to relevant hazardous material regulations. Shipping typically requires temperature control and secondary containment to prevent leaks or spills, ensuring environmental and personnel safety.
    Storage **Storage for Phenol, 5-Ethyl-2-Fluoro-:** Store in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep container tightly closed, protected from light, heat, and moisture. Use corrosion-resistant shelving and clearly label the container. Avoid exposure to direct sunlight. Ensure emergency equipment (eyewash, showers) is accessible in storage areas.
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    Certification & Compliance
    More Introduction

    Phenol, 5-Ethyl-2-Fluoro-: Our Experience as a Manufacturer

    Phenols never stop teaching you respect. On the production floor, subtle changes in structure can lead to very different behaviors in the batch reactor. Our team manufactures Phenol, 5-Ethyl-2-Fluoro- (CAS 1615-89-4), also referred to in-house by its model name, PE2F. Years of handling this compound taught us how its unique properties stem straight from its chemistry: the combination of a fluorine atom in the ortho position and an ethyl group on the ring brings more than a name; it shifts the entire performance profile. The first time we scaled up PE2F, flow rates and temperature controls needed adjustment compared to traditional mono- or di-substituted phenols—aromatic substitution truly matters.

    What Makes Phenol, 5-Ethyl-2-Fluoro- Distinct

    PE2F distinguishes itself from classic phenolics, including unsubstituted phenols, by combining electron-withdrawing and electron-donating effects right on the ring. Chemically, the introduction of fluorine at position 2 increases stability against oxidative degradation. We observe this firsthand: in storage, PE2F resists the yellowing that quickly mars basic phenol packages, letting us guarantee a longer shelf life and reduced waste for downstream partners. The ethyl group at position 5 contributes bulk, which modifies boiling and melting points. For instance, our batches typically purify above 99% and present as clean, white crystalline solids at room temperature—a visible sign of careful substitution.

    Most applications for PE2F tap into these physical and electronic tweaks. Customers in the agrochemical sector requested replacements for more reactive, easily oxidized phenolic intermediates. PE2F’s stability solved handling problems. Electronic properties shift the reactivity profile, making this compound a step above simple phenols when building specialty chemicals. For resin scientists, the altered electron density creates condensation behaviors not found in standard alkylated or fluorinated phenols, opening up fresh polymer architectures.

    Production Observations in Our Facility

    Switching from multi-ton runs of para-alkylphenols to PE2F taught us the need to respect new distillation curves. The vapor pressure profile does not simply interpolate between base phenol and ethylphenol; the presence of fluorine sharpens the separation window. In our processing suites, distillation columns benefit from extra control loops, and condenser fouling dropped compared to heavier, multi-alkylated analogs.

    Our operators know the character of this material—PE2F forms sharp, well-defined crystals after final purification, an advantage in solid-state reaction setups. Dust control during packaging pays dividends, as even a little material loss over a year adds up in specialty production. All phenols emit a distinct odor; PE2F’s scent comes off gentler than that of unsubstituted phenol, helpful for plant operators during bulk handling.

    Uses and Technical Advantages

    PE2F’s primary uses line up with sectors where selective reactivity is everything. In our experience, research and development teams in the pharmaceutical field explored PE2F as a precursor for fluorinated building blocks, where the site-selective placement of both fluorine and ethyl groups plays into the biological profile of targeted molecules. Lab partners found that PE2F provided higher yields in key transformations than similar mono-substituted phenols. That means fewer byproducts, easier purification downstream, and ultimately tighter controls on finished purity.

    Agrochemical companies have also pushed this molecule into pilot-scale syntheses of novel fungicides. The push-pull effect on the aromatic ring, from both ethyl and fluoro substituents, led to faster coupling reactions when making more complex target molecules. That reduces turnaround time and material costs.

    For advanced polymer work, R&D chemists praise PE2F’s predictable reactivity in condensation chemistry. It delivers backbone rigidity in specialty resins where shelf life and chemical resistance must outlast harsh outdoor exposure. Our direct feedback from resin formulators notes fewer side reactions and lower color development in accelerated aging tests, which we attribute to the combined electronic and steric influence of the two substitutions on the ring.

    How PE2F Differs from Other Phenolic Compounds

    Every manufacturer comes to know the character of phenolic materials personally. Standard phenol serves as a backbone of many industries thanks to its simplicity, but it comes with safety concerns around volatility and toxicity. The addition of an ethyl group alone, as in 5-ethylphenol, nudges up melting and boiling points, yet little changes at the bench other than physical handling. The story alters dramatically when fluorine enters. Mono-fluorophenols carry increased stability but frequently run into limitations in terms of reactivity with certain partners, making them a bottleneck for multistep syntheses.

    PE2F strikes a balance, a point made plain during pilot programs with our partners. This molecule behaves more safely in storage than base phenol, owing to suppressed volatility and reduced susceptibility to color and odor development. This doesn’t sound glamorous but, for supply managers, it means lower hazard ratings, less concern over regulatory storage, and greater reliability for just-in-time production schedules.

    In the laboratory, PE2F’s mixed substituents lead to sharper, more controllable selectivity in downstream reactions—not too sluggish, not so reactive that side products take over. This balance allows for the invention of new processes that would fail or give poor yields with unsubstituted or mono-substituted analogs. For example, processes that require regioselective activation of only certain sites on the ring see higher selectivity and improved overall conversion. That means fewer repurifications and better returns on invested raw material and labor hours.

    One challenge stands clear—a higher synthetic entry cost. The complexity of introducing both fluorine and ethyl groups on the ring ramps up the multi-step synthesis, requiring more tightly controlled reactors and higher purity reagents. We overcame early bottleneck stages through modifications in catalyst design and careful optimization of the fluorination step. Recoveries reached production scale faster by designing crystallization regimes matched to the compound’s unique behavior. The investment at this stage returns clear value to downstream partners, who see better yield, less waste, and safer materials to handle throughout the life of the product.

    Environmental Considerations and Handling

    Operating as a manufacturer, chemical responsibility is core to our process. The inclusion of fluorine in aromatic compounds often raises questions over persistence in the environment. As a facility, we continuously monitor effluent streams for fluorinated residues and work with external partners on the reduction of byproducts at the source. During initial process development for PE2F, changes in waste treatment were necessary—advanced oxidation and activated carbon systems capture unreacted materials, leading to measured reductions in effluent fluorine content.

    PE2F’s solid-state at room temperature brings handling advantages. Storage in lined steel containers has shown no compatibility issues, and its resistance to ordinary air oxidation extends storage intervals, resulting in less frequent batch rework. Our logistics team finds that, unlike some di-alkylated phenols, PE2F avoids the sticky residues that challenge packaging lines and prolong turnover times. As for safety, OEL (Occupational Exposure Limit) recommendations remain close to those found for related alkyl- or fluoro-phenols, supported by regular plant air monitoring and personal protective equipment requirements in accordance with best industry practice.

    Supporting Reliability for End Users

    Our partners rely not just on the physical supply of PE2F but on the entire support network behind it. From our vantage point in chemical manufacturing, one investment stands above others: rigorous QC at each stage, starting from incoming raw material. Small impurities at the fluorination or alkylation steps can cause downstream cascade issues. Our custom-designed NMR and GC-MS protocols ensure each batch adheres to specifications, with no detectable contamination from chlorinated or higher alkyl byproducts.

    Shipping professionals appreciate the ease with which PE2F batches meet transportation regulations. The solid form and high chemical stability reduce hazard classification under many transport codes, lowering documentation time and simplifying international logistics. That’s a win for R&D programs that need rapid, global deployment.

    R&D Feedback and Ongoing Improvements

    As new partner applications emerge, we refine our process and product offering. Several collaborative research projects with universities and contract research labs allowed us to trial PE2F in emerging organic electronics. There, demanding purity standards test every link in our supply chain. Feedback about trace metal content led to upgrades in both purification and packaging; a new polytetrafluoroethylene (PTFE) lining prevented unwanted metal leaching during storage.

    Fine-tuning particle size proved valuable to customers developing catalytic supports or requiring precise dosing. Our horizontal crystallizer system lets us adjust crystal morphology without introducing additives that could compromise downstream reactivity. This is particularly important for projects migrating into regulated pharmaceutical or food-contact resin sectors, where even trace impurities or lingering reagents must be avoided. Almost every advance we make here comes from listening to real, on-the-ground chemists and responding directly to needs they raise as they test and deploy PE2F in challenging new contexts.

    Future Tech and Sustainability Prospects

    The synthetic routes to PE2F, like many functionalized aromatics, carry a natural resource footprint. Our research staff engages directly with green chemistry advocates, both internally and from client-side R&D. Recent efforts focused on minimizing waste in the fluorination step, where, historically, stoichiometric reagents led to high byproduct formation. The introduction of catalytic fluorine donors, particularly those leveraging soluble metal complexes, decreased waste load per kilo of product shipped. >As manufacturers, efficiency at scale directly supports both environmental performance and cost competitiveness.

    Exploring solvent recycling in the alkylation stage brought another benefit—instead of sending spent solvents to off-site disposal, closed-loop vapor recovery enables us to recapture valuable materials, lower emissions, and cut feedstock costs. For us, these aren’t abstract sustainability pledges but day-by-day changes, tracked on spreadsheets and process monitors in real time. The trusted relationships built with ESG auditors and environmental engineers help us keep pace with evolving regional guidelines and ensure our end users enjoy a secure, future-ready supply of critical phenolic intermediates.

    Lessons Learned from Scale-Up and Commercialization

    Starting production of a new aromatic, even for an experienced phenol player, brings new learning curves. For PE2F, silicone-lined reactors outperformed steel once minor corrosion was traced back to trace acid from the fluorination step. Initial pilot-scale batches alerted us to vapor emission points during high-temperature distillation; fixing these issues early saved hundreds of hours of downtime later. Lab-to-plant translation means assigning teams not just to the physical run itself, but to analytics, logistics, and continuous process improvement.

    Shipping large volumes worldwide requires deep integration between synthesis, QA, regulatory affairs, and commercial logistics. Documents that comply with destination market regulations require collaboration between several departments. PE2F’s inherent chemical stability proved one of its most important assets—lower likelihood of spoilage or off-specification return shipments streamlines relationships between us as the manufacturer and our downstream customers.

    What End Users Gain from Our Experience

    Decades in phenolic manufacturing shape our approach to each compound, but PE2F stands out for its flexibility in advanced synthetic uses and for its safety and storage benefits in commercial-scale applications. The feedback loop between our operations, technical support teams, and application chemists ensures that the material we supply meets more than a checklist—it genuinely makes a difference in bench chemistry, pilot production, and commercial operations across industries.

    Our customers know every batch of PE2F starts from quality feedstocks, backed by strict process controls that minimize both unwanted byproducts and off-target substitutions. Batch consistency tightens up time spent in downstream QC, while process changes—like upgrades to purification protocols—translate right into easier regulatory filings and safer products for end users. By opening our labs and production lines to outside audits and fostering open technical exchanges, we build reliability and trust right into the molecule’s value chain.

    Final Perspective

    Phenol, 5-Ethyl-2-Fluoro-, as we have come to know it, reflects decades of practical lessons in managing specialized aromatic chemistry. The unique combination of fluorine and ethyl substitution pushes both the boundaries of synthetic application and the details of safe, reliable manufacturing. Practical experience, attention to material behavior, direct engagement with customer feedback, and a commitment to clean, stable supply underpin our approach each day. Every drum shipped represents more than chemical content; it stands for years of expertise, customer collaboration, and a drive toward solutions that respect the needs of researchers, formulators, and plant engineers alike.