Anhui Liwei Chemical Co., Limited
Products

2-(2,2,2-Trifluoroethoxy)Phenol


    • Product Name 2-(2,2,2-Trifluoroethoxy)Phenol
    • Alias 2-Hydroxyphenyl 2,2,2-trifluoroethyl ether
    • Einecs 629-334-2
    • 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

    222045

    Chemicalname 2-(2,2,2-Trifluoroethoxy)Phenol
    Casnumber 161326-26-7
    Molecularformula C8H7F3O2
    Molecularweight 192.14
    Appearance Colorless to pale yellow liquid
    Boilingpoint 207-208°C
    Density 1.324 g/cm3
    Refractiveindex 1.467
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC=C(C(=C1)O)OCC(F)(F)F
    Inchi InChI=1S/C8H7F3O2/c9-8(10,11)5-13-7-4-2-1-3-6(7)12/h1-4,12H,5H2

    As an accredited 2-(2,2,2-Trifluoroethoxy)Phenol 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-(2,2,2-Trifluoroethoxy)Phenol, sealed with a screw cap, labeled with safety information.
    Shipping 2-(2,2,2-Trifluoroethoxy)phenol should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be handled in accordance with all safety regulations, labeled properly, and accompanied by the proper documentation. Transport should comply with local, national, and international chemical shipping guidelines to ensure safe delivery.
    Storage 2-(2,2,2-Trifluoroethoxy)phenol should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it separate from incompatible substances such as strong oxidizers and bases. Properly label the container and avoid exposure to heat or sources of ignition. Store in accordance with local chemical safety guidelines.
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    Certification & Compliance
    More Introduction

    2-(2,2,2-Trifluoroethoxy)Phenol: Experience From the Manufacturer’s Floor

    Understanding the Essence of 2-(2,2,2-Trifluoroethoxy)Phenol

    As a team deeply involved in the daily reality of chemical production, we have learned that making 2-(2,2,2-Trifluoroethoxy)Phenol is more than a process—it’s a confluence of chemistry, market needs, and safety concerns. In the world of ether-phenols, the trifluoroethoxy group does much more than tweak a formula. It transforms the physical and chemical behavior of the phenol moiety entirely. Our decision to focus on this molecule grew from repeated requests from specialized users needing a phenol with high thermal resilience and distinct reactivity in their synthesis chain. Building experience batch by batch, we have seen innovation right in front of us, watching how subtle changes—like introducing a trifluoroethoxy group—open doors to new applications that demanded real solutions from real chemists.

    Model and Specifications: Direct Lessons From Daily Manufacturing

    Our standard for 2-(2,2,2-Trifluoroethoxy)Phenol always comes down to two things: purity and consistency. Every time we talk about the product, we talk about the numbers we control in production. We never consider purity in vague terms; our lab routinely generates product with GC purity above 98.5%, which is not pulled from brochures but from weeks and months of batch histories. Moisture content means more to us than a number on a sheet, since a single point higher on the scale can ruin an entire process downstream. Our people watch for water, test for residual solvents, and rerun purification steps until the sample reads out exactly what we trust. There isn’t tolerance for fuzziness.

    Weight, appearance, and solubility are facts we check not for catalog gloss but because experienced buyers give feedback we use to tune our material. The crystalline powder holds a faint, instantly recognizable aroma—field chemists say it has a sharper nose than standard phenol, a clue to its changed electronic structure. Our internal standard batch sits at a melting point of 48 to 50 degrees Celsius, and every operator, from synthesis to packaging, knows it has to look right before it ever leaves the floor.

    Putting It To Work: Function and Value

    Customers from the pharmaceutical and agrochemical fields keep returning for 2-(2,2,2-Trifluoroethoxy)Phenol, often telling us about their own in-house experiments. In pharmaceuticals, putting a trifluoroethoxy group on a ring structure usually changes both the metabolic stability and the way a molecule slots into enzyme binding sites. A senior customer working on new CNS-active compounds once showed us the difference between running reactions with ordinary phenol derivatives versus our product. His team found that the fluoroalkoxy group altered lipophilicity so much that their lead compound’s absorption profile shifted completely. That result didn’t just mean a better hit rate; it meant a shot at a pipeline breakthrough.

    In crop protection, synthesis teams have noticed that the electron-withdrawing nature of the trifluoro group means they can design phenolic units that resist unwanted oxidation or degradation out in the field. This translates into product shelf-life and maintains efficacy long after spraying. We do hear from research labs exploring wholly new cross-coupling routes, and these groups appreciate the reactivity differences, reporting that our phenol’s lower nucleophilicity keeps side reactions at bay and allows for selective functionalization at positions that would otherwise prove tricky. As a manufacturing team, hearing these long chain stories, stretching from our reactor to harvest or dosage studies, makes the late-night maintenance and constant batch sampling worth the grind.

    What Sets 2-(2,2,2-Trifluoroethoxy)Phenol Apart

    Working with dozens of substituted phenols over the years, the ones bearing a trifluoroethoxy group grab our attention because of their robust chemical personality. Compared to standard ethoxyphenols or plain hydroxybenzenes, 2-(2,2,2-Trifluoroethoxy)Phenol shows improved resistance to oxidative breakdown. This comes straight from the properties of the trifluoro group, where the tight bond strength resists conditions that would quickly degrade other phenol derivatives. One time, a large-scale project switched from an ordinary ethoxy-derivative to our trifluoroethoxy material and immediately cut down process impurities by 40 percent. The difference wasn’t theoretical. It ran through the columns, changed the time on the rotavap, and made waste handling less risky.

    Handling is another point that real-world staff care about. Certain phenols are notorious for rapid air-oxidation and give off alarming smells in the storage area. 2-(2,2,2-Trifluoroethoxy)Phenol, in our experience, stores cleanly under nitrogen for extended periods. Bottles opened three months earlier still present the same color and scent—there’s minimal browning or sticky residue around the neck, a clear improvement compared to less stable analogues. There’s immediate operational savings from not having to discard discolored, partially degraded product.

    Production Realities and Quality Insights

    The reality of producing this specialty chemical involves a commitment to mastering each link in supply. Over the last decade, we have learned that even small slips in precursor purity or water ingress ruin reaction yields and lead to costly rework. Our staff have built a practice of double-checking starting material certificates and checking every drum of trifluoroethanol for unintended acid impurities. As a result, production yields climbed from an average of 71% to over 80% in recent years—a gain not by accident but by learning hard lessons batch-by-batch.

    Scaling synthesis from kilogram lab runs to full-scale manufacturing brought its own set of headaches. A solvent ratio that works on 10 grams surprised us by fouling up stirring at 10 kilos. It’s not glamorous, but more than half of our process refinements came from technicians who noticed subtle shifts in crystal morphology during slow cooling. Switching out a common filtration aid sounds minor—until you see a half-ton filter cake that just won’t wash clean. We live these details.

    Supporting Responsible Use and Meeting Industry Trends

    The drive for greener, safer chemicals shapes how we optimize this product. The environmental profile of fluorinated organics attracts scrutiny, so all residuals are tracked with care. Our operators train on spill and waste handling beyond regulatory minimums, and our facilities invest in effluent treatment that neutralizes traces before anything leaves the plant. We take this responsibility seriously, because over the years, a few grams leaking upstream could cause real consequences downstream.

    Regulators and end users ask sharp questions about each component and its lifecycle. The presence of trifluoro units requires explaining to auditors and corporate partners. Not only have we logged in-house migration rates for fluorinated residues, but we have also participated in roundtables with customers and environmental chemists, working on safer product applications and tighter effluent controls.

    On top of that, the movement toward greener solvents and more energy-efficient synthesis routes has us constantly surveying the literature and attending industry seminars. Our lab teams have introduced several cycles where we cut down solvent volume, replaced chlorinated wash agents, and recycled mother liquor without risking product purity. These steps don’t just check compliance boxes—they keep costs stable and build trust among the people who rely on chemical integrity and safety above all else.

    Why 2-(2,2,2-Trifluoroethoxy)Phenol Earns Its Place In Modern Synthesis

    From a manufacturer’s view, this product has proven itself in versatility and reliability. Colleagues in medicinal chemistry depend on it to drive selectivity into syntheses where standard phenols fall short. Agrochemical researchers say it means longer field performance and less frequent reapplication. Importantly, when our customers return for repeat batches, they focus on the same process advantages: less disposal, better columns, and fewer headaches in downstream purification.

    We also hear from university labs running scaled-down process development. They praise the molecule’s reactivity profile, which allows for direct coupling to electrophiles in ways that cut out extra steps. Over and over, experienced scientists mention the lower rate of decomposition products compared to non-fluorinated counterparts. It’s a difference that shows up not just in yields, but in the headaches avoided during analysis and regulatory reporting. Their feedback has helped us tweak our routine, guiding our R&D chemists as they experiment with improved crystallization and drying sequences.

    Direct Dialogue: Listening Makes All The Difference

    Feedback from the people actually using the material—who see the good and the bad—shapes how we plan batch production and decide on investments in analytics and reactor upgrades. Through years of phone calls, plant visits, and pilot-scale troubleshooting, certain patterns became clear. Consistency from batch to batch tops every user’s wish list. No one welcomes surprises, especially at the stage where a process must pass strict validation. This drumbeat for predictability pushed us to install inline monitoring equipment and build an archive of every batch’s analytical run, open to customer audit anytime. Some users now log into our remote access database to review their own historic data sets, trusting in the long relationship to back up each delivery.

    We also pay attention to voice-of-the-customer requests for smaller or larger packaging. Research labs often want sub-kilo jars, while production sites shift to drum quantities. Fulfilling both ends of the scale forced upgrades in cleanroom dispensing and packaging automation. These investments pay back in loyalty, and every now and then, in shared discoveries—once, a customer tracing a subtle byproduct shared their NMR, which prompted a switch in our washing sequence.

    Staying Ahead Without Cutting Corners

    Any specialty chemical rises and falls by the reputation of those making it. Over years of effort and thousands of kilos made, we have resisted the urge to cut corners, knowing that one slip not only ruins a batch but damages trust built over countless phone calls and face-to-face conversations. Our investment runs to site audits, training for every new regulation, and handover meetings between shifts.

    We carry out in-house impurity profiling with updated technology, mapping minor peaks that sometimes escape routine checks. Customers have asked us to spot-check new potential impurities that appeared on mass spec screens overseas. Our team enjoys the challenge, sending feedback and collaborating with buyers toward better solutions for every application sector. The confidence in every drum rests on checks, rechecks, and hands-on ownership—not just management meetings, but shop floor pride.

    Challenges Ahead and How We’re Facing Them

    Demand for high-purity 2-(2,2,2-Trifluoroethoxy)Phenol continues to rise alongside the expectations for safety and traceability. Regulatory agencies in several regions ask for expanded documentation and transparent reporting of trace contaminants. Preparing for this, our analytic team has expanded trace analysis to sub-ppm detection. We educate our workforce about evolving environmental regulations, staying ahead of new protocols in both production and waste management.

    Another challenge involves raw material markets, as supply chain volatility sometimes threatens the regular delivery of key precursors. With years of relationships behind us, we build redundancy through multiple suppliers, forward-purchased contracts, and local stock. Production doesn’t halt for want of a key fluorinated intermediate; planning and storage always come ahead of schedule crunches, learned the hard way through past shortages.

    Finally, reaching new global customers means crossing language, regulatory, and customs barriers. Our documentation now runs in multiple languages and local compliance officers regularly check paperwork before shipping. Nothing gets loaded for export without front-line staff confirming every detail lines up with the local market’s requirements. By grounding every challenge in the daily practice of hands-on chemistry, we keep moving forward.

    Real-World Differences Between Our Product and Other Phenols

    Over the years, we have compared our product to other phenolic compounds, both in-house and in customer application trials. The changes driven by the trifluoroethoxy group aren’t just academic. Non-fluorinated phenols give lower oxidative stability, and even a simple ethoxy-derivative can rapidly lose performance under harsh processing conditions. In side-by-side stability tests, aliquots of our product consistently outlast straight phenol or p-ethoxyphenol, both under high-heat and in light-exposed stockrooms.

    In multi-step synthesis workflows, the difference emerges in downstream recovery and overall yield. Our customers report that the desired phenol doesn’t require heavy post-processing steps to remove oxidized brown tars, and the lessened loss leads to a steady drop in overall operational expense. The true impact of switching to a trifluoroethoxy phenol emerges only after several batches, when fewer complaints reach the technical support desk and efficiency improvements start appearing on production dashboards.

    Analytical feedback supports what hands-on synthesis teams see—reactions move with fewer side products, and NMR purity meets benchmarks more often than with older standards. Industrial-scale operators appreciate spending less time troubleshooting and more time pushing forward new product lines. These differences mean that, over time, new users rarely go back to non-fluorinated alternatives once they’ve converted to this molecule.

    Looking Ahead: Ongoing Commitment From The Inside Out

    Each drum of 2-(2,2,2-Trifluoroethoxy)Phenol carries the fingerprints of dozens of hands—those who cleaned vessels, checked GC traces, adjusted pH, logged storage conditions, and took late-night emergency calls. From the shop floor to the lab bench, everyone knows the product’s importance across core industries, and each new process adjustment grew from lived experience, not theory alone.

    We stay committed to providing material that stands up to real-world challenges. The stories we hear from users—whether in drug discovery or agrichemical synthesis—remind us why every detail matters, from purity assurance to transparent batch tracking and responsible waste handling. The field keeps changing and so do we, always listening and learning with each new request. In the end, our success comes from respect for the molecule, the process, and everyone who builds trust into every batch.