Anhui Liwei Chemical Co., Limited
Products

4-(Trifluoromethoxy)Phenole


    • Product Name 4-(Trifluoromethoxy)Phenole
    • Alias 4-(Trifluoromethoxy)phenol
    • Einecs 211-995-7
    • 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

    833488

    Chemical Name 4-(Trifluoromethoxy)phenol
    Molecular Formula C7H5F3O2
    Molecular Weight 178.11 g/mol
    Cas Number 828-90-0
    Appearance White to off-white crystalline powder
    Melting Point 63-66 °C
    Boiling Point 222-223 °C
    Solubility In Water Slightly soluble
    Density 1.422 g/cm3
    Purity Typically ≥98%
    Smiles C1=CC(=CC=C1O)OC(F)(F)F
    Refractive Index 1.525 (estimated)
    Flash Point 109 °C
    Storage Conditions Store in a cool, dry place, tightly closed
    Synonyms 4-Hydroxyphenyl trifluoromethyl ether

    As an accredited 4-(Trifluoromethoxy)Phenole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle contains 25g of 4-(Trifluoromethoxy)phenol; tightly sealed with a screw cap and labeled with safety information.
    Shipping 4-(Trifluoromethoxy)phenol is shipped in tightly sealed, inert containers to prevent moisture and air exposure. Packages comply with international chemical safety regulations and include appropriate hazard labeling. The chemical is transported under controlled temperature conditions, with documentation detailing handling precautions and emergency procedures as required for laboratory and industrial use.
    Storage 4-(Trifluoromethoxy)phenol should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and bases. Keep the container tightly closed and protected from light and moisture. Store in a chemical-resistant, labeled container. Use secondary containment to prevent spillage. Always follow local regulations and safety guidelines for hazardous chemicals.
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    Certification & Compliance
    More Introduction

    4-(Trifluoromethoxy)Phenol: Manufacturing Insight and Product Commentary

    Working in chemical manufacturing means seeing the intricate process behind each compound that leaves our facility. 4-(Trifluoromethoxy)phenol, known in the industry for its unique combination of chemical activity and stability, stands out in the lineup of functionalized phenols. In the world of fine chemicals, people often seek improvements on the old standards. Our version of 4-(Trifluoromethoxy)phenol, with its chemical formula C7H5F3O2 and CAS number 827-99-6, reveals what happens when a laboratory’s craft directs itself toward purity, consistency, and customer application needs.

    Reflecting on the Importance of 4-(Trifluoromethoxy)Phenol in Synthesis

    Manufacturing phenolic compounds for decades sharpens one’s sense for what works in the reaction vessel. We have watched chemists look for that balance between reactivity and manageability when building more elaborate molecules. Fluorinated phenols in particular have drawn interest from pharmaceutical and agrochemical developers. The trifluoromethoxy group on the para position—a structure not found in simple phenols—alters both the electronic properties and lipophilicity of the molecule. This small change matters. The group pulls electron density, shifting pKa and influencing where and how the phenol participates in further synthesis.

    Comparison between standard phenol and 4-(Trifluoromethoxy)phenol highlights these differences. Plain phenol rarely shows the same chemical persistence or aromatic stability under harsher reagents. By producing the 4-trifluoromethoxy derivative, we help chemists introduce a robust, electron-deficient aromatic core into active ingredients. Demand has risen as researchers integrate such groups into kinase inhibitors, antiviral agents, and new materials that demand exotic substitution patterns for specialized function.

    The Path from Raw Material to Consistent Product

    Reproducibility separates an average supplier from a dedicated manufacturer. We source raw fluorinated building blocks directly. After years in production, we developed a stepwise, controlled process for producing 4-(Trifluoromethoxy)phenol. The process starts with strict lot qualification for halogenated anisoles, and we monitor water and impurity content at every step. Operators manage reaction temperature and pressure closely, since the trifluoromethoxy moiety, though sturdy, does not tolerate carelessness in the presence of strong acids or bases. Post-synthesis, we rely on solid-liquid separation technology tailored to fine organic solids, then employ continuous-flow washing to reach a residual salt level well below typical benchmarks.

    Our crystalline product carries high assay (at least 99% by HPLC) and offers low moisture content. Over the years, trial and error has led us away from processes that gave only irregular particle sizes or poor filterability. The current route yields a free-flowing white to off-white solid, ready for scaling applications and tailored for solution or melt blending in downstream steps.

    Applications: What Chemists Actually Do With 4-(Trifluoromethoxy)Phenol

    We have worked alongside customers who feed our product into pilot and production-scale reactors. The compound sees common use as an intermediate. Medicinal chemistry programs use it to develop ether or thioether linkages, extend aromatic rings, and introduce strong electron-withdrawing effects in active pharmacophores. Agrochemical makers see benefit in its resistance to oxidative breakdown, giving their final compounds longer effective lifetimes. Material scientists incorporate it when fabricating specialty polymers where the aromatic system’s polarity and hydrophobicity must be fine-tuned for niche applications.

    Some makers prepare aryl ethers or carbonates with this starting point, exploiting its relatively low acidity compared to unsubstituted phenols. Others use it to generate cross-coupled products using Suzuki or Buchwald-Hartwig reactions, since the substitution pattern directs regioselectivity more predictably. Unlike earlier phenol derivatives, the trifluoromethoxy modification delivers robust compatibility with modern Pd catalysis without requiring extra protecting groups. This reduces reaction steps and minimizes purification headaches downstream.

    Comparing 4-(Trifluoromethoxy)Phenol to Varied Alternatives

    In our history as a producer, we tested related compounds for the same target applications. 2-(Trifluoromethoxy)phenol, where the group sits ortho instead of para, doesn’t grant the same synthetic flexibility. It suffers from unwelcome side reactions and offers a less accessible hydroxyl group. Meanwhile, the typical 4-nitrophenol or 4-chlorophenol are far less hydrophobic, and they lack the added stability against metabolic or oxidative stress. Substituting a methoxy or ethoxy for the trifluoromethoxy falls short when chemists want maximal fluorine content driving their molecular design or when clinical testing targets improved pharmacokinetics.

    For those seeking more robust electron withdrawal, some turn to 4-trifluoromethylphenol. But in daily operations, we see increased handling hazards and lower product yields at scale. The presence of an oxygen atom in the trifluoromethoxy group tempers reactivity. Over dozens of production runs, the balance between product safety, performance, and availability tips in favor of 4-(Trifluoromethoxy)phenol.

    Specification: Delivering Reliability and Understanding Customer Demands

    Our model offers a purity listed consistently above 99% by area normalization in HPLC testing, an advantage borne from tight process controls and rigorous QA practices, not loose sourcing. We ship in high-barrier containers, minimizing exposure to atmospheric moisture and limiting risk of contamination. Chemists prefer the absence of extraneous peaks in their NMR and mass spec readouts. Repeat customers point out that even a few tenths of a percent less water than a competing lot can sometimes spare hours in solvent exchanges or pause workups. Stable color and solid consistency have saved clients money by reducing pre-processing steps.

    Some teams request particle size adjustments or modified drying conditions. Our plant makes these feasible, as we invested in filtration and drying capacity tailored to batch flexibility. When new customers come with unorthodox requests—say, sub-50 micron product for catalytic testing—we collaborate directly with both process and R&D teams to meet practical parameters instead of sending out a one-formula-fits-all product.

    Handling Safety and Storage: Manufacturer’s Perspective

    Producing and shipping 4-(Trifluoromethoxy)phenol requires diligence and careful design. Though non-volatile compared to low-mass ethers, trifluoromethoxyphenols possess enough reactivity in their hydroxyl group to demand closed handling and proper PPE throughout production. As a manufacturer, we monitor dust control in each area and provide sealed packaging to prevent air and light degradation. Thanks to investments in ventilation and spill-collection, our operators have not suffered incidents during transfers or clean-up in many years. This translates to safer experiences for our clients when they use, transfer, or store the product at their own facilities.

    Our supply chain steps up to the challenge of global shipping. Bulk containers are lined for chemical compatibility and shipped under temperature-stable conditions. This prevents unexpected cold-flow or caking seen with some suppliers’ less stable lots. We advise customers to store the product in cool, dry, and well-ventilated spaces, and we regularly check that shelf life matches our published test results. By collaborating closely with technical teams, we have developed procedures for lab-scale and process-scale delivery that keep both material and personnel safe without undue extra protocols or paperwork burdens for our clients.

    Continuous Improvement: Listening to Chemists and Responding

    Direct customer feedback shapes every upgrade we make. Several years ago, recurring requests focused on easier weighing and charging of the product in automated synthesis setups. By fine-tuning drying cycles and particle size distribution, we managed to achieve near-clump-free flow. Some clients in Japan noted color drift in batches exposed to high humidity in port customs—our response included upgraded packaging foil and humidity indicators. Other customers—a few with unconventional downstream chemistry—asked for removal of trace halogenated byproducts. Our QA team invested in new GC-MS protocols to drive identification and purification beyond what was considered industry standard at the time, shrinking the analytical gap between our product and the theoretical profile.

    We participate in cross-industry discussions about raw material supply, waste handling, and environmental impacts. By eliminating unnecessary solvent steps and optimizing post-processing for minimal waste, our teams keep environmental footprint low without sacrificing purity or throughput. Several projects over the past decade focused on circular economy principles, reclaiming byproducts into other process streams. This pays off not only in savings but also in regulatory compliance and market trust, reinforcing the value of direct manufacturer engagement.

    What Sets a Manufacturer Apart

    Handling demands on both volume and turnaround time has transformed our facility from a basic chemical plant to a connected partner for research and scale-up teams. Unlike brokers or trading houses, we keep control over each reaction and purification, cutting out unpredictable lead times and mixed-batch risk. When a customer calls about a unique impurity spec, our production, QA, and logistics teams all participate, shortening the problem-solving loop. Cumulative experience means we track subtle clues—like a shift in melting point or new UV absorbance—before they could affect a pilot run or full registration batch at the customer site.

    We see clients return for 4-(Trifluoromethoxy)phenol not because it carries flashy branding, but because they can rely on its attributes batch after batch. Reliable sourcing from a primary maker means less downtime and fewer disappointments in multi-step synthetic plans. In the competitive landscape of specialty chemicals, having this kind of trust lets both manufacturer and client push chemistry farther, faster. Flexibility in packaging, guidance on storage, and regular lot performance data support not only smooth internal operations, but also the innovation that our own customers chase in their respective markets.

    Adapting Strategies for a Changing Market

    Our experience as a direct manufacturer goes beyond chemical transformations. Regulatory expectations, REACH registration, and regional compliance require robust documentation and agile data management. Years of customer auditing have taught us the value of full traceability—from reactor logs to final shipment certificates. Regulatory pressure on fluorinated organic chemicals increases each year, due in part to both safety and environmental concerns. We remain proactive, tracking international guidelines, ensuring our emissions are monitored, and conducting regular safety drills for our teams. Clients have come to expect this level of diligence, and we use these systems to improve not only accreditation, but also the way each shipment is produced and delivered.

    Engagement with academic and industrial partners sheds light on new application areas. Recent research in advanced materials, surface science, and photoactive compounds draws heavily on the modular reactivity that compounds like 4-(Trifluoromethoxy)phenol make possible. Direct interaction with these partners helps us update our analytical techniques and production controls. Rather than remain satisfied with current purity markers, we test for emerging contaminants, facilitate chain-of-custody data sharing, and refine lot labeling for straightforward import across diverse jurisdictions. This cycle of feedback and adaptation keeps us ahead in a competitive field.

    Balancing Tradition and Innovation in Chemical Manufacturing

    Over years of operation, our perspective has shifted from mere output to delivering impact. Building 4-(Trifluoromethoxy)phenol with the reliability and nuance demanded by advanced chemical synthesis challenges us to think about chemistry not as a commodity, but as a service. Every adjustment to drying times, every new analytical run, and every shipping detail is informed directly by experience and the drive to help chemists meet more complex goals than ever before. That focus makes all the difference for downstream efficiency, yield, and final product quality.

    We understand that for many customers, choosing 4-(Trifluoromethoxy)phenol is as much about supplier confidence as about molecular structure. In a sea of options, reliability is earned, not advertised. By anchoring production in evidence-based upgrades and authentic chemistry experience, we continue to provide a product that supports innovation—not just inside our own walls, but throughout every lab and plant that partners with us.