Anhui Liwei Chemical Co., Limited
Products

Phenol, 5-Fluoro-2-(Trifluoromethyl)-


    • Product Name Phenol, 5-Fluoro-2-(Trifluoromethyl)-
    • Alias 5-Fluoro-2-(trifluoromethyl)phenol
    • Einecs 242-354-4
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
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    Specifications

    HS Code

    594367

    Chemical Name Phenol, 5-Fluoro-2-(Trifluoromethyl)-
    Cas Number 345-92-6
    Molecular Formula C7H4F4O
    Molecular Weight 180.10 g/mol
    Appearance Colorless to light yellow liquid
    Boiling Point 168-170°C
    Density 1.453 g/cm3
    Solubility In Water Slightly soluble
    Flash Point 71°C
    Refractive Index 1.457
    Purity Typically ≥98%
    Synonyms 5-Fluoro-2-(trifluoromethyl)phenol
    Smiles OC1=CC(C(F)(F)F)=CC(F)=C1

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

    Packing & Storage
    Packing The packaging is a 25-gram amber glass bottle with a secure screw cap, labeled "Phenol, 5-Fluoro-2-(Trifluoromethyl)-".
    Shipping Shipping of Phenol, 5-Fluoro-2-(Trifluoromethyl)- requires secure, leak-proof containers, typically made of compatible plastic or glass. It should be labeled as a hazardous chemical and protected from heat, moisture, and incompatible substances. Transport should comply with local and international regulations, including proper documentation and hazard classification.
    Storage Phenol, 5-Fluoro-2-(trifluoromethyl)- should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and bases. Keep the container tightly closed and protected from moisture and direct sunlight. Store in a chemical-resistant container, properly labeled, and adhere to all relevant safety and local regulatory guidelines.
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    Certification & Compliance
    More Introduction

    Phenol, 5-Fluoro-2-(Trifluoromethyl)-: A Closer Look from the Manufacturer's Perspective

    Introduction to Phenol, 5-Fluoro-2-(Trifluoromethyl)-

    Working directly with the synthesis and production of Phenol, 5-Fluoro-2-(Trifluoromethyl)- over the years has provided a first-hand understanding of its unique value for advanced chemical research and manufacturing. The interest in substituted phenols like this compound continues to grow, as the quest for precision and reproducibility in aromatic building blocks becomes more demanding. Our facility operates at the interface of process chemistry and real-world performance, with hands literally on the glassware and reactors, looking to control purity, batch consistency, and response to customer-specific feedback. Phenol, 5-Fluoro-2-(Trifluoromethyl)-, thanks to its fluorinated profile, stands out among phenolic intermediates for specialized synthesis pathways, especially for those seeking to build robust, high-performance molecules with applications in modern pharmaceuticals, agrochemicals, and advanced materials.

    The Unique Structure and Its Impact

    Taking a deep look at the structure, the 5-fluoro and 2-trifluoromethyl pattern reshapes the chemical character of the underlying phenol. Small changes in aromatic substitution can bring big shifts in reactivity and physical properties. Sitting at the bench, handling both the raw and refined forms, it’s clear that the presence of these substituents increases both the electron-withdrawing effect and steric bulk, making it more than just another phenol. This arrangement tunes the acidity, offers greater resistance to oxidative degradation, and can influence solubility compared to the standard phenol or other mono-substituted versions. Plus, the distinct fingerprint in NMR and mass spectrometry streamlines batch verification and ongoing quality assurance.

    Specifications: Getting the Details Right

    Customers in pharmaceutical, agrochemical, or polymer discovery have commented time and again that consistency from batch to batch makes or breaks research timelines. Our production focuses on maintaining a high-purity standard—generally exceeding 98% purity by GC and 99% by HPLC. Careful attention goes into minimizing moisture and residual solvents. Handling extra fluorinated aromatics comes with its own logistical needs: glass lines, fluorine-resistant seals, and precise, low-oxygen packaging. Feedback from partner labs and direct customers has shaped how we test for trace byproducts and decide our main specification criteria, not just because of regulatory requirements, but because problematic impurities can impact downstream coupling, arylation, or protection chemistries meant to use this intermediate.

    Model Variants, Batch Profiles, and Practical Selection

    From firsthand observation, the real demand for Phenol, 5-Fluoro-2-(Trifluoromethyl)- grows out of its adaptability. Whether in small pilot batches or multi-kilogram production runs, we’ve seen R&D teams requesting tailored packaging and purity grades. Some synthetic chemists prefer slightly higher water content for solubility, some call for an anhydrous grade for sensitive reactions—so batch selection often reflects downstream use, not simple catalog numbers. Having learned from orders for just a few grams to truckloads, we keep close communication with customers about storage conditions: this compound’s volatility is lower than base phenol, which aids handling but the trifluoromethyl and fluorine groups make it sensitive to trace acids or bases.

    Applications and Practical Insights From the Plant Floor

    Making this compound has taught the team a lot about the scale-up challenges of halogenated aromatics. Our customers put it to work in Suzuki couplings, etherifications, or further functionalizations—building blocks for active components in medicinal chemistry and crop chemistry often trace their roots to such fluorinated phenols. There’s been a visible shift towards these intermediates, especially in exploring new lead compounds with better metabolic stability and improved pharmacokinetics. With the right substitution, researchers see increased bioavailability and persistence both in biological targets and chemical processes.

    For those creating advanced monomers or targeted dyes, the compound’s resistance to light-induced degradation brings tangible benefits. During pilot projects for new high-performance coatings, users have shared that their results—less yellowing, stronger chemical stability—directly link to the role played by the trifluoromethyl group at the ortho position. R&D specialists regularly visit our facility for technical exchanges, discussing not only the expected reactivity but also the downstream surprises, such as small shifts in melting point or unexpected reactivity in electrophilic aromatic substitutions.

    Why This Compound Stands Apart

    Sitting in the plant, surrounded by drums of both basic phenol and its more sophisticated derivatives, people ask: What makes this substitute truly different? Many suppliers stock a range of halogenated phenols, but the dual substitution pattern influences virtually every phase, from synthesis through final application.

    Fluorination at the 5-position not only alters the electron density but also impacts hydrogen bonding and reaction scope, especially compared to non-fluorinated or singly-fluorinated analogues. The 2-trifluoromethyl group further increases hydrophobicity, imparting distinct partitioning behavior in both liquid extractions and biological contexts. In direct industry trials with focus on pesticide discovery, this molecule helped researchers tune selectivity and reduce off-target effects simply by swapping out less robust substituents for this combination.

    Early on, we noticed that researchers working with standard 2-chloro or 4-bromo phenols sometimes ran into poor yields or stability issues during catalytic transformations. Offering Phenol, 5-Fluoro-2-(Trifluoromethyl)-, with clear technical data provided by our own chemists, let customers try direct substitutes in their syntheses—leading to reproducible improvements in several multi-step programs. These real-world successes, backed by open technical discussions, have driven demand more than generic catalog listings ever could.

    Ongoing Challenges in Manufacturing

    Every fluorinated aromatic brings up unique safety and environmental concerns, both for us and end users, and that’s something we address with targeted investments. Waste minimization, exhaust gas scrubbing, and personal safety training have become more critical each year. Mercury-based reagents found in old literature never belong in our practice—modern, safer fluorination techniques, stricter cleaning protocols, and containment procedures remain front and center every day.

    Anyone making multi-kilogram lots of electrophilic intermediates has stories to tell about exothermic steps and waste streams. We regularly invest in analytical upgrades and process improvements to keep impurities controlled below customer-defined limits. Our chemists are always present during scale-up, walking the line to confirm no deviation from agreed specifications. Close, ongoing feedback between QC staff and production managers means issues get fixed in process, not on paper, which builds real trust with partners.

    Customer Feedback and Collaboration

    Partnerships with both major and small-volume buyers have shaped the way this compound is manufactured and supported. Over the years, university labs and multinationals alike have come back with hands-on feedback from real experiments, real failures, and real successes. Adjustment of drying steps, revisiting fractional distillation conditions, and taking extra care with trace metal content have all come from direct user input.

    In project meetings, questions usually focus less on technical jargon and more on real questions: Is this lot dry enough for a sodium hydride reaction? Will residual toluene show up in final testing? Our batch records track every production variable, with records stretching back over a decade, so repeat customers know which tweaks to request for their next order. This ongoing, two-way communication goes far beyond just data sheets—it’s a partnership built on hands-on problem-solving and proven batch history.

    Comparing to Other Phenolic Compounds and Alternatives

    Conversations with process chemists at both innovation labs and established plants often circle back to the broader context—why pick this compound over alternatives? While plenty of substituted phenols exist, the precise arrangement of the fluoro and trifluoromethyl groups reroutes chemical reactivity, impacts metabolic fate, and affects overall process safety. In multiple screens against standard halogenated phenols, this product demonstrated higher thermal stability and less tendency to form problematic side products in cross-coupling regimes.

    Looking beyond straightforward cost comparisons, the use of Phenol, 5-Fluoro-2-(Trifluoromethyl)- frequently reduces the total number of purification steps needed following key transformations—yielding cleaner intermediates, especially in Suzuki or Buchwald-Hartwig conditions. Users shared data from ongoing syntheses where more basic halogenated phenols resulted in downstream chromatographic headaches or batch-to-batch drift—issues substantially reduced when switching to our compound.

    There are situations where more basic phenols fit the bill perfectly. Yet as complexity rises—especially in the pharmaceutical or specialty materials sectors—the added investment in a doubly-substituted, highly pure intermediate can cut costs over the long haul by reducing rework, improving reproducibility, and supporting tighter regulatory filings. This feedback, back and forth between plant floor and lab bench, shapes the ongoing evolution of not only our synthesis but also shipping, storage, and post-sale support.

    Logistics, Packaging, and Supply Chain Reality

    It’s easy to underappreciate the practical challenges of moving sensitive, high-value chemicals from the reactor to the customer’s bench. Our experience delivering Phenol, 5-Fluoro-2-(Trifluoromethyl)- across continents has highlighted packaging as more than just an afterthought. From glass ampoules, crimp-sealed metal cans, to fluoropolymer linings for industrial totes, each packaging type grew out of requests by customers who learned the hard way about product loss, contamination, or stability deteriorations during shipping.

    Direct coordination with logistics partners, tracked shipments, and a willingness to troubleshoot customs issues in real-time has cut delivery times and made repeat orders more predictable. As a manufacturer, visiting labs and plant sites across multiple regions provides first-hand insight into what works and what requires another look. Quality doesn’t stop at the production line—it covers every step through to the receiving dock and the user’s own hands.

    Responsible Practices and the Path Forward

    From day one, making Phenol, 5-Fluoro-2-(Trifluoromethyl)- at commercial scale built a sense of duty to both our industry and the environment. Regulatory landscapes keep shifting. The European drive for substance registration, Asian customs scrutiny, and the North American regulatory focus on traceability all converge on the need for transparency and stewardship.

    Practical, everyday improvements matter. Moving to closed reactors, reusing solvent where possible, and investing in fume abatement has real downstream impact—not just to environmental metrics but to the safety and morale of our team. Regular, no-shortcut internal audits and public sustainability reports create a cycle of continual learning. Peer review, feedback from cross-industry consortia, and involvement in technical conferences keep us nimble, always comparing notes with others pushing the boundaries of specialty chemical manufacturing.

    Technical Support and Ongoing Learning

    A deep-rooted part of our manufacturing philosophy centers on not simply shipping a product, but offering enduring technical support and problem-solving—this comes directly from being hands-on with the synthesis, not just reading about it. Customers running into specific synthetic bottlenecks—whether solubility hiccups or unexpected NMR shifts—have found our bench chemists to be an invaluable resource.

    Directly exchanging spectral data, discussing optimal base or catalyst choices, and troubleshooting purification methods come up frequently in technical calls. These conversations often reveal new insights that shape our internal protocols and guide batch improvements. There’s a real pride in knowing the feedback loop stretches from our reactors right into the customer’s notebook, multiplying the compound’s value well beyond its chemical formula.

    The Real Value: Experience and Partnership

    Being deeply involved in every step of the manufacturing process brings a perspective that product sheets alone can’t offer. Practical adjustments on the line, open doors to visiting chemists, and the willingness to rethink protocols after every customer experience help us stay ahead as demand for complex, fluorinated intermediates rises. The communities working with substituted phenols are small but ever more demanding; their challenges, openly discussed in technical exchanges, shape new approaches to safety, quality, and logistics.

    For many in the chemical industry, sourcing the best raw materials is just the beginning. The real differentiator comes with technical dialogue, an openness to experimentation, and a shared goal to push technological and scientific boundaries. Phenol, 5-Fluoro-2-(Trifluoromethyl)-, crafted with direct input from those using it at the front lines of research and production, stands as a product built not just by formula, but by hard-won experience and a real commitment to partnership.