|
HS Code |
266041 |
| Chemicalname | Phenol, 2-Fluoro-4-(Trifluoromethyl)- |
| Molecularformula | C7H4F4O |
| Molecularweight | 180.10 g/mol |
| Casnumber | 2924-16-5 |
| Appearance | Colorless to pale yellow liquid |
| Meltingpoint | 18-20°C |
| Boilingpoint | 137-139°C at 20 mmHg |
| Density | 1.421 g/cm3 at 25°C |
| Solubility | Slightly soluble in water |
| Flashpoint | 70°C (closed cup) |
| Refractiveindex | 1.4750 |
| Smiles | CC1=CC(=C(C=C1O)F)C(F)(F)F |
As an accredited Phenol,2-Fluoro-4-(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of Phenol, 2-Fluoro-4-(Trifluoromethyl)-, tightly sealed, labeled with hazard and safety information. |
| Shipping | The chemical *Phenol, 2-Fluoro-4-(Trifluoromethyl)-* is shipped as a hazardous material in tightly sealed, chemically compatible containers. Packaging complies with international regulations (such as IATA, DOT, and IMDG). Proper labeling and documentation are included, and transport is conducted by licensed carriers to ensure safety and environmental protection. |
| Storage | Store Phenol, 2-Fluoro-4-(Trifluoromethyl)- in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers and bases. Keep the container tightly closed and protected from light and moisture. Use only approved, chemically resistant containers. Store under inert atmosphere if possible, and follow all relevant safety and regulatory guidelines. |
Competitive Phenol,2-Fluoro-4-(Trifluoromethyl)- prices that fit your budget—flexible terms and customized quotes for every order.
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Every year, thousands of customers in the pharmaceutical and advanced materials industries come searching for functional building blocks that can handle increasing requirements for selectivity, stability, and reactivity. Among these sought-after specialty intermediates, Phenol, 2-Fluoro-4-(Trifluoromethyl)-, recognized in our shop under model number variations according to custom purities and packaging standards, takes on requests that demand more than just standard phenols.
As a chemical manufacturer with thirty years of hands-on experience, our deep involvement in the day-to-day complexities of halogenated phenol production makes us aware of practical hurdles often overlooked by end-users and R&D managers. Questions usually concern not just pricing, but reliability in purity, batch uniformity, and consistent analytical performance. These are answered directly by robust process controls from the first stages of synthesis through every step of fractional distillation and drying.
In our production system, Phenol, 2-Fluoro-4-(Trifluoromethyl)- carries the CAS number 79784-66-6. Batches manufactured here typically achieve a minimum purity that meets HPLC specifications and GC-MS traceability, with most lots passing the 98.5% mark as confirmed by in-house and third-party labs. Experienced process chemists on our team calibrate not just reactivity and heat transfer, but also monitor contaminant profiles such as ortho- and para-isomers, moisture, and trace metals. Consistent results depend on strict supervision of reagent quality, inert gas atmospheres, and the kind of small procedural tweaks that only show up over hundreds of pilot and commercial runs.
We prepare this compound in solid crystalline form. Handling procedures and packaging account for its volatility and sensitivity to atmospheric moisture. Over years of feedback from buyers, we switched to improved inert-gas packaging and non-static bags for large drums and resin-lined, nitrogen-blanketed bottles for smaller requests. Standard packs start from 100 grams for R&D; multi-kilogram drums are arranged by annual or long-term contract.
Many customers ask about the distinction between this compound and its close relatives – for example, plain trifluoromethyl phenols, or other ortho-fluorinated phenols. What has become evident through decades of custom orders is that the dual electron-withdrawing power of fluorine and trifluoromethyl on the aromatic ring opens unique routes in stepwise fluorination, etherification, and coupling chemistry. The presence of both groups modulates the phenolic proton in a way that impacts pKa and affects subsequent transformations. For certain target molecules, minor changes in electron density mean huge downstream differences in selectivity during Suzuki or Buchwald–Hartwig couplings, as well as protection/deprotection strategies.
In analytical sciences, trace impurities in phenolic systems often cause headaches. Our regular customers surface the same concern: does the compound carry over persistent by-products that would appear on LC-MS traces? We run routine analyses and share raw data for full transparency. Chemists at pharmaceutical and agrochemical labs rely on our background checks and are assured that the house processes leave minimal residual solvents, with by-products staying within thresholds updated as regulatory standards evolve.
Working directly with both process and bench-scale users, we have learned how 2-Fluoro-4-(Trifluoromethyl) Phenol brings uncommon value in key synthesis steps. It acts as a starting material for complex heterocycles, selective inhibitors, and next-generation crop protection agents. Medicinal chemistry teams often use it to introduce matched polarity and steric bulk for analog development. Agrochemical formulators appreciate the stability and clean transformation possible when coupling via ether or amide linkages.
Several long-term partners in the fragrance and flavors sector have pointed out the clean, crisp aromatic notes that can be achieved through methylation or further fluorination of the phenolic ring. This selectivity is difficult to match using alternative phenols that lack the same substitution pattern.
In the realm of polymer and specialty material science, this compound often appeals to teams designing monomers for high-performance resins or fluorinated coatings. Early discussions in joint development projects made it clear: using our 2-Fluoro-4-(Trifluoromethyl) Phenol as a core raw material produced more consistent molecular weights and lower dispersities, compared to starting from non-fluorinated precursors. Thermal stability and chemical resistance show measurable improvements when the trifluoromethyl and fluorine are precisely located on the ring, as demonstrated by our internal DSC and TGA datasets.
Scaling from kilo to ton batches, each step introduces new challenges. Chemists not familiar with halogenated aromatics sometimes expect these syntheses to mirror simpler phenol chemistry. In reality, both fluorine and trifluoromethyl substituents alter reaction pathways, reactivity, and, most importantly, the safety profile. We train our operators rigorously on temperature ramp rates and vent design to handle exotherms and fumes that may arise from unexpected side reactions. Equipment maintenance schedules reflect the need for upgraded seals and corrosion-resistant components, based on years learning from failures in legacy setup.
Feedback from our technical support hotline underscores the importance of clear material handling protocols. Mistakes in water exclusion or transfer under air can introduce hydrolysis or discoloration that an NMR or GC trace will later reveal. On the positive side, challenges often have straightforward fixes: careful control of process gas, tight container seals, and routine moisture checks. As a supplier, we share short handling guides with every shipment, and our team stands by to walk labs through process troubleshooting, drawing from real incidents rather than just manual reviews.
Over the last ten years, changing expectations around purity, batch traceability, and environmental safety have led us to revise nearly every SOP in the plant. Regulatory guidelines for impurities, including fluorinated residuals, have tightened, especially as more applications focus on pharmaceutical and agrochemical pathways. Our quality managers and plant chemists collaborate to ensure our control measures are mapped to the latest international guidelines, with audit trails for each production lot.
Direct experience with regional audits, especially in the EU and North America, has built a respect for thorough documentation. End users now demand transparency not just in certificates of analysis, but also in supply chain cleanliness and documentation of by-product waste handling. Years ago, an “in spec” batch could be shipped with just a single chromatogram. Now we provide full impurity profiles, residual solvent analyses, and heavy metal content for every drum sold, prepared by our in-house quality team whose expertise comes from decades in pharmaceutical synthesis and validation.
Working with halogenated and perfluorinated chemistry comes with responsibilities. We have learned that adopting new technologies in waste treatment reduces both emissions and liability. In our plant, solvent recovery systems reclaim and refine process solvents, and activated carbon beds trap low-level vapor losses. Staff in the waste-handling team receive monthly practical training, and we run quarterly safety drills that reflect lessons learned from historical incidents.
Customers and regulators today prioritize data. Annual environmental impact reviews, published publicly and open to independent inspection, highlight our commitment to lowest-impact synthesis. Industry partners appreciate practical efforts to minimize waste volumes and carefully document neutralization steps for spent acids or halogenated by-products.
Production managers, heads of R&D, and senior scientists all value prompt, firsthand technical support. Our approach comes from having solved countless batch issues, from unpredicted coloration in storage to lab-scale variation in melting points due to subtle differences in pre-crystallization cooling rates. The support team has former plant chemists, not call-center agents, answering who have seen product from the inside out.
All technical discussions are rooted in actual incidents and test data, not just reference papers. Should an issue arise in a customer’s plant, users speak directly with manufacturing engineers who have guided the same product from raw material to finished lot. This practical knowledge shortens troubleshooting time and reflects our commitment to reliability and openness.
Direct comparisons with other substituted phenols sometimes yield surprising differences. Take the example of simple 4-trifluoromethylphenol or 2-fluorophenol. We have seen that only with the correct pairing of the ortho-fluorine and para-trifluoromethyl does the molecule exhibit the desired shifts in both reactivity and solubility for certain critical chemistries. This specificity grants chemists more freedom in fine-tuning intermediate properties, whether blocking groups, activators, or handles for further derivatization.
Historically, labs using less highly substituted phenols reported higher side reaction rates and lower yields during cross-coupling or nucleophilic aromatic substitution. Several customers recounted experiences where only after switching to our model did impurity levels drop below critical thresholds. Consistency in the physical state, color, and melting point – all impacted by the dual substitution pattern – matters for scaling from early R&D to plant-scale runs.
We maintain supply chains for similar compounds but have seen a clear trend: Teams focused on high-value applications migrate to the 2-Fluoro-4-(Trifluoromethyl) configuration because of its unique performance and predictable downstream steps. Our plant experience shows that subtle molecular tweaks, including the precise placement of electron-withdrawing groups on the phenolic ring, deliver substantial downstream impact not only in synthetic yield but in ease of purification and formulation stability.
What often gets overlooked is the direct effect of subtle process variables on finished product quality. By obsessively refining temperature control, solvent selection, and workup protocols, our manufacturing team continually pushes down by-product levels and batch-to-batch variation. The investment in monitored air-handling, dynamic mixing, and custom filtration setups isn’t just overhead—it makes the difference between a batch that flies through a pharmaceutical QC lab and one that stalls due to an unexpected peak in the trace chromatogram.
Time and effort spent sampling and analyzing each lot lets us anticipate out-of-spec scenarios. This has enabled smoother scale-ups, fewer customer complaints, and better data for continuous improvement discussions. We try to lead the conversation with practical insight, not sales talk, because our own productivity depends on keeping the lines running smoothly.
Supply chain managers and technical procurement staff engage us about risk controls—how raw material fluctuations, freight bottlenecks, or energy price swings might impact their own project timelines. Decades spent developing relationships with global fluorine and hydrocarbon suppliers allows us to lock in raw stocks and buffer critical intermediates. When global logistics snarls threaten timelines, we often switch to pre-positioned stocks at regional distribution points.
Shipping halogenated and perfluorinated chemicals brings regulatory and practical hurdles. We have built relationships with certified transporters who understand the need for strict temperature and moisture controls on the road and in the air. Shipments arrive with temperature data loggers and tamper-evident seals because small deviations can affect final assay and regulatory acceptance. Our investment in quality logistics grows out of hard lessons learned, not slide deck promises.
End-users in labs, pilot facilities, and production plants share a common goal: materials that deliver on their promise every time, without surprises. As a manufacturer, we find that delivering on these expectations requires practical engagement—site visits, joint troubleshooting sessions, and in some cases, pilot-lot support. The evolution in customer support, from just order fulfillment to active collaboration, reflects changes in our own approach over the years.
Hands-on project experience with partners, from kilo samples to multi-ton trials, reveals insights impossible to glean from written reports. Our teams arrive on-site to assess, measure, and troubleshoot right at the reactor, bringing the full toolkit of production knowledge into your process setting.
Investments in direct engagement pay off in smoother project launches and faster problem identification, both for us and for customers.
Decades of refining the craft of making and supplying Phenol, 2-Fluoro-4-(Trifluoromethyl)- mean the compound stands out for customers with challenging synthesis or production demands. What began as a specialty intermediate for a narrow group of users has grown into a toolbox staple for teams in pharmaceuticals, agrochemicals, specialty polymers, and advanced materials. Each industry we serve brings fresh perspectives, asking for innovations in purity, reactivity, and sustainability.
Lessons learned through active engagement with customer labs and production engineers continue to shape our practices, from upstream sourcing to supply chain logistics, from analytical protocol updates to waste-handling investments. By anchoring every decision in lived practical experience, not just compliance paperwork, we can deliver a product that meets the high bar set by demanding regulatory bodies and innovative scientists.
For technical teams evaluating the next phenolic intermediate, Phenol, 2-Fluoro-4-(Trifluoromethyl)- offers more than a chemical formula. It represents years of manufacturing experience, trial, and documentation that aim to move your project from concept to production with real-world reliability.