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HS Code |
633157 |
| Cas Number | 98-17-9 |
| Molecular Formula | C7H5F3O |
| Molecular Weight | 162.11 g/mol |
| Iupac Name | 3-(Trifluoromethyl)phenol |
| Appearance | White to off-white solid |
| Melting Point | 31-34 °C |
| Boiling Point | 180-182 °C |
| Density | 1.37 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 74 °C |
| Smiles | C1=CC(=CC(=C1)O)C(F)(F)F |
| Synonyms | m-(Trifluoromethyl)phenol |
| Refractive Index | 1.482 |
| Pubchem Cid | 72595 |
| Ec Number | 202-649-8 |
As an accredited 3-Trifluoromethylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Trifluoromethylphenol is supplied in a 100g amber glass bottle with a secure screw cap, labeled with hazard warnings. |
| Shipping | 3-Trifluoromethylphenol is shipped in tightly sealed containers to prevent leaks and contamination. It should be stored and transported in a cool, well-ventilated area, away from heat and incompatible materials. Packaging complies with relevant chemical regulations, and handling typically requires appropriate labeling, safety documentation, and protective measures during shipment. |
| Storage | 3-Trifluoromethylphenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Recommended storage temperature is below 25°C. Ensure proper labeling and access only to trained personnel, following all relevant chemical safety protocols. |
Applications of 3-Trifluoromethylphenol in Industrial Manufacturing3-Trifluoromethylphenol supports key transformations in advanced industrial manufacturing, delivering targeted chemical properties to pharmaceutical synthesis, specialty agrochemicals, liquid crystal monomers, and advanced polymer production. Below, we detail specific downstream scenarios where 3-Trifluoromethylphenol is integrated and highlight the precise compliance, dosage, process, and product requirements as observed by commercial users. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisGlobal pharmaceutical manufacturers use 3-Trifluoromethylphenol as a core building block in the synthesis of several APIs, especially in producing molecules with fluorinated aromatic rings for enhanced metabolic stability. This compound undergoes specific electrophilic substitution or coupling reactions to introduce trifluoromethylphenol moieties into key intermediates required in high-value patented drugs. Industry compliance standards
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2. Agrochemical Synthesis for Herbicide and Fungicide Active IngredientsProducers in the crop protection sector use 3-Trifluoromethylphenol as a starting point for manufacturing selective herbicides and fungicides demanding fluorine-containing aromatic scaffolds. The chemical enters chlorination or esterification steps, conferring improved bioactivity, persistence, and plant uptake to the final molecules in commercial formulations. Industry compliance standards
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3. Monomer for Liquid Crystal Display (LCD) MaterialsDownstream electronics material firms incorporate 3-Trifluoromethylphenol in the development of monomers forming the core of nematic and smectic liquid crystals. The objective is to introduce the trifluoromethyl group to the aromatic core, which impacts dielectric anisotropy, viscosity, and temperature stability critical for high-performance display devices. Industry compliance standards
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4. Advanced Polymer Additive and High-Performance Resin ManufacturingSpecialty chemical companies use 3-Trifluoromethylphenol to introduce fluorinated functionalities into engineering polymers and resins where exceptional chemical resistance or low surface energy are required for specialized coatings, adhesives, and sealants. The compound is co-polymerized through phenol-formaldehyde reactions or directly embedded as a functional chain terminator or modifier. Industry compliance standards
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Speaking from inside the chemical plant, we rarely come across a molecule that brings as much utility to fine chemical synthesis as 3-Trifluoromethylphenol. Known to many as MFP or by its structural formula C7H5F3O, this aromatic compound has earned a unique place on our production lines for both its chemical profile and the flexibility it affords downstream applications. In our experience, handling the entire lifecycle of this product—from raw fluorinated precursors to packaged material ready for shipment—unlocks distinctive advantages for the chemists and material scientists who rely on it.
The value of 3-Trifluoromethylphenol begins at the molecular level. Its benzene ring bears a trifluoromethyl group in the meta position and a hydroxy group. The trifluoromethyl moiety is not just a cosmetic modification; in our work we’ve found that this group provides robust electron-withdrawing effects, which can dramatically alter the reactivity of the molecule’s core. This has substantial consequences for synthesis routes in agrochemical, pharmaceutical, and specialty materials sectors where nuanced control of reactivity defines the outcome.
Our batches maintain a minimum purity of 99%, and we adhere to rigorous quality checks in every step — from distillation to final assay. This ensures both the hydroxy and trifluoromethyl functional groups remain intact, critical for any customer relying on predictable downstream derivatization. Having worked through enough synthesis trials, we know that small deviations in composition can lead to significant consequences for product yield or impurity profiles in later steps.
Manufacturing this material demands both technical rigor and practical know-how. Every reactor load starts with a clear audit of incoming fluorinated bulk chemicals. Only select grades make it past our raw material validators, as any trace of halogenated side-products or water can compromise both the purity and the shelf-life of the final phenol. Years of in-plant experience have shown that even slight impurities at the raw stage can catalyze undesired side reactions, raising purification costs downstream.
Our process pivots around controlled aromatic substitution, where temperature control is everything. Operators do not cut corners here: improper heat gradients or incomplete mixing show up as off-ratios of the para- and ortho-isomers in the crude product. Inline NMR monitoring lets us catch and correct these before isolation even begins. This level of plant integration creates batch-to-batch reproducibility — a trait our customers now expect with each shipment.
The material itself comes as a white to off-white crystalline powder, free-flowing but sensitive to contamination. Even though the trifluoromethyl group helps with stability, we store finished product in airtight, moisture-free containers to prevent any hydrolysis or yellowing over time. From direct experience, exposure to trace moisture leads to color changes and, more critically, can start to generate insoluble byproducts. Workers in our packaging lines insist on double-layer sealed drums to help buyers avoid these headaches later.
Handling at scale also calls for care with dust control—this powder has a habit of clinging to surfaces, which is a recipe for cross-contamination in multipurpose plants. We use dedicated equipment on the discharge line and perform manual swabbing between campaign runs. Avoiding cross-over with other fluorinated compounds is key, especially for API or regulated feedstock markets, as the slightest trace of a similar-structure byproduct can upend entire downstream syntheses.
While many buyers ask for a basic data sheet, it’s the real-life results that matter most for a production chemist. Our in-house analytical team measures melting point, moisture, bulk density, and purity using both HPLC and GC. The melting range of 51–54°C consistently shows up in finished batches, giving users confidence in recrystallization steps. Moisture readings sit below 0.1%, as any higher content triggers a root-cause audit in our drying rooms.
We deliberately avoid using stabilizers or modifying additives, having found through trial that these can influence the reactivity—especially for end-users who need untouched, virgin material for highly sensitive syntheses. Every lot’s certificate matches the actual drum contents; samples rarely deviate from the spec, though we are quick to rework or scrap anything that falls outside our limits.
For those outside the plant, 3-Trifluoromethylphenol may seem like another entry in the phenolic building block catalog. From here on the production floor, the applications come into sharper focus. In pharmaceutical research, it serves as an intermediate for the synthesis of selective kinase inhibitors and as a fine-tuning agent for bioactive molecule scaffolds. One common example involves its role as a precursor in the Suzuki-Miyaura cross-coupling, a method heavily used to elaborate aromatic rings in clinical candidate drugs. If the upstream phenol isn’t pure, we’ve seen firsthand how yields crumble and side product profiles balloon, increasing both the isolation headaches and regulatory scrutiny.
Agrochemical labs come to us looking for the same material to build more selective herbicidal or fungicidal agents. Here, the trifluoromethyl group isn't mere window dressing — it confers improved metabolic stability and impacts the biologically relevant pKa of active molecules. Test chemists who trialed lower-grade sources in pilot plant settings often came back reporting batch failures or inconsistent assay results. Our production-grade consistency helps them maintain reproducibility across entire product campaigns, avoiding both waste and regulatory mishaps.
From a materials science viewpoint, derivatives of 3-Trifluoromethylphenol appear in specialty monomers for high-performance coatings and electronics. The precise electronic and steric influence of the CF3 group lets formulators push boundaries on dielectric constant, solubility, and environmental resistance. Our direct feedback from users confirms that small variability in starting phenol purity can skew downstream polymerization ratios and ultimately affect the finished device or coating performance.
Every smart buyer weighs options between meta-, para-, and ortho-substituted analogs or even looks to non-fluorinated phenols when price becomes the main criterion. For us, manufacturing meta-substituted 3-Trifluoromethylphenol pivots on its distinct reactivity profile. Compared with the para and ortho configurations, our meta product gives unique selectivity in electrophilic aromatic substitution. Customers synthesizing downstream sulfonates or amides learn quickly that the meta position yields different regiochemical outcomes, making our compound the tool of choice in many medicinal or agrochemical routes.
Looking at other fluorinated phenols, such as 2-Trifluoromethylphenol or 4-Trifluoromethylphenol, the location of the CF3 group matters. Through trial, customers see drastic differences in both reactivity and ultimate biological activity, especially in medicinal chemistry, where subtle changes can define IP space or functional activity. Our in-plant records show that mixing isomers or using blended grades causes more headaches than savings, especially if using the product in regulated synthesis steps. Recrystallization does not fully resolve co-eluting isomeric impurities, so strict upstream control is the needed solution — something we invest considerable effort to guarantee.
Buyers sometimes ask about using non-fluorinated analogs to cut costs. Experience across several specialty synthesis workshops demonstrates this path rarely pays off, as the trifluoromethyl group’s electronic influence determines solubility and target binding in many pharmaceuticals or agro-active molecules. This difference plays out in both bench and pilot runs, with end-product properties changing unpredictably if a standard phenol swaps in during scale-up.
Producing 3-Trifluoromethylphenol at commercial scale is not without daily challenges. One persistent hurdle is managing trace halogenated impurities through both synthesis and packaging, since these can react in later stages or catalyze unwanted downstream transformations. Our team’s direct hands-on approach—continuous monitoring, batch sampling, and in-house purification—keeps impurities below detection thresholds. Years ago early plant batches suffered yield losses and customer complaints over small but impactful levels of unidentified impurities. We have since overhauled the entire solvent recovery system and now treat all process effluent as a critical quality determinant, not just a waste stream.
Worker safety and environmental handling mark another area where our perspective differs from outside observers. This material, while not classified as acutely toxic, generates strong odors and demands strict containment to protect both personnel and the surrounding community. Regular operator training and exhaust scrubbing keep downtime rare, but we stay vigilant for leaks or uncontrolled emissions, especially in hot summer months when vapor pressures fluctuate. Inspections rarely reveal issues, and rapid maintenance response helps keep every campaign on track.
A third challenge involves transportation. High-purity material needs secure, sealed transport to ensure no exposure to humidity or rogue vapors en route. Over a decade, multiple logistics partners have cycled through our chain, and we only retain the few who deliver on schedule and without incident. Even small transit mishaps can erode product quality and lead to costly customer returns. That is why shipping rooms coordinate closely with production and QA teams, making last-minute adjustments to packaging or shipping mode based on real-world conditions rather than a theoretical checklist.
Working day-in and day-out as a direct manufacturer allows us to serve as more than a raw materials supplier. Many process development teams keep us on speed dial during scale-up campaigns, seeking not just a reliable supply, but access to real-world application data. Our teams regularly host joint troubleshooting sessions to refine process adaptations, from solvent switchovers to alternative coupling strategies. This hands-on, problem-solving approach arms our customers with reliable outcomes, rather than just a product spec.
In one recent example, a pharmaceutical company sought to scale a synthesis route but encountered a persistent impurity spike during triflation. A cooperative investigation traced the root cause to the barely-perceptible increase in water content after a shipping delay. Batch records and moisture logs proved decisive in flagging the issue early, helping the customer avoid extensive downtime or requalification of finished batches.
Sometimes, R&D teams pilot new derivatization sequences using various phenolic precursors, only to hit unforeseen hurdles at scale. We offer both technical guidance and rapid sample turnaround, drawing from our firsthand plant data rather than generic white-paper advice. Our experience shows that investing expertise alongside product supply leads to solutions that meet both regulatory and commercial standards.
Recent shifts in global chemical regulation and corporate responsibility drive us to improve process safety and sustainability. For 3-Trifluoromethylphenol, that means optimizing solvent selection for lower emissions and minimizing effluent toxicity. Decades of running high-volume batches bred a keen awareness of where older processes created waste. By switching to solvent recycling and installing real-time emission sensors, we trimmed both costs and environmental impact. This isn’t just regulatory box-ticking: our experience shows that newer, greener processes reduce downtime and long-term liability, in addition to supporting broader industry commitments to safer, more responsible manufacturing.
Scrutiny on fluorinated intermediates, both from environmental regulators and the public, keeps us attentive to lifecycle stewardship. Our current plant structure prioritizes closed-loop solvent handling and high-efficiency abatement technologies to capture any stray emissions. Regular audits benchmark us against the best available practices and push us to innovate further, particularly around fluorinated waste minimization and safe material stewardship.
Working day after day as actual hands-on producers of 3-Trifluoromethylphenol, we know where the real strengths and pitfalls of this compound lie. Its value exists not only in chemical structure or paper specifications but in the reproducibility, collaboration, and traceability we bring to every batch that leaves our gate. Understanding the quirks of this phenol, from reactivity to best handling practices, is not theoretical—it's the lived experience of our team on the production floor, the test bench, and the road to our customers. For those ready to translate molecular precision into tangible results, the combination of deep plant experience, practical supply capabilities, and end-user partnership makes a real difference, far beyond what any catalog entry could reveal.