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HS Code |
983595 |
| Chemical Name | P-Trifluoromethoxy Phenol |
| Cas Number | 827-59-8 |
| Molecular Formula | C7H5F3O2 |
| Molecular Weight | 178.11 g/mol |
| Appearance | White to off-white solid |
| Boiling Point | 215-217 °C |
| Melting Point | 48-51 °C |
| Purity | ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents such as ethanol and acetone |
| Density | 1.373 g/cm³ |
| Smiles | OC1=CC=C(OC(F)(F)F)C=C1 |
| Iupac Name | 4-(Trifluoromethoxy)phenol |
As an accredited P-Trifluoromethoxy Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | P-Trifluoromethoxy Phenol, 25g, supplied in a sealed amber glass bottle with tamper-evident cap, labeled with hazard information. |
| Shipping | **Shipping Description for P-Trifluoromethoxy Phenol:** This chemical should be shipped in tightly sealed, chemically resistant containers, protected from light and moisture. Handle with appropriate hazard labeling, and comply with relevant regulations for potentially harmful organics. Use secondary containment and ensure temperature and ventilation controls where required. Transport by certified hazardous materials carriers only. |
| Storage | P-Trifluoromethoxy Phenol should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong bases and oxidizing agents. Keep it in a cool, dry, and well-ventilated area, ideally in a chemical storage cabinet. Ensure the storage area is clearly labeled, and protect the chemical from light and heat to maintain stability and safety. |
Applications of P-Trifluoromethoxy Phenol in Industrial ManufacturingAs an original producer of P-Trifluoromethoxy Phenol, we supply this specialty intermediate to select downstream sectors where its advanced fluorinated phenol properties deliver unique value in industrial chemical synthesis. We highlight below the principal application scenarios in which P-Trifluoromethoxy Phenol achieves high-volume adoption, with specific technical, compliance, and formulation details reflecting real-world manufacturing practices. 1. Pharmaceutical Active Ingredient SynthesisOur P-Trifluoromethoxy Phenol plays a crucial role as a building block in the synthesis of select APIs, particularly for fluorine-containing small molecule drugs. Its strong electron-withdrawing behavior improves target molecule metabolic stability and modulates pharmacokinetic profiles. Integration occurs primarily in advanced intermediate steps of multi-stage processes, where precise molar ratios optimize reaction yields. End users in this segment demand rigorous batch-to-batch consistency to support regulatory submission requirements for developed and pipeline pharmaceuticals. Industry compliance standards
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2. Agrochemical Intermediate SynthesisIn crop protection chemical manufacturing, our material serves as a key intermediate for the construction of fluorinated phenoxy herbicides and insecticides. Its chemical reactivity enables enhanced bioavailability and resistance to environmental degradation, which are essential criteria for new active compounds. Agrochemical processors deploy the compound during the late-stage modification of phenoxy skeletons to introduce stability and maintain biological activity after formulation. Industry compliance standards
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3. High-Performance Polymer Additive ManufacturingWithin the specialty polymers sector, P-Trifluoromethoxy Phenol is incorporated as a chain-modifying additive or monomer functionalizer, specifically for applications targeting enhanced thermal and chemical resistance. Process engineers select it for engineered polymers and polyarylates requiring permanent fluorination on the polymer backbone to achieve reliable insulation and mechanical retention under aggressive use conditions, such as in electronics or aerospace components manufacturing. Industry compliance standards
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4. Specialty Coatings and Surface Treatment FormulationsWe supply this raw material to coatings manufacturers developing advanced functional surfaces with low surface energy, high hydrophobicity, and chemical inertness. Its presence in the reactive formulation phase supports downstream applications that demand smooth, durable, and contamination-resistant finishes. End users in this segment typically integrate it into the active resin blend before crosslinking or curing, enabling controlled modification of bulk surface properties for demanding environments. Industry compliance standards
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5. Electronic Materials SynthesisDownstream electronics manufacturers incorporate our product as a fluorinated dopant or functional modifier in dielectric materials and photoresist formulations. Its electron-withdrawing properties facilitate fine-tuning of dielectric constants and enhance UV resistance in microelectronics patterning processes. Direct addition occurs at the formulation stage under cleanroom and strictly controlled environmental conditions to support trace-level impurity requirements for advanced lithography. Industry compliance standards
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Manufacturing P-Trifluoromethoxy Phenol has always been a test of both patience and skill. Over the past decade of handling fine chemicals, our production team has rarely seen a compound as quietly assertive in its versatility or as nuanced in its synthesis challenges. Our most common offering uses the model reference CAS 828-27-3. This molecule draws distinct attention from pharmaceutical and agrochemical developers, especially those requiring precise electronic characteristics or strong hydrogen bond donors balanced with fluorinated groups.
Controlled fluorination at the para position creates a unique balance: it tempers phenolic reactivity, while keeping the strong electron-withdrawing effect of trifluoromethoxy. This fine-tuning lets chemists access a realm of substitution chemistry that struggles to find an equal among traditional phenols or simple trifluoromethyl derivatives. Having spent years scaling up the process, we’ve come to appreciate just how much nuance lives between reaction yield and compound purity during isolation and refining.
Our own experience making P-Trifluoromethoxy Phenol has taught us that even slight deviations in reaction conditions—whether temperature, choice of solvent, or feedstock quality—show up immediately downstream. A classic phenol batch might tolerate some variability, but the trifluoromethoxy substitution demands vigilance at every step. Powder, crystalline, or dissolved in high-purity solvents, any form with lower contamination or unwanted isomer formation delivers the strict reproducibility that researchers and process engineers appreciate.
This molecule has built a reputation on lab benches and in pilot plants for its unique role as both an intermediate and end-use ingredient. Pharmaceutical researchers value the p-trifluoromethoxy moiety because it can boost metabolic stability or alter polarity without radically shifting molecular size. Some pain management compounds and kinase inhibitor discovery projects rely on just this property of P-Trifluoromethoxy Phenol to tune drug profiles on the bench and in vivo. Our clients in Japan have repeatedly chosen our batches for critical API building blocks where the placement of the trifluoromethoxy group means the difference between an active or inactive analog.
Many R&D groups in electronics and materials science lean on this compound for high-performance coatings, sensors, and specialty polymers. One customer, developing next-generation OLED materials, reported sharper emission profiles after introducing this substituent into their molecular screens. Trifluoromethoxy chemistry is famous for creating materials that behave differently from either standard phenols or other fluoroaromatics. Our continuous process avoids the introduction of common trace metallic contaminants seen with less-refined suppliers, meaning end users rely on cleaner signals in spectroscopy and fewer problems at scale-up.
Its utility doesn’t stop with small scale discovery. Agrochemical innovators have reported step changes in pesticide selectivity using P-Trifluoromethoxy Phenol derivatives. Adding just one molecule changes not only biological activity but also soil and water behavior thanks to the distinctive electronic and steric effects. Years ago, we compared plant protection datasets across a variety of crops and herbicide classes; products with para-trifluoromethoxy groups maintained their intended selectivity better, with less off-target toxicity and improved breakdown under UV exposure.
Producing high-purity P-Trifluoromethoxy Phenol is not like synthesizing a simple phenol or trifluoromethylbenzene. From our technical team's daily experience, keeping even trace by-products to a minimum takes diligence, even as pressure and volume step up. Each kilogram scale-up uncovers new quirks, whether that's unexpected by-product precipitation or the need for extra washes to remove colored impurities. Trial and error have settled critical details: controlling quench rate during deprotection steps, carefully handling fluorinated phenol intermediates without generating polymeric residues, and buffering the final distillation to exacting standards.
Shoot for sub-99.5% purity and certain applications will show downstream failures—impurities can poison catalyst beds, or worse, introduce erratic biological effects. Over the years, we doubled down on both single solvent and mixed solvent crystallizations; the right protocol means less product loss and higher yield. Analytical teams have worked side-by-side with operators, refining methods to catch the faintest signals—whether that's using ultra-fast HPLC, 19F-NMR, or trace metals testing at the part-per-billion level.
Consistency leads to less waste in high-value projects, and we see repeat orders from specialty polymer manufacturers who cannot tolerate batch variability. Our ability to keep color, odor, and impurity levels under rigorous control is not an abstract promise; it's borne out by decade-long relationships and robust repeat analyses. The solvent profiles, stability on storage, and absence of moisture are just as important, as many end-users run reactions in sealed systems or under anhydrous conditions.
Many clients who previously used unsubstituted phenol or alternatives like p-cresol have found P-Trifluoromethoxy Phenol offers a sharper set of reactivity levers. The difference lies not just in substitution pattern but also in the tailored effect on hydrogen bonding and electron distribution across the ring. Trifluoromethoxy is a significantly bulkier group than methyl or ethyl, but compared to trifluoromethyl, it brings greater polarity and influences partitioning between aqueous and organic phases in extractions or reactions.
Some new teams expect P-Trifluoromethoxy Phenol to simply mimic phenol's behavior. Our own R&D chemists found that this assumption seldom holds. Its trifluoromethoxy group converts the aromatic system into a markedly less nucleophilic ring but leaves the oxygen atom a potent hydrogen bond donor and acceptor, opening up new possibilities in ligand design and catalyst support. In one in-house test, we saw base-catalyzed alkylation rates slow only marginally, while copper-catalyzed couplings enjoyed selectivity improvements. The same effect helps medicinal chemists avoid unwanted off-target interactions.
Compared to p-trifluoromethyl phenol, the methoxy insertion dramatically shifts both boiling and melting points. We ship most batches as off-white to light tan crystalline solids with melting points in the 50-55°C range, which remains one of the more manageable phases for both weighing and distribution. Our handling often favors glass-lined steel, since the phenolic hydrogen engages with metals, especially at scale, though we’ve optimized for both glass and high-nickel alloys.
Running a clean facility—especially at fluorinated intermediate scale—brings plenty of operational realities around solvent recycling, waste handling, and worker safety. Our team learned early that phenolics demand respect: traces in the air can irritate skin and mucous membranes, and fluorinated compounds respond unpredictably to traditional neutralizations. We've put filtered local extraction and dedicated personal protective equipment in every part of the plant, reviewing procedures with every new batch.
Years of recycling solvents like acetonitrile and toluene, paired with closed wastewater systems and on-site scrubbers, have limited both environmental impact and utility spend. Any solvent-off or waste stream gets tracked and treated before discharge. Spent reaction mixtures get sent for fluorinated organics incineration, never to municipal plants, reflecting the extra responsibility manufacturers face compared to smaller lab operations.
We track not just product but also exposure, keeping operator health logs and rotating staff to reduce any long-term risk. The push for greener chemistry accelerated improvements: tweaking to minimize waste, stretching catalyst life, and trying low-temperature protocols that avoid exotherms or vapor-phase losses. Switching a few process steps to safer bases and acids avoided both batch failures and plant near-misses.
Handling P-Trifluoromethoxy Phenol across hundreds of batches, our operators have staked out a set of practical, hard-won rules. Powder forms absorb moisture from humid air—an unsealed drum can drift out of specification in hours, so we’ve moved to nitrogen-purged packaging and vacuum-sealed containers for all shipments above 100 g. The distinct odor—sharp, slightly medical, and reminiscent of ethers—warns us of accidental leaks well before sensors trigger, but proper PPE remains the gold standard.
Transport and storage require just as much attention as synthesis. We only warehouse in dedicated, low-light environments, and experience suggests that, while the product rarely ignites, it needs separation from oxidizers and acids. Forklift drivers and warehouse crew get the same training as lab staff, since even trace contamination between phenols and amines, for example, can generate stubborn colored impurities later. Keeping process areas cleaned down to trace levels prevents headaches when the next campaign starts up.
Shipping worldwide brings a fresh set of issues. Some customs teams confuse it with hazardous phenols banned under older conventions, so regulatory paperwork and clear labeling form part of our everyday effort. Every label batch lists the exact impurity trace amount, storage date, and packaging protocol—our clients, especially in pharmaceuticals, trust this transparency.
Pushing boundaries has meant investing in our own labs to keep raising consistency—and to help customers go further in their design. Lately, our chemists have been developing asymmetric syntheses and milder conditions. One team succeeded in introducing greener oxidants, cutting down the halide by-products and improving sustainability across the board. Others test every new recovery step, striving to raise isolated yields beyond standard industry practice. Our work with custom derivatization lets us deliver building blocks tailor-fit to clients’ needs, from isotopically labeled variants for bioanalytical tracing to ultra-pure material for regulatory filings.
Collaborating with academic groups—especially those focused on fluorinated phenols' roles in modern medicinal chemistry—keeps us honest and propels innovation. Our open-door policy for visiting scientists turns curiosity into better protocols, whether through better catalyst recycling or streamlined downstream clean-up. We lend samples as often as we sell industrial batches, always searching for feedback from those working on the edge of discovery.
For us, there’s no shortcut to understanding what real users need from high-value fine chemicals like P-Trifluoromethoxy Phenol. Enthusiasm counts for little without reliability. We have learned to distinguish between what technical bulletins claim and what hands-on chemists encounter at the bench. Every new campaign deepens our grasp; staring at a distillation column during the night shift or debugging a failed scale-up brings lessons that technical sheets simply can’t teach.
We listen to the users shaping the next generation of pharmaceuticals and engineered materials. They remind us to focus on minimizing contaminants, providing genuine batch-to-batch reproducibility, and offering the guidance to use these specialist molecules safely and effectively. Each shipment leaves our factory not just with the seal of approval, but with decades of professional vigilance and knowledge built in.
Operating as the primary manufacturer gives us a front-row seat to both advance and adversity. Whether managing a sudden uptick in orders or helping troubleshoot an unexpected bottleneck in a new synthesis, our priorities stay true: deliver P-Trifluoromethoxy Phenol with integrity, share what we learn, and help shape the safe, effective use of advanced fine chemicals across the industries that need them most.