|
HS Code |
942281 |
| Chemicalname | Phenol, 2,5-Bis(Trifluoromethyl)- |
| Casnumber | 1635-61-6 |
| Molecularformula | C8H4F6O |
| Molecularweight | 230.11 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 58-60 °C |
| Boilingpoint | 176-178 °C at 19 mmHg |
| Density | 1.55 g/cm³ |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Refractiveindex | 1.440 (at 20 °C) |
| Smiles | CC1=CC(=C(C=C1O)C(F)(F)F)C(F)(F)F |
| Inchi | InChI=1S/C8H4F6O/c9-7(10,11)4-1-6(14)5(2-8(12,13)3-4)15/h1-3,14H |
| Pubchemcid | 148956 |
| Synonyms | 2,5-Bis(trifluoromethyl)phenol |
| Flashpoint | 81 °C |
As an accredited Phenol, 2,5-Bis(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a secure screw cap, labeled “Phenol, 2,5-Bis(Trifluoromethyl)-,” and hazard information. |
| Shipping | Phenol, 2,5-Bis(Trifluoromethyl)- should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It is typically transported as a hazardous material according to relevant regulations (e.g., DOT, IATA, IMDG). Proper labeling, documentation, and use of secondary containment are required to ensure safe handling and prevent leaks or exposure during transit. |
| Storage | Phenol, 2,5-Bis(Trifluoromethyl)- should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Avoid exposure to direct sunlight and moisture. Use appropriate materials such as glass or compatible plastic for containers. Clearly label storage areas and containers to ensure safe handling and identification. |
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Working directly with chemicals every day, you remember which compounds truly set themselves apart among a dizzying array of similar names and molecules that land on your bench. Phenol, 2,5-Bis(Trifluoromethyl)- is one of those. Among chemists and in production facilities, it’s often called 2,5-bis(trifluoromethyl)phenol, model CAS 2403-89-6. Watching its crisp, crystalline grains flow in a reaction or seeing its transparent white purity after recrystallization, you understand why so many teams keep coming back to this compound. For those looking closely at the fluorinated organics scene, having this product in the lineup means access to a building block that consistently delivers in applications where reliability, reactivity, and exacting purity can't be gambled.
There’s an ongoing need for phenolic intermediates in the pharmaceutical, agrochemical, and specialty materials markets. We’re not dealing with ordinary phenols here. Incorporating two trifluoromethyl groups onto a phenol skeleton delivers a distinctive set of chemical properties—high electron-withdrawing character, substantial increases in chemical strength, and a remarkable boost in metabolic stability when used in active compounds. From the manufacturer’s viewpoint, the choice of substituents makes a night-and-day difference in real-world trials. Products with lesser electron-withdrawing groups can’t compete on the same reactivity, and simple phenol doesn’t come close in terms of hydrophobicity or thermal stability.
Firms making pharmaceuticals or designing crop protection agents invest in phenols outfitted with trifluoromethyl groups because these functionalities transform how molecules behave in a human or environmental system. Steric demand and strong electron-withdrawing effects combine to reduce non-specific degradation. That’s particularly valuable in drug discovery, where one extra half-life or one less metabolic byproduct can make or break a candidate’s progress. As the actual team working up batch after batch, we have watched researchers approach us looking for clean, predictable sources of this molecule. Commercial-scale production consistently emphasizes chemical reliability; repeated NMRs and chromatography results back that up before shipments leave the plant. Industry giants and universities alike don’t gamble on brokers piecing together their supply from unpredictable sources when their reputations are on the line.
Stepping into the lab or plant and seeing the process through—synthesizing, purifying, and testing each lot—gives you an appreciation for what a high standard means for those relying on these chemicals downstream. For 2,5-bis(trifluoromethyl)phenol, keeping trace metal content and residual halide levels extraordinarily low isn't just a check-box for certificates of analysis. Impurities can derail sensitive coupling reactions or spark off unwanted polymerization at later stages. We control synthetic parameters closely and run extended chromatographic purifications to yield product that matches strictest expectations batch-to-batch.
Years of hands-on work show that customer demand doesn’t end at 97% purity. Medicinal chemists, process engineers, and formulation teams all drive requests for higher, analytic-grade standards—frequently above 99%-99.5%. That magnitude of difference, invisible to casual eyes, registers with our process engineers as longer shelf-life, more reliable assay results, and smother downstream derivatization. Packaging matters, too; we use high-barrier materials, shield against atmospheric moisture, and minimize particle attrition during transport to help customers avoid contamination right up to the moment the drum opens.
Those new to trifluoromethyl-substituted phenols often ask what really distinguishes 2,5-bis(trifluoromethyl)phenol from its mono-substituted siblings—or even unsubstituted phenol. The answer, proven repeatedly in bench and pilot-scale settings, boils down to the reinforced electronegativity and unique spatial arrangement the two CF3 groups introduce. Aromatic substitution patterns affect both the reactivity and the physical properties. This particular molecule slots into synthetic sequences that call for increased resistance to oxidation and deprotonation, benefiting from the additive effects of two electron-withdrawing arms. Attempts to mimic these effects with just one trifluoromethyl, or with variations at different ring positions, simply fall short for demanding targets.
From a manufacturer’s perspective, the difference isn’t theoretical. Synthesis protocols sometimes need sharp adjustment—temperature gradients must be monitored carefully, catalysts tweaked, and fine-tuned quenching stages performed to obtain proper yields without introducing isomeric contamination or heavier byproducts. Experience shows that attempts to ‘substitute down’ with lower-cost, single-substituted analogs often fail when exposed to harsh downstream chemistry or under industrial sterilization. Our technical staff has fielded panicked inquiries from customers whose previous sources delivered substandard variants. That often results in days or weeks lost repeating syntheses and costly downtime.
Talking to end users and industry partners gives clear confirmation—phenol, 2,5-bis(trifluoromethyl)- holds a niche born out of necessity, not just hypothetical research. In agricultural chemistry, integration of the two CF3 groups on an aromatic core blocks off sites susceptible to microbial degradation, making the active ingredient persist in field conditions long enough for assured pest or weed control. In medicinal chemistry, substituting this phenol backbone into lead structures helps achieve immune evasion or metabolic stability, which turns into longer-acting, less frequent dosing for patients.
Materials scientists, too, reach for this product when designing high-performance polymers that withstand elevated temperatures or aggressive solvents. The double trifluoromethyl configuration proves particularly tough against hydrolysis, finding its place as a precursor or intermediate for specialty resins, high-durability coatings, or films requiring finely tuned dielectric properties. It’s hard to find other phenolic platforms that stand up as well under long-term exposure to heat or strong acids.
Production plants and labs see their own side of the logistical story. Phenol, 2,5-bis(trifluoromethyl)-, because of its twin fluorinated groups, demands careful process management from the first charges through final pack-out. Fluorinated aromatic systems can degrade ordinary seals and process hardware, especially when scaling up outside the pilot reactor. We’ve adapted our equipment—using specific elastomers and lined vessels—to guard against losses. During the distillation and crystallization stages, patience and tight thermal control keep volatile losses minimal and product integrity intact.
Storage and transport carry their own concerns. High-purity phenolic intermediates do not like exposure to environmental moisture or light for extended periods; yellowing, clumping, or surface oxidation can result. Our warehouse team tracks inventory closely and rotates any product that approaches beyond six months in storage—no one wants to take risks with degraded feedstocks, particularly at large scale. By keeping material away from UV and oxygen triggers and sealing every drum under inert gas, we make sure what arrives on the customer’s dock mirrors what left our line.
Many companies talk about providing chemicals “off-the-shelf.” From our manufacturing vantage point, the reality is more nuanced. Customers frequently request tailored particle sizes for suspension formulations, specific crystallinity levels for flowability in automated reactors, or adjustments in moisture content. One pharma client, for example, struggled with clumping in their feeder system. We reviewed their process details and switched from a finer-grind to a slightly coarser cut, which eliminated feed blockages at scale.
Traceability backs up every shipment. We track each drum to the exact batch, tying together the series of raw material, reaction, isolation, and test data. This isn’t just a matter of regulatory compliance—although that certainly matters in an age of global supply chain scrutiny. It means users can trust the full history of what they’re working with, down to the lot and operator. This level of oversight now plays into audits from both pharma and agrochemical players, who rightly want to manage their own quality as tightly as possible.
Companies relying on key intermediates face fewer surprises when they work directly with the manufacturer. Years of practice show how direct dialogue—with no extra steps between plant and end user—prevents misunderstandings about product form, package types, or purity guarantees. We receive immediate feedback from users and can swiftly tweak a parameter or offer technical guidance if a problem surfaces. Communication goes in both directions: features that help one customer often translate into valuable upgrades for many others.
Often, resellers focus on a price list and move on, with little understanding of the practical differences that one synthetic route or purification tweak can mean. We’ve seen customers burned by inconsistent materials and slow, roundabout troubleshooting through layers of distribution. Working as a true partner means offering chemistry knowledge as much as shipping drums—whether it’s helping scale a process safely, troubleshooting an intractable side-reaction, or sending a sample for early-stage validation.
The innovations driving modern medicine and agricultural science draw from a handful of molecules that set the stage for more advanced chemistry. 2,5-bis(trifluoromethyl)phenol’s popularity among leading labs and companies isn’t by accident. Each new therapy or crop protection product relies on raw materials that meet rigorous performance standards time after time. We talk with formulators and synthetic chemists working on the next-generation of antifungal agents, kinase inhibitors, or herbicide scaffolds—and this compound shows up in molecular libraries again and again. They need to know every gram they buy acts consistently, holds up to exacting standards, and matches the proof-of-concept established at discovery.
Startup materials developers also benefit. One team turned to phenol, 2,5-bis(trifluoromethyl)- as a key monomer precursor in producing a fluorinated polyarylether for fuel cell membranes. The resulting polymer offered higher operating temperatures and lower gas permeability than conventional backbones. Scale-up only worked because they could count on the reproducibility of the upstream phenol.
Manufacturers face evolving demands around sustainability, traceability, and supply assurance. Newer generations of chemists and end users ask sharper questions: What is the environmental profile of this process? Can you provide assurance on responsible sourcing? We respond by optimizing reaction conditions for atom economy, substituting greener solvents, and reducing waste. Our technical staff pushes to recover solvents, recycle packing, and invest in energy-efficient plant upgrades. Several years ago, we re-worked purification protocols to eliminate a halogenated solvent, saving thousands of liters of hazardous waste annually. The market expects this level of stewardship now, and rightly so.
Supply assurance means operating redundant production trains for critical materials and holding strategic inventory for our most consistent users. Upstream shortages—whether from geopolitical tension, shipping bottlenecks, or raw material price spikes—don’t hit customers as hard when the manufacturer manages capacity closely. Our team keeps open channels with both local and international suppliers, qualifying new material sources and stress-testing production workflows to prevent downtime.
Reality in chemical plants includes plenty of hard work ensuring worker safety and environmental compliance. Phenolic compounds, even highly substituted ones like 2,5-bis(trifluoromethyl)phenol, command respect in handling. Our plant operates with robust engineering controls: fume extraction, gloves and goggles, and closed transfer systems at scale. Waste streams go through trained staff and careful neutralization, not just straightforward disposal.
Product stewardship teams keep on top of evolving reg-ulatory frameworks. Whether a customer operates in North America, Europe, or Asia-Pacific, questions on allowable trace levels and import certifications don’t go unanswered. We involve our compliance officers early—for example, helping one multinational file a new dossier for a plant protection product incorporating this phenol as a key intermediate. Documentation—SDS, analytical reports, and process detail—always aligns with real manufacturing realities, not just boilerplate regulatory language.
Researchers continue to push past limits: higher solubility, narrower particle size control, or specialized derivatives of the original molecule. We hear from labs developing custom analogs—adding methoxy, carboxyl, or nitro groups along with the base CF3 units—seeking even sharper property tuning for next-generation candidates. Because our manufacturing staff designs and adapts processes directly, it’s possible to develop custom modifications rooted in hands-on understanding, not just theoretical feasibility. This ongoing feedback loop tightens connections between plant and bench scientist, raising industry standards across the board.
In summary, Phenol, 2,5-bis(trifluoromethyl)- gives scientists, engineers, and innovators a reliable platform to build on. It’s not a commodity; it’s a trusted backbone with a proven track record of supporting progress across multiple industries. By focusing on hands-on manufacturing, practical purity, responsive support, and a commitment to sustainable operations, those working inside the chemical plant help move science forward, one precise batch at a time.