|
HS Code |
628807 |
| Chemicalname | 2-Fluoro-5-(Trifluoromethyl)Phenol |
| Casnumber | 771-02-0 |
| Molecularformula | C7H4F4O |
| Molecularweight | 180.10 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 135-137°C at 760 mmHg |
| Meltingpoint | -15°C |
| Density | 1.445 g/cm3 at 25°C |
| Purity | ≥98% |
| Refractiveindex | 1.4640 at 20°C |
| Solubility | Slightly soluble in water |
| Smiles | C1=C(C=C(C=C1F)O)C(F)(F)F |
| Inchi | InChI=1S/C7H4F4O/c8-5-2-1-4(7(9,10)11)3-6(5)12/h1-3,12H |
| Synonyms | 5-(Trifluoromethyl)-2-fluorophenol |
| Flashpoint | 59°C |
As an accredited 2-Fluoro-5-(Trifluoromethyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Fluoro-5-(Trifluoromethyl)Phenol, sealed with a screw cap and tamper-evident label. |
| Shipping | 2-Fluoro-5-(Trifluoromethyl)Phenol is shipped in tightly sealed, chemically resistant containers to prevent leaks and exposure. The package is labeled according to hazardous material regulations and includes safety documentation. Shipping is conducted via approved carriers, ensuring compliance with local, national, and international chemical transport guidelines for safe and secure delivery. |
| Storage | Store **2-Fluoro-5-(trifluoromethyl)phenol** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and bases. Ensure the storage area is equipped with appropriate spill containment and clearly labeled. Avoid exposure to moisture and sources of ignition. Recommended storage temperature is 2–8°C (refrigerated). |
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Every batch of 2-Fluoro-5-(Trifluoromethyl)Phenol we produce runs through our own reactors. This isn’t just a matter of pride; it’s the plain reality that start-to-finish control in a chemical facility creates tangible reliability from raw material to packaged phenol. The molecular structure—one fluorine at the ortho position, a trifluoromethyl at the meta—isn’t an obscure detail, it shapes the way this compound reacts in synthesis and defines much of its industrial value. Our chemists work with this molecule in its pure crystalline or liquid form—depending on specific storage and shipping requirements—and we monitor every reaction stage for impurities.
2-Fluoro-5-(Trifluoromethyl)Phenol, with CAS 1623-19-4, strikes a balance between activity and stability that makes it a prized component for pharmaceutical growers and agrochemical researchers. Its melting point, boiling range, and moisture content have a direct impact on processing yields and reproducibility. We’ve seen requests from early synthetic work through to manufacturing scale—some value the electron-withdrawing effect of trifluoromethyl for growing more selective target molecules, others seek reactivity with the phenolic hydroxyl group.
Plenty of phenolic compounds float in the global market, but 2-Fluoro-5-(Trifluoromethyl)Phenol stands out for anyone focusing on downstream reactivity. The addition of both fluorine and a trifluoromethyl group changes not just the boiling point but the way the molecule participates in coupling reactions. In aromatic halogenations and cross-coupling, this structure resists many of the side-reactions that slow down scale-up. Our facility doesn’t just follow a recipe; our operators adjust temperatures and solvent ratios based on feedback from previous batches, because to meet a pharmaceutical spec, one kind of ‘good enough’ won’t do.
Customers routinely talk about the difference this compound makes in their synthesis flow. We hear from medicinal chemists developing kinase inhibitors and crop science teams engineering molecules for advanced herbicides. Our own R&D has explored it in nucleophilic aromatic substitution, where the leaving group’s influence can make or break the yield. We analyze for trace metals, hydrolytic stability, and overall purity using in-house equipment. Since this isn’t always supplied in drum quantities, small R&D lots matter just as much, and we make sure the product coming out of the vessel matches the real needs of the bench chemist.
Lab reports and QA sheets can outline melting points, assay percentages, and trace impurity levels, but in a practical sense, what matters most is the reproducibility of the product. We usually crystallize the material for most applications, aiming for purity levels above 98 percent—GC and NMR provide confirmation, and our experience tells us what counts as a genuine deviation and what’s simple analytical drift.
Handling fluorinated aromatic compounds isn’t for the uninitiated. The presence of trifluoromethyl drives volatility higher than basic phenols, and that needs close management during isolation and drying. Over the years we’ve shifted from basic vacuum ovens to more robust isolation protocols, so loss is minimized and contamination is checked at each transfer point. This gets more important in agrochemical R&D, where every fraction gram can affect the final biological screen of an active candidate.
The reasons customers turn to us aren’t theoretical. In drug synthesis, 2-Fluoro-5-(Trifluoromethyl)Phenol serves either as a direct starting material or as a modifier in more complex routes. Our team has worked with pharma partners who need a reactive fluorinated nucleus for exploring new kinase inhibitors. In one project, our phenol’s precise substitution pattern let an API team install a specific ether bond without unwanted rearrangements. Agrochemical development follows a similar logic—this compound’s electron configuration introduces resistance to metabolic breakdown in field trials, letting a single synthetic modification translate into weeks of additional weed control without extra post-harvest residues.
We supply both in-lab quantities and multi-kilogram lots. Some of our customers run high-throughput screening, needing consistent fifty-gram lots. Others bring in a hundred kilos at a time to shift projects from bench to pilot scale. Our production lines adjust to these shifts, with solvent and purification routines tweaked to guarantee material is on spec regardless of order size. Regular feedback from users shapes our SOPs—one example: we introduced a two-stage washing process for the crystalline product after users reported trace entrapment between mother liquor and crystal faces.
Too many buyers underestimate the role of supply chain transparency in specialty organics. Every bag or drum from our facility can be traced to the reactor it was made in, the chemists on shift, and the precise conditions logged in the plant database. This traceability matters—especially since many of our customers face regulatory filings where product lineage gets scrutinized as much as composition. We keep retained samples from each lot, stored at reference conditions, and we reference these for stability checks and any quality disputes.
Safety isn’t just regulatory compliance. Our operators face the reality of handling aggressive fluorinated aromatics, so our plant uses closed systems, full containment during charge, and constant air monitoring around vent lines. Years ago we learned from an unexpected pressure spike; since then, our batch records feature interlocks based on both pressure and temperature, not just fill level. That experience shapes every run and every final pack.
Standard product spec sheets never tell the whole story. We invest in flexible packaging—amber glass bottles for high-purity small scale work, HDPE drums for large-scale development lots, and inert atmosphere packaging for sensitive applications. It’s never only about purity numbers. Consistent handling properties, safe storage life, and real-world performance in downstream syntheses matter.
Our production engineers have been asked to fine-tune batch crystallization rates to meet very narrow particle size distribution requests. Though it might seem trivial on paper, in a flow chemistry process or pilot-scale continuous application, the consistency of suspended material can dictate reactor clogging or smooth progress. We tune grind, particle flow, and additional sieving steps in direct response to practical reports from our partners.
The landscape for substituted phenols is crowded, from 4-fluoro variants to methylated phenols, yet our years on the line show clear reasons for selecting the 2-fluoro-5-(trifluoromethyl) isomer. The electron-withdrawing group at the para position to the hydroxyl adds unique properties—sharper acidity, altered nucleophilicity, and increased resistance to oxidation. These details aren’t academic; they reshape the kinetic and thermodynamic profiles in multi-step syntheses. We’ve seen process yields in nucleophilic aromatic substitution and Pd-catalyzed cross-couplings improve after switching to our product. Several pharmaceutical scale-ups reported less tar and improved crystallinity just by shifting to our phenol variant.
Many products on the market feature trace residual halides or solvents. Years of in-house process improvements mean our output stays consistent batch-to-batch, with impurity content below detection by LCMS and GC-MS at standard low ppm levels. We enforce both ICH guidelines and in-house specs born from actual customer syntheses—not just arbitrary spec sheet numbers.
Some researchers once believed they could substitute an unfluorinated or mono-fluoro analog and see similar downstream yields. Direct experiments, including side-by-side scale-up at our customer’s pilot plants, have shown otherwise. The specific reactivity and selectivity of the 2-fluoro-5-(trifluoromethyl)phenol molecule save days of downstream purification and increase the final active fraction in many medicinal chemistry assays. Every time we deliver a freshly produced lot, we follow up to track if the material delivers observed yield or conversion improvements against their prior phenolic intermediates. That closing of the manufacturing and end-use feedback cycle keeps our quality high.
Research chemists know the frustration of working with commercial samples that drift batch to batch. Over the last decade, we have standardized our raw material supply, reaction conditions, and purification train, specifically for the needs of customers scaling up programs from ten grams to several hundred. These aren’t high-volume commodity runs. The care given by our operators, along with a real understanding of the work happening in our customers’ labs—makes the difference.
It’s become routine for our technical staff to field direct consultation requests. Chemists working on heteroaryl synthesis often face bottlenecks in stepwise deprotection or functionalization. Our on-site chemists have deep practical knowledge of 2-Fluoro-5-(Trifluoromethyl)Phenol’s lability under various conditions: acidic, basic, and oxidative. Direct answers, not theoretical ones, save time when a downstream process throws unexpected results. When a client recently ran into phase separation issues during scale-up, our technical team checked for undetected water by Karl Fischer titration, providing insight on necessary process tweaks.
Making fluorinated organics comes with environmental responsibility. Our plant minimizes volatile emissions through closed-loop scrubbers, and we reclaim solvents whenever possible. Spent mother liquors are recycled, and aqueous waste passes through multiple stages before disposal. Decades spent in the specialty fine chemical business taught us that every percentage point of yield and gram of waste influence the real cost of each kilogram we deliver.
Worker exposure to fine particulates and volatile organic compounds gets managed by a layered approach. Ventilation rates and air quality checks aren’t just scribbled in a log; they tie directly back to bonuses and performance metrics for our operators. This builds real attention to detail because those working closest to the materials know where minor process tweaks can remove the greatest risk.
Some of the best process improvements come from end users. One medicinal chemistry group flagged an issue with trace ionic contamination interfering with a late-stage metal-catalyzed coupling. We trialed a revised wash route and reduced their column fouling, cutting several purification steps. Pilot customers aiming for green chemistry benchmarks pressed us to cut residual solvents below target limits. In one case, changes to drying atmosphere and additional evacuation steps dropped DCM content by 90 percent, facilitating their regulatory pathway.
Quality audits and repeat orders speak louder than brochures. If an API developer or crop science team tells us a subtle lot-to-lot difference changed their yield by two percent, that’s real-world evidence more meaningful than just certificate numbers. Our production staff, often with more than a decade on the plant floor, know how every line on the batch sheet has a direct impact on each synthesized molecule’s journey from raw material to final use.
2-Fluoro-5-(Trifluoromethyl)Phenol isn’t a theoretical entry in a catalog; our team’s years of accumulated hands-on know-how drive every lot out the door. Whether the end user cares about purity in an exploratory NCE, resilience during a scale-up run, or subtle handling in an industrial pilot, our chemists and engineers measure their own standards by the performance of the compounds we produce. Starting with a simple feedstock, through solid reaction reliability, disciplined isolation, and honest response to every customer query, we build both product and trusted relationships batch after batch.
Every order of this compound reflects direct engagement with the actual demands of chemists pushing boundaries in synthesis. Behind the bottle or drum, you’ll find a team that relies on its own laboratory experience and plant discipline—so every specification, every data point, and every packed container carries the weight of our ongoing commitment to performance and transparency. To us, 2-Fluoro-5-(Trifluoromethyl)Phenol is not only a chemical—it’s a reflection of the standards we’ve set, sharpened by the results our customers achieve.