|
HS Code |
812295 |
| Chemical Name | 5-Fluoro-2-Trifluoromethyl-Phenol |
| Cas Number | 700-90-5 |
| Molecular Formula | C7H4F4O |
| Molecular Weight | 180.10 |
| Appearance | White to off-white solid |
| Boiling Point | 162-164°C |
| Melting Point | 39-42°C |
| Density | 1.47 g/cm3 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC1=CC(=C(C=C1F)O)F |
| Inchi | InChI=1S/C7H4F4O/c8-5-1-2-6(7(9,10)11)4(12)3-5/h1-3,12H |
| Refractive Index | n20/D 1.452 |
| Storage Conditions | Store at room temperature, keep tightly closed |
| Synonyms | 2-(Trifluoromethyl)-5-fluorophenol |
| Pubchem Cid | 120341 |
As an accredited 5-Fluoro-2-Trifluoromethyl-Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 25 grams of 5-Fluoro-2-Trifluoromethyl-Phenol, sealed with a screw cap, labeled with hazard warnings. |
| Shipping | 5-Fluoro-2-Trifluoromethyl-Phenol is shipped in tightly sealed, chemical-resistant containers to prevent leaks and degradation. Packages are clearly labeled and comply with international transport regulations. The chemical is stored in a cool, dry environment, protected from heat and direct sunlight during transit, ensuring product integrity upon arrival. |
| Storage | 5-Fluoro-2-trifluoromethyl-phenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers and bases. Protect from moisture and light. Use appropriate chemical-resistant containers and store at room temperature, unless otherwise specified by the manufacturer’s safety guidelines. Always follow standard laboratory chemical storage protocols. |
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As a chemical manufacturer covering every step from raw material sourcing to final purification, we approach specialty intermediates with a focus on both detail and reliability. Our experience stretches across numerous aromatic fluorinated compounds. 5-Fluoro-2-Trifluoromethyl-Phenol, recognized by its model identifier and molecular signature, stands out within the phenolic derivatives group for reasons deeply tied to structure and process chemistry.
5-Fluoro-2-Trifluoromethyl-Phenol carries a unique combination of a fluoro substituent at position five and a trifluoromethyl group at position two on the aromatic ring. This arrangement changes both reactivity and stability, and influences practical outcomes later on during application and downstream modification. Aromatic phenols attract attention in synthetic chemistry because the hydroxyl group lends itself to a wide range of transformations. By introducing both a fluorine atom and a trifluoromethyl group, the molecule’s electronic environment shifts in a way that enables very targeted reactions in complex molecule construction.
Synthesis of this compound calls for strict control of each stage, especially during halogenation and hydroxy functionalization. In our plant, we use proprietary processes to guide substitution toward the desired regio-isomer, with thorough in-process analytics ensuring selectivity. Starting materials have to be traceable and consistently pure; otherwise, side reactions increase, yield drops, or impurities complicate downstream purification.
The phenolic product leaves our reactors as a crystalline solid, often off-white or faintly yellow, determined by tiny amounts of byproducts. Purity checks routinely run beyond common industrial thresholds. Practically, purity means fewer disruptions for our partners engaged in pharmaceutical research or agrochemical synthesis. Impurities—even marginal ones—add variables to sensitive reactions or affect catalyst performance.
Typical bottlenecks during scale-up involve not only reaction control but also the separation of closely related fluoro-aromatic isomers. Our QC group deploys advanced HPLC and NMR methods, never relying only on melting point or traditional thin-layer chromatography. This approach comes from direct feedback: customers in API (active pharmaceutical ingredient) discovery have told us about failed reactions traced back to trace impurities in earlier material.
Downstream users turn to 5-Fluoro-2-Trifluoromethyl-Phenol mainly for its versatility as a building block. In pharmaceuticals, the combination of fluorine and a trifluoromethyl group on an aromatic ring influences metabolic stability, bioavailability, and receptor binding. Medicinal chemists find that introducing this group helps them tweak lead compounds for better in vivo performance, crucial for candidates targeting central nervous system pathways or anti-infective screens.
Crop science groups utilize this molecule in herbicide and fungicide discovery. The electronic impact of the fluoro and trifluoromethyl groups can modulate biological activity and environmental persistence. When used for life science research, the specific substitution pattern opens up coupling possibilities that are not accessible with non-fluorinated phenols or simple fluorophenols.
Material scientists investigating new polymer and liquid crystal structures also request this intermediate for its ability to adjust thermal and dielectric properties. In this context, differences between mono-fluorinated and trifluoromethylated aromatics determine bulk material performance. Some customers have remarked that performance hinges on using the exact isomer, rather than any compound with similar functional groups—underscoring that not all fluoro-phenols are interchangeable.
Basic phenol lacks the electron-deficient nature seen in its fluorinated variants. Introducing a trifluoromethyl group at the ortho position, alongside a fluoro group, boosts the molecule’s overall hydrophobicity, making it less soluble in water but easier to process in certain organic solvents. This hydrophobicity affects extraction, crystallization, and even the taste and smell if used as an intermediate for flavor or fragrance compounds. In our operations, we have found that the product requires less aggressive drying compared to other phenols, due to rapid phase separation during workup.
In contrast to 4-fluoro-2-trifluoromethyl-phenol or 2,4,6-trifluorophenol, our product offers a very particular balance in nucleophilicity and steric effects at the para and ortho positions. Chemists have told us this impacts selective coupling chemistry, such as in Suzuki or Ullmann reactions. Because the -CF3 group sits adjacent to the hydroxyl, its electron-withdrawing nature lowers the phenol’s pKa, allowing for milder reaction conditions in O-alkylation or acylation. In our large-scale reactions, we have observed higher conversions under gentler alkaline conditions relative to other fluorophenols.
We have collaborated closely with research teams in both academic and industrial arenas. While the chemical looks like a small part of a bigger puzzle, feedback from project leaders reaffirms that the reproducibility of our batches makes a real-world difference in research timelines. A material that crystallizes cleanly and presents a narrow NMR profile means process chemists can move faster toward data generation.
Over years of production, adjustments in our purification lines—continuous extraction, flash chromatography, final crystallization—arose directly from customer feedback. One large pharma group found their catalyst life extended after switching to batches manufactured on our modified protocol, due to lower metal impurity content. These iterative improvements show up in more stable, predictable outcomes for every user, whether they run a milligram test batch or a 100-liter pilot run.
Reproducibility takes center stage for medicinal and agrochemical discovery. We see research cycles slow down or speed up based on the consistency of their starting materials. Once a Japanese contract research firm shared how their screening campaign aligned with our supply cycles to avoid months of revalidation. From our own experience, the performance gap between lots made with fully-integrated analytics versus spot-verified lots gives a practical reminder: even a small impurity in a “research grade” material can mislead a multi-million dollar campaign. To support the most demanding users, every batch ties back to a full analytical archive.
During scale-up, green chemistry constraints have become more pronounced. Users ask about residual solvents, byproduct profiles, and even lifecycle analytics for sustainability reporting. Our approach incorporates solvent recovery, reprocessing of mother liquors, and minimization of halogenated waste. Direct feedback from European buyers convinced us to modernize our distillation and incorporate in-line solvent recycling. By investing in these upgrades, we make sure our footprint matches buyers’ downstream compliance needs.
Our operations reflect a zero-compromise approach to safety. While some phenolic intermediates drift toward instability as molecular weight increases, 5-Fluoro-2-Trifluoromethyl-Phenol retains thermal robustness through purification and packaging. Early in our production ramp-up, we evaluated batch-to-batch thermal stability using DSC and TGA. These readings then guided storage and shipping protocols. Customer audits tell us that the clarity of our documentation—covering not just batch records but also impurity tracking—defuses issues before they appear.
Transparency with buyers, especially for pharmaceutical intermediates, establishes trust. We provide detailed profiles upon request, including elemental analyses and comprehensive chromatographic signatures. Not every company asks, but those preparing for regulatory filings in the US, Europe, or Japan often require it. Our lab teams remain available for follow-ups if any discrepancies show up during a partner's process or analytical checks.
Fluorinated intermediates attract scrutiny for their environmental persistence. In response, our process designers reworked solvent flows and waste byproduct management. Flushing steps now channel solvents into closed-loop recovery instead of single-use waste. Fluoride-rich wastes are neutralized and scrapped under local compliance protocols. In partnership with several downstream users, we began lifecycle reporting for bulk runs: not a regulatory requirement yet, but often a negotiation point in supply contracts.
Some material engineers aligned their procurement policies to restrict “non-essential” fluorinated chemicals. We consult with their teams to clarify downstream use and justify the selection where the physical or bioactive properties cannot be recreated using non-fluorinated alternatives. The chemical’s performance often anchors critical components in medical or agricultural innovation pipelines, so the collaborative approach enables innovation while respecting compliance objectives.
Chemicals containing both fluorine and phenolic groups sometimes display volatility or acidity that leads to packaging or handling concerns. In our storage areas, 5-Fluoro-2-Trifluoromethyl-Phenol remains nonhygroscopic with minimal odor or off-gassing. We ship in high-density containers, sealed under inert gas for bulk shipments to eliminate oxidative risk. Routine transit into North America, Europe, and Asia gives us firsthand experience navigating customs and compliance hurdles. Rapid turnarounds on documentation and familiarity with import requirements help buyers avoid holdups that delay project milestones.
Our logistics group manages supply chain resilience through direct links with producers of upstream raw materials. Each year, supply challenges emerge as geopolitical events or natural disruptions unsettle logistics, so over time, we established buffer stocks as a safeguard. Buyers benefit by locking in consistent access to specialty intermediates that few suppliers can replicate at scale.
Every year, we collect feedback from teams using our phenolic intermediates in new syntheses or pilot-scale testing. One customer in the United States, advancing an antipsychotic candidate, shared analytical results confirming that trace levels of a side isomer affected their yield after cross-coupling. We adapted our purification train, cutting the out-of-spec lots to near zero within four months of their alert. Another collaborator in European agrochemical R&D team documented an uptick in formulation stability upon switching to our material: the specific isomer conferred a shelf-life edge and reduced unwanted degradation, which in turn affected their registration data positively.
Several academic chemists highlighted the importance of clear spectral data and batch traceability. For research protocols destined for patent filings, batch-specific NMR, GC-MS, and even IR data make it easier to defend inventive step or confirm reproducibility. We listen and upgrade our batch record system continuously, making sure end-users receive this documentation with every delivery.
Emerging research explores derivatives synthesized from 5-Fluoro-2-Trifluoromethyl-Phenol as core fragments for kinase inhibitor scaffolds, perfluoroalkylated polymers, and photo-catalytic materials. In these fields, a small difference in the aromatic substitution pattern amplifies into major distinctions in downstream reactivity or function. Companies developing OLED materials or advanced diagnostics inquire about minor structural analogs; our plant can pivot production lines to accommodate short-run custom lots without sacrificing quality or purity.
Every custom project brings fresh challenges that reveal more about the chemical’s tolerances—how it behaves under high-pressure hydrogenation, its resistance to oxidant quenching under metal-catalyzed couplings, or stability during halogenation. Sharing this empirical knowledge back to our buyers sets a feedback loop for continuous improvement. As manufacturing engineers and chemists, we pay attention to the “nuts and bolts” at every step, drawing a direct connection from upstream production to the performance buyers see at the bench or in formulation tanks.
Access to specialty intermediates like this phenol hinges on more than just manufacturing output or inventory levels. Navigating shifting regulatory and trade environments calls for supplier transparency, robust documentation, and technical support that extends beyond spot purchasing. Research customers repeatedly tell us how documented reproducibility and fast, knowledgeable technical support reduce their risk during method validation, patent drafting, or early regulatory submissions.
As direct manufacturers, we recognize the growing complexity in expectations from new pharmaceutical and agrochemical development. A reliable supply of a single intermediate—especially one with non-standard substitution—determines whether a research project launches, grows, or stalls. We see ourselves not just as suppliers, but as direct partners in solving the chemistry that underpins tomorrow’s technology and health advances.
5-Fluoro-2-Trifluoromethyl-Phenol will remain a vital part of discovery chemistry. Every batch tells a story of evolving process knowledge and practical responsiveness. As chemists, we invest in the details because every improvement in purity, documentation, or supply continuity reflects lessons learned in actual manufacturing runs, not abstract theory. Downstream progress—lower process risk, improved product performance, speedier synthesis—follows from these choices. For those pushing the frontiers of pharmaceuticals, agrochemicals, or advanced polymer science, our experience stands behind every shipment.