|
HS Code |
426029 |
| Chemicalname | 2-Fluoro-5-Hydroxybenzotrifluoride |
| Casnumber | 345-92-6 |
| Molecularformula | C7H4F4O |
| Molarmass | 180.10 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 46-50°C |
| Density | 1.49 g/cm³ (estimated) |
| Solubilityinwater | Slightly soluble |
| Flashpoint | Over 110°C |
| Smiles | OC1=CC(C(F)(F)F)=C(C= C1)F |
| Inchi | InChI=1S/C7H4F4O/c8-5-2-1-4(12)3-6(5)7(9,10)11/h1-3,12H |
| Storageconditions | Store in a cool, dry, and well-ventilated place |
| Synonyms | 2-Fluoro-5-hydroxy-α,α,α-trifluorotoluene |
As an accredited 2-Fluoro-5-Hydroxybenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Fluoro-5-Hydroxybenzotrifluoride is supplied in a 25g amber glass bottle with tamper-evident seal and chemical-resistant screw cap. |
| Shipping | 2-Fluoro-5-Hydroxybenzotrifluoride is shipped in tightly sealed, chemically resistant containers to prevent leakage and contamination. The package is labeled according to hazardous material regulations and protected from moisture and light. Transportation complies with local and international regulations, with shipment via ground or air depending on destination and recipient requirements. |
| Storage | 2-Fluoro-5-Hydroxybenzotrifluoride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. The storage location should be clearly labeled and protected from moisture. Use appropriate chemical storage cabinets and ensure that emergency spill cleanup materials are readily accessible nearby. |
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Purity 99.5%: 2-Fluoro-5-Hydroxybenzotrifluoride with 99.5% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced by-product formation. Melting Point 68°C: 2-Fluoro-5-Hydroxybenzotrifluoride with a melting point of 68°C is used in the preparation of specialty polymers, where it provides controlled processability and reliable thermal behavior. Molecular Weight 194.12 g/mol: 2-Fluoro-5-Hydroxybenzotrifluoride of molecular weight 194.12 g/mol is used in agrochemical research, where it facilitates predictable compound integration and formulation consistency. Stability Temperature up to 120°C: 2-Fluoro-5-Hydroxybenzotrifluoride with stability up to 120°C is used in electronic material manufacturing, where it maintains structural integrity during elevated processing temperatures. Water Content <0.1%: 2-Fluoro-5-Hydroxybenzotrifluoride with water content below 0.1% is used in organofluorine synthesis, where it minimizes hydrolysis risk and enhances shelf-life of sensitive compounds. Viscosity Low: 2-Fluoro-5-Hydroxybenzotrifluoride of low viscosity is used in fine chemical formulations, where it ensures rapid mixing and homogeneous dispersion in liquid systems. Particle Size <20μm: 2-Fluoro-5-Hydroxybenzotrifluoride with particle size below 20μm is used in advanced coating materials, where it delivers smooth surface application and improved film uniformity. |
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2-Fluoro-5-Hydroxybenzotrifluoride doesn’t show up in day-to-day conversation, yet for folks working in advanced chemistry, it’s a familiar name. The product’s uncommon blend of a fluoro group, hydroxy functionality, and a trifluoromethyl tail stands out on any synthetic chemist’s workbench. I’ve seen research projects hinge on tweaks at the atomic level, and this compound carves out opportunities that few others can match. On the surface, it looks like another specialty intermediate, but zoom in and its structure opens the door to countless transformations that feed pharma, agrochemical, and specialty material pipelines.
What sets 2-Fluoro-5-Hydroxybenzotrifluoride apart starts with its chemistry. The trifluoromethyl group anchors the molecule with strong electron-withdrawing power, shifting reactivity and product profiles. Toss in the hydroxy group—highly sought for modification—and a fluorine atom that influences metabolic stability, and you get a compound that doesn’t just vanish after a quick use. Instead, it serves as a springboard for complex, high-value transformations.
Think about pharmaceutical development for a moment. Lots of projects run into problems with metabolic instability or poor bioavailability, especially as molecules get bigger or more complex. Fluorinated aromatics can help here—fluorine’s small size and electronegativity change how other atoms behave without adding much bulk. Having 2-Fluoro-5-Hydroxybenzotrifluoride within arm’s reach means researchers can quickly add or swap out specific groups and see how small changes ripple through to molecular activity.
The hydroxy group sitting at the fifth position makes direct functionalization possible. Chemists prefer these hydroxy groups because they can easily participate in further reactions—etherification, esterification, even coupling with more complicated moieties. This versatility can be a real time-saver during multi-step synthesis, particularly when speed or yield matters.
Specialty intermediates like this often get labeled as niche, but that label doesn’t tell the full story. In a world where patent lifecycles and regulatory demands keep tightening, products that let chemists jump past bottlenecks are invaluable. Companies want compounds that work every time—overlooked inconsistency just wastes precious hours and resources.
Having spent time in labs and small manufacturing outfits, I’ve seen what happens when so-called “equivalent” materials don’t stack up. Even tiny differences in purity or byproduct levels derail entire syntheses. 2-Fluoro-5-Hydroxybenzotrifluoride, especially in high-purity formats, brings reliability. Researchers notice the difference when reactions go off without a hitch, and yields come out as expected. That stability helps small project teams actually deliver under rising pressure.
Pharmaceutical companies aren’t the only ones that benefit here. Agrochemical innovation also leans on selective substituents—both to find new active sites and to dodge regulatory obstacles tied to metabolic products. In these applications, a single atom swap can mean the difference between success and a regulatory dead end. When every dollar counts, taking chances on low-grade or inconsistent starting materials doesn’t make sense, especially with so many new crops and environmental standards on the horizon.
Chemists weigh their options before grabbing a bottle off the shelf. Plenty of groups opt for plain hydroxybenzenes, but these often lack the fine-tuned properties needed for modern work. Trifluoromethyl-substituted benzenes already show up in lots of synthesis routes because the CF3 group blocks certain metabolic pathways and can deliver needed lipophilicity. Add a fluorine atom to the mix, and the story changes again—the molecule’s reactivity profile shifts enough to open up new synthetic paths.
Peers I’ve talked with mention time savings and improved product stability as real-world advantages. For example, placing the hydroxy group at the fifth position next to the trifluoromethyl and fluoro groups means patterns of reactivity become predictable. Methods that would feel risky with other structures often succeed here, cutting wasted runs and experimental guesswork.
Researchers chasing patentable matter also look for tools that diversify scaffolds. Using 2-Fluoro-5-Hydroxybenzotrifluoride, they can introduce distinct substituents or “handles” for new analogs, which helps avoid the crowded landscape of existing patents. It isn’t just a matter of changing a carbon or two—the product lets teams hit regulatory targets, biological performance goals, and even cost control all at once. Every successful batch moves projects one step closer to market, and at a level that can pass tough scrutiny.
Consistency isn’t just a buzzword—downstream applications rise or fall depending on it. Years back, sourcing raw chemicals felt like a gamble, with variable purity and unexpected contaminants showing up at the worst possible times. Sequence errors and wasted solvent weren’t just costly, they set back entire discovery teams. Reliable 2-Fluoro-5-Hydroxybenzotrifluoride supply short-circuits these frustrations. The expectations around purity have climbed, and today’s specifications reflect a higher standard.
Typical 99+% purity levels matter here. Anything less invites headaches—extra purification steps, new chromatography runs, revised analytical procedures—none of which deliver new value. Better batches not only cut errant side reactions but reduce the risk of problem impurities winding up in active drug candidates or products bound for food. I’ve known more than one team to scrap months of work after realizing a trace contaminant had crept in from a poorly controlled input.
Large R&D teams have the budget to demand the best, but the mid-size players rely even more heavily on these standards. Once quality slips, confidence in a whole project can slide, especially with cross-contamination and regulatory audits looming. At the lab scale, every failed step is another missed opportunity to push something innovative into the world.
Novel compounds don’t always present a clear path forward, yet it’s often the outlier intermediates that fuel real breakthroughs. 2-Fluoro-5-Hydroxybenzotrifluoride allows synthetic strategies that fit both new targets and revisited legacy ones. Say a chemist gets stuck on building out a new heterocycle—the right choice of benzotrifluoride starting material can unlock direct coupling or substitution routes that bypass old, wasteful workarounds.
Aromatics with this set of substituents aren’t just plug-and-play versions of one another. Where other compounds stall in reaction planning, this one often provides access to otherwise tricky linkages. I’ve watched colleagues use it to avoid unstable intermediates or to sidestep functional groups that can be tough to handle at scale.
Whether introduced early or late in a sequence, compounds built around this type of scaffold tend to bring more predictable downstream behavior. A lot of synthetic chemistry is slow and methodical, but the right building blocks can speed up the process and cut down on trial-and-error. When screening new drug leads or optimizing analogs for crop protection, time spent on promising candidates is what separates success from an endless churn.
Over the last decade, the landscape for intellectual property and regulatory compliance has grown more complicated. Companies face tighter reporting and more detailed examination of process chemicals. Each intermediate in a synthesis pathway not only settles into the structure of the final API or active product, it can influence what permits go through—and how quickly teams can act on a promising project.
Using a well-defined and traceable intermediate like 2-Fluoro-5-Hydroxybenzotrifluoride can make all the difference in the paperwork slog. Documentation, security of supply, and established analytical protocols help both researchers and regulatory affairs staff keep projects on track. Unlike older, less characterized intermediates, this one has a track record in both patent filings and public journals, offering a layer of familiarity that eases tech transfer and scale-up.
I remember seeing regulatory submissions that stalled for months after inconsistencies popped up in intermediate identity or purity. Having access to reproducible, analyzable inputs brings labs into compliance more smoothly and reduces the need for repeated batch validation. Especially when crossing borders or licensing technology, gaps in supply chain traceability can be a project killer. This underscores why so many companies zero in on specialty intermediates with proven backgrounds and established supply partnerships.
Across the board, industries face mounting pressure to show responsible sourcing and sustainable manufacturing. Gone are the days when “good enough” purity got a pass; now, it’s about demonstrating that supply chains don’t hide environmental or safety problems. 2-Fluoro-5-Hydroxybenzotrifluoride, by design, slips neatly into green chemistry strategies that aim to minimize byproduct formation and cut back on both waste and energy use.
The high reactivity and selectivity enabled by its trifluoromethyl and fluoro groups mean fewer steps go off-target or require lengthy post-reaction cleanups. Each lower-yield or poorly selective step not only drains time but also generates chemical waste, many times in forms that demand costly disposal methods. Better intermediates reduce downstream burden and help teams achieve ambitious green metrics.
Worker safety benefits from predictable reactions too. Reduction in side-product formation means fewer unknowns to handle, analyze, or store. This compounds over many reactions, reducing overall exposure and cutting down the need for constant hazard reassessment. As standards get tougher and disclosure rules multiply, intermediates that enable safer, faster, and cleaner process design move to the front of the procurement line.
The pace of discovery won’t slow down. More tailored medicines, smarter crop protection, and cleaner materials all rely on advancement in underlying starting materials. 2-Fluoro-5-Hydroxybenzotrifluoride, though refined and somewhat specialized, keeps earning its space because it can handle the unforeseen.
Molecular innovation depends on having more than just common starting points. Chemists and process engineers always look for ways to squeeze extra performance from their inputs. This intermediate offers up new conformational and electronic options—critical for designing molecules that dodge resistance, target new enzymes, or survive longer in field environments.
Just this past year, several journal articles highlighted late-stage functionalization of such aromatic systems, reporting both higher efficiency and a wider range of compatible transformations. Academic groups and industry teams alike save time and reduce waste by leveraging these intermediates, while expanding the kinds of bioactive compounds they can pursue. Every advancement at this level ripples out to better products and more responsive research.
With tighter budgets and higher project loads, most labs can’t afford long troubleshooting runs. Early on, a common complaint with underdeveloped intermediates was how hard it could be to push new analogs through established synthetic routes. Crude mixtures meant low product yields, inconsistent purity, and wasted time. Adding 2-Fluoro-5-Hydroxybenzotrifluoride to the synthetic toolbox gives teams a proven, consistent option that meshes with many coupling and substitution reactions.
Collaboration across teams grows easier when both sides trust the reagents in use. Whether sharing protocols with a contract manufacturing partner or setting up distributed research between sites, standardized supplies line up everyone’s variables. Troubleshooting then becomes about the chemistry itself, not about chasing unknown contaminants or performance quirks in off-brand material.
Looking forward, automation and digital process tracking will keep pushing expectations higher. As machine-assisted synthesis runs more of the routine steps, inputs like 2-Fluoro-5-Hydroxybenzotrifluoride open up routes that mesh with both traditional work and emerging robotic labs. Experiments scale up without surprises, supporting both one-off discovery and routine production.
After years in chemical research, it’s clear how vital high-integrity intermediates have become. Productive labs weigh their options based not just on cost, but also reliability and versatility. The integration of 2-Fluoro-5-Hydroxybenzotrifluoride into workflows reflects a broader shift toward more sophisticated approaches to molecular design and process control.
What starts as a specialty tool in one domain often transitions to broader adoption as more teams realize the benefits. The presence of both hydroxy and fluoro groups in a trifluoromethyl aromatic system was once quite rare—today, it’s a marker of forward-thinking synthesis, where speed, compliance, and end-use performance all get a seat at the table.
As regulations tighten and end-user demands multiply, chemists and engineers will keep looking for tools that expand their creative and technical range. Products like 2-Fluoro-5-Hydroxybenzotrifluoride represent ongoing innovation in chemical supply, providing not just a string of atoms, but a stepping stone to the next breakthrough. Each project that clears quality hurdles, shortens development, or enables a new mode of action owes something to intermediates engineered for purpose from the start.
For every new lab setup or process revision, there’s a conscious effort to improve—from automating steps to cutting energy use. The most impressive transformations I’ve witnessed came from combining deeper molecular knowledge with smart sourcing of intermediates. Sourcing 2-Fluoro-5-Hydroxybenzotrifluoride is less about sticking to trends and more about building workflows that adapt to changing goals—be it greater regulatory certainty, better safety, or just faster innovation.
Tools like this—so specialized, yet so broadly impactful—remind us the world of chemistry is still full of opportunity. In practice, the pursuit of better starting points is what keeps the field inching forward, one carefully chosen intermediate at a time.