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HS Code |
587828 |
| Productname | 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone |
| Casnumber | 1166229-10-6 |
| Molecularformula | C10H6F4O |
| Molecularweight | 218.15 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 128-130°C at 10 mmHg |
| Density | 1.325 g/cm³ (approximate) |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol) |
| Flashpoint | >110°C |
| Refractiveindex | 1.439 (approximate) |
As an accredited 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25g of 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone, securely sealed in an amber glass bottle with tamper-evident cap and hazard labeling. |
| Shipping | **Shipping Description for 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone:** This chemical is securely packaged in sealed containers, compliant with chemical transport regulations. It is shipped via certified carriers, ensuring protection from moisture, light, and extreme temperatures. Proper labeling and documentation are included for safe and traceable transport, in accordance with relevant safety, environmental, and customs guidelines. |
| Storage | Store **2'-Fluoro-4'-(Trifluoromethyl)propiophenone** in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of heat or ignition. Protect from light and moisture. Store separately from incompatible substances such as strong oxidizers and acids. Ensure that appropriate safety and spill containment measures are in place in the storage area. |
Applications of 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone in Industrial ManufacturingAs a chemical raw material manufacturer, we supply 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone for specialized synthetic routes in pharmaceutical intermediates, agrochemical synthesis, advanced material chemistry, and fine chemical research. Our production focuses on purity control and traceability to support leading global industrial users. 1. Pharmaceutical API Intermediate SynthesisPharmaceutical manufacturers primarily apply this compound as an advanced intermediate in the synthesis of fluoro-containing APIs, including CNS-active derivatives and anti-infective agents. The characteristic fluoroaromatic and ketone functional groups provide critical selectivity in late-stage transformations, especially for constructing pharmacophores via Grignard addition, reductive amination, or coupling chemistry. Our supply chain integration ensures consistent molecular quality, supporting cGMP custom synthesis and commercial-scale API production for regulated markets. Industry compliance standards
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2. Agrochemical and Crop Protection SynthesisProducers of crop protection molecules use the compound as a key intermediate in the synthesis of new-generation organofluorine pesticides and herbicides. The unique combination of a fluoroaryl ring and trifluoromethyl group allows the synthesis of highly selective, photostable lead structures with enhanced environmental fate. The building block integrates late in the process to construct target heterocycles or aromatic scaffolds needed for patented agrochemical agents. Industry compliance standards
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3. Advanced Materials for Organic ElectronicsR&D programs in high-performance materials incorporate this aromatic ketone as a molecular anchor in constructing optoelectronic polymers and functional monomers. The strong electron-withdrawing trifluoromethyl substituent adjusts electronic properties, critical for engineering charge-transport materials used in OLED and organic solar cell fabrication. End-users in specialty polymer manufacturing demand high assay and low-metal content to meet tight specifications for functional material synthesis. Industry compliance standards
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4. Fine Chemical Intermediates for Custom SynthesisCustom synthesis organizations and specialty chemical producers value this fluorinated ketone as a reactive building block for designing structurally complex fine chemicals. Its controlled reactivity enables selective introduction of fluorine and trifluoromethyl groups onto advanced aromatic motifs, instrumental in research-scale compound libraries and pilot-scale specialty chemical manufacturing. High-purity specifications and batch reproducibility are critical for successful downstream transformations. Industry compliance standards
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In fine chemical manufacturing, subtle changes at the molecular level often drive new capabilities for pharmaceutical and agrochemical discovery. 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone holds a distinct place in our product line, crafted with careful attention to purity and consistent structure. Our expertise in halogenated aromatics lets us produce this compound at a scale and quality that speaks clearly to demanding researchers and formulation teams. Each batch draws on process control that grew from decades of hands-on experience with aromatic ketones.
Our production process for this compound pivots on direct fluorination of appropriately substituted propiophenone precursors. We employ state-of-the-art reactors designed for both safety and the selectivity that this structure demands. The result aligns with tight expectation values for molecular weight, appearance, and impurity profiles. This compound’s crystalline solid form and sharp melting point reflect both raw material selection and the repeated improvement of filtration and crystallization steps—a focus that comes from repeated engagement with real-world bottlenecks, not assumptions. Each lot undergoes analysis by NMR, GC-MS, and HPLC to exclude process-related by-products, pyrogenic residues, or halogen exchange byproducts.
As manufacturers working closely with medicinal chemists and process development teams, we’ve found that subtle changes like a fluorine at the ortho-position and a trifluoromethyl group in the para position bring not only increased metabolic stability but also impact on lipophilicity and receptor binding. This molecular profile distinguishes 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone from the straightforward 4'-trifluoromethyl variant. Bond strength and electron distribution shift, making this compound a favored cornerstone for researchers needing more resistant scaffolds or looking to fine-tune bioactivity across a family of analogues.
Process chemists in our facilities handle these two groups as more than molecular decorations. The strong electron-withdrawing effect from the CF3 group offsets the more moderate impact of the fluorine. During scale-up, we observed that reactivity and purification challenges differ significantly from the parent propiophenone or from singly-substituted variants. By controlling the introduction sequence of these halogens, unwanted side products—especially those resulting from competitive ortho substitution—become far less concerning. This repeatedly saves time and solvent during workup, fitting the environmental and commercial goals most customers demand.
Chemists at the bench in our plant routinely witness the difference between theory and application with specialty intermediates. 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone shows its strengths in several recurring projects. Innovators in custom synthesis regularly select this molecule as a precursor in constructing more complex heterocycles; the halogenated aromatic allows for selective cross-coupling, while the ketone moiety offers leverage through condensations and reductive amination. One customer worked with us to adapt a patented Friedel-Crafts route, observing higher yields and a dramatic reduction in TFA-related byproducts compared with earlier, less functionalized analogues. This wasn’t theory; it was the outcome of repeated feedback, process tweaks, and instrument readouts.
We often field questions about where this compound stands in a landscape crowded with aromatic ketones. Its greatest strengths appear in designing advanced pharmaceutical leads and agrochemical intermediates where metabolic stability and resistance to oxidation or hydrolysis matter. The combination of the two halogen groups builds in resistance to oxidative metabolism at both the ortho and para positions, making it more robust in the face of aggressive biological or environmental breakdown. Our repeated pilot plant runs reveal that this stability comes alongside a strong, consistent crystallinity—even after repeated solvent washes or recoveries, the compound maintains a fine, easily filtered grain size. Consistent particle morphology reduces headaches on automated filling lines and helps maintain batch-to-batch reproducibility for downstream users.
What sets the manufacturing of 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone apart is the concrete way it challenges a production plant. Introduction of both fluoro and trifluoromethyl groups can trigger unwanted side reactions if conditions slip outside a small temperature or pH window. Early process attempts in our plant highlighted the need for continuous in-process controls—temperature, pH, and halide ion monitoring became standard. We adopted in-line analytics because sample-based quality checks, though thorough, missed fleeting process shifts. GC-MS snapshots at each stage allow real-time interventions, keeping downstream purification manageable and yields high.
The experience taught us to build redundant failsafes into our reactors and storage systems. Initial scale-up generated more acidic, non-volatile residues than theory predicted. Our operators responded by reworking solvent recovery and introducing additional neutralization points. Years of these lessons flow directly into our standard operating procedure. Each synthesized batch now leaves our plant with comprehensive analytical documentation, but the foundation stands on the series of incremental gains made by hands-on chemists, not only desk-bound QCs.
Every kilogram of this compound shipped ends up in the hands of a chemist who is part of a larger story—whether it's early-stage pharma research or pesticide development. Our role doesn’t stop at the reactor vessel; we’ve invested in listening closely to repetitive user feedback. Some customers need very fine controls on impurity levels to pass regulatory submission hurdles. Others pursue green chemistry, and so they seek guidance on solvent swaps or ways to reduce energy inputs. We don’t lay down abstract claims about “exceeding industry norms”—we share results from our waste solvent recovery setups and explain trade-offs we’ve actually encountered in filtration, re-crystallization, or solvent exchange protocols.
An international partner once required an unusually tight control on moisture content for automated handling. In response, our team revamped drying and packaging protocols—a solution born from customer dialogue rather than defaulting to a one-size-fits-all approach. Such projects rarely show up in glossy brochures, but they end up improving our baseline product for all users. The biggest impacts come from adapting in response to real-world bottlenecks.
Experienced users recognize quickly that 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone stands apart from standard aromatic ketones and even from other fluorinated or trifluoromethylated compounds. Feedback from synthetic routes consistently shows higher selectivity and less need for input purification—critical at bigger scales. Small-scale experiments in drug candidate libraries show the molecule’s stability under oxidative or basic workup, providing a reliable backbone for more exotic group introductions.
Our process also sidesteps common pitfalls associated with uncontrolled exotherm or halogen migration during synthesis—problems frequently cited in industry reviews but less often addressed by direct manufacturer action. Instead of fighting recurring contamination or persistent off-odors, we targeted process variables, invested in air handling, and upgraded containment. These measures reflect practical decision-making, not marketing narratives.
Any technical manufacturing journey runs up against limits. Our runs with 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone flagged practical bottlenecks and boundary conditions worth noting. Solubility issues at scale impacted solvent choices and could alter purification protocols unexpectedly. We answered by maintaining an ongoing log of solvent behavior—hexanes, toluene, acetone—during both crystallization and re-dissolving stages. Rather than masking these as theoretical risks, we document them for process engineers and offer detailed histories for those who need to tweak their own downstream applications.
Waste treatment also ranks high on the real-world problem list. Halogen-heavy compounds raise persistent disposal issues; we address them with both on-site incineration and contracted specialized waste services. Sharing this operational information equips informed buyers and partners with the facts they need to build more robust safety and environmental programs. Industry frameworks today demand this openness, not just for compliance but for the trust that comes when sharing long-term operational lessons.
Those who use 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone with regularity see consistent performance as a direct result of controls over synthesis, crystallization, and packaging—all in a facility able to pivot quickly based on feedback. We don't offer empty promises—every batch is documented with real, repeatable data, and every improvement is shared openly with partners. Having worked through multiple iterations, we know firsthand where the bottlenecks lie and how small adjustments—whether in raw material preparation, process temperature profiles, or downstream filtration—translate to meaningful outcomes.
Process engineers, not just salespeople, talk directly to users who need reliable feedback routes. We conduct annual process reviews, root cause analyses following any deviation, and encourage cross-team mentorship—something less visible in third-party supply chains. Our commitment comes from seeing so many projects improve, survive, or even thrive due to direct manufacturer involvement long after initial delivery.
Crafting 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone didn’t appear overnight. Its repeated reinvention, process re-design, and adaptation owe much to the demands of pharmaceutical and advanced materials innovation. Supply doesn’t rely on distant tollers; all steps, from precursor formation through purification and packaging, take place within our direct oversight. That means learning from every hiccup in the process and making those improvements the ground floor of every subsequent batch.
Feedback also comes from academia. Academic teams chase the next generation of receptor modulators, enzyme inhibitors, or materials components; their requests often drive rare derivative exploration or push for higher chiral purity. We support these calls directly, explaining why certain modifications raise costs or cut yields, or how to spread risk through pilot runs. This open dialogue sharpens our manufacturing edge, keeping us aligned with both cutting-edge research and day-to-day production realities.
The path from raw feedstock to pure 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone is defined as much by setbacks as successes. Years ago, our operators found that filtration media occasionally failed to exclude fine, polar impurities unique to this structure. Redundant washing steps and monitoring helped us clear this hurdle, but the lesson endured—standard routines do not suffice for all chemistries. This compound taught us the value of active listening between plant operators and the laboratory team, aligning theory with practical recoveries and yields.
Logistics always makes an impact. Packaging protocols evolved over multiple iterations in response to customer reports about caking or moisture pickup mid-shipment. Switching to layered barrier packaging and adding real-time moisture indicators weren't theoretical improvements—they cut incidental losses and improved shelf stability. Hands-on solutions from transport and storage teams gave rise to measurable changes in both customer satisfaction and re-order rates.
Our efforts with 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone go beyond maintaining the status quo. Researchers and process chemists expect not only material but support with test data, troubleshooting, and best-practice advice. Collaborations with both academic and industrial players lead to real advances—better yields, reduced solvent needs, smarter purification. Open lines of communication reduce guesswork and foster a community of problem-solvers instead of isolated end users.
With regulatory expectations growing sharper and downstream requirements shifting, manufacturers with hands-on experience offer more than raw material—they contribute insight and risk reduction. Constant dialogue with up- and downstream partners sharpens our protocols and keeps our operations agile. The cycle of inquiry and feedback keeps 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone a reliable workhorse, not just an item on a shelf.
The foundation of trust for this material rests in transparency, consistent quality, and an authentic commitment to process-driven improvement, not in abstract marketing terms. Through setbacks and milestones, we anchor our production of 2'-Fluoro-4'-(Trifluoromethyl)Propiophenone in evidence from real projects, not just lab diaries or brochures. Each improvement—whether in handling, documentation, or technical troubleshooting—represents one more step toward compounds that do more than meet minimum standards; they enable the next round of scientific progress.
Supplying specialty compounds like this involves more than following regulatory playbooks. Each milestone in the compound's manufacture reflects a blend of chemical insight, logistics problem-solving, and open exchange between experts who know both the process and the changing needs of research and industry. This path, built by working chemists and anchored in practical, observed data, lets the compound keep pace with, and occasionally drive, the evolving challenges of modern synthesis and discovery.