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HS Code |
191496 |
| Cas Number | 653-46-3 |
| Molecular Formula | C8H5F3O |
| Molecular Weight | 174.12 |
| Iupac Name | 1-(2,3,6-trifluorophenyl)ethan-1-one |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 69-71°C at 20 mmHg |
| Melting Point | -14°C |
| Density | 1.312 g/cm3 at 25°C |
| Refractive Index | 1.470 |
| Flash Point | 86°C |
| Smiles | CC(=O)C1=C(C(=C(C=C1)F)F)F |
| Solubility | Slightly soluble in water, soluble in organic solvents |
As an accredited 2',3',6'-Trifluoroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2',3',6'-Trifluoroacetophenone (5 grams) is a tightly sealed amber glass bottle, labeled with proper hazard and safety information. |
| Shipping | **Shipping Description for 2',3',6'-Trifluoroacetophenone:** This chemical should be shipped in a tightly sealed container, protected from moisture and light. Follow all relevant regulations for transport of organic chemicals. Label clearly and include safety data. Compatible packaging materials are essential to prevent leaks or reactions. Avoid extreme temperatures during shipment. |
| Storage | **2',3',6'-Trifluoroacetophenone** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition or heat. Protect from moisture and incompatible substances such as strong oxidizers. Store at room temperature and keep away from direct sunlight. Ensure appropriate labeling and access is limited to trained personnel using proper protective equipment. |
Applications of 2',3',6'-Trifluoroacetophenone in Industrial Manufacturing2',3',6'-Trifluoroacetophenone is a specialized fluorinated building block used in select high-value sectors where its reactivity and unique substitution pattern enable advanced synthesis routes. As a direct manufacturer, we supply only to processes with proven downstream utility, each subject to specific regulatory and compositional demands. The following are the principal application scenarios implemented by our industrial partners. 1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)Chemical firms incorporate this compound as a key intermediate when constructing fluorinated aromatic fragments, which enhance metabolic stability and bioavailability in modern APIs. The molecule enters multi-step organic syntheses, commonly within Suzuki-Miyaura or Buchwald-Hartwig coupling protocols, contributing to leading compounds under late-stage development or commercial production, including select central nervous system and anti-inflammatory agents. Industry compliance standards
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2. Agrochemical Research and ProductionR&D and contract manufacturing organizations in agrochemicals employ this fluorinated acetophenone for constructing target pesticides and herbicides, particularly where fluorine incorporation improves biological persistence and selectivity. The molecule is utilized in heterocycle assembly for insecticidal or fungicidal actives, where it influences both potency and environmental degradation profile. Industry compliance standards
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3. OLED Material PrecursorsSpecialty electronic material manufacturers exploit the trifluorinated acetophenone structure during building block assembly for organic light-emitting diodes (OLEDs). Fluorine-modified aromatics impart enhanced electronic performance and film stability in high-value OLED emitters and transport layers. The raw material typically undergoes nucleophilic aromatic substitution or is coupled to heteronuclear systems aiming for precise photophysical characteristics. Industry compliance standards
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4. Advanced Liquid Crystal Material SynthesisAdvanced display material producers source this compound to tailor the dielectric and optical properties within liquid crystal monomers used in high-performance display panels. The trifluorinated moiety enables tight control over nematic range and viscosity, improving panel response times and thermal stability for automotive and large-format displays. Industry compliance standards
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5. Fluorinated Polymer Modifier in Specialty CoatingsCoatings formulators target this acetophenone as a reactive monomer or precursor to insert trifluoromethyl functionalities into performance polymers. The fluorine content imparts low surface energy and chemical resistance, particularly valuable in anti-graffiti finishes, selective release coatings, and exposure-resistant surface films. Controlled introduction at the backbone modification or chain termination step ensures reproducible properties for high-specification applications. Industry compliance standards
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Among the range of aromatic ketones we’ve scaled up at our manufacturing site, 2',3',6'-Trifluoroacetophenone stands out for the subtle but significant role its fluorination pattern plays in downstream chemistry. This molecule—often referenced by its CAS number 199105-85-2 in research circles—has carved its niche in the synthetic toolkit for laboratories and production teams tackling complex targets that demand both selectivity and reactivity. Drawing from years on the line, handling and producing this acetophenone variant, I have seen where its unique structural features stack up and where it diverges from the crowd.
As producers, we pay close attention to the integrity of each batch of 2',3',6'-Trifluoroacetophenone. Our model typically runs with a purity well above 98%, monitored by gas chromatography as standard for this class of compounds. The solid yields and reliability under scale-up conditions come from persistent work on solvent management, hydrogen fluoride containment, and heating regimes during trifluoromethylation. You notice the difference when you open a fresh drum—the acetophenone’s faint, sharp odor gives it away, with the light yellow to colorless look confirming minimal contaminants. The trifluoro substitutions at the 2, 3, and 6 primes lead to both steric and electronic effects, which you can see play out in reaction selectivity or crystallization behavior. This directly feeds into higher yields downstream, especially for pharmaceutical intermediates or advanced agrochemical scaffolds.
Every batch is more than just numbers on a certificate; what matters is how it performs in the reactor. Our product typically comes with tightly controlled moisture levels and is shipped in sealed, inert-lined containers that allow direct transfer into dry rooms. From regular conversations with process chemists, I know small amounts of residual moisture or side products can throw off metal-catalyzed coupling reactions or downstream carbonyl manipulations. We go well beyond routine HPLC checks to screen for trace by-products, especially any related to incomplete fluorination or aromatic impurities, because those have been known to inhibit certain palladium or nickel catalysts. Some may overlook the physical form, but free-flowing, stable powder is critical for high-throughput dosing systems in continuous flow plants. We saw first-hand how clumped material wastes time and reduces safety margins, especially on automated platforms that measure by weight rather than volume.
I’ve shipped this compound to customers synthesizing fine chemicals, developing high-performance polymers, and investigating leads in pharmaceutical R&D. The pattern of fluorine atoms boosts metabolic stability for many targets and changes how aromatic rings behave under further functionalization. For instance, placing fluorines at these specific positions reduces electron density on the benzene ring, enhancing selectivity in electrophilic substitution. I’ve seen medicinal chemists use this effect to push regioselective halogenation or nitration even in challenging systems. The combination of electron-withdrawing and ortho effects from the trifluorine setup also raises its value in materials science, facilitating the design of specialty monomers or cross-linkers for advanced polymers, especially where thermal and oxidative stability is critical.
We also serve groups experimenting with advanced catalysts or organometallic systems, where a very clean starting material prevents side reactions that waste time in laborious purifications later. The ketone moiety’s resilience under both acidic and basic conditions means the molecule survives multistep sequences, including reductions, halogenations, or even Suzuki couplings. This robustness relieves headaches, especially during scale-up, when process deviations can cost days of troubleshooting and lost batches if starting material variabilities seep into later steps.
We’ve produced several trifluorinated and monofluorinated acetophenone analogs, and the distinctions become obvious both in handling and chemical behavior. Many chemists reach for para- or mono-fluorinated versions, but single-position fluorine can’t deliver the same balance between ring activation and steric hindrance. Some see cost as the only differentiator, but the consistent gains in product yield and reproducibility reported back from our partners using 2',3',6'-Trifluoroacetophenone show the extra fluorines at these positions are doing real chemical work. With the three fluorine atoms, solubility profiles also shift, especially in nonpolar or slightly polar organic solvents. Sometimes, this means longer dissolution times during set-up, but the trade-off returns in improved selectivity during late-stage functionalization.
Many alternative ketones attract nucleophiles more aggressively or undergo side condensation, complicating the synthesis of structurally elaborate end products. Our product tends to hold up against unintended side reactions even when run under conditions involving strong bases or temperature swings, which appeals to teams running variable pilot runs. In contrast, unsubstituted acetophenone or simple derivatives suffer from instability under harsh environments, producing more by-products that slow down purification and raise costs. The physical stability of 2',3',6'-Trifluoroacetophenone extends shelf life as well, letting R&D teams buy in bulk for multi-quarter projects and avoid last-minute stockouts. This kind of operational reliability often gets undervalued in cost calculations yet matters hugely when project delivery schedules are on the line.
Saying a compound is “safe” ignores the reality producers experience. We’ve designed our production and packaging to minimize risk from possible exposure. On the plant floor, we use enclosed transfer systems and reinforced PPE during large-scale handling, as the powdered form can irritate skin or airways if not respected. Shipping protocols stick to strict labeling and tamper-proof closures after one close call with a compromised shipment. Our ongoing safety reviews drill down into any incident data. Regular team training focuses on spill procedures and first-responder communication inside the facility—practical details, not clipboard theory. Smaller research packages get internal double-bagging and desiccant packs to protect integrity during shipping even if storage conditions aren’t perfect on the client side. This hands-on, prevention-based mindset reduces stock losses and prevents delays for our customers, particularly those juggling tight timelines in preclinical or pilot plant settings.
2',3',6'-Trifluoroacetophenone’s scalable synthesis isn’t as straightforward as some off-the-shelf acetophenones. We’ve refined a multi-step process, relying on selective fluorination of precursor aromatic systems under carefully controlled temperatures and pressures. Some in the trade bypass careful separation steps, but we never shortcut solvent swaps or distillations. The reward is cleaner product without the lingering acidic or oxidized by-products that users report slow down chromatography or poison catalysts. We source our feedstock from established domestic partners, keeping supply chains tight and cutting down on unexpected impurities that sometimes slip in from unknown origins. Raw material quality trumps low prices in this context—one bad lot can jeopardize not just one run, but weeks of scheduled downstream work. As the actual manufacturer, we stay locked into every stage, from raw material selection up to lot release, because reputation rides on every delivered load.
As regulatory demand increases for traceability and process transparency, our team already records batch genealogy from the ground up. We keep digital and hard-copy logs of every critical process parameter for each batch, tying this record-keeping directly to lot number and shipment. This routine discipline doesn’t just satisfy regulatory audits—it gives our technical support team the context to troubleshoot or retrace steps whenever a customer encounters even a slight deviation in their process. More than once, this data trail has enabled rapid adjustments for clients developing new routes, keeping their trials on track rather than spiraling through costly delays caused by spec drift or unclear provenance.
Pharma and agrochemical developers often approach us seeking insights on introducing fluorinated scaffolds such as 2',3',6'-Trifluoroacetophenone into their chemistries. Drawing from our own R&D work and stories shared by customers, we pay special attention to solvent choice, ratio of reactants, and order of addition in pilot-scale ketone alkylation reactions. Reaction exotherm management plays a unique role: the trifluoroaromatic ring changes heat release compared to less substituted counterparts. We’ve collaborated with clients to help adjust their protocols for lower hot-spot risks, using slow-dosing and staged dilution rather than relying on catch-up cooling at the end. With growing demand for robust synthesis options for clinical trial supply, many companies want to bypass lengthier protection-deprotection protocols, and the resilience of this acetophenone core lets them pare down steps. Our technical teams provide real-time batch analysis, making quick corrections to process drift and resolving minor issues before they become full-scale batch failures. Custom support at this level comes not from generic documentation but from hands-on knowledge developed through repeating, observing, and troubleshooting these systems firsthand.
No chemical product discussion can skip over environmental considerations, especially with fluorinated compounds. Our production lines include routine checks for atmospheric emissions and waste streams. Recovery units for hydrogen fluoride and spent acids run at every stage, with neutralization and containment protocols written and tested by in-house teams—not copied from generic manuals. After a period of trial and error, recycle loops and neutralization beds recover and destroy much of the spent process acid, transforming uncontrolled waste into managed by-products. These steps aren’t about regulatory box-ticking but keeping pace with higher expectations from clients and the community. Environmental reporting isn’t confined to management reports; we share targets and progress with shop floor operators so every member sees the bigger picture. Continuous improvement comes directly from team feedback on waste minimization and resource efficiency—ideas tested and adopted after firsthand use, not as abstract “initiatives.”
Unlike distributors who hand off product without context, our technical teams track and log customer feedback. A few years back, tighter customer specs on particle size and moisture sent us on a campaign to upgrade our drying equipment. Minor changes at the process level, like gentler mixing and inert gas sweeps, dramatically reduced both batch variability and user complaints. We hold quarterly review meetings with key customers to debrief on engine-room experiences, not just procurement metrics. More often than not, practical suggestions from those running actual chemistry drive changes to how we filter, package, and transport this compound. Some customer R&D teams need materials for small-batch exploratory work; others push for guaranteed lot scalability for multi-ton production. We answer both needs by running both pilot and large-production lines side-by-side, sampling each batch for cross-comparison. The confidence our scale-up success gives to project managers, especially during make-or-break launches, grows straight out of this deep manufacturing involvement—not marketing spin.
Handling the actual chemistry, batch after batch, teaches lessons you do not learn from reading product blurb sheets. The real-world consistency, backed by active data tracking, sets us apart from volume-driven commodity players. Whether the next destination is a pharma pilot plant, an academic research lab, or an industrial polymer development floor, we treat every batch as if it were heading for our own use—a mindset born from the pride of making something that actually pushes innovation forward.
2',3',6'-Trifluoroacetophenone demonstrates how thoughtful manufacturing and lived experience can add value, protect downstream processes, and anticipate customer needs well in advance. This product represents more than a chemical; it embodies years of practical refinement, direct user engagement, and a culture that values operational clarity, transparency, and continuous learning. As regulations tighten and chemical development grows ever more complex, these qualities separate reliable manufacturers from those just moving commodities. Our job isn’t done with shipment. We stay hands-on, open to feedback, always pushing for the next incremental gain in both process and product quality for our partners, large and small.