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HS Code |
969848 |
| Product Name | 3,4,5-Trifluorobenzophenone |
| Cas Number | 147028-57-5 |
| Molecular Formula | C13H7F3O |
| Molar Mass | 236.19 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 68-71°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=CC=C(C=C1)C(=O)C2=CC(=C(C(=C2)F)F)F |
| Inchi | InChI=1S/C13H7F3O/c14-11-7-10(12(15)13(16)8-11)9-5-3-2-4-6-9/h2-8H |
As an accredited 3,4,5-Trifluorobenzophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3,4,5-Trifluorobenzophenone is supplied in a 25g amber glass bottle with a secure screw cap and safety labeling. |
| Shipping | 3,4,5-Trifluorobenzophenone is shipped in tightly sealed containers, protected from light and moisture, and handled according to regulations for non-hazardous chemicals. Packages are clearly labeled and cushioned to prevent damage during transit. Ensure compliance with local, national, and international shipping regulations for laboratory chemicals to guarantee safe delivery. |
| Storage | 3,4,5-Trifluorobenzophenone should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep separate from incompatible substances such as strong oxidizing agents. Ensure storage conditions minimize the risk of ignition or chemical reaction. Proper labeling and adherence to local chemical storage regulations are recommended for safety. |
Applications of 3,4,5-Trifluorobenzophenone in Industrial ManufacturingAs a dedicated producer of 3,4,5-trifluorobenzophenone, we support industrial partners in key markets requiring reliable fluoroaromatic building blocks. Our production ensures consistent purity and supply chain stability for downstream synthesis in specialized application areas. Below are the main sectors where our material integrates into advanced manufacturing routes. 1. Pharmaceutical Intermediate for Anti-Tumor AgentsPharmaceutical companies use this compound as a core intermediate for the synthesis of kinase inhibitors and other anti-cancer APIs. The material’s trifluoromethyl substitutions are essential for influencing target molecule bioactivity, metabolic stability, and selectivity. It enters the route at the aromatic coupling stage, serving as a precursor for heterocycle assembly or further derivatization. Manufacturing partners employ precise stoichiometry to manage regulatory residual limits and ensure batch reproducibility. Industry compliance standards
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2. Synthesis of Organic PhotoinitiatorsManufacturers of UV-curing systems use this compound as a structural fragment in photoinitiator molecules. Its electronic properties enable efficient UV absorption and radical generation during polymerization. Production teams blend it into multi-step synthesis starting from ketone coupling, followed by functionalization to introduce desired absorption peaks for specific curing applications. Strict handling is required to comply with product and process safety standards for photochemical feedstocks. Industry compliance standards
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3. Agrochemical Synthesis – Herbicide PrecursorAgrochemical formulators integrate this compound as a key aromatic scaffold while creating new-generation fluorinated herbicides. Its trifluorinated aromatic ring supports metabolic persistence and enhances selectivity for target weeds. The raw material is introduced during the condensation or halogenation stage, allowing precise incorporation into multi-line synthetic routes. Quality control teams monitor purity and solvent residue as required by agro-product legislation to guarantee safety for field application. Industry compliance standards
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4. Liquid Crystal Material IntermediateProducers of advanced display technologies select this fluoroaromatic ketone as a foundational intermediate for synthesizing high-performance liquid crystal compounds. The molecular structure promotes tailored dielectric anisotropy and thermal stability, which are critical for the alignment and response behavior of liquid crystals in modern LCD panels. Entry into the process occurs during aromatic core formation. Synthesis adjustments ensure purity aligns with stringent electronics industry parameters, preventing optical and performance defects in final modules. Industry compliance standards
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5. Fine Chemical Intermediate for Specialty PolymersManufacturers in specialty polymer sectors incorporate this material during custom monomer synthesis, targeting applications that demand a high level of chemical resistance, UV stability, and unique dielectric properties. The trifluorinated aromatic functionality can impart advanced performance to engineered resins and coatings. Typical usage occurs in the early monomer modification stages, with downstream checks on integration efficiency and residuals in accordance with application-specific certification systems. Industry compliance standards
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At our manufacturing facility, the development and production of 3,4,5-Trifluorobenzophenone has proven to be a key part of supporting a variety of industries with dependable building blocks. Our team approaches every batch with a focus on purity and practical application, reflecting years spent at the bench, troubleshooting scale-up and refining every stage of processing. Consistency and quality matter to us because the end-users trust our expertise and the capabilities of our plant.
We produce 3,4,5-Trifluorobenzophenone to the requirements of research and commercial laboratories that demand low impurity profiles. This compound appears as an off-white to pale yellow crystalline solid and has a molecular formula of C13H7F3O, with a molecular weight of 236.19 g/mol. We standardize purification methods like column chromatography with solvents that do not introduce trace contaminants, and we routinely check melting points and NMR profiles during scale-up. Liquid handling systems are maintained for batch sizes from a few kilos to much larger production lots without deviation from specification.
Handling this product requires experience since the trifluorinated ring introduces a new set of physicochemical traits. We pay close attention to moisture and light sensitivity; warehouse conditions reflect this, keeping samples and drums in tightly sealed, inert containers. Our quality control lab employs HPLC and GC to detect any byproducts down to the ppm level, so what leaves the loading bay matches what was approved by QC.
Synthetic chemists select 3,4,5-Trifluorobenzophenone for both its reactivity and its resistance to unwanted side reactions. We first began producing this molecule for a customer developing specialty benzophenone-based UV-absorbers, and usage has grown from there. Its three fluorine atoms provide distinct electronic effects, which alters the reactivity in Friedel–Crafts acylations and Grignard additions compared to unsubstituted analogs. This property found traction in pharmaceutical R&D, where research teams rely on subtle electronic tweaks to unlock new lead compounds. We have seen the molecule moving into agricultural intermediates as well, especially where chemical resistance is needed in final products.
Researchers involved in medicinal chemistry often cite the advantages of fluorinated scaffolds for fine-tuning bioactivity. Trifluoromethyl and trifluorophenyl groups resist metabolic cleavage in vivo, which simplifies the path toward candidates with longer half-lives. The addition of the trifluorinated benzoyl group directly influences the physical properties of drug templates, and during plant trials, our technical support helps customers dial in reaction conditions that maximize yield without sacrificing purity.
During pilot projects, chemists often weigh the choice between mono-, di-, or trifluoro substitution on the phenyl ring. We have run systematic trials with our own team at the scale-up stage to compare recovery rates, melting points, and chromatographic profiles among 2,4,5- and 3,4,5-substituted benzophenones. Out of all tested analogs, 3,4,5-Trifluorobenzophenone solidifies with the fewest polymorphic forms, which improves ease of isolation and storage. Solubility in common organic solvents surpasses that of many alternatives, especially when methanol, acetonitrile, or DCM are used as process solvents during downstream modifications.
In the working environment, these differences translate into shorter purification steps and lower rates of reaction side products. Cost of waste disposal can drop because of the cleaner profiles. Documented by our own process engineers, this trend has saved both time and solvent over repeated campaigns. Competitors may offer other variants, but direct head-to-head data shows our product line maintains narrower batch-to-batch variation, which is critical for users scaling from milligram to kilogram quantities.
Working around specialty fluorinated ketones takes training and an eye for detail. Our process chemistry team regularly reviews new findings on environmental fate and toxicity to help downstream users adapt safe handling protocols. Although the compound offers a largely manageable risk profile, we advise against long storage at elevated temperatures and work to minimize human exposure through secure packaging designs.
We invest in education, both for our own staff and for our customers. Our technical panels review the performance of 3,4,5-Trifluorobenzophenone under a range of synthetic conditions and pass on observations about yields, stability, and compatibility with metal catalysts. This practical support streamlines scale-up for end-users, often avoiding common roadblocks encountered in sulfonation or metal-catalyzed couplings.
Production of fluorinated aromatics can require specialized equipment, and our team continuously works to reduce the energy and waste produced. Solvent recovery systems operate at every production stage. Where possible, we switch to lower-impact reagents and minimize halogenated byproducts. Researchers who care about the broader impact of their chemical use find our analysis of cradle-to-gate emissions informative when planning supply chain strategies.
Close communication with buyers has helped us identify opportunities to collect empty drums and work towards circular supply chain models. We encourage bulk orders when it makes sense, as this scaling reduces packaging waste and transport costs per kilogram delivered. The consistent quality we deliver not only serves immediate applications but supports environmental targets through reduced batch failures and fewer off-spec shipments.
Maintaining agility in production meets the evolving needs of both research teams and commercial clients. We have structured our facility so that we can rapidly adjust to both sudden influxes in demand and precise batch customization. This often proves crucial during patent races, where delays in raw material deliveries may impact a new drug candidate’s progress.
We supply 3,4,5-Trifluorobenzophenone directly from our own lines, not from external brokers. This vertical integration translates into shorter lead times, lower development risks, and fewer quality deviations. Clients have remarked on the peace of mind that stems from established communication lines and the transparency of our inventory process.
Advanced trifluorinated compounds present synthetic hurdles, especially during scale-up that rarely show in bench-scale trials. We often confront issues such as incomplete fluorination, unexpected hydrolysis, and catalyst fouling. Over the years, iterative problem-solving has led us to optimize our route to 3,4,5-Trifluorobenzophenone. We do not shy away from sharing our setbacks and improvements—it is part of how we build long-term relationships with advanced chemical developers.
Every improvement in synthesis targets end-user needs. Lower residual solvent, higher batch purity, and consistent color all influence downstream performance. Each time an unexpected challenge arises, our chemists and operators meet face-to-face to resolve it using both academic understanding and real-world experience acquired across many years of specialty chemical manufacturing.
Feedback matters. We encourage every lab and commercial site using our 3,4,5-Trifluorobenzophenone to share their experiences. When a customer reported an issue with isolation due to polymorphism, we revisited our crystallization protocols and adopted a refined seeding method that improved both yield and reproducibility for future lots. Direct dialogue enables us to adapt rapidly and align our product with both novel and established processing protocols.
Our technical staff remains accessible during new process launches, offering advice on scale conversion, solvent swaps, or alternative workup methods. Ongoing partnerships with academic labs and industrial innovators help us track where new bottlenecks appear and how our products hold up in demanding syntheses. This approach sets our production apart from faceless commodity suppliers; the feedback we receive shapes our future runs.
Our experience in supplying this compound has shown that it bridges a unique gap for those developing next-generation materials and pharmaceuticals. Its electronic profile means that chemists can precisely modulate it through organic transformations like reductions, condensations, and couplings. This flexibility allows researchers to access a wider array of target molecules without having to continually change core reagents.
We have consistently found that 3,4,5-Trifluorobenzophenone outperforms non-fluorinated or singly fluorinated variants in specific reaction environments, especially in terms of final product purity and ease of isolation. Because we are involved directly with the manufacture and refinement of this molecule, we bring forward observations about solvent effects, temperature windows, and catalyst compatibility that save downstream users weeks of method development. Real economies show up when both the starting material and the technical support come from the same experienced source.
As a chemical producer, we know that no compound is truly “plug and play.” Every lot matters, every feedback loop improves future production, and every tweak in process can pay dividends for hundreds of users. Our approach to 3,4,5-Trifluorobenzophenone blends technical reliability with the flexibility required by modern synthetic chemistry.
We remain invested in refining both our manufacturing routes and our technical communication. The goal is to supply a product that chemists want to use, because it performs precisely as expected in highly variable environments. Supplying directly means fewer opportunities for error or misinformation, and our team stands behind every drum and bottle that leaves the factory.
Users regularly highlight the difference that comes with working directly with those who not only provide the product, but also solve problems when they arise, and help drive innovation in the sector. This is how we believe 3,4,5-Trifluorobenzophenone should be delivered: with the knowledge, transparency, and attention to detail earned through years of focused, practical chemical manufacturing.