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HS Code |
459424 |
| Chemical Name | 2,5-Difluorobenzophenone |
| Cas Number | 348-51-6 |
| Molecular Formula | C13H8F2O |
| Molecular Weight | 218.20 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 64-67 °C |
| Boiling Point | 328 °C |
| Density | 1.25 g/cm³ |
| Solubility In Water | Insoluble |
| Purity | Typically ≥98% |
| Smiles | O=C(c1ccccc1)c2cc(F)ccc2F |
| Refractive Index | 1.595 (estimated) |
| Storage Temperature | Store at room temperature |
| Flash Point | 148 °C |
| Pubchem Id | 11760 |
As an accredited 2,5-Difluorobenzophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle sealed with a screw cap, labeled "2,5-Difluorobenzophenone, CAS 345-92-6," with hazard and handling instructions. |
| Shipping | 2,5-Difluorobenzophenone is shipped in tightly sealed containers, protected from light and moisture. It should be transported according to regulations for chemicals, including labeling for hazardous materials if applicable. Handle with care to avoid spillage or breakage. Store in a cool, dry place away from incompatible substances during transit. |
| Storage | 2,5-Difluorobenzophenone should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store it in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizing agents. Always label the container clearly and follow all relevant chemical storage and safety guidelines to prevent environmental contamination or accidental exposure. |
Applications of 2,5-Difluorobenzophenone in Industrial Manufacturing2,5-Difluorobenzophenone serves as a key intermediate in several advanced material sectors, where its unique structural properties enable demanding downstream synthesis routes. Below, we detail the primary, commercially proven application scenarios, referencing concrete compliance benchmarks, practical formulation guidance, precise processing stages, and finished product outputs based on real-world large-scale adoption. 1. High-Performance Polyetheretherketone (PEEK) Resin SynthesisIn the specialty polymer sector, manufacturers use this compound as a principal monomer in the production of polyetheretherketone. Its difluoro substitution improves melt-processability and enhances the final polymer’s mechanical stability and chemical resistance. The input ratio adapts to the molecular weight targets of each customer’s batch but remains a critical factor in resin consistency. Process engineers introduce the raw material at the initial polymerization stage, employing nucleophilic aromatic substitution with bisphenolates under anhydrous and inert atmosphere conditions. The resulting PEEK finds principal use in demanding environments such as medical device housings, aircraft interior parts, pump components, and precision electronics insulation. Industry compliance standards
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2. Liquid Crystal Polymer (LCP) Synthesis for ElectronicsWith its rigid, planar structure and high fluorine content, the intermediate supports the synthesis of liquid crystal polymers prized for superior thermal stability and dielectric performance. Formulators select the addition ratio according to requirements for melt viscosity and molecular orientation. Synthetic chemists introduce the compound at the condensation step with hydroquinone or similar comonomers under high-temperature, low-moisture conditions to maximize molecular alignment. Downstream producers extrude, spin, or injection mold the resulting polymers to serve as microelectronics connectors, high-frequency circuit substrates, and advanced microwave components. Industry compliance standards
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3. Building Block in Advanced Pharmaceutical SynthesisProcess chemists employ the compound as a sophisticated building block during multi-step syntheses, mainly for producing next-generation active pharmaceutical ingredients where the difluorinated aryl ketone moiety demands precise substitution. The incorporation ratio varies depending on molecule complexity and process scale, often being determined by retrosynthetic route analysis. The intermediate is introduced at a defined cyclization or coupling stage, commonly under controlled temperature and strictly monitored purity conditions. Manufacturers purify and isolate downstream forms for transformation into regulated drug substances addressing therapeutic targets such as CNS disorders and metabolic diseases. Industry compliance standards
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4. Reactive UV-Curable Oligomer Production for Industrial CoatingsIn specialty coatings technology, formulators use the difluorinated ketone as a reactive linker in the synthesis of UV-curable oligomers with enhanced chemical durability and weather resistance. By manipulating feed ratios, R&D teams tune hardness and gloss for flooring, optical, or protective coatings. The compound enters amid the polycondensation reaction or as a chain-terminating agent in prepolymer prep, with strict attention to impurity control and acrylation yields. The final UV-cured products serve as high-spec films and varnishes for electronics, automotive plastics, and industrial flooring. Industry compliance standards
Typical usage ratio
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