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2,5-Difluorobenzophenone

    • Product Name 2,5-Difluorobenzophenone
    • Alias DFBP
    • Einecs 250-241-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    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 & Storage
    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.
    Application of 2,5-Difluorobenzophenone

    Applications of 2,5-Difluorobenzophenone in Industrial Manufacturing

    2,5-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 Synthesis

    In 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

    • ASTM D6262 (Standard Specification for PEEK Molding and Extrusion Materials)
    • FDA 21 CFR 177.2415 (PEEK Plastics for Food Contact)
    • ISO 10993 (Biocompatibility for Medical Applications)
    • EN 45545-2 (Fire Performance for Railway Applications)

    Typical usage ratio

    • Usually 45–55 mol% of total aryl ketone monomer feed, adjusted based on target molecular structure and mechanical requirements.

    Downstream process integration

    • Charged at the primary monomer introduction step of nucleophilic aromatic substitution polymerization, using high-purity solvents and deoxygenation protocols.

    Final product types

    • PEEK pellets for injection molding
    • PEEK powder for extrusion
    • Machined PEEK rods and sheets
    • Performance films for electronics and aerospace

    2. Liquid Crystal Polymer (LCP) Synthesis for Electronics

    With 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

    • IEC 61249-2-11 (LCP Base Materials for Printed Wiring Boards)
    • UL 94 V-0 (Flame Retardant Certification for Plastics)
    • RoHS Directive (Restriction of Hazardous Substances in Electronics)
    • IPC-4103 (Specification for LCP Laminates and Prepregs)

    Typical usage ratio

    • Ranges from 35–50 mol% of monomer batch; chemists adjust according to melt flow and thermal resistance targets for each run.

    Downstream process integration

    • Fed directly into the condensation polymerization reactor alongside comonomers and catalysts during LCP backbone formation.

    Final product types

    • High-speed data connector housings
    • BGA substrate laminates
    • RF antenna moldings
    • Thin LCP films for flexible circuits

    3. Building Block in Advanced Pharmaceutical Synthesis

    Process 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

    • ICH Q7A (GMP for Active Pharmaceutical Ingredients)
    • USP–NF Monograph Requirements
    • Ph. Eur. quality guidelines for raw materials
    • FDA cGMP Part 210/211 (Finished Pharmaceuticals)

    Typical usage ratio

    • Dosage depends on synthetic pathway, commonly 0.6–1.2 equivalents relative to the main reactant in the key coupling step; optimal ratio controlled by batch optimization trials.

    Downstream process integration

    • Charged during Suzuki, Friedel-Crafts, or other aromatic acylation steps within API intermediate synthesis, under monitored reaction atmospheres with GMP-compliant documentation.

    Final product types

    • Pharmaceutical intermediates bearing difluoroketone motifs
    • API building blocks for CNS, antidiabetic, and anticancer drugs
    • Reference standards for regulated synthesis routes
    • Custom small-molecule libraries for drug discovery

    4. Reactive UV-Curable Oligomer Production for Industrial Coatings

    In 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

    • ISO 9001:2015 (Quality Management System for Coating Production)
    • REACH (Registration, Evaluation, Authorisation of Chemicals) Registration
    • EN 1504-2 (Surface Protection Systems for Concrete)
    • ISO 16000-9 (Indoor Air Quality – VOC Emissions)

    Typical usage ratio

    • Incorporation level usually 10–20 mol% of the prepolymer feed, modifiable depending on target crosslink density and desired mechanical properties.

    Downstream process integration

    • Added during oligomer synthesis or as a terminal modifier during prepolymer formation, subject to exhaustive QC and monitoring of residual monomers.

    Final product types

    • Scratch-resistant UV-cured films
    • Protective varnishes for electronics
    • Industrial floor coatings
    • Glossy topcoats for automotive decorative plastics
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