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Ethyl (Pentafluorobenzoyl)Acetate

    • Product Name Ethyl (Pentafluorobenzoyl)Acetate
    • Alias EPBA
    • Einecs 402-500-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    381876

    Productname Ethyl (Pentafluorobenzoyl)Acetate
    Casnumber 151119-73-2
    Molecularformula C11H7F5O3
    Molecularweight 282.16
    Appearance Colorless to pale yellow liquid
    Boilingpoint 117-119°C (at 18 mmHg)
    Density 1.461 g/cm³
    Refractiveindex 1.400-1.420
    Purity Typically ≥97%
    Smiles CCOC(=O)CC(=O)C1=C(F)C(=F)C(=F)C(=F)C1=F

    As an accredited Ethyl (Pentafluorobenzoyl)Acetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Clear glass bottle with a secure screw cap, white label marked "Ethyl (Pentafluorobenzoyl)Acetate, 25g," hazard symbols, and batch number.
    Shipping Ethyl (Pentafluorobenzoyl)acetate should be shipped in tightly sealed, chemically resistant containers, protected from moisture and light. Transport according to local, national, and international regulations for hazardous chemicals. Ensure clear labeling and include appropriate safety documentation (SDS). Handle and store in a cool, dry place away from incompatible materials.
    Storage Ethyl (Pentafluorobenzoyl)acetate should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong bases or oxidizing agents. Keep it in a cool, dry, well-ventilated area, preferably in a chemical storage refrigerator or designated flammable liquids cabinet. Ensure appropriate chemical labeling and access only to trained personnel using suitable personal protective equipment (PPE).
    Application of Ethyl (Pentafluorobenzoyl)Acetate

    Applications of Ethyl (Pentafluorobenzoyl)Acetate in Industrial Manufacturing

    Ethyl (Pentafluorobenzoyl)Acetate serves as a specialized intermediate in several industrial markets. Its unique pentafluorinated structure and reactive functionalities support advanced synthesis routes in organic chemistry, agrochemicals, pharmaceuticals, and specialty coatings production. Our material is manufactured according to strict process controls to meet stringent technical and regulatory demands in these downstream applications.

    1. Pharma Intermediate Synthesis

    Commercial pharmaceutical manufacturers frequently use this material as a fluorinated building block for small-molecule active pharmaceutical ingredient (API) intermediates. The strong electron-withdrawing properties facilitate functional group transformations, particularly during key acylation and condensation steps in API synthesis. Strict traceability and impurity controls are enforced to support regulatory submissions and clinical trial requirements in regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters where applicable
    • European Pharmacopoeia (Ph. Eur.) for starting materials
    • REACH regulation for supply into the EU

    Typical usage ratio

    • Usage typically ranges from 0.1 to 2.5 molar equivalents depending on the target API's synthetic route and the step involved. The ratio adjusts according to the specific reactivity and desired yield at each stage.

    Downstream process integration

    • Material generally enters the process during Stage 2–3 of multi-step syntheses. It reacts with nucleophilic partners under controlled temperature and solvent systems within reactor vessels equipped for GMP operations.

    Final product types

    • Small-molecule APIs containing fluorinated aromatic rings
    • Advanced pharmaceutical intermediates for oncology and CNS drugs
    • Library compounds for medicinal chemistry R&D
    • Key side-chains for late-stage functionalization

    2. Agrochemical Active Ingredient Manufacture

    Leading agrochemical producers incorporate this intermediate during the manufacture of advanced herbicide, insecticide, and fungicide actives. Its electron-withdrawing fluoroaromatic structure enables high selectivity in coupling reactions for structure-activity-optimized agrochemical actives. Close coordination with customer safety assessment teams ensures consistent quality and documentation for finite residue regulatory dossiers worldwide.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • OECD GLP (Good Laboratory Practice) for toxicological studies
    • EPA 40 CFR Part 158 (United States FIFRA regulation)
    • China GB/T 1606-2001 (Agricultural Chemicals - Technical Specification)

    Typical usage ratio

    • Typical loadings range from 0.2 to 3.0 equivalents relative to primary nucleophiles. The level is optimized based on target molecule structure and environmental fate profiles.

    Downstream process integration

    • Raw material is charged to synthesis reactors during key acylation, esterification, or coupling steps. It is subsequently reacted under anhydrous or controlled-pH conditions with other pesticide-active intermediates.

    Final product types

    • Fluorinated herbicide actives for broadleaf weed control
    • Fungicide molecules with advanced resistance management features
    • Insecticide compounds exhibiting improved target selectivity
    • Precursor blocks for field-tested combination products

    3. Specialty Polymer Synthesis

    Producers develop advanced functional polymers by introducing this compound as a pendant group precursor or end-capping agent. The pentafluorobenzoyl functionality imparts increased hydrophobicity, weather resistance, and chemical inertness, supporting specialty projects in electronics and performance coatings segments. All production follows strict batch recording for traceability to downstream functional testing and certifications.

    Industry compliance standards

    • ISO 9001:2015-certified QC protocols
    • RoHS Directive 2011/65/EU for electronic applications
    • UL 94 Flame Retardancy Standard (where used in coatings/polymer insulation)
    • TSCA compliance for polymer raw materials in North America

    Typical usage ratio

    • Industrial polymerizations utilize this intermediate at 0.5–4% weight percentage, adjusted for desired degree of fluorination and end-use performance testing.

    Downstream process integration

    • Integrated in main monomer batch feed or used during post-polymerization modification steps. Introduced under precisely monitored temperature and agitation for uniform distribution within polymer chains.

    Final product types

    • Fluorinated acrylic copolymers for anti-graffiti coatings
    • Hydrophobic surface-active agents in electronics encapsulation resins
    • Damping materials for automotive component housings
    • Protective films with UV and chemical resistance

    4. Organic Electronics & Advanced Materials

    Advanced materials developers leverage this raw material for synthesizing fluorinated compounds used in organic thin films, OLEDs, and optoelectronic devices. It directly contributes to improved material charge mobility, moisture resistance, and processability. Applications require documented low-residual solvents and comprehensive spectral data to confirm purity for electronic-grade materials manufacturing.

    Industry compliance standards

    • IEC 61249-2-21 (Requirements for base materials used in electronic components)
    • IPC-4101D for plastic laminate sheets
    • ISO/TS 80004-8:2013 for nano-enabled electronic materials
    • REACH registration for supplied advanced monomers

    Typical usage ratio

    • Utilization varies from 1.0% to 7.5% by mol for functional layer synthesis, depending on the desired fluorination level in the functional polymeric or small-molecule organic layer.

    Downstream process integration

    • Added during advanced organic synthesis, typically preceding vacuum deposition or solution casting. Key for introducing pentafluorinated aromatic segments into the polymer or small molecule backbone.

    Final product types

    • Charge transport layers in OLED display fabrication
    • Moisture-resistant dielectric coatings for flexible circuits
    • Organic photovoltaic active materials
    • Nano-structured interface modifiers for printed electronics
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