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1-(2-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione

    • Product Name 1-(2-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione
    • Alias TFMPD
    • Einecs 629-035-6
    • 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

    703570

    Chemical Name 1-(2-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione
    Molecular Formula C11H6F3NO2
    Molecular Weight 241.17 g/mol
    Cas Number 134194-13-7
    Appearance White to off-white solid
    Melting Point 110-114°C
    Solubility Slightly soluble in polar organic solvents
    Purity Typically ≥98%
    Smiles FC(F)(F)c1ccccc1N2C(=O)C=CC2=O
    Inchi InChI=1S/C11H6F3NO2/c12-11(13,14)8-4-2-1-3-7(8)15-9(16)5-6-10(15)17/h1-6H
    Storage Condition Store in a cool, dry place, tightly closed

    As an accredited 1-(2-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled with chemical name, hazard symbols, and weight: 25 grams. Store cool, dry.
    Shipping Shipping of 1-(2-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione requires secure, airtight packaging, compliant with chemical safety regulations. The container should be clearly labeled with hazard information. Transport should be via certified carriers, protected from extreme temperatures and moisture, and accompanied by a Safety Data Sheet (SDS) to ensure proper handling and emergency response.
    Storage Store 1-(2-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers or bases. Ensure appropriate labeling and secondary containment. Use only in a chemical fume hood. Follow all relevant safety and storage protocols as specified by your institution or supplier.
    Application of 1-(2-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione

    Applications of 1-(2-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione in Industrial Manufacturing

    Our direct manufacturing facility produces 1-(2-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione supporting key segments in chemical process industries. Below we outline specific downstream application fields where this compound is incorporated according to validated industrial practice, covering compliance, formulation guidance, integration steps, and the end product focus for each manufacturing sector.

    1. High-Performance Polyimide Monomers for Advanced Electronics

    This raw material functions as a critical monomer precursor in synthesizing high-performance polyimides used in flexible electronic substrates, display components, and insulating films. Customers typically utilize it to impart superior thermal stability and chemical resistance needed for next-generation microelectronics.

    Industry compliance standards

    • IEC 61249-2-51:2017 (Requirements for Polyimide Films in Flexible Printed Circuit Boards)
    • RoHS 2015/863/EU (Restriction of Hazardous Substances Directive for electronics)
    • IPC-4101E (Requirements for Base Materials for Rigid and Multilayer Printed Boards)
    • ISO 9001 (Quality Management Systems in Electronic Materials Manufacturing)

    Typical usage ratio

    • 5–25 wt% in the dianhydride/diamine monomer feed blend, adjusted by desired film thickness and dielectric property target

    Downstream process integration

    • Introduced at the monomer blending phase before thermal imidization; precise dosing and mixing are managed by in-line dosing systems to meet lamination or casting requirements

    Final product types

    • Flexible printed circuits, polyimide flexible display substrates, insulation films for microelectronic packaging, coverlay films for automotive control units

    2. Specialty Agrochemical Intermediate Synthesis

    Producers of advanced crop-protection agents and specialty agro-intermediates use this compound as a nucleus for selective synthesis of triazole, pyrrole, and imide-based active ingredients. The molecular scaffold promotes both biological activity and environmental stability in the downstream actives.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC 1907/2006) for new chemical entity registration in Europe
    • China ICAMA pesticide production license standards
    • ISO 9001 (Agrochemical Manufacturing Quality)

    Typical usage ratio

    • 8–16 mol% as a core building block in key-step ring closure, with adjustments based on specific active substance design and synthetic route

    Downstream process integration

    • Charged at the heterocycle formation or functionalization stage, typically in batch or flow reactors; monitored via real-time HPLC or GC for conversion optimization

    Final product types

    • Herbicide and fungicide actives containing trifluoromethyl-phenyl-imide functionalities, other specialty agrochemical intermediates used in seed dressing and foliar sprays

    3. Advanced Organic Photovoltaic (OPV) Materials

    Manufacturers of organic solar films incorporate this compound in donor/acceptor semiconducting layers. Its electron-deficient structure and fluorinated aromatic system enhance the charge transport, leading to higher efficiency in flexible solar modules.

    Industry compliance standards

    • IEC 61215 (Photovoltaic module qualification standards)
    • RoHS (Directive 2011/65/EU for solar industry)
    • ISO 14001 (Environmental Management for photovoltaic chemical processing)
    • UL 1703 (Flat-Plate Photovoltaic Modules)

    Typical usage ratio

    • 1–10 wt% in OPV active layer formulation, optimized by target bandgap/charge mobility parameters and absorption characteristics

    Downstream process integration

    • Added during the solution-processing phase for bulk-heterojunction blends, followed by spin coating, drying, and lamination in controlled environments

    Final product types

    • Organic thin-film solar panels, flexible module rolls, integrated photovoltaic building materials

    4. Pharmaceutical Impurity Profiling and Reference Standard Sourcing

    In API and pharmaceutical finished product manufacturing, this compound is synthesized and supplied as an impurity reference material for regulatory submission and batch release quality assessments. Its unique structure provides a traceability marker for process validation studies in regulated pharmaceutical environments.

    Industry compliance standards

    • ICH Q3A/B (Impurities in New Drug Substances/Products)
    • USP/NF and EP (Pharmaceutical Reference Standard Requirements)
    • cGMP (21 CFR 210/211) for API and FDF manufacturing
    • ISO/IEC 17025 for analytical laboratories producing impurity reference materials

    Typical usage ratio

    • 0.01–0.20 wt% spiked for HPLC, GC, or LC-MS validation—ratio based on method sensitivity and regulatory guidance for impurity thresholds

    Downstream process integration

    • Dosed as a standard or process marker at the analytical quality control stage, including release testing and method validation for impurities and residuals

    Final product types

    • Pharmaceutical reference standards, research-grade impurity kits, internal QC analytical kits for multinational pharmaceutical companies

    5. Fluorinated Specialty Dye and Pigment Synthesis

    This compound serves as a key synthetic intermediate for the production of fluorine-containing dyes and pigments, which deliver enhanced lightfastness and solvent resistance, particularly needed in high-value printing, security inks, and specialty coatings.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile dye safety
    • EN 71-3 (Safety of toys—Migration of certain elements for pigment safety)
    • REACH Annex XVII (Restriction of hazardous aromatic amines in colorants)
    • ISO 18314-1 (Analytical methods for colorants in industrial applications)

    Typical usage ratio

    • 3–12 mol% in key coupling reactions and condensation steps, adjusted for desired chromophore yield and formulation depth

    Downstream process integration

    • Added to the main synthetic batch as a fluorinated core substrate; integrated into dye intermediate sequences with real-time colorimetric and purity monitoring

    Final product types

    • High-performance textile dyes, anti-counterfeit security pigments, fluorinated pigment dispersions for plastics and printing inks
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