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(2-Trifluoromethyl-Benzoimidazol-1-Yl)-Acetic Acid

    • Product Name (2-Trifluoromethyl-Benzoimidazol-1-Yl)-Acetic Acid
    • Alias CF3-BzImAcOH
    • Einecs 624-682-5
    • 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
    VTB
    Specifications

    HS Code

    225988

    Chemical Name (2-Trifluoromethyl-Benzoimidazol-1-Yl)-Acetic Acid
    Molecular Formula C10H7F3N2O2
    Molecular Weight 244.17 g/mol
    Appearance White to off-white powder
    Cas Number 104010-37-7
    Purity Typically ≥98%
    Melting Point 175-178°C
    Solubility Slightly soluble in water, soluble in DMSO and methanol
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Smiles FC(F)(F)c1cc2n(cnc2cc1)CC(=O)O

    As an accredited (2-Trifluoromethyl-Benzoimidazol-1-Yl)-Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5g package features a sealed amber glass bottle, labeled with chemical name, purity, batch number, and hazard warnings for safe handling.
    Shipping (2-Trifluoromethyl-Benzoimidazol-1-Yl)-Acetic Acid is shipped in secure, airtight containers to prevent contamination and moisture absorption. It should be handled as a chemical product, complying with relevant safety regulations. The package is labeled with hazard information and shipped by certified carriers, ensuring safe and prompt delivery to laboratory or industrial destinations.
    Storage (2-Trifluoromethyl-Benzoimidazol-1-yl)-Acetic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep at room temperature (15–25°C). Protect from moisture and heat. Ensure proper chemical labeling and access is restricted to trained personnel in a laboratory or chemical storage facility.
    Application of (2-Trifluoromethyl-Benzoimidazol-1-Yl)-Acetic Acid

    Applications of (2-Trifluoromethyl-Benzoimidazol-1-Yl)-Acetic Acid in Industrial Manufacturing

    (2-Trifluoromethyl-Benzoimidazol-1-Yl)-Acetic Acid serves as a specialized intermediate and functional building block across tightly defined industrial sectors. Our production meets large-volume and niche requirements in the pharmaceutical, agrochemical, specialty polymer, advanced electronics, and dye manufacturing value chains. Each downstream application employs this material under unique regulatory, ratio, and process constraints to achieve specific product quality and performance outcomes.

    1. API Intermediate for Antifungal Pharmaceutical Synthesis

    This molecule plays a key role as an intermediate in the synthesis of triazole or benzimidazole-derived antifungal medications. Downstream pharmaceutical manufacturers apply it in direct amidation or N-alkylation steps to construct complex active pharmaceutical ingredients (APIs) targeting fungal cell wall biosynthesis. Precise purity management and process analytics ensure consistent conversion rates and compound integrity during batch or continuous flow production.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (U.S. FDA GMP for drugs)
    • Chinese Pharmacopoeia (ChP) strict impurity limits
    • EU EudraLex Volume 4 for GMP standards

    Typical usage ratio

    • 10–25% molar equivalent, adjusted by target API route and yield optimization
    • Excess reagent may be used for reaction completion and then removed during purification

    Downstream process integration

    • Charged into reaction vessels during key coupling and cyclization steps
    • Inline and at-line QC monitoring for residual intermediates and by-products
    • Solvent selection tailored for scale-up and impurity control
    • Material handled under validated cleaning and containment protocols

    Final product types

    • Oral and topical antifungal tablets
    • Injectable antifungal preparations
    • Veterinary antifungal suspensions
    • Solid oral controlled-release antifungal formulations

    2. Herbicide and Fungicide Agrochemical Intermediate

    Within the agrochemical industry, downstream formulators utilize this substance as an intermediate during the multi-step synthesis of heteroaryl-acetic acid herbicides and crop protection agents. These include products with selective activity against fungal infestations or broadleaf weed species. Rigid control of reaction conditions and impurity profiles is essential to comply with agricultural chemical legislation.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications & Evaluations
    • ISO 17025 for laboratory testing traceability
    • Chinese Ministry of Agriculture (GB 2763) pesticide residue limits
    • European Regulation (EC) No 1107/2009—plant protection product standards

    Typical usage ratio

    • 5–18% mole fraction, precisely adjusted based on target active ingredient yield
    • Stoichiometry calibrated according to downstream scale and specific herbicide synthesis

    Downstream process integration

    • Used as a core structure in stepwise N-acylation and condensation reactions
    • Feeds directly into multi-kilogram batch syntheses under inert atmosphere
    • Quality assurance monitoring for halogenated by-products and unreacted intermediates
    • Incorporated at the penultimate synthetic step to maximize conversion

    Final product types

    • Selective herbicide granules
    • Emulsifiable fungicide concentrates
    • Suspension concentrates for crop protection
    • Ready-to-use foliar spray pesticides

    3. Specialty Polymer Modification Additive

    Formulators in the specialty polymer sector add this compound as a modifying monomer or end-group blocker to municipal-grade and electronic-grade polymer chains. Its incorporation provides fluorinated and benzimidazole moieties, improving polymer dielectric properties, hydrophobicity, and resistance to aggressive chemicals. Batch consistency is vital to enable high performance in completed resins, membranes, or engineered plastics.

    Industry compliance standards

    • ASTM D638 (Polymer tensile property requirements)
    • REACH Annex XVII (European Registration, Evaluation, Authorisation & Restriction of Chemicals restrictions)
    • RoHS Directive 2011/65/EU for electronics applications
    • UL Yellow Card – Fire and electrical performance safety for plastics

    Typical usage ratio

    • 0.5–3.5% by weight in custom polymer blends
    • Exact loadings determined by desired functionalization and application-specific properties
    • Small-scale pilot runs to optimize mechanical and electrical targets

    Downstream process integration

    • Dosed into polymerization reactors as co-monomer or terminal chain modifier
    • Mixing and dispersion calibrated to avoid raw material agglomeration
    • Monitored with real-time FTIR and NMR to confirm functional group incorporation
    • Controlled cooling and curing cycles to minimize volatility loss

    Final product types

    • High-voltage insulating films
    • Perfluorinated resin-based membranes
    • Chemically resistant engineering thermoplastics
    • Antistatic or hydrophobic coatings for electronics and medical plastics

    4. Intermediate for High-Performance Organic Electronic Materials

    Leading-edge electronics and display manufacturers utilize this molecule as a critical intermediate in the fabrication of organic semiconductors and functional dyes for OLED and photovoltaic devices. The trifluoromethyl group and benzimidazole linkage impart specific charge transport and thermal stability attributes. Stringent process management and trace-level purity control are enforced to prevent contaminant introduction in cleanroom environments.

    Industry compliance standards

    • IEC 62631 — Electrical insulation materials for electronics
    • IATF 16949:2016 (Automotive electronics supplier requirements)
    • ISO 9001:2015 for electronic material manufacturing
    • SEMATECH Guidelines for electronic chemical purity

    Typical usage ratio

    • 1.0–8.0% relative to target dye or semiconductor precursor
    • Adjustment based on required charge carrier mobility and color properties
    • Pilot-scale screening to validate optoelectronic performance

    Downstream process integration

    • Introduced at dye coupling or acylation steps in organic semiconductor synthesis
    • Solid-liquid blending conducted in nitrogen-filled glove boxes
    • Material traceability maintained throughout multilayer device stack assembly
    • In-line purity checks for metallic and organic contamination below parts-per-million levels

    Final product types

    • OLED emitter or transport layers for next-generation displays
    • Organic photovoltaic active layers
    • Photoresist dyes for semiconductor lithography
    • Thin-film transistor substrates

    5. Intermediate for Performance Dye and Pigment Manufacturing

    Producers in the high-performance dye and pigment industry employ this intermediate to introduce the trifluoromethyl-benzimidazole unit into specialty colorant molecules. These target enhanced photostability, solvent resistance, and specific wavelength absorption for use in coatings, plastics, and textile applications. Process reproducibility and impurity limitation are rigorously managed to deliver consistent color and performance attributes at scale.

    Industry compliance standards

    • ETAD Code of Ethics for dye and pigment manufacturers
    • EN 71-3 (Toy safety — migration of certain elements in colored coatings)
    • REACH Annex XVII and SVHC requirements
    • SQB Certification for regulated pigment usage in textiles and plastics

    Typical usage ratio

    • 2–10% weight percent in downstream pigment synthesis
    • Batch scale and target chromatic properties determine loading
    • QC feedback loop guides continuous ratio refinement

    Downstream process integration

    • Condensation or diazotization step for performance pigment core construction
    • Integration with chromophore extension and stabilization agents
    • Material dosing automated via gravimetric feeders in pigment reactors
    • Final color properties validated with spectroscopic and accelerated weathering tests

    Final product types

    • UV-stable automotive coatings
    • Plastic compounding pigments
    • Technical printing inks
    • Outdoor textile colorants
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