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3'-(Trifluoromethyl)Acetophenone

    • Product Name 3'-(Trifluoromethyl)Acetophenone
    • Einecs 214-129-6
    • 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
    VTB
    Specifications

    HS Code

    782068

    Cas Number 14309-87-6
    Molecular Formula C9H7F3O
    Molecular Weight 188.15
    Iupac Name 1-[3-(trifluoromethyl)phenyl]ethan-1-one
    Appearance Colorless to pale yellow liquid
    Boiling Point 92-94 °C at 17 mmHg
    Melting Point -10 °C
    Density 1.217 g/cm3 at 25 °C
    Refractive Index 1.4740-1.4760
    Solubility Insoluble in water, soluble in organic solvents
    Purity Typically >98%
    Smiles CC(=O)C1=CC(=CC=C1)C(F)(F)F

    As an accredited 3'-(Trifluoromethyl)Acetophenone 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 screw cap containing 25 grams of 3'-(Trifluoromethyl)Acetophenone, labeled with chemical name, hazard symbols, and batch number.
    Shipping 3'-(Trifluoromethyl)Acetophenone is shipped in sealed, chemical-resistant containers compliant with international safety regulations. Packaging ensures protection from moisture and light, with clear hazard labeling. Transport follows guidelines for flammable organic compounds. Temperature is controlled as required, and all documentation, including Safety Data Sheets (SDS), accompanies the shipment for safe handling and receipt.
    Storage Store **3'-(Trifluoromethyl)acetophenone** in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep out of direct sunlight and moisture. Use appropriate chemical-resistant gloves and safety goggles when handling. Ensure proper labeling and follow all local regulations for storage of organic chemicals.
    Application of 3'-(Trifluoromethyl)Acetophenone

    Applications of 3'-(Trifluoromethyl)Acetophenone in Industrial Manufacturing

    As the direct manufacturer of 3'-(Trifluoromethyl)Acetophenone, we serve leading industrial partners across multiple sectors where stringent material sourcing and precision chemical integration are imperative. Below, we present key application areas, each demonstrating specialized requirements in regulatory compliance, formulation, production methodology, and downstream product development.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies source this material as a building block for synthesizing fluorinated APIs, particularly within anti-inflammatory, antiviral, and central nervous system (CNS) therapeutic classes. Its incorporation typically takes place early in multi-step organic synthesis, where electronic and lipophilic modification via the trifluoromethyl group directly impacts the pharmacological profile and metabolic stability of the target compound. Manufacturing sites must validate trace impurities and thoroughly document batch production processes to meet global regulatory demands.

    Industry compliance standards

    • ICH Q7 - Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • China Pharmacopoeia (ChP)
    • EU EudraLex Volume 4

    Typical usage ratio

    • 10%–30% molar equivalence in coupling reactions, adjusted based on the specific target’s synthetic route and desired yield

    Downstream process integration

    • Merged in the key step of aromatic fluorination or ketone functionalization during multi-step batch or continuous-flow synthesis of APIs

    Final product types

    • Trifluoromethylated CNS drugs
    • Novel anti-inflammatory agents
    • High-value pharmaceutical R&D intermediates
    • Preclinical drug candidates

    2. Agrochemical Intermediate for Herbicide and Pesticide Synthesis

    Agrochemical formulators utilize this intermediate chiefly for the preparation of advanced fluorinated herbicides and fungicides, which require precise fluorine placement to achieve target bioactivity and environmental persistence. During large-scale synthesis, technicians add it during the acylation or aromatic substitution stage, often requiring on-site purification and waste management controls to comply with environmental discharge limits and product registration guidelines.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)
    • REACH (EC 1907/2006) registration for chemical intermediates
    • China National Standards for Agrochemical Products (GB)

    Typical usage ratio

    • 5%–15% by mass as a precursor in the synthetic pathway, depending on product selectivity and downstream derivatization needs

    Downstream process integration

    • Introduced in catalytic coupling or Friedel–Crafts acylation steps, followed by downstream derivatization and formulation for field applications

    Final product types

    • Selective pre-emergent and post-emergent herbicides
    • Trifluoromethylated fungicides
    • Crop-protection intermediates for global markets
    • Seed coating and soil treatment solutions

    3. Specialty Chemical Synthesis for Liquid Crystal Materials

    Manufacturers of advanced display technologies incorporate this raw material for the design of liquid crystal (LC) compounds used in TFT-LCD and OLED displays. The introduction of the trifluoromethyl aromatic segment imparts distinct dielectric and phase-transition characteristics vital to screen performance and energy consumption. Production teams control addition during the primary condensation or aromatic substitution phase within restricted-access cleanrooms.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for Electronic Materials
    • RoHS Directive 2011/65/EU (for restriction of hazardous substances in electronics)
    • JEDEC JESD 625B Contamination Control Program
    • IPC-4101B for base materials in electronic assemblies

    Typical usage ratio

    • 2%–6% by weight, depending on desired optical anisotropy and LC viscosity

    Downstream process integration

    • Participates in the main aromatic core building stage, followed by purification and blending into bespoke LC mixtures for direct use in panel manufacturing

    Final product types

    • TFT-LCD liquid crystal mixtures
    • OLED precursor compounds
    • High-resolution display panel chemicals
    • Advanced optical films

    4. Fine Fragrance and Aromatic Chemicals Development

    Fragrance compounders include this acetophenone derivative during top-note and heart-note molecule synthesis, leveraging the unique sensory profile introduced by the trifluoromethyl group. Processing typically happens within regulated fragrance laboratories, focusing on purity, stability, and compliance with international fragrance ingredient safety standards, followed by robust quality control during blending for end-user products.

    Industry compliance standards

    • IFRA (International Fragrance Association) Safety Standards
    • EU Cosmetics Regulation (EC) No. 1223/2009
    • US FDA Title 21 CFR for Fragrance Ingredients
    • REACH Annex XVII for restricted substances in consumer products

    Typical usage ratio

    • Up to 3% by mass for aroma modification, dynamically adjusted during sensory evaluation and in line with regulatory thresholds

    Downstream process integration

    • Blended during the mid-stage of aroma molecule synthesis and integrated into bulk fragrance concentrates, then passed to compounding for branded product development

    Final product types

    • Luxury fine fragrances for personal care
    • Specialty aroma compounds for candles
    • Perfumer’s intermediate blends
    • Premium air freshener formulations
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