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3-(Trifluoromethyl)Phenacyl Bromide

    • Product Name 3-(Trifluoromethyl)Phenacyl Bromide
    • Alias TFMPB
    • Einecs 236-012-8
    • 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

    111352

    Chemical Name 3-(Trifluoromethyl)Phenacyl Bromide
    Cas Number 349-15-5
    Molecular Formula C9H6BrF3O
    Molecular Weight 267.04
    Appearance White to off-white crystalline powder
    Purity Typically ≥98%
    Melting Point 52-56 °C
    Boiling Point No data (decomposes)
    Solubility Soluble in organic solvents such as dichloromethane and ethanol
    Density 1.69 g/cm³
    Synonyms 2-Bromo-1-[3-(trifluoromethyl)phenyl]ethanone
    Storage Conditions Store in a cool, dry place, tightly closed
    Hazard Statements Causes skin and eye irritation
    Ec Number 206-477-3

    As an accredited 3-(Trifluoromethyl)Phenacyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 3-(Trifluoromethyl)Phenacyl Bromide is packaged in a tightly sealed amber glass bottle with a hazard label.
    Shipping 3-(Trifluoromethyl)Phenacyl Bromide is shipped in tightly sealed, chemically resistant containers to prevent moisture and light exposure. It is classified as a hazardous material and handled under applicable transport regulations, including proper labeling and documentation. Shipments are typically made via certified couriers with special handling for hazardous chemicals to ensure safety and compliance.
    Storage 3-(Trifluoromethyl)phenacyl bromide should be stored in a cool, dry, and well-ventilated area, away from sources of heat and incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and protect it from light and moisture. Store it in a designated flammable or chemical storage cabinet and label the container clearly to ensure safe handling and access.
    Application of 3-(Trifluoromethyl)Phenacyl Bromide

    Applications of 3-(Trifluoromethyl)Phenacyl Bromide in Industrial Manufacturing

    3-(Trifluoromethyl)Phenacyl Bromide serves as a high-value synthetic intermediate in the chemical industry. Our factory supplies this material for a range of specialized downstream sectors, supporting fine and industrial chemical manufacturing globally. Below we detail its primary industrial applications, regulatory environment, and typical integration parameters.

    1. Pharmaceutical Intermediate in Antifungal API Synthesis

    Many pharmaceutical manufacturers use this compound as a key intermediate for producing triazole-based antifungal active pharmaceutical ingredients. The reactivity of the trifluoromethyl and bromo moieties enables efficient substitution and cyclization reactions in multi-step synthesis of pharmaceutical actives, including fluconazole derivatives and related triazoles. Production adheres to strict quality control and regulatory compliance for APIs, with process controls at each stage to minimize impurities and ensure traceability through to the final formulated drug.

    Industry compliance standards

    • ICH Q7A for good manufacturing practice in active pharmaceutical ingredient production
    • Current Good Manufacturing Practice (cGMP, 21 CFR Part 210/211, US FDA)
    • European Pharmacopoeia (Ph. Eur.) monographs for triazole-based APIs
    • REACH Regulation (EC 1907/2006) for chemical safety in Europe

    Typical usage ratio

    • Applied at 0.8–1.5 molar equivalents relative to the targeted API intermediate, adjusted according to yield optimization in each batch scale

    Downstream process integration

    • Weigh and add into the main condensation or alkylation step under controlled pH and temperature, followed by work-up and purification steps compliant with GMP documentation

    Final product types

    • Fluconazole and its analogs
    • Voriconazole pre-intermediates
    • Research-grade triazole standards
    • Commercial triazole antifungal APIs

    2. Agrochemical Synthesis: Triazole Fungicides

    This compound acts as a core building block for the agrochemical sector, especially in the synthesis of triazole fungicides such as flutriafol, cyproconazole, and similar crop protection chemicals. Its high electrophilicity allows for clean incorporation into the heterocyclic structures required for potent systemic fungicides, supporting large-scale, cost-efficient agrochemical manufacturing with strict supply chain traceability.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 for process and quality management systems
    • REACH (EC 1907/2006) for approved agricultural intermediates
    • OECD Guidelines for the Testing of Chemicals (Pesticide Active Ingredients)

    Typical usage ratio

    • Concentration ranges between 1.0–2.3 molar equivalents per batch, with adjustments based on the specific fungicide structure and downstream conversion rates

    Downstream process integration

    • Charged into the initial ring-forming step or as an electrophilic reactant in key coupling reactions; process monitored for stage purity and compliance with effluent controls

    Final product types

    • Technical grade triazole fungicidal concentrates
    • Formulated crop protection products (emulsifiable concentrates, suspension concentrates)
    • Seed treatment chemicals
    • Blends for broad-spectrum antifungal protection in cereal and fruit crops

    3. Specialty Dye Intermediate for Fluorescent Markers

    Manufacturers of specialty fluorescent dyes incorporate this trifluoromethyl phenacyl bromide as a selective reagent for functional group modifications during dye precursor synthesis. The compound’s high reactivity with nucleophilic aromatic substrates enables fine-tuned dye spectral properties, supporting product development in life sciences, textile tracing, and analytical chemistry where label performance and signal intensity are critical.

    Industry compliance standards

    • ISO 9001:2015 quality management for dye manufacturing
    • EN 71-3 for chemical safety in toy and textile dyes (where applicable)
    • RoHS Directive 2011/65/EU for restricted hazardous substances (for electronic tracer dyes)
    • GLP (Good Laboratory Practice) certification for analytical dye products

    Typical usage ratio

    • Used at 0.5–1.0 molar equivalent relative to dye core molecules; adjusted per chromophore structure and desired fluorescence yield

    Downstream process integration

    • Introduced at the functionalization or side-chain modification step, often via phase-transfer or organic solvent systems with controlled temperature and reaction time

    Final product types

    • Fluorescent dyes for HPLC and microscopy
    • Textile marking reagents
    • Biochemical fluorescent labeling compounds
    • Tracer dyes for environmental and water flow studies

    4. Fine Chemical Intermediate in Benzophenone Derivative Synthesis

    Chemical manufacturers utilize this compound as a precursor in the preparation of benzophenone derivatives and related fine chemicals. The compound enters Friedel-Crafts acylation or nucleophilic substitution reactions, providing a trifluoromethyl-substituted aromatic scaffold for downstream use in UV absorbers, photoinitiators, and specialty polymer additives. Stringent process protocols ensure purity and lot traceability at each transformation stage.

    Industry compliance standards

    • ISO 14001 for environmental management in chemical handling
    • ISO 9001:2015 certification for quality assurance
    • Chemical Facility Anti-Terrorism Standards (CFATS, US Department of Homeland Security) for precursor chemicals
    • EU Regulation (EC) 1272/2008 (CLP) for hazard classification and labeling

    Typical usage ratio

    • Formulated at 1.2–1.8 molar equivalents depending on desired substitution level in benzophenone target molecules

    Downstream process integration

    • Dosed into batch or continuous reactors during controlled acylation and subsequent purification process; continuous QC ensures correct structure and minimal byproducts

    Final product types

    • UV absorber additives (for polymers and coatings)
    • Photoinitiators for inks and adhesives
    • Benzophenone photo-crosslinking agents
    • Intermediate resins for specialty plastics
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