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4-(Trifluoromethyl)Phenacyl Bromide

    • Product Name 4-(Trifluoromethyl)Phenacyl Bromide
    • Alias p-(Trifluoromethyl)phenacyl bromide
    • Einecs 239-272-3
    • 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

    164240

    Chemicalname 4-(Trifluoromethyl)Phenacyl Bromide
    Casnumber 1535-73-5
    Molecularformula C9H6BrF3O
    Molecularweight 267.04
    Appearance White to light yellow crystalline powder
    Meltingpoint 71-75°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.64 g/cm³
    Purity Typically >98%
    Smiles C1=CC(=CC=C1C(=O)CBr)C(F)(F)F
    Inchi InChI=1S/C9H6BrF3O/c10-6-9(14)7-3-1-2-5-8(7)4-11(12,13)15/h1-3,5H,4,6H2

    As an accredited 4-(Trifluoromethyl)Phenacyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 4-(Trifluoromethyl)Phenacyl Bromide, labeled with hazard warnings and chemical information.
    Shipping 4-(Trifluoromethyl)Phenacyl Bromide is shipped in secure, airtight containers to prevent moisture and light exposure. It is classified as hazardous and must be transported with appropriate labeling, documentation, and within regulatory guidelines for chemicals. Shipping typically requires temperature control and limited handling to ensure safety and product integrity.
    Storage 4-(Trifluoromethyl)Phenacyl Bromide should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong bases and oxidizers. Store at 2–8 °C (refrigerator). It should be clearly labeled as toxic and irritant, and handled only in a chemical fume hood with proper protective equipment.
    Application of 4-(Trifluoromethyl)Phenacyl Bromide

    Applications of 4-(Trifluoromethyl)Phenacyl Bromide in Industrial Manufacturing

    As a specialized manufacturer of 4-(Trifluoromethyl)Phenacyl Bromide (TFMPB), we supply this fine chemical to several integral segments of the chemical and pharmaceutical industries. Below are its established applications, based on established customer usage patterns and regulatory environments worldwide.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers leverage TFMPB as a critical α,β-unsaturated ketone intermediate in multi-step syntheses for various APIs, particularly in anti-inflammatory and central nervous system drug development. Its para-trifluoromethyl group offers electron-withdrawing properties essential for constructing molecular scaffolds with high activity, streamlining subsequent transformations and improving target selectivity. TFMPB is most often integrated during condensation and coupling steps, requiring strict process and quality control throughout.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA requirements)
    • European Pharmacopoeia (Ph. Eur.) monograph references for starting materials
    • Chinese Pharmacopoeia Chapter V standards for process intermediates

    Typical usage ratio

    • Batch processes typically introduce TFMPB at 0.5–1.5 molar equivalents relative to the key amine or nucleophile substrate. Labs adjust charge based on yield optimization and target impurity profile.

    Downstream process integration

    • TFMPB enters the synthetic route post-halogenation or aromatic substitution and participates in Friedel-Crafts alkylations or nucleophilic substitutions under controlled thermal reaction conditions. Purification occurs after intermediate isolation, prior to final assembly or cyclization.

    Final product types

    • Nonsteroidal anti-inflammatory drug (NSAID) intermediates
    • Central nervous system (CNS) active APIs
    • Specialty pharmaceutical building blocks for oncology drugs

    2. Agrochemical Intermediate Production

    TFMPB is a favored synthetic block in the crop protection industry, particularly for the creation of fluorinated ketone structures in insecticide and herbicidal compound pipelines. The introduction of the trifluoromethyl group into the molecular backbone enhances metabolic stability and field persistence, answering regulatory and agronomic requirements for efficacy and environmental behavior. Production lines commonly handle this compound in intermediate coupling steps with precision to prevent side product formation and ensure downstream yield.

    Industry compliance standards

    • ISO 9001:2015 quality management systems
    • FAO/WHO specifications for pesticide manufacturing
    • OECD GLP (Good Laboratory Practice) for chemistry studies
    • Local environmental authority regulations on fluorinated materials

    Typical usage ratio

    • Standard processes utilize 0.7–1.2 equivalents relative to the alkylation or condensation partner; process development adjusts this ratio for structural diversity or impurity minimization.

    Downstream process integration

    • Integrated into stepwise fluorination or phenacylation reactions early in synthesis chains, often prior to halogen exchange or heterocycle formation. Process requires efficient solvent control to comply with waste minimization regulations.

    Final product types

    • Selective insecticide precursors
    • Herbicide intermediates containing trifluoromethyl moieties
    • Stabilizers for fungicides and pesticidal actives

    3. Fluorinated Dye and Pigment Manufacture

    Chemical producers use TFMPB as a key functional group donor for synthesizing specialty dyes and pigments with enhanced photostability. Its molecular structure introduces electron-withdrawing effects that enable formulating colorants with long-term resistance to fading and degradation under UV exposure. Such dyes meet industrial textile and printing requirements where resistance to extreme light and chemical environments is critical.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textile dyes and finishes)
    • ISO 14001:2015 for environmental management
    • REACH Annex XVII restrictions on hazardous dye intermediates
    • RoHS guidelines for electronics-compatible pigments

    Typical usage ratio

    • Scale-up productions typically dose 1.0–1.3 equivalents as the primary arylating agent, with ratio tuning for target tint strength or solubility in finished formulations.

    Downstream process integration

    • TFMPB enters pigment synthesis at the nucleophilic acylation or condensation stage. Subsequent processing steps include high-temperature coupling, filtration, and crystallization for pure dye isolation.

    Final product types

    • High-fastness disperse dyes for polyester fibers
    • Specialty organic pigments for automotive coatings
    • Photostable printing inks for industrial packaging

    4. Fluorinated Analytical Reagent Synthesis

    Research chemical and diagnostic kit manufacturers select TFMPB to produce fluorinated carbonyl compounds serving as key derivatizing agents in GC and LC methods. Its strong electron-withdrawing effect helps create reagents that facilitate identification and quantitation of amines, amino acids, steroids, and other analytes through enhanced detection sensitivity. These compounds are especially relevant for regulated laboratories operating under quality benchmarks for trace analysis and clinical diagnostics.

    Industry compliance standards

    • ISO/IEC 17025 for chemical analysis laboratories
    • USP/NF monographs for analytical reagent grades
    • CLSI (Clinical and Laboratory Standards Institute) specifications
    • Pharmaceutical Analytical Method Validation Guidelines (e.g., ICH Q2(R1))

    Typical usage ratio

    • Lab and production batches add 0.8–1.5 equivalents depending on the analyte’s functional group density and desired derivatization efficiency; adjustments based on reaction time and analytical protocol.

    Downstream process integration

    • Used principally in the derivatization step prior to chromatographic analysis; typically followed by liquid–liquid extraction and purification via distillation or recrystallization.

    Final product types

    • GC and LC derivatization kits
    • Fluorinated analytical marker agents
    • Diagnostic reference standards for clinical and food analysis labs

    5. Specialty Polymer Modifier Synthesis

    Some advanced materials manufacturers utilize TFMPB for the synthesis of functional monomers and oligomers designed to impart fluorinated properties to specialty acrylics, urethanes, and epoxies. By introducing bulky and electronegative groups during the polymer precursor phase, end-use properties such as chemical resistance, weatherability, and surface energy are improved. These modifications are critical in producing engineered films, coatings, and laminates that operate in aggressive service environments, including electronics and aerospace applications.

    Industry compliance standards

    • ISO 9001 for quality management in polymer production
    • ASTM D256 for impact resistance testing
    • UL 94 for flame retardancy requirements (where applicable)
    • RoHS and REACH for restricted substance compliance

    Typical usage ratio

    • Modifier feed ratios generally fall between 0.2–0.8 molar equivalents, depending on targeted polymer end-group density and mechanical property enhancement profiles.

    Downstream process integration

    • TFMPB is introduced during oligomerization or monomer preparation by reaction with base polymer backbones under inert atmosphere. Crosslinking or copolymerization typically follows to lock in desirable performance attributes.

    Final product types

    • High-durability fluorinated coatings for automotive parts
    • Low surface energy laminates for electronics
    • UV-resistant polymer films for architectural glazing
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