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4-Bromo-2-Fluorobenzotrifluoride

    • Product Name 4-Bromo-2-Fluorobenzotrifluoride
    • Alias 4-Bromo-2-fluoro-1-(trifluoromethyl)benzene
    • Einecs 624-306-5
    • 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

    755465

    Cas Number 401-89-8
    Molecular Formula C7H3BrF4
    Molecular Weight 243.00 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 153-156 °C
    Melting Point -5 °C
    Density 1.66 g/cm³ at 25 °C
    Purity 98% (typical)
    Refractive Index 1.486
    Flash Point 64 °C
    Solubility Insoluble in water
    Smiles FC1=CC=C(C(F)(F)F)C=C1Br
    Synonyms 2-Fluoro-4-bromobenzotrifluoride
    Ec Number 254-839-2
    Un Number 3272

    As an accredited 4-Bromo-2-Fluorobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 4-Bromo-2-Fluorobenzotrifluoride is supplied in a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 4-Bromo-2-Fluorobenzotrifluoride is shipped in compliance with chemical safety regulations. It is securely packaged in sealed containers to prevent leaks and is labeled as hazardous material. Shipping is typically by ground or air, subject to availability, and requires appropriate documentation and handling by trained personnel to ensure safe transport.
    Storage 4-Bromo-2-Fluorobenzotrifluoride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep away from sources of ignition and heat. Ensure proper labeling and prevent exposure to moisture. Store at room temperature and follow all standard chemical storage protocols for hazardous materials.
    Application of 4-Bromo-2-Fluorobenzotrifluoride

    Applications of 4-Bromo-2-Fluorobenzotrifluoride in Industrial Manufacturing

    As an experienced manufacturer of specialty fluoroaromatic intermediates, we supply 4-Bromo-2-Fluorobenzotrifluoride for targeted downstream applications in the agrochemical, pharmaceutical, electronics, and polymer sectors. Each industrial use reflects stringent compliance, process demands, and finished product standards unique to its field.

    1. Synthesis of Agrochemical Active Ingredients

    This material acts as a crucial halogenated intermediate for selective herbicides and fungicides. It enables the construction of trifluoromethyl-substituted aromatic cores favored in modern crop protection, enhancing bioactivity and environmental stability. Agrochemical manufacturers incorporate this compound in multi-step syntheses requiring high purity materials and reproducible reactivity.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Intermediates
    • ISO 9001-certified quality management for synthesis and traceability
    • REACH Regulation (EC) No. 1907/2006 for chemical safety and registration in the EU
    • US EPA TSCA Inventory Listing

    Typical usage ratio

    • 10–25% by input weight in the targeted halogen-exchange or nucleophilic aromatic substitution stage, adjusted for specific pathway requirements and downstream functionalization steps

    Downstream process integration

    • Feeds directly into Grignard or palladium-catalyzed coupling for aryl-substituted pesticide scaffolds
    • Subjected to selective nucleophilic or oxidative substitutions
    • Requires controlled addition to minimize competing side reactions

    Final product types

    • Trifluoromethyl-substituted phenoxy herbicides
    • New-generation cereal fungicide actives
    • Intermediate blocks for cereal and soybean protection chemicals

    2. Pharmaceutical Intermediate for API Synthesis

    This compound serves as a building block for pharmaceutical companies producing advanced intermediates and APIs containing trifluoromethyl aromatic motifs. Its presence introduces metabolic stability and favorable ADMET properties, crucial for today’s oncology, anti-inflammatory, and CNS therapies. Pharmaceutical process chemists demand batch consistency, regulatory traceability, and controlled impurity profiles.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for API intermediates
    • European Pharmacopoeia (Ph. Eur.) monograph for fluorinated building blocks
    • US FDA Drug Master File (DMF) registration procedures
    • Controlled Substance Act compliance when used in regulated compounds

    Typical usage ratio

    • 15–40% of stage input, determined by stoichiometry of coupling reactions or halogen exchange, and further adjusted for scalability in pilot and commercial manufacturing

    Downstream process integration

    • Introduced at the initial aromatic functionalization step in multi-step synthesis
    • Undergoes Suzuki, Sonogashira, or Buchwald-Hartwig cross-coupling for side-chain installation
    • Requires solvent and temperature management for API impurity control

    Final product types

    • Pre-cursor intermediates for fluorinated kinase inhibitors
    • Active pharmaceutical ingredients for targeted cancer therapy
    • Raw materials for CNS and anti-viral medicines

    3. Advanced Electronic Chemicals Production

    Electronic chemical manufacturers use this raw material to synthesize specialty materials for photoresist components and other semiconductor process chemicals. The trifluoromethyl and halogen functionalities improve electronic performance and etch resistance, which are vital for photolithography and IC fabrication. The material must meet semiconductor-grade requirements for purity and particle content.

    Industry compliance standards

    • SEMI C93-0819 Specification for Electronic Grade Organics
    • ISO 9001:2015 for process documentation and lot traceability
    • RoHS Directive 2011/65/EU for heavy metal and halogen content
    • Chinese GB/T 31464-2015 for chemical purity in chip manufacturing

    Typical usage ratio

    • 2–8% in functional monomer or photoactive compound mixtures, adjusted by desired resist profile and film thickness

    Downstream process integration

    • Enters organometallic or metal-free coupling steps for producing advanced resist functionalities
    • Requires contamination controls in cleanroom blending and purification
    • Often recrystallized or vacuum distilled for critical electronic applications

    Final product types

    • Photoresist monomers and oligomers
    • Dielectric layer additives for flat panel displays
    • Etch-resistant coatings for integrated circuits

    4. High-Performance Polymer Synthesis

    In the polymer industry, this fluorinated benzotrifluoride acts as a halogenated aromatic monomer for specialty engineering polymers. Its structure imparts high chemical resistance and low surface energy, preferred in fluoropolymer blends. Manufacturers require tight control over material properties and impurity levels to meet end-user reliability demands.

    Industry compliance standards

    • ASTM D5676 for aromatic monomer purity verification
    • ISO 14001 for environmental management during polymer synthesis
    • EU REACH listing for monomers in plastics
    • UL 94 for final polymer fire resistance if used in electronics applications

    Typical usage ratio

    • 3–12% of total monomer input for copolymerization, adjusted for target polymer architecture and mechanical property demands

    Downstream process integration

    • Added during solution or emulsion polymerization with comonomers such as styrene, acrylates, or other fluorinated aromatics
    • Feeds directly to chain extension or crosslinking reactions
    • Requires precise dosing to control molecular weight and end-group functionality

    Final product types

    • Fluorinated engineering plastics
    • Low-energy coatings for industrial equipment
    • Specialty films for chemical process industry

    5. Fine Chemical and Specialty Intermediate Production

    Producers in the fine chemicals sector implement this compound for building customized molecules with trifluoromethyl and halogen patterns. These intermediates support varied synthesis routes in pigments, liquid crystals, and advanced materials requiring precise molecular architecture. Material purity and analytical documentation are essential for multi-industry supply.

    Industry compliance standards

    • ISO 17025-accredited analytical protocols for batch release
    • GMP manufacturing where applicable to intermediary supply
    • Specific Standard Operating Procedures (SOPs) for documentation
    • REACH pre-registration for targeted volume and European market compliance

    Typical usage ratio

    • 5–18% depending on target molecule complexity, synthetic pathway, and overall chemical conversion efficiency

    Downstream process integration

    • Participates in stepwise halogen exchange, nucleophilic aromatic substitution, or palladium-catalyzed cross-couplings
    • Further functionalization may include oxidation, reduction, or coupling with advanced nucleophiles
    • Blending and purification involve column chromatography or vacuum stripping

    Final product types

    • Intermediates for specialty pigments and liquid crystals
    • Halogenated aromatic compounds for research laboratories
    • Fine chemical blocks for advanced performance materials
    Free Quote

    Competitive 4-Bromo-2-Fluorobenzotrifluoride prices that fit your budget—flexible terms and customized quotes for every order.

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