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2,4,5-Trifluorobenzyl Bromide

    • Product Name 2,4,5-Trifluorobenzyl Bromide
    • Alias TFBB
    • Einecs 246-804-4
    • 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

    445575

    Product Name 2,4,5-Trifluorobenzyl Bromide
    Cas Number 1191-41-9
    Molecular Formula C7H4BrF3
    Molecular Weight 225.01
    Appearance Colorless to pale yellow liquid
    Boiling Point 79-81°C at 13 mmHg
    Density 1.632 g/cm3 at 25°C
    Refractive Index 1.5220
    Purity Typically ≥ 98%
    Smiles C1=C(C(=CC(=C1F)F)F)CBr
    Storage Conditions Store in a cool, dry place, tightly closed container
    Synonyms α-Bromo-2,4,5-trifluorotoluene

    As an accredited 2,4,5-Trifluorobenzyl Bromide 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, labeled “2,4,5-Trifluorobenzyl Bromide, 25g.” Includes hazard warnings and manufacturer details.
    Shipping 2,4,5-Trifluorobenzyl Bromide is shipped in tightly sealed containers to prevent leakage and exposure. It should be packaged according to hazardous materials regulations, typically under UN 3265, Class 8 (corrosive). The packaging must be clearly labeled and accompanied by appropriate safety documentation to ensure compliance with transport and safety standards.
    Storage Store 2,4,5-Trifluorobenzyl Bromide in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and bases. Keep the container tightly closed and protected from moisture and light. Use corrosion-resistant shelves and avoid exposure to heat sources. Clearly label storage containers and ensure appropriate spill containment and emergency procedures are in place.
    Application of 2,4,5-Trifluorobenzyl Bromide

    Applications of 2,4,5-Trifluorobenzyl Bromide in Industrial Manufacturing

    2,4,5-Trifluorobenzyl Bromide serves as a specialized intermediate across several high-value chemical sectors. Our manufacturing process ensures tight impurity control and consistent supply, responding directly to formulation, regulatory, and supply-chain priorities at industrial scale. Below are key downstream tracks where this raw material integrates into exacting manufacturing flows.

    1. Agrochemical Active Ingredients Synthesis

    This compound enters as a nucleophilic alkylating agent in the synthesis of specific triazole and pyridine-based fungicides and herbicides. Our customers formulate crop protection molecules requiring selective benzylation, where fluorine patterning enhances environmental stability and field performance. Processing occurs primarily during phase-transfer catalysis or with strong base deprotonation, followed by coupling with nitrogen-containing heterocycle cores. Full traceability and batch-to-batch consistency support field and export registrations across regulated markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • U.S. EPA 40 CFR Part 180 – Tolerances and Exemptions for Pesticide Chemical Residues
    • EU Regulation (EC) No. 1107/2009 (Plant Protection Products)
    • ISO 17034:2016 for Reference Material Producers (where final products undergo residue testing)

    Typical usage ratio

    • 0.1–0.4 mole per mole of target triazole or pyridine intermediate; range adjustment based on conversion yield, expected substitution position, and process scale from kilogram to multi-ton.

    Downstream process integration

    • Alkylation steps in custom synthesis blocks; charged via jacketed glass-lined reactors, with real-time monitoring for bromide recovery and fluorinated by-product separation.

    Final product types

    • Fungicides: difenoconazole derivatives
    • Herbicides: fluorinated pyridines
    • Pre-emergent weed control actives
    • Custom synthesis advanced intermediates for field-ready agro-product formulations

    2. Pharmaceutical Intermediate for CNS Drugs

    Many pharmaceutical manufacturers use this benzyl bromide in producing fluorine-rich building blocks for central nervous system drug APIs, particularly where trifluorinated aromatic motifs improve blood-brain barrier penetration or metabolic stability. The intermediate reacts via nucleophilic substitution to introduce the benzyl group at a late API synthetic stage. Process chemists require high purity and low residual moisture to avoid downstream degradation, while our plant’s comprehensive batch records support API DMF submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monographs for API intermediates
    • EudraLex Volume 4 (EU GMP Guidelines)
    • U.S. FDA DMF (Type II) filing compatibility

    Typical usage ratio

    • 0.8–1.2 equivalent per key amine or oxygen nucleophile during benzylation; ratio controlled for selectivity versus over-alkylation for final CNS-active molecule.

    Downstream process integration

    • Nucleophilic substitution step following condensation and protection chemistry, using dry aprotic solvents under nitrogen atmosphere; often in kilo-scale glass reactors with in-process GC/HPLC monitoring of conversion.

    Final product types

    • Fluorinated benzylamine and benzyl ether API key intermediates
    • Precursors for antipsychotic and antidepressant drugs
    • Building blocks in development-stage CNS molecules for clinical pipelines
    • Chemical reference standards for pharmacopoeial studies

    3. Electronic Chemicals: Liquid Crystal Monomer Synthesis

    High-performance display manufacturers use this halobenzyl intermediate to assemble custom fluorinated aromatic monomers, essential for advanced liquid crystal formulations in LCD and OLED panels. The material’s high chemical reactivity under controlled Grignard or Ullmann-type coupling allows precise substitution into precursor frameworks. Our strict handling protocols prevent ionic contamination, supporting defect-free downstream device production.

    Industry compliance standards

    • SEMI C3 Standard (Specifications for Electronic Chemicals)
    • JEDEC JESD625 (Requirements for Handling Electrostatic-Discharge-Sensitive Devices)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001:2015 for batch quality traceability

    Typical usage ratio

    • Stoichiometric 1:1 input per terminal phenol or alkoxide group; fine-tuned in pilot scale for optimal substitution without excess bromide carryover.

    Downstream process integration

    • Coupling reaction after pre-functionalization of aromatic monomers; reacted under dry and inert conditions on glass/ceramic equipment; end-use validated by downstream physical property testing (dielectric, viscosity, ESD, etc.).

    Final product types

    • Fluorinated liquid crystal monomers and oligomers
    • Intermediate compounds for alignment layer agents in LCDs
    • Specialty materials for OLED panel fabrication
    • Photoalignment materials for optical films

    4. Specialty Polymer Synthesis for Fluorinated Resins

    This raw material reacts as a functional group donor in the production of specialty fluoropolymer resins and thermosetting plastics. Industrial sites incorporate it into step-growth or free-radical polymerizations, where fluorinated benzyl units enhance resistance to chemicals, UV, and thermal cycling. Its high reactivity and low impurity profile minimize polymer color and defect rates, critical for downstream molding and extrusion operations in electronics and automotive ventures.

    Industry compliance standards

    • ASTM D543 – Resistance of Plastics to Chemical Reagents
    • IEC 60695-11-10 (Flammability of polymeric materials for electrical equipment)
    • UL 94 (Standard for Safety of Flammability of Plastic Materials)
    • REACH Regulation (EC) No. 1907/2006 (EU chemicals registration)

    Typical usage ratio

    • 2–10 wt% as a co-monomer or chain-end functionalizer; level depends on resin architecture and required surface energy or chemical resistance.

    Downstream process integration

    • Fed into prepolymer reactors or extruders during the compounding stage; compatible with both batch and continuous production using automated dosing for consistent copolymer composition.

    Final product types

    • Fluorinated thermoplastic pellets and granules
    • High chemical resistance polymer films and sheets
    • Wire insulation and cable jackets for electronics
    • Automotive gaskets and seals with extended service life
    Free Quote

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