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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 | 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. |
Applications of 2,4,5-Trifluorobenzyl Bromide in Industrial Manufacturing2,4,5-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 SynthesisThis 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
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2. Pharmaceutical Intermediate for CNS DrugsMany 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
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3. Electronic Chemicals: Liquid Crystal Monomer SynthesisHigh-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
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4. Specialty Polymer Synthesis for Fluorinated ResinsThis 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
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