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HS Code |
225676 |
| Product Name | 2-Bromo-4-Fluorobenzoic Acid |
| Cas Number | 1673-32-9 |
| Molecular Formula | C7H4BrFO2 |
| Molecular Weight | 219.01 |
| Appearance | White to off-white solid |
| Melting Point | 155-159°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.779 g/cm³ |
| Smiles | C1=CC(=C(C=C1Br)C(=O)O)F |
| Inchi | InChI=1S/C7H4BrFO2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,(H,10,11) |
| Storage Conditions | Store at room temperature, tightly closed, in a dry place |
As an accredited 2-Bromo-4-Fluorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Bromo-4-Fluorobenzoic Acid, securely sealed, labeled with CAS number and hazard symbols. |
| Shipping | 2-Bromo-4-Fluorobenzoic Acid is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material and handled according to regulatory requirements, including appropriate labeling and documentation. Shipment is typically via ground or air freight, ensuring temperature control and compliance with chemical transport regulations. |
| Storage | 2-Bromo-4-Fluorobenzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases and oxidizing agents. Keep away from moisture and direct sunlight. Store at room temperature or as specified on the chemical's safety data sheet. Proper labeling and secondary containment are recommended to prevent spills and contamination. |
Applications of 2-Bromo-4-Fluorobenzoic Acid in Industrial Manufacturing2-Bromo-4-fluorobenzoic acid is a specialty intermediate used primarily in the synthesis of complex organic compounds. Our manufacturing expertise ensures highly consistent quality for industrial downstream processes. Below are detailed application scenarios supported by practical standards, process details, and end-use outcomes. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisThis compound is widely integrated into the synthetic routes of several pharmaceutical APIs, particularly within anti-inflammatory and anti-neoplastic research pipelines. Its aryl halide structure provides a crucial blocking group, facilitating site-selective reactions such as Suzuki coupling and amidation during the creation of functionalized benzamides. QC departments in API production closely monitor the acid’s purity profile, isomer content, and residual solvent levels to meet drug master file (DMF) requirements. Industry compliance standards
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2. Agrochemical Synthesis for Herbicide and Fungicide Active CompoundsManufacturers of advanced crop protection agents incorporate this benzoic acid derivative for constructing highly substituted aromatic systems. In particular, the compound’s ortho-bromo and para-fluoro arrangement allows for selective aromatic substitution and functionalization, opening pathways for halogenated benzene cores within herbicide scaffolds. Plant protection formula technicians adjust process parameters to optimize reactivity and minimize byproducts, especially at scale-up campaign phases. Industry compliance standards
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3. Electronic Chemicals for Organic Synthesis in OLED PrecursorsThe compound’s structural motif, with electron-withdrawing groups at key positions, is leveraged in the development of advanced organic motifs for optoelectronics and OLED emitter production. Material engineers employ the acid in the functionalization of biphenyl, carbazole, or fluorene building blocks, vital for charge transport layers and emissive molecular design. Consistency in halogen content and ultra-low metal impurity is mandatory for downstream electronic material performance. Industry compliance standards
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4. Specialty Fine Chemicals: Advanced Dye and Pigment IntermediatesChemical manufacturers involved in dye and pigment sectors utilize this benzoic acid derivative during the construction of complex aromatic frameworks. It plays a critical role where selective halogenation and reactive group positioning are required in pigment intermediates, ensuring superior chromophore performance and lightfastness. Laboratories specify purity, trace halogen, and moisture level controls to meet rigorous color industry requirements. Industry compliance standards
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