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HS Code |
811034 |
| Product Name | 4-(2-Bromoethyl)Benzoic Acid |
| Cas Number | 52711-18-9 |
| Molecular Formula | C9H9BrO2 |
| Molecular Weight | 229.07 |
| Appearance | White to off-white solid |
| Melting Point | 134-138°C |
| Boiling Point | No data available |
| Density | No data available |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in DMSO and DMF |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Smiles | C1=CC(=CC=C1CCBr)C(=O)O |
| Inchi | InChI=1S/C9H9BrO2/c10-6-5-7-1-3-8(4-2-7)9(11)12/h1-4H,5-6H2,(H,11,12) |
| Refractive Index | No data available |
As an accredited 4-(2-Bromoethyl)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 4-(2-Bromoethyl)benzoic acid is supplied in a sealed amber glass bottle with a secure screw cap label. |
| Shipping | 4-(2-Bromoethyl)benzoic acid is shipped in tightly sealed, chemically resistant containers to ensure safety and maintain product integrity. Packaging adheres to relevant regulatory standards for hazardous materials. The shipment is clearly labeled, accompanied by a Safety Data Sheet (SDS), and typically requires ground or specialized courier transport suitable for chemical substances. |
| Storage | 4-(2-Bromoethyl)benzoic acid should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances like strong oxidizing agents. Avoid moisture exposure. Store at room temperature, preferably between 2–8°C. Ensure proper labeling and handle with gloves and eye protection to prevent skin and eye contact. |
Applications of 4-(2-Bromoethyl)Benzoic Acid in Industrial ManufacturingAs a key intermediate produced in-house, 4-(2-Bromoethyl)benzoic acid finds wide use in fine chemical synthesis across the pharmaceutical, agrochemical, and specialty polymer sectors. Our plant engineers work alongside downstream manufacturers for material selection, formulation guidance, and technical optimization. The following sections detail proven industrial environments where this compound supports cost-effective, standard-compliant production of advanced end products. 1. Pharmaceutical Intermediate for Antihypertensive API SynthesisDownstream pharmaceutical manufacturers incorporate this compound in multi-step syntheses of certain angiotensin receptor blockers and other antihypertensive active pharmaceutical ingredients (APIs). The benzylic bromide functionality is crucial for N-alkylation or C–C coupling stages, enabling structural diversity in various proprietary intermediates for final API assembly. Manufacturers optimize charge ratios and reaction sequences by referencing validated process development data, ensuring efficiency and regulatory traceability throughout the value chain. Industry compliance standards
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2. Synthesis of Specialty Agrochemical Building BlocksMajor agrochemical formulators utilize our compound as a halogenated intermediate in the multi-step production of plant-protecting agents such as selective herbicides and growth modulators. Its reactivity towards nucleophilic aromatic substitution and Grignard chemistry allows direct access to key molecular frameworks required for active ingredient development. Downstream protocol optimization focuses on minimizing byproduct content in accordance with international export specifications. Industry compliance standards
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3. Custom Monomer Preparation for Advanced Polymer SynthesisSpecialty polymer manufacturers deploy this crystalline acid as an activated aromatic building block in the preparation of functionalized monomers used for engineering plastics and performance coatings. The bromoethyl group enables controlled co-monomer formation via substitution with nucleophilic agents, delivering macromolecules with designed pendant functionalities. Process engineers optimize reaction kinetics and contamination control as part of stringent polymer QC protocols to meet application-specific needs in automotive, electronic, and industrial surfaces. Industry compliance standards
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4. Functionalized Ligand Synthesis for Catalysis and Process ChemistryChemical process catalyst developers rely on this specialty intermediate to introduce bromoalkyl groups into aromatic ligand frameworks, supporting production of proprietary complex ligands for transition metal catalysis. The compound’s benzylic bromide unit reacts cleanly with amines, phosphines, and carbanion equivalents, facilitating installation of versatile coordination sites. Precise control of reagent stoichiometry and purity is critical to finished catalyst activity and batch traceability in compliance-sensitive markets. Industry compliance standards
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5. Fine Chemical Intermediate for Synthesis of Colorants and DyesManufacturers of specialty colorants exploit the reactivity of this benzoic acid derivative to build complex aromatic scaffolds via nucleophilic displacement or transition-metal mediated cross-coupling. Its precise introduction into the dye precursor synthesis route supports consistent batch-to-batch color quality and stability. Formulators rely on validated process analytics and international product safety standards due to widespread end-use in textiles, plastics, and coatings. Industry compliance standards
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