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HS Code |
120125 |
| Cas Number | 17169-80-3 |
| Molecular Formula | C9H9BrO2 |
| Molecular Weight | 229.07 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 280-282°C |
| Density | 1.483 g/cm3 |
| Refractive Index | 1.560 |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water; soluble in organic solvents |
As an accredited Ethyl 3-Bromobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ethyl 3-Bromobenzoate, 25g, is supplied in a sealed amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | Ethyl 3-Bromobenzoate is shipped in tightly sealed containers, protected from light and moisture. It is packaged following hazardous material guidelines due to its chemical nature. During transport, care is taken to maintain stable temperatures and prevent leaks or spills. Proper labeling and documentation ensure compliance with safety and regulatory requirements. |
| Storage | Ethyl 3-Bromobenzoate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep out of direct sunlight and moisture. Proper chemical storage protocols, including appropriate labeling and secondary containment, should be followed to prevent leaks, spills, and contamination. |
Applications of Ethyl 3-Bromobenzoate in Industrial ManufacturingEthyl 3-Bromobenzoate serves as a key intermediate in the synthesis of advanced chemicals for fine chemical, pharmaceutical, agrochemical, dye, and material science industries. The following sections present detailed and specific industrial scenarios, with technical data derived from direct production and customer application feedback. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers rely on ethyl 3-bromobenzoate in the preparation of specialty benzene ring intermediates, which form the core structure for many active pharmaceutical ingredients (APIs). The raw material enters key steps such as Suzuki coupling and further derivatization to produce anti-inflammatory, anti-hypertensive, or anti-epileptic drug molecules. Processes require strict compliance with GMP guidelines, and QC ensures residual bromide levels meet pharmacopoeial specifications. Manufacturers critically monitor raw material input, solvent ratio, and downstream crystallization to optimize purity and minimize impurities. Final goods undergo release testing for regulatory submission. Industry compliance standards
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2. Agrochemical SynthesisAgricultural chemical manufacturers utilize ethyl 3-bromobenzoate as a scaffold for constructing selective herbicides and insecticides. The compound’s halogenated aromatic ring structure offers an essential handle for further functionalization, especially via nucleophilic aromatic substitution. Control over reaction temperature, phase, and reagent ratio ensures consistent yield in multi-step processes. Post-reaction, the intermediate feeds into acylation or amination steps for final active ingredient (AI) synthesis. Production records align with OECD and FAO batch documentation guidelines, ensuring downstream traceability from raw material intake to formulated crop protection product. Industry compliance standards
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3. Dyes and Pigments ManufacturingDye and pigment producers integrate ethyl 3-bromobenzoate in the manufacture of specialized aromatic chromophores for high-performance textile, ink, and polymer coloration. Process engineers introduce this raw material during key halogenation or esterification stages, using controlled conditions to maximize chromogenic group attachment and minimize ring substitution side products. Quality assurance teams conduct spectroscopic and chromatographic monitoring during reaction and post-synthesis to maintain batch-to-batch color strength and stability. Documentation aligns with chemical compliance for global distribution and end-user safety. Industry compliance standards
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4. Material Science and Advanced PolymersProducers of high-value performance materials use ethyl 3-bromobenzoate in the functionalization of aromatic monomers that impart rigidity and thermal stability to engineering plastics and specialty resins. The ester acts as a leaving group for subsequent polycondensation, enabling the integration of brominated blocks for flame resistance or surface modification. Automated batch tracking ensures regulatory material ID throughout polymer chain design, and sample analyses verify incorporation per specification. The approach supports material certification necessary for automotive, construction, and electronics sectors. Industry compliance standards
Typical usage ratio
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