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Ethyl 3-Bromobenzoate

    • Product Name Ethyl 3-Bromobenzoate
    • Alias Ester, ethyl 3-bromobenzoic acid
    • Einecs 247-297-8
    • 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

    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 & Storage
    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.
    Application of Ethyl 3-Bromobenzoate

    Applications of Ethyl 3-Bromobenzoate in Industrial Manufacturing

    Ethyl 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 Synthesis

    Pharmaceutical 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

    • ICH Q7 GMP Guidelines for API Manufacturing
    • USP and European Pharmacopoeia Residual Solvent/Bromide Limits
    • FDA 21 CFR Part 210/211
    • EDQM Certification for European Distribution

    Typical usage ratio

    • 0.7–1.2 molar equivalent per target intermediate, adjusted based on step yield and downstream loss

    Downstream process integration

    • Charged in stage two or three during aromatic intermediate synthesis
    • Involved in Pd-catalyzed cross-coupling, followed by purification and conversion

    Final product types

    • Nonsteroidal anti-inflammatory drug precursors (NSAIDs)
    • CNS-active intermediates
    • Selective receptor modulator backbone compounds

    2. Agrochemical Synthesis

    Agricultural 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

    • FAO/WHO Specification for Agricultural Pesticides
    • REACH (EC 1907/2006) for Chemical Registration
    • ISO 9001 Quality Management System
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • 1.0 equivalent relative to aromatic base compound; process may require 10–20% excess if side reaction risk observed during scale-up

    Downstream process integration

    • Fed into Grignard or nucleophilic substitution units as primary halogenated source
    • Converted into ring-substituted phenoxy or carboxamide groups

    Final product types

    • Precursor to substituted benzoic acid herbicides
    • Building blocks for pyrazole or triazole-based insecticides
    • Starting material for fungicidal heterocycles

    3. Dyes and Pigments Manufacturing

    Dye 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

    • OEKO-TEX Standard 100 for Restricted Substances
    • EN 71-3 Toy Safety for Migratable Elements in Pigments
    • ISO 9001:2015 Certified Production System
    • REACH Annex XVII for Chemical Restrictions

    Typical usage ratio

    • 5–15% by weight in primary aromatic intermediate blend; loading varies by desired color intensity and application

    Downstream process integration

    • Introduced in step one or two of chromophore assembly reactions
    • Incorporated prior to final condensation or sulfonation stages

    Final product types

    • Reactive dyes for cellulose fibers
    • Azo pigment intermediates for high-fastness printing inks
    • Specialty colorants for plastics and synthetic fibers

    4. Material Science and Advanced Polymers

    Producers 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

    • UL 94 Flammability Standards for Plastics
    • RoHS Directive (2011/65/EU) Substance Restrictions
    • ISO 14001 Environmental Management in Chemical Manufacturing
    • ASTM E595 Outgassing Testing (for electronics applications)

    Typical usage ratio

    • 3–10 mol% in aromatic monomer feedstock; adjusted to target desired flame retardance and polymer performance

    Downstream process integration

    • Input at pre-polymer synthesis using melt or solution reaction technology
    • Linked in controlled order to maximize molecular weight and functionality

    Final product types

    • Brominated polyesters and polyamides
    • Specialty engineering thermoplastics
    • Functional polymer additives for high-heat applications
    Free Quote

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