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3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester

    • Product Name 3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester
    • Alias Ethyl 3-(3-bromophenyl)-3-oxopropanoate
    • Einecs 416-050-0
    • 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
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    Specifications

    HS Code

    287399

    Product Name 3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester
    Cas Number 35343-04-7
    Molecular Formula C11H11BrO3
    Molecular Weight 271.11
    Appearance Pale yellow to yellow liquid
    Purity ≥98%
    Boiling Point 337.3°C at 760 mmHg
    Density 1.444 g/cm3
    Refractive Index 1.537
    Smiles CCOC(=O)CC(=O)C1=CC(=CC=C1)Br
    Storage Temperature 2-8°C

    As an accredited 3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g of 3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester is packaged in a sealed amber glass bottle with tamper-evident cap.
    Shipping The chemical **3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester** is shipped in tightly sealed, chemically resistant containers, clearly labeled and securely cushioned to prevent damage. It is transported in compliance with all relevant hazardous materials regulations, accompanied by safety documentation (MSDS), and typically shipped via certified courier to ensure safe and timely delivery.
    Storage **Storage information for 3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester:** Store in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible materials (such as strong oxidizing agents and bases). Protect from light and moisture. Recommended storage temperature: 2–8°C (refrigerator). Use personal protective equipment when handling. Follow all relevant local, state, and federal guidelines for chemical storage.
    Application of 3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester

    Applications of 3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester in Industrial Manufacturing

    Produced in-house with tightly monitored batch controls, 3-(3-Bromo-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester serves as a specialty building block in downstream industries requiring high-purity intermediates for advanced organic syntheses. Below, we detail real-world use cases across four core sectors where our raw material integrates directly into established commercial production flows, with strict adherence to regulatory, operational, and quality benchmarks.

    1. Pharmaceutical Intermediate for Anti-Inflammatory Drugs

    Many pharmaceutical clients utilize this compound as a strategic intermediate in synthesizing targeted non-steroidal anti-inflammatory drug (NSAID) actives due to its functionalized aromatic structure. It enters the process following initial condensation reactions, playing a key role before API finalization.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • United States Pharmacopeia (USP) guidelines for drug substance intermediates
    • European Pharmacopoeia (Ph. Eur.) monographs for API synthesis steps
    • ICH Q3A/B Impurity Guidelines

    Typical usage ratio

    • 0.7–3.5 molar equivalents relative to the downstream core structure, adjusted based on the target molecule’s synthetic route and third-step yield optimization protocols

    Downstream process integration

    • Implemented at the third or fourth synthesis step post-halogen exchange, typically introduced after initial Grignard or Friedel–Crafts steps and prior to purification and API cyclization

    Final product types

    • Finished API bulk powder for NSAIDs (such as advanced arylpropionic acid derivatives)
    • Tablet-grade bulk ingredients
    • Capsule and suspension drug formulations (after further downstream processing)

    2. Agrochemical Active Ingredient Synthesis

    Agrochemical manufacturers incorporate this raw material as a precursor in the production of certain advanced herbicide and pesticide analogs, leveraging its bromo-aryl and keto functionalities for rapid coupling reactions in microwaves or catalytic settings.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Active Ingredients (JMPR/FAO/WHO)
    • European Crop Protection Association (ECPA) quality procedures
    • ISO 9001:2015 for agrochemical raw material processing
    • REACH (EC Regulation No 1907/2006) substance registration (Europe)

    Typical usage ratio

    • 5–8% by mass in the key active ingredient precursor batch; ratio varies with the molecular weight target and the extent of aryl group incorporation during pre-purification phases

    Downstream process integration

    • Loaded into closed reactor systems following initial alkylation, entering in the core intermediate formation stage before hydrogenation or halogen removal processing

    Final product types

    • Technical-grade herbicide concentrates
    • Active pesticide matrix formulations
    • Granular and liquid crop protection additives

    3. Synthesis of Specialty Aromatic Ketones for Polymer Additives

    Our material acts as a crucial intermediate for custom aromatic ketone compounds incorporated into high-performance polymer additives, especially where chemical resistance and thermal stability improvements for engineering plastics are required.

    Industry compliance standards

    • ASTM D6319 and D638 standards for plastics chemical additives
    • RoHS Directive (2011/65/EU) for restricted substance validation
    • ISO 14001 for environmental management in chemical production
    • UL 94 certification prerequisites for flame-retardant plastics

    Typical usage ratio

    • 1.5–4.5% by weight in the additive synthesis stage; fine-tuned based on desired polymer compatibility and additive performance in melt-processing lines

    Downstream process integration

    • Blended in post-monomer addition step during polycondensation, typically after the main polymer backbone is assembled and prior to extrusion or molding masterbatch granulation

    Final product types

    • Anti-aging masterbatch additive concentrates
    • Specialty thermoplastic resins for automotive parts
    • Industrial-grade flame-retardant plastic pellets

    4. Development of Advanced Liquid Crystal Compounds

    Electronics-grade manufacturers deploy this ester as a functionalized synthon to introduce precise aryl bromide groups at the pre-fabrication stage of liquid crystal compound synthesis, facilitating the creation of high-performance display molecules for TFT and OLED technologies.

    Industry compliance standards

    • IEC 62321 for hazardous substances testing in electronics chemicals
    • IPC-1752A material declaration for electronics manufacturing
    • ISO 9001:2015 for specialty chemical synthesis
    • RoHS compliance for electronic-grade raw materials

    Typical usage ratio

    • 0.3–2.0 mol % depending on the mesogen structure and birefringence requirements for end-user pixel technology

    Downstream process integration

    • Enters during the principal arylation or ester-exchange phase, prior to the introduction of nitro- or cyano-groups, and remains throughout column purification and final molecular fractionation

    Final product types

    • Liquid crystal mixture precursors
    • High-purity dopant materials for LCD/TFT/OLED displays
    • Electronic-grade custom intermediates for specialty display panel manufacturing
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