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4-(2-Bromoethyl)Benzoic Acid

    • Product Name 4-(2-Bromoethyl)Benzoic Acid
    • Alias 4-(2-Bromoethyl)benzoic acid
    • Einecs 610-041-7
    • 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

    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 & Storage
    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.
    Application of 4-(2-Bromoethyl)Benzoic Acid

    Applications of 4-(2-Bromoethyl)Benzoic Acid in Industrial Manufacturing

    As 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 Synthesis

    Downstream 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) Monographs for relevant APIs
    • US FDA 21 CFR Part 211 for drug product manufacture
    • Chinese Pharmacopoeia (ChP) for domestic regulatory submission

    Typical usage ratio

    • Used at 0.9–1.4 molar equivalents in the N-alkylation or coupling stage relative to the nucleophilic reactant, with precise adjustment based on impurity control and yield requirements as defined by route-specific process validation.

    Downstream process integration

    • Integrated as an electrophilic reagent in controlled addition at the intermediate synthesis stage, following initial condensation but before deprotection or final ring closure operations.

    Final product types

    • Losartan potassium intermediate
    • Telmisartan precursor compound
    • Multiple benzimidazole- or biphenyl-derived antihypertensive intermediates

    2. Synthesis of Specialty Agrochemical Building Blocks

    Major 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

    • FAO/WHO Codex Alimentarius international standards for active ingredient purity
    • ISO 9001:2015 certified QC systems for agro-intermediate output
    • REACH (EC No. 1907/2006) registration for European market supply
    • OECD Test Guidelines for residual analysis

    Typical usage ratio

    • Employed at 1.05–1.2 equivalents versus the target nucleophile in coupling or condensation reactions; stoichiometry controlled based on process mass balance and required crop protection activity profile.

    Downstream process integration

    • Charged after initial aromatic framework construction but before terminal heterocycle formation; introduced in batch or continuous flow reactors equipped with controlled temperature and inert atmosphere systems.

    Final product types

    • Pyridine- and triazole-derived herbicide intermediates
    • Precursors for synthetic plant growth regulators
    • Key intermediates for post-patent fungicide development

    3. Custom Monomer Preparation for Advanced Polymer Synthesis

    Specialty 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

    • ISO 9001:2015 for production quality systems
    • EN 10204:2004 for material certification in specialty polymers
    • RoHS (Directive 2011/65/EU) for end-use in electrical components
    • UL Yellow Card for flame retardant and functional polymer grades (as applicable)

    Typical usage ratio

    • Dosed at 2–8 wt% in co-polymerization mixes or as the limiting agent in step-growth polymerization, with batch size and molecular weight target determining scale and frequency of addition.

    Downstream process integration

    • Added during monomer functionalization either pre-polymerization or as a reactive pendant group donor; processed using jacketed stainless steel reactors with vacuum/controlled agitation for molecular weight control.

    Final product types

    • High-performance engineering thermoplastics with halogenated side chains
    • UV-resistant polymer coatings
    • Customized block copolymers for high-tech industrial applications

    4. Functionalized Ligand Synthesis for Catalysis and Process Chemistry

    Chemical 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

    • ISO 17025:2017 for laboratory testing and batch certification
    • Responsible Care® certification for catalyst handling safety
    • REACH registration for single-site catalyst supply in Europe
    • Internal QC–QA per the downstream manufacturer’s catalyst release specification

    Typical usage ratio

    • Applied at 1.0–1.1 equivalents relative to the ligand precursor in single-step or stepwise alkylation, measured by real-time NMR or HPLC analysis to confirm completion and reduce residual impurity risk.

    Downstream process integration

    • Introduced post-core ligand assembly as an alkylation or substitution agent, followed by filtration, solvent exchange, and purification per customer-defined ligand specifications for downstream metal complexation.

    Final product types

    • Bidentate and tridentate phosphine/amine ligands
    • Precatalysts for olefin polymerization
    • Custom ligands for fine chemical and pharmaceutical catalysis

    5. Fine Chemical Intermediate for Synthesis of Colorants and Dyes

    Manufacturers 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

    • REACH compliance for colorant registration in EU markets
    • OEKO-TEX® Standard 100 for dyestuff safety in textiles
    • ISO 787/ISO 105 test series for pigment and dye performance
    • RoHS and heavy metal content regulations for electronics applications

    Typical usage ratio

    • Used at 1.0–1.3 equivalents for coupling with amine or aryl functional groups, with real-time analytics ensuring high chromophore yield and minimal residual starting material.

    Downstream process integration

    • Added following diazo coupling or aromatic amination in the dye intermediate manufacturing train, with solvent control and filtration for purity enhancement.

    Final product types

    • Substituted anthraquinone, azo, and phthalocyanine dye intermediates
    • Performance organic pigments for plastics and coatings
    • Colorant precursors for inkjet and industrial marking fluids
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