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2-Bromo-4-Fluorobenzoic Acid

    • Product Name 2-Bromo-4-Fluorobenzoic Acid
    • Alias 2-Bromo-4-fluorobenzoicacid
    • Einecs 249-801-6
    • 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

    225676

    Product Name 2-Bromo-4-Fluorobenzoic Acid
    Cas Number 1673-32-9
    Molecular Formula C7H4BrFO2
    Molecular Weight 219.01
    Appearance White to off-white solid
    Melting Point 155-159°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.779 g/cm³
    Smiles C1=CC(=C(C=C1Br)C(=O)O)F
    Inchi InChI=1S/C7H4BrFO2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,(H,10,11)
    Storage Conditions Store at room temperature, tightly closed, in a dry place

    As an accredited 2-Bromo-4-Fluorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-Bromo-4-Fluorobenzoic Acid, securely sealed, labeled with CAS number and hazard symbols.
    Shipping 2-Bromo-4-Fluorobenzoic Acid is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material and handled according to regulatory requirements, including appropriate labeling and documentation. Shipment is typically via ground or air freight, ensuring temperature control and compliance with chemical transport regulations.
    Storage 2-Bromo-4-Fluorobenzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases and oxidizing agents. Keep away from moisture and direct sunlight. Store at room temperature or as specified on the chemical's safety data sheet. Proper labeling and secondary containment are recommended to prevent spills and contamination.
    Application of 2-Bromo-4-Fluorobenzoic Acid

    Applications of 2-Bromo-4-Fluorobenzoic Acid in Industrial Manufacturing

    2-Bromo-4-fluorobenzoic acid is a specialty intermediate used primarily in the synthesis of complex organic compounds. Our manufacturing expertise ensures highly consistent quality for industrial downstream processes. Below are detailed application scenarios supported by practical standards, process details, and end-use outcomes.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    This compound is widely integrated into the synthetic routes of several pharmaceutical APIs, particularly within anti-inflammatory and anti-neoplastic research pipelines. Its aryl halide structure provides a crucial blocking group, facilitating site-selective reactions such as Suzuki coupling and amidation during the creation of functionalized benzamides. QC departments in API production closely monitor the acid’s purity profile, isomer content, and residual solvent levels to meet drug master file (DMF) requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) Guide for Active Pharmaceutical Ingredients
    • USP General Notices (for pharmaceutical intermediate controls)
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals GMPs)
    • Local Drug Regulatory Authority registration requirements (e.g., EMA, NMPA)

    Typical usage ratio

    • Employed at 1–4 mole equivalents with respect to the main aromatic scaffold, depending on the targeted API’s synthetic pathway and downstream functionality requirements

    Downstream process integration

    • Feeding into the arylation or amidation steps of multi-stage API synthesis, particularly after halogen-exchange activation or prior to amide bond formation; excess is typically recovered and purified

    Final product types

    • Small-molecule kinase inhibitors
    • Non-steroidal anti-inflammatory APIs (advanced intermediates)
    • Customized benzamide research compounds
    • Targeted cancer therapy intermediates

    2. Agrochemical Synthesis for Herbicide and Fungicide Active Compounds

    Manufacturers of advanced crop protection agents incorporate this benzoic acid derivative for constructing highly substituted aromatic systems. In particular, the compound’s ortho-bromo and para-fluoro arrangement allows for selective aromatic substitution and functionalization, opening pathways for halogenated benzene cores within herbicide scaffolds. Plant protection formula technicians adjust process parameters to optimize reactivity and minimize byproducts, especially at scale-up campaign phases.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides (JMPS)
    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 (Quality Management for Agrochemical Industry)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Product Registration)

    Typical usage ratio

    • Generally 5–10% w/w of the total coupling reactants in the synthesis of benzoyl-core agrochemical intermediates; specific ratios depend on process batch size, desired herbicide loading, and post-reaction workup efficiency

    Downstream process integration

    • Integration during the aromatic substitution or halogen exchange phase, preceding esterification or carbamate formation necessary for finished agrochemical actives

    Final product types

    • Halogenated herbicide precursors
    • Fungicide intermediates for field crop protection
    • Benzoyl-aryl carbamate building blocks
    • Formulated herbicidal blends for resistant weed management

    3. Electronic Chemicals for Organic Synthesis in OLED Precursors

    The compound’s structural motif, with electron-withdrawing groups at key positions, is leveraged in the development of advanced organic motifs for optoelectronics and OLED emitter production. Material engineers employ the acid in the functionalization of biphenyl, carbazole, or fluorene building blocks, vital for charge transport layers and emissive molecular design. Consistency in halogen content and ultra-low metal impurity is mandatory for downstream electronic material performance.

    Industry compliance standards

    • IEC 62474 Material Declaration for Electronic Equipment
    • RoHS Directive (2011/65/EU) compliance for hazardous substance restriction
    • SEMATECH purity requirements for organic electronic materials
    • ISO 14001 (Environmental Management System for chemical process)

    Typical usage ratio

    • Used at 0.5–3 mole equivalents relative to the OLED core precursor, depending on design of electron/hole transport segments and the presence of additional halogenation steps

    Downstream process integration

    • Addition in aryl-coupling or amidation stages where halogen selectivity is essential; often deployed prior to cyclization or chain extension for OLED backbone synthesis

    Final product types

    • Intermediate benzene cores for OLED emitters
    • Electron transport material building blocks
    • Precursor molecules for blue and green emission layers
    • Specialty materials for thin-film organic semiconductors

    4. Specialty Fine Chemicals: Advanced Dye and Pigment Intermediates

    Chemical manufacturers involved in dye and pigment sectors utilize this benzoic acid derivative during the construction of complex aromatic frameworks. It plays a critical role where selective halogenation and reactive group positioning are required in pigment intermediates, ensuring superior chromophore performance and lightfastness. Laboratories specify purity, trace halogen, and moisture level controls to meet rigorous color industry requirements.

    Industry compliance standards

    • ISO 12040:1997 (Industrial Dyes – Test Methods)
    • REACH Regulation (EC) No 1907/2006 (for aromatic chemical intermediates)
    • ASTM D3134 (Specification for Organic Pigments)
    • ZDH (German Institute for Pigment and Colour Standardization)

    Typical usage ratio

    • Typically 2–7% by weight of the intermediate mass in the multi-step pigment synthesis, with adjustment depending on process scale and target pigment chromaticity

    Downstream process integration

    • Entry point in halogenated aromatic coupling or acylation, prior to core diazotization or azo coupling steps involved in high-performance dye manufacturing

    Final product types

    • Advanced azo dye precursors
    • Benzoyl functional pigments for automotive coatings
    • Specialty colorants for plastics and printing inks
    • Lightfast materials for fiber and textile coloration
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