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4-Bromo-3-Nitroanisole

    • Product Name 4-Bromo-3-Nitroanisole
    • Alias p-Bromo-m-nitroanisole
    • Einecs 629-024-6
    • 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
    VTB
    Specifications

    HS Code

    417919

    Chemical Name 4-Bromo-3-Nitroanisole
    Molecular Formula C7H6BrNO3
    Molecular Weight 232.03 g/mol
    Cas Number 6305-34-4
    Appearance Yellow solid
    Melting Point 75-79°C
    Solubility Slightly soluble in water
    Density 1.73 g/cm³ (approximate)
    Smiles COC1=CC(=C(C=C1)Br)[N+](=O)[O-]
    Inchi InChI=1S/C7H6BrNO3/c1-12-7-3-2-5(8)6(4-7)9(10)11/h2-4H,1H3
    Storage Conditions Store at room temperature in a dry place
    Hazard Class Irritant
    Synonyms 1-Bromo-2-methoxy-5-nitrobenzene

    As an accredited 4-Bromo-3-Nitroanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle, sealed, with a white screw cap, displaying hazard symbols and labeled "4-Bromo-3-Nitroanisole, ≥98%".
    Shipping 4-Bromo-3-Nitroanisole is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported according to regulatory guidelines for hazardous chemicals, with appropriate labeling and documentation. During transit, temperature and handling precautions are observed to ensure safety and preserve chemical integrity.
    Storage 4-Bromo-3-nitroanisole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep away from heat, sparks, and sources of ignition. Protect from moisture and direct sunlight. Store at room temperature and label the container clearly to avoid accidental misuse.
    Application of 4-Bromo-3-Nitroanisole

    Applications of 4-Bromo-3-Nitroanisole in Industrial Manufacturing

    As an established manufacturer of 4-Bromo-3-Nitroanisole, we supply pharmaceutical, agrochemical, and specialty materials industries with this key aromatic intermediate. Our product meets the process-critical requirements of advanced downstream applications, supporting the synthesis of value-added compounds in regulated and high-purity environments.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    4-Bromo-3-Nitroanisole serves as a controlled aromatic building block in the multi-step synthesis of certain pharmaceutical APIs, particularly where electron-withdrawing activities or directed ortho metalation are required. Large-scale GMP-compliant plants utilize this intermediate at defined process stages where the bromine and nitro functionalities enable regioselective modifications, including nucleophilic substitutions or further reductions for complex molecule assembly.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients (APIs)
    • EU EudraLex, Volume 4 (GMP)
    • US FDA 21 CFR Part 210/211 for Drug Products
    • Relevant pharmacopoeias for downstream APIs

    Typical usage ratio

    • Ranges from 0.8 – 2.5 molar equivalents per step; final ratio depends on specific reaction design and desired API yield
    • Adjusted for process scale and impurity control

    Downstream process integration

    • Charged into bromination or nitro-group transformation steps after purification
    • Utilized during aromatic substitution and heterocycle-forming reactions in multi-kilo API campaigns

    Final product types

    • Generic and branded APIs (oxidative CNS drugs, anti-allergy molecules, advanced pain management molecules)
    • Intermediates for later-stage pharmaceutical synthesis

    2. Agrochemical Intermediate Manufacturing

    Numerous agrochemical producers rely on this aromatic intermediate to direct the synthesis of selective herbicide actives and fungicide scaffolds. The compound’s halogenated nitroaromatic structure lends itself to the formation of diverse substitution patterns, favoring precision in the development of active agrochemical ingredients designed for regulatory compliance and field stability requirements.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (e.g., active ingredient content, impurity profile)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products authorization)
    • ISO 9001:2015 for process and quality control

    Typical usage ratio

    • 0.5 – 1.4 molar equivalents per batch, fine-tuned based on crop-protection active design and targeted impurity thresholds

    Downstream process integration

    • Fed to the nucleophilic aromatic substitution step to introduce further nitrogen or sulfur groups
    • Converted into more complex benzenoid intermediates prior to formulation

    Final product types

    • Herbicide pre-cursors (for rice, maize, and wheat fields)
    • Fungicide technical concentrates
    • Active intermediates for post-patent agrochemicals

    3. Specialty Dye and Pigment Synthesis

    Manufacturers of performance dyes and pigments leverage the brominated and nitro-functionalized ring for the generation of custom-designed colorants, which require defined substitution on aromatic cores. Specialty pigment makers rely on the reactivity of this intermediate for stepwise introduction of further substituents or as a key precursor in azo or anthraquinone-based colorant synthesis.

    Industry compliance standards

    • EN 71-3: Toy Safety – Migration of Certain Elements (for pigments in toys)
    • REACH Regulation (EC) No 1907/2006 for chemical safety, SVHC absence
    • ISO 9001:2015 for colorant manufacturing QA/QC processes

    Typical usage ratio

    • 1.0 molar equivalent standard charge; can increase up to 2.0 equivalents in chromatism-critical applications

    Downstream process integration

    • Integrated in early-phase diazotization or coupling stages
    • Utilized in halogenated nitroaromatic derivatization before final pigment crystallization

    Final product types

    • Specialty organic pigments (textiles, inks, coatings)
    • High-purity dyes for analytical or electronic applications

    4. Electronic Chemical Intermediates

    Producers of fine electronic chemicals select this compound as a precursor in the synthesis of functionalized aromatic monomers for use in color display technologies and specialty polymers. The electron-rich anisole group, combined with halogen and nitro substituents, enables precise monomer modification required for rigid electronic devices and high-performance materials.

    Industry compliance standards

    • IEC 62474: Material Declaration for Electronic Products
    • RoHS Directive 2011/65/EU (Hazardous Substances in Electronics)
    • ISO 14001:2015 for environmental and process management systems

    Typical usage ratio

    • 0.3 – 1.0 molar equivalents per synthesis, controlled for chain length in polymer or monomer applications

    Downstream process integration

    • Fed into Suzuki-type cross-coupling or nucleophilic substitution at pre-polymerization stages
    • Purified and incorporated as an electronic-grade intermediate before final end-capping or polymerization

    Final product types

    • OLED intermediates
    • Dielectric monomer building blocks
    • High-performance specialty polymers for electronics

    5. Development of Analytical Standards and Reference Materials

    Producers of certified reference materials and analytical standards utilize this compound in the calibration and validation of quantitative analytical methods, especially in laboratories testing for trace-level organobromine or nitroaromatic residues in complex matrices. The chemical’s consistent structure and purity specifications help support regulatory and industry-driven monitoring programs.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • IUPAC recommendations for chemical purity and reference materials
    • Guidelines by AOAC International for analytical standards

    Typical usage ratio

    • Preparation of standard solutions at concentrations from 1 μg/mL to 100 mg/mL, adjusted to detection limits

    Downstream process integration

    • Introduced during standard solution preparation, purity verification, and system suitability testing
    • Employed in method validation, calibration curve establishment, and laboratory proficiency testing

    Final product types

    • Chemical reference standards for QC laboratories
    • Certified analytical reference materials for instrument calibration
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