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4-Bromo-3-Methoxyaniline

    • Product Name 4-Bromo-3-Methoxyaniline
    • Alias 4-Bromo-3-methoxybenzenamine
    • Einecs 620-062-5
    • 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

    302899

    Productname 4-Bromo-3-Methoxyaniline
    Casnumber 22948-16-5
    Molecularformula C7H8BrNO
    Molecularweight 202.05
    Appearance Light yellow to brown solid
    Meltingpoint 66-69°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Synonyms 4-Bromo-m-anisidine; 3-Methoxy-4-bromoaniline
    Smiles COC1=CC(=C(C=C1)Br)N
    Inchikey XOGRWTWTZAZPKG-UHFFFAOYSA-N
    Storagetemperature Store at 2-8°C
    Hazardclass Irritant

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

    Packing & Storage
    Packing The 50g 4-Bromo-3-Methoxyaniline is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 4-Bromo-3-Methoxyaniline is shipped in tightly sealed containers, typically under ambient conditions, and protected from moisture and light. The chemical is classified as hazardous; therefore, shipping follows strict regulatory guidelines (such as DOT and IATA), including appropriate labeling, documentation, and handling by certified carriers to ensure safe transportation.
    Storage 4-Bromo-3-methoxyaniline should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers and acids. Keep it in a cool, well-ventilated, and dry area, ideally in a chemical storage cabinet designed for hazardous or organic compounds. Clearly label the container and handle with appropriate personal protective equipment (PPE).
    Application of 4-Bromo-3-Methoxyaniline

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

    4-Bromo-3-Methoxyaniline serves as a key intermediate in multiple value chains across the pharmaceutical, agrochemical, pigment, and specialty chemical sectors. As a direct manufacturer, we deliver this product to formulators and producers seeking reliable integration into synthesis routes that demand consistency, purity, and compliance with stringent industry protocols.

    1. Pharmaceutical Intermediates for Targeted APIs

    Pharmaceutical manufacturers use this compound as a core building block in the multi-step synthesis of selected branded and generic active pharmaceutical ingredients, including certain kinase inhibitors and CNS therapies. The material enters acylation or coupling reactions where control of substitutions is critical for therapeutic activity. Formulators adjust charge levels to balance purity targets, meet batch volume demands, and avoid unwanted byproducts, especially under cGMP regimes. Our supply chain assures full traceability and documentation, meeting regulatory demands for registration and commercial production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211: Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs
    • EU GMP Part II: Basic Requirements for Active Substances
    • Japanese Pharmacopoeia (JP17), as relevant to precursor use

    Typical usage ratio

    • 0.1–1.5 molar equivalents, adjusted per target API yield and impurity requirements
    • Process engineers may increase ratio by up to 20% to compensate for secondary reaction losses

    Downstream process integration

    • Feedstock in nucleophilic aromatic substitution and amide coupling steps
    • Introduced after initial ring activation stage, prior to key condensation or cyclization

    Final product types

    • Small-molecule kinase inhibitor APIs
    • Central nervous system drug substances
    • Oncology therapeutic intermediates
    • Patent-protected pharmaceutical actives

    2. Agrochemical Synthesis Intermediates

    Major crop-protection formulators integrate this brominated aniline in the synthesis of advanced herbicides and fungicide actives, where electron-rich anilines act as scaffold modifiers. Downstream chemists apply precise weighing to match theoretical yields and ensure no negative impact on subsequent chlorination or alkylation steps. Regulatory teams review lot documentation and impurity profile data, as many geographies have mandatory requirements for raw material traceability.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA 40 CFR Part 158: Data Requirements for Pesticides
    • REACH Regulation EC 1907/2006 for chemical registration (EU)
    • ISO 9001:2015 Quality Management for Agricultural Chemical Production

    Typical usage ratio

    • 0.6–1.2 molar equivalents depending on target molecule and downstream reaction efficiency
    • Formulations for new actives may require up to 1.5 equivalents to ensure conversion

    Downstream process integration

    • Charged into aromatic substitution phases for heterocycle or quinoline derivative synthesis
    • Participates in coupling reactions for functionalized aniline-based herbicide intermediates

    Final product types

    • Selective herbicides for cereals and broadacre crops
    • Systemic fungicides targeting powdery mildew and leaf spot pathogens
    • Pesticide active ingredients for export and domestic registration
    • Intermediate compounds for third-party synthesis finishing

    3. Pigment and Dye Intermediate Manufacturing

    Industrial pigment producers use 4-Bromo-3-Methoxyaniline to construct high-performance azo and polycyclic pigment intermediates, feeding into colorant lines where thermal and light stability are priorities. Technologists optimize dosing based on color yield efficiency, target C.I. structure, and reduction of side product formation. Analytical QC monitors residual bromide to avoid product contamination. Adherence to REACH, TSCA, and local colorant safety standards is verified for each batch.

    Industry compliance standards

    • REACH Regulation EC 1907/2006 for industrial colorants
    • US Toxic Substances Control Act (TSCA) Section 8(b)
    • EN 71-3:2019 for migration of certain elements in pigments used in toys and printing inks
    • ISO 1248:2016 on technical requirements for pigments

    Typical usage ratio

    • 0.8–1.1 molar equivalents against diazotization or coupling agent
    • Colour yield targets may drive use up to 1.3 equivalents in high-intensity pigments

    Downstream process integration

    • Introduced in colorant synthesis post-diazotization
    • Key input in the creation of azo and metal complex pigments

    Final product types

    • Organic yellow, orange, and red pigments for plastics and coatings
    • Dyes for specialty textile printing
    • Toner colorants for electrophotographic printers
    • Color filter materials for electronics

    4. Specialty Chemical Building Blocks

    Manufacturers of fine chemicals harness 4-Bromo-3-Methoxyaniline in constructing customized aromatic amine derivatives, facilitating flexible synthesis in materials science, electronic chemicals, and photoinitiator precursors. Chemists select batch sizes and stoichiometry based on project-specific molecular design, with regulatory checks under GHS and transport directives. Customers require material that supports downstream scale-up with robust documentation and COA data to satisfy ISO scrutiny.

    Industry compliance standards

    • GHS (Globally Harmonized System) labeling and documentation
    • ISO 9001:2015 Quality Management for specialty chemical production
    • Safe Transport of Dangerous Goods (UN Recommendations, ADR/RID as applicable)
    • EU CLP Regulation (EC) No 1272/2008 for classification and labeling

    Typical usage ratio

    • 0.5–1.0 molar equivalents in functional group introduction steps
    • Projects requiring higher selectivity may increase ratio to 1.2 equivalents

    Downstream process integration

    • Used after pre-coupling functionalization for targeted amine synthesis
    • Integrated in N-arylation and etherification routes for oligomers and specialty monomers

    Final product types

    • Electronic-grade intermediates for OLED and photoresist manufacture
    • Polymer additives and specialty resins
    • Photoactive compounds for imaging and lithographic applications
    • Custom-designed fine chemicals for R&D and commercial scale

    5. Flavors and Fragrances Synthesis (Regulated Non-food Additives)

    The fine fragrance sector employs this aniline as a precursor for aromatic aldehyde and ketone intermediates in the synthesis of high-value perfumery bases. Dosage and purity are tightly controlled to avoid noncompliance with IFRA (International Fragrance Association) safety standards, and all deliveries are accompanied by impurity and allergen statements. End users rely on defined impurity thresholds and batch-to-batch consistency to satisfy both internal QC and regulatory filing for fragrance compositions.

    Industry compliance standards

    • IFRA Standards (Amendment 51 for non-food flavor/fragrance intermediates)
    • EU Regulation 1223/2009 on cosmetic products (for perfumery applications)
    • Cosmetic Ingredient Review (CIR) safety guidance
    • ISO 22716:2007 Cosmetics—Good Manufacturing Practices

    Typical usage ratio

    • 0.3–0.9 molar equivalents per batch as determined by desired aldehyde/ketone intermediate yield
    • Purity optimization may require dropwise addition at lower volumes for pilot fragrance lines

    Downstream process integration

    • Introduced post-coupling in aromatic ring modification steps
    • Used in regulated non-food pathways—excluded from food chain contact grades

    Final product types

    • Fine fragrance base intermediates for perfumery compounds
    • Aromatic aldehydes/ketones for high-performance scent ingredients
    • Cosmetic aroma additives for regulated skincare and body care
    • Intermediate compounds for further downstream transformation in fragrance houses
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