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7-Bromo-1-Tetralone

    • Product Name 7-Bromo-1-Tetralone
    • Einecs 609-208-9
    • 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

    337412

    Product Name 7-Bromo-1-Tetralone
    Cas Number 51768-04-4
    Molecular Formula C10H9BrO
    Molecular Weight 225.08
    Appearance White to off-white solid
    Melting Point 82-86°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g. ethanol, dichloromethane)
    Storage Conditions Store at room temperature, away from light and moisture
    Synonyms 7-Bromo-3,4-dihydro-1(2H)-naphthalenone
    Smiles Brc1ccc2c(=O)cccc2c1
    Inchi InChI=1S/C10H9BrO/c11-8-3-1-2-7-4-5-9(12)6-10(7)8/h1-3,6H,4-5H2

    As an accredited 7-Bromo-1-Tetralone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 7-Bromo-1-Tetralone, 25g, is packaged in an amber glass bottle with a tamper-evident cap and chemical hazard labeling.
    Shipping 7-Bromo-1-Tetralone is shipped in tightly sealed containers to prevent leaks or contamination, protected from light and moisture. It is classified as a hazardous chemical and requires compliant labeling, documentation, and handling according to regulatory standards. Transport is typically via ground or air, following all safety and shipping regulations.
    Storage 7-Bromo-1-tetralone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat or ignition. Keep it away from incompatible substances such as strong oxidizing agents. Ensure proper labeling and secondary containment to prevent spills. Access should be limited to trained personnel using appropriate personal protective equipment.
    Application of 7-Bromo-1-Tetralone

    Applications of 7-Bromo-1-Tetralone in Industrial Manufacturing

    As a specialized manufacturer, we recognize the critical roles of 7-Bromo-1-Tetralone across advanced industrial chemical synthesis sectors. This intermediate enables targeted molecular construction for downstream applications in pharmaceuticals, agrochemicals, specialty dyes, and advanced materials. Below, we detail specific industry scenarios where 7-Bromo-1-Tetralone enters production, emphasizing compliance, usage ratios, integration workflows, and end-product outputs.

    1. Pharmaceutical Intermediate for CNS Active Compounds

    Pharmaceutical companies select our 7-Bromo-1-Tetralone to synthesize central nervous system (CNS) active molecules. Its bromo-ketone structure allows for efficient functional group transformations, supporting heterocycle assembly and aryl substitution, both critical in drug development. Manufacturers introduce this intermediate during the stepwise construction of tricyclic and tetracyclic pharmaceutical scaffolds, especially in antipsychotic and antidepressant drug pipelines. The material undergoes strict input control and traceability during multistep organic reactions under GMP settings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 – GMP Guidelines
    • United States Pharmacopeia (USP) monograph specifications for intermediates
    • Relevant local FDA and EMA precursor control lists

    Typical usage ratio

    • 0.20–0.40 molar equivalents relative to core amines or hydrazines, with precise adjustment based on reaction scale and substrate reactivity

    Downstream process integration

    • Enters as the electrophilic partner in Grignard addition or Suzuki coupling in the intermediate stage of API synthesis, following raw material QC release and reactor charging

    Final product types

    • Antidepressant and antipsychotic APIs, such as tetracyclic derivatives
    • Pipeline CNS modulators in clinical development
    • Advanced intermediates for generic drug synthesis
    • Reference standards for pharmaceutical QC

    2. Building Block for Agrochemical Synthesis

    Agrochemical formulators utilize 7-Bromo-1-Tetralone as a starting block for selective fungicide and herbicide molecules. Its aromatic bromo functionality permits efficient substitution, enabling downstream extension into benzyl-substituted heterocycles and oxygenated aromatic rings. Typical industrial scale reactions require careful attention to product purity to prevent active residue concerns in regulated field applications.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • OECD Guidelines for the Testing of Chemicals (Section 2: Effects on Biotic Systems)
    • ISO 9001:2015 certified quality system for raw material manufacturing
    • National agroscience ingredient import/export controls

    Typical usage ratio

    • 10–25% w/w relative to total synthetic batch, adjusted for pathway yield and downstream coupling efficiency

    Downstream process integration

    • Charged at step two or three of multi-stage synthesis, typically after the initial condensation phase when extending the aromatic structure or introducing functionalized rings

    Final product types

    • Systemic fungicidal actives (triazole, strobilurin skeletons)
    • Aryloxyphenoxypropionic acid class herbicide intermediates
    • Custom synthesis intermediates for contract agrochemical projects
    • Analytical standards for residue analysis

    3. Dye Intermediate in Specialty Colorant Manufacturing

    Colorant manufacturers apply 7-Bromo-1-Tetralone as a specialty intermediate for constructing high-performance dyes, especially in applications requiring unique red and purple hues. Reactivity at the bromo position enables downstream coupling with azo or thiol groups, supporting the precise structure modification required for light-fastness and solvent-resistance in textile or plastics coloration. Close process control of halogen content and impurities is maintained to meet stringent end-use requirements.

    Industry compliance standards

    • Oeko-Tex Standard 100 (for textile applications)
    • REACH Regulation (EC) No 1907/2006 for chemical safety in EU markets
    • ISO 9001:2015 and ISO 14001:2015 for manufacturer quality and environmental management
    • ZDHC Chemical Management Protocol (where applicable)

    Typical usage ratio

    • 5–12% w/w in batch colorant synthesis, varying by dye architecture and downstream reactivity

    Downstream process integration

    • Utilized in intermediate coupling stages, typically following aromatic ring functionalization and prior to azo or thioether bond formation in dye molecule assembly

    Final product types

    • High-fastness anthraquinone dyes for industrial textiles
    • Specialty pigments for plastics and coatings
    • Colorant components for digital printing inks
    • Precursor intermediates for advanced color matching formulations

    4. Advanced Materials: Precursor for Organic Electronics

    Manufacturers of organic electronic materials rely on 7-Bromo-1-Tetralone to introduce brominated aryl motifs into conductive small molecules and polymers. Its controlled reactivity promotes incorporation into conjugated backbones, which is essential for enhancing charge mobility and film-forming characteristics in organic semiconductors and OLED materials. The product’s trace metal and halide specification integrity supports reliable device-grade material synthesis.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substances restriction in electronics
    • IEC 62474 Material Declaration for the Electrical and Electronics Industry
    • ISO 9001:2015 for material quality assurance
    • Customer-specific purity and contaminant control specifications (ppb–ppm level)

    Typical usage ratio

    • 2–6 mol% loaded during active layer precursor synthesis, based on polymer chain length and device specification needs

    Downstream process integration

    • Feeds into Stille or Suzuki cross-coupling protocols as the aryl bromide donor during monomer chain building for conjugated polymer backbones

    Final product types

    • Organic light-emitting diode (OLED) materials
    • Organic photovoltaic (OPV) active layer precursors
    • Conducting polymers for flexible electronics
    • Specialty semiconductors for display technologies
    Free Quote

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