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6-Bromo-2-Tetralone

    • Product Name 6-Bromo-2-Tetralone
    • Einecs 253-732-0
    • 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
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    VTB
    Specifications

    HS Code

    238953

    Chemical Name 6-Bromo-2-Tetralone
    Cas Number 57191-11-4
    Molecular Formula C10H9BrO
    Molecular Weight 225.08 g/mol
    Appearance White to off-white solid
    Melting Point 87-90°C
    Purity Typically >98%
    Solubility Soluble in organic solvents like DMSO and ethanol
    Smiles O=C1CCc2cc(Br)ccc2C1
    Inchi InChI=1S/C10H9BrO/c11-8-2-3-9-7(6-8)4-1-5-10(9)12/h2-3,6H,1,4-5H2
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms 6-Bromo-3,4-dihydro-2H-naphthalen-1-one

    As an accredited 6-Bromo-2-Tetralone 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 25g of 6-Bromo-2-Tetralone, sealed with a screw cap, labeled with hazard and product information.
    Shipping 6-Bromo-2-Tetralone is shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent contamination. Packages are labeled according to regulatory requirements. The chemical is protected from light, heat, and moisture during transit. Transportation complies with local and international hazardous material regulations to guarantee safe delivery to the end user.
    Storage 6-Bromo-2-Tetralone should be stored in a tightly closed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers. Store at room temperature or as directed on the manufacturer’s label to ensure chemical stability and prevent degradation. Always follow standard chemical safety guidelines.
    Application of 6-Bromo-2-Tetralone

    Applications of 6-Bromo-2-Tetralone in Industrial Manufacturing

    6-Bromo-2-Tetralone is a specialty intermediate valued in multiple chemical manufacturing sectors. It serves as a critical building block in regulated pharmaceutical synthesis, dye and pigment manufacturing, specialty agrochemical production, as well as in advanced fragrance formulation. The following application scenarios demonstrate actual downstream use cases, relevant industrial standards, dosage practices, process stages, and finished product types.

    1. Pharmaceutical APIs: Synthesis of Central Nervous System Agents

    The pharmaceutical sector implements 6-Bromo-2-Tetralone primarily to manufacture intermediates for central nervous system active ingredients, notably for atypical antipsychotics and anti-Parkinson compounds. Manufacturers utilize its substituted tetralone structure for targeted molecular transformations during multi-step synthesis. This use case focuses on stringent process controls with attention to reaction selectivity, impurity profile, and traceable documentation to support registration filings and tech transfer.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US cGMPs for finished pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monographs for API intermediates
    • US FDA Drug Master File (DMF) submission requirements

    Typical usage ratio

    • 0.4–1.2 molar equivalents per target intermediate; adjusted for conversion yield and side-reaction minimization in sequence reactions.

    Downstream process integration

    • Introduced during key ring closure or halogenation steps, followed by purification and further derivatization.
    • Utilized in batch or semi-continuous reactors with in-process HPLC monitoring.
    • Process validation includes stability of the intermediate and metal catalyst scavenging steps.

    Final product types

    • Pharmaceutical grade API precursors, such as substituted tetrahydronaphthalene derivatives
    • Bulk APIs for central nervous system disorder treatments
    • Regulatory starting materials for patented drug substances

    2. Dye and Pigment Industry: Intermediate for Anthraquinone-Based Compounds

    Manufacturers in the dye and pigment sector use 6-Bromo-2-Tetralone as an intermediate for high-performance anthraquinone-based colorants. Its unique bromo substitution facilitates selective coupling and functional group transformations that enhance chromophore properties. The process chain includes tight emission control and waste stream tracking due to halogenated material handling, fulfilling regulatory and customer audit demands.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006, Annex VII and VIII (Europe)
    • OEKO-TEX® Standard 100 Restricted Substance List
    • ISO 9001:2015 Quality Management Systems for manufacturing/process control

    Typical usage ratio

    • 5–20% molar basis relative to final dye core; variable based on target hue and functionalization route.

    Downstream process integration

    • Engaged during condensation reactions to introduce bromo functionality.
    • Transferred through solvent extractions and crystallization steps prior to oxidative finishing.
    • Endpoint analytical control using UV-Vis and HPLC/GC techniques.

    Final product types

    • High-performance vat dyes for textile and fiber coloration
    • Specialty pigments for coatings and plastics applications
    • Anthraquinone lake colorants for inks and industrial printing

    3. Agrochemical Synthesis: Building Block for Herbicide Intermediates

    The agrochemical sector adopts 6-Bromo-2-Tetralone for the synthesis of selective herbicide intermediates, especially for naphthalene and phthalide-based product lines. The compound acts as a key precursor in structural modification steps that provide desired biological activity and selective binding properties. Process operations prioritize batch tractability, cross-contamination checks, and governmental registration standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • US EPA 40 CFR Part 158 (Data Requirements for Pesticide Registration)
    • ISO 17065:2012 (Certification of plant protection products supply chains)

    Typical usage ratio

    • 8–15% by weight in multi-component synthesis; adapted based on biotransformation efficiency and crystallization yield.

    Downstream process integration

    • Added in ring formation or substitution reactions to introduce halogenation.
    • Transfer through continuous stirred-tank reactors (CSTR) and automated filtration units.
    • In-line GC-MS employed to ensure intermediate stage purity before scale-up.

    Final product types

    • Active agrochemical intermediates for further downstream formulation
    • Pre-formulated technical herbicide concentrates
    • Regulatory reference standards for residue analysis

    4. Fragrance and Aroma Chemicals: Scent Molecule Synthesis

    Advanced fragrance chemical manufacturers leverage 6-Bromo-2-Tetralone in the custom synthesis of musk and floral aroma building blocks. Its tetralone backbone enables tailored cyclization and reduction steps to yield complex macrocyclic musks, with established routes minimizing by-product contamination and olfactory off-notes. Customer specifications demand tight impurity control, high batch reproducibility, and thorough documentation for international shipment and cosmetics registration.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association) for material safety and purity
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9001:2015 for batch release and traceability

    Typical usage ratio

    • 2–10% loading in precursor stages; depends on target macrocycle and conversion selectivity required by fragrance formulators.

    Downstream process integration

    • Used in lactonization or Grignard coupling reactions, followed by downstream hydrogenation.
    • Controlled distillation and vacuum drying exclude volatile impurities prior to finishing.
    • Gas chromatography-olfactometry (GC-O) supports batch release approval.

    Final product types

    • Cyclic musk aroma ingredients for fine fragrance blends
    • Floral and woody note intermediates for household and personal care perfumes
    • Custom macrocyclic compounds for F&F industry applications
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