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2-Methyl-1-Tetralone

    • Product Name 2-Methyl-1-Tetralone
    • Einecs 239-623-2
    • 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

    843279

    Chemical Name 2-Methyl-1-tetralone
    Molecular Formula C11H12O
    Molecular Weight 160.21 g/mol
    Cas Number 5293-55-6
    Appearance Pale yellow to yellow crystalline solid
    Melting Point 38-41 °C
    Boiling Point 150-153 °C at 2 mmHg
    Density 1.09 g/cm³
    Synonyms 2-Methyltetralone, 2-Methyl-1,2,3,4-tetrahydronaphthalen-1-one
    Smiles CC1CCc2ccccc2C1=O
    Inchi InChI=1S/C11H12O/c1-8-6-7-10-4-2-3-5-9(10)11(8)12/h2-5,8H,6-7H2,1H3
    Refractive Index 1.578 (predicted)
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store in a cool, dry place, keep container tightly closed

    As an accredited 2-Methyl-1-Tetralone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 2-Methyl-1-Tetralone (25g) features an amber glass bottle with a secure screw cap and clear hazard labeling.
    Shipping 2-Methyl-1-Tetralone is shipped in tightly sealed, chemically resistant containers to prevent leaks and contamination. It should be transported under ambient conditions, away from ignition sources, oxidizers, and direct sunlight. Proper labeling and documentation compliant with hazardous material regulations are required. Handle with care to avoid spills during transit.
    Storage 2-Methyl-1-Tetralone should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and direct sunlight. Keep the container tightly closed and clearly labeled. Store separately from oxidizing agents and strong acids or bases. Use appropriate chemical-resistant containers and avoid exposure to moisture. Ensure access to suitable spill containment and safety equipment in the storage area.
    Application of 2-Methyl-1-Tetralone

    Applications of 2-Methyl-1-Tetralone in Industrial Manufacturing

    As a direct manufacturer with large-scale synthesis capabilities, we supply 2-Methyl-1-Tetralone to multiple industrial segments where its high purity and consistent chemical structure are critical to customer operations. Below, we outline key application areas, specification requirements, production flows, and common downstream product forms that our clientele demand in international markets.

    1. Pharmaceutical Intermediate for Antihypertensive APIs

    2-Methyl-1-Tetralone is used extensively as a core intermediate in the synthesis of certain antihypertensive active pharmaceutical ingredients, especially in pathways that require naphthalene-based ketones as building blocks. Process engineers employ the compound in key Friedel–Crafts and Grignard reactions, controlling material quality at each stage to adhere to regulatory submission standards. Strict batch consistency, impurity profile management, and validated cleaning protocols are maintained during its conversion into API precursors. Customers in global pharmaceutical supply chains require transparent traceability and regulatory-compliant documentation for each batch processed through GMP environments.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (US FDA CGMP for Finished Pharmaceuticals)
    • EU GMP Part II (Basic Requirements for Active Substances)
    • Ph. Eur., USP, JP—Raw material and impurity control as per applicable monographs in API synthesis

    Typical usage ratio

    • Ranges from 0.8 to 1.2 molar equivalents per API synthesis stage, adjusted by target yield and process selectivity; client process QC determines final charge amount per batch.

    Downstream process integration

    • Charged into initial condensation or alkylation steps post-solubilization;
    • Purity checked via in-process HPLC/GC before further reduction or cyclization;
    • Material proceeds through isolation, purification, and transformation into the final API structure.

    Final product types

    • Finished antihypertensive active pharmaceutical ingredients (e.g., naphthyl derivatives);
    • Intermediates for cardiovascular drug candidates;
    • Pharmaceutical-grade bulk intermediates for contract manufacturing organization (CMO) partners.

    2. Fine Fragrance Ingredients Synthesis

    Fragrance compound manufacturers rely on 2-Methyl-1-Tetralone for constructing high-impact aroma chemicals, particularly those based on musky and amber notes. It serves as a precursor for ketonic and bicyclic aromatic blends, undergoing controlled catalytic hydrogenation and acylation to impart desired olfactory profiles. The downstream process emphasizes minimal contaminant carryover and thorough organoleptic assessment, as end-use applications are closely regulated under international cosmetic standards and require IFRA certification for individual fragrance molecules.

    Industry compliance standards

    • IFRA Code of Practice and Annexes (International Fragrance Association);
    • EU REACH registration for usage in finished fragrance compounds;
    • ISO 22716 (Cosmetic GMP) for facilities integrating fragrance ingredients;
    • Cosmetics Regulation (EC) No 1223/2009 for ingredient safety and labeling.

    Typical usage ratio

    • Generally 3–10% by mass in aroma chemical synthesis steps, fine-tuned according to target molecule structure and downstream concentration requirements.

    Downstream process integration

    • Added to reaction vessels for controlled hydrogenation or side-chain modification;
    • Undergoes continuous distillation and purification to meet fragrance-grade specifications;
    • Blended into complex mixtures by flavorists after stability testing.

    Final product types

    • High-purity aroma chemicals for fine fragrance bases;
    • Musky ketones in luxury perfumes and colognes;
    • Synthetic amber notes for home and personal care applications.

    3. Agrochemical Active Ingredient Manufacturing

    Major agrochemical producers use 2-Methyl-1-Tetralone to develop intermediate structures in the synthesis of growth regulation and pest management actives. The compound’s naphthalene backbone supports the construction of heterocyclic scaffolds used in selective herbicides and insecticides. Downstream formulation leverages strict analytical controls to minimize by-product residues, as finished actives require global registration for field use and are monitored for environmental toxicity according to international pesticide regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products;
    • OECD Principles of Good Laboratory Practice (GLP);
    • China GB Standard for Pesticide Residues;
    • EU Regulation EC 1107/2009 (placing of plant protection products on the market).

    Typical usage ratio

    • Used at 1.5–2.8 equivalents per targeted coupling stage, directly correlated with throughput and conversion rate per seasonal production campaign.

    Downstream process integration

    • Charged at controlled temperature for first-stage etherification or cyclization;
    • Incorporated into multi-step synthesis for active construction, monitored via batch tracking;
    • Extensive in-process analysis for residuals before formulation into stable concentrates or dispersibles.

    Final product types

    • Technical-grade herbicide and insecticide actives;
    • Pre-formulated sprayable crop protection products;
    • Environmental safety-tested bioactive intermediates for market registration.

    4. Dyes & Pigments Precursor for Industrial Colorants

    Several large-scale dye manufacturers incorporate 2-Methyl-1-Tetralone into the synthesis of high-performance organic pigments, targeting textile, plastics, and coatings segments. The compound enters via nucleophilic substitution and oxidation reactions, building key chromophoric groups essential for lightfastness and brilliance. Batch-specific traceability assures customers reliable integration into pigment plants, where compliance with heavy metal restrictions and global ecolabel standards for export drive the requirements for feedstock quality documentation.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for restriction of hazardous substances in dyes);
    • EU Regulation (EC) No 1907/2006 (REACH) for pigments and additives;
    • ISO 9001 (Quality Management in Colorant Manufacturing);
    • US CPSIA Lead and Phthalates Standards—applicable to exported colorant goods.

    Typical usage ratio

    • 0.5–3 weight% in pigment precursor reactions, adjusted based on end-use concentration, performance requirements, and desired spectrum properties.

    Downstream process integration

    • Enters early-stage syntheses for chromophore construction;
    • Subjected to oxidative or reductive pathway as per pigment design;
    • Integrated into final pigment dispersion units for quality finishing and packaging.

    Final product types

    • High-fastness organic pigments for textile dyeing;
    • Masterbatch colorants for plastics processing lines;
    • Specialty industrial coatings and inkjet printing dyes.

    5. Specialty Polymer and Resin Synthesis

    Advanced materials producers in the specialty polymer sector employ 2-Methyl-1-Tetralone in the creation of structural monomers for high-thermal stability resins. It serves as a modifier in resin backbone systems used in automotive composites, electronics encapsulants, and performance adhesives. Formulation sections require accurate mass-balance calculations and integration with polymerization initiators, as regulatory control over process emissions and extractables remains strict for many high-tech and export-oriented applications.

    Industry compliance standards

    • ISO 14001 (Environmental Management for Industrial Production);
    • EN 45545-2 (Fire Safety for Railway Polymer Applications);
    • ASTM D638 and D790 (Standard Test Methods for Polymers);
    • EU RoHS for electronics-use restricts hazardous monomer content and by-products.

    Typical usage ratio

    • Used at 2–6 mol% relative to total monomer charge in resin or thermoset formulations, with adjustments based on customer mechanical and thermal property targets.

    Downstream process integration

    • Directly charged to pre-polymer mixture prior to catalyst or crosslinker addition;
    • Cured under controlled temperature/atmosphere with in-line monitoring of conversion;
    • Integrated into continuous or batch extrusion as needed for downstream fabrication.

    Final product types

    • Epoxy and polyester resins with enhanced impact and heat resistance;
    • Composite structural parts for automotive and aerospace industries;
    • Encapsulants and thermally stable adhesives for electronics assembly.
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