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3-Methoxyphenylacetone

    • Product Name 3-Methoxyphenylacetone
    • Alias 3-methoxy-1-phenylpropan-2-one
    • Einecs 217-950-5
    • 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
    VTB
    Specifications

    HS Code

    291885

    Iupac Name 1-(3-methoxyphenyl)propan-2-one
    Molecular Formula C10H12O2
    Molar Mass 164.20 g/mol
    Cas Number 832-26-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 274 °C
    Density 1.061 g/cm³
    Solubility In Water Slightly soluble
    Flash Point 117 °C
    Smiles COC1=CC=CC(=C1)CC(=O)C
    Pubchem Cid 70108

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

    Packing & Storage
    Packing The 100g bottle of 3-Methoxyphenylacetone is packaged in an amber glass container with a secure, tamper-evident screw cap.
    Shipping 3-Methoxyphenylacetone is shipped in tightly sealed, chemical-resistant containers to prevent contamination and evaporation. The packaging complies with hazardous material regulations, ensuring safe transit. It is labeled with the appropriate hazard and handling information and is typically shipped with temperature control, avoiding extreme heat or cold, and adhering to all applicable transport guidelines.
    Storage 3-Methoxyphenylacetone should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizers. Keep the container tightly closed and protected from direct sunlight. Store at room temperature, ideally between 2–8°C. Use appropriate chemical-resistant containers, and ensure proper labeling to avoid accidental misuse or contamination.
    Application of 3-Methoxyphenylacetone

    Applications of 3-Methoxyphenylacetone in Industrial Manufacturing

    3-Methoxyphenylacetone is a specialty intermediate widely used in downstream industrial synthesis. Sourced directly from our precision chemical facilities, this compound meets stringent global regulations for several end-markets. Below, we outline the key application segments where this material plays an integral, documented role in fine chemical production and advanced manufacturing.

    1. Pharmaceutical API Intermediate Synthesis

    Major pharmaceutical manufacturers use this intermediate in the synthesis of select central nervous system active pharmaceutical ingredients. The aromatic ketone structure supports key condensation reactions in the assembly of small-molecule APIs. Route selection and integration depend on final molecule design and regulatory strategy, with attention to impurity profiles and validated cleaning standards during scale-up. Quality control centers on both EU GMP and USP monograph expectations for incoming intermediates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Directive 2003/94/EC and EudraLex Volume 4
    • United States Pharmacopeia (USP) General Chapters on Impurities and Residual Solvents
    • ICH Q3A/B for impurities and residuals

    Typical usage ratio

    • 10–30% by weight in multi-step synthesis, dosage determined by stoichiometry and targeted API yield
    • Adjusted for side-product management and batch-to-batch consistency

    Downstream process integration

    • Entry at condensation stage with amine partners using reductive amination or Grignard reaction
    • Co-processing under controlled temperature and solvent systems, followed by isolation and purification

    Final product types

    • Phenethylamine-class CNS APIs (for regulated prescription formulations)
    • Specialty pharmaceutical intermediate building blocks
    • Precursors for patented CNS and psychiatric disorder therapies

    2. Fragrance Ingredient Manufacturing

    Fragrance chemical producers utilize this ketone as a key precursor for the synthesis of complex musks and specialty aroma compounds. The methoxy-substitution provides a foundation for downstream methylation, isomerization, and cyclization, contributing depth to fine fragrance bases. All processes must adhere to IFRA guidelines, and production requires strict allergen control and batch tracing.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • EU Cosmetics Regulation (EC) No. 1223/2009 – Annexes II and III for fragrance allergens
    • ISO 9001:2015 for fragrance raw materials traceability
    • REACH Registration compliance for fragrance intermediates

    Typical usage ratio

    • 5–20% in ketone-based aroma synthesis routes
    • Content varies with target olfactory note and purity requirements

    Downstream process integration

    • Initiates the synthesis by methylation, or cyclization with aldehyde or alcohol moieties
    • Utilized in batch reaction systems to maximize aroma intensity and minimize by-products

    Final product types

    • Specialty musks for luxury perfumes
    • Aroma base chemicals for detergent and personal care fragrances
    • Blended perfumery concentrates for consumer products

    3. Agrochemical Intermediate Synthesis

    Agrochemical formulators select 3-methoxyphenylacetone for the construction of advanced herbicide and fungicide scaffolds. The molecule's controlled reactivity supports functional group transformation and side chain elongation, allowing efficient design of next-generation crop protection compounds. Compliance emphasizes toxicological evaluation and adherence to international pesticide manufacturing norms.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 for agrochemical process management
    • OECD Good Laboratory Practice Guidelines
    • Globally Harmonized System (GHS) for chemical labeling and safety data sheets

    Typical usage ratio

    • 8–25% per batch, depending on the designed herbicide or fungicide side chain requirements
    • Ratio optimized for active moiety introduction and environmental fate

    Downstream process integration

    • Applied in precursor alkylation or oxidation steps before incorporation into final active substances
    • Monitored via HPLC to track residuals and intermediate conversion rates

    Final product types

    • Active intermediates for selective herbicides
    • Precursor compounds for novel systemic fungicides
    • Seed treatment chemical building blocks

    4. Specialty Polymer and Resin Additives

    Producers of functional polymers and cross-linked resins employ this aromatic ketone as a monomer modifier. Its molecular structure enhances flexibility or introduces UV-absorbing functionality for adhesives and coatings. Blending requires precise control of monomer feed ratios and full traceability under industrial hygiene standards for plastic additive production.

    Industry compliance standards

    • REACH (Regulation (EC) No. 1907/2006) compliance for polymer additives
    • ISO 14001 Environmental Management for resin plants
    • FDA 21 CFR Part 177 for indirect food contact in specialty polymer applications (if applicable)
    • Quality system based on ISO 9001 for batch reproducibility

    Typical usage ratio

    • 2–10% of total monomer feed, determined by required flexibility or UV-absorption performance
    • Adjusted following QC analysis of batch polymer characteristics

    Downstream process integration

    • Incorporated via in situ polymerization as a reactive diluent or chain modifier
    • Dosed during resin pre-polymer blending or masterbatch preparation

    Final product types

    • UV-stabilized coatings and clear adhesives
    • Thermoset and thermoplastic resin systems for automotive and electronics
    • High-performance construction sealants
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