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5,6-Dimethoxy-1-Indanone

    • Product Name 5,6-Dimethoxy-1-Indanone
    • Alias 5,6-Dimethoxyindan-1-one
    • Einecs 220-786-7
    • 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

    547134

    Cas Number 20721-46-2
    Molecular Formula C11H12O3
    Molecular Weight 192.21 g/mol
    Iupac Name 5,6-dimethoxy-2,3-dihydro-1H-inden-1-one
    Appearance White to off-white solid
    Melting Point 95-97°C
    Boiling Point Unknown
    Solubility Soluble in organic solvents such as ethanol and dichloromethane
    Density Unknown
    Smiles COc1cc2c(cc1OC)C(=O)CC2
    Inchi InChI=1S/C11H12O3/c1-13-8-3-7-4-5-11(12)10(7)9(8)14-2/h3-4H,5-6H2,1-2H3
    Ec Number 244-094-8

    As an accredited 5,6-Dimethoxy-1-Indanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 5,6-Dimethoxy-1-Indanone is packaged in a tightly sealed, amber glass bottle with clear hazard labeling.
    Shipping 5,6-Dimethoxy-1-Indanone is typically shipped in tightly sealed containers to protect it from moisture and light. It should be handled and transported in accordance with standard chemical safety protocols, including labeling and documentation. Shipping must comply with local and international regulations for non-hazardous laboratory chemicals. Store in a cool, dry place upon arrival.
    Storage 5,6-Dimethoxy-1-Indanone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Protect from moisture and incompatible substances such as strong oxidizers. Store at recommended room temperature, and always follow standard laboratory safety protocols when handling or storing this compound.
    Application of 5,6-Dimethoxy-1-Indanone

    Applications of 5,6-Dimethoxy-1-Indanone in Industrial Manufacturing

    5,6-Dimethoxy-1-Indanone functions as a key intermediate for multiple specialized sectors requiring rigorous quality, traceability, and reliable supply chain integration. Below we outline verified downstream applications, together with compliance, dosing, process stage, and end product details relevant to each manufacturing field.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical companies employ 5,6-Dimethoxy-1-Indanone as a core building block in the synthesis of complex indanone derivatives for anti-inflammatory and neuroprotective drug discovery. Its role is central in the formation of specific cyclic ketone scaffolds through substituted indanone condensation reactions. In R&D and commercial-scale GMP processes, precise stoichiometry and reaction control are required to ensure drug substance purity and batch-to-batch repeatability. This raw material is utilized for the preparation of small molecule drugs subjected to strict regulatory auditing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monograph Guidance for Intermediates
    • 21 CFR Part 210/211 (FDA Drug Manufacturing)
    • EU EMA Guidelines for Starting Materials in Medicinal Products

    Typical usage ratio

    • 10–30% molar basis relative to target API precursors; exact ratio depends on downstream target molecule complexity

    Downstream process integration

    • Introduced during condensation, cyclization, and derivatization steps in the synthetic route for new chemical entities

    Final product types

    • Active pharmaceutical ingredients for anti-parkinsonian and anti-inflammatory medications
    • Intermediates for central nervous system drug candidates
    • Finished pharmaceutical tablets and capsules

    2. Agrochemical Intermediate Manufacturing

    Leading agrochemical firms integrate 5,6-Dimethoxy-1-Indanone into synthesis pathways for pyridyl and indanone-based herbicide and pesticide actives. These structurally unique compounds target weed and pest resistance in crops. Manufacturers rely on this material for key condensation reactions enabling scalable production under rigorous quality and environmental controls. Trace level impurities must be managed due to their direct impact on final agrochemical efficacy and regulatory registration acceptance.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice
    • ISO 9001:2015 Quality Management for Agrochemical Manufacturing
    • National Maxwell Standard GB 20671 for Pesticide Raw Materials (CN)
    • FAO/WHO Specifications for Plant Protection Products

    Typical usage ratio

    • 5–20% mass balance in intermediate coupling reactions, depending on the crop protection formulation and target molecule

    Downstream process integration

    • Charged into stage-specific reactors during the construction of indanone herbicides and insecticides, ahead of formulation blending

    Final product types

    • Technical grade herbicide and pesticide actives
    • Emulsifiable concentrate and wettable powder crop protection formulations
    • Seed treatment chemical agents

    3. Fine Chemical Synthesis for Dye and Pigment Bases

    The dye and pigment sector uses 5,6-Dimethoxy-1-Indanone as a precursor in the synthesis of advanced aromatic systems. These targeted syntheses produce colorants employed in specialty inks and high-stability coatings, where colorfastness and batch uniformity are critical. This intermediate participates in Friedel-Crafts acylation and cyclization schemes to introduce methoxy substituents that enhance pigment stability under UV exposure and in harsh process environments.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • EN 71-3 Safety of Toys for Colorant Components (EU)
    • Global Harmonized System (GHS) for Chemical Labeling
    • Manufacturing Restricted Substances List (MRSL) Compliance for Textile Dyes

    Typical usage ratio

    • 15–25% precursor composition by weight in dyestuff synthesis batches; modifiable for pigment shade and solubility characteristics

    Downstream process integration

    • Incorporated at the cyclization step of pigment base synthesis before azo-coupling or further derivatization

    Final product types

    • Specialty ink colorants for industrial printing
    • Automotive and architectural coating pigments
    • High-performance plastic and textile dyes

    4. Fragrance and Aromatic Chemicals Manufacture

    Fragrance compound producers use 5,6-Dimethoxy-1-Indanone as a core intermediate for synthesizing aromatic ketones and indanone derivatives found in fine fragrances, cosmetic aromas, and household scents. The methoxy-substituted structure enables downstream reactions yielding musky and woody base notes with high odor stability. Manufacturing lines must meet IFRA and REACH criteria for traceability and composition safety, and production teams control input ratios according to olfactory target profiles and consumer product safety data.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • EU REACH Regulation (EC No 1907/2006)
    • ISO 22716 Good Manufacturing Practice for Cosmetics
    • US EPA TSCA for Aroma Chemicals

    Typical usage ratio

    • 2–10% by mass in precursor blend; proportion adjusted based on intended aromatic note strength and base formulation

    Downstream process integration

    • Fed into condensation reactors for production of indanone musk components and aromatic ketones prior to final blending and dilution

    Final product types

    • Fine fragrance compositions for perfumery
    • Cosmetic base aroma ingredients
    • Fragrance oil blends for home and fabric care
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