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4-Methyl-1-Indanone

    • Product Name 4-Methyl-1-Indanone
    • Einecs 210-266-3
    • 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

    755850

    Cas Number 2503-29-9
    Molecular Formula C10H10O
    Molecular Weight 146.19 g/mol
    Iupac Name 4-methyl-1-indanone
    Appearance White to off-white solid
    Melting Point 41-44°C
    Boiling Point 296°C
    Density 1.13 g/cm³
    Refractive Index 1.576
    Purity Typically ≥98%
    Synonyms 4-Methylindan-1-one
    Smiles CC1=CC2=C(C=C1)C(=O)CC2
    Solubility Slightly soluble in water, soluble in organic solvents
    Flash Point 134°C
    Storage Conditions Store at room temperature, in a dry place

    As an accredited 4-Methyl-1-Indanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle labeled "4-Methyl-1-Indanone," features hazard pictograms, CAS number, lot number, and safety instructions.
    Shipping 4-Methyl-1-Indanone is typically shipped in tightly sealed, chemical-resistant containers to prevent leakage or contamination. It should be kept away from heat, sparks, and open flames, and stored in a cool, well-ventilated area. Proper labeling and documentation are required according to local and international transportation regulations.
    Storage 4-Methyl-1-indanone should be stored in a cool, dry, and well-ventilated area away from sources of ignition or heat. Keep the container tightly closed and protected from light and moisture. Store separately from strong oxidizing agents and acids. Use appropriate chemical-resistant containers and label clearly. Follow all standard chemical storage regulations and safety guidelines.
    Application of 4-Methyl-1-Indanone

    Applications of 4-Methyl-1-Indanone in Industrial Manufacturing

    4-Methyl-1-Indanone is applied as an essential raw material across several advanced chemical manufacturing sectors. Our material is produced consistently in compliance with international quality benchmarks, enabling downstream partners to achieve precise performance targets in fine chemicals, electronic intermediates, fragrance synthesis, and pharmaceutical intermediates.

    1. Synthesis of High-Performance Organic Electronic Intermediates

    This compound establishes itself as a building block for advanced electronic chemicals, especially in the production of OLED and conductive polymer intermediates. In this field, manufacturers apply it in C–C coupling reactions and selective oxidation processes to produce functionalized indanone derivatives, supporting electronic characteristics required for next-generation displays and organic devices. The process requires strict purity control and analytical verification to ensure consistent electronic grade specification, with continual in-line monitoring during preparation and final purification.

    Industry compliance standards

    • IEC 60747 (Semiconductor Devices)
    • IPC-4552 (Organic Solderability Preservatives)
    • RoHS Directive (2011/65/EU) for hazardous substances
    • REACH Regulation (EC) No. 1907/2006

    Typical usage ratio

    • 15–25% by mol count in indanone precursor synthesis; proportions adjusted by electronic function group requirements and yield optimization.

    Downstream process integration

    • Introduced at early-stage organometallic coupling; processed through multi-step synthesis, then refined under inert atmospheres with real-time GC-MS tracking.

    Final product types

    • OLED emitter intermediates
    • Organic field-effect transistor (OFET) precursors
    • Photoresist materials
    • Polyfunctional indanone-based electronic chemicals

    2. Aroma Chemicals and Fragrance Intermediate Production

    Major fragrance manufacturers utilize this raw material to develop high-value musk and jasmine aroma intermediates. Catalytic hydrogenation and downstream acylation reactions convert the input material into complex aroma molecules. Production scales require batch consistency, identity testing, and routine sensory evaluations, especially when qualifying for food-contact and cosmetic-grade materials.

    Industry compliance standards

    • IFRA Code of Practice (latest update)
    • EU Cosmetic Regulation (EC) No. 1223/2009
    • US Food Chemicals Codex (FCC)
    • ISO 9001 Quality Management System for fragrance supply

    Typical usage ratio

    • 8–18% by mass in aroma intermediate synthesis; exact ratios depend on synthetic pathway efficiency and required fragrance intensity.

    Downstream process integration

    • Fed into catalytic batch reactors for Friedel–Crafts or Grignard modifications, followed by fractional vacuum distillation, adsorption, and QC on headspace GC.

    Final product types

    • Jasmine-type ketone intermediates
    • Synthetic musk bases
    • Fine fragrance base stocks
    • Flavor-and-fragrance approved indanone derivatives

    3. Pharmaceutical Intermediate Manufacturing

    Several API producers integrate this raw material during the multi-stage synthesis of neurological and anti-inflammatory drug intermediates. Its reactive methylene and carbonyl groups enable selective modifications for regulated bioactive molecule construction. On-site compliance documentation requires monitoring for trace impurities, full batch record retention, and rigorous alignment to GMP standards. Each process stage mandates reference standard comparison and isolation of critical intermediates via preparative HPLC.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide
    • USP General Chapter <1086> Impurities in Drug Substances
    • EU GMP Volume 4
    • CFDA Chemical Drug Registration classification

    Typical usage ratio

    • 10–22% by mol basis in key intermediate stage; ratio varies per targeted API scaffold and side-chain length requirements.

    Downstream process integration

    • Added post-initial alkylation, enabling further condensation/functionalization steps before conversion to final API intermediates; all processing according to sanitation and containment protocols.

    Final product types

    • Neuroprotective agent intermediates
    • Non-steroidal anti-inflammatory (NSAID) precursors
    • Psychoactive indanone derivative drug candidates
    • Regulatory-submitted API building blocks

    4. Agrochemical Synthesis and Plant Protection Intermediate Formulation

    Agrochemical formulators employ this molecule in synthesis of selective herbicide and fungicide intermediates. It contributes to the indanone moiety in bioactive compounds, supporting targeted mechanisms of action crucial for resistance management in crop protection programs. Each batch passes impurity profiling and stability testing to meet sector safety allowances for residual materials in formulated goods.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • OECD Test Guidelines for Chemicals
    • US EPA PR Notice 94-4 (Production safety and quality for pesticide chemicals)
    • ISO 17025 Laboratory Accreditation

    Typical usage ratio

    • 12–20% by mol contribution in intermediate synthesis; adjusted as per herbicide efficacy trials and structure-activity relation data.

    Downstream process integration

    • Reacted with specific acyl, nitrogen, or halide agents in protected reactors; further processed via hydrolysis, crystallization, and technical-grade purification prior to downstream formulation or stabilization.

    Final product types

    • Selective herbicide intermediates
    • Fungicide precursor bases
    • Plant growth regulator intermediates
    • Custom indanone-based active ingredient building blocks

    5. Specialty Polymer Additive and Resin Modifier Manufacturing

    This material enables synthesis of high-refractive, thermally stable resin modifiers and UV-absorbing polymer additives. It is introduced to improve the physical and chemical characteristics of engineering plastics and specialty coatings. Each formulation adheres to batch consistency and residual solvent limits, while downstream product testing ensures end-use compatibility with intended optical, mechanical, or UV-protective functionalities.

    Industry compliance standards

    • UL 94 Flammability Testing
    • RoHS (2011/65/EU) and WEEE (2012/19/EU) directives
    • ISO 4892 Weathering and UV Testing
    • REACH SVHC Assessment

    Typical usage ratio

    • 5–13% by weight in monomer/polymer blends; adjusted based on required additive concentration to meet target optical or mechanical specifications.

    Downstream process integration

    • Pre-mixed into bulk monomer feed, or added post-polymerization for masterbatch production; underwent extrusion or melt blending, then pelletized before quality assessment.

    Final product types

    • UV-absorber additive concentrates
    • Thermally stable polyester resins
    • High-refractive index plastic components
    • Specialty engineering polymer formulations
    Free Quote

    Competitive 4-Methyl-1-Indanone prices that fit your budget—flexible terms and customized quotes for every order.

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