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3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene

    • Product Name 3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene
    • Alias 3,4-DIMETHOXY-β-METHYL-β-NITROSTYRENE
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    695259

    Chemical Name 3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene
    Molecular Formula C11H13NO4
    Molecular Weight 223.23 g/mol
    Appearance Yellow crystalline solid
    Melting Point 91-93°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Structure Contains a nitrostyrene core substituted with methoxy groups at the 3 and 4 positions and a methyl group at the beta position
    Iupac Name 1-(3,4-dimethoxyphenyl)-2-nitropropene
    Smiles COC1=CC=C(C=C1OC)C(C)=[N+](O)[O-]

    As an accredited 3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A tightly sealed, amber glass bottle labeled "3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene, 10g" with chemical safety and handling instructions.
    Shipping **3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene** should be shipped in sealed, chemical-resistant containers, labeled according to relevant chemical safety standards. Protect from moisture, heat, and light during transit. Comply with local and international regulations for the transport of potentially hazardous substances, and provide appropriate documentation for safe and legal shipping.
    Storage 3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene should be stored in a tightly sealed container, away from light, heat, and moisture. Store in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong acids or oxidizers. Label the container clearly, and keep it in a secure location to prevent unauthorized access. Follow all relevant safety guidelines.
    Application of 3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene

    Applications of 3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene in Industrial Manufacturing

    As a core intermediate engineered in our facilities, 3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene supports high-value industrial production streams. Our consistent synthesis and QC systems meet the narrow demands of advanced material, pharmaceutical, and specialty chemical industries that depend on validated raw materials for downstream integration.

    1. Production of Pharmaceutical Intermediates for CNS Active Compounds

    The compound serves as a precursor in the synthesis route of several central nervous system (CNS) active molecules, particularly within the phenethylamine and amphetamine derivative classes. Manufacturers use this intermediate for condensation and reduction steps, finely controlling batch purity and optical isomer separation. Regulatory authorities strictly monitor the sourcing, batch records, and material traceability for all scheduled substance intermediates in this downstream track.

    Industry compliance standards

    • US DEA List I Chemical compliance (21 CFR 1310)
    • EU EMEA GMP Part II (Active Substances)
    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • Chinese Pharmacopoeia (ChP, for APIs/intermediates)

    Typical usage ratio

    • 0.9–1.5 molar equivalents relative to product yield, fine-tuned by target intermediate and byproduct minimization

    Downstream process integration

    • Charged as a key substrate at the initial condensation stage in small molecule CNS drug synthesis, followed by reduction and cyclization steps

    Final product types

    • API intermediates for neurological therapeutics
    • Bulk APIs for psychiatric and anti-migraine medications

    2. Advanced Material Synthesis for Organic Electronics

    The raw material participates in the formation of complex aromatic scaffolds used in research and pilot production of organic semiconductors, OLED precursors, and specialty polymers. Process chemists require high-purity, low-residual nitro compounds with controlled methoxy substitution patterns for step-growth and cross-coupling reactions. Stringent material conformity and traceability to batch-level become mandatory for integration into electronics manufacturing chains.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronic devices
    • REACH Regulation (EC No 1907/2006) substance registration
    • INCI labeling for relevant downstream additives
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 20–45 wt% as an advanced building block per oligomer batch, adjusted by device architecture and substrate compatibility

    Downstream process integration

    • Introduced at the monomer coupling or functionalization step for manufacturing precursors to OLED emitters and charge transport materials

    Final product types

    • OLED small molecule emitters and hole transport layers
    • Organic semiconducting polymers for flexible electronics

    3. Specialty Dye Intermediate Manufacturing

    Large-scale colorant producers use 3,4-Dimethoxy-Beta-Methyl-Beta-Nitrostyrene as a selective intermediate for the preparation of high-purity azo and nitro dyes. The tailored methoxy and methyl-nitro substitution enhances bathochromic shift and color stability, making it suitable for industrial textile and ink applications. Production adheres to strict effluent handling and worker safety monitoring according to dye chemistry EHS regulations.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for dye residues
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, Manufacturing Restricted Substances List)
    • EU REACH Sapphire List for azo dye restrictions
    • GHS SDS hazard communication

    Typical usage ratio

    • 15–30 mol% based on total dye component loading, varied by desired shade intensity and substrate

    Downstream process integration

    • Reacted during the diazotization or coupling stage in synthetic dye production streams

    Final product types

    • Industrial textile dyes for cellulose and synthetic fibers
    • Solvent-based printing inks

    4. Custom Synthesis of Analytical Reference Standards

    Accredited analytical labs and reference standard providers utilize the material for controlled synthesis of analytical markers. It is employed where the methoxy-nitro aromatic motif is required as part of internal standards or impurity profiling for regulated trace analysis—especially in impurity testing and forensic toxicology. Strict documentation, validated COA, and analytical traceability are central to each lot transition.

    Industry compliance standards

    • ISO/IEC 17025 laboratory accreditation
    • USP Reference Standard procedures
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals, Laboratories)
    • IUPAC Chemical Identifier best practices

    Typical usage ratio

    • Sub-milligram to gram scale, adjusted case-by-case by validation protocol and instrument detection limits

    Downstream process integration

    • Charged into multi-step synthesis for production of analyte reference compounds required in HPLC, GC-MS, and NMR quality control

    Final product types

    • Certified analytical reference materials (ARMs)
    • Trace-level process impurities and metabolite markers
    Free Quote

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    Tel: +8615371019725

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