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5-Methoxy-2-Methylindole

    • Product Name 5-Methoxy-2-Methylindole
    • Alias 5-Methoxy-2-Methylindole
    • Einecs 247-897-9
    • 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

    318702

    Name 5-Methoxy-2-Methylindole
    Cas Number 3188-14-9
    Molecular Formula C10H11NO
    Molecular Weight 161.20
    Appearance White to off-white solid
    Boiling Point 334.3 °C at 760 mmHg
    Melting Point 60-64 °C
    Density 1.16 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC1=CC2=C(C=C1)C=CN2OC
    Iupac Name 5-methoxy-2-methyl-1H-indole
    Pubchem Cid 39783

    As an accredited 5-Methoxy-2-Methylindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-Methoxy-2-Methylindole (25g) is supplied in a sealed amber glass bottle, labeled with hazard symbols and safety information.
    Shipping 5-Methoxy-2-Methylindole is shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent leakage. It is handled according to standard hazardous material regulations, protected from light, heat, and moisture, with appropriate labeling. Transport follows relevant legal and safety guidelines for shipping laboratory chemicals.
    Storage 5-Methoxy-2-Methylindole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect from light and moisture. Label the container clearly. Personal protective equipment (PPE) should be used when handling, and access should be restricted to trained personnel only.
    Application of 5-Methoxy-2-Methylindole

    Applications of 5-Methoxy-2-Methylindole in Industrial Manufacturing

    As the direct manufacturer of 5-Methoxy-2-Methylindole, we support the integration of this intermediate into regulated specialty chemical segments. Our focus is on proven downstream applications in pharmaceutical synthesis, advanced dye intermediates, research reagents, and agrochemical building blocks. Below, we provide comprehensive scenario-specific insights into each sector, including regulatory standards, industrial usage ratios, precise incorporation points in manufacturing, and the real-world nature of final products adopted by our global B2B partners.

    1. Pharmaceutical Intermediates: Active Pharmaceutical Ingredient (API) Synthesis

    Our material serves as a critical intermediate in multistep syntheses for selective serotonin receptor modulators and related API scaffolds. Leading pharma manufacturers use it due to its reliable indole core functionalization within route design for CNS-targeted small molecules. Maintaining traceability and purity is essential, since incorporation typically happens early in syntheses, which is tightly monitored under GMP frameworks. Process chemists control the addition based on specific batch demands, with purification and analytical tracking ensuring compliance until the final API stage.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP) as specified in ICH Q7 and US FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur.) certificate of suitability when relevant
    • Risk assessments following ECHA-REACH requirements for intermediates
    • Auditable supply chain per ISO 9001:2015 quality management system

    Typical usage ratio

    • 3–10 mol% relative to the target molecule’s indole precursor stage, precision adjusted for each custom synthesis protocol depending on yield, selectivity, and end-use pharmacopoeial standards

    Downstream process integration

    • Directly introduced during early heterocycle assembly or late-stage indole derivatization, engaged via Suzuki coupling or methylation steps before final salt formation and purification

    Final product types

    • Serotonin 5-HT receptor antagonists/agonists
    • Triptan-class CNS therapeutics
    • Custom indole-based APIs in clinical development
    • Reference standards for pharmaceutical analytics

    2. Advanced Dye and Pigment Intermediates

    Specialty colorant manufacturers utilize this compound as a structural intermediate in synthesizing high-performance indole-based dyes and pigments, valued for their unique methoxy-substituted chromophores. Jacketing with functionalized indoles enhances lightfastness and solubility required for digital textile printing and electronic display coatings. Regulatory controls focus on purity and by-product management due to potential downstream use in regulatory-sensitive applications for consumer and industrial textiles.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex 4 (input material restrictions for textile dyes)
    • REACH Annex XVII compliance for aromatic amine derivatives
    • ZDHC MRSL (Manufacturing Restricted Substances List) conformance
    • ISO 9001-based quality inspection for colorant input streams

    Typical usage ratio

    • 0.5–2% weight addition relative to primary aromatic feedstock for pigment or dye couplers, optimized based on desired tonality and final coverage strength in the finished product

    Downstream process integration

    • Added post-nitration before diazotization steps or as a direct indole donor in colorant coupling; subsequent filtration and crystallization align with final product application protocols

    Final product types

    • Reactive and acid dyes for digital textile printing
    • OLED display pigment concentrates
    • Industrial inks with indole-based colorants
    • Custom pigment dispersions for decorative coatings

    3. Research and Diagnostic Chemical Reagent Production

    Chemical supply labs formulate analytical reagents and biochemical assay kits using this compound as a model indole derivative. Its unique substitution enables precise chromogenic and fluorogenic responses, supporting in vitro research, pathway tracking, and enzymatic activity screens. Production demands batch consistency, reference documentation, and lot release testing for trace impurities to meet research-grade purity requirements and international transportation standards.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • GHS/CLP classification and safety data adherence (EU Regulation 1272/2008)
    • JIS K 0125 (Japanese Industrial Standard for reagent specification)
    • ISO/IEC 17025 accreditation for analytical verification

    Typical usage ratio

    • 0.1–1% by weight in diagnostic kit formulations, modified according to detection sensitivity for calibration standards and synthetic control compounds

    Downstream process integration

    • Enters reagent formulation during marker conjugation protocols or as a benchmark control in kit manufacturing, followed by aliquoting, freeze-drying, and QC release

    Final product types

    • Synthetic enzyme substrates for laboratory research
    • Calibration standards for chromatographic analysis
    • In vitro diagnostic assay components
    • Batch-labeled reference materials for scientific use

    4. Agrochemical Intermediate for Crop Protection R&D

    In the crop protection sector, producers use this specialty indole as an intermediate within custom synthesis programs for potential new-class herbicides and fungicidal actives. Candidates derived from its scaffold undergo structure-activity relationship (SAR) studies and metabolic fate evaluations. Scale-up takes place under stringent environmental and occupational safety controls, with full accountability to agricultural input regulatory bodies before bulk formulation.

    Industry compliance standards

    • OECD GLP (Good Laboratory Practice) for agrochemical synthesis and testing
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • EU Regulation (EC) No 1107/2009 for plant protection product intermediates
    • ISO 14001 for environmental management throughout the supply chain

    Typical usage ratio

    • 2–6 mol% as a branded scaffold relative to parent aromatic substrate within SAR synthesis libraries, adjusted to compound series and in vivo efficacy outcomes

    Downstream process integration

    • Introduced as the initiating building block in synthetic routes for lead diversification; processing includes condensation, halogenation, and subsequent formulation under containment for bioactivity screening

    Final product types

    • Herbicidal and fungicidal R&D candidates
    • Small-quantity advanced agrochemical intermediates
    • Screening standards for field trial evaluation
    • Discovery-stage crop protection chemical libraries
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