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6-Methoxy-2-Oxindole

    • Product Name 6-Methoxy-2-Oxindole
    • Alias 6-Methoxyindolin-2-one
    • Einecs 629-082-6
    • 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
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    Specifications

    HS Code

    595046

    Product Name 6-Methoxy-2-Oxindole
    Cas Number 2562-34-9
    Molecular Formula C9H9NO2
    Molecular Weight 163.18 g/mol
    Appearance Off-white to pale yellow solid
    Melting Point 178-182°C
    Purity Typically ≥98%
    Boiling Point Decomposes before boiling
    Solubility Soluble in DMSO, slightly soluble in water
    Smiles COc1ccc2c(c1)[C@@H](=O)NC2
    Inchi InChI=1S/C9H9NO2/c1-12-6-2-3-7-8(4-6)9(11)10-5-7/h2-4,10H,5H2,1H3
    Storage Condition Store at 2-8°C, protected from light and moisture
    Synonyms 6-Methoxyoxindole

    As an accredited 6-Methoxy-2-Oxindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 6-Methoxy-2-Oxindole (5 grams) is a sealed amber glass vial with a tamper-evident screw cap, clearly labeled.
    Shipping **Shipping Description for 6-Methoxy-2-Oxindole:** This chemical is shipped in secure, tightly sealed containers to prevent moisture and contamination. Packaging complies with standard chemical safety regulations. The shipment includes a material safety data sheet (MSDS) and clear hazard labeling. Transportation is arranged via certified carriers to ensure safe and compliant delivery.
    Storage 6-Methoxy-2-Oxindole should be stored in a tightly sealed container, away from light, moisture, heat, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably in a chemical fume hood or dedicated storage cabinet. Proper labeling and handling procedures should be followed to ensure safety and prevent contamination or degradation.
    Application of 6-Methoxy-2-Oxindole

    Applications of 6-Methoxy-2-Oxindole in Industrial Manufacturing

    6-Methoxy-2-Oxindole serves as a key synthetic intermediate for several segments within the pharmaceutical, fine chemical, agrochemical, and specialty dye industries. Our expertise as a direct manufacturer enables precise compliance and integration into complex downstream workflows. Below, we detail specific application scenarios and the requirements for each sector.

    1. Pharmaceutical API Intermediate for Tetrahydro-β-Carboline Derivatives

    Pharmaceutical companies use this compound in the production of tetrahydro-β-carboline APIs, including those used in neurology and oncology research. It acts as an advanced intermediate during multistep synthesis. Strict batch-controlled processes and compliance with regulatory documentation are standard throughout. Customer SOPs for intermediate isolation ensure traceability and consistent impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP and EP monographs for intermediates
    • FDA DMF (Drug Master File) submission protocols
    • REACH registration for handling and exposure

    Typical usage ratio

    • 5% – 18% of total reaction mass, adjusted according to desired substitution pattern and process scale
    • Process development phase may require up to 25% excess to optimize yield and purity

    Downstream process integration

    • Introduced after indole ring construction during fused ring closure steps
    • Integrated into batch reactors at nitrogen-protected stages to prevent oxidation
    • Material held under inert atmosphere during alkylation and cyclization

    Final product types

    • Anticancer and neuropharmacological drug substances
    • Research active pharmaceutical ingredients
    • Advanced heterocyclic intermediates

    2. Intermediate in Agrochemical Synthesis (Plant Growth Regulators)

    Major agrochemical manufacturers incorporate this oxindole derivative to construct key skeletons present in indole-based plant growth regulators. It enables introduction of methoxy groups, enhancing plant hormone mimicry. All sourcing and use adhere to agrochemical industry safety and disclosure rules. Our analysts assist with Form F235 regulatory dossiers and full traceability documentation as required by regional bodies.

    Industry compliance standards

    • EPA pesticide registration (40 CFR Part 152)
    • OECD Principles of Good Laboratory Practice (GLP)
    • Chinese Ministry of Agriculture ICAMA review
    • ISO 9001:2015 certified production

    Typical usage ratio

    • 2% – 12% in synthesis of target phytohormonal actives
    • Modified based on degree of substitution and final product purity requirements

    Downstream process integration

    • Charged post-feedstock blending in the main cyclization stage of IAA-related compounds
    • Used in acid or base-catalyzed condensation reactors
    • QC sampling controls for methoxy group placement

    Final product types

    • Indole-3-acetic acid analogues
    • Substituted auxin compounds
    • Precursor to plant stimulant formulations

    3. Substrate for Fine Chemical Synthesis in Specialty Dye Manufacturing

    Producers of specialty dyes utilize 6-Methoxy-2-Oxindole as a building block for functional indole-based chromophores. It provides specific electron-donating properties required in functional materials and organic pigments. Manufacturer technical staff collaborate in HPLC-monitored process optimization for batch-to-batch color consistency and purity validation.

    Industry compliance standards

    • REACH Annex VII/VIII regulatory framework
    • EN 71-3:2019 (for toy and consumer safety dyes in EU)
    • ASTM D4287 (dye purity testing)
    • ISO 9001 quality management during batch release

    Typical usage ratio

    • 10% – 30% of total input mass for desired dye structures
    • Scaled by target chromophore substitution and desired shade depth

    Downstream process integration

    • Dosed at high temperature during oxidative ring closure
    • Participates in direct condensation with sulfonic acid derivatives
    • Final purification via column chromatography to ensure pigment stability

    Final product types

    • Indole-based synthetic dyes for specialty inks
    • Organic pigments for security printing
    • Colorants for electronics and optoelectronic applications

    4. Isatin Derivative Manufacturing for Chemical Research and Development

    Research chemical manufacturers use this oxindole as a core scaffold for synthesizing substituted isatins and related heterocycles. It supports exploration of new reaction pathways and serves as a key starting point for the discovery of prospective molecules in medicinal chemistry. Analytical QC, NMR structure validation, and detailed COA documentation accompany each batch.

    Industry compliance standards

    • ISO 17025 for laboratory analysis
    • GLP (Good Laboratory Practice) for analytical verification
    • Material Safety Data Sheet (MSDS) and CLP labeling compliance (EC 1272/2008)
    • Applicable regional chemical inventory registration (e.g., TSCA, IECSC)

    Typical usage ratio

    • 3% – 20% depending on research protocol and downstream transformations
    • Experimental procedures may vary ratios based on target molecule complexity

    Downstream process integration

    • Used as the initial input in oxidative or reductive transformation series
    • Forms basis for Grignard additions and halogenation studies
    • Aligned with HPLC/LCMS QC checkpoints to maintain chemical integrity

    Final product types

    • N-substituted isatin intermediates
    • Indole-based small molecule libraries
    • Reference standards for pharmaceutical and academic research
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