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Oxindole

    • Product Name Oxindole
    • Alias 1H-indol-2-one
    • Einecs 202-308-0
    • 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

    300787

    Name Oxindole
    Chemical Formula C8H7NO
    Molecular Weight 133.15 g/mol
    Cas Number 59-48-3
    Appearance White to light yellow solid
    Melting Point 120-122 °C
    Solubility In Water Slightly soluble
    Boiling Point 375 °C
    Density 1.32 g/cm³
    Iupac Name 1,3-dihydro-2H-indol-2-one

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

    Packing & Storage
    Packing A 250g amber glass bottle with a screw cap, labeled "Oxindole," includes hazard symbols, batch number, and storage instructions.
    Shipping Oxindole is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is typically transported as a solid under ambient conditions. Proper labeling and documentation are required in accordance with local, national, and international regulations. Handle with appropriate safety precautions to avoid inhalation, ingestion, or skin contact.
    Storage Oxindole should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from incompatible substances such as strong oxidizing agents. Ensure proper labeling and secure storage to prevent accidental exposure or spillage. Use appropriate personal protective equipment when handling.
    Application of Oxindole

    Applications of Oxindole in Industrial Manufacturing

    Oxindole serves as a critical intermediate for a range of specialized industries. Our production is tailored to meet the strict expectations of pharmaceutical syntheses, industrial dye precursors, agricultural chemicals, pigment formulations, and advanced polymer research. Below, we outline precise downstream pathways where oxindole plays an essential and compliant role, supported by up-to-date industry standards.

    1. Synthesis of Active Pharmaceutical Ingredients (APIs)

    Oxindole is a valuable core building block in pharmaceutical manufacturing, especially in the synthesis of spirooxindole and substituted oxindole APIs. Multinational pharmaceutical companies integrate it during the construction of alkaloids, anti-inflammatory agents, and kinase inhibitors. The intermediate undergoes condensation or cyclization reactions under GMP environments, with stringent control of purity, impurities, and storage conditions by automated process controls. Manufacturers rely on detailed analytical profiles and validated isolation protocols to ensure consistent product quality, as required for finished drug authorities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • European Pharmacopoeia Ph. Eur. 11.0 (as intermediate limits)
    • 21 CFR Part 211 US FDA cGMP
    • EDQM Certification of Suitability, where applicable

    Typical usage ratio

    • Oxindole loading ranges from 0.8 to 1.2 molar equivalents based on target API yield and synthesis stage.
    • Fine-tuned according to impurity profile and reaction kinetics in large-scale batch reactors.

    Downstream process integration

    • Fed into the initial or mid-stage reaction vessel during small-molecule synthesis.
    • Incorporated before key cyclization or ring-closure steps.
    • Temperature and pH tightly monitored to prevent side-product formation.

    Final product types

    • Antitumor agents (e.g., indirubin analogs, selective kinase inhibitors)
    • Anti-inflammatory and anti-allergy medications
    • Neurological disorder drugs (investigational compounds)
    • Complex alkaloid-type finished pharmaceuticals

    2. Industrial Dye and Pigment Precursors

    Dye and pigment manufacturers use oxindole as a precursor for the production of specific indigoid and indoline dyes required in the textile and plastics sector. Its reactivity allows for controlled substitution patterns and consistent chromophore development during sulfonation or halogenation stages. Production adheres to environmental and workplace safety standards, with color intensity and stability tested for each batch, providing material suitable for high-specification coloration of synthetic fibers and engineering plastics.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems – Colorants Industry
    • REACH (EC 1907/2006) Substance Registration and Safety Data Compliance in EU
    • ZDHC Manufacturing Restricted Substances List for textiles
    • Oeko-Tex Standard 100 certification, relevant pigments

    Typical usage ratio

    • 0.5% to 2% by mass of total dye batch, adjusted based on desired shade strength and fastness specifications.
    • Higher ratios for deep blue and violet tone formulations.

    Downstream process integration

    • Oxindole introduced during the condensation or coupling stage of colorant synthesis.
    • Requires controlled feed rates and staged temperature ramps in glass-lined reactors.
    • Often followed by filtration, grinding, and spray-drying in pigment plants.

    Final product types

    • Indoline and indigoid dyes for synthetic and cellulosic fiber dyeing
    • Pigment dispersions for engineering plastics
    • Masterbatch concentrates for fiber extrusion
    • Colorants for automotive coatings

    3. Agricultural Chemicals & Plant Growth Regulators

    Oxindole acts as a precursor for manufacturing select plant growth regulators and biocidal agents. Agrochemical companies deploy it as a ring-closed intermediate before final functionalization. The raw material supports the synthesis of tryptophan-derived growth stimulants, introduced into field-ready formulations following rigorous screening for environmental persistence and phytotoxicity. Our process allows production streams with minimized residuals, enabling partners to achieve reliable active ingredient incorporation following GLP standards.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) guidelines
    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 14001:2015 Environmental Management Systems
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)

    Typical usage ratio

    • Ranges between 0.3% and 1.5% by weight in precursor batches for regulator synthesis.
    • Ratio optimized for conversion efficiency and minimal residue in the final active substance.

    Downstream process integration

    • Charged into the main reaction during precursor synthesis for indole-derivative regulators.
    • Precursor complexes purified before esterification and formulation steps.
    • Sequential solvent removal and stabilization as required by downstream crop species.

    Final product types

    • Auxin-type plant growth stimulants
    • Seed treatment agents
    • Herbicide precursors and metabolite-blockers
    • Foliar application formulations

    4. Specialty Polymers & Advanced Materials Synthesis

    Oxindole provides a crucial aromatic structure for the design of high-performance polymers and heterocyclic additives in advanced materials R&D. Chemical engineers working on electronics and specialty coatings exploit its structural rigidity and multifunctional groups for targeted polymer backbone modification. The raw material undergoes condensation polymerizations or controlled radical processes in strictly monitored pilot lines, complying with customer QC and environmental release limits.

    Industry compliance standards

    • ISO 13485:2016 (for medical-grade polymer applications)
    • RoHS (Directive 2011/65/EU) for electrical and electronic equipment
    • ASTM D638 Polyester and Polyamide Testing Standards
    • GMP guidelines for pharmaceutical-contact polymers

    Typical usage ratio

    • Typically 0.1 to 1.0 molar equivalents within the polymer feedstock, depending on desired polymer chain length and mechanical properties.
    • Lower ratios maintained for flexible film applications; higher ratios for rigid composites.

    Downstream process integration

    • Integrated into pre-polymerization reactors during heterocyclic incorporation steps.
    • Often requires real-time viscosity and molecular weight monitoring via GPC.
    • Excess reactant recycled for process optimization.

    Final product types

    • High temperature-resistant specialty films
    • Electronic encapsulation resins
    • Conductive polymer composites
    • Medical device coatings and implantable polymer components
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