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5-Carboxyoxindole

    • Product Name 5-Carboxyoxindole
    • Alias Oxindole-5-carboxylic acid
    • Einecs 217-984-5
    • 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
    VTB
    Specifications

    HS Code

    113703

    Name 5-Carboxyoxindole
    Cas Number 4007-69-0
    Molecular Formula C9H7NO3
    Molecular Weight 177.16 g/mol
    Appearance White to off-white solid
    Melting Point 270-274°C (decomposes)
    Solubility Slightly soluble in water; soluble in DMSO, methanol
    Iupac Name 1,3-Dihydro-2H-indole-5-carboxylic acid-2-one
    Pubchem Cid 314526
    Smiles C1C(=O)NC2=CC=C(C=C21)C(=O)O
    Inchi InChI=1S/C9H7NO3/c11-9-7-3-1-5(9)2-4-6(7)8(12)10-9/h1-4H,(H,10,11,12)
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 5-Oxo-2,3-dihydro-1H-indole-5-carboxylic acid

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

    Packing & Storage
    Packing 5-Carboxyoxindole, 25g: Supplied in a high-quality, amber glass bottle with a secure screw cap, labeled with hazard and identification details.
    Shipping 5-Carboxyoxindole is shipped in secure, sealed containers, compliant with chemical safety regulations. Packaging ensures protection from moisture and contamination. Accompanied by a Safety Data Sheet (SDS), it is transported via approved carriers, with labeling in accordance with international and domestic hazardous material shipping standards. Handle with appropriate protective equipment upon receipt.
    Storage 5-Carboxyoxindole should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Store it in a cool, dry, well-ventilated area, preferably at room temperature or lower. Avoid moisture and incompatible materials like strong oxidizers. Proper chemical labeling and adherence to safety protocols are essential for safe handling and storage.
    Application of 5-Carboxyoxindole

    Applications of 5-Carboxyoxindole in Industrial Manufacturing

    As a direct manufacturer specializing in the production of 5-Carboxyoxindole, we supply this intermediate for specialized applications in pharmaceutical synthesis, agrochemical formulation, pigment production, and advanced chemical research. Below, we detail major downstream use cases across diverse industrial sectors, referencing applicable compliance frameworks, batch formulation practices, and integrated process steps based on established industry operations.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    5-Carboxyoxindole serves as an advanced intermediate in the synthesis of select APIs, particularly in the realm of oncology and anti-inflammatory agents. In GMP-compliant facilities, it is incorporated at the heterocycle-building stage where precise structural formation is critical to biological activity. Manufacturers integrate this compound during key amidation or acylation steps, maintaining strict control on impurity profiles and residual solvents during the multi-stage synthesis process. Formulation teams adjust the inclusion ratio based on API target specifications and downstream hydrolysis requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs (relevant APIs)
    • US FDA CFR Title 21, Part 211 (Finished Pharmaceuticals)
    • EU GMP Part II – Basic Requirements for Active Substances

    Typical usage ratio

    • 10-30% mole equivalent in step-wise synthesis, adjustable based on target API yield and process efficiency; final ratio determined by the nature of subsequent condensation reactions.

    Downstream process integration

    • Introduced at Stage II or III of the synthetic route, typically following formation or activation of a key heterocycle precursor.
    • Crystallization and purification steps customized to ensure minimal carryover of unreacted intermediates.

    Final product types

    • Chemotherapeutic agents (e.g., indole alkaloid derivatives)
    • Non-steroidal anti-inflammatory drugs
    • Novel small-molecule therapeutics

    2. Agrochemical Intermediate Manufacturing

    In the agrochemical sector, 5-Carboxyoxindole acts as a building block for the synthesis of new-generation herbicides and plant growth regulators incorporating indole structures. The material is introduced in high-shear reactors as a nucleophilic substrate, participating in selective alkylation and cyclization pathways. Process chemists monitor the stoichiometric ratio closely to manage the conversion efficiency and minimize formation of by-products, especially when scaling up to production volumes targeting regulatory review.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for Chemical Production
    • OECD Test Guidelines for Chemical Safety Assessment
    • REACH (EC 1907/2006) Registration for Agrochemical Components
    • FAO/WHO Specifications for Pesticide Ingredients

    Typical usage ratio

    • 5-15% w/w relative to total reactants in early-stage cyclization; optimal ratio tested via pilot batch runs for desired active content in end-use formulation.

    Downstream process integration

    • Added post-neutralization, before condensation or esterification steps in multi-step processes.
    • Filtration, solvent exchange, and post-reaction pH adjustment are calibrated to meet downstream conversion criteria.

    Final product types

    • Selective herbicides containing indole-based active moieties
    • Plant growth regulation compounds
    • Seed treatment adjuvants employing substituted oxindole structures

    3. Advanced Organic Pigments Production

    5-Carboxyoxindole is integral to the synthesis of high-purity indole-based pigments used in specialty inks and high-performance coatings. In pigment manufacture, formulation chemists use the carboxyl functional group for coupling with diazonium salts to achieve precise shade and fastness properties. Quality teams implement tight in-process controls on particle morphology and free acid content. Adjustment of the usage level takes into account desired hue intensity and application substrate compatibility.

    Industry compliance standards

    • ISO 1248:2006 (Pigments – Specifications and methods of test)
    • EU Regulation (EC) No 1272/2008 on Classification, Labeling and Packaging (CLP)
    • ASTM D3871-07: Standard Test Method for Pigment Content
    • RoHS Directive (for electronic ink applications)

    Typical usage ratio

    • 3-12% of pigment mass, custom-fitted according to color saturation requirements and formulation batch volume.

    Downstream process integration

    • Introduced in the diazotization or condensation stage, prior to drying and milling operations.
    • Subjected to controlled thermal treatment during pigment particle formation.

    Final product types

    • Specialty printing inks (security, textile, art)
    • High-performance industrial coatings
    • Fine chemical pigments for plastics compounding

    4. Research and Development of Fine Organic Synthesis

    Academic and corporate R&D centers use 5-Carboxyoxindole as a core skeleton for synthesizing new heterocyclic molecules, focused on lead discovery and route optimization studies. Scientists employ this raw material as a nucleophile or electrophile in constructing novel frameworks via metal-catalyzed cross-coupling or organocatalytic transformations. Researchers frequently vary the introduction amount to screen for optimal yields, regioselectivity, and access to structurally unique analogues under laboratory-scale and semi-pilot conditions.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for chemical research
    • ISO/IEC 17025:2017 (Laboratory Testing and Calibration)
    • Institutional chemical safety protocols (MSDS adherence, handling standards)
    • Local and national environmental waste disposal regulations

    Typical usage ratio

    • 0.2-2 mmol scale per reaction in method development, up to 100 g/L in larger screening campaigns; proportion adapted to reaction type and combinatorial throughput needs.

    Downstream process integration

    • Initial scaffold input in reaction screening arrays, directly influencing yield and structure of discovery compounds.
    • Work-up includes advanced purification steps such as HPLC or flash chromatography before downstream bioactivity screening.

    Final product types

    • New heterocyclic compound libraries for drug screening
    • Targeted synthesis of potential agrochemical actives
    • Advanced organic materials for electronics research
    Free Quote

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