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Rhodanine

    • Product Name Rhodanine
    • Alias NSC-67338
    • Einecs 207-924-1
    • 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

    896385

    Chemicalname Rhodanine
    Casnumber 1192-93-2
    Molecularformula C3H3NOS2
    Molarmass 133.19 g/mol
    Appearance Yellow crystalline solid
    Meltingpoint 165-166°C
    Boilingpoint Decomposes before boiling
    Solubility Slightly soluble in water, soluble in ethanol and acetone
    Density 1.67 g/cm³
    Smiles C1C(=O)SC(=S)N1
    Iupacname 2-thioxo-4-thiazolidinone
    Storageconditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing Rhodanine, 25g, is packaged in a sealed amber glass bottle with a screw cap and a printed hazard label for safety.
    Shipping Rhodanine is shipped in tightly sealed containers, protected from light and moisture to maintain stability. The packages are labeled according to safety regulations and handled as laboratory chemicals, requiring standard precautions to avoid inhalation or skin contact. Transport complies with international and local chemical shipping guidelines to ensure safe delivery.
    Storage Rhodanine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure the storage area is clearly labeled, and limit access to trained personnel. Proper storage prolongs its stability and minimizes risks associated with chemical handling.
    Application of Rhodanine

    Applications of Rhodanine in Industrial Manufacturing

    Rhodanine supports key production processes across pharmaceutical intermediates, agrochemical synthesis, colorant manufacture, and specialty fine chemicals. The following sections outline how industrial clients integrate this material into their operational workflows.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers rely on this compound as a building block for the construction of thiazolidinone scaffolds in active pharmaceutical ingredient (API) synthesis. During medicinal chemistry campaigns, it facilitates the assembly of heterocyclic frameworks for a range of antibacterials, antivirals, and enzyme inhibitors. Researchers integrate it during multicomponent reactions, leveraging its nucleophilic reactivity in Knoevenagel and Michael addition steps. Scale-up production uses controlled batch processes, with dedicated filtration and crystallization units to prevent cross-contamination under GMP. Downstream, APIs proceed through isolation, purification, and micronization lines ahead of formulation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) Source Material Standards
    • European Pharmacopoeia (Ph. Eur.) Monograph Procedures
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • 10%–35% of intermediate batch weight; proportion set by molar requirements of target thiazolidinone assembly route

    Downstream process integration

    • Introduced during early-stage intermediate assembly (Knoevenagel condensation or Michael-type additions)
    • Purified with solvent extraction, then isolated for onward coupling in heterocycle synthesis

    Final product types

    • Beta-lactam antibiotics
    • Antiviral API intermediates
    • Thiazolidinedione-based antidiabetics
    • Research-grade screening compounds for pharmaceutical R&D

    2. Agrochemical Active Ingredient Synthesis

    Formulators in the agrochemical sector use this material as a precursor for plant protection compounds, particularly in the synthesis of heterocyclic pesticides and fungicides. The incorporation occurs during the construction of 2-thioxo-thiazolidinone rings, a recurring motif in modern crop actives. Manufacturers target high selectivity by adjusting reaction pH and temperature while ensuring full conversion through analytical monitoring. Typically, the material feeds multi-step syntheses where downstream steps include acetylation, halogenation, or alkylation before formulation into wettable powders or emulsifiable concentrates for field application.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No 1107/2009 (EU Plant Protection Product Authorization)
    • OECD Principles of Good Laboratory Practice (GLP) for active ingredient development
    • REACH Regulation (EC) No 1907/2006-Annexes VII-X for chemical safety

    Typical usage ratio

    • 15%–45% of total precursor weight; adjusted for desired yield in thiazolidinone ring formation

    Downstream process integration

    • Added at the main heterocycle-forming reaction, often as the limiting reagent for regioselective synthesis
    • Intermediate processed via filtration, solvent exchange, and finally formulated into granular or concentrated products

    Final product types

    • Fungicidal technical concentrates (e.g., containing thiazolidinone moiety)
    • New-generation pesticide active ingredients
    • Seed treatment actives with enhanced persistence

    3. Specialty Dye and Pigment Production

    Colorant and pigment manufacturers employ this building block for the creation of sulfur-containing dye intermediates and specialty organic pigments. It reacts with aromatic aldehydes and amines under controlled condensation conditions, promoting the formation of dye molecules with vivid chromatic properties and strong fastness. Chemical engineers adjust solvent parameters and reactant loading to generate pure pigment intermediates, which later undergo sulfonation or additional ring closure steps. End-use includes the textile, plastic, and leather industries, demanding high batch-to-batch consistency and purity to comply with environmental and application regulations.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textiles and leathers
    • REACH Annex XVII (restricted substances in pigments and dyes)
    • ISO 9001 Quality Management for pigment manufacture
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)

    Typical usage ratio

    • 5%–20% of dye or pigment intermediate reaction mass; optimized per target chromophore synthesis route

    Downstream process integration

    • Feedstock to condensation reactions for pigment base synthesis
    • Isolated pigment intermediates undergo post-treatment such as granulation, heat setting, or dispersion blending

    Final product types

    • Sulfur dyes for textile coloration
    • Organic pigments for plastics and coatings
    • Specialty colorants for inkjet printer formulations

    4. Fine Chemicals and Analytical Reagents

    Producers of analytical reagents and specialty fine chemicals integrate this compound for constructing bespoke chelating agents and as a standard reagent in metal ion analysis. In laboratory settings, it participates in the synthesis of metal complexing agents, used as chromogenic indicators for heavy metal detection. The process entails dissolution and reaction with target ions under controlled pH and solvent conditions. Manufacturers ensure production with trace impurity monitoring, delivering high-purity grades for research and industrial laboratories, as well as for QC across multiple sectors including environmental, food, and pharmaceutical analysis.

    Industry compliance standards

    • ISO 17034 (General requirements for the competence of reference material producers)
    • ISO/IEC 17025 (Testing and calibration laboratory standards)
    • ASTM D1687 (Standard Test Methods for Chromium in Water, applicable to chelating reagents)

    Typical usage ratio

    • 0.1%–1% in reagent formulation; concentration tailored to analytical sensitivity requirements

    Downstream process integration

    • Added at reagent blending or complexation step under pH-controlled conditions
    • Packed in air-tight vials post-purification and QC approval

    Final product types

    • Chromogenic metal detection kits (for Cr, Cu, etc.)
    • Bespoke chelating agents for heavy metal remediation
    • Reference materials for laboratory calibration
    Free Quote

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