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Phenolphthalein Disulfate Tripotassium Salt Trihydrate

    • Product Name Phenolphthalein Disulfate Tripotassium Salt Trihydrate
    • Alias PTK
    • Einecs 242-749-5
    • 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

    164246

    Chemical Name Phenolphthalein Disulfate Tripotassium Salt Trihydrate
    Chemical Formula C20H12K3O10S2·3H2O
    Molar Mass 670.80 g/mol
    Appearance White to off-white powder
    Solubility In Water Soluble
    Cas Number 16292-19-6
    Storage Conditions Store at 2-8°C, dry conditions
    Purity Typically ≥98%
    Usage pH indicator, analytical reagent
    Melting Point Decomposes before melting (approx. >200°C)
    Stability Stable under recommended storage conditions
    Synonyms Phenolphthalein disulfonic acid tripotassium salt trihydrate
    Hazard Statements May cause eye irritation
    Color Change Ph Range pH 0.5 - 2.0 (yellow to colorless)
    Inchi Key BCNAHASHYMROSL-UHFFFAOYSA-K

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

    Packing & Storage
    Packing 250g of Phenolphthalein Disulfate Tripotassium Salt Trihydrate is supplied in a tightly sealed, amber-capped HDPE bottle with hazard labeling.
    Shipping Phenolphthalein Disulfate Tripotassium Salt Trihydrate is shipped in tightly sealed, chemically-resistant containers to prevent moisture exposure and contamination. Packaging complies with relevant regulations for chemical transport. It is typically shipped via ground or air freight, accompanied by a safety data sheet and appropriate hazard labeling to ensure secure and compliant delivery.
    Storage Phenolphthalein Disulfate Tripotassium Salt Trihydrate should be stored in a tightly sealed container, protected from light, heat, and moisture. Keep it at room temperature, in a well-ventilated, dry area, away from incompatible substances such as strong acids and oxidizers. Ensure the storage area is clearly labeled and restrict access to trained personnel only. Follow all relevant safety and regulatory guidelines.
    Application of Phenolphthalein Disulfate Tripotassium Salt Trihydrate

    Applications of Phenolphthalein Disulfate Tripotassium Salt Trihydrate in Industrial Manufacturing

    As a specialized manufacturer, we deliver Phenolphthalein Disulfate Tripotassium Salt Trihydrate of consistent quality and purity for precise integration in advanced downstream sectors. Our expertise ensures reliable material performance to meet stringent demands, particularly in analytical chemistry, automated water quality monitoring, in-vitro diagnostic reagent preparation, and biochemical automation lines. Below we detail the focused applications where this material provides critical technical benefits, including regulatory frameworks, established formulation ratios, processing points, and end product types suited to the actual operating standards of the global market.

    1. Laboratory Analytical Reagents for Titrimetric Analysis

    In analytical chemistry laboratories, this compound serves as a high-sensitivity acid-base indicator in titrimetry, including but not limited to potentiometric and visual endpoint analysis. Its unique sulfonated structure enhances solubility and stability in aqueous media, supporting precision titrations for quality control testing in chemical, pharmaceutical, and food sectors. Formulators rely on its reproducibility under laboratory benchmarks for accurate endpoint detection.

    Industry compliance standards

    • ISO 17025 (Testing and Calibration Laboratories)
    • ACS (American Chemical Society) Reagent Standards
    • European Pharmacopoeia (monographs for analytical reagents)
    • British Pharmacopoeia analytical reagent sections

    Typical usage ratio

    • 0.02%–0.04% w/v according to titration method sensitivity; adjusted based on sample concentration and endpoint visibility requirements

    Downstream process integration

    • Dissolve the salt in deionized water during indicator solution formulation or premix with buffer for pH calibration standards before bottling for laboratory supply

    Final product types

    • Pre-mixed titration indicator solutions
    • Concentrated analytical kits for laboratory use
    • pH endpoint detection vials
    • Reference standards for quality control laboratories

    2. Automated Water and Wastewater Analyzer Reagents

    Municipal and industrial water testing operators use this material in field and online automated water analysis systems. The compound acts as a reliable endpoint indicator for alkalinity and acidity titrations in environmental monitoring, offering compatibility with automated dosing and optical sensing platforms due to its stability and low interference in complex matrices.

    Industry compliance standards

    • US EPA Method 310.1 (Alkalinity, Automated Titrimetric, Potentiometric, and Colorimetric Method)
    • ISO 9963-1:1994 (Water quality — Determination of alkalinity)
    • Standard Methods for the Examination of Water and Wastewater (APHA 2320 B)
    • DIN EN ISO 10523 (pH measurement in water)

    Typical usage ratio

    • 0.025%–0.05% in ready-to-use indicator cartridges, varying with instrument design and sample load

    Downstream process integration

    • Integrate during automated reagent system filling, either as a pre-prepared solution or in concentrated form for dilution onsite, directly feeding analyzer units equipped with microfluidic or optical sensors

    Final product types

    • Sealed indicator cartridges for in-line analyzers
    • On-site water quality reagent packs for auto-analyzers
    • Colorimetric reagent vials for portable water monitoring kits
    • Lab-on-chip test module components

    3. In-Vitro Diagnostic (IVD) Systems and Biochemistry Assay Kits

    Medical diagnostic kit manufacturers incorporate this material as a chromogenic component in pH-based biochemical assays and CNFEs (colorimetric nucleic acid functional enzyme) test protocols for clinical chemistry. Its certified purity enables use in highly regulated manufacturing environments, supporting visual endpoint analysis of enzymatic activity and specific metabolic pathways that require defined color shift responses under controlled laboratory conditions.

    Industry compliance standards

    • ISO 13485 (Medical device quality management systems)
    • CE-IVD (EU Directive 98/79/EC for in vitro diagnostic devices)
    • US FDA 21 CFR Part 820 (Quality System Regulation for Medical Devices)
    • China NMPA IVD Product Registration Regulations

    Typical usage ratio

    • 0.01%–0.03% in diagnostic ready-mix solutions, optimized per assay kit protocol to minimize interference and maintain endpoint clarity

    Downstream process integration

    • Blend into biochemical substrate solution during kit assembly or dose into microplate wells in automated reagent dispensing steps before freeze-drying or liquid filling

    Final product types

    • pH indicator assay kits for serum and plasma diagnostics
    • Colorimetric substrate packs for clinical biochemistry analyzers
    • Rapid diagnostic reagent strips (lateral flow, microfluidic)
    • Enzyme activity detection kits

    4. Biochemical Automation and Screening Platforms

    High-throughput screening platforms, particularly in pharmaceutical development and biotechnology R&D, rely on this compound as a non-interfering colorimetric marker during enzyme kinetics studies and automated pH trace monitoring. Producers of liquid handling platforms and reagent manufacturers deploy it for assay traceability during multi-well plate readout, requiring consistent batch quality to support automated robotic processes and long-cycle operation.

    Industry compliance standards

    • GLP (Good Laboratory Practice, OECD and FDA parts 58)
    • USP General Chapter <797> (Pharmaceutical Compounding-Sterile Preparations, when relevant for automated system QC)
    • ISO 15189 (Medical Laboratories)
    • DIN EN ISO 9001 (Quality Management Systems)

    Typical usage ratio

    • 0.015%–0.035%, selected based on assay microplate design, liquid volume range, and detection platform optical requirements

    Downstream process integration

    • Add as a traceable dye component at master mix preparation, or premix in system-specific reagent cartridges before aliquoting across automated screening plates or test arrays

    Final product types

    • Robotic assay system reagent modules
    • Microplate colorimetric QC controls for drug screening
    • Prepackaged biochemical screening kits for high-throughput discovery
    • Lab automation consumables with color marker trace
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