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O-Phenanthroline Monohydrochloride Monohydrate

    • Product Name O-Phenanthroline Monohydrochloride Monohydrate
    • Alias 1,10-Phenanthroline hydrochloride monohydrate
    • Einecs 237-523-0
    • 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

    457651

    Chemical Name O-Phenanthroline Monohydrochloride Monohydrate
    Molecular Formula C12H9N2·HCl·H2O
    Molar Mass 243.7 g/mol
    Cas Number 3829-86-5
    Appearance White to pale yellow crystalline powder
    Solubility In Water Soluble
    Melting Point About 240 °C (decomposes)
    Storage Conditions Store at room temperature, keep container tightly closed
    Ph 1 In Water Approx. 5
    Synonyms 1,10-Phenanthroline monohydrochloride monohydrate

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

    Packing & Storage
    Packing 100 g white plastic bottle with red cap, labeled "O-Phenanthroline Monohydrochloride Monohydrate," safety symbols, and product details.
    Shipping O-Phenanthroline Monohydrochloride Monohydrate is shipped in tightly sealed containers, protected from light and moisture. It should be transported at room temperature and handled as a non-hazardous chemical, following standard laboratory safety procedures. Ensure secure packaging and labeling in compliance with chemical shipping regulations to prevent contamination or accidental release.
    Storage O-Phenanthroline Monohydrochloride Monohydrate should be stored in a tightly sealed container, away from moisture and incompatible substances. Keep it in a cool, dry, well-ventilated area, protected from direct sunlight and sources of ignition. Ensure containers are clearly labeled. Store at room temperature, and avoid exposure to oxidizing agents and acids to maintain chemical stability and safety.
    Application of O-Phenanthroline Monohydrochloride Monohydrate

    Applications of O-Phenanthroline Monohydrochloride Monohydrate in Industrial Manufacturing

    As a manufacturer of high-purity O-Phenanthroline Monohydrochloride Monohydrate, we supply this specialty chelating reagent to advanced sectors requiring precise coordination chemistry. Our material plays a critical role in several well-established industrial processes, supporting both qualitative and quantitative methodologies integral to final product consistency. The following segments provide a comprehensive overview of application pathways, compliance benchmarks, formulation practices, and end-product classifications for this chemical in commercial downstream scenarios.

    1. Spectrophotometric Determination of Iron in Environmental Analysis

    Environmental monitoring laboratories and water treatment plants utilize this reagent for colorimetric iron determination. Its strong binding affinity to ferrous ions forms intensely colored coordination complexes, which analytical teams detect and quantify by absorption in the visible spectrum. The ingredient delivers high specificity for Fe(II), supporting regulatory reporting of trace metals in drinking water and industrial effluents, where matrix interference presents a common challenge.

    Industry compliance standards

    • USEPA Method 315B (Determination of Iron by 1,10-Phenanthroline Method in Water Testing)
    • Standard Methods for the Examination of Water and Wastewater, APHA-AWWA-WEF, Method 3500-Fe B
    • ISO 6332:1988 (Water quality—Determination of iron—Spectrometric method using 1,10-phenanthroline)
    • EN 1233 (Water Quality – Determination of Iron)

    Typical usage ratio

    • 0.002–0.008% w/v reagent concentration in aqueous analytical formulations, tailored according to expected iron content and matrix complexity

    Downstream process integration

    • Direct addition into buffered water samples post-filtration; complex forms in situ before absorbance measurement at 510 nm using UV-Vis spectrophotometers

    Final product types

    • Certified water quality analytical results and environmental compliance reports
    • Packaged water quality monitoring kits for field and laboratory use
    • Reference standards for proficiency testing laboratories

    2. Pharmaceutical Quality Control of Metal Impurities

    Pharmacopeial laboratories apply this compound as a colorimetric indicator for quantifying trace iron and related metals during API and excipient quality testing. It forms a complex with iron(II) under acidic conditions, enabling accurate detection of contamination that could compromise final product purity or lead to regulatory non-conformities. The procedure aligns with global monographs to meet stringent market requirements for heavy metal limits.

    Industry compliance standards

    • United States Pharmacopeia (USP) <730> Plasma Spectrochemistry
    • European Pharmacopoeia (Ph. Eur.) 2.4.9 Iron
    • Japanese Pharmacopoeia (JP) 17th edition, General Notices 2.49
    • Current Good Manufacturing Practice (cGMP) regulations

    Typical usage ratio

    • 0.001–0.002% w/v relative to sample weight, adjusted according to the detection limit needed and sample matrix characteristics

    Downstream process integration

    • Sample solution preparation with addition of standardized indicator solution during iron limit testing, followed by visual or instrument-based color assessment

    Final product types

    • Active pharmaceutical ingredients (APIs) certified for trace metal content
    • Pharma-grade excipients and solvent batches with documented analytical reports
    • Batch release documentation for solid, semi-solid, and liquid dosage forms

    3. Electroplating Bath Monitoring in Metal Finishing Industries

    Manufacturers of electronic components and automotive parts rely on this reagent for real-time determination of iron levels in electroplating baths. Excess ferrous ions disrupt plating uniformity and surface integrity, so accurate in-process monitoring is essential during production runs. The rapid-test format ensures operators maintain tight bath chemistry control, minimizing rework or defect rates for high-value substrates.

    Industry compliance standards

    • ISO 4527:2014 (Metallic and other inorganic coatings—Electroplated coatings of nickel plus chromium and of copper plus nickel plus chromium—Specification and test methods)
    • ASTM B322 (Standard Practice for Cleaning Metals Prior to Electroplating)
    • IATF 16949:2016 (Automotive Quality Management Systems for finishing line traceability)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)

    Typical usage ratio

    • 0.003–0.007% w/v in working bath samples; adjusted depending on bath turnover frequency and process volume

    Downstream process integration

    • Addition to on-line bath samples collected at set intervals; formation of colored chelate allows spectrophotometric or visual estimation of iron content before corrective dosing or filtration passes

    Final product types

    • Decorative and functional metal-coated parts for electronics, automotive, and appliance applications
    • Process documentation and quality certificates for ISO-audited metal finishing lines
    • Routine analysis protocols for electroplating plant management

    4. Chemical Reagent and Diagnostic Kit Production

    Producers of laboratory diagnostics and standardized chemical test kits use this material as a central chromogenic component. Its ability to generate clearly defined coloring upon metal complexation supports end-users in executing straightforward color tests for iron presence in educational, clinical, and industrial environments. Formulators must ensure ingredient consistency to maintain calibration and test reliability, especially for multi-component kit assembly.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for applied chemical kit manufacturing)
    • ISO 13485:2016 (Medical devices—Quality management systems for in vitro diagnostic reagents, where applicable)
    • CE Marking – IVD Directive (for medical diagnostic kits in the EU)
    • GB/T 6682-2008 (Chinese National Standards for Laboratory Water and Reagent Quality)

    Typical usage ratio

    • Customarily 0.005–0.015% by total kit weight, adjusted during formulation standardization according to the detection range and target market

    Downstream process integration

    • Measured incorporation into the chromogenic component solution during kit blending; subsequent aliquoting into unit-dose vials or droppers under controlled environments to preserve reagent stability

    Final product types

    • Pre-packed iron testing kits for clinical, field, or educational applications
    • Multi-component water analysis testing panels
    • Color test reagents for academic chemistry and environmental monitoring
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