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    Chondroitin Sulfate COA

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    m.shahin8888
    This document provides a certificate of analysis for a batch of chondroitin sulfate sodium. It details the specifications, test methods, and results for the product to ensure it meets USP41 requirements for identity, purity, quality, and microbiological limits.

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    © All Rights Reserved
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    Chondroitin Sulfate COA

    Uploaded by

    m.shahin8888
    39 views1 page
    This document provides a certificate of analysis for a batch of chondroitin sulfate sodium. It details the specifications, test methods, and results for the product to ensure it meets USP41 requirements for identity, purity, quality, and microbiological limits.

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    Chondroitin sulfate COA

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    This document provides a certificate of analysis for a batch of chondroitin sulfate sodium. It details the specifications, test methods, and results for the product to ensure it meets USP41 requirements for identity, purity, quality, and microbiological limits.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    39 views1 page

    Chondroitin Sulfate COA

    Uploaded by

    m.shahin8888
    This document provides a certificate of analysis for a batch of chondroitin sulfate sodium. It details the specifications, test methods, and results for the product to ensure it meets USP41 requirements for identity, purity, quality, and microbiological limits.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
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    JIAXING HENGJIE BIOPHARMACEUTICAL CO., LTD.

    CERTIFICATE OF ANALYSIS
    COA NO.: HS2011137
    Product: CHONDROITIN SULPHATE SODIUM
    Original Bovine(Terrestrial) Report Date 2020/11/27
    Batch No.: HS2011137 Quantity: 1000KG
    Net Weight: 25KG/DRUM Gross weight: 27.5KG/DRUM
    Manufacturing Date: 2020/11/20 Expiry Date: 2023/05/31

    ITEMS SPECIFICATIONS (TEST METHOD) RESULT


    Appearance White to off-white powder Pass
    Identification Infra Red Confirmed (USP197K) Pass
    Sodium reaction (USP191) Positive
    Assay(ODB) NLT98% (CPC) 99.0%
    Loss on drying Less than7%(USP731) 6.1%
    Protein NMT6.0%(USP41) 2.3%
    Heavy Metal NMT20PPM (MethodIIUSP231) Pass
    PH (1%H2O solution) 5.5-7.5(USP791) 6.2
    Chloride NMT0.5%(USP221) Pass
    Sulfates NMT0.24%(USP221) Pass
    Specific Rotation - 20°~ -30°(USP781S) -27.1°
    Residue on Ignition 20%-30%(USP281) 25.5%
    Clarity (5%H2O solution) <0.35@420nm 0.1
    Electrophoretic purity NMT2.0%(USP726) Pass
    Total Bacteria Count <1000CFU/g (USP2021) Pass
    Yeast & Mold <100CFU/g (USP2021) Pass
    Salmonella Negative (USP2022) Negative
    E.Coli Negative (USP2022） Negative
    Staphylococcus Aureus Negative (USP2022） Negative
    Particle size 100% through 80 mesh Pass
    Storage: keep in an airtight container, protected from light.

    CONCLUSION: CONFORM TO USP 41 REQUIREMENTS

    CHECKER: PRINCIPAL:

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