|Product Name:||EP Grade Chondroitin Sulfate||Origin:||Bovine Cartilage|
|Purity Of Chondroitin:||≥95%||Protein Content:||≤3.0%|
|Registration Documents:||DMF Documentation Available||GMP Status:||Pharma GMP Available|
|Application:||Pharma Tablet Or Capsules||Function:||Improve Bone Density, Maintain Function Of Joints|
Drug Chondroitin Sulfate Sodium,
Bovine Chondroitin Sulfate Sodium,
Bovine chondroitin sulfate sodium salt
Pharmaceutical Grade Chondroitin Sulfate Sodium extracted from Bovine Trachea for Drug Products
We Beyond Biopharma is a manufacturer of EP grade chondroitin sulfate for pharmaceutical products. We have the Pharma GMP and DMF available for registration purposes.
Our Pharmaceutical grade chondroitin sulfate is produced from bovine trachea with 95% purity by CPC titration method. The protein content in the chondroitin sulfate is controlled to be less than 3.0% in order to meet the pharma standard.
We have the registration experiences of pharma grade chondroitin sulfate is CIS countries such as Russia, Ukraine and Belarus. We can provide documentation support and help you to register our pharma chondroitin sulfate in your country.
Our Pharma Grade Chondroitin sulfate is in total compliance with EP standard, and is commonly used in pharmaceutical finished dosage form such as tablet and capsules.
|Appearance||White or almost white, hygroscopic powder.|
|Solubility||Freely soluble in water, practically insoluble in acetone and in ethanol (96 per cent).|
A: Infrared absorption spectrophotometry
B. Solution S1 gives reaction (b) of sodium
C. Examine the electropherograms obtained in the test for related substances.
|Intrinsic viscosity||0.01m3/kg to 0.15 m3/kg|
|Specific rotation||Between-20.0º and -30.0º(determined on solution S1. )|
Total viable aerobic count
Yeast and Mold
Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli,
|pH||Between 5.5 and 7.5 (determined on solution S1. )|
|Loss on drying||12.0% max.(determined on 1.000 g by drying in an oven at 100-105 °C for 4 h. )|
|Heavy metals||20ppm max.|
|Protein||3.0% max.(dried substance)|
|Content||95% to 105% (dried substance).|
|Any secondary band in the electropherogram obtained with the test solution is not more intense than the band in the electropherogram obtained with reference solution (b) (2 per cent).
Quick Details of Pharma Grade Chondroitin Sulfate
|Product Name||Chondroitin Sulfate Soidum|
|Quality Standard||Pharma Grade EP Standard|
|Appearance||White to off white powder|
|Production process||enzymatic hydrolysis process|
|Protein Content||≥ 95% by EP Standard|
|Loss on Drying||≤10%|
|Function||Joint health Support, Cartilage and Bone Health|
|Application||Pharma Grade in Tablet, Capsules, or Powder|
|Halal Certificate||Yes, Halal Verified|
|GMP Status||Pharma GMP Available|
|Health Certificate||Yes, Health certificate is available for custom clearance purpose|
|Shelf Life||24 months from production date|
|Packing||25KG/Drum, Inner Packing: Double PE BAGS, Outer Packing: Paper Drum
Contact Person: Eric Lee