Derived from premium bovine cartilage, our Bovine Chondroitin Sulfate is manufactured to meet stringent USP and EP quality standards, with an assay ranging from 90% to 105%. As a direct manufacturer with over 20 years of production and global export experience, we ensure consistent batch-to-batch quality under ISO, GMP, and HACCP quality management systems. Every shipment is supported by comprehensive documentation, including COA, TDS, and MSDS, helping nutraceutical, pharmaceutical, and veterinary manufacturers meet international quality and regulatory requirements with confidence.
Chondroitin sulfate bovine is a natural glycosaminoglycan extracted from bovine cartilage. It is used in joint health supplements due to its role in supporting cartilage structure and joint mobility. This 90% grade material is suitable for commercial procurement and industrial applications in the nutraceutical sector.
The product is available in powder form with customizable particle sizes, allowing integration into various production processes. Batch-to-batch consistency is maintained through standardized extraction and purification protocols, supporting steady business operations for formulation teams.
Test Items | Specifications |
|---|---|
Appearance | White or almost white powder, hygroscopic powder |
Solubility | Freely soluble in water, practically insoluble in acetone and in ethanol 96% |
Infrared Identification | The infrared absorption spectrum is consistent with that obtained with USP Chondroitin Sulfate Sodium RS |
Sodium Identification | Positive |
Assay by CPC (dry basis) | 90.0-105.0% |
Clarity and Color | <0.35 at 420nm |
Limit of protein | ≤6.0% |
Specific Rotation | -20.0° - -30.0° |
pH | 5.5-7.5 |
Heavy Metals | ≤20ppm |
Residue on Ignition | 20.0-30.0% |
Loss on Drying | <12.0% |
Chlorides | <0.50% |
Sulfate | <0.24% |
Electrophoretic Purity | ≤2% |
Limit of Nonspecific Dissaccharides | ≤10.0% |
Residual Solvents | ≤0.5% |
Bulk Density | ≥0.60g/ml |
Particle Size | 100% thru 80 Mesh or customize |
Total Plate Count | ≤1000 CFU/g |
Yeast and Mold | ≤100 CFU/g |
E. Coli | Negative |
Salmonella | Negative |
S. aureus | Negative |
P. aeruginosa | Negative |
The product conforms to USP and EP quality requirements. Assay testing is performed using CPC and HPLC methods, with results traceable to reference standards. Each production batch undergoes full testing before release.
Manufacturing facilities operate under ISO-certified quality management systems. Production follows GMP standards, and food safety management follows HACCP principles. Halal and Kosher certifications are available upon request for specific market requirements.
Each shipment includes a batch-specific Certificate of Analysis (COA), Technical Data Sheet (TDS), and Material Safety Data Sheet (MSDS). Additional documentation for regulatory submissions can be provided upon request to support market entry processes.
Bovine chondroitin sulfate 90% is used in joint health supplement products. It can be incorporated into single-ingredient formulations or combined with other active materials.
The powder is suitable for tablet, capsule, and powder blend formulations. Particle size can be adjusted to match specific production equipment and processing requirements.
The material works in combined formulas with glucosamine, MSM, collagen, and other joint health ingredients. The purity profile supports formulation flexibility for various product concepts.
Factory-direct production allows for bulk supply capability with controlled lead times. Long-term cooperation arrangements are available for enterprise customers with consistent volume requirements.
With 20 years of export experience across global markets, the team provides support for documentation preparation and logistics coordination. Quotation requests receive response within standard business hours.
Particle size, packaging specifications, and documentation formats can be adjusted to meet specific commercial procurement needs. Technical consultation for formulation development is also available.
Assay testing is performed using the CPC (cetylpyridinium chloride) titration method and HPLC method, consistent with USP and EP monograph requirements. Each batch is tested before release.
Yes, the 90% grade bovine chondroitin sulfate is formulated for nutraceutical and dietary supplement production. The impurity and microbiology profiles meet the requirements for dietary supplement and functional food applications.
Production facilities hold ISO, GMP, and HACCP certifications. Halal and Kosher certifications are available upon request. The product itself conforms to USP and EP quality standards.
Yes, standard particle size is 100% through 80 mesh. Custom particle size specifications can be arranged based on production volume and specific processing requirements.
Each shipment includes a batch-specific Certificate of Analysis (COA), Technical Data Sheet (TDS), and Material Safety Data Sheet (MSDS). Additional regulatory documentation can be provided upon request.
Yes, the chondroitin sulfate is extracted from bovine cartilage. The source material is traceable, and production follows established animal-derived material handling protocols.
