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Chondroitin Sulfate Sodium
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| Place of Origin | China |
| Brand Name | HS |
| Certification | NSF-GMP |
| Model Number | 95% |
95% Purity Chondroitin Sulfate Sodium Extracted from Bovine Cartilages for Joint Supplements
The Chondroitin sulfate sodium is extracted from bovine cartilages with 95% purity. It is a ingredient used for joint health supplements.
The specification of bovine chondroitin sulfate with 95% assay is listed as below. All the testing items are the same as USP grade chondroitin sulfate 90%, except for the assay testing which is 95%.
| Product: | Chondroitin Sulfate sodium | |||||||
| Original | Bovine(Terrestrial) | Report Date | 2017/04/17 | |||||
| Batch No.: | HS1704035 | Quantity: | 1000KGS | |||||
| Net Weight: | 25KG/DRUM | Gross weight: | 27.5KG/DRUM | |||||
| Manufacturing Date: | 2017/04/12 | Expiry Date: | 2019/04/11 | |||||
ITEMS |
SPECIFICATIONS (TEST METHOD) |
RESULT |
||||||
| Appearance | White to off-white powder | Pass | ||||||
| Identification | Infra Red Confirmed (USP197K). | Pass | ||||||
| Sodium reaction (USP191) | Positive | |||||||
| The chromatogram of the enzymatically digested sample solution as obtained in the test for the limit of nonspecific disaccharides shows three main peaks corresponding to △DI-4S, △DI-6S,△DI-OS in the enzymatically digested standard solution. By peak area response, △ DI-4S is the most abundant, followed by the △ DI-6S, with △ DI-OS being the least abundant of the three | ||||||||
| Assay(ODB) |
NLT95% (CPC Titration) | 96.6% | ||||||
| Loss on drying |
Less than12%(USP731) | 8.5% | ||||||
| Nonespecific Dissaccharides | NMT10% | 7.1% | ||||||
| Protein |
NMT6.0%(USP38) | 4.8% | ||||||
| Sulfate |
＜0.24%(USP221) | ＜0.24 | ||||||
| Chloride |
＜0.5% (USP221) | ＜0.5% | ||||||
| Heavy Metal |
NMT20PPM (Method I USP231) | Pass | ||||||
| PH (1%H2O solution) |
5.5-7.5(USP791) | 6.3 | ||||||
| Specific Rotation |
- 20°~ -30°(USP781S) | -23.5° | ||||||
| Residue on Ignition |
20%-30%(dry base)(USP281) | 26.4% | ||||||
| OrganicVolatile Residual(Ethanol) |
NMT0.5% (USP467) | PASS | ||||||
| Clarity (5%H2O solution) |
<0.35@420nm | 0.22 | ||||||
| Electrophoretic purity | NMT2.0%(USP726) | Pass | ||||||
| Bulk Density | NLT 0.5g/ml | 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 | ||||||
| Enterobacteria |
Negative in 1 gram (USP2022) | Negative | ||||||
| Particle size | 100% through 80 mesh | Pass | ||||||
| Storage: 25kg/drum, keep in an airtight container, protected from light. | ||||||||
The advantage of our bovine chondroitin sulfate 95% :
1. Produced in the GMP Workshop, according to NSF-GMP standards.
2. None Irradiation. our bovine chondroitin sulfate 95% is produced in the clean GMP workshop, the bacterial is well controlled, no irradiation is needed.
3. The DMF documentation. We have DMF documenation for the bovine chondroitin sulfate 95%.
4. Warehouse and inventory in the USA and EU. We have warehouse and inventory int he USA and EU
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