| ITEMS | SPECIFICATIONS (TEST METHOD) |
|---|---|
| Appearance | White to off-white powder (USP 197K) |
| Identification | A: Infrared Absorption (197K) B: It meets the requirements of the tests for chloride (191) C: The retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, as obtained in the Assay. (USP) |
| Solubility: | Very soluble in water, sparingly soluble in methanol, practically insoluble in acetone. |
| Assay | 98%-102% (HPLC) |
| Specific Rotation | 70°– 73° (USP781S) |
| PH (2%, 25°) | 3.0-5.0 (USP791) |
| Loss on drying | Less than 1.0% (USP731) |
| Residue on Ignition | NMT 0.1% (USP281) |
| Sulfates | NMT 0.24% (USP221) |
| Chloride | < 17.0% (USP) |
| Heavy Metal | NMT 10PPM (USP231) |
| Lead | NMT 0.5PPM (USP211) |
| Mercury | NMT 1.0ppm (USP211) |
| Cadmium | NMT 1.0PPM (USP211) |
| Total Bacteria Count | < 1000CFU/g (USP2021) |
| Yeast & Mold | < 100CFU/g (USP2021) |
| Salmonella | Negative (USP2022) |
| E.Coli | Negative (USP2022) |
| Staphylococcus Aureus | Negative (USP2022) |
| Bulk Density | NLT 0.8g/ml (IN-HOUSE) |
| Particle size | 100% through 80 mesh (Pass) |
We guarantee our product is manufactured in a facility with strict allergen control protocols, ensuring zero cross-contamination with shellfish or animal products..
Our multi-stage crystallization and purification process results in a consistent, white, free-flowing powder that meets the highest standards of the USP (United States Pharmacopeia) and EP (European Pharmacopoeia).
We maintain a fully traceable supply chain, from the sourcing of non-GMO corn feedstock to the final packaged powder, providing complete transparency and quality assurance.
Standard packaging includes 25KG net weight fiber drums or cartons, sealed with inner double-layer food-grade polyethylene bags for moisture protection.