Products – Anmol Chemicals Private Limited
Sodium Hyaluronate BP
Identity
Chemical Name: Sodium Hyaluronate
Mol. Formula: C28H44N2NaO23
Mol. Weight: 799.641 g/mol
CAS No.: 9067-32-7
General Specifications:
Test | Specification |
Characters | It occurs as a white or almost white, very hygroscopic powder or fibrous aggregate. |
Identification
Test A Test B |
a. Infrared absorption spectrophotometry b. It gives reaction of sodium. |
Solubility | Sparingly soluble or soluble in water, practically insoluble in acetone and in anhydrous ethanol. |
Appearance of solution | Solution is clear and its absorbance at 600 nm is not greater than 0.01. |
pH | Between 5.0 to 8.5. |
Intrinsic viscosity | Specified Test. |
Sulfated glycosaminoglycans | Not more than 1.0 % |
Nucleic acids | The absorbance of solution at 260 nm is maximum 0.5 |
Protein | Not more than 0.3% |
Chlorides | Not more than 0.5% |
Iron | Not more than 80 ppm |
Loss on drying | Not more than 20.0% |
Assay | Not less than 95.0 % and not more than 105.0 % (dried substances) |
Shelf life, Storage and Packing
It should be stored in a segregated area in a cool and ventilated place away from combustible materials. Keep in a tightly closed container, sealed until ready for use. It is packed in 25kg or 50kg HDPE bags or drums as required.
Other
We Manufacture Bulk Dugs/API, Excipients, pharmaceuticals (IP/BP/USP/NF/PH. EUR./JP), Speciality Chemicals (Pure/AR/ACS), mineral fortifiers (FCC). our manufacturing facility is GLP, GMP (FDA) approved, ISO 9001, ISO 14001, ISO 22000, FSSC 22000, FSSAI, kosher, halal, COPP and WHO-GMP certified.
Good Manufacturing Practice Certified by World Health Organization (WHO-GMP)
Written Confirmation Certification (WC)
Good Manufacturing Practice (EXCiPACT cGMP)
Good Manufacturing Practice (cGMP)
Good Laboratory Practice (GLP)