| Creatinine USP-NF PARENTEX 1KG | |||
| P7504SR100 | 43221A901DX | ||
| USP-NF PARENTEX | 43221A9 | ||
| 60-27-5 | 102460 | ||
| C4H7N3O | April 2024 | ||
| 113.12 | March 2027 | ||
| Sr.No. | Test | Result | Specification |
|---|---|---|---|
| 1 | Description | White crystalline powder, odorless | White crystals or crystalline powder, odorless |
| 2 | Solubility | Complies | Soluble in water, slightly soluble in alcohol, practically insoluble in acetone, in ether, and in chloroform |
| 3 | Identification A (By IR) | Complies | IR spectra of the sample should be concomitant with IR spectra of the standard |
| 4 | Assay (on dry basis) | 99.4% | 98.5%-102.0% |
| 5 | Residue on ignition | 0.1% | NMT 0.2% |
| 6 | Loss on drying (105°C, 3 Hrs) | 0.1% | NMT 3.0% |
| 7 | Total aerobic microbial count | Less than 100 CFU/gm | NMT 100 CFU/gm |
| 8 | Total Yeast & mold count | Less than 10 CFU/gm | NMT 10 CFU/gm |
| 9 | Bacterial endotoxins | Less than 2.5 EU/gm | NMT 2.5 EU/gm |
Remarks: THE CAPTIONED BATCH MATERIAL COMPLIES WITH THE PRESCRIBED QUALITY OF THE ABOVE SPECIFICATION AS WELL AS USP-NF SPECIFICATION.
FINAR provides this analytical report in good faith and to the best of its knowledge. It should not be substituted for the users own raw material quality control.
| Tested By (Chemist - Quality Control) | Approved By (Head - Quality Control) |
Computer Generated Report - Does not require Signature.
