| Creatinine USP-NF PARENTEX 1KG | |||
| P7504SR100 | 48281A925BZ | ||
| USP-NF PARENTEX | 48281A9 | ||
| 60-27-5 | 118766 | ||
| C4H7N3O | February 2026 | ||
| 113.12 | January 2029 | ||
| Sr.No. | Test | Result | Specification | Method Reference |
|---|---|---|---|---|
| 1 | Description | White crystalline powder, odorless | White crystals or crystalline powder, odorless | USP-NF |
| 2 | Solubility | Complies | Soluble in water, slightly soluble in alcohol, practically insoluble in acetone, in ether, and in chloroform | USP-NF |
| 3 | Identification A (By IR) | Complies | IR spectra of the sample should be concomitant with IR spectra of the standard | USP-NF |
| 4 | Assay (on dry basis) | 101.5% | 98.5%-102.0% | USP-NF |
| 5 | Residue on ignition | 0.08% | NMT 0.2% | USP-NF |
| 6 | Loss on drying (105°C, 3 Hrs) | 0.2% | NMT 3.0% | USP-NF |
| 7 | Total aerobic microbial count | Less than 100 CFU/gm | NMT 100 CFU/gm | In-house |
| 8 | Total Yeast & mold count | Less than 10 CFU/gm | NMT 10 CFU/gm | In-house |
| 9 | Bacterial endotoxins | Less than 2.5 EU/gm | NMT 2.5 EU/gm | In-house |
Remarks: THE CAPTIONED BATCH MATERIAL COMPLIES WITH THE PRESCRIBED QUALITY OF THE ABOVE SPECIFICATION AS WELL AS USP-NF SPECIFICATION.
Actylis 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.
