| Calcium chloride dihydrate USP/Ph.Eur 5KG | |||
| 90430SR500 | 474497107JY | ||
| USP/Ph.Eur | 4744971 | ||
| 10035-04-8 | 116114 | ||
| CaCl2.2H2O | October 2025 | ||
| 147.02 | September 2028 | ||
| Sr.No. | Test | Result | Specification | Method Reference |
|---|---|---|---|---|
| 1 | Description | White crystalline powder. Is deliquescent and hygroscopic. | white, hard, odorless fragments or granules or crystalline powder. Is deliquecent and hygroscopic. | USP/ Ph.Eur |
| 2 | Solubility | Complies | Freely soluble in water, in alcohol and in boiling alcohol; Very soluble in boiling water Soluble in ethanol (96%) | USP/ Ph.Eur |
| 3 | Appearance of solution | Complies | Solution should be clear and not more intensely coloured than reference solution Y6. | Ph.Eur |
| 4 | Identification (Calcium 1) | Complies | Precipitate should insoluble in 6N acetic acid while soluble in hydrochloric acid | USP |
| 5 | Identification (Calcium 2) | Complies | The chloroform layer should coloured red. | Ph.Eur |
| 6 | Identification (Calcium 3) | Complies | A white crystalline precipitate should form. | Ph.Eur |
| 7 | Identification (Chloride) | Complies | A curdy white precipitate should insoluble in nitric acid but soluble in 6N ammonium hydroxide | USP/ Ph.Eur |
| 8 | pH (5% aq soln) | 5.25 | 4.5 - 9.2 | USP |
| 9 | Assay | 100.9% | 99.0% - 107.0% of CaCl2.2H2O | USP |
| 10 | Acidity or Alkalinity | 0.1 mL of 0.01 M sodium hydroxide required | Not more than 0.2 mL of 0.01 M sodium hydroxide or 0.01M Hydrochloric acid should require to turn solution red | Ph.Eur |
| 11 | Iron, Aluminum & Phosphate | Complies | No turbidity or precipitate should produce. | USP |
| 12 | Magnesium & alkali metals | 0.16% | NMT 0.5% | Ph.Eur |
| 13 | Sulfates | Less than 300 ppm | NMT 300ppm | Ph.Eur |
| 14 | Barium(Ba) | Complies | Any opalescence in the solution is not more intense than reference solution | Ph.Eur |
| 15 | Iron (Fe) | Less than 10 ppm | NMT 10ppm | Ph.Eur |
Remarks: THE CAPTIONED MATERIAL COMPLIES WITH THE PRESCRIBED QUALITY OF USP AND PH.EUR 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.
