| Alginic acid USP-NF/Ph.Eur/BP 5KG | |||
| M1077SR500 | 48674A615DZ | ||
| USP-NF/Ph.Eur/BP | 48674A6 | ||
| 9005-32-7 | 120690 | ||
| (C6H8O6)n | April 2026 | ||
| 10000-60000 g/mol | March 2029 | ||
| Sr.No. | Test | Result | Specification | Method Reference |
|---|---|---|---|---|
| 1 | Appearance | Yellowish-white, amorphous powder. | White to yellowish-white, white or pale yellowish-brown, crystalline or amorphous powder or fibrous powder. | USP-NF/Ph.Eur/BP |
| 2 | Solubility | Complies | It dissolves in 10% KOH. | In-house |
| 3 | Identification (By IR) | Complies | IR spectra of the sample should be concomitant with IR spectra of the corresponding standard. | USP-NF |
| 4 | Identification (By chemical test 1) | Complies | A voluminous, gelatinous precipitate should form. | USP-NF/Ph.Eur/BP |
| 5 | Identification (By chemical test 2) | Complies | A heavy, gelatinous precipitate should form. | USP-NF |
| 6 | Identification (By chemical test 3) | Complies | No Voluminous gelatinous mass should form. | Ph.Eur/BP |
| 7 | Identification (By chemical test 4) | Complies | The isopropyl ether extract exhibits a deeper purplish hue than that from a blank. | USP-NF/Ph.Eur/BP |
| 8 | Arsenic | Not detected | NMT 3ppm | USP-NF/In-house |
| 9 | Lead | 0.13 ppm | NMT 10ppm | USP-NF/In-house |
| 10 | chloride | 0.58% | NMT 1.0% | Ph.Eur/BP |
| 11 | pH | 2.12 | 1.5 - 3.5 | USP-NF |
| 12 | Loss on drying (105 °C, 4 hrs) | 11.03% | NMT 15.0% | USP-NF/Ph.Eur/BP |
| 13 | Sulfated ash | 5.73% | NMT 8.0% | Ph.Eur/BP |
| 14 | Total Ash | 2.37% | NMT 4.0% | USP-NF |
| 15 | Acid value | 286 | NLT 230 on the dried basis | USP-NF |
| 16 | Assay (on dried basis) | 20.2% | 19.0 - 25.0% | Ph.Eur/BP |
| 17 | Total aerobic microbial count | Less than 200 CFU/gm | NMT 200 CFU/gm | In-house |
| 18 | Salmonella | Absent/10gm | should be absent/10gm | In-house |
| 19 | Escherichia coli | Absent/gm | should be absent/gm | In-house |
| 20 | Particle Size Distribution | 100% | 99 - 100% (Thru 120 mesh) | In-house |
Remarks: THE CAPTIONED MATERIAL COMPLIES WITH THE PRESCRIBED QUALITY OF USP-NF, PH.EUR AND BP 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.
