| Benzyl Benzoate (Low Benzaldehyde) USP/Ph.Eur/BP PARENTEX PLUS 2.5LT | |||
| I1293LC250 | 45600B127BY | ||
| USP/Ph.Eur/BP PARENTEX PLUS | 45600B1 | ||
| 120-51-4 | 110321 | ||
| C6H5COOCH2C6H5 | February 2025 | ||
| 212.3 | January 2027 | ||
| Sr.No. | Test | Result | Specification | Method Reference |
|---|---|---|---|---|
| 1 | Appearance/Description | Clear, colorless oily liquid having a slight aromatic odor. | Colourless or almost colourless crystals,clear colorless or almost colourless,oily liquid having a slight aromatic odor. | USP/Ph.Eur/BP |
| 2 | Solubility | Complies | Practically insoluble in water and in glycerin. Miscible with alcohol, Ethanol (96%), with ether, and with chloroform with methylene chloride and with fatty and essential oils. | USP/Ph.Eur/BP |
| 3 | Identification A (By IR) | Complies | IR Spectra of the sample should be concomitant with IR spectra of the standard | USP/Ph.Eur/BP |
| 4 | Identification B (By Chemical test) | 122.4°C | Dried precipitate should melt between 121°C to 124°C | Ph.Eur/BP |
| 5 | Identification C (By Chemical test) | 122.9°C | Dried precipitate should melt between 121°C to 124°C | Ph.Eur/BP |
| 6 | Assay (By Titration) | 99.6% | 99.0% - 100.5% | USP/Ph.Eur/BP |
| 7 | Limit of Aldehydes (As benzaldehyde content) | B.L.Q (Q.L=30ppm) | NMT 250 ppm | In-house |
| 8 | Specific gravity, 25°C | 1.118 | 1.116 to 1.120 | USP |
| 9 | Relative density, 20°C | 1.120 | 1.118 to 1.122 | Ph.Eur/BP |
| 10 | Congealing temperature | 18.4°C | NLT 18.0°C | USP |
| 11 | Freezing point | 17.8°C | NLT 17.0°C | Ph.Eur/BP |
| 12 | Refractive index,20° C | 1.569 | 1.568 - 1.570 | USP/Ph.Eur/BP |
| 13 | Acidity 1 | 0.07ml of 0.1M NaOH required | NMT 0.2ml of 0.1M NaOH should required to change the colour of indicator to pink. | Ph.Eur/BP |
| 14 | Acidity 2 | 0.7 ml of 0.020 N sodium hydroxide required | NMT 1.5 ml of 0.020 N sodium hydroxide should require to restore the pink color. | USP |
| 15 | Boiling point | 320.9°C | About 320°C | Ph.Eur/BP |
| 16 | Sulphated ash | 0.02% | NMT 0.1% | Ph.Eur/BP |
| 17 | Total aerobic microbial count | Less than 100 CFU/ml | NMT 100 CFU/ml | In-house |
| 18 | Total combined yeast and molds count | Less than 10 CFU/ml | NMT 10 CFU/ml | In-house |
| 19 | Bacterial endotoxins | Less than 0.25 EU/ml | NMT 0.25 EU/ml | In-house |
| 20 | Escherichia coli | Absent/ml | should be Absent/ml | In-house |
| 21 | Salmonella | Absent/10ml | should be Absent/10ml | In-house |
| 22 | Staphylococcus aureus | Absent/ml | should be Absent/ml | In-house |
| 23 | Pseud. aeruginosa | Absent/ml | should be Absent/ml | In-house |
Remarks: THE CAPTIONED BATCH MATERIAL COMPLIES WITH THE PRESCRIBED QUALITY OF THE ABOVE SPECIFICATION AS WELL AS USP, Ph.Eur, 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.
