| Benzyl alcohol CDMF PARENTEX 500ML | |||
| P3290LM500 | 47971C312AZ | ||
| CDMF PARENTEX | 47971C3 | ||
| 100-51-6 | 118503 | ||
| C6H5CH2OH | January 2026 | ||
| 108.14 | December 2027 | ||
| Sr.No. | Test | Result | Specification | Method Reference |
|---|---|---|---|---|
| 1 | Appearance | A colorless liquid. | A colorless liquid. (CP) | |
| 2 | Solubility | Complies | Sparingly soluble in water. Miscible with ethanol (96%) and with fatty and essential oils with ether and with chloroform. Freely soluble in 50% alcohol. (USP-NF/Ph.Eur) | |
| 3 | Relative density, 20°C | 1.045 | 1.043 - 1.050 (CP) | |
| 4 | Boiling range | 96% distilled at 203°C - 206°C | NLT 95% (mL/mL) is distilled at 203°C - 206°C. (CP) | |
| 5 | Identification by Chemical test | Complies | The benzylaldehyde characteristic odour should perceptible. (CP) | |
| 6 | Identification by IR | Complies | IR spectra of the sample should be concomittant with IR spectra of the standard. (CP) | |
| 7 | Appearance of solution | Complies | The solution is clear and colorless. (USP-NF/Ph.Eur) | |
| 8 | Refractive index, 20°C | 1.541 | 1.538 - 1.541 (USP-NF/Ph.Eur) | |
| 9 | Assay | 98.93% | NLT 98.0% on anhydrous basis. (CP) | |
| 10 | Acidity | 0.1 mL of 0.1M sodium hydroxide required. | NMT 0.2 mL of 0.1M sodium hydroxide should required to change the color of the indicator to pink. (CP) | |
| 11 | Fats & Fixed oils (Peroxide value) | 0.5 | NMT 5 (USP/Ph.Eur) | |
| 12 | Residue on evaporation | 0.005% | NMT 0.05% (USP-NF/Ph.Eur) | |
| 13 | Chlorides | Less than 0.003% | NMT 0.003% (CP) | |
| 14 | Water | 0.045% | NMT 0.5% (CP) | |
| 15 | Related substances: Benzaldehyde | 0.02% | NMT 0.05% (CP) | |
| 16 | Related substances: Any other impurity | 0.008% | NMT 0.01% (CP) | |
| 17 | Related substances: the total amount of all other impurities | 0.01% | NMT 0.05% (CP) | |
| 18 | Total aerobic microbial count | Less than 100 CFU/g | NMT 100 CFU/g (In-house) | |
| 19 | Total combined yeast and molds count | Less than 10 CFU/g | NMT 10 CFU/g (In-house) | |
| 20 | Bacterial endotoxins | Less than 0.1 EU/mg | NMT 0.1 EU/mg (CP) |
Remarks: THE CAPTIONED BATCH MATERIAL COMPLIES WITH THE PRESCRIBED QUALITY OF THE ABOVE 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.
