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Glycerin synthetic CDMF PARENTEX PLUS 2.5LT
I3721LC25042439B402LW
CDMF PARENTEX PLUS42439B4
56-81-599865
C3H8O3December 2023
92.10November 2025
Sr.No.TestResultSpecification
1DescriptionClear, colourless, syrupy liquid, unctuous to the touch, having a sweet taste. Has not more than a slight charactersitic odor, which is neither harsh nor disagreeable. Is hygroscopic. Its solutions are neutral to litmus.Clear, colourless, syrupy liquid, unctuous to the touch, having a sweet taste. Has not more than a slight characteristic odor, which is neither harsh nor disagreeable. Is hygroscopic. Its solutions are neutral to litmus.
2SolubilityCompliesMiscible with water, ethanol (96%) and with alcohol. Slightly soluble in acetone. Insoluble in fatty oils, in essential oils, in chloroform, in ether and in fixed and volatile oils.
3Identification (By IR)CompliesIR spectra of the sample should be concomitant with IR spectra of the standard.
4Identification (Diethylene glycol)Not detectedNMT 0.10%
5Identification (Ethylene glycol)Not detectedNMT 0.10%
6Identification (By GC Chromatogram)CompliesThe retention time of the glycerine peak of the Sample solution corresponds to that obtained in the Standard solution.
7Appearance of solutionCompliesClear and colorless solution.
8ColorCompliesThe colour should not be darker than reference solution.
9Acidity or alkalinityCompliesPink colour should produce after adding 0.2 mL of 0.1 mol/L sodium hydroxide solution..
10Refractive index, 20°C1.4741.470 - 1.475
11Relative density, 20°C1.2611.258 - 1.268
12Aldehydes and reducing substancesCompliesThe light absorption of the test solution at 655 nm should not be more than that of 2.0 mL of the reference solution.
13Fatty acids and estersCompliesNMT 2.0 mL of sodium hydroxide (0.1 mol/L) VS should require.
14Related substances: Impurity A (Diethylene glycol)Not detectedNMT 0.1%
15Related substances: Any other impurity with a retention time less than the retention time of glycerol0.01%NMT 0.1%
16Related substances: Total of all impurities with retention times greater than the retention time of glycerol0.06%NMT 0.5%
17Related substances: Individual impurity0.02%NMT 0.1%
18Related substances: Total impurities0.1%NMT 1.0%
19Aldehyde residues (Glyceraldehyde)Not detectedNMT 5ppm
20Aldehyde residues (Formaldehyde)Not detetcedNMT 2ppm
21Aldehyde residues (Hydroxyacetone)Not detectedNMT 5ppm
22Aldehyde residues (Dihydroxyacetone)Not detectedNMT 5ppm
23Halogenated compoundsLess than 35ppmNMT 35 ppm
24SugarsCompliesThe solution should remain blue and no precipitate should form.
25ChloridesLess than 0.0006%NMT 0.0006%
26SulphateLess than 0.002%NMT 0.002%
27Water0.3%NMT 2.0%
28Residue on ignition0.001%NMT 0.01%
29Assay (Anhydrous basis)99.8%99.0% - 101.0%
30Chlorinated substancesLess than 0.003%NMT 0.003%
31Readily carbonizable substancesCompliesAny colour produced should not more intense than that of an equal volume of a reference solution.
32AmmoniumCompliesNo odour of ammonia should produced.
33CalciumCompliesThe solution should be clear.
34IronLess than 0.00005%NMT 0.00005%
35Total aerobic microbial countLess than 100 CFU/gmNMT 100 CFU/gm
36Total combined yeast and mold countLess than 10 CFU/gmNMT 10 CFU/gm
37Bacterial endotoxinsLess than 5 EU/gmNMT 5 EU/gm
38E.coliAbsentShould not be detected.
Remarks: THE CAPTIONED BATCH MATERIAL COMPLIES WITH THE PRESCRIBED QUALITY OF THE ABOVE SPECIFICATION AS WELL AS USP, Ph.Eur AND Ch.P SPECIFICATION.
FINAR 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.
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