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Benzyl Benzoate CDMF PARENTEX PLUS 2L
I3293LC20045885B403DY
CDMF PARENTEX PLUS45885B4
120-51-4111338
C14H12O2April 2025
212.2March 2027
Sr.No.TestResultSpecificationMethod Reference
1DescriptionClear, colorless, oily liquid having a slight aromatic odor.Clear, colorless, oily liquid having a slight aromatic odor.USP
2SolubilityCompliesPractically insoluble in water and in glycerin. Miscible with alcohol,with ether, and with chloroform.USP
3Identification A (By IR)CompliesIR Spectra of the sample should be concomitant with IR spectra of the corresponding standardUSP
4Assay99.80%99.0%-100.5%USP
5Limit of Aldehydes (As benzaldehyde)Less than 0.05%NMT 0.05%USP
6Specific gravity, 25°C1.1181.116-1.120USP
7Congealing temperature18.4°CNot less than 18.0°CUSP
8Refractive index,20° C1.5691.568-1.570USP
9Acidity1.1 mL of 0.02N sodium hydroxide requiredNMT 1.5 mL of 0.02N sodium hydroxide should require to restore the pink colorUSP
10Residue on ignition0.05%NMT 0.1%CP
11Total aerobic microbial countLess than 100 CFU/mlNMT 100 CFU/mlIn-house
12Total combined yeast and molds countLess than 10 CFU/mlNMT 10 CFU/mlIn-house
13Bacterial endotoxinsLess than 0.25 EU/mlNMT 0.25 EU/mlIn-house
14E.coliAbsent/mlshould be Absent/mlIn-house
15SalmonellaAbsent/10mlshould be Absent/10mlIn-house
16Staphylococcus aureusAbsent/mlshould be Absent/mlIn-house
17Pseud. aeruginosaAbsent/mlshould be Absent/mlIn-house
18Purity (By GC)99.94%NLT 99.8%In-house
19Any individual impurity (By GC)0.015%NMT 0.10%In-house
Remarks: THE CAPTIONED MATERIAL COMPLIES WITH THE PRESCRIBED QUALITY OF USP AND CP 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.
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