Clarity of solution
[NOTEThe
Test solution is to be compared to
Reference suspension 1 in diffused daylight 5 minutes after preparation of
Reference suspension 1.]
Hydrazine solution
Transfer 1.0 g of hydrazine sulfate to a 100-mL volumetric flask, dissolve in and dilute with water to volume, and mix. Allow to stand 4 to 6 hours before use.
Methenamine solution
Transfer 2.5 g of methenamine to a 100-mL glass-stoppered flask, add 25.0 mL of water, insert the glass stopper, and mix to dissolve.
Primary opalescent suspension
[NOTEThis suspension is stable for 2 months, provided it is stored in a glass container free from surface defects. The suspension must not adhere to the glass and must be well mixed before use.] Transfer 25.0 mL of Hydrazine solution to the Methenamine solution in the 100-mL glass-stoppered flask. Mix, and allow to stand for 24 hours.
Opalescence standard
[NOTEThis suspension should not be used beyond 24 hours after preparation.] Transfer 15.0 mL of the Primary opalescent suspension to a 1000-mL volumetric flask, dilute with water to volume, and mix.
Reference suspensions
Transfer 5.0 mL of the Opalescence standard to a 100-mL volumetric flask, dilute with water to volume, and mix to obtain Reference suspension 1. Transfer 10.0 mL of the Opalescence standard to a second 100-mL volumetric flask, dilute with water to volume, and mix to obtain Reference suspension 2.
Test solution
Dissolve 2.0 g of Benzyl Alcohol in 60 mL of water, and mix.
Procedure
Transfer a sufficient portion of the
Test solution to a test tube of colorless, transparent, neutral glass with a flat base and an internal diameter of 15 mm to 25 mm, to obtain a depth of 40 mm. Similarly transfer portions of
Reference suspension 1, Reference suspension 2, and water to separate matching test tubes. Compare the
Test solution, Reference suspension 1, Reference suspension 2, and water in diffused daylight, viewing vertically against a black background (see
Visual Comparison under
Spectrophotometry and Light-Scattering 851).
[NOTEThe diffusion of light must be such that
Reference suspension 1 can readily be distinguished from water, and that
Reference suspension 2 can readily be distinguished from
Reference suspension 1.] The
Test solution shows the same clarity as that of water, or its opalescence is not more pronounced than that of
Reference suspension 1.
Limit of nonvolatile residue
[NOTEEnsure that the Benzyl Alcohol to be examined complies with the test for
Peroxide value 401 before performing this test.
] Evaporate 10.0 g of Benzyl Alcohol on a water bath to dryness, and dry the residue at 105
for 1 hour. Cool in a desiccator, and weigh. The residue weighs not more than 5 mg: not more than 0.05% of nonvolatile residue is found.
Related compounds
Test solution
Use the Benzyl Alcohol specimen under examination.
Ethylbenzene solution
Transfer 100 mg of ethylbenzene, accurately weighed, to a 10-mL volumetric flask, dissolve in and dilute with Test solution to volume, and mix. Transfer 1.0 mL of this solution to a 10-mL volumetric flask, dilute with Test solution to volume, and mix.
Dicyclohexyl solution
Transfer 2.0 g of dicyclohexyl to a 10-mL volumetric flask, dissolve in and dilute with Test solution to volume, and mix. Transfer 1.0 mL of this solution to a 10-mL volumetric flask, dilute with Test solution to volume, and mix.
Standard solution 1
Transfer 750 mg of benzaldehyde, accurately weighed, and 500 mg of cyclohexylmethanol, accurately weighed, to a 25-mL volumetric flask, dissolve in and dilute with Test solution to volume, and mix. Transfer 0.5 mL of this solution to a 10-mL volumetric flask, add 1.0 mL of Ethylbenzene solution and 1.5 mL of Dicyclohexyl solution, dilute with Test solution to volume, and mix.
Standard solution 2 (where the Benzyl Alcohol under test is intended for use in the manufacture of injectable dosage forms)
Transfer about 250 mg of benzaldehyde, accurately weighed, and about 500 mg of cyclohexylmethanol, accurately weighed, to a 25-mL volumetric flask, dissolve in and dilute with Test solution to volume, and mix. Transfer 0.5 mL of this solution to a 10-mL volumetric flask, add 1.0 mL of Ethylbenzene solution and 1.0 mL of Dicyclohexyl solution, dilute with Test solution to volume, and mix.
Chromatographic system (see Chromatography 621)
The gas chromatograph is equipped with a flame-ionization detector and a 0.32-mm × 30-m column coated with a 0.5-µm film of G16. Helium is used as the carrier gas flowing at a rate of 1.2 mL per minute at 50
. The injection port and detector temperatures are maintained at about 200
and 310
, respectively. The column temperature is programmed to increase linearly from 50
to 220
at a rate of 5
per minute, and is maintained at 220
for 35 minutes. Chromatograph the appropriate
Standard solution, and record the peak responses as directed for
Procedure: the relative retention times are about 0.28 for ethylbenzene, 0.59 for dicyclohexyl, 0.68 for benzaldehyde, 0.71 for cyclohexylmethanol, and 1.0 for benzyl alcohol; and the resolution,
R, between benzaldehyde and cyclohexylmethanol is not less than 3.0.
Procedure
Separately inject equal volumes (about 0.1 µL) of the appropriate
Standard solution and the
Test solution into the chromatograph, record the chromatograms, and measure the areas for the major peaks.
[NOTEDisregard any peak having an area less than 0.01 times the area of the ethylbenzene peak in the chromatogram of the appropriate
Standard solution. In the chromatogram of the
Test solution, verify that there are no peaks with the same retention times as those of ethylbenzene or dicyclohexyl.
]
In the chromatogram of the Test solution, the area of any peak corresponding to benzaldehyde is not greater than the difference between the area of the peak due to benzaldehyde in the chromatogram of Standard solution 1 (0.15%) or in the chromatogram of Standard solution 2 (0.05%) and the area of the peak due to benzaldehyde in the chromatogram of the Test solution.
In the chromatogram of the Test solution, the area of any peak corresponding to cyclohexylmethanol is not greater than the difference between the area of the peak due to cyclohexylmethanol in the chromatogram of Standard solution 1 (0.10%) or in the chromatogram of Standard solution 2 (0.10%) and the area of the peak due to cyclohexylmethanol in the chromatogram of the Test solution.
In the chromatogram of the Test solution, the sum of the areas of any peaks with retention times less than that of benzyl alcohol, excluding the peaks due to benzaldehyde and cyclohexylmethanol, is not greater than four times the area of the ethylbenzene peak in the chromatogram of Standard solution 1 (0.04%) or is not greater than two times the area of the ethylbenzene peak in the chromatogram of Standard solution 2 (0.02%).
In the chromatogram of the Test solution, the sum of the areas of any peaks with retention times greater than that of benzyl alcohol is not greater than the area of the dicyclohexyl peak in the chromatogram of Standard solution 1 (0.3%) or in the chromatogram of Standard solution 2 (0.2%).
Assay
To about 900 mg of Benzyl Alcohol, accurately weighed, add 15.0 mL of a freshly prepared mixture of pyridine and acetic anhydride (7:1), and boil under reflux for 30 minutes. Cool, add 25 mL of water, add 0.25 mL of a phenolphthalein solution prepared by dissolving 100 mg of phenolphthalein in 80 mL of alcohol and diluting with water to 100 mL, and titrate with 1 N sodium hydroxide VS. Perform a blank determination (see
Titrimetry 541). Calculate the percentage of C
7H
8O taken by the formula:
10.81
N(
VB VU)/
W,
in which
VU and
VB are the number of mL of 1 N sodium hydroxide used for the Benzyl Alcohol and the blank, respectively; and
W is the weight, in g, of Benzyl Alcohol taken.