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Avobenzone
1,3-Propanedione, 1-[4-(1,1-dimethylethyl)phenyl]-3-(4-methoxyphenyl)-. 1-(p-tert-Butylphenyl)-3-(p-methoxyphenyl)-1,3-propanedione » Avobenzone contains not less than 95.0 percent and not more than 105.0 percent of C20H22O3, calculated on the dried basis.
Packaging and storage
Preserve in tight, light-resistant containers.
Identification
B:
Ultraviolet Absorption
Solution:
5 µg per mL.
Medium:
alcohol.
Absorptivities at 360 nm do not differ by more than 3.0%.
Loss on drying
Chromatographic purity
Test solution
Proceed as directed for Assay preparation in the Assay.
Chromatographic system (see Chromatography
Procedure
Inject a volume (about 1 µL) of Test solution into the chromatograph, record the chromatogram, and measure the peak responses. Calculate the percentage of each impurity in the portion of Avobenzone taken by the formula:
100(rI / rS)
in which rI is the response of each individual peak, other than the avobenzone peak, in the chromatogram of the Test solution; and rS is the sum of the responses of all of the peaks in the chromatogram of the Test solution: not more than 3.0% of any individual impurity is found, and the sum of all of the impurities is not more than 4.5%.
Assay
Standard preparation
Dilute an accurately measured quantity of USP Avobenzone RS in acetone, and dilute quantitatively, and stepwise if necessary, with acetone to obtain a solution having a known concentration of about 50 mg per mL.
Assay preparation
Transfer about 500 mg of Avobenzone, accurately weighed, to a 10-mL volumetric flask, dilute with acetone to volume, and mix.
Chromatographic system (see Chromatography
Procedure
Separately inject equal volumes (about 1 µL) of the Standard preparation and the Assay preparation into the chromatograph, record the chromatograms, and measure the responses for the major peaks. Calculate the quantity, in mg, of C20H22O3 in the portion of Avobenzone taken by the formula:
10C (rU / rS)
in which C is the concentration, in mg per mL, of USP Avobenzone RS in the Standard preparation; and rU and rS are the peak responses obtained from the Assay preparation and the Standard preparation, respectively.
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
USP32NF27 Page 1608
Pharmacopeial Forum: Volume No. 33(5) Page 872
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