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Thioridazine Hydrochloride
(thye'' oh rid' a zeen hye'' droe klor' ide).
C21H26N2S2·HCl
10H-Phenothiazine, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-, monohydrochloride. 10-[2-(1-Methyl-2-piperidyl)ethyl]-2-(methylthio)phenothiazine monohydrochloride » Thioridazine Hydrochloride contains not less than 99.0 percent and not more than 101.0 percent of C21H26N2S2·HCl, calculated on the dried basis.
Packaging and storage
Preserve in tight, light-resistant containers.
USP Reference standards
[noteThroughout the following procedures, protect test or assay specimens, the Reference Standard, and solutions containing them, by conducting the procedures without delay, under subdued light, or by using low-actinic glassware. ]
Identification
B:
A solution (1 in 100) in a mixture of water and alcohol (1:1) responds to the test for Chloride
Melting range
pH
Loss on drying
Residue on ignition
Selenium
Chromatographic purity
[noteConduct this procedure in subdued lighting without delay. ]
Diluting solution:
a mixture of methanol and ammonium hydroxide (49:1).
Test solution
Transfer 100 mg of Thioridazine Hydrochloride, accurately weighed, to a 5-mL volumetric flask. Dissolve in and dilute with Diluting solution to volume, and mix.
Standard solutions
Dissolve an accurately weighed quantity of USP Thioridazine Hydrochloride RS in Diluting solution, and dilute quantitatively, and stepwise if necessary, with Diluting solution to obtain a solution having a known concentration of 20.0 mg per mL (Standard solution A). Dilute appropriate portions of this solution quantitatively with Diluting solution to obtain five Standard solutions B to F having known concentrations of 0.1, 0.067, 0.025, 0.02 and 0.01 mg per mL, respectively. The final concentrations of Standard solutions B to F represent 0.5%, 0.33%, 0.125%, 0.1% and 0.05% concentration of Standard solution A, respectively.
Application volume:
5 µL.
Developing solvent system:
a mixture of chloroform, isopropyl alcohol, and ammonium hydroxide (74:25:1).
Procedure
Apply equal spots of the Test solution and Standard solutions A to F as directed under Ordinary Impurities
Assay
Dissolve about 350 mg of Thioridazine Hydrochloride, accurately weighed, in 80 mL of a solution of equal parts of glacial acetic acid and acetic anhydride, and titrate with 0.1 N perchloric acid VS, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary correction. Each mL of 0.1 N perchloric acid is equivalent to 40.70 mg of C21H26N2S2·HCl.
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
USP35NF30 Page 4848
Pharmacopeial Forum: Volume No. 31(3) Page 798
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