Triflupromazine Hydrochloride
C18H19F3N2S·HCl
388.88
388.8810H-Phenothiazine-10-propanamine, N,N-dimethyl-2-(trifluoromethyl)-, monohydrochloride.
10-[3-(Dimethylamino)propyl]-2-(trifluoromethyl)phenothiazine monohydrochloride
[1098-60-8].» Triflupromazine Hydrochloride contains not less than 97.0 percent and not more than 103.0 percent of C18H19F3N2S·HCl, calculated on the dried basis.
Packaging and storage—
Preserve in well-closed, light-resistant glass containers.
USP Reference standards 
11
—
USP Triflupromazine Hydrochloride RS.
11—
USP Triflupromazine Hydrochloride RS.
note—Throughout 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:
Ultraviolet Absorption 197U—
197U—
Solution:
10 µg per mL.
Medium:
0.5 N sulfuric acid.
Absorptivities at 255 nm, calculated on the dried basis, do not differ by more than 3.0%.
C:
Prepare a solution of Triflupromazine Hydrochloride in methanol containing 10 mg per mL. Apply 10 µL each of this solution and a Standard solution of USP Triflupromazine Hydrochloride RS in methanol containing 10 mg per mL to a suitable thin-layer chromatographic plate (see Chromatography 621) coated with a 0.25-mm layer of chromatographic silica gel mixture. Allow the spots to dry, and develop the chromatogram in a solvent system consisting of a mixture of n-propyl alcohol, water, and ammonium hydroxide (88:11:1) until the solvent front has moved about three-fourths of the length of the plate. Remove the plate from the developing chamber, mark the solvent front, and allow the solvent to evaporate. Locate the spots on the plate by spraying lightly with dilute methanolic sulfuric acid (4 in 10) and then heating for 15 minutes: the RF value and color (pink-orange) of the principal spot obtained from the test solution correspond to that obtained from the Standard solution.
621) coated with a 0.25-mm layer of chromatographic silica gel mixture. Allow the spots to dry, and develop the chromatogram in a solvent system consisting of a mixture of n-propyl alcohol, water, and ammonium hydroxide (88:11:1) until the solvent front has moved about three-fourths of the length of the plate. Remove the plate from the developing chamber, mark the solvent front, and allow the solvent to evaporate. Locate the spots on the plate by spraying lightly with dilute methanolic sulfuric acid (4 in 10) and then heating for 15 minutes: the RF value and color (pink-orange) of the principal spot obtained from the test solution correspond to that obtained from the Standard solution.
Loss on drying 731—
Dry it at 100
for 2 hours: it loses not more than 0.5% of its weight.
731—
Dry it at 100 for 2 hours: it loses not more than 0.5% of its weight.
Residue on ignition 281:
not more than 0.1%.
281:
not more than 0.1%.
Ordinary impurities 466—
466—
Test solution:
acetone.
Standard solution:
acetone.
Eluant:
a mixture of chloroform and methanol (4:1).
Visualization:
1.
Assay—
Dissolve about 800 mg of Triflupromazine Hydrochloride, accurately weighed, in 100 mL of glacial acetic acid. Add 10 mL of mercuric acetate TS and 1 drop of crystal violet TS, and titrate with 0.1 N perchloric acid VS to a blue endpoint. Perform a blank determination, and make any necessary correction. Each mL of 0.1 N perchloric acid is equivalent to 38.89 mg of C18H19F3N2S·HCl.
Auxiliary Information—
Please check for your question in the FAQs before contacting USP.
Chromatographic Column—
| Topic/Question | Contact | Expert Committee |
| Monograph | Ravi Ravichandran, Ph.D.
Senior Scientist 1-301-816-8330 |
(MDPP05) Monograph Development-Psychiatrics and Psychoactives |
| Reference Standards | Lili Wang, Technical Services Scientist 1-301-816-8129 RSTech@usp.org |
USP32–NF27 Page 3802
Pharmacopeial Forum: Volume No. 29(6) Page 1994
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.