{"id":15041,"date":"2025-10-16T12:08:00","date_gmt":"2025-10-16T05:08:00","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=15041"},"modified":"2025-10-16T12:08:00","modified_gmt":"2025-10-16T05:08:00","slug":"flupentixol-hydrochloride","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/flupentixol-hydrochloride\/","title":{"rendered":"Flupentixol Hydrochloride"},"content":{"rendered":"<p><em>(Flupentixol Dihydrochloride, Ph. Eur. monograph 1693)<\/em><\/p>\n<p>C<sub>23<\/sub>H<sub>27<\/sub>Cl<sub>2<\/sub>F<sub>3<\/sub>N<sub>2<\/sub>OS 507.4 2413-38-9<\/p>\n<p><strong>Action and use<\/strong><\/p>\n<p>Dopamine receptor antagonist; neuroleptic.<\/p>\n<p><strong>Preparation<\/strong><\/p>\n<p>Flupentixol Tablets<\/p>\n<h2>DEFINITION<\/h2>\n<p>2-[4-[3-[(EZ)-2-(Trifluoromethyl)-9H-thioxanthen-9-ylidene]propyl]piperazin-1-yl]ethan-1-ol dihydrochloride.<\/p>\n<h3>Content<\/h3>\n<p>\u2014 flupentixol dihydrochloride: 99.0 per cent to 101.0 per cent (dried substance);<\/p>\n<p>\u2014 (Z)-isomer: 42.0 per cent to 52.0 per cent.<\/p>\n<h2>CHARACTERS<\/h2>\n<h3>Appearance<\/h3>\n<p>White or almost white powder.<\/p>\n<h3>Solubility<\/h3>\n<p>Very soluble in water, soluble in ethanol (96 per cent), practically insoluble in methylene chloride.<\/p>\n<h2>IDENTIFICATION<\/h2>\n<p>First identification: A, D.<\/p>\n<p>Second identification: B, C, D.<\/p>\n<p>A. Infrared absorption spectrophotometry (2.2.24).<\/p>\n<p>Comparison flupentixol dihydrochloride CRS.<\/p>\n<p>B. Thin-layer chromatography (2.2.27).<\/p>\n<p>Test solution: Dissolve 20 mg of the substance to be examined in methanol R and dilute to 10 mL with the same solvent.<\/p>\n<p>Reference solution: Dissolve 20 mg of flupentixol dihydrochloride CRS in methanol R and dilute to 10 mL with the same solvent.<\/p>\n<p>Plate: TLC silica gel F254 plate R.<\/p>\n<p>Mobile phase: water R, diethylamine R, methyl ethyl ketone R (1:4:95 V\/V\/V).<\/p>\n<p>Application: 2 \u03bcL.<\/p>\n<p>Development: Twice over 3\/4 of the plate.<\/p>\n<p>Drying: In air.<\/p>\n<p>Detection A: Examine in ultraviolet light at 254 nm.<\/p>\n<p>Results A: The principal spot in the chromatogram obtained with the test solution is similar in position and size to the principal spot in the chromatogram obtained with the reference solution. Doubling of the spot may be observed in both chromatograms.<\/p>\n<p>Detection B: Spray with alcoholic solution of sulfuric acid R; heat at 110 \u00b0C for 5 min and allow to cool; examine in ultraviolet light at 365 nm.<\/p>\n<p>Results B: The principal spot in the chromatogram obtained with the test solution is similar in position and size to the principal spot in the chromatogram obtained with the reference solution. Doubling of the spot may be observed in both chromatograms.<\/p>\n<p>C. Mix about 5 mg with 45 mg of heavy magnesium oxide R and ignite in a crucible until an almost white residue is obtained (usually less than 5 min). Allow to cool, add 1 mL of water R, 0.05 mL of phenolphthalein solution R1 and about 1 mL of dilute hydrochloric acid R to render the solution colourless. Filter and add to the filtrate a freshly prepared mixture of 0.1 mL of alizarin S solution R and 0.1 mL of zirconyl nitrate solution R. Mix, allow to stand for 5 min and compare the colour of the solution with that of a blank prepared in the same manner. The test solution is yellow. The blank is red.<\/p>\n<p>D. It gives reaction (a) of chlorides (2.3.1).<\/p>\n<h2>TESTS<\/h2>\n<h3>Appearance of solution<\/h3>\n<p>The solution is clear (2.2.1) and its absorbance (2.2.25) at 410 nm is not greater than 0.125.<\/p>\n<p>Dissolve 0.500 g in 5.0 mL of water R.<\/p>\n<h3>pH (2.2.3)<\/h3>\n<p>2.0 to 3.0.<\/p>\n<p>Dissolve 0.5 g in carbon dioxide-free water R and dilute to 50 mL with the same solvent.<\/p>\n<h3>Related substances<\/h3>\n<p>Liquid chromatography (2.2.29). Carry out the test protected from light and prepare the solutions immediately before use.<\/p>\n<p>Buffer solution: Dissolve 6.3 g of ammonium formate R in about 900 mL of water for chromatography R, adjust to pH 8.2 with concentrated ammonia R and dilute to 1000 mL with water for chromatography R.<\/p>\n<p>Test solution: Dissolve 58.0 mg of the substance to be examined in mobile phase A and dilute to 50.0 mL with mobile phase A.<\/p>\n<p>Reference solution (a): Dilute 1.0 mL of the test solution to 100.0 mL with mobile phase A. Dilute 1.0 mL of this solution to 10.0 mL with mobile phase A.<\/p>\n<p>Reference solution (b): Dissolve the contents of a vial of flupentixol for system suitability CRS (containing impurities A, C, H and I) in 1 mL of mobile phase A.<\/p>\n<p>Column:<\/p>\n<p>\u2014 size: l = 0.15 m, \u00d8 = 4.6 mm;<\/p>\n<p>\u2014 stationary phase: end-capped octadecylsilyl silica gel for chromatography R (3 \u03bcm);<\/p>\n<p>\u2014 temperature: 40 \u00b0C.<\/p>\n<p>Mobile phase:<\/p>\n<p>\u2014 mobile phase A: buffer solution, acetonitrile for chromatography R, water for chromatography R (58:420:522 V\/V\/V);<\/p>\n<p>\u2014 mobile phase B: buffer solution, acetonitrile for chromatography R (100:900 V\/V);<\/p>\n<table style=\"border-collapse: collapse; width: 100%; height: 64px;\">\n<tbody>\n<tr style=\"height: 43px;\">\n<td style=\"width: 33.3333%; height: 43px; text-align: center;\"><strong>Time<\/strong><\/p>\n<p><strong>(min)<\/strong><\/td>\n<td style=\"width: 33.3333%; height: 43px; text-align: center;\"><strong>Mobile phase A<\/strong><\/p>\n<p><strong>(per cent V\/V)<\/strong><\/td>\n<td style=\"width: 33.3333%; height: 43px; text-align: center;\"><strong>Mobile phase B<\/strong><\/p>\n<p><strong>(per cent V\/V)<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 21px;\">\n<td style=\"width: 33.3333%; height: 21px; text-align: center;\">0 &#8211; 40<\/td>\n<td style=\"width: 33.3333%; height: 21px; text-align: center;\">90 \u2192 5<\/td>\n<td style=\"width: 33.3333%; height: 21px; text-align: center;\">10 \u2192 95<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Flow rate: 0.8 mL\/min.<\/p>\n<p>Detection: Spectrophotometer at 230 nm.<\/p>\n<p>Injection: 20 \u03bcL.<\/p>\n<p>Identification of peaks: Use the chromatogram supplied with flupentixol for system suitability CRS and the chromatogram obtained with reference solution (b) to identify the peaks due to both isomers of flupentixol and impurities A, C + I, and H.<\/p>\n<p>Relative retention: With reference to flupentixol (Z)-isomer (retention time = about 11 min): impurity A = about 0.83; impurity H = about 0.90; impurities C and I = about 0.97; flupentixol (E)-isomer = about 1.04.<\/p>\n<p>System suitability: Reference solution (b):<\/p>\n<p>\u2014 resolution: minimum 2.5 between the peaks due to impurities A and H;<\/p>\n<p>\u2014 peak-to-valley ratio: minimum 10.0, where Hp = height above the baseline of the peak due to impurities C+I and Hv = height above the baseline of the lowest point of the curve separating this peak from the peak due to flupentixol (Z)-isomer.<\/p>\n<p>Calculation of percentage contents:<\/p>\n<p>\u2014 correction factors: multiply the peak areas of the following impurities by the corresponding correction factor: impurities C and I = 2.0; impurity H = 2.0;<\/p>\n<p>\u2014 for each impurity, use the concentration of flupentixol dihydrochloride (both isomers) in reference solution (a).<\/p>\n<p>Limits:<\/p>\n<p>\u2014 impurity H: maximum 0.5 per cent;<\/p>\n<p>\u2014 sum of impurities C and I: maximum 0.3 per cent;<\/p>\n<p>\u2014 unspecified impurities: for each impurity, maximum 0.10 per cent;<\/p>\n<p>\u2014 total: maximum 1.0 per cent;<\/p>\n<p>\u2014 reporting threshold: 0.05 per cent.<\/p>\n<h3>Loss on drying (2.2.32)<\/h3>\n<p>Maximum 2.0 per cent, determined on 1.000 g by drying in an oven at 105 \u00b0C.<\/p>\n<h3>Sulfated ash (2.4.14)<\/h3>\n<p>Maximum 0.1 per cent, determined on 1.0 g in a platinum crucible.<\/p>\n<h2>ASSAY<\/h2>\n<h3>Flupentixol dihydrochloride<\/h3>\n<p>Dissolve 0.200 g in 30 mL of ethanol (96 per cent) R. Carry out a potentiometric titration (2.2.20), using 0.1 M sodium hydroxide. Read the volume added between the 2 points of inflexion.<\/p>\n<p>1 mL of 0.1 M sodium hydroxide is equivalent to 50.74 mg of C23H27Cl2F3N2OS.<\/p>\n<h3>(Z)-Isomer<\/h3>\n<p>Liquid chromatography (2.2.29).<\/p>\n<p>Test solution: Dissolve 20.0 mg of the substance to be examined in the mobile phase and dilute to 50.0 mL with the mobile phase.<\/p>\n<p>Reference solution: Dissolve 20.0 mg of flupentixol dihydrochloride CRS in the mobile phase and dilute to 50.0 mL with the mobile phase.<\/p>\n<p>Column:<\/p>\n<p>\u2014 size: l = 0.25 m, \u00d8 = 4.0 mm;<\/p>\n<p>\u2014 stationary phase: silica gel for chromatography R (5 \u03bcm).<\/p>\n<p>Mobile phase: water for chromatography R, concentrated ammonia R, 2-propanol R, heptane R (2:4:150:850 V\/V\/V\/V).<\/p>\n<p>Flow rate: 1.5 mL\/min.<\/p>\n<p>Detection: Spectrophotometer at 254 nm.<\/p>\n<p>Injection: 20 \u03bcL.<\/p>\n<p>Run time: 1.5 times the retention time of flupentixol (Z)-isomer.<\/p>\n<p>Identification of peaks: Use the chromatogram supplied with flupentixol dihydrochloride CRS and the chromatogram obtained with the reference solution to identify the peaks due to both isomers of flupentixol.<\/p>\n<p>Relative retention: With reference to flupentixol (Z)-isomer (retention time = about 6 min): flupentixol (E)- isomer = about 1.2.<\/p>\n<p>System suitability: Reference solution:<\/p>\n<p>\u2014 resolution: minimum 3.0 between the peaks due to flupentixol (Z)-isomer and flupentixol (E)-isomer.<\/p>\n<p>Calculate the percentage content of the (Z)-isomer of C<sub>23<\/sub>H<sub>27<\/sub>Cl<sub>2<\/sub>F<sub>3<\/sub>N<sub>2<\/sub>OS taking into account the assigned content of flupentixol (Z)-isomer in flupentixol dihydrochloride CRS.<\/p>\n<h2>STORAGE<\/h2>\n<p>Protected from light.<\/p>\n<h2>IMPURITIES<\/h2>\n<p>Specified impurities C, H, I.<\/p>\n<p>Other detectable impurities (the following substances would, if present at a sufficient level, be detected by one or other of the tests in the monograph. They are limited by the general acceptance criterion for other\/unspecified impurities and\/or by the general monograph Substances for pharmaceutical use (2034). It is therefore not necessary to identify these impurities for demonstration of compliance. See also 5.10. Control of impurities in substances for pharmaceutical use) A, B, E, G.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-15083\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/2-209-300x163.jpg\" alt=\"Flupentixol Hydrochloride \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/2-209-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/2-209-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/2-209-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/2-209.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>A. (9RS)-9-[3-(dimethylamino)propyl]-2-(trifluoromethyl)-9H-thioxanthen-9-ol,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-15084\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/3-196-300x163.jpg\" alt=\"Flupentixol Hydrochloride \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/3-196-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/3-196-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/3-196-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/3-196.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>B. N,N-dimethyl-3-[(EZ)-2-(trifluoromethyl)-9H-thioxanthen-9-ylidene]propan-1-amine,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-15085\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/4-178-300x163.jpg\" alt=\"Flupentixol Hydrochloride \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/4-178-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/4-178-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/4-178-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/4-178.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>C. 1-[3-[(EZ)-2-(trifluoromethyl)-9H-thioxanthen-9-ylidene]propyl]piperazine,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-15086\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/5-143-300x163.jpg\" alt=\"Flupentixol Hydrochloride \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/5-143-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/5-143-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/5-143-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/5-143.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>E. 2-[4-[3-[(EZ)-2-(trifluoromethyl)-9H-thioxanthen-9-ylidene]propyl]piperazin-1-yl]ethyl acetate,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-15087\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/6-112-300x163.jpg\" alt=\"Flupentixol Hydrochloride \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/6-112-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/6-112-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/6-112-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/10\/6-112.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>G. 2-(trifluoromethyl)-9H-thioxanthen-9-one,<\/p>\n<p>H. either 2-[4-[(E)-3-[(9RS)-2-(trifluoromethyl)-9H-thioxanthen-9-yl]prop-2-en-1-yl]piperazin-1-yl]ethan-1-ol or 2-[4-[(Z)-3- [(9RS)-2-(trifluoromethyl)-9H-thioxanthen-9-yl]prop-2-en-1-yl]piperazin-1-yl]ethan-1-ol,<\/p>\n<p>I. either 2-[4-[(E)-3-[(9RS)-2-(trifluoromethyl)-9H-thioxanthen-9-yl]prop-2-en-1-yl]piperazin-1-yl]ethan-1-ol or 2-[4-[(Z)-3-[(9RS)-2-(trifluoromethyl)-9H-thioxanthen-9-yl]prop-2-en-1-yl]piperazin-1-yl]ethan-1-ol.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>(Flupentixol Dihydrochloride, Ph. Eur. monograph 1693) C23H27Cl2F3N2OS 507.4 2413-38-9 Action and use Dopamine receptor antagonist; neuroleptic. Preparation Flupentixol Tablets DEFINITION 2-[4-[3-[(EZ)-2-(Trifluoromethyl)-9H-thioxanthen-9-ylidene]propyl]piperazin-1-yl]ethan-1-ol dihydrochloride. Content \u2014 flupentixol dihydrochloride: 99.0 per cent to 101.0 per cent (dried substance); \u2014 (Z)-isomer: 42.0 per cent to 52.0 per cent. CHARACTERS Appearance White or almost white powder. Solubility Very soluble in&#8230;<\/p>\n","protected":false},"author":4,"featured_media":15082,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-15041","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-medicinal-substances"],"acf":[],"_links":{"self":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/15041","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/comments?post=15041"}],"version-history":[{"count":3,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/15041\/revisions"}],"predecessor-version":[{"id":15094,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/15041\/revisions\/15094"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/15082"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=15041"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=15041"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=15041"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}