{"id":25445,"date":"2025-11-04T14:48:54","date_gmt":"2025-11-04T07:48:54","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=25445"},"modified":"2025-11-04T14:48:54","modified_gmt":"2025-11-04T07:48:54","slug":"nilutamide","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/nilutamide\/","title":{"rendered":"Nilutamide"},"content":{"rendered":"

(Ph. Eur. monograph 2256)<\/p>\n

C12<\/sub>H10<\/sub>F3<\/sub>N3<\/sub>O4<\/sub>\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 317.2\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a063612-50-0<\/p>\n

Action and use<\/strong><\/p>\n

Cytotoxic.<\/p>\n

DEFINITION<\/h2>\n

5,5-Dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione.<\/p>\n

Content<\/h3>\n

98.0 per cent to 102.0 per cent (anhydrous substance).<\/p>\n

CHARACTERS<\/h2>\n

Appearance<\/h3>\n

White or almost white powder.<\/p>\n

Solubility<\/h3>\n

Very slightly soluble in water, freely soluble in acetone, soluble in anhydrous ethanol.<\/p>\n

IDENTIFICATION<\/h2>\n

Infrared absorption spectrophotometry (2.2.24).<\/p>\n

Comparison: nilutamide CRS.<\/p>\n

TESTS<\/h2>\n

Related substances<\/h3>\n

Liquid chromatography (2.2.29). Prepare the solutions immediately before use.<\/p>\n

Solvent mixture: acetonitrile for chromatography R, water R (35:65 V\/V).<\/p>\n

Test solution: Dissolve 0.10 g of the substance to be examined in the solvent mixture and dilute to 100 mL with the solvent mixture.<\/p>\n

Reference solution (a): Dilute 20.0 mL of the test solution to 100.0 mL with the solvent mixture. Dilute 1.0 mL of this solution to 100.0 mL with the solvent mixture.<\/p>\n

Reference solution (b): Dissolve 2 mg of the substance to be examined and 2 mg of nilutamide impurity B CRS in the solvent mixture and dilute to 50 mL with the solvent mixture.<\/p>\n

Column:<\/p>\n

\u2014 size: l = 0.15 m, \u00d8 = 4.6 mm;<\/p>\n

\u2014 stationary phase: spherical octadecylsilyl silica gel for chromatography R (5 \u03bcm).<\/p>\n

Mobile phase:<\/p>\n

\u2014 mobile phase A: 2.0 g\/L solution of potassium dihydrogen phosphate R adjusted to pH 7.5 with 1 M sodium hydroxide;<\/p>\n

\u2014 mobile phase B: acetonitrile for chromatography R;<\/p>\n\n\n\n\n\n
Time<\/strong>
\n(min)<\/strong><\/td>\n		Mobile phase A<\/strong>
\n(per cent V\/V)<\/strong><\/td>\n		Mobile phase B<\/strong>
\n(per cent V\/V)<\/strong><\/td>\n<\/tr>\n
0 – 8<\/td>\n55<\/td>\n45<\/td>\n<\/tr>\n
8 – 30<\/td>\n55 \u2192 30<\/td>\n45 \u2192 70<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

Flow rate: 1.5 mL\/min.<\/p>\n

Detection: Spectrophotometer at 230 nm.<\/p>\n

Injection: 20 \u03bcL.<\/p>\n

Relative retention: With reference to nilutamide (retention time = about 5.3 min): impurity B = about 0.9.<\/p>\n

System suitability: Reference solution (b):<\/p>\n

\u2014 resolution: minimum 3.0 between the peaks due to impurity B and nilutamide.<\/p>\n

Limits:<\/p>\n

\u2014 unspecified impurities: for each impurity, not more than 0.5 times the area of the principal peak in the chromatogram obtained with reference solution (a) (0.10 per cent);<\/p>\n

\u2014 total: not more than 1.5 times the area of the principal peak in the chromatogram obtained with reference solution (a) (0.3 per cent);<\/p>\n

\u2014 disregard limit: 0.25 times the area of the principal peak in the chromatogram obtained with reference solution (a) (0.05 per cent).<\/p>\n

Water (2.5.12)<\/h4>\n

Maximum 0.5 per cent, determined on 0.500 g.<\/p>\n

Sulfated ash (2.4.14)<\/h4>\n

Maximum 0.1 per cent, determined on 1.0 g in a platinum crucible.<\/p>\n

ASSAY<\/h2>\n

Liquid chromatography (2.2.29). The solutions are stable for 24 h at room temperature and in daylight.<\/p>\n

Solvent mixture: acetonitrile for chromatography R, water R (35:65 V\/V).<\/p>\n

Test solution: Dissolve 50.0 mg of the substance to be examined in the solvent mixture and dilute to 100.0 mL with the solvent mixture.<\/p>\n

Reference solution: Dissolve 50.0 mg of nilutamide CRS in the solvent mixture and dilute to 100.0 mL with the solvent mixture.<\/p>\n

Column:<\/p>\n

\u2014 size: l = 0.15 m, \u00d8 = 4.6 mm;<\/p>\n

\u2014 stationary phase: spherical octadecylsilyl silica gel for chromatography R (5 \u03bcm).<\/p>\n

Mobile phase: Mix 40 volumes of acetonitrile R and 60 volumes of a 2.0 g\/L solution of potassium dihydrogen phosphate R adjusted to pH 7.5 with 1 M sodium hydroxide.<\/p>\n

Flow rate: 1.5 mL\/min.<\/p>\n

Detection: Spectrophotometer at 267 nm.<\/p>\n

Injection: 20 \u03bcL.<\/p>\n

Retention time: About 9 min.<\/p>\n

Calculate the percentage content of C12<\/sub>H10<\/sub>F3<\/sub>N3<\/sub>O4<\/sub> from the declared content of nilutamide CRS.<\/p>\n

STORAGE<\/h2>\n

Protected from light.<\/p>\n

IMPURITIES<\/h2>\n

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, C, D.<\/p>\n

\"Nilutamide\"<\/p>\n

A. 5-imino-4,4-dimethyl-1-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidin-2-one,<\/p>\n

\"Nilutamide\"<\/p>\n

B. 4-nitro-3-(trifluoromethyl)aniline (nifeline),<\/p>\n

\"Nilutamide\"<\/p>\n

C. 5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]oxazolidine-2,4-dione,<\/p>\n

\"Nilutamide\"<\/p>\n

D. 1,3-bis[4-nitro-3-(trifluoromethyl)phenyl]urea.<\/p>\n","protected":false},"excerpt":{"rendered":"

(Ph. Eur. monograph 2256) C12H10F3N3O4\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 317.2\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a063612-50-0 Action and use Cytotoxic. DEFINITION 5,5-Dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione. Content 98.0 per cent to 102.0 per cent (anhydrous substance). CHARACTERS Appearance White or almost white powder. Solubility Very slightly soluble in water, freely soluble in acetone, soluble in anhydrous ethanol. IDENTIFICATION…<\/p>\n","protected":false},"author":2,"featured_media":25465,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-25445","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\/25445","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\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/comments?post=25445"}],"version-history":[{"count":2,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/25445\/revisions"}],"predecessor-version":[{"id":25467,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/25445\/revisions\/25467"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/25465"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=25445"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=25445"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=25445"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}