{"id":25338,"date":"2025-11-04T13:42:26","date_gmt":"2025-11-04T06:42:26","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=25338"},"modified":"2025-11-04T13:42:26","modified_gmt":"2025-11-04T06:42:26","slug":"niflumic-acid","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/niflumic-acid\/","title":{"rendered":"Niflumic Acid"},"content":{"rendered":"

(Ph. Eur. monograph 2115)<\/p>\n

C13<\/sub>H9<\/sub>F3<\/sub>N2<\/sub>O2\u00a0<\/sub> \u00a0 \u00a0 \u00a0 \u00a0 \u00a0282.2\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 4394-00-7<\/p>\n

DEFINITION<\/h3>\n

2-[[3-(Trifluoromethyl)phenyl]amino]pyridine-3-carboxylic acid.<\/p>\n

Content<\/h3>\n

98.5 per cent to 101.5 per cent (dried substance).<\/p>\n

CHARACTERS<\/h2>\n

Appearance<\/h3>\n

Pale yellow, crystalline powder.<\/p>\n

Solubility<\/h3>\n

Practically insoluble in water, freely soluble in acetone, soluble in ethanol (96 per cent) and in methanol.<\/p>\n

Melting point (2.2.15)<\/h3>\n

About 204 \u00b0C.<\/p>\n

IDENTIFICATION<\/h2>\n

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

Comparison: niflumic acid CRS.<\/p>\n

TESTS<\/h2>\n

Impurity C<\/h3>\n

Thin-layer chromatography (2.2.27).<\/p>\n

Test solution: Dissolve 0.50 g of the substance to be examined in 5 mL of methanol R and dilute to 10.0 mL with the same solvent.<\/p>\n

Reference solution: Dissolve 25 mg of 3-trifluoromethylaniline R (impurity C) in 20 mL of methanol R and dilute to 100 mL with the same solvent. Dilute 1.0 mL of the solution to 100 mL with methanol R.<\/p>\n

Plate: TLC silica gel F254<\/sub> plate R.<\/p>\n

Mobile phase: acetic acid R, ethyl acetate R, toluene R (5:25:90 V\/V\/V).<\/p>\n

Application: 10 \u03bcL.<\/p>\n

Development: Over 3\/4 of the plate.<\/p>\n

Drying: In air, until the solvents have evaporated.<\/p>\n

Detection: Spray with 4-dimethylaminocinnamaldehyde solution R and heat at 60 \u00b0C for 10 min.<\/p>\n

Limit:<\/p>\n

\u2014 impurity C: any spot due to impurity C is not more intense than the principal spot in the chromatogram obtained with the reference solution (50 ppm).<\/p>\n

Related substances<\/h3>\n

Liquid chromatography (2.2.29).<\/p>\n

Test solution: Dissolve 20.0 mg of the substance to be examined in 10 mL of acetonitrile R and dilute to 20.0 mL with water R.<\/p>\n

Reference solution: Dissolve 5.0 mg of niflumic acid impurity A CRS, 5.0 mg of niflumic acid impurity B CRS and 6.0 mg of niflumic acid impurity E CRS in 20 mL of acetonitrile R, add 5.0 mL of the test solution and dilute to 50.0 mL with water R. Dilute 1.0 mL of this solution to 100.0 mL with a mixture of equal volumes of acetonitrile R and water R.<\/p>\n

Column:<\/p>\n

\u2014 size: l = 0.125 m, \u00d8 = 4.0 mm;<\/p>\n

\u2014 stationary phase: octylsilyl silica gel for chromatography R (5 \u03bcm);<\/p>\n

\u2014 temperature: 25 \u00b0C.<\/p>\n

Mobile phase: phosphoric acid R, acetonitrile R, water for chromatography R (2.5:500:500 V\/V\/V).<\/p>\n

Flow rate: 1.0 mL\/min.<\/p>\n

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

Injection: 10 \u03bcL.<\/p>\n

Run time: 4 times the retention time of niflumic acid.<\/p>\n

Relative retention: With reference to niflumic acid (retention time = about 3.5 min): impurity A = about 0.4; impurity E = about 0.7; impurity B = about 0.8 (the peaks due to impurities E and B may be inverted).<\/p>\n

System suitability: Reference solution:<\/p>\n

\u2014 resolution: minimum 1.5 between the peaks due to impurities E and B.<\/p>\n

Limits:<\/p>\n

\u2014 impurity B: not more than 4 times the area of the corresponding peak in the chromatogram obtained with the reference solution (0.4 per cent);<\/p>\n

\u2014 impurity A: not more than the area of the corresponding peak in the chromatogram obtained with the reference solution (0.1 per cent);<\/p>\n

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

\u2014 sum of impurities other than B: not more than twice the area of the peak due to niflumic acid in the chromatogram obtained with the reference solution (0.2 per cent);<\/p>\n

\u2014 disregard limit: 0.5 times the area of the peak due to niflumic acid in the chromatogram obtained with the reference solution (0.05 per cent).<\/p>\n

Chlorides (2.4.4)<\/h3>\n

Maximum 200 ppm.<\/p>\n

Dissolve 0.5 g in a mixture of 1 mL of nitric acid R and 10 mL of methanol R and dilute to 20 mL with water R. To 10 mL of the solution add 5 mL of water R.<\/p>\n

Phosphates (2.4.11)<\/h3>\n

Maximum 100 ppm.<\/p>\n

Dilute 1.0 mL of the test solution prepared as described in general chapter 2.4.8 (method C) to 100 mL with water R.<\/p>\n

Loss on drying (2.2.32)<\/h4>\n

Maximum 0.3 per cent, determined on 2.000 g by drying in an oven at 105 \u00b0C.<\/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

Dissolve 0.200 g in a mixture of 10 mL of water R and 40 mL of ethanol (96 per cent) R. Titrate with 0.1 M sodium hydroxide, determining the end-point potentiometrically (2.2.20).<\/p>\n

1 mL of 0.1 M sodium hydroxide is equivalent to 28.22 mg of C13<\/sub>H9<\/sub>F3<\/sub>N2<\/sub>O2<\/sub>.<\/p>\n

IMPURITIES<\/h2>\n

Specified impurities A, B, C.<\/p>\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) E, F.<\/p>\n

\"Niflumic<\/p>\n

A. 2-chloropyridine-3-carboxylic acid,<\/p>\n

\"Niflumic<\/p>\n

B. 2-hydroxy-N-[3-(trifluoromethyl)phenyl]pyridine-3-carboxamide,<\/p>\n

\"Niflumic<\/p>\n

C. 3-(trifluoromethyl)aniline,<\/p>\n

\"Niflumic<\/p>\n

E. 6-[[3-(trifluoromethyl)phenyl]amino]pyridine-3-carboxylic acid,<\/p>\n

\"Niflumic<\/p>\n

F. methyl 2-[[3-(trifluoromethyl)phenyl]amino]pyridine-3-carboxylate.<\/p>\n","protected":false},"excerpt":{"rendered":"

(Ph. Eur. monograph 2115) C13H9F3N2O2\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0282.2\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 4394-00-7 DEFINITION 2-[[3-(Trifluoromethyl)phenyl]amino]pyridine-3-carboxylic acid. Content 98.5 per cent to 101.5 per cent (dried substance). CHARACTERS Appearance Pale yellow, crystalline powder. Solubility Practically insoluble in water, freely soluble in acetone, soluble in ethanol (96 per cent) and in methanol. Melting point…<\/p>\n","protected":false},"author":2,"featured_media":25345,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-25338","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\/25338","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=25338"}],"version-history":[{"count":3,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/25338\/revisions"}],"predecessor-version":[{"id":25365,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/25338\/revisions\/25365"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/25345"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=25338"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=25338"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=25338"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}