{"id":17156,"date":"2025-10-21T16:55:01","date_gmt":"2025-10-21T09:55:01","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=17156"},"modified":"2025-10-21T16:55:01","modified_gmt":"2025-10-21T09:55:01","slug":"ketorolac-trometamol","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/ketorolac-trometamol\/","title":{"rendered":"Ketorolac Trometamol"},"content":{"rendered":"

(Ph. Eur. monograph 1755)<\/em><\/p>\n

C19<\/sub>H24<\/sub>N2<\/sub>O6<\/sub> 376.4 74103-07-4<\/p>\n

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

Cyclo-oxygenase inhibitor; analgesic; anti-inflammatory.<\/p>\n

DEFINITION<\/h2>\n

2-Amino-2-(hydroxymethyl)propane-1,3-diol (1RS)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylate.<\/p>\n

Content<\/h3>\n

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

CHARACTERS<\/h2>\n

Appearance<\/h3>\n

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

Solubility<\/h3>\n

Freely soluble in water and in methanol, slightly soluble in ethanol (96 per cent), practically insoluble in<\/p>\n

methylene chloride.<\/p>\n

IDENTIFICATION<\/h2>\n

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

Comparison: ketorolac trometamol CRS.<\/p>\n

TESTS<\/h2>\n

Solution S<\/h3>\n

Dissolve 0.75 g in carbon dioxide-free water R and dilute to 25.0 mL with the same solvent.<\/p>\n

Appearance of solution<\/h3>\n

Solution S is clear (2.2.1).<\/p>\n

pH (2.2.3)<\/h3>\n

5.7 to 6.7.<\/p>\n

Dilute 5 mL of solution S to 15 mL with carbon dioxide-free water R.<\/p>\n

Absorbance (2.2.25)<\/h3>\n

Maximum 0.10, determined at 430 nm for solution S.<\/p>\n

Related substances<\/h3>\n

Liquid chromatography (2.2.29). Protect the solutions from bright light.<\/p>\n

Solvent mixture tetrahydrofuran R, water R (30:70 V\/V).<\/p>\n

Test solution: Dissolve 20 mg of the substance to be examined in the solvent mixture and dilute to 50 mL with the solvent mixture.<\/p>\n

Reference solution (a): Dilute 1.0 mL of the test solution to 10.0 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 ketorolac trometamol for peak identification CRS (containing impurities A, B, C and D) in 5 mL of the solvent mixture.<\/p>\n

Column:<\/p>\n

\u2014 size: l = 0.25 m, \u00d8 = 4.6 mm;<\/p>\n

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

\u2014 temperature: 40 \u00b0C.<\/p>\n

Mobile phase: Mix 30 volumes of tetrahydrofuran R with 70 volumes of a solution prepared as follows: dissolve 5.75 g of ammonium dihydrogen phosphate R in 900 mL of water R, adjust to pH 3.0 with phosphoric acid R and dilute to 1000 mL with water R.<\/p>\n

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

Detection: Spectrophotometer at 313 nm.<\/p>\n

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

Run time: 3 times the retention time of ketorolac.<\/p>\n

Identification of impurities: Use the chromatogram supplied with ketorolac trometamol for peak identification CRS and the chromatogram obtained with reference solution (b) to identify the peaks due to
\nimpurities A, B, C and D.<\/p>\n

Relative retention: With reference to ketorolac (retention time = about 10 min): impurity C = about 0.5; impurity A = about 0.6; impurity D = about 0.7; impurity B = about 0.9.<\/p>\n

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

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

Limits:<\/p>\n

\u2014 correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity A = 0.67; impurity B = 0.52; impurity C = 2.2;<\/p>\n

\u2014 impurities A, B, C, D: for each impurity, not more than the area of the principal peak in the chromatogram obtained with reference solution (a) (0.1 per cent);<\/p>\n

\u2014 unspecified impurities: for each impurity, not more than 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 10 times the area of the principal peak in the chromatogram obtained with reference solution (a) (1.0 per cent);<\/p>\n

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

Loss on drying (2.2.32)<\/h3>\n

Maximum 0.5 per cent, determined on 1.000 g by drying in vacuo at 60 \u00b0C for 3 h.<\/p>\n

Sulfated ash (2.4.14)<\/h3>\n

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

ASSAY<\/h2>\n

Dissolve 0.300 g in 60 mL of anhydrous acetic acid R. Titrate with 0.1 M perchloric acid, determining the end-point potentiometrically (2.2.20).<\/p>\n

1 mL of 0.1 M perchloric acid is equivalent to 37.64 mg of C19<\/sub>H24<\/sub>N2<\/sub>O6<\/sub>.<\/p>\n

STORAGE<\/h2>\n

Protected from light.<\/p>\n

IMPURITIES<\/h2>\n

Specified impurities A, B, C, D.<\/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, G, H, I, J.<\/p>\n

\"Ketorolac<\/p>\n

A. (1RS)-5-benzoyl-2,3-dihydro-1H-pyrrolizin-1-ol,<\/p>\n

\"Ketorolac<\/p>\n

B. 5-benzoyl-2,3-dihydro-1H-pyrrolizin-1-one,<\/p>\n

\"Ketorolac<\/p>\n

C. (1RS)-6-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid,<\/p>\n

\"Ketorolac<\/p>\n

D. (1RS)-5-benzoyl-1-methoxy-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid,<\/p>\n

\"Ketorolac<\/p>\n

E. (1RS)-5-benzoyl-N-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl]-2,3-dihydro-1H-pyrrolizine-1-carboxamide,<\/p>\n

\"Ketorolac<\/p>\n

F. (1RS)-7-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid,<\/p>\n

\"Ketorolac<\/p>\n

G. methyl (1RS)-5-benzoyl-1-hydroxy2,3-dihydro-1H-pyrrolizine-1-carboxylate,<\/p>\n

\"Ketorolac<\/p>\n

H. methyl (1RS)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylate,<\/p>\n

\"Ketorolac<\/p>\n

I. phenyl(2,3-dihydro-1H-pyrrolizin-5-yl)methanone,<\/p>\n

\"Ketorolac<\/p>\n

J. ethyl (1RS)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylate.<\/p>\n","protected":false},"excerpt":{"rendered":"

(Ph. Eur. monograph 1755) C19H24N2O6 376.4 74103-07-4 Action and use Cyclo-oxygenase inhibitor; analgesic; anti-inflammatory. DEFINITION 2-Amino-2-(hydroxymethyl)propane-1,3-diol (1RS)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylate. Content 98.5 per cent to 101.5 per cent (dried substance). CHARACTERS Appearance White or almost white, crystalline powder. Solubility Freely soluble in water and in methanol, slightly soluble in ethanol (96 per cent), practically insoluble in methylene chloride….<\/p>\n","protected":false},"author":4,"featured_media":17162,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-17156","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\/17156","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=17156"}],"version-history":[{"count":2,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/17156\/revisions"}],"predecessor-version":[{"id":17177,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/17156\/revisions\/17177"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/17162"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=17156"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=17156"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=17156"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}