{"id":24704,"date":"2025-11-03T15:18:43","date_gmt":"2025-11-03T08:18:43","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=24704"},"modified":"2025-11-03T15:18:43","modified_gmt":"2025-11-03T08:18:43","slug":"triclabendazole","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/triclabendazole\/","title":{"rendered":"Triclabendazole"},"content":{"rendered":"

Triclabendazole for Veterinary Use<\/p>\n

(Ph. Eur. monograph 2609)<\/em><\/p>\n

C14<\/sub>H9<\/sub>Cl3<\/sub>N2<\/sub>OS 359.7 68786-66-3<\/p>\n

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

Benzimidazole antihelminthic.<\/p>\n

DEFINITION<\/h2>\n

5-Chloro-6-(2,3-dichlorophenoxy)-2-(methylsulfanyl)-1H-benzimidazole.<\/p>\n

Content<\/h3>\n

99.0 per cent to 101.0 per cent (dried substance).<\/p>\n

CHARACTERS<\/h2>\n

Appearance<\/h3>\n

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

Solubility<\/h3>\n

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

IDENTIFICATION<\/h2>\n

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

Comparison triclabendazole CRS.<\/p>\n

TESTS<\/h2>\n

Related substances<\/h3>\n

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

Test solution: Dissolve 50.0 mg of the substance to be examined in 10 mL of acetonitrile R and dilute to 25.0 mL with the mobile phase.<\/p>\n

Reference solution (a): Dilute 1.0 mL of the test solution to 50.0 mL with the mobile phase. Dilute 1.0 mL of this solution to 10.0 mL with the mobile phase.<\/p>\n

Reference solution (b): Dissolve the contents of a vial of triclabendazole for system suitability CRS ( impurities A, B and D) in 1.0 mL of the mobile phase.<\/p>\n

Column:<\/p>\n

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

\u2014 stationary phase: base-deactivated end-capped octadecylsilyl silica gel for chromatography R (5 \u03bcm).<\/p>\n

Mobile phase: Dissolve 0.77 g of ammonium acetate R in 800 mL of water for chromatography R, add 1 mL of triethylamine R and mix; adjust to pH 4.5 with glacial acetic acid R and dilute to 1 L with water for chromatography R. Mix 40 volumes of this solution and 60 volumes of acetonitrile R.<\/p>\n

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

Detection: Spectrophotometer at 305 nm.<\/p>\n

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

Run time: 2.5 times the retention time of triclabendazole.<\/p>\n

Identification of impurities: Use the chromatogram supplied with triclabendazole for system suitability CRS and the chromatogram obtained with reference solution (b) to identify the peaks due to impurities A, B and D.<\/p>\n

Relative retention: With reference to triclabendazole (retention time = about 10 min): impurity A = about 0.6; impurity B = about 0.7; impurity D = about 1.9.<\/p>\n

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

\u2014 resolution: minimum 2.5 between the peaks due to impurities A and B.<\/p>\n

Calculation of percentage contents:<\/p>\n

\u2014 correction factors: multiply the peak areas of the following impurities by the corresponding correction factor: impurity A = 1.9; impurity D = 2.7;<\/p>\n

\u2014 for each impurity, use the concentration of triclabendazole in reference solution (a).<\/p>\n

Limits:<\/p>\n

\u2014 impurities A, D: for each impurity, maximum 0.3 per cent;<\/p>\n

\u2014 unspecified impurities: for each impurity, maximum 0.20 per cent;<\/p>\n

\u2014 total: maximum 1.0 per cent;<\/p>\n

\u2014 reporting threshold: 0.10 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 an oven at 105 \u00b0C for 6 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 0.280 g in 50 mL of anhydrous acetic acid R. Allow to cool and 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 35.97 mg of C14<\/sub>H9<\/sub>Cl3<\/sub>N2<\/sub>OS.<\/p>\n

STORAGE<\/h2>\n

Protected from light.<\/p>\n

IMPURITIES<\/h2>\n

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

\"Triclabendazole\"<\/p>\n

A. 5-chloro-6-(2,3-dichlorophenoxy)-2-(methylsulfinyl)-1H-benzimidazole,<\/p>\n

\"Triclabendazole<\/p>\n

B. 5-chloro-6-(2,3-dichlorophenoxy)-1H-benzimidazole-2-thiol,<\/p>\n

\"Triclabendazole\"<\/p>\n

D. 4-chloro-5-(2,3-dichlorophenoxy)-2-nitroaniline.<\/p>\n","protected":false},"excerpt":{"rendered":"

Triclabendazole for Veterinary Use (Ph. Eur. monograph 2609) C14H9Cl3N2OS 359.7 68786-66-3 Action and use Benzimidazole antihelminthic. DEFINITION 5-Chloro-6-(2,3-dichlorophenoxy)-2-(methylsulfanyl)-1H-benzimidazole. Content 99.0 per cent to 101.0 per cent (dried substance). CHARACTERS Appearance White or almost white, crystalline powder. Solubility Practically insoluble in water, soluble in acetone, sparingly soluble in ethanol (96 per cent). IDENTIFICATION Infrared absorption spectrophotometry…<\/p>\n","protected":false},"author":4,"featured_media":24736,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[176],"tags":[],"class_list":["post-24704","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-british-pharmacopoeia-veterinary-2020"],"acf":[],"_links":{"self":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/24704","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=24704"}],"version-history":[{"count":2,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/24704\/revisions"}],"predecessor-version":[{"id":24742,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/24704\/revisions\/24742"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/24736"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=24704"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=24704"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=24704"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}