{"id":3599,"date":"2025-09-24T15:04:04","date_gmt":"2025-09-24T08:04:04","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=3599"},"modified":"2025-10-04T12:00:49","modified_gmt":"2025-10-04T05:00:49","slug":"benazepril-hydrochloride","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/benazepril-hydrochloride\/","title":{"rendered":"Benazepril Hydrochloride"},"content":{"rendered":"<p><em>(Ph. Eur. monograph 2388)<\/em><\/p>\n<p>C<sub>24<\/sub>H<sub>29<\/sub>ClN<sub>2<\/sub>O<sub>5<\/sub> 461.0 86541-74-4<\/p>\n<p><strong>Action and use<\/strong><\/p>\n<p>Angiotensin converting enzyme inhibitor.<\/p>\n<h2>DEFINITION<\/h2>\n[(3S)-3-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetic acid hydrochloride.<\/p>\n<h3>Content<\/h3>\n<p>97.5 per cent to 102.0 per cent (dried substance).<\/p>\n<h2>CHARACTERS<\/h2>\n<h3>Appearance<\/h3>\n<p>White or almost white, crystalline powder, hygroscopic.<\/p>\n<h3>Solubility<\/h3>\n<p>Slightly soluble in water, freely soluble in anhydrous ethanol, very slightly soluble in ethyl acetate, practically insoluble in cyclohexane.<\/p>\n<p>It shows polymorphism (5.9).<\/p>\n<h2>IDENTIFICATION<\/h2>\n<p>Carry out either tests A, B, D or tests B, C, D.<\/p>\n<p>A. Specific optical rotation (2.2.7): -141 to -136 (dried substance).<\/p>\n<p>Dissolve 1.000 g in anhydrous ethanol R and dilute to 50.0 mL with the same solvent.<\/p>\n<p>B. Infrared absorption spectrophotometry (2.2.24).<\/p>\n<p>Comparison: benazepril hydrochloride CRS.<\/p>\n<p>If the spectra obtained in the solid state show differences, dissolve the substance to be examined and the reference substance separately in methanol R, evaporate to dryness and record new spectra using the residues.<\/p>\n<p>C. Enantiomeric purity (see Tests).<\/p>\n<p>D. It gives reaction (a) of chlorides (2.3.1).<\/p>\n<h2>TESTS<\/h2>\n<h3>Related substances<\/h3>\n<p>Liquid chromatography (2.2.29).<\/p>\n<p>Test solution (a): Dissolve 50.0 mg of the substance to be examined in the mobile phase and dilute to 50.0 mL with the mobile phase.<\/p>\n<p>Test solution (b): Dilute 10.0 mL of test solution (a) to 100.0 mL with the mobile phase.<\/p>\n<p>Reference solution (a): Dissolve 50.0 mg of benazepril hydrochloride CRS in the mobile phase and dilute to 50.0 mL with the mobile phase. Dilute 10.0 mL of this solution to 100.0 mL with the mobile phase.<\/p>\n<p>Reference solution (b): Dissolve the contents of a vial of benazepril for system suitability CRS (containing impurities B, C, D, E, F and G) in 1.0 mL of test solution (a).<\/p>\n<p>Reference solution (c): Dilute 1.0 mL of reference solution (a) to 50.0 mL with the mobile phase.<\/p>\n<p>Column:<\/p>\n<p>\u2014 size: l = 0.30 m, \u00d8 = 3.9 mm;<\/p>\n<p>\u2014 stationary phase: end-capped octadecylsilyl silica gel for chromatography R (10 \u03bcm).<\/p>\n<p>Mobile phase: Add 0.2 mL of glacial acetic acid R to 1000 mL of a mixture of 360 volumes of water R and 640 volumes of methanol R2; add 0.81 g of tetrabutylammonium bromide R and stir to dissolve.<\/p>\n<p>Flow rate: 1.0 mL\/min.<\/p>\n<p>Detection: Spectrophotometer at 240 nm.<\/p>\n<p>Injection: 25 \u03bcL of test solution (a) and reference solutions (b) and (c).<\/p>\n<p>Run time: 3 times the retention time of benazepril.<\/p>\n<p>Relative retention: With reference to benazepril (retention time = about 6 min): impurity E = about 0.3; impurity F = about 0.4; impurity C = about 0.5; impurity B = about 1.8; impurity D = about 2.0; impurity G = about 2.5.<\/p>\n<p>Identification of impurities: Use the chromatogram supplied with benazepril for system suitability CRS and the chromatogram obtained with reference solution (b) to identify the peaks due to impurities B, C, D, E, F and G.<\/p>\n<p>System suitability Reference solution (b):<\/p>\n<p>\u2014 resolution: minimum 2.5 between the peaks due to benazepril and impurity B and minimum 1.5 between the peaks due to impurities E and F.<\/p>\n<p>Limits:<\/p>\n<p>\u2014 correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity E = 0.5; impurity F = 0.7;<\/p>\n<p>\u2014 impurity B: not more than 2.5 times the area of the principal peak in the chromatogram obtained with reference solution (c) (0.5 per cent);<\/p>\n<p>\u2014 impurity C: not more than 1.5 times the area of the principal peak in the chromatogram obtained with reference solution (c) (0.3 per cent);<\/p>\n<p>\u2014 impurities D, E, F, G: for each impurity, not more than the area of the principal peak in the chromatogram obtained with reference solution (c) (0.2 per cent);<\/p>\n<p>\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 (c)(0.10 per cent);<\/p>\n<p>\u2014 total: not more than 10 times the area of the principal peak in the chromatogram obtained with reference solution (c) (2.0 per cent);<\/p>\n<p>\u2014 disregard limit: 0.25 times the area of the principal peak in the chromatogram obtained with reference solution (c) (0.05 per cent).<\/p>\n<h3>Enantiomeric purity<\/h3>\n<p>Liquid chromatography (2.2.29).<\/p>\n<p>Buffer solution pH 6.0 Dissolve 3.58 g of disodium hydrogen phosphate dodecahydrate R and 9.66 g of potassium dihydrogen phosphate R in water R and dilute to 1000.0 mL with the same solvent.<\/p>\n<p>Test solution: Dissolve 50.0 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 (a): Dissolve 5.0 mg of benazepril impurity A CRS in the mobile phase and dilute to 50.0 mL with the mobile phase.<\/p>\n<p>Reference solution (b): Dilute 1.0 mL of reference solution (a) to 100.0 mL with the mobile phase.<\/p>\n<p>Reference solution (c): Dilute 1.0 mL of reference solution (a) to 10.0 mL with the mobile phase. Dilute 1.0 mL of this solution to 10.0 mL with the test solution.<\/p>\n<p>Column:<\/p>\n<p>\u2014 size: l = 0.10 m, \u00d8 = 4.0 mm;<\/p>\n<p>\u2014 stationary phase: spherical silica gel AGP for chiral chromatography R (5 \u03bcm);<\/p>\n<p>\u2014 temperature: 30 \u00b0C.<\/p>\n<p>Mobile phase methanol R2, buffer solution pH 6.0 (20:80 V\/V).<\/p>\n<p>Flow rate 0.9 mL\/min.<\/p>\n<p>Detection Spectrophotometer at 240 nm.<\/p>\n<p>Injection 50 \u03bcL of the test solution and reference solutions (b) and (c).<\/p>\n<p>Run time 3.5 times the retention time of benazepril.<\/p>\n<p>Relative retention: With reference to benazepril (retention time = about 6 min): impurity A = about 1.9.<\/p>\n<p>System suitability: Reference solution (c):<\/p>\n<p>\u2014 peak-to-valley ratio: minimum 2.5, where Hp = height above the baseline of the peak due to impurity A and<\/p>\n<p>Hv = height above the baseline of the lowest point of the curve separating this peak from the peak due to benazepril.<\/p>\n<p>Limit:<\/p>\n<p>\u2014 impurity A: not more than the area of the corresponding peak in the chromatogram obtained with reference solution (b) (0.1 per cent).<\/p>\n<h3>Loss on drying (2.2.32)<\/h3>\n<p>Maximum 1.5 per cent, determined on 1.000 g by drying in vacuo at 105 \u00b0C for 3 h.<\/p>\n<h3>Sulfated ash (2.4.14)<\/h3>\n<p>Maximum 0.1 per cent, determined on 1.0 g.<\/p>\n<h2>ASSAY<\/h2>\n<p>Liquid chromatography (2.2.29) as described in the test for related substances with the following modification.<\/p>\n<p>Injection: Test solution (b) and reference solution (a).<\/p>\n<p>Calculate the percentage content of C<sub>24<\/sub>H<sub>29<\/sub>ClN<sub>2<\/sub>O<sub>5<\/sub> from the declared content of benazepril hydrochloride CRS.<\/p>\n<h2>STORAGE<\/h2>\n<p>Protected from light, in an airtight container.<\/p>\n<h2>IMPURITIES<\/h2>\n<p>Specified impurities A, B, C, D, E, F, G.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-8973\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/1-186-300x163.jpg\" alt=\"Benazepril Hydrochloride\" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/1-186-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/1-186-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/1-186-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/1-186.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>A. [(3R)-3-[[(1R)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-8974\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/2-229-300x163.jpg\" alt=\"Benazepril Hydrochloride\" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/2-229-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/2-229-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/2-229-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/2-229.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>B. [(3RS)-3-[[(1SR)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-8975\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/3-235-300x163.jpg\" alt=\"Benazepril Hydrochloride\" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/3-235-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/3-235-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/3-235-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/3-235.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>C. (2S)-2-[[(3S)-1-(carboxymethyl)-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-3-yl]amino]-4-phenylbutanoic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-8987\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/Benazepril-Hydrochloride-300x163.jpg\" alt=\"Benazepril Hydrochloride\" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/Benazepril-Hydrochloride-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/Benazepril-Hydrochloride-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/Benazepril-Hydrochloride-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/Benazepril-Hydrochloride.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>D. [(3S)-3-[[(1S)-3-cyclohexyl-1-(ethoxycarbonyl)propyl]amino]-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-8976\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/4-210-300x163.jpg\" alt=\"Benazepril Hydrochloride\" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/4-210-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/4-210-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/4-210-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/4-210.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>E. [(3S)-3-amino-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-8977\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/5-183-300x163.jpg\" alt=\"Benazepril Hydrochloride\" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/5-183-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/5-183-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/5-183-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/5-183.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>F. 1,1-dimethylethyl [(3S)-3-amino-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetate,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-8978\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/6-163-300x163.jpg\" alt=\"Benazepril Hydrochloride\" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/6-163-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/6-163-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/6-163-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/09\/6-163.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>G. ethyl (2S)-2-[[(3S)-1-(2-ethoxy-2-oxoethyl)-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-3-yl]amino]-4-phenylbutanoate.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>(Ph. Eur. monograph 2388) C24H29ClN2O5 461.0 86541-74-4 Action and use Angiotensin converting enzyme inhibitor. DEFINITION [(3S)-3-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetic acid hydrochloride. Content 97.5 per cent to 102.0 per cent (dried substance). CHARACTERS Appearance White or almost white, crystalline powder, hygroscopic. Solubility Slightly soluble in water, freely soluble in anhydrous ethanol, very slightly soluble in ethyl acetate, practically insoluble&#8230;<\/p>\n","protected":false},"author":4,"featured_media":3620,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-3599","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\/3599","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=3599"}],"version-history":[{"count":4,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/3599\/revisions"}],"predecessor-version":[{"id":8989,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/3599\/revisions\/8989"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/3620"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=3599"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=3599"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=3599"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}