{"id":26513,"date":"2025-11-06T08:51:14","date_gmt":"2025-11-06T01:51:14","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=26513"},"modified":"2025-11-06T08:51:14","modified_gmt":"2025-11-06T01:51:14","slug":"perindopril-erbumine","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/perindopril-erbumine\/","title":{"rendered":"Perindopril Erbumine"},"content":{"rendered":"<p><em>(Perindopril tert-Butylamine, Ph. Eur. monograph 2019)<\/em><\/p>\n<p>C<sub>23<\/sub>H<sub>43<\/sub>N<sub>3<\/sub>O<sub>5<\/sub> 441.6 107133-36-8<\/p>\n<p><strong>Action and use<\/strong><\/p>\n<p>Angiotensin converting enzyme inhibitor.<\/p>\n<p><strong>Preparation<\/strong><\/p>\n<p>Perindopril Erbumine Tablets<\/p>\n<h2>DEFINITION<\/h2>\n<p>2-Methylpropan-2-amine (2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)butyl]amino]propanoyl]octahydro-1H-indole-2- carboxylate.<\/p>\n<h3>Content<\/h3>\n<p>99.0 per cent to 101.0 per cent (anhydrous substance).<\/p>\n<h2>CHARACTERS<\/h2>\n<h3>Appearance<\/h3>\n<p>White or almost white, slightly hygroscopic, crystalline powder.<\/p>\n<h3>Solubility<\/h3>\n<p>Freely soluble in water and in ethanol (96 per cent), soluble or sparingly soluble in methylene chloride.<\/p>\n<p>It shows polymorphism (5.9).<\/p>\n<h2>IDENTIFICATION<\/h2>\n<p>A. Specific optical rotation (2.2.7): -69 to -66 (anhydrous substance).<\/p>\n<p>Dissolve 0.250 g in ethanol (96 per cent) R and dilute to 25.0 mL with the same solvent.<\/p>\n<p>B. Infrared absorption spectrophotometry (2.2.24).<\/p>\n<p>Comparison: perindopril tert-butylamine CRS.<\/p>\n<p>If the spectra obtained show differences, dissolve the substance to be examined and the reference substance separately in methylene chloride R, evaporate to dryness and record new spectra using the residues.<\/p>\n<p>C. Examine the chromatograms obtained in the test for impurity A.<\/p>\n<p>Results: In the chromatogram obtained with the test solution a spot is observed with the same RF as the spot with the higher RF in the chromatogram obtained with reference solution (c) (tert-butylamine).<\/p>\n<h2>TESTS<\/h2>\n<h3>Impurity A<\/h3>\n<p>Thin-layer chromatography (2.2.27).<\/p>\n<p>Test solution: Dissolve 0.20 g of the substance to be examined in methanol R and dilute to 10.0 mL with the same solvent.<\/p>\n<p>Reference solution (a): Dissolve 5 mg of perindopril impurity A CRS in methanol R and dilute to 25.0 mL with the same solvent.<\/p>\n<p>Reference solution (b): Dilute 5.0 mL of reference solution (a) to 20.0 mL with methanol R.<\/p>\n<p>Reference solution (c): To 5 mL of reference solution (a) add 5 mL of a 20 g\/L solution of 1,1-dimethylethylamine R in methanol R.<\/p>\n<p>Plate: TLC silica gel plate R.<\/p>\n<p>Mobile phase: glacial acetic acid R, toluene R, methanol R (1:40:60 V\/V\/V).<\/p>\n<p>Application: 10 \u03bcL of the test solution and reference solutions (b) and (c).<\/p>\n<p>Development: Over 2\/3 of the plate.<\/p>\n<p>Drying: In a current of warm air.<\/p>\n<p>Detection: Expose to iodine vapour for at least 20 h.<\/p>\n<p>System suitability: Reference solution (c):<\/p>\n<p>\u2014 the chromatogram shows 2 clearly separated spots.<\/p>\n<p>Limit:<\/p>\n<p>\u2014 impurity A: any spot due to impurity A is not more intense than the spot in the chromatogram obtained with reference solution (b) (0.25 per cent).<\/p>\n<h3>Stereochemical purity<\/h3>\n<p>Liquid chromatography (2.2.29).<\/p>\n<p>Test solution: Dissolve 20 mg of the substance to be examined in ethanol (96 per cent) R and dilute to 10.0 mL with the same solvent.<\/p>\n<p>Reference solution (a): Dilute 1.0 mL of the test solution to 100.0 mL with ethanol (96 per cent) R. Dilute 1.0 mL of this solution to 10.0 mL with ethanol (96 per cent) R.<\/p>\n<p>Reference solution (b): Dissolve 10 mg of perindopril for stereochemical purity CRS (containing impurity I) in ethanol (96 per cent) R and dilute to 5 mL with the same solvent.<\/p>\n<p>Column:<\/p>\n<p>\u2014 size: l = 0.25 m, \u00d8 = 4.6 mm;<\/p>\n<p>\u2014 stationary phase: base-deactivated end-capped octadecylsilyl silica gel for chromatography R (5 \u03bcm);<\/p>\n<p>\u2014 temperature: 50 \u00b0C for the column and the tubing preceding the column (the method has been developed with a temperature of 50 \u00b0C for at least 30 cm of the tubing preceding the column).<\/p>\n<p>Mobile phase: Mix, in the following order, 21.7 volumes of acetonitrile R1, 0.3 volumes of pentanol R, and 78 volumes of a 1.50 g\/L solution of sodium heptanesulfonate R previously adjusted to pH 2.0 with a mixture of equal volumes of perchloric acid R and water for chromatography R.<\/p>\n<p>Flow rate: 0.8 mL\/min.<\/p>\n<p>Detection: Spectrophotometer at 215 nm.<\/p>\n<p>Equilibration: Minimum 4 h.<\/p>\n<p>Injection: 10 \u03bcL.<\/p>\n<p>Identification of impurities: Use the chromatogram supplied with perindopril for stereochemical purity CRS and the chromatogram obtained with reference solution (b) to identify the peak due to impurity I.<\/p>\n<p>Run time: 1.5 times the retention time of perindopril.<\/p>\n<p>Relative retention: With reference to perindopril (retention time = about 100 min): impurity I = about 0.9.<\/p>\n<p>System suitability:<\/p>\n<p>\u2014 the chromatogram obtained with reference solution (b) is similar to the chromatogram supplied with perindopril for stereochemical purity CRS;<\/p>\n<p>\u2014 signal-to-noise ratio: minimum 3 for the principal peak in the chromatogram obtained with reference solution (a);<\/p>\n<p>\u2014 peak-to-valley ratio: minimum 3, where Hp = height above the baseline of the peak due to impurity I and Hv = height above the baseline of the lowest point of the curve separating this peak from the peak due to perindopril in the chromatogram obtained with reference solution (b).<\/p>\n<p>Limits:<\/p>\n<p>\u2014 impurity I: not more than the area of the principal peak in the chromatogram obtained with reference solution (a) (0.1 per cent);<\/p>\n<p>\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<p>\u2014 disregard limit: disregard any peak with a relative retention with reference to perindopril of less than 0.6 or more than 1.4.<\/p>\n<h3>Related substances<\/h3>\n<p>Liquid chromatography (2.2.29). Prepare the solutions immediately before use or maintain them at a temperature below 10 \u00b0C.<\/p>\n<p>Test solution: Dissolve 60 mg of the substance to be examined in mobile phase A and dilute to 20.0 mL with mobile phase A.<\/p>\n<p>Reference solution (a): Dissolve 3 mg of perindopril for peak identification CRS (containing impurities B, E, F, H and K) in 1 mL of mobile phase A.<\/p>\n<p>Reference solution (b): Dilute 1.0 mL of the test solution to 200.0 mL with mobile phase A.<\/p>\n<p>Reference solution (c): Dilute 1.0 mL of reference solution (b) to 10.0 mL with mobile phase A.<\/p>\n<p>Column:<\/p>\n<p>\u2014 size: l = 0.15 m, \u00d8 = 4 mm;<\/p>\n<p>\u2014 stationary phase: end-capped octylsilyl silica gel for chromatography R (5 \u03bcm);<\/p>\n<p>\u2014 temperature: 60 \u00b0C for the column and the tubing preceding the column.<\/p>\n<p>Mobile phase:<\/p>\n<p>\u2014 mobile phase A: water for chromatography R adjusted to pH 2.5 with a mixture of equal volumes of perchloric acid R; and water for chromatography R;<\/p>\n<p>\u2014 mobile phase B: 0.03 per cent V\/V solution of perchloric acid R in acetonitrile R1;<\/p>\n<table style=\"border-collapse: collapse; width: 100%; height: 85px;\">\n<tbody>\n<tr style=\"height: 43px;\">\n<td style=\"width: 33.3333%; text-align: center; height: 43px;\"><strong>Time<\/strong><br \/>\n<strong>(min)<\/strong><\/td>\n<td style=\"width: 33.3333%; text-align: center; height: 43px;\"><strong>Mobile phase A<\/strong><br \/>\n<strong>(per cent V\/V)<\/strong><\/td>\n<td style=\"width: 33.3333%; text-align: center; height: 43px;\"><strong>Mobile phase B<\/strong><br \/>\n<strong>(per cent V\/V)<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 21px;\">\n<td style=\"width: 33.3333%; height: 21px; text-align: center;\">0 &#8211; 5<\/td>\n<td style=\"width: 33.3333%; height: 21px; text-align: center;\">95<\/td>\n<td style=\"width: 33.3333%; height: 21px; text-align: center;\">5<\/td>\n<\/tr>\n<tr style=\"height: 21px;\">\n<td style=\"width: 33.3333%; height: 21px; text-align: center;\">5 &#8211; 60<\/td>\n<td style=\"width: 33.3333%; height: 21px; text-align: center;\">95 \u2192 40<\/td>\n<td style=\"width: 33.3333%; height: 21px; text-align: center;\">5 \u2192 60<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Flow rate: 1.0 mL\/min.<\/p>\n<p>Detection: Spectrophotometer at 215 nm.<\/p>\n<p>Injection: 20 \u03bcL.<\/p>\n<p>Identification of impurities: Use the chromatogram supplied with perindopril for peak identification CRS and the chromatogram obtained with reference solution (a) to identify the peaks due to impurities B, E, F, H and K.<\/p>\n<p>Relative retention: With reference to perindopril (retention time = about 25 min): impurity B = about 0.68; impurity K = about 0.72; impurity E = about 1.2; impurity F = about 1.6; impurity H = about 1.8 (impurity H may be eluted as 1 or 2 peaks).<\/p>\n<p>System suitability: Reference solution (a):<\/p>\n<p>\u2014 peak-to-valley ratio: minimum 3, where Hp = height above the baseline of the peak due to impurity B and Hv = height above the baseline of the lowest point of the curve separating this peak from the peak due to impurity K.<\/p>\n<p>Limits:<\/p>\n<p>\u2014 impurity E: not more than 0.8 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.4 per cent);<\/p>\n<p>\u2014 impurity B: not more than 0.6 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.3 per cent);<\/p>\n<p>\u2014 impurities F, H: for each impurity, not more than 0.4 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.2 per cent);<\/p>\n<p>\u2014 unspecified impurities: for each impurity, not more than 0.2 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.10 per cent);<\/p>\n<p>\u2014 total: not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (1.0 per cent);<\/p>\n<p>\u2014 disregard limit: the area of the principal peak in the chromatogram obtained with reference solution (c) (0.05 per cent).<\/p>\n<h3>Water (2.5.12)<\/h3>\n<p>Maximum 1.0 per cent, determined on 0.50 g.<\/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>Dissolve 0.160 g in 50 mL of anhydrous acetic acid R. Titrate with 0.1 M perchloric acid, determining the end-point potentiometrically (2.2.20).<\/p>\n<p>1 mL of 0.1 M perchloric acid is equivalent to 22.08 mg of C<sub>23<\/sub>H<sub>43<\/sub>N<sub>3<\/sub>O<sub>5<\/sub>.<\/p>\n<h2>STORAGE<\/h2>\n<p>In an airtight container.<\/p>\n<h2>IMPURITIES<\/h2>\n<p>Specified impurities A, B, E, F, H, I.<\/p>\n<p>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) C, D, G, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y, Z, AA, BB, CC.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26691\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/2-24-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/2-24-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/2-24-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/2-24-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/2-24.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>A. (2S,3aS,7aS)-octahydro-1H-indole-2-carboxylic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26692\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/3-23-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/3-23-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/3-23-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/3-23-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/3-23.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>B. (2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-carboxybutyl]amino]propanoyl]octahydro-1H-indole-2-carboxylic acid (perindoprilat),<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26693\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/4-22-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/4-22-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/4-22-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/4-22-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/4-22.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>C. (2S)-2-[(3S,5aS,9aS,10aS)-3-methyl-1,4-dioxodecahydropyrazino[1,2-a]indol-2(1H)-yl]pentanoic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26694\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/5-21-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/5-21-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/5-21-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/5-21-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/5-21.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>D. (2S)-2-[(3S,5aS,9aS,10aR)-3-methyl-1,4-dioxodecahydropyrazino[1,2-a]indol-2(1H)-yl]pentanoic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26695\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/6-17-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/6-17-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/6-17-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/6-17-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/6-17.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>E. (2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-[(1-methylethoxy)carbonyl]butyl]amino]propanoyl]octahydro-1H-indole-2-carboxylic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26696\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/7-15-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/7-15-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/7-15-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/7-15-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/7-15.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>F. ethyl (2S)-2-[(3S,5aS,9aS,10aS)-3-methyl-1,4-dioxodecahydropyrazino[1,2-a]indol-2(1H)-yl]pentanoate,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26697\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/8-12-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/8-12-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/8-12-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/8-12-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/8-12.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>G. (2S,3aS,7aS)-1-[(2S)-2-[(5RS)-3-cyclohexyl-2,4-dioxo-5-propylimidazolidin-1-yl]propanoyl]octahydro-1H-indole-2- carboxylic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26698\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/9-11-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/9-11-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/9-11-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/9-11-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/9-11.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>H. (2S,3aS,7aS)-1-[(2S)-2-[(5RS)-3-cyclohexyl-2-(cyclohexylimino)-4-oxo-5-propylimidazolidin-1-yl]propanoyl]octahydro-1H-indole-2-carboxylic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26699\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/10-9-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/10-9-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/10-9-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/10-9-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/10-9.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>I. (2RS,3aRS,7aRS)-1-[(2RS)-2-[[(1SR)-1-(ethoxycarbonyl)butyl]amino]propanoyl]octahydro-1H-indole-2-carboxylic acid ((\u00b1)-1\u2032\u2032-epi-perindopril),<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26700\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/11-7-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/11-7-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/11-7-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/11-7-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/11-7.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>J. (2S,3aS,7aS)-1-[(2S)-2-aminopropanoyl]octahydro-1H-indole-2-carboxylic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26701\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/12-5-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/12-5-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/12-5-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/12-5-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/12-5.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>K. (3S,5aS,9aS,10aS)-3-methyldecahydropyrazino[1,2-a]indole-1,4-dione,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26702\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/13-3-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/13-3-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/13-3-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/13-3-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/13-3.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>L. (2S,3aS,7aS)-1-acetyloctahydro-1H-indole-2-carboxylic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26703\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/14-3-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/14-3-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/14-3-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/14-3-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/14-3.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>M. (2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-(methoxycarbonyl)butyl]amino]propanoyl]octahydro-1H-indole-2-carboxylic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26704\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/15-3-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/15-3-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/15-3-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/15-3-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/15-3.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>N. (2S)-3-cyclohexyl-2-[[(2S)-2-[[(1S)-1-(ethoxycarbonyl)butyl]amino]propanoyl]amino]propanoic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26705\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/16-3-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/16-3-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/16-3-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/16-3-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/16-3.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>O. (2S,3aS,7aS)-1-[[(2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)butyl]amino]propanoyl]octahydro-1H-indol-2-yl]carbonyl]octahydro-1H-indole-2-carboxylic acid,<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-26706\" src=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/17-3-300x163.jpg\" alt=\"Perindopril Erbumine \" width=\"300\" height=\"163\" srcset=\"https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/17-3-300x163.jpg 300w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/17-3-1024x555.jpg 1024w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/17-3-768x416.jpg 768w, https:\/\/nhathuocngocanh.com\/bp\/wp-content\/uploads\/2025\/11\/17-3.jpg 1200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>1-[2-[[1-(ethoxycarbonyl)butyl]amino]propanoyl]octahydro-1H-indole-2-carboxylic acid,<\/p>\n<p>P. (2RS,3aRS,7aRS)-, (2\u2032SR)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-2\u2032-epi-perindopril,<\/p>\n<p>Q. (2RS,3aRS,7aSR)-, (2\u2032RS)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-7a-epi-perindopril,<\/p>\n<p>R. (2RS,3aSR,7aRS)-, (2\u2032RS)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-3a-epi-perindopril,<\/p>\n<p>S. (2SR,3aRS,7aRS)-, (2\u2032RS)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-2-epi-perindopril,<\/p>\n<p>T. (2RS,3aRS,7aRS)-, (2\u2032SR)-, (1\u2032\u2032SR)-:<\/p>\n<p>(\u00b1)-1\u2032\u2032,2\u2032-di-epi-perindopril,<\/p>\n<p>U. (2RS,3aRS,7aSR)-, (2\u2032RS)-, (1\u2032\u2032SR)-:<\/p>\n<p>(\u00b1)-1\u2032\u2032,7a-di-epi-perindopril,<\/p>\n<p>V. (2SR,3aSR,7aRS)-, (2\u2032RS)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-2,3a-di-epi-perindopril,<\/p>\n<p>W. (2SR,3aRS,7aRS)-, (2\u2032RS)-, (1\u2032\u2032SR)-:<\/p>\n<p>(\u00b1)-1\u2032\u2032,2-di-epi-perindopril,<\/p>\n<p>X. (2SR,3aRS,7aSR)-, (2\u2032RS)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-2,7a-di-epi-perindopril,<\/p>\n<p>Y. (2SR,3aRS,7aRS)-, (2\u2032SR)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-2,2\u2032-di-epi-perindopril,<\/p>\n<p>Z. (2RS,3aSR,7aRS)-, (2\u2032RS)-, (1\u2032\u2032SR)-:<\/p>\n<p>(\u00b1)-1\u2032\u2032,3a-di-epi-perindopril,<\/p>\n<p>AA. (2RS,3aSR,7aSR)-, (2\u2032RS)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-3a,7a-di-epi-perindopril,<\/p>\n<p>BB. (2RS,3aSR,7aRS)-, (2\u2032SR)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-2\u2032,3a-di-epi-perindopril,<\/p>\n<p>CC. (2RS,3aRS,7aSR)-, (2\u2032SR)-, (1\u2032\u2032RS)-:<\/p>\n<p>(\u00b1)-2\u2032,7a-di-epi-perindopril.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>(Perindopril tert-Butylamine, Ph. Eur. monograph 2019) C23H43N3O5 441.6 107133-36-8 Action and use Angiotensin converting enzyme inhibitor. Preparation Perindopril Erbumine Tablets DEFINITION 2-Methylpropan-2-amine (2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)butyl]amino]propanoyl]octahydro-1H-indole-2- carboxylate. Content 99.0 per cent to 101.0 per cent (anhydrous substance). CHARACTERS Appearance White or almost white, slightly hygroscopic, crystalline powder. Solubility Freely soluble in water and in ethanol (96 per cent),&#8230;<\/p>\n","protected":false},"author":4,"featured_media":26690,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-26513","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\/26513","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=26513"}],"version-history":[{"count":2,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/26513\/revisions"}],"predecessor-version":[{"id":26708,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/26513\/revisions\/26708"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/26690"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=26513"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=26513"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=26513"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}