{"id":11139,"date":"2025-10-09T10:05:15","date_gmt":"2025-10-09T03:05:15","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=11139"},"modified":"2025-10-09T10:05:15","modified_gmt":"2025-10-09T03:05:15","slug":"ethacridine-lactate-monohydrate","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/ethacridine-lactate-monohydrate\/","title":{"rendered":"Ethacridine Lactate Monohydrate"},"content":{"rendered":"

(Ph. Eur. monograph 1591)<\/p>\n

C18<\/sub>H21<\/sub>N3<\/sub>O4<\/sub>,H2<\/sub>O\u00a0 \u00a0361.4\u00a0 \u00a06402-23-9<\/p>\n

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

Antiseptic.<\/p>\n

DEFINITION<\/h2>\n

7-Ethoxyacridine-3,9-diamine (2RS)-2-hydroxypropanoate monohydrate.<\/p>\n

Content<\/h3>\n

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

CHARACTERS<\/h2>\n

Appearance<\/h3>\n

Yellow crystalline powder.<\/p>\n

Solubility<\/h3>\n

Sparingly soluble in water, very slightly soluble in ethanol (96 per cent), practically insoluble in methylene chloride.<\/p>\n

IDENTIFICATION<\/h2>\n

First identification: A.<\/p>\n

Second identification: B, C.<\/p>\n

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

Comparison ethacridine lactate monohydrate CRS.<\/p>\n

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

Test solution: Dissolve 5 mg of the substance to be examined in 2 mL of water R and dilute to 10 mL with methanol R.<\/p>\n

Reference solution: Dissolve 5 mg of ethacridine lactate monohydrate CRS in 2 mL of water R and dilute to 10 mL with methanol R.<\/p>\n

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

Mobile phase glacial acetic acid R, water R, butanol R (17:17:66 V\/V\/V).<\/p>\n

Application 2 \u03bcL; the volume can be adapted based on the type of plate used.<\/p>\n

Development Over 2\/3 of the plate.<\/p>\n

Drying At 100-105 \u00b0C.<\/p>\n

Detection A: Examine in daylight.<\/p>\n

Results A: The principal spot in the chromatogram obtained with the test solution is similar in position and size to the principal spot in the chromatogram obtained with the reference solution.<\/p>\n

Detection B: Examine in ultraviolet light at 254 nm and at 366 nm.<\/p>\n

Results B: The principal spot in the chromatogram obtained with the test solution is similar in position, colour and size to the principal spot in the chromatogram obtained with the reference solution.<\/p>\n

C. To 50 mL of solution S (see Tests) add 10 mL of dilute sodium hydroxide solution R. Filter. To 5 mL of the filtrate, add 1 mL of dilute sulfuric acid R. 5 mL of the solution obtained gives the reaction of lactates (2.3.1).<\/p>\n

TESTS<\/h2>\n

Solution S<\/h3>\n

Dissolve 2.0 g in carbon dioxide-free water R and dilute to 100.0 mL with the same solvent.<\/p>\n

pH (2.2.3)<\/h3>\n

5.5 to 7.0 for solution S.<\/p>\n

Related substances<\/h3>\n

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

Test solution: Dissolve 10.0 mg of the substance to be examined in the mobile phase and dilute to 25.0 mL with the mobile phase.<\/p>\n

Reference solution (a): Dilute 1.0 mL of the test solution to 100.0 mL with the mobile phase.<\/p>\n

Reference solution (b): Dilute 1.0 mL of reference solution (a) to 10.0 mL with 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 1.0 g of sodium octanesulfonate R in a mixture of 300 mL of acetonitrile R and 700 mL of phosphate buffer solution pH 2.8 R.<\/p>\n

Flow rate 1 mL\/min.<\/p>\n

Detection Spectrophotometer at 268 nm.<\/p>\n

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

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

Retention time Ethacridine = about 15 min.<\/p>\n

Limits:<\/p>\n

\u2014 any impurity: not more than 3 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.3 per cent);<\/p>\n

\u2014 total: not more than the area of the principal peak in the chromatogram obtained with reference solution (a) (1 per cent);<\/p>\n

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

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

4.5 per cent to 5.5 per cent, determined on 1.000 g by drying in vacuo at 105 \u00b0C.<\/p>\n

Sulfated ash (2.4.14)<\/h4>\n

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

ASSAY<\/h2>\n

Dissolve 0.270 g in 5.0 mL of anhydrous formic acid R. Add 60.0 mL of acetic anhydride R 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 34.34 mg of C18<\/sub>H21<\/sub>N3<\/sub>O4<\/sub>.<\/p>\n

STORAGE<\/h2>\n

Protected from light.<\/p>\n

IMPURITIES<\/h2>\n

\"Ethacridine<\/p>\n

A. 6-amino-2-ethoxyacridin-9(10H)-one,<\/p>\n

\"Ethacridine<\/p>\n

B. 6-chloro-2-ethoxyacridin-9-amine,<\/p>\n

\"Ethacridine<\/p>\n

C. 2-[(9-amino-7-ethoxyacridin-3-yl)oxy]ethan-1-ol.<\/p>\n","protected":false},"excerpt":{"rendered":"

(Ph. Eur. monograph 1591) C18H21N3O4,H2O\u00a0 \u00a0361.4\u00a0 \u00a06402-23-9 Action and use Antiseptic. DEFINITION 7-Ethoxyacridine-3,9-diamine (2RS)-2-hydroxypropanoate monohydrate. Content 99.0 per cent to 101.0 per cent (dried substance). CHARACTERS Appearance Yellow crystalline powder. Solubility Sparingly soluble in water, very slightly soluble in ethanol (96 per cent), practically insoluble in methylene chloride. IDENTIFICATION First identification: A. Second identification: B,…<\/p>\n","protected":false},"author":3,"featured_media":11155,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-11139","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\/11139","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\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/comments?post=11139"}],"version-history":[{"count":2,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/11139\/revisions"}],"predecessor-version":[{"id":11157,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/11139\/revisions\/11157"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/11155"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=11139"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=11139"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=11139"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}