{"id":2850,"date":"2025-09-22T15:57:53","date_gmt":"2025-09-22T08:57:53","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=2850"},"modified":"2025-10-02T14:05:36","modified_gmt":"2025-10-02T07:05:36","slug":"betahistine-dihydrochloride","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/betahistine-dihydrochloride\/","title":{"rendered":"Betahistine Dihydrochloride"},"content":{"rendered":"

(Ph. Eur. monograph 1665)<\/p>\n

C8<\/sub>H14<\/sub>Cl2<\/sub>N2<\/sub>\u00a0 \u00a0 209.1\u00a0 \u00a0 5579-84-0<\/p>\n

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

Histamine H1 receptor antagonist; antihistamine.<\/p>\n

Preparation<\/strong><\/p>\n

Betahistine Dihydrochloride Tablets<\/p>\n

DEFINITION<\/h2>\n

N-Methyl-2-(pyridin-2-yl)ethanamine dihydrochloride.<\/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 slightly yellow powder, very hygroscopic.<\/p>\n

Solubility<\/h3>\n

Very soluble in water, soluble in ethanol (96 per cent), practically insoluble in 2-propanol.<\/p>\n

IDENTIFICATION<\/h2>\n

First identification: B, D.<\/p>\n

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

A. Melting point (2.2.14): 150 \u00b0C to 154 \u00b0C.<\/p>\n

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

Comparison betahistine dihydrochloride CRS.<\/p>\n

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

Test solution: Dissolve 10 mg of the substance to be examined in 2 mL of ethanol (96 per cent) R.<\/p>\n

Reference solution: Dissolve 10 mg of betahistine dihydrochloride CRS in 2 mL of ethanol (96 per cent) R.<\/p>\n

Plate: TLC silica gel GF254 plate R.<\/p>\n

Mobile phase concentrated ammonia R, ethyl acetate R, methanol R (0.75:15:30 V\/V\/V).<\/p>\n

Application: 2 \u03bcL.<\/p>\n

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

Drying: At 110 \u00b0C for 10 min.<\/p>\n

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

Results: 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

D. It gives reaction (a) of chlorides (2.3.1).<\/p>\n

TESTS<\/h2>\n

Solution S<\/h3>\n

Dissolve 5.0 g in carbon dioxide-free water R, and dilute to 50 mL with the same solvent.<\/p>\n

Appearance of solution<\/h3>\n

Solution S is clear (2.2.1) and not more intensely coloured than reference solution B8 (2.2.2, Method II).<\/p>\n

pH (2.2.3)<\/h4>\n

2.0 to 3.0 for solution S.<\/p>\n

Related substances<\/h3>\n

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

Test solution Dissolve 25 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): Dissolve 10 mg of betahistine dihydrochloride CRS and 10 mg of 2-vinylpyridine R in the mobile phase and dilute to 50.0 mL with the mobile phase. Dilute 2.0 mL of the solution to 50.0 mL with the mobile phase.<\/p>\n

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

Reference solution (c): Dilute 2.0 mL of reference solution (b) to 10.0 mL with the mobile phase.
\nColumn:<\/p>\n

\u2014 size: l = 0.15 m, \u00d8 = 3.0 mm;<\/p>\n

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

Mobile phase Dissolve 2.0 g of sodium dodecyl sulfate R in a mixture of 15 mL of a 10 per cent V\/V solution of sulfuric acid R, 35 mL of a 17 g\/L solution of tetrabutylammonium hydrogen sulfate R and 650 mL of water R; adjust to pH 3.3 using dilute sodium hydroxide solution R and mix with 300 mL of acetonitrile R.<\/p>\n

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

Detection: Spectrophotometer at 260 nm.<\/p>\n

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

Run time: 4 times the retention time of betahistine.<\/p>\n

Relative retention: With reference to betahistine (retention time = about 7 min): impurity B = about 0.2; impurity A = about 0.3; impurity C = about 3.<\/p>\n

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

\u2014 resolution: minimum 3.5 between the peaks due to 2-vinylpyridine and betahistine.<\/p>\n

Limits:<\/p>\n

\u2014 correction factor: for the calculation of content, multiply the peak area of impurity B by 0.4;<\/p>\n

\u2014 impurities A, B, C: 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

\u2014 unspecified impurities: for each impurity, not more than 0.5 times of the area of the principal peak in the
\nchromatogram obtained with reference solution (c) (0.10 per cent);<\/p>\n

\u2014 total: not more than 0.5 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.5 per cent);<\/p>\n

\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

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

Maximum 1.0 per cent, determined on 1.000 g by drying in an oven 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 80.0 mg in 50 mL of ethanol (96 per cent) R. Titrate with 0.1 M sodium hydroxide, determining the end-point potentiometrically (2.2.20). Read the volume added to reach the second point of inflexion.
\n1 mL of 0.1 M sodium hydroxide is equivalent to 10.46 mg of C8H14Cl2N2.<\/p>\n

STORAGE<\/h2>\n

In an airtight container.<\/p>\n

IMPURITIES<\/h2>\n

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

\"Betahistine<\/p>\n

A. 2-ethenylpyridine (2-vinylpyridine),<\/p>\n

\"Betahistine<\/p>\n

B. 2-(pyridin-2-yl)ethanol,<\/p>\n

\"Betahistine<\/p>\n

C. N-methyl-2-(pyridin-2-yl)-N-[2-(pyridin-2-yl)ethyl]ethanamine.<\/p>\n","protected":false},"excerpt":{"rendered":"

(Ph. Eur. monograph 1665) C8H14Cl2N2\u00a0 \u00a0 209.1\u00a0 \u00a0 5579-84-0 Action and use Histamine H1 receptor antagonist; antihistamine. Preparation Betahistine Dihydrochloride Tablets DEFINITION N-Methyl-2-(pyridin-2-yl)ethanamine dihydrochloride. Content 99.0 per cent to 101.0 per cent (dried substance). CHARACTERS Appearance White or slightly yellow powder, very hygroscopic. Solubility Very soluble in water, soluble in ethanol (96 per cent), practically…<\/p>\n","protected":false},"author":3,"featured_media":2863,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-2850","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\/2850","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=2850"}],"version-history":[{"count":5,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/2850\/revisions"}],"predecessor-version":[{"id":7841,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/2850\/revisions\/7841"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/2863"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=2850"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=2850"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=2850"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}