{"id":29554,"date":"2025-11-10T17:22:17","date_gmt":"2025-11-10T10:22:17","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=29554"},"modified":"2025-11-10T17:22:17","modified_gmt":"2025-11-10T10:22:17","slug":"testosterone-decanoate","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/testosterone-decanoate\/","title":{"rendered":"Testosterone Decanoate"},"content":{"rendered":"

Edition: BP 2025 (Ph. Eur. 11.6 update)<\/span><\/p>\n

General Notices<\/span><\/p>\n

(Ph. Eur. monograph 1736)<\/span><\/p>\n

C29<\/sub>H46<\/sub>O3<\/sub> 442.7<\/span><\/p>\n

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

Androgen.<\/span><\/p>\n

DEFINITION<\/span><\/h2>\n

3-Oxoandrost-4-en-17p-yl decanoate.<\/span><\/p>\n

Content<\/span><\/h3>\n

97.0 per cent to 102.0 per cent (dried substance).<\/span><\/p>\n

CHARACTERS<\/span><\/h2>\n

Appearance<\/span><\/h3>\n

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

Solubility<\/span><\/h3>\n

Practically insoluble in water, very soluble in acetone, in methylene chloride and in anhydrous ethanol, freely soluble in fatty oils.<\/span><\/p>\n

IDENTIFICATION<\/span><\/h2>\n

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

Comparison testosterone decanoate CRS.<\/span><\/p>\n

B. Examine the chromatograms obtained in the assay.<\/span><\/p>\n

Results The principal peak in the chromatogram obtained with the test solution is similar in retention time and size to the principal peak in the chromatogram obtained with reference solution (c).<\/span><\/p>\n

TESTS<\/span><\/h2>\n

Appearance of solution<\/span><\/h3>\n

The solution is clear (2.2.1) and not more intensely coloured than reference solution BY6 (2.2.2, Method II).<\/span><\/p>\n

Dissolve 0.20 g in 20 mL of methanol R.<\/span><\/p>\n

Specific optical rotation (2.2.7)<\/span><\/p>\n

+ 75.0 to + 80.0 (dried substance).<\/span><\/p>\n

Dissolve 0.200 g in anhydrous ethanol R and dilute to 20.0 mL with the same solvent.<\/span><\/p>\n

Related substances<\/span><\/h3>\n

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

Test solution Dissolve 20.0 mg of the substance to be examined in the mobile phase and dilute to 50.0 mL with the mobile phase.<\/span><\/p>\n

Reference solution (a) Dissolve the contents of a vial of testosterone decanoate for system suitability CRS (containing impurities A, B, C, D, E and F) in 1 mL of the mobile phase.<\/span><\/p>\n

Reference solution (b) Dilute 10.0 mL of the test solution to 100.0 mL with the mobile phase. Dilute 1.0 mL of this solution to 20.0 mL with the mobile phase.<\/span><\/p>\n

Reference solution (c) Dissolve 20.0 mg of testosterone decanoate CRS in the mobile phase and dilute to 50.0 mL with the mobile phase.<\/span><\/p>\n

Column:<\/span><\/p>\n

\u2014<\/span> size: l = 0.25 m, 0 = 4.6 mm;<\/span><\/p>\n

\u2014<\/span> stationary phase: end-capped octadecylsilyl silica gel for chromatography R (5 pm);<\/span><\/p>\n

\u2014<\/span> temperature: 40 \u00b0C.<\/span><\/p>\n

Mobile phase water R, acetonitrile R (5:95 V\/V).<\/span><\/p>\n

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

Detection Spectrophotometer at 240 nm.<\/span><\/p>\n

Injection 20 pL of the test solution and reference solutions (a) and (b).<\/span><\/p>\n

Run time Twice the retention time of testosterone decanoate.<\/span><\/p>\n

Identification of impurities Use the chromatogram supplied with testosterone decanoate for system suitability CRS and the chromatogram obtained with reference solution (a) to identify the peaks due to impurities A, B, C, D, E and F.<\/span><\/p>\n

Relative retention With reference to testosterone decanoate (retention time = about 20 min): impurity A = about 0.2; impurity B = about 0.6; impurities C and G = about 0.79; impurity D = about 0.83; impurity E = about 1.3;<\/span><\/p>\n

impurity F = about 1.7.<\/span><\/p>\n

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

\u2014<\/span> resolution: minimum 1.5 between the peaks due to impurities C and D.<\/span><\/p>\n

Limits:<\/span><\/p>\n

\u2014<\/span> correction factors: for the calculation of content, multiply the peak area of impurity A by 0.7;<\/span><\/p>\n

\u2014<\/span> impurities A, B, D, E, F: for each impurity, not more than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.5 per cent);<\/span><\/p>\n

\u2014<\/span> sum of impurities C and G: not more than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.5 per cent);<\/span><\/p>\n

\u2014<\/span> 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);<\/span><\/p>\n

\u2014<\/span> total: not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (1.0 per cent);<\/span><\/p>\n

\u2014<\/span> disregard limit: 0.1 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.05 per cent).<\/span><\/p>\n

Free acid<\/span><\/h3>\n

Dissolve 0.65 g in 10 mL of ethanol (96 per cent) R, previously neutralised to bromothymol blue solution R3, and titrate immediately with 0.01 M sodium hydroxide, using 0.1 mL of bromothymol blue solution R3 as indicator. Not more than 0.6 mL of 0.01 M sodium hydroxide is required to change the colour of the indicator to blue.<\/span><\/p>\n

Loss on drying (2.2.32)<\/span><\/h3>\n

Maximum 0.5 per cent, determined on 1.000 g by drying in vacuo at a pressure not exceeding 0.7 kPa.<\/span><\/p>\n

ASSAY<\/span><\/h2>\n

Liquid chromatography (2.2.29) as described in the test for related substances with the following modification.<\/span><\/p>\n

Injection 20 pL of the test solution and reference solution (c).<\/span><\/p>\n

Calculate the percentage content of C29H46O3 from the declared content of testosterone decanoate CRS.<\/span><\/p>\n

STORAGE<\/span><\/h2>\n

At a temperature of 2 \u00b0C to 8 \u00b0C.<\/span><\/p>\n

IMPURITIES<\/span><\/h2>\n

Specified impurities A, B, C, D, E, F G.<\/span><\/p>\n

\"testosterone-decanoate\"<\/p>\n

A. testosterone,\u2003<\/span><\/p>\n

\"testosterone-decanoate\"<\/span><\/p>\n

B. 3-oxoandrost-4-en-17p-yl octanoate (testosterone octanoate),<\/span><\/p>\n

\"testosterone-decanoate\"<\/span><\/p>\n

C. 3-oxoandrost-4-en-17p-yl nonanoate (testosterone nonanoate),<\/span><\/p>\n

\"testosterone-decanoate\"<\/span><\/p>\n

D. 3-oxoandrost-4-en-17p-yl undec-10-enoate (testosterone undecylenate),<\/span><\/p>\n

\"testosterone-decanoate\"<\/span><\/p>\n

E. 3-oxoandrost-4-en-17p-yl undecanoate (testosterone undecanoate),<\/span><\/p>\n

\"testosterone-decanoate\"<\/span><\/p>\n

F. 3-oxoandrost-4-en-17p-yl dodecanoate (testosterone laurate),\u2003<\/span><\/p>\n

\"testosterone-decanoate\"<\/span><\/p>\n

G. 3-oxoandrost-4-en-17a-yl decanoate (epitestosterone decanoate).<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"

Edition: BP 2025 (Ph. Eur. 11.6 update) General Notices (Ph. Eur. monograph 1736) C29H46O3 442.7 Action and use Androgen. DEFINITION 3-Oxoandrost-4-en-17p-yl decanoate. Content 97.0 per cent to 102.0 per cent (dried substance). CHARACTERS Appearance White or almost white powder. Solubility Practically insoluble in water, very soluble in acetone, in methylene chloride and in anhydrous ethanol,…<\/p>\n","protected":false},"author":5,"featured_media":29555,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-29554","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\/29554","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\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/comments?post=29554"}],"version-history":[{"count":2,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/29554\/revisions"}],"predecessor-version":[{"id":29570,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/29554\/revisions\/29570"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/29555"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=29554"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=29554"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=29554"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}