{"id":12677,"date":"2025-10-11T11:36:34","date_gmt":"2025-10-11T04:36:34","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=12677"},"modified":"2025-10-11T11:36:34","modified_gmt":"2025-10-11T04:36:34","slug":"ethylenediamine","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/ethylenediamine\/","title":{"rendered":"Ethylenediamine"},"content":{"rendered":"

(Ph. Eur. monograph 0716)<\/p>\n

C2<\/sub>H8<\/sub>N2<\/sub>\u00a0 \u00a0 \u00a0 \u00a060.1\u00a0 \u00a0 \u00a0 \u00a0 107-15-3<\/p>\n

DEFINITION<\/h2>\n

Ethane-1,2-diamine.<\/p>\n

Content<\/h3>\n

98.0 per cent to 101.0 per cent.<\/p>\n

CHARACTERS<\/h2>\n

Appearance<\/h3>\n

Clear, colourless or slightly yellow liquid, hygroscopic.<\/p>\n

Solubility<\/h3>\n

Miscible with water and with anhydrous ethanol.<\/p>\n

On exposure to air, white fumes are evolved. On heating, it evaporates completely.<\/p>\n

IDENTIFICATION<\/h2>\n

A. Relative density (2.2.5): 0.895 to 0.905.<\/p>\n

B. Boiling point (2.2.12): 116 \u00b0C to 118 \u00b0C.<\/p>\n

C. To 0.2 mL add 0.5 mL of acetic anhydride R. Boil. A crystalline mass forms after cooling, which dissolves in 5 mL of 2- propanol R with heating. Cool the solution and add 5 mL of ether R. If necessary, initiate crystallisation by scratching the walls of the test-tube with a glass rod. Filter through a sintered-glass filter (2.1.2), wash with several portions of ether R
\nand dry at 100-105 \u00b0C. The residue melts (2.2.14) at 173 \u00b0C to 177 \u00b0C.<\/p>\n

TESTS<\/h2>\n

Solution S<\/h3>\n

Mix 10 g with carbon dioxide-free water R and dilute to 100 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 the reference solution BY6<\/sub> (2.2.2, Method II).<\/p>\n

Carbonate<\/h3>\n

A mixture of 4 mL of solution S and 6 mL of calcium hydroxide solution R is not more opalescent than reference suspension II (2.2.1).<\/p>\n

Chlorides (2.4.4)<\/h3>\n

Maximum 100 ppm.<\/p>\n

To 5 mL of solution S add 5 mL of dilute nitric acid R and dilute to 15 mL with water R.<\/p>\n

Ammonia and other bases<\/h3>\n

Dissolve 1.2 g in 20 mL of ethanol (96 per cent) R and add, dropwise with stirring, 4.5 mL of hydrochloric acid R.<\/p>\n

Evaporate to dryness on a water-bath, breaking up any resulting cake with a glass rod, and dry at 100-105 \u00b0C for 1 h. 1 g of the residue is equivalent to 0.4518 g of C2<\/sub>H8<\/sub>N2<\/sub>. Calculate the percentage content of C2H8N2: it does not vary by more than 0.5 from the percentage content determined in the assay.<\/p>\n

Iron (2.4.9)<\/h3>\n

Maximum 10 ppm, determined on solution S.<\/p>\n

Residue on evaporation<\/h4>\n

Maximum 0.3 per cent.<\/p>\n

Evaporate 5.00 g to dryness on a water-bath and dry at 100-105 \u00b0C for 1 h. The residue weighs a maximum of 15 mg.<\/p>\n

ASSAY<\/h2>\n

Place 25.0 mL of 1 M hydrochloric acid and 0.2 mL of methyl red mixed solution R in a flask. Add 0.600 g of the substance to be examined. Titrate with 1 M sodium hydroxide until the colour changes from violet-red to green.<\/p>\n

1 mL of 1 M hydrochloric acid is equivalent to 30.05 mg of C2<\/sub>H8<\/sub>N2<\/sub>.<\/p>\n

STORAGE<\/h2>\n

In an airtight container, protected from light.<\/p>\n","protected":false},"excerpt":{"rendered":"

(Ph. Eur. monograph 0716) C2H8N2\u00a0 \u00a0 \u00a0 \u00a060.1\u00a0 \u00a0 \u00a0 \u00a0 107-15-3 DEFINITION Ethane-1,2-diamine. Content 98.0 per cent to 101.0 per cent. CHARACTERS Appearance Clear, colourless or slightly yellow liquid, hygroscopic. Solubility Miscible with water and with anhydrous ethanol. On exposure to air, white fumes are evolved. On heating, it evaporates completely. IDENTIFICATION A. Relative…<\/p>\n","protected":false},"author":2,"featured_media":12681,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-12677","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\/12677","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\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/comments?post=12677"}],"version-history":[{"count":2,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/12677\/revisions"}],"predecessor-version":[{"id":12683,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/12677\/revisions\/12683"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/12681"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=12677"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=12677"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=12677"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}