{"id":14018,"date":"2025-10-14T15:28:44","date_gmt":"2025-10-14T08:28:44","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=14018"},"modified":"2025-10-14T15:28:44","modified_gmt":"2025-10-14T08:28:44","slug":"gestodene","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/gestodene\/","title":{"rendered":"Gestodene"},"content":{"rendered":"

(Ph. Eur. monograph 1726)<\/p>\n

C_{21<\/sub>H_{26<\/sub>O_{2<\/sub>\u00a0 \u00a0 \u00a0 \u00a0310.4\u00a0 \u00a0 \u00a0 \u00a060282-87-3<\/p>\n}}}

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

Progestogen.<\/p>\n

DEFINITION<\/h2>\n
13-Ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-4,15-dien-20-yn-3-one.<\/p>\n
Content<\/h3>\n
97.5 per cent to 102.0 per cent (dried substance).<\/p>\n
CHARACTERS<\/h2>\n
Appearance<\/h3>\n
White or yellowish, crystalline powder.<\/p>\n
Solubility<\/h3>\n
Practically insoluble in water, freely soluble in methylene chloride, soluble in methanol, sparingly soluble in ethanol (96 per cent).<\/p>\n
It shows polymorphism (5.9).<\/p>\n
IDENTIFICATION<\/h2>\n
A. Specific optical rotation (see Tests).<\/p>\n
B. Infrared absorption spectrophotometry (2.2.24).<\/p>\n
Comparison: gestodene CRS.<\/p>\n
If the spectra obtained in the solid state show differences, dissolve the substance to be examined and the reference substance separately in acetone R, evaporate to dryness and record new spectra using the residues.<\/p>\n
TESTS<\/h2>\n
Specific optical rotation (2.2.7)<\/h3>\n
-188 to -198 (dried substance).<\/p>\n
Dissolve 0.100 g in methanol R and dilute to 10.0 mL with the same solvent.<\/p>\n
Related substances<\/h3>\n
Liquid chromatography (2.2.29).<\/p>\n
Solvent mixture: acetonitrile R1, water R (50:50 V\/V).<\/p>\n
Test solution (a): Dissolve 30.0 mg of the substance to be examined in 5 mL of acetonitrile R1 and dilute to 10.0 mL with water R.<\/p>\n
Test solution (b): Dilute 1.0 mL of test solution (a) to 10.0 mL with the solvent mixture.<\/p>\n
Reference solution (a): Dissolve 3 mg of gestodene for system suitability CRS (containing impurities A, B, C and L) in 0.5 mL of acetonitrile R1 and dilute to 1.0 mL with water R.<\/p>\n
Reference solution (b): Dilute 1.0 mL of test solution (a) to 100.0 mL with the solvent mixture. Dilute 1.0 mL of this solution to 10.0 mL with the solvent mixture.<\/p>\n
Reference solution (c): Dissolve 30.0 mg of gestodene CRS in 5 mL of acetonitrile R1 and dilute to 10.0 mL with water R. Dilute 1.0 mL of this solution to 10.0 mL with the solvent mixture.<\/p>\n
Reference solution (d): Dissolve the contents of a vial of gestodene impurity I CRS in 1.0 mL of the solvent mixture.<\/p>\n
Column:<\/p>\n
\u2014 size: l = 0.15 m, \u00d8 = 4.6 mm;<\/p>\n
\u2014 stationary phase: spherical end-capped octylsilyl silica gel for chromatography R (3.5 \u03bcm).<\/p>\n
Mobile phase:<\/p>\n
\u2014 mobile phase A: water R;<\/p>\n
\u2014 mobile phase B: acetonitrile R1;<\/p>\n\n\n\n\n\n\n\n
Time<\/strong>
\n(min)<\/strong><\/td>\n Mobile phase A<\/strong>
\n(per cent V\/V)<\/strong><\/td>\n Mobile phase B<\/strong>
\n(per cent V\/V)<\/strong><\/td>\n<\/tr>\n
0 – 2<\/td>\n 62<\/td>\n 38<\/td>\n<\/tr>\n
2 – 20<\/td>\n 62 \u2192 58<\/td>\n 38 \u2192 42<\/td>\n<\/tr>\n
20 – 24<\/td>\n 58 \u2192 30<\/td>\n 42 \u2192 70<\/td>\n<\/tr>\n
24 – 32<\/td>\n 30<\/td>\n 70<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
Flow rate: 1.0 mL\/min.<\/p>\n
Detection: Spectrophotometer at 205 nm and at 254 nm.<\/p>\n
Injection: 10 \u03bcL of test solution (a) and reference solutions (a), (b) and (d).<\/p>\n
Identification of impurities: Use the chromatogram supplied with gestodene for system suitability CRS and the chromatogram obtained with reference solution (a) to identify the peaks due to impurities A, B, C and L; use the chromatogram obtained with reference solution (d) to identify the peak due to impurity I.<\/p>\n
Relative retention: With reference to gestodene (retention time = about 12.5 min): impurity A = about 0.9; impurity C = about 1.1; impurity I = about 1.2; impurity L = about 1.46; impurity B = about 1.53.<\/p>\n
System suitability: Reference solution (a):<\/p>\n
\u2014 resolution: minimum 2.0 between the peaks due to impurity A and gestodene.<\/p>\n
Limits:<\/p>\n
\u2014 correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity A = 2.2; impurity I = 1.3;<\/p>\n
\u2014 impurity A at 254 nm: 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 impurity B at 205 nm: not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (0.2 per cent);<\/p>\n
\u2014 impurity C at 254 nm: not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (0.2 per cent);<\/p>\n
\u2014 impurities I, L at 205 nm: for each impurity, not more than 1.5 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.15 per cent);<\/p>\n
\u2014 unspecified impurities at 254 nm: for each impurity, not more than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.10 per cent);<\/p>\n
\u2014 total at 254 nm: not more than 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 at 254 nm: 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
Maximum 0.5 per cent, determined on 1.000 g by drying in an oven at 105 \u00b0C for 3 h.<\/p>\n
ASSAY<\/h2>\n
Liquid chromatography (2.2.29) as described in the test for related substances with the following modifications.<\/p>\n
Injection: Test solution (b) and reference solution (c).<\/p>\n
Detection: Spectrophotometer at 254 nm.<\/p>\n
Calculate the percentage content of C_{21<\/sub>H_{26<\/sub>O_{2<\/sub> from the declared content of gestodene CRS.<\/p>\n}}}
IMPURITIES<\/h2>\n
Specified impurities A, B, C, I, L.<\/p>\n
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)<\/p>\n
\u2014 at 205 nm: G, J, K;<\/p>\n
\u2014 at 254 nm: D, E, F, H.<\/p>\n
$\"Gestodene\"$ <\/p>\n
A. 13-ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-4,6,15-trien-20-yn-3-one (\u03946-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
B. 13-ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-5(10),15-dien-20-yn-3-one (\u03945(10)-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
C. 13-ethyl-17-hydroxy-2\u03b1-(1-hydroxy-1-methylethyl)-18,19-dinor-17\u03b1-pregna-4,15-dien-20-yn-3-one (2-isopropanol-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
D. 13-ethyl-6\u03b2,17-dihydroxy-18,19-dinor-17\u03b1-pregna-4,15-dien-20-yn-3-one (6\u03b2-hydroxy-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
E. 13-ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-4,15-dien-20-yne-3,6-dione (6-keto-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
F. 13-ethyl-17-hydroxy-3-oxo-18,19-dinor-17\u03b1-pregn-4-en-20-yn-15\u03b1-yl acetate (15\u03b1-acetoxy-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
G. 13-ethyl-3-methoxy-18,19-dinor-17\u03b1-pregna-1,3,5(10),15-tetraen-20-yn-17-o1 (A-aromatic-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
H. 13-ethyl-3-ethynyl-18,19-dinor-17\u03b1-pregna-3,5,15-trien-20-yn-17-o1 (diethynyl-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
I. 13-ethyl-17-hydroxy-5-methoxy-18,19-dinor-5\u03b1,17\u03b1-pregn-15-en-20-yn-3-one (5-methoxy-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
J. 13-ethylspiro(18,19-dinor-17\u03b1-pregna-5,15-dien-20-yne-3,2\u2032-[1,3]dioxolan)-17-ol and 13-ethylspiro(18,19-dinor-17\u03b1-pregna-5(10),15-dien-20-yne-3,2\u2032-[1,3]dioxolan)-17-ol (gestodene ketal),<\/p>\n
$\"Gestodene\"$ <\/p>\n
K. 13-ethyl-3,17-dihydroxy-18,19-dinor-17\u03b1-pregna-1,3,5(10),15-tetraen-20-yn-6-one (aromatic 6-keto-gestodene),<\/p>\n
$\"Gestodene\"$ <\/p>\n
L. 13-ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-5,15-dien-20-yn-3-one (\u03945(6)-gestodene).<\/p>\n","protected":false},"excerpt":{"rendered":"
(Ph. Eur. monograph 1726) C21H26O2\u00a0 \u00a0 \u00a0 \u00a0310.4\u00a0 \u00a0 \u00a0 \u00a060282-87-3 Action and use Progestogen. DEFINITION 13-Ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-4,15-dien-20-yn-3-one. Content 97.5 per cent to 102.0 per cent (dried substance). CHARACTERS Appearance White or yellowish, crystalline powder. Solubility Practically insoluble in water, freely soluble in methylene chloride, soluble in methanol, sparingly soluble in ethanol (96 per cent). It…<\/p>\n","protected":false},"author":2,"featured_media":14061,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-14018","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\/14018","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=14018"}],"version-history":[{"count":2,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/14018\/revisions"}],"predecessor-version":[{"id":14077,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/14018\/revisions\/14077"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/14061"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=14018"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=14018"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=14018"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}

Time<\/strong> \n(min)<\/strong><\/td>\n	Mobile phase A<\/strong> \n(per cent V\/V)<\/strong><\/td>\n	Mobile phase B<\/strong> \n(per cent V\/V)<\/strong><\/td>\n<\/tr>\n
0 – 2<\/td>\n	62<\/td>\n	38<\/td>\n<\/tr>\n
2 – 20<\/td>\n	62 \u2192 58<\/td>\n	38 \u2192 42<\/td>\n<\/tr>\n
20 – 24<\/td>\n	58 \u2192 30<\/td>\n	42 \u2192 70<\/td>\n<\/tr>\n
24 – 32<\/td>\n	30<\/td>\n	70<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n Flow rate: 1.0 mL\/min.<\/p>\n Detection: Spectrophotometer at 205 nm and at 254 nm.<\/p>\n Injection: 10 \u03bcL of test solution (a) and reference solutions (a), (b) and (d).<\/p>\n Identification of impurities: Use the chromatogram supplied with gestodene for system suitability CRS and the chromatogram obtained with reference solution (a) to identify the peaks due to impurities A, B, C and L; use the chromatogram obtained with reference solution (d) to identify the peak due to impurity I.<\/p>\n Relative retention: With reference to gestodene (retention time = about 12.5 min): impurity A = about 0.9; impurity C = about 1.1; impurity I = about 1.2; impurity L = about 1.46; impurity B = about 1.53.<\/p>\n System suitability: Reference solution (a):<\/p>\n \u2014 resolution: minimum 2.0 between the peaks due to impurity A and gestodene.<\/p>\n Limits:<\/p>\n \u2014 correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity A = 2.2; impurity I = 1.3;<\/p>\n \u2014 impurity A at 254 nm: 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 impurity B at 205 nm: not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (0.2 per cent);<\/p>\n \u2014 impurity C at 254 nm: not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (0.2 per cent);<\/p>\n \u2014 impurities I, L at 205 nm: for each impurity, not more than 1.5 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.15 per cent);<\/p>\n \u2014 unspecified impurities at 254 nm: for each impurity, not more than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.10 per cent);<\/p>\n \u2014 total at 254 nm: not more than 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 at 254 nm: 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 Maximum 0.5 per cent, determined on 1.000 g by drying in an oven at 105 \u00b0C for 3 h.<\/p>\n ASSAY<\/h2>\n Liquid chromatography (2.2.29) as described in the test for related substances with the following modifications.<\/p>\n Injection: Test solution (b) and reference solution (c).<\/p>\n Detection: Spectrophotometer at 254 nm.<\/p>\n Calculate the percentage content of C_{21<\/sub>H_{26<\/sub>O_{2<\/sub> from the declared content of gestodene CRS.<\/p>\n}}} IMPURITIES<\/h2>\n Specified impurities A, B, C, I, L.<\/p>\n 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)<\/p>\n \u2014 at 205 nm: G, J, K;<\/p>\n \u2014 at 254 nm: D, E, F, H.<\/p>\n $\"Gestodene\"$ <\/p>\n A. 13-ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-4,6,15-trien-20-yn-3-one (\u03946-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n B. 13-ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-5(10),15-dien-20-yn-3-one (\u03945(10)-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n C. 13-ethyl-17-hydroxy-2\u03b1-(1-hydroxy-1-methylethyl)-18,19-dinor-17\u03b1-pregna-4,15-dien-20-yn-3-one (2-isopropanol-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n D. 13-ethyl-6\u03b2,17-dihydroxy-18,19-dinor-17\u03b1-pregna-4,15-dien-20-yn-3-one (6\u03b2-hydroxy-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n E. 13-ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-4,15-dien-20-yne-3,6-dione (6-keto-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n F. 13-ethyl-17-hydroxy-3-oxo-18,19-dinor-17\u03b1-pregn-4-en-20-yn-15\u03b1-yl acetate (15\u03b1-acetoxy-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n G. 13-ethyl-3-methoxy-18,19-dinor-17\u03b1-pregna-1,3,5(10),15-tetraen-20-yn-17-o1 (A-aromatic-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n H. 13-ethyl-3-ethynyl-18,19-dinor-17\u03b1-pregna-3,5,15-trien-20-yn-17-o1 (diethynyl-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n I. 13-ethyl-17-hydroxy-5-methoxy-18,19-dinor-5\u03b1,17\u03b1-pregn-15-en-20-yn-3-one (5-methoxy-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n J. 13-ethylspiro(18,19-dinor-17\u03b1-pregna-5,15-dien-20-yne-3,2\u2032-[1,3]dioxolan)-17-ol and 13-ethylspiro(18,19-dinor-17\u03b1-pregna-5(10),15-dien-20-yne-3,2\u2032-[1,3]dioxolan)-17-ol (gestodene ketal),<\/p>\n $\"Gestodene\"$ <\/p>\n K. 13-ethyl-3,17-dihydroxy-18,19-dinor-17\u03b1-pregna-1,3,5(10),15-tetraen-20-yn-6-one (aromatic 6-keto-gestodene),<\/p>\n $\"Gestodene\"$ <\/p>\n L. 13-ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-5,15-dien-20-yn-3-one (\u03945(6)-gestodene).<\/p>\n","protected":false},"excerpt":{"rendered":" (Ph. Eur. monograph 1726) C21H26O2\u00a0 \u00a0 \u00a0 \u00a0310.4\u00a0 \u00a0 \u00a0 \u00a060282-87-3 Action and use Progestogen. DEFINITION 13-Ethyl-17-hydroxy-18,19-dinor-17\u03b1-pregna-4,15-dien-20-yn-3-one. Content 97.5 per cent to 102.0 per cent (dried substance). CHARACTERS Appearance White or yellowish, crystalline powder. Solubility Practically insoluble in water, freely soluble in methylene chloride, soluble in methanol, sparingly soluble in ethanol (96 per cent). It…<\/p>\n","protected":false},"author":2,"featured_media":14061,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-14018","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\/14018","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=14018"}],"version-history":[{"count":2,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/14018\/revisions"}],"predecessor-version":[{"id":14077,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/14018\/revisions\/14077"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/14061"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=14018"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=14018"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=14018"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}

Content<\/h3>\n97.5 per cent to 102.0 per cent (dried substance).<\/p>\n

CHARACTERS<\/h2>\n

Appearance<\/h3>\nWhite or yellowish, crystalline powder.<\/p>\n

Solubility<\/h3>\nPractically insoluble in water, freely soluble in methylene chloride, soluble in methanol, sparingly soluble in ethanol (96 per cent).<\/p>\nIt shows polymorphism (5.9).<\/p>\n

TESTS<\/h2>\n

Specific optical rotation (2.2.7)<\/h3>\n-188 to -198 (dried substance).<\/p>\nDissolve 0.100 g in methanol R and dilute to 10.0 mL with the same solvent.<\/p>\n

Loss on drying (2.2.32)<\/h4>\nMaximum 0.5 per cent, determined on 1.000 g by drying in an oven at 105 \u00b0C for 3 h.<\/p>\n

Content<\/h3>\n
97.5 per cent to 102.0 per cent (dried substance).<\/p>\n

Appearance<\/h3>\n
White or yellowish, crystalline powder.<\/p>\n

Solubility<\/h3>\n
Practically insoluble in water, freely soluble in methylene chloride, soluble in methanol, sparingly soluble in ethanol (96 per cent).<\/p>\n
It shows polymorphism (5.9).<\/p>\n

Specific optical rotation (2.2.7)<\/h3>\n
-188 to -198 (dried substance).<\/p>\n
Dissolve 0.100 g in methanol R and dilute to 10.0 mL with the same solvent.<\/p>\n

Loss on drying (2.2.32)<\/h4>\n
Maximum 0.5 per cent, determined on 1.000 g by drying in an oven at 105 \u00b0C for 3 h.<\/p>\n