Introduction:Basic information about Lynestrenol CAS 52-76-6, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Lynestrenol Basic information
| Product Name: | Lynestrenol |
| Synonyms: | 4-ESTREN-17-ALPHA-ETHYNYL-17-BETA-OL;4-ESTREN-17A-ETHINYL-17BETA-OL;19-nor-17-alpha-pregn-4-en-20-yn-17-l;ETHINYLESTRENOL;LYNOESTRENOL;LYNESTRENOL;(17-alpha)-19-norpregn-4-en-20-yn-17-ol;17-alpha-ethinyl-17-beta-hydroxyestr-4-ene |
| CAS: | 52-76-6 |
| MF: | C20H28O |
| MW: | 284.44 |
| EINECS: | 200-151-4 |
| Product Categories: | Steroids;Hormone;Intracellular receptor |
| Mol File: | 52-76-6.mol |
|
Lynestrenol Chemical Properties
| Melting point | 158°C |
| alpha | D -13° (chloroform) |
| Boiling point | 366.92°C (rough estimate) |
| density | 1.0083 (rough estimate) |
| refractive index | 1.4500 (estimate) |
| storage temp. | 2-8°C |
| solubility | Practically insoluble in water, soluble in acetone and in ethanol (96 per cent). |
| pka | 13.12±0.40(Predicted) |
| form | Solid |
| color | Crystals from MeOH |
| Merck | 14,5629 |
| Major Application | pharmaceutical (small molecule) |
| InChI | 1S/C20H28O/c1-3-20(21)13-11-18-17-9-8-14-6-4-5-7-15(14)16(17)10-12-19(18,20)2/h1,6,15-18,21H,4-5,7-13H2,2H3/t15-,16+,17+,18-,19-,20-/m0/s1 |
| InChIKey | YNVGQYHLRCDXFQ-XGXHKTLJSA-N |
| SMILES | O[C@@]1([C@@]2([C@H]([C@H]3[C@@H]([C@H]4CCCC=C4CC3)CC2)CC1)C)C#C |
| CAS DataBase Reference | 52-76-6 |
| EPA Substance Registry System | Lynestrenol (52-76-6) |
Safety Information
| RTECS | RC8964300 |
| HS Code | 2937230000 |
| Hazardous Substances Data | 52-76-6(Hazardous Substances Data) |
Lynestrenol Usage And Synthesis
| Chemical Properties | White or almost white, crystalline powder. |
| Uses | Lynestrenol is an orally available progestogen hormone used in contraception to avoid hereditary angiodema as well as in treatment of ischemic stroke. |
| Uses | Progestogen;Antioestrogen |
| Definition | ChEBI: Lynestrenol is a steroid. It derives from a hydride of an estrane. |
| Brand name | Anacycline 101;Anacylin 101;Anacylin 28;Ancylin;Athilyn;Endometril;Exluton (a);Fysiognens;Fysionorm;Gestrol;Lindiol 2.5;Lyn_ratiopharm;Lyn_ratiophram_sequenz;Lyndeol;Lyndile tt;Lyndiol e.;Lyndiolett;Lynoenstrenol;Lyn-ratiopharm;Mini pregnon;Minifol;Minilyn;Neo lyndiol;Neo-lindiol;Neo-lynobol;Nonovulet;Noracyclin 22;Normophasic;Novostat;Org 485-50;Orgaluton;Orgametrol;Ovamezzo;Ovanone;Ovanon-e;Ovariostat;Ovoresta micro;Ovostat-28;Ovostat-micro;Phasicon;Physiostat;Physistat;Pregnon-28;Restovar. |
| World Health Organization (WHO) | Lynestrenol, a synthetic progestogen, was introduced in the early1960s as a component in oral contraceptive preparations. In 1967, as a result ofnew regulations required by the United States Food and Drug Administration,lynestrenol was submitted to long-term toxicity studies and by the early 1970s itwas shown to be associated with an increased incidence of mammary tumours inbeagle bitches which led to its withdrawal by at least one regulatory authority.Subsequently the validity of the beagle bitch model as a predictor ofcarcinogenicity of steroid contraceptives has been contested by many nationalregulatory authorities and lynestrenol remains available in some countries forcontraceptive and other purposes.(Reference: (WHODI) WHO Drug Information, 1-3, 5-7, 1984) |
| Safety Profile | An experimental teratogen.Experimental reproductive effects. Human reproductiveeffects by ingestion and implant routes: menstrual cyclechanges or disorders, female fertility index, other fertilitychanges and effects on females. Questionable carcinoge |
Lynestrenol Preparation Products And Raw materials