| Nom |
2'H-Androst-2-eno[3,2-c]pyrazol-17-ol,17-méthyl-, (5a,17b)-? |
| Synonymes |
2'H-5a-Androst-2-eno[3,2-c]pyrazol-17b-ol, 17-méthyl- (8CI)?; Cyclopenta[7,8]phénanthro[2,3-c]pyrazol-1-ol,1,2,3,3a,3b,4,5,5a,6,7,10,10a,10b,11,12,12a-hexadécahydro-1,10a,12a-triméthyl-(6CI,7CI)?; 17-méthyl-5a-androstano[3,2-c]pyrazol-17b-ol?; 17-méthyl-pyrazolo[4',3'?:2,3]-5a-androstan-17b-ol?; 17a-méthyl-17b-hydroxy-5a-androstano(3,2-c)pyrazole?; 17b-hydroxy-17-méthyl-5a-androstano[3,2-c]pyrazole?; 17b-hydroxy-17a-méthyl-5a-androstano[3,2-c]pyrazole?; Anabol?; Androstanazol?; Androstanazole?; l’androstanazolestanazol?; Estazol?; NSC233046?; Stanabolique?; le stanazolol?; le stanozolol?; Stromba?; Strombaject?; Tevabolin?; Victoire 14833?; Winstro?de?; Winstrol?; Dép?t de Winstrol?; Winstrol V |
| Nom anglais |
2'H-Androst-2-eno[3,2-c]pyrazol-17-ol,17-methyl-, (5a,17b)-;2'H-5a-Androst-2-eno[3,2-c]pyrazol-17b-ol, 17-methyl- (8CI); Cyclopenta[7,8]phenanthro[2,3-c]pyrazol-1-ol,1,2,3,3a,3b,4,5,5a,6,7,10,10a,10b,11,12,12a-hexadecahydro-1,10a,12a-trimethyl-(6CI,7CI); 17-Methyl-5a-androstano[3,2-c]pyrazol-17b-ol; 17-Methyl-pyrazolo[4',3':2,3]-5a-androstan-17b-ol; 17a-Methyl-17b-hydroxy-5a-androstano(3,2-c)pyrazole; 17b-Hydroxy-17-methyl-5a-androstano[3,2-c]pyrazole; 17b-Hydroxy-17a-methyl-5a-androstano[3,2-c]pyrazole; Anabol; Androstanazol; Androstanazole; Androstanazolestanazol; Estazol; NSC233046; Stanabolic; Stanazolol; Stanozolol; Stromba; Strombaject; Tevabolin; Win 14833; Winstroid; Winstrol; Winstrol Depot; Winstrol V |
| Formule moléculaire |
C21H32N2O |
| Poids Moléculaire |
328.55 |
| Numéro de registre CAS |
302-96-5 |
| Structure moléculaire |
![302-96-5 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol,17-méthyl-, (5a,17b)-?](https://images-a.chemnet.com/suppliers/chembase/cas178/302-96-5.jpg)
|
| Densité |
1.129g/cm3 |
| Point d'ébullition |
490.8°Cat760mmHg |
| Point d'éclair |
250.7°C |
| Les symboles de danger |
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| Codes des risques |
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| Description de sécurité |
x." target="_blank">Human systemic effects by ingestion: jaundice. An experimental teratogen. Other experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx.:;
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