| Nombre del producto |
2'H-Androst-2-eno[3,2-c]pyrazol-17-ol,17-metil-, (5a,17b)- |
| Sinónimos |
2'H-5a-Androst-2-eno[3,2-c]pirazol-17b-ol, 17-metil- (8CI); Ciclopenta[7,8]fenantro[2,3-c]pirazol-1-ol,1,2,3,3a,3b,4,5,5a,6,7,10,10a,10b,11,12,12a-hexadecahidro-1,10a,12a-trimetil-(6CI,7CI); 17-metil-5a-androstano[3,2-c]pirazol-17b-ol; 17-metil-pirazolo[4',3':2,3]-5a-androstan-17b-ol; 17a-metil-17b-hidroxi-5a-androstano(3,2-c)pirazol; 17b-hidroxi-17-metil-5a-androstano[3,2-c]pirazol; 17b-hidroxi-17a-metil-5a-androstano[3,2-c]pirazol; Anabol; Androstanazol; Androstanazol; Androstanazolestanazol; Estazol; NSC233046; Estanabólico; Stanazolol; Estanozolol; Stromba; Strombaject; Tevabolin; Gana 14833; Winstroid; Winstrol; Depósito de Winstrol; Winstrol V |
| Nombre en inglés |
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 |
| Fórmula molecular |
C21H32N2O |
| Peso Molecular |
328.55 |
| Número de registro CAS |
302-96-5 |
| Estructura Molecular |
![302-96-5 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol,17-metil-, (5a,17b)-](https://images-a.chemnet.com/suppliers/chembase/cas178/302-96-5.jpg)
|
| Densidad |
1.129g/cm3 |
| Punto de ebullición |
490.8°Cat760mmHg |
| Punto de inflamación |
250.7°C |
| Símbolos de Peligro |
|
| Códigos de Riesgos |
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| Descripción de Seguridad |
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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