| Name | Mestanolone |
|---|---|
| Synonyms | 17ALPHA-METHYLANDROSTAN-17BETA-OL-3-ONE 17ALPHA-METHYLDIHYDROTESTOSTERONE 17a-methyl-5a-androstan-17b-ol-3-one 17A-METHYLANDROSTAN-17B-OL-3-ONE 17a-methyldihydrotestosterone 17BETA-HYDROXY-17ALPHA-METHYL-5ALPHA-ANDROSTAN-3-ONE 17-HYDROXY-10,13,17-TRIMETHYLHEXADECAHYDROCYCLOPENTA[A]PHENANTHREN-3-ONE 3-KETO-17B-HYDROXY-17A-METHYL-5A-ANDROSTANE 5-ALPHA-ANDROSTAN-17-ALPHA-METHYL-17-BETA-OL-3-ONE 5ALPHA-ANDROSTANE-17ALPHA-METHYL-17BETA-OL-3-ONE MESTALINE MESTANOLONE METHYLANDROSTANOLONE METHYLDIHYDROTESTOSTERONE 17alpha-Methyl-17beta-hydroxy-5alpha-androstan-3-one 17alpha-Methyl-5alpha-dihydrotestosterone 17a-methylandrostan-17b-ol-3-one--dea*scheduleii 17-beta-hydroxy-17-methyl-5-alpha-androstan-3-on 17-beta-hydroxy-17-methyl-5-alpha-androstan-3-one 17beta-Hydroxy-17-methyl-5alpha-androstan-3-one |
| CAS NO | 521-11-9 |
| EINECS(EC#) | 208-302-6 |
| MDL Number | MFCD00021158 |
| Molecular Weight | 304.47 |
| Molecular Formula | C20H32O2 |
| Mestanolone Chemical Properties | |
|---|---|
| Melting point | 191 °C |
| density | 1.0279 (rough estimate) |
| Boiling point | 385.28°C (rough estimate) |
| storage temp | Controlled Substance, -20?C Freezer |
| CAS DataBase Reference | 521-11-9(CAS DataBase Reference) |
| refractive index | 1.4824 (estimate) |
| pka | 15.15±0.60(Predicted) |
| form | neat |
| InChIKey | WYZDXEKUWRCKOB-YDSAWKJFSA-N |
| Merck | 5915 |
| NIST Chemistry Reference | Mestanolone(521-11-9) |
| Safety Information | |
|---|---|
| Hazard Codes | Xn |
| Risk Statements | 40 |
| Safety Statements | 22-36 |
| WGK Germany | 3 |
| HS Code | 29372900 |
| RTECS | BV8064500 |
| Mestanolone Usage And Synthesis | |
|---|---|
| Description | Mestanolone is an orally active anabolic-androgenic steroid and the 17α-methylated derivative of dihydrotestosterone (DHT), which is an endogenous androgen sex steroid and hormone. It is capable of increasing testosterone benefit, suppressing estrogen effect, leaning muscle tissue, increasing strength as well as improving drive and focus. It is mainly used for the treatment of male hypogonadism and decreased sperm infertility. |
| Chemical Properties | White Solid |
| Uses | Anabolic steroid. Controlled substance. |
| Purification Methods | Dissolve mestanolone in Et2O, wash it with N NaOH, H2O, dry it (Na2SO4), evaporate and recrystallise it from EtOAc. The semicarbazone has m 235-236o (from EtOH). [Ruzicka et al. Helv Chim Acta 18 1487 1935.] |
| Mestanolone Preparation Products And Raw materials | |
|---|---|
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