| Name | Androsterone |
|---|---|
| Synonyms | 3A-HYDROXY-5A-ANDROSTAN-17-ONE 3ALPHA-HYDROXY-5ALPHA-ANDROSTAN-17-ONE 3-ALPHA-HYDROXYETIOALLOCHOLAN-17-ONE 5A-ANDROSTAN-3A-OL-17-ONE 5ALPHA-ANDROSTAN-3ALPHA-OL-17-ONE 5ALPHA-ANDROSTAN-3ALPHA-OL-17-ONE-16,16-D2 androstan-3a-ol-17-one ANDROSTERINE ANDROSTEROLONE ANDROSTERONE CIS-ANDROSTERONE 3-alpha-hydroxy-17-androstanone 3alpha-Hydroxy-17-androstanone 3-alpha-hydroxy-5-alpha-androstan-17-on 3-Epihydroxyetioallocholan-17-one 3-hydroxy-,(3-alpha,5-alpha)-androstan-17-on 3-hydroxy-,(3alpha,5alpha)-androstan-17-on 5alpha-Androstan-17-one, 3alpha-hydroxy- 5alpha-Androstane-3alpha-ol-17-one 5alpha-Androsterone |
| CAS NO | 53-41-8 |
| MDL Number | MFCD01317504 |
| Molecular Weight | 290.44 |
| Molecular Formula | C19H30O2 |
| Androsterone Chemical Properties | |
|---|---|
| Melting point | 181-184 °C(lit.) |
| alpha | 96 º (c=1, C2H5OH) |
| density | 1.0320 (rough estimate) |
| Boiling poin | 372.52°C (rough estimate) |
| storage temp | −20°C |
| CAS DataBase Reference | 53-41-8(CAS DataBase Reference) |
| refractive index | 1.4709 (estimate) |
| pka | 15.14±0.60(Predicted) |
| form | neat |
| Water Solubility | 11.5mg/L(23.5 ºC) |
| Merck | 13,645 |
| NIST Chemistry Reference | Androsterone(53-41-8) |
| BRN | 2217626 |
| EPA Substance Registry System | Androsterone (53-41-8) |
| Safety Information | |
|---|---|
| Hazard Codes | Xi |
| Risk Statements | 36/37/38-43 |
| Safety Statements | 22-24/25-36/37-26 |
| RTECS | BV8053000 |
| WGK Germany | 3 |
| HS Code | 29379000 |
| F | 3-21 |
| Androsterone Usage And Synthesis | |
|---|---|
| Chemical Properties | white to light beige crystalline powder |
| Uses | It was isolated from male urine after removed of the phenolic estrogen fraction. |
| Uses | Antihypertensor |
| Definition | ChEBI: An androstanoid that is 5alpha-androstane having a hydroxy substituent at the 3alpha-position and an oxo group at the 17-position. It is a metabolite of dehydroepiandrosterone |
| Purification Methods | Crystallise androsterone from Me2CO/Et2O or Me2CO and sublime it in high vacuum. The acetate [1164-95-0] crystallises from Et2O, Me2CO/Et2O or aqueous EtOH and sublimes in high vacuum with m 165-166o, [] D 25 +87o (c 2, EtOH). |
| Package method |
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