| Identification | More | [Name]
Androsterone | [CAS]
53-41-8 | [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 | [EINECS(EC#)]
200-173-4 | [Molecular Formula]
C19H30O2 | [MDL Number]
MFCD01317504 | [Molecular Weight]
290.44 | [MOL File]
53-41-8.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light beige crystalline powder | [Melting point ]
181-184 °C(lit.)
| [alpha ]
96 º (c=1, C2H5OH) | [Boiling point ]
372.52°C (rough estimate) | [density ]
1.0320 (rough estimate) | [refractive index ]
1.4709 (estimate) | [storage temp. ]
−20°C
| [solubility ]
Acetonitrile: 1 mg/ml; Ethanol: 1 mg/ml; Methanol: 1 mg/ml | [form ]
neat | [pka]
15.14±0.60(Predicted) | [Water Solubility ]
11.5mg/L(23.5 ºC) | [Merck ]
13,645 | [BRN ]
2217626 | [CAS DataBase Reference]
53-41-8(CAS DataBase Reference) | [NIST Chemistry Reference]
Androsterone(53-41-8) | [EPA Substance Registry System]
53-41-8(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
36/37/38-43 | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
BV8053000
| [F ]
3-21 | [HS Code ]
29379000 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light beige crystalline powder | [Uses]
Antihypertensor | [Uses]
It was isolated from male urine after removed of the phenolic estrogen fraction. | [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). [Ruzicka Helv Chim Acta 17 1389 1934, Marker J Am Chem Soc 57 1755 1935, Gnds & Orr J Chem Soc Chem Commun 1239 1982, Beilstein 8 IV 462.] |
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