Androsterone
Androsterone Basic information
- Product Name:
- Androsterone
- Synonyms:
-
- 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-10,13-dimethylperhydrocyclopenta[a]phenanthren-17-one
- ANDROSTERONE,98%(BULK
- (3R,5S,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one
- CAS:
- 53-41-8
- MF:
- C19H30O2
- MW:
- 290.44
- EINECS:
- 200-173-4
- Product Categories:
-
- Steroids & Hormones - 13C & 2H
- Steroids
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Mol File:
- 53-41-8.mol
Androsterone Chemical Properties
- 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
- 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
- Androsterone (53-41-8)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-43
- Safety Statements
- 22-24/25-36/37-26
- WGK Germany
- 3
- RTECS
- BV8053000
- F
- 3-21
- HS Code
- 29379000
MSDS
- Language:English Provider:Androstan-3a-ol-17-one
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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
Uses
Typical urinary 17-oxosteroid, formed by the metabolic reduction of testosterone. Less potent than testosterone.
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.]
AndrosteroneSupplier
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Androsterone(53-41-8)Related Product Information
- Androstenedione
- Diphenolic acid
- 4-(Diethylamino)salicylaldehyde
- Pralmorelin
- DL-α-Tocopherol
- 5-Chlorovaleric acid
- CHLOROPHOSPHONAZO III
- Androsterone-2,2,4,4-d4
- d4-Androsterone
- Androsterone-[d4] Glucuronide Sodium Salt
- ANDROSTERONE GLUCURONIDE CRYSTALLINE
- Epiandrosterone acetate
- Metandienone
- Dehydroepiandrosterone
- Epiandrosterone
- Dehydroepiandrosterone acetate
- 7-alpha-Hydroxydehydroepiandrosterone
- 7-Keto-dehydroepiandrosterone