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 Structure
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
pka15.14±0.60(Predicted)
form neat
Water Solubility 11.5mg/L(23.5 ºC)
Merck 13,645
BRN 2217626
CAS DataBase Reference53-41-8(CAS DataBase Reference)
NIST Chemistry ReferenceAndrosterone(53-41-8)
EPA Substance Registry SystemAndrosterone (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
3-21
HS Code 29379000
MSDS Information
ProviderLanguage
Androstan-3a-ol-17-one English
SigmaAldrich English
ACROS English
Androsterone Usage And Synthesis
Chemical Propertieswhite to light beige crystalline powder
UsesIt was isolated from male urine after removed of the phenolic estrogen fraction.
UsesAntihypertensor
UsesTypical urinary 17-oxosteroid, formed by the metabolic reduction of testosterone. Less potent than testosterone.
DefinitionChEBI: 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 MethodsCrystallise 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.]
Androsterone Preparation Products And Raw materials
Preparation Products5alpha-Androstan-3alpha,17beta-diol 3-acetate-->5ALPHA-Androstan-3ALPHA-ol
Metandienone Pralmorelin Dehydroepiandrosterone ANDROSTERONE TOSYLATE 5-ALPHA-ANDROSTAN-3-ALPHA, 11-BETA-DIOL-17-ONE 3-ACETATE 5-ALPHA-ANDROSTAN-3,17-DIONE 3-DIMETHYL KETAL Epiandrosterone acetate ETHYLENEDIAMINE TETRAKIS(PROPOXYLATE-BLOCK-ETHOXYLATE) TETROL Diphenolic acid 4-(Diethylamino)salicylaldehyde 11-BETA-HYDROXYANDROSTERONE 11-KETOANDROSTERONE BETA-D-GLUCURONIDE 11-KETOANDROSTERONE 16α-Hydroxy Androsterone ANDROSTERONE SULFATE SODIUM CRYSTALLINE ANDROSTERONE ACETATE,androsterone acetate crystalline,ANDROSTERONE 3-ACETATE VETRANAL, 100 MG,ANDROSTERONE 3-ACETATE Androstenedione 5ALPHA-ANDROSTAN-3ALPHA,11ALPHA-DIOL-17-ONE

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