Androst-4-en-3,11,17-trion

Adrenosterone Struktur
382-45-6
CAS-Nr.
382-45-6
Bezeichnung:
Androst-4-en-3,11,17-trion
Englisch Name:
Adrenosterone
Synonyma:
11-KETOANDROSTENEDIONE;ANDROST-4-ENE-3,11,17-TRIONE;Nsc12166;s substance G;ADRENOSTERONE;Andrenosterone;Reichstein'REICHSTEIN'S 'G';(+)-ADRENOSTERONE;Adrenosterone >
CBNumber:
CB1765508
Summenformel:
C19H24O3
Molgewicht:
300.39
MOL-Datei:
382-45-6.mol

Androst-4-en-3,11,17-trion Eigenschaften

Schmelzpunkt:
219-222 °C(lit.)
alpha 
300 º (c=1 in chloroform)
Siedepunkt:
381.62°C (rough estimate)
Dichte
1.1381 (rough estimate)
Brechungsindex
290 ° (C=0.2, EtOH)
storage temp. 
Sealed in dry,Room Temperature
Löslichkeit
Chloroform (Slightly), Ethyl Acetate (Slightly)
Aggregatzustand
Solid
Farbe
White to Off-White
Optische Rotation
[α]20/D +300°, c = 1 in chloroform
Wasserlöslichkeit
98.49mg/L(23.5 ºC)
Merck 
14,176
InChIKey
RZRPTBIGEANTGU-IRIMSJTPSA-N
CAS Datenbank
382-45-6(CAS DataBase Reference)
NIST chemische Informationen
Androst-4-ene-3,11,17-trione(382-45-6)

Sicherheit

WGK Germany  3

Androst-4-en-3,11,17-trion Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

Off-White to Pale Yellow Solid

Verwenden

Androstenedione is a steroid hormone. It is used to make medicine. Androstenedione is used to increase the production of the hormone testosterone to enhance athletic performance, increase energy, keep red blood cells healthy, enhance recovery and growth from exercise, and increase sexual desire and performance.

benefits

Adrenosterone is sold as a dietary supplement since 2007 as a fat loss and muscle gaining supplement. It is thought to be a competitive selective 11βHSD1 inhibitor, which is responsible for activation of cortisol from cortisone. Thus preventing muscle breakdown, and contributing to a majority of its effects.

läuterung methode

Dissolve adrenosterone i n Me2CO, decolorise it with charcoal, filter, add H2O, Me2CO evaporate and the solid is recrystallised from aqueous EtOH. Also recrystallise it from Et2O or Et2O/pentane and dry it at 110o/0.1mm for 2hours. It can be sublimed under high vacuum. [Reichstein Helv Chim Acta 20 953, 979 1937, Mason et al. J Biol Chem 116 267 1936, Beilstein 7 III 4601.]

Androst-4-en-3,11,17-trion Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Androst-4-en-3,11,17-trion Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 163)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
career henan chemical co
+86-0371-86658258
factory@coreychem.com China 29780 58
TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000
marketing@targetmol.com United States 32431 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +86-189 4982 3763
sales@tnjchem.com China 34526 58
Wuhan Aoliqisi New Material Technology Co., Ltd.
+86-13545906766; 13545906766
sales@whaop.com China 257 58
RongNa Biotechnology Co.,Ltd
+86-86-13583358881 +8618560316533
Brad@rongnabiotech.com China 3374 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 17705817739
info@dycnchem.com China 52693 58
Dingwang Technology (Wuhan) Co., Ltd.
+undefined-27-2786652399 +undefined13627115097
market02@senwayer.com China 886 58
HANGZHOU LEAP CHEM CO., LTD.
+86-571-87711850 +86-15355479329
market18@leapchem.com China 43303 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+86-18621343501
product@acmec-e.com China 33301 58
Shandong Hanjiang Chemical Co., Ltd
+86-0533-2066820 +8618369939125
hanson@sdhanjiang.com China 998 58

382-45-6(Androst-4-en-3,11,17-trion)Verwandte Suche:


  • Nsc12166
  • ADRENOSTERONE (11-OXO)
  • 11-Keto-4-androstene-3,17-dione
  • 11-Oxo-4-androstene-3,17-dione
  • 4-Androstene-3,11,17-trione Reichstein's Substance G
  • Reichstein&apos
  • s substance G
  • (8S,9S,10R,13S,14S)-10,13-dimethyl-1,2,6,7,8,9,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,11,17-trione
  • REICHSTEIN'S SUBSTANCE G
  • REICHSTEIN'S SUBSTANCE 'G'
  • REICHSTEIN'S ''G''
  • REICHSTEIN'S 'G'
  • 11-Oxo/Adrenosterone
  • sodium (6R,7R)-3-(acetyloxymethyl)-7-[(2-cyano-1-oxo-2-phenylethyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
  • (+)-ADRENOSTERONE
  • Adrenosterone ((+)-Adrenosterone)
  • 4-ANDROSTENE-3,11,17-TRIONE
  • 4-ANDROSTEN-3,11,17-TRIONE
  • ADRENOSTERONE
  • 11-Oxy-4-androstenedione
  • Adrenosterone;Androst-4-ene-3,11,17-trione;Reichstein's substance G
  • 11-Ketoandrostenedione, 4-Androstene-3,11,17-trione, Androst-4-ene-3,11,17-trione, Reichsteins substance G
  • (8β,9α,10β,14α,13β)-Androsta-4-ene-3,11,17-trione
  • Andrenosterone
  • 11-OXO Prohormones Adrenosterone
  • Androsten-3,11,17-trione (Solution)
  • Adrenosterone >
  • Androsten-3,11,17-trione
  • 11-oxoandrostenedione
  • (8S,9S,10R,13S,14S)-10,13-Dimethyl-7,8,10,12,13,14,15,16-octahydro-1H-cyclopenta[a]phenanthrene-3,11,17(2H,6H,9H)-trione
  • 11-Ketoandrostenedione-[2.3.4-13C3]
  • Adrenosterone, 10 mM in DMSO
  • 1-D,3,4-13C2-Adrenosterone
  • 11-KETOANDROSTENEDIONE
  • ANDROST-4-ENE-3,11,17-TRIONE
  • 382-45-6
  • 328-45-6
  • Steroids
  • 17-Ketosteroids
  • Chiral Building Blocks
  • Asymmetric Synthesis
  • Complex Molecules
  • 17-Ketosteroids
  • Biochemistry
  • Pharmaceutical Intermediates
  • Steroids
  • Inhibitors
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