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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;Nsc12166;s substance G;ADRENOSTERONE;Andrenosterone;Reichstein'REICHSTEIN'S 'G';(+)-ADRENOSTERONE;Adrenosterone >REICHSTEIN'S ''G''
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
L?slichkeit
Chloroform (Slightly), Ethyl Acetate (Slightly)
Aggregatzustand
Solid
Farbe
White to Off-White
Optische Aktivit?t
[α]20/D +300°, c = 1 in chloroform
Wasserl?slichkeit
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.

l?uterung 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 H?ndler.

Global( 163)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Nanjing Shizhou Biotechnology Co., Ltd
+86-15850508050 +86-15850508050
sean.lv@synzest.com China 323 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-18789408387
1057@dideu.com China 3959 58
Hebei Mojin Biotechnology Co., Ltd
+86 13288715578 +8613288715578
sales@hbmojin.com China 12834 58
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28172 58
career henan chemical co
+86-0371-86658258 +8613203830695
factory@coreychem.com China 29810 58
Hebei Bonster Technology Co.,Limited
+8613315996897
bsterltd.wendy@gmail.com China 792 58
WUHAN CIRCLE POWDER TECHNOLOGY CO.,LTD
+8615377521700
wangwendy93@gmail.com China 868 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000
marketing@targetmol.com United States 32161 58
WUHAN CIRCLE POWDER TECHNOLOGY CO.,LTD
+8618007166089
circlepowder01@gmail.com China 229 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763
sales@tnjchem.com China 34563 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
  • 4-ANDROSTENE-3,11,17-TRIONE
  • 4-ANDROSTEN-3,11,17-TRIONE
  • ANDROST-4-ENE-3,11,17-TRIONE
  • ADRENOSTERONE
  • 11-Oxy-4-androstenedione
  • 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
  • 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)
  • 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
  • Adrenosterone;Androst-4-ene-3,11,17-trione;Reichstein's substance G
  • 11-KETOANDROSTENEDIONE
  • 11-Ketoandrostenedione-[2.3.4-13C3]
  • 382-45-6
  • 328-45-6
  • Steroids
  • 17-Ketosteroids
  • Chiral Building Blocks
  • Asymmetric Synthesis
  • Complex Molecules
  • 17-Ketosteroids
  • Biochemistry
  • Pharmaceutical Intermediates
  • Steroids
  • Inhibitors
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
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