Adrenosterone

Adrenosterone Structure
CAS No.
382-45-6
Chemical Name:
Adrenosterone
Synonyms
11-KETOANDROSTENEDIONE;Nsc12166;s substance G;ADRENOSTERONE;Andrenosterone;Reichstein'REICHSTEIN'S 'G';(+)-ADRENOSTERONE;Adrenosterone >REICHSTEIN'S ''G''
CBNumber:
CB1765508
Molecular Formula:
C19H24O3
Molecular Weight:
300.39
MOL File:
382-45-6.mol
Modify Date:
2024/7/2 14:09:54

Adrenosterone Properties

Melting point 219-222 °C(lit.)
alpha 300 º (c=1 in chloroform)
Boiling point 381.62°C (rough estimate)
Density 1.1381 (rough estimate)
refractive index 290 ° (C=0.2, EtOH)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
form Solid
color White to Off-White
optical activity [α]20/D +300°, c = 1 in chloroform
Water Solubility 98.49mg/L(23.5 ºC)
Merck 14,176
InChIKey RZRPTBIGEANTGU-IRIMSJTPSA-N
CAS DataBase Reference 382-45-6(CAS DataBase Reference)
NIST Chemistry Reference Androst-4-ene-3,11,17-trione(382-45-6)

SAFETY

Risk and Safety Statements

WGK Germany  3

Adrenosterone price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 284998 Adrenosterone 98% 382-45-6 5G ₹10738.4 2022-06-14 Buy
TCI Chemicals (India) A1397 Adrenosterone 382-45-6 1G ₹4800 2022-05-26 Buy
Product number Packaging Price Buy
284998 5G ₹10738.4 Buy
A1397 1G ₹4800 Buy

Adrenosterone Chemical Properties,Uses,Production

Chemical Properties

Off-White to Pale Yellow Solid

Uses

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.

Purification Methods

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.]

Adrenosterone Preparation Products And Raw materials

Global( 161)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6100 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6257 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6768 58 Inquiry
Nanjing Shizhou Biotechnology Co., Ltd +86-15850508050 +86-15850508050 China 323 58 Inquiry
Shaanxi Dideu Medichem Co. Ltd +86-029-81138252 +86-18789408387 China 3922 58 Inquiry
Hebei Mujin Biotechnology Co.,Ltd +86 13288715578 +8613288715578 China 12809 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29808 58 Inquiry
Hebei Bonster Technology Co.,Limited +8613315996897 China 792 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 32159 58 Inquiry
Hefei TNJ Chemical Industry Co.,Ltd. +86-0551-65418671 +8618949823763 China 34563 58 Inquiry
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] Adrenosterone, 10 mM in DMSO 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