4-Androstenedione(4AD) 63-05-8 98%
Androstenedione Basic information
Biological Metabolism
Product Name: Androstenedione
Synonyms: 3,17-Dioxoandrost-4-Ene;Androstenedione (CRM);Testosterone EP Impurity A;4-Androstene-3;4-androsten-3,17-dione (4-AD);4-Androstene-3,17-dione Solution, 100ppm;Androstenedione solution ;4-androstene-3,17-dione(4-AD)
CAS: 63-05-8
MF: C19H26O2
MW: 286.41
EINECS: 200-554-5
Product Categories: API;Metabolites & Impurities;Pharmaceutical Intermediates;Steroids;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File: 63-05-8.mol
Androstenedione Chemical Properties
Melting point 170-171 °C(lit.)
Boiling point 368.77°C (rough estimate)
alpha D30 +199° (in chloroform)
density 1.0655 (rough estimate)
refractive index 1.4709 (estimate)
Fp 2℃
storage temp. Controlled Substance, -20°C Freezer
color Dimorphous: Needles from acetone, or crystalsfrom hexane
Water Solubility 57.28mg/L(25 ºC)
Merck 13,643
InChIKey AEMFNILZOJDQLW-QAGGRKNESA-N
CAS DataBase Reference 63-05-8(CAS DataBase Reference)
NIST Chemistry Reference Androst-4-ene-3,17-dione(63-05-8)
EPA Substance Registry System 4-Androstenedione (63-05-8)
Safety Information
Hazard Codes Xn,T,F
Risk Statements 40-64-52-22-61-60-36-20/21/22-11
Safety Statements 22-24/25-36-45-36/37-53-26-16
RIDADR UN 1648 3 / PGII
WGK Germany 3
RTECS BV8150000
HS Code 29372900
Hazardous Substances Data 63-05-8(Hazardous Substances Data)
MSDS Information
Provider Language
Androstenedione English
SigmaAldrich English
Androstenedione Usage And Synthesis
Biological Metabolism The in vitro perfusion of the human placental lobule with 7-ethoxycoumarin gives 7-hydroxycoumarin, and perfusion with androstenedione gives the conversion products, estrone, estradiol, and testosterone. The human placenta has only a limited capacity for the metabolism of xenobiotics.
Description Androstenedione (CRM) (Item No. ISO60161) is a certified reference material categorized as an anabolic androgenic steroid. Androstenedione is a precursor of testosterone (Item Nos. ISO60154 | ISO00154 | 15645) and estrone . Androstenedione is regulated as a Schedule III compound in the United States. Androstenedione (CRM) (Item No. ISO60161) is provided as a DEA exempt preparation. This product is intended for research and forensic applications.
Chemical Properties White to Off-White Solid
Uses Testosterone precursor and metabolite with androgenic activity. Controlled substance (anabolic sterid)
Definition ChEBI: A 3-oxo Delta4-steroid that is androst-4-ene substituted by oxo groups at positions 3 and 17. It is a steroid hormone synthesized in the adrenal glands and gonads.
Safety Profile An experimental teratogen. Otherexperimental reproductive effects. Questionablecarcinogen with experimental tumorigenic data. Whenheated to decomposition it emits acrid smoke andirritating fumes.
Purification Methods Crystallise the dione from hexane. It is soluble in *C6H6, CHCl3 and EtOH. It has max at 239nm. It is a precursor of estrone or testosterone and has androgenic activity. [Ruzicka & Wettstein Helv Chim Acta 18 980 1935, Beilstein 7 III 3636, 7 IV 2381.]
Androstenedione Preparation Products And Raw materials
Raw materials beta-Sitosterol-->3-keto-23,24-bisnorchol-4-en-22-ol-->CAMPESTEROL-->Cholesterol-->(8S,9R,10S,13S,14S,17S)-9,17-dihydroxy-10,13-dimethyl-2,6,7,8,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-one
Preparation Products Spironolactone-->5B-ANDROSTANE-3,17-DIONE-->Androsta-1,4-diene-3,17-dione-->Testosterone undecanoate-->Androst-3-en-17-one,(5)-->5α-Androstane-3,6,17-trione-->11α-Hydroxyandrost-4-ene-317-dione-->Methyl 3-oxo-4-androstene-17beta-carboxylate-->6-METHYLENEANDROST-4-ENE-3,17-DIONE
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