Home > Name List By other > (8R,9S,10R,13S,14S)-10,13-dimethyl-2,6,7,8,9,11,12,14,15, 16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione Germany

CAS No 63-05-8 , (8R,9S,10R,13S,14S)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,
16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione Search by region : Germany

  • Name: (8R,9S,10R,13S,14S)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,
    16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione
  • Synonyms: Fecundin; 63-05-8; SKF 2170; 4-Androstenedione; 3,17-Dioxoandrost-4-ene; Androtex; 4-Androstene-3,17-dione;Androst-4-ene-3,17-dione;(8R,9S,10R,13S,14S)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,
    16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione;
  • CAS Registry Number:
  • Melting Point: 170-173 ºC
  • Flash Point: 161.1 ºC
  • Boiling Point: 431.4 ºC at 760 mmHg
  • Density: 1.11 g/cm3
  • Refractive index: 1.551
  • Safety Statements: An experimental teratogen. Other experimental reproductive effects. Questionable carcinogen with experimental tumorigenic data. When heated to decomposition it emits acrid smoke and irritating fumes.
  • Hazard Symbols: Xn
  • Flash Point: 161.1 ºC
  • EINECS: 200-554-5
  • Molecular Weight: 286.40854
  • InchiKey: AEMFNILZOJDQLW-QAGGRKNESA-N
  • InChI: InChI=1S/C19H26O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,
    2)10-8-16(14)18/h11,14-16H,3-10H2,1-2H3/t14-,15-,16-,18-,19-/m0/s1
  • Risk Statements: 40
  • Molecular Formula: C19H26O2
  • Molecular Structure:CAS No:63-05-8 (8R,9S,10R,13S,14S)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,<br />16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione

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References of (8R,9S,10R,13S,14S)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,
16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione
Title: Androstenedione
CAS Registry Number: 63-05-8
CAS Name: Androst-4-ene-3,17-dione
Synonyms: D4-androstenedione; D4-etiocholendione-3,17
Molecular Formula: C19H26O2
Molecular Weight: 286.41
Percent Composition: C 79.68%, H 9.15%, O 11.17%
Literature References: Weak androgen produced by the adrenal gland; converted in peripheral tissues to testosterone or estrone, q.q.v. Prepn: L. Ruzicka, A. Wettstein, Helv. Chim. Acta 18, 986 (1935); E. S. Wallis, E. Fernholz, J. Am. Chem. Soc. 57, 1511 (1935); and physiological activity: A. Butenandt, H. Kudszus, Z. Physiol. Chem. 237, 75 (1935). Isoln from adrenal cortex: J. von Euw, T. Reichstein, Helv. Chim. Acta 24, 879 (1941). Physiology: V. H. T. James, A. B. Goodall in Proc. 9th Congr. Hung. Soc. Endocrinol. Metab., F. A. Laszlo, Ed. (Akad. Kiado, Budapest, 1979) pp 235-241. HPLC determn in plasma or serum: V. R. Walker et al., Anal. Biochem. 234, 194 (1996). Discussion of use as dietary supplement: L. Schnirring, Physician Sportsmed. 26, 15-18 (1998). Clinical effect of oral supplement on blood chemistry: D. S. King et al., J. Am. Med. Assoc. 281, 2020 (1999).
Properties: Crystals from hexane, mp 173-174°. [a]D30 +199° (in chloroform).
Melting point: mp 173-174°
Optical Rotation: [a]D30 +199° (in chloroform)
NOTE: This is a controlled substance (anabolic steroid): 21 CFR, 1308.13, as defined in 1300.01.