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17β-Dihydroepiandrosterone
SpectraBase Compound ID 2Vx5Zb8JUXV
InChI InChI=1S/C19H32O2/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/h12-17,20-21H,3-11H2,1-2H3/t12-,13-,14-,15-,16-,17-,18-,19-/m0/s1
InChIKey CBMYJHIOYJEBSB-YSZCXEEOSA-N
Mol Weight 292.5 g/mol
Molecular Formula C19H32O2
Exact Mass 292.24023 g/mol
Enantiomer InChIKey CBMYJHIOYJEBSB-IMECAPTFSA-N
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number A1220-000
Copyright Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number A1220-000
Copyright Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids
Source of Spectrum Forensic Spectral Research
Catalog Number A1220-000
Technique KBr1 0.64mg
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Prof. Spiteller, University Bayreuth, Germany
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Dr. Makin, London Hospital Medical College, UK
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SWG-33-2104-0
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
  • 5α-Androstan-3β,17β-diol
  • 5a-Androstane-3b,17b-diol
  • 5α-Androstan-3α,17β-diol
  • 3.beta.,17.beta.-dihydroxy-5.alpha.-androstane
  • Androstane-3,17-diol
  • (3S,5S,8R,9S,10S,13S,14S,17S)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol
Title Journal or Book Year
Molecular docking simulation studies on potent butyrylcholinesterase inhibitors obtained from microbial transformation of dihydrotestosterone Chemistry Central Journal 2013
Transformation of a series of saturated isomeric steroidal diols by Aspergillus tamarii KITA reveals a precise stereochemical requirement for entrance into the lactonization pathway The Journal of Steroid Biochemistry and Molecular Biology 2010
An unusual ring—A opening and other reactions in steroid transformation by the thermophilic fungus Myceliophthora thermophila The Journal of Steroid Biochemistry and Molecular Biology 2009
13C n.m.r. spectra of steroids —a survey and commentary Organic Magnetic Resonance 1977
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