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4-Androsten-6α,17β-diol-3-one

Compound with spectra: 2 NMR, 2 FTIR, 2 Raman, and 2 MS (GC)

4-Androsten-6α,17β-diol-3-one
SpectraBase Compound ID Fk1NZek82bH
InChI InChI=1S/C19H28O3/c1-18-7-5-11(20)9-15(18)16(21)10-12-13-3-4-17(22)19(13,2)8-6-14(12)18/h9,12-14,16-17,21-22H,3-8,10H2,1-2H3/t12-,13-,14-,16-,17-,18+,19-/m0/s1
InChIKey XSEGWEUVSZRCBC-QXROXWLYSA-N
Mol Weight 304.43 g/mol
Molecular Formula C19H28O3
Exact Mass 304.203845 g/mol
Enantiomer InChIKey XSEGWEUVSZRCBC-QUZMDVADSA-N

View Spectrum of 4-Androsten-6α,17β-diol-3-one

ATR-IR Spectrum
Copyright Copyright © 2014-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number A5732-000

View Spectrum of 4-Androsten-6α,17β-diol-3-one

ATR-IR Spectrum
Copyright Copyright © 2019-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids
Source of Spectrum Forensic Spectral Research
Catalog Number A5732-000

View Spectrum of 4-Androsten-6α,17β-diol-3-one

Raman Spectrum
Copyright Copyright © 2015-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number A5732-000

View Spectrum of 4-Androsten-6α,17β-diol-3-one

Raman Spectrum
Copyright Copyright © 2015-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids
Source of Spectrum Forensic Spectral Research
Catalog Number A5732-000

View Spectrum of 4-Androsten-6α,17β-diol-3-one

MS (GC) Spectrum
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Prof. Spiteller, University Bayreuth, Germany

View Spectrum of 4-Androsten-6α,17β-diol-3-one

MS (GC) Spectrum
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Dr. Makin, London Hospital Medical College, UK

View Spectrum of 4-Androsten-6α,17β-diol-3-one

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.

View Spectrum of 4-Androsten-6α,17β-diol-3-one

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 6α-Hydroxyandrosterone
  • 6α-Hydroxytestosterone
  • 6-ALPHA,17-BETA-DIHYDROXY-ANDROST-4-EN-3-ONE
  • 6.ALPHA.,17.BETA.-DIHYDROXY-ANDROST-4-ENE-3-ONE
  • ANDROST-4-ENE-6.ALPHA.,17.BETA.-DIOL-3-ONE
  • (6S,8R,9S,10R,13S,14S,17S)-6,17-dihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
  • 6,17-DIHYDROXYANDROST-4-EN-3-ONE
6β-Hydroxyandrosterone
6.ALPHA.,17.BETA.-DIHYDROXY-ANDROST-4-ENE-3-ONE
6α-Hydroxytestosterone
6-BETA,17-BETA-DIHYDROXYANDROST-4-EN-3-ONE
6β-Hydroxytestosterone
Androst-4-ene-3,6,17-triol
6.beta.-Methylpregn-4-en-3-one
6-METHYLENE-ANDROST-4-ENE-17-BETA-OL-3-ONE
6-BETA-CHLORO-ANDROSTAN-4-ENE-3,17-DIONE
6α-bromoandrost-4-ene-3,17-dione
6β-bromoandrost-4-ene-3,17-dione
4-FLUORO-5-ANDROSTEN-17-BETA-OL-3-ONE
ANDROST-4-ENE-6.BETA.-OL-3-ONE-TRIMETHYLSILYL ETHER
ANDROST-4-ENE-6.BETA.-OL-3-ONE(6.BETA.-TRIMETHYLSILYL ETHER)
Title Journal or Book Year
Hydroxylation of steroids by Fusarium oxysporum, Exophiala jeanselmei and Ceratocystis paradoxa Steroids 2011
Metabolism of anabolic steroids in humans: Synthesis of 6β-hydroxy metabolites of 4-chloro-1,2-dehydro-17α-methyltestosterone, fluoxymesterone, and metandienone Steroids 1995
6α-Hydroxytestosterone
6.ALPHA.,17.BETA.-DIHYDROXY-ANDROST-4-ENE-3-ONE
6β-Hydroxyandrosterone
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