Estrone

• Formula: C₁₈H₂₂O₂
• Molecular weight: 270.3661
• IUPAC Standard InChI: InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3 Copy

  
• IUPAC Standard InChIKey: DNXHEGUUPJUMQT-UHFFFAOYSA-N Copy
• CAS Registry Number: 53-16-7
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: Estra-1,3,5(10)-trien-17-one, 3-hydroxy-; Aquacrine; Crinovaryl; Cristallovar; Crystogen; Destrone; Disynformon; Endofolliculina; Esterone; Estrol; Estron; Estrovarin; Estrugenone; Estrusol; Femestrone injection; Femidyn; Folikrin; Folipex; Folisan; Follestrine; Follestrol; Follicular hormone; Folliculin; Follicunodis; Follidrin; Glandubolin; Hiestrone; Hormofollin; Hormovarine; Kestrone; Ketodestrin; Ketohydroxyestrin; Kolpon; Menagen; Menformon; Oestrin; Oestroform; Oestrone; Oestroperos; Ovifollin; Perlatan; Solliculin; Theelin; Thelykinin; Thynestron; Tokokin; Unden; Unden (pharmaceutical); Wynestron; 1,3,5(10)-Estratrien-3-ol-17-one; delta-1,3,5-Estratrien-3β-ol-17-one; delta-1,3,5-Oestratrien-3β-ol-17-one; Estrona; Estrone-A; Fem-O-Gen; Hormestrin; Ketohydroxy-Estratriene; Menformon A; Mestronaq; Thelestrin; 1,3,5(10)-Oestratrien-3-ol-17-one; 3-Hydroxy-oestra-1,3,5(10)-trien-17-one; 3-Hydroxy-1,3,5(10)-oestratrien-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; 3-Hydroxy-17-keto-oestra-1,3,5-triene; 3-Hydroxyestra-1,3,5(10)-trien-17-one; E(sub 1); Estrin; Folliculine; Folliculine benzoate; Ketohydroxyoestrin; 1,3,5-Oestratrien-3-ol-17-one; 3-Hydroxyestra-1,3,5(10)-triene-17-one; Femestrone inj.; Fermidyn; Follidrin (tablets); WAY 164397; Δ-1,3,5(10)-Estratrien-3-ol-17-one; (+)-Estrone; Folliculinum
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• Information on this page:
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
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IR Spectrum

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Coblentz Society, Inc.

Condensed Phase Spectrum

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Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. More information on the manner in which spectra in this collection were collected can be found here.

Notice: Concentration information is not available for this spectrum and, therefore, molar absorptivity values cannot be derived.

Additional Data

Mass spectrum (electron ionization)

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

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Van Den Dool and Kratz RI, non-polar column, custom temperature program

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Novakovic, Tvrzicka, et al., 1995
Novakovic, J.; Tvrzicka, E.; Vsetecka, V.; Pouzar, V.; Feltl, L., Capillary gas-chromatographic retention behavior and physico-chemical properties of underivatized equine estrogens, Collect. Czech. Chem. Commun., 1995, 60, 5, 813-819, https://doi.org/10.1135/cccc19950813 . [all data]

Tret'yakov, 2007
Tret'yakov, K.V., Retention Data. NIST Mass Spectrometry Data Center., NIST Mass Spectrometry Data Center, 2007. [all data]

Notes

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