Estriol

• Formula: C₁₈H₂₄O₃
• Molecular weight: 288.3814
• IUPAC Standard InChI: InChI=1S/C18H24O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-17,19-21H,2,4,6-7,9H2,1H3/t13?,14?,15?,16-,17+,18?/m0/s1 Copy

  
• IUPAC Standard InChIKey: PROQIPRRNZUXQM-PVGHXWSTSA-N Copy
• CAS Registry Number: 50-27-1
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Stereoisomers:
  • Epiestriol
• Other names: Estra-1,3,5(10)-triene-3,16,17-triol, (16α,17β)-; Destriol; Estra-1,3,5(10)-trien-3,16α,17β-triol; Estra-1,3,5(10)-triene-3,16α,17β-triol; Estratriol; Follicular hormone hydrate; NSC-12169; Orestin; Ovestin; OE3; Theelol; Tridestrin; Trihydroxyestrin; 1,3,5(10)-Estratriene-3,16α,17β-Triol; 16α-Estriol; 16α-Hydroxy-17β-estradiol; 16α,17β-Estriol; 3,16α,17β-Estriol; 3,16α,17β-Trihydroxyestra-1,3,5(10)-triene; Oestriol; 1,3,5(10)-Estratrien-3,16α,17β-triol; (16α,17β)-Estra-1,3,5(10)-triene-3,16,17-triol; (16α,17β)-Oestra-1,3,5(10)-triene-3,16,17-triol; A 13610; Aacifemine; Deuslon A; Oestra-1,3,5(10)-triene-3,16α, 17β-triol; Oestratriol; Ortho-Gynest; Overstin; Ovestrion; Thulol; 1,3,5-Estratriene-3β,16-α,17-β-triol; 1,3,5-Oestratriene-3-β,16α,17β-triol; 16α-Hydroxyestradiol; 16α-Hydroxyoestradiol; 16α,17β-Oestriol; 3,16α,17β-Trihydroxy-δ-1,3,5-estratriene; 3,16α,17β-Trihydroxy-δ-1,3,5-oestratriene; 3,16α,17β-Trihydroxy-1,3,5(10)-estratriene; Estra-1,3,5(10)-triene-3,16-α, l7-β-triol; Estriolo; Gynaesan; Hemostyptanon; Holin; Hormomed; Hormonin; Klimoral; 3,16-α,17-β-Oestriol; Orgastyptin; Ovesterin; Stiptanon; Synapause; 3,16-α,17-β-Trihydroxyoestra-1,3,5(10)-triene; Trihydroxyoestrin; Triodurin; Triovex; Colpogyn; Gynasan; Klimax E; Oekolp; Ovo-Vinces; Estriel; Incurin; Folicular hormone; Colpovister; Ovestinon; Estra-1(10),2,4-triene-3,16,17-triol
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• Information on this page:
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
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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

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

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Normal alkane 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.

Tret'yakov, 2008
Tret'yakov, K.V., Retention Data. NIST Mass Spectrometry Data Center., NIST Mass Spectrometry Data Center, 2008. [all data]

Waggott and Davies, 1984
Waggott, A.; Davies, I.W., Identification of organic pollutants using linear temperature programmed retention indices (LTPRIs) - Part II, 1984, retrieved from http://dwi.defra.gov.uk/research/completed-research/reports/dwi0383.pdf. [all data]

Ardrey and Moffat, 1981
Ardrey, R.E.; Moffat, A.C., Gas-liquid chromatographic retention indices of 1318 substances of toxicological interest on SE-30 or OV-1 stationary phase, J. Chromatogr., 1981, 220, 3, 195-252, https://doi.org/10.1016/S0021-9673(00)81925-1 . [all data]

Notes

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