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:
  • Normal alkane RI, non-polar column, custom temperature program
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Normal alkane RI, non-polar column, custom temperature program

Go To: Top, References, Notes

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

References

Go To: Top, Normal alkane RI, non-polar column, custom temperature program, Notes

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

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

Go To: Top, Normal alkane RI, non-polar column, custom temperature program, References

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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