5β-Androst-1-ene-3α,17β-diol,bis-TMS


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

Normal alkane RI, non-polar column, temperature ramp

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Column type Active phase I Reference Comment
CapillaryUltra-12529.Parr, Zapp, et al., 200717. m/0.2 mm/0.11 μm, He, 20. K/min, 320. C @ 2. min; Tstart: 140. C
CapillaryHP-5MS2583.Parr, Zapp, et al., 200716.5 m/0.25 mm/0.25 μm, He, 20. K/min, 320. C @ 2. min; Tstart: 140. C
CapillarySE-542548.Schänzer and Donike, 199220. m/0.25 mm/0.33 μm, He, 5. K/min; Tstart: 200. C; Tend: 300. C
CapillarySE-542555.Schänzer and Donike, 199215. m/0.2 mm/0.33 μm, He, 5. K/min; Tstart: 200. C; Tend: 300. C

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.

Parr, Zapp, et al., 2007
Parr, M.K.; Zapp, J.; Becker, M.; Opfermann, G.; Bartz, U.; Schanzer, W., Steroidal isomers with uniform mass spectra of their per-TMS derivatives: Synthesis of 17-hydroxyandrostan-3-ones, androst-1-, and -4-ene-3,17-diols, Steroids, 2007, 72, 6-7, 545-551, https://doi.org/10.1016/j.steroids.2007.03.006 . [all data]

Schänzer and Donike, 1992
Schänzer, W.; Donike, M., Metabolism of boldenone in man: gas chromatographic/mass spectrometric identification of urinary excreted metabolites and determination of excretion rates, Biol. Mass Spectrom., 1992, 21, 1, 3-16, https://doi.org/10.1002/bms.1200210104 . [all data]


Notes

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