Suitability of N,O-bis(trimethylsilyl)trifluoroacetamide and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide as derivatization reagents for the determination of the estrogens estrone and 17alpha-ethinylestradiol by gas chromatography-mass spectrometry.J Chromatogr A. 2004 Feb 13; 1026(1-2):295-300.JC
Abstract
This paper describes apreviously unreported problem with the use of N,O-bis-(trimethylsilyl)trifluoroacetamide (BSTFA) and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) to derivatise the natural hormone estrone (E1) and the synthetic estrogen 17alpha-ethinylestradiol (EE2). The resulting trimethylsilyl (TMS) and t-butyldimethylsilyl (TBS) derivatives of EE2 were partially converted to their respective El derivatives. Therefore, these reagents may not be suitable for simultaneous determination of estrogens in environmental samples, which raises questions about the reliability of results from some earlier studies.
MeSH
Pub Type(s)
Journal Article
Language
eng
PubMed ID
14763757
Citation
Shareef, Ali, et al. "Suitability of N,O-bis(trimethylsilyl)trifluoroacetamide and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide as Derivatization Reagents for the Determination of the Estrogens Estrone and 17alpha-ethinylestradiol By Gas Chromatography-mass Spectrometry." Journal of Chromatography. A, vol. 1026, no. 1-2, 2004, pp. 295-300.
Shareef A, Parnis CJ, Angove MJ, et al. Suitability of N,O-bis(trimethylsilyl)trifluoroacetamide and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide as derivatization reagents for the determination of the estrogens estrone and 17alpha-ethinylestradiol by gas chromatography-mass spectrometry. J Chromatogr A. 2004;1026(1-2):295-300.
Shareef, A., Parnis, C. J., Angove, M. J., Wells, J. D., & Johnson, B. B. (2004). Suitability of N,O-bis(trimethylsilyl)trifluoroacetamide and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide as derivatization reagents for the determination of the estrogens estrone and 17alpha-ethinylestradiol by gas chromatography-mass spectrometry. Journal of Chromatography. A, 1026(1-2), 295-300.
Shareef A, et al. Suitability of N,O-bis(trimethylsilyl)trifluoroacetamide and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide as Derivatization Reagents for the Determination of the Estrogens Estrone and 17alpha-ethinylestradiol By Gas Chromatography-mass Spectrometry. J Chromatogr A. 2004 Feb 13;1026(1-2):295-300. PubMed PMID: 14763757.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Suitability of N,O-bis(trimethylsilyl)trifluoroacetamide and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide as derivatization reagents for the determination of the estrogens estrone and 17alpha-ethinylestradiol by gas chromatography-mass spectrometry.
AU - Shareef,Ali,
AU - Parnis,Craig J,
AU - Angove,Michael J,
AU - Wells,John D,
AU - Johnson,Bruce B,
PY - 2004/2/7/pubmed
PY - 2004/12/16/medline
PY - 2004/2/7/entrez
SP - 295
EP - 300
JF - Journal of chromatography. A
JO - J Chromatogr A
VL - 1026
IS - 1-2
N2 - This paper describes apreviously unreported problem with the use of N,O-bis-(trimethylsilyl)trifluoroacetamide (BSTFA) and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) to derivatise the natural hormone estrone (E1) and the synthetic estrogen 17alpha-ethinylestradiol (EE2). The resulting trimethylsilyl (TMS) and t-butyldimethylsilyl (TBS) derivatives of EE2 were partially converted to their respective El derivatives. Therefore, these reagents may not be suitable for simultaneous determination of estrogens in environmental samples, which raises questions about the reliability of results from some earlier studies.
SN - 0021-9673
UR - https://www.unboundmedicine.com/medline/citation/14763757/Suitability_of_NO_bis_trimethylsilyl_trifluoroacetamide_and_N__tert_butyldimethylsilyl__N_methyltrifluoroacetamide_as_derivatization_reagents_for_the_determination_of_the_estrogens_estrone_and_17alpha_ethinylestradiol_by_gas_chromatography_mass_spectrometry_
DB - PRIME
DP - Unbound Medicine
ER -