1976
DOI: 10.1021/ac50005a038
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Qualitative and quantitative analyses of bansyl derivatives of dopamine and some of its metabolites in urine samples by electron impact and field desorption mass spectrometry

Abstract: The derivatives of dopamine, 3-O-methyldopamlne, and 4-O-methyldopamine produced by reaction with 5-di-n-butylamlnonaphthalene-1-sulfonyl chloride (BANS-CI) were separated by thin-layer chromatography and identified by electron Impact and field desorption mass spectrometry. The base peaks In the electron impact spectra were formed by loss of C3H7 from the molecular Ion. In contrast, the field desorption spectra showed only the molecular Ions. The BANS derivatives

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Cited by 31 publications
(2 citation statements)
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References 23 publications
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“…Using this technique, the sample (unknown amount) and standard (known amount) are desorbed from the FD emitter in one measurement under identical conditions. Previously, it has been shown that stable isotope dilution is the method of choice for quantitative determinations in FD-MS (12)(13)(14)(15).…”
Section: Resultsmentioning
confidence: 99%
“…Using this technique, the sample (unknown amount) and standard (known amount) are desorbed from the FD emitter in one measurement under identical conditions. Previously, it has been shown that stable isotope dilution is the method of choice for quantitative determinations in FD-MS (12)(13)(14)(15).…”
Section: Resultsmentioning
confidence: 99%
“…Mixtures of dopamine added to urine at the 10-ng//uL level have been determined via the FD method using dopamine-d4 as the internal standard. After formation of the tris-bansyl derivative and TLC cleanup, the relative error was 5% (22).…”
Section: Analytical Applicationsmentioning
confidence: 99%