2009
DOI: 10.1016/j.jchromb.2008.12.064
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Determination of biogenic amines in beer with pre-column derivatization by high performance liquid chromatography

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Cited by 77 publications
(41 citation statements)
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“…It can react with amines in low concentration to form stable derivatives under alkaline conditions, and the excess reagent is hydrolyzed to the corresponding phenol without any other by-products and interferences Sun et al 2009;Tang et al 2009). The hydrolysis compound can be written as (CNBF)OH.…”
Section: Derivatives and Derivatization Conditionsmentioning
confidence: 99%
“…It can react with amines in low concentration to form stable derivatives under alkaline conditions, and the excess reagent is hydrolyzed to the corresponding phenol without any other by-products and interferences Sun et al 2009;Tang et al 2009). The hydrolysis compound can be written as (CNBF)OH.…”
Section: Derivatives and Derivatization Conditionsmentioning
confidence: 99%
“…The CNBF derivatization was rapid at moderate temperature, along with the resultant derivatives being very stable and of high ultraviolet and fluorescent absorption [41][42][43][44][45][46][47]. There were not any multiple derivatives and by-products except CNBF hydrolysis compound in the reaction, while excess reagent and its hydrolysis compound could not disturb the separation.…”
Section: Introductionmentioning
confidence: 96%
“…Biogenic amines are usually determined by thin layer chromatography (TLC) [6,7], capillary electrophoresis (CE) [8][9][10], gas chromatography (GC) [11,12] and liquid chromatography (LC) with ultra-violet (UV) or fluorescence detection [13][14][15][16][17][18][19][20][21][22][23]25]. Among these methods, LC is the most popular and frequently used for the separation and quantification of biogenic amines.…”
Section: Introductionmentioning
confidence: 99%
“…There are many derivatization reagents usually applied for biogenic amines analysis such as bis-3,5-dinitrobenzoyl chloride (DNBZ-Cl) [13], dabsyl chloride (Dbs-Cl) [14], benzoyl chloride [15], 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate (AQC) [16], [2-ethylhexyl] sulphosuccinate (AOT) [17], dansyl chloride (Dns-Cl) [18], 9-fluorenylmethyl chloroformate (FMOC) [19], o-phthalaldehyde (OPA) [20], N-hydroxysuccinimidyl fluorescein-o-acetate (SIFA) [21], 1,2-naphthoquinone-4-sulfonate (NOS) [22] and 4-chloro-3, 5-dinitrobenzotrifluoride (CNBF) [23]. In spite of the popularity of these pre-column methods, there have also been many reports describing various shortcomings in their applications, such as short detection wavelengths, poor reproducibility and stability, redundant hydrolysates, incomplete reactions and serious interference for the determination of real samples.…”
Section: Introductionmentioning
confidence: 99%