Stavric B, Klassen R, Miles W
J Assoc Off Anal Chem. 1979 Sep;62(5):1020-6.
A method is described for the simultaneous quantitation of trace amounts of alpha- (alpha-NA) and beta-naphthylamines (beta-NA) with detectability in the 0.1 ppb range and sensitivity of 50 picomoles in certified food grade amaranth (FD&C Red No. 2; C.I. Food Red 9; CI 16185). The amaranth sample is extracted with benzene, and the evoporated residue is derivatized with perfluorooctanoic anhydride. The resulting derivatives are separated by gas-liquid chromatography and identified and quantitated by mass spectrometric monitoring of the m/e at 539.04. The method was used for quantitation of alpha-NA and beta-NA in randomly chosen samples of amaranth. Of 11 samples from different manufacturers, 5 were free of the beta-isomer; the remaining samples contained up to 1.2 ppb beta-NA. The concentration of alpha-NA ranged from no detectable amount to 970 ppb; the majority of the samples contained less than 7 ppb.
描述了一种同时定量痕量α-萘胺(α-NA)和β-萘胺(β-NA)的方法,该方法在认证食品级苋菜红(FD&C红2号;C.I.食品红9;CI 16185)中的检测限在0.1 ppb范围内,灵敏度为50皮摩尔。用苯萃取苋菜红样品,蒸发残渣用全氟辛酸酐衍生化。所得衍生物通过气液色谱分离,并通过对m/e为539.04处的质谱监测进行鉴定和定量。该方法用于定量随机选择的苋菜红样品中的α-NA和β-NA。在来自不同制造商的11个样品中,5个不含β-异构体;其余样品中β-NA含量高达1.2 ppb。α-NA的浓度范围从检测不到到970 ppb;大多数样品含量低于7 ppb。