Scher A L
J Assoc Off Anal Chem. 1985 May-Jun;68(3):474-7.
A method is described for the determination of the intermediates in D&C Orange No. 17 by reverse phase liquid chromatography. The pigment is dissolved in boiling dioxane and then precipitated. The filtrate is chromatographed by isocratic elution, which is followed by a wash and equilibration. Peak area calibrations were linear. At the provisional specification levels, 99% prediction limits were 0.200 +/- 0.0012% 2,4-dinitroaniline (2,4-DNA) and 0.200 +/- 0.006% 2-naphthol. The limits of determination were 0.0023% for 2,4-DNA and 0.013% for 2-naphthol at the 99.5% confidence level. Recoveries were 98-100% for 2,4-DNA added at the 0.005-2% level, and 93-103% for 2-naphthol added at the 0.025-2% level. A survey of certified D&C Orange No. 17 samples showed that the lots contained higher levels of the intermediates than were determined previously by a cellulose column method, in which the pigment is not dissolved.
描述了一种通过反相液相色谱法测定D&C橙黄17号中间体的方法。将该色素溶解于沸腾的二氧六环中,然后沉淀。滤液通过等度洗脱进行色谱分析,随后进行冲洗和平衡。峰面积校准呈线性。在暂定规格水平下,99%的预测限为2,4 - 二硝基苯胺(2,4 - DNA)0.200±0.0012%和2 - 萘酚0.200±0.006%。在99.5%置信水平下,2,4 - DNA的测定限为0.0023%,2 - 萘酚的测定限为0.013%。对于添加水平为0.005 - 2%的2,4 - DNA,回收率为98 - 100%;对于添加水平为0.025 - 2%的2 - 萘酚,回收率为93 - 103%。对已认证的D&C橙黄17号样品的调查表明,这些批次中中间体的含量高于先前通过纤维素柱法测定的结果,在纤维素柱法中该色素未溶解。