National Institute of Health Sciences, 1-18-1, Kami-yoga, Setagaya-ku, Tokyo 158-8501, Japan.
San-Ei Gen F.F.I Co, Ltd., 1-1-11, Sanwa-cho, Toyonaka City, Osaka 561-8588, Japan.
Food Chem. 2017 Dec 15;237:733-742. doi: 10.1016/j.foodchem.2017.05.084. Epub 2017 May 17.
The main subsidiary color of structure in Food Red No. 106 (R106) was identified to be a desethyl derivative (R106-SubA). High-performance liquid chromatography (HPLC) was performed for the quantitative determination of benzaldehyde-2,4-disulfonic acid, N,N-diethyl-m-aminophenol, leuco acid, pyrone acid, R106-SubA, etc. in R106. An ammonium acetate solution (20mM) and acetonitrile:water (7:3) were used to stabilize the retention time of the HPLC analytes. The linearity of the calibration curves was in the range of 0.05-10μg/mL, with good correlation coefficients (R>0.9983). The recoveries of impurities at levels 0.1%, 0.5% and 1% ranged from 94.2% to 106.6% with relative standard deviations of 0.1%-1.0%. While surveying commercial R106, the amounts obtained by area% determination were similar to those obtained by the calibration-curve determination. The area% determination by HPLC for the determinations of impurities in R106 is a simple and reliable method and can be applied in routine analysis.
食品红 106(R106)结构中的主要副产物颜色被鉴定为去乙基衍生物(R106-SubA)。采用高效液相色谱法(HPLC)对苯甲醛-2,4-二磺酸、N,N-二乙基-m-氨基酚、隐色酸、吡喃酸、R106-SubA 等进行定量测定。采用 20mM 乙酸铵溶液和乙腈:水(7:3)来稳定 HPLC 分析物的保留时间。校准曲线的线性范围为 0.05-10μg/mL,相关系数良好(R>0.9983)。杂质在 0.1%、0.5%和 1%水平的回收率在 94.2%-106.6%之间,相对标准偏差在 0.1%-1.0%之间。在对商业 R106 进行调查时,通过面积%测定得到的数量与通过校准曲线测定得到的数量相似。HPLC 用于测定 R106 中杂质的面积%测定是一种简单可靠的方法,可应用于常规分析。