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[高效液相色谱法测定和检测偶氮染料食用色素中的起始原料、中间体及辅助色素]

[Determination and survey of starting materials, intermediates, and subsidiary colors in food color of azo dye by high performance liquid chromatography].

作者信息

Ishimitsu S, Mishima I, Tsuji S, Shibata T

出版信息

Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku. 1997(115):175-80.

PMID:9641837
Abstract

A method for determination of starting materials, intermediates and subsidiary colors in food color of azo dye was developed by use of HPLC. The following conditions were used for analysis: column, L-column ODS (4.6 mm phi x 250 mmL); mobile phase, 0.02 M ammonium acetate (A), acetonitrile (B); concentration gradient, perform the linear concentration gradient from A:B (100:0) to (60:40) for 40 min; detection, starting materials and intermediates at 239 nm, and subsidiary colors at 510 nm. Standard material, domestic product and imported product were analyzed by the present HPLC method and impurities were measured. Recoveries of each impurity from azo dye averaged 99.1-103.5%. The detection limit was 0.05 microgram/g for each impurity.

摘要

建立了一种利用高效液相色谱法测定偶氮染料食用色素中起始原料、中间体和副色的方法。分析采用以下条件:色谱柱,L-column ODS(4.6mm内径×250mm长);流动相,0.02M醋酸铵(A)、乙腈(B);浓度梯度,从A:B(100:0)到(60:40)进行40分钟的线性浓度梯度;检测,起始原料和中间体在239nm处检测,副色在510nm处检测。采用本高效液相色谱法分析了标准物质、国产产品和进口产品,并测定了杂质。偶氮染料中各杂质的回收率平均为99.1-103.5%。各杂质的检测限为0.05微克/克。

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