Chromatographic fingerprints of industrial toluic acids established for their quality control

被引:24
作者
Lian, Hongzhen
Wei, Yuna
机构
[1] Nanjing Univ, Key Lab Analyt Chem Life Sci, Educ Minist China, Sch Chem & Chem Engn, Nanjing 210093, Peoples R China
[2] Nanjing Univ, Ctr Mat Anal, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金;
关键词
chromatographic fingerprint; fine chemical intermediate; o-toluic acid; m-toluic acid; p-toluic acid; HPLC; ultraviolet spectrum;
D O I
10.1016/j.talanta.2006.03.054
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
The chromatographic fingerprints of industrial o-toluic acid, m-toluic acid and p-toluic acid have been established by HPLC-UV detection according to their impurity groups. HPLC separation of all relative substances involved in the groups was developed on a Kromasil CIS column by using methanol-water-NH4Ac-HAc buffer (100 mM, pH 4.70) 15/65/20 (v/v/v) as the mobile phase at a flow rate of 1.5 mL/min, and detection was operated by UV adsorption at a wavelength of 254 nm. The ultraviolet spectra corresponding to each chromatographic peak were also recorded for further identification of all components. Whether the limits of relative impurities residues in a toluic acid product are qualified or not can be intuitively estimated by analyzing its chromatogram, with comparison to the fingerprint. This protocol has successfully provided some Chinese manufacturers with a simple and feasible method for quality control of toluic acids for industrial use. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:264 / 269
页数:6
相关论文
共 16 条
[1]
CHEN MJ, 2002, TRADIT PAT MED, V24, P905
[2]
DU GH, 1998, PETROCHEM TECHNOL, V27, P82
[3]
[杜曦 Du Xi], 2004, [化学研究与应用, Chemical Research and Application], V16, P107
[4]
Gas-chromatographic fatty-acid fingerprints and partial least squares modeling as a basis for the simultaneous determination of edible oil mixtures [J].
Hajimahmoodi, M ;
Vander Heyden, Y ;
Sadeghi, N ;
Jannat, B ;
Oveisi, MR ;
Shahbazian, S .
TALANTA, 2005, 66 (05) :1108-1116
[5]
Direct continuous supercritical fluid extraction as a novel method of wine analysis -: Comparison with conventional indirect extraction and implications for wine variety identification [J].
Karásek, P ;
Planeta, J ;
Ostrá, EV ;
Mikesová, M ;
Goliás, J ;
Roth, M ;
Vejrosta, J .
JOURNAL OF CHROMATOGRAPHY A, 2003, 1002 (1-2) :13-23
[6]
LIAN HZ, 2000, FINE CHEM INTERMED, V34, P1
[7]
LIAN HZ, 2005, FINE SPEC CHEM, V13, P6
[8]
Quality control of herbal medicines [J].
Liang, YZ ;
Xie, PS ;
Chan, K .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 812 (1-2) :53-70
[9]
Identification of impurities in acarbose by using an integrated liquid chromatography-nuclear magnetic resonance and liquid chromatography-mass spectrometry approach [J].
Novak, P ;
Cindric, M ;
Tepes, P ;
Dragojevic, S ;
Ilijas, M ;
Mihaljevic, K .
JOURNAL OF SEPARATION SCIENCE, 2005, 28 (13) :1442-1447
[10]
Combined use of liquid chromatography-nuclear magnetic resonance spectroscopy and liquid chromatography-mass spectrometry for the characterization of an acarbose degradation product [J].
Novak, P ;
Tepes, P ;
Cindric, M ;
Ilijas, M ;
Dragojevic, S ;
Mihaljevic, K .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1033 (02) :299-303