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机构地区:[1]上海应用技术学院,上海200235 [2]上海香料研究所,上海200232
出 处:《化学世界》2010年第2期87-90,86,共5页Chemical World
基 金:上海市教委基金项目资助(05D205009)
摘 要:建立同时测定反应香精中2-胺基-3,4,8-三甲基-3H-咪唑并[4,5-F]喹喔啉(4,8-DiMeIQx)和2-胺基-1-甲基-6-苯基咪唑[4,5-b]嘧啶(PhIP)的高效液相色谱(HPLC)分析方法。用强酸水解反应香精,在碱性环境下用二氯甲烷萃取分析物,弱酸净化。以乙腈和pH3.44的醋酸-醋酸胺缓冲溶液梯度洗脱,264 nm(测定4,8-DiMeIQx)和312 nm(测定PhIP)双波长扫描,进行高效液相色谱检测。4,8-DiMeIQx和PhIP在反应香精中的检出限均为0.01 mg/L;加标回收率分别为87.25%和102%。用该法对国内不同公司的不同产品进行检验适用性良好。A high-performance liquid chromatography (HPLC) analytical method for,determination of 2- amino-l-methyl-:6-phenylimidazo [-4,5-b] pyridine (PhIP) and 2-amino-3,4,8-trimethyl-3H-imidazo [-4,5-F] quino xaline (4, 8-DiMeIQx) in process flavor was estalliohed. The process fla,;or samples were hydrolyzed by a strong acid. The sample was extracted from the solution after treatment by dichloromethane in alkaline environment, and then purified by a weak acid. Acetonitrile and pH3.44 acetic acid-ammonium acetate buffer solution were used as the mobile phase, and 264 nm (determining 4, 8- DiMeIQx) and 312nm (determining PhIP) were the detective wavelengths. The detective limitation values for the two heterocyclic amines (HCAs) in process flavor were both 0. 01 mg/L, and the recovery was 87.25% for 4, 8-DiMeIQx and 102 % for PhiP. This technique was usable for the determination of process flavor products supplied from different companies.
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