2,2'-Dithiobiscl-amine-4,5-dimethoxybenzene) was synthesized as a highly sensitive, selective and stable fluorescence derivatization reagent for aromatic aldehydes in liquid chromatography. The reagent reacts selectively with aromatic aldehydes in acidic media in the presence of tri-n-butylphosphine
2-(5-Hydrazinocarbonyl-2-thienyl) -5, 6-methylenedioxybenzofuran and 2-(5-hydrazinocarbonyl-2-furyl)-5, 6-methylenedioxybenzofuran as novel fluorescence derivatisation reagents for carboxylic acids in liquid chromatography
โ Scribed by Mikihiko Saito; Tamano Ushijima; Kazumi Sasamoto; Kenshi Yakata; Yosuke Ohkura; Keiyu Ueno
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 756 KB
- Volume
- 300
- Category
- Article
- ISSN
- 0003-2670
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โฆ Synopsis
The new acid hydrazides, 2-( S-hydrazinocarbonyl-2-thienyl) -5,6-methylenedioxybenzofuran (TMBH) and 2-( S-hydrazinocarbonyl-Zfuryl) -5,6-methylenedioxybenzofuran (FMBH) , were synthesized as precolumn fluorescence derivatisation reagents for carboxylic acids in liquid chromatography. These compounds readily react with carboxylic acids in the presence of a coupling reagent under mild conditions in aqueous solution to give fluorescent derivatives. The detection limits of lauric acid were both 0.1 pmol per 10 ~1 injection volume at a signal-to-noise ratio of 3. The methods in which these compounds are used were applied to the assay of a standard mixture of prostaglandins (25 PM) and prostaglandins in a human seminal fluid.
๐ SIMILAR VOLUMES
A highly sensitive fluorescent labeling reagent, 4-(5,6-dimethoxy-2-phthalimidinyl)-2-methoxyphenylsulfonyl chloride (DMS-Cl), for determination of amino acids by HPLC has been developed. DMS-Cl reacted with amino acids in the basic medium to produce the corresponding fluorescent sulfonamides (excit