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-Amino-4,5-ethylenedioxyphenol as fluorescence derivatization reagent for aromatic aldehydes in liquid chromatography
โ Scribed by Hitoshi Nohta; Fumie Sakai; Masaaki Kai; Yosuke Ohkura; Mikihiko Saito
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 435 KB
- Volume
- 287
- Category
- Article
- ISSN
- 0003-2670
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โฆ Synopsis
2-Amino-4,5ethylenedioxyphenol was found to be useful as a precolumn fluorescence derivatization reagent for aromatic aldehydes in liquid chromatography. The reagent reacts selectively with the aldehydes in two steps: first, heating WMIT) for 45 min in methanol solution in the presence of dicyclohexylcarbodiimide; secondly, standing for more than 1 min at room temperature after acidification. The fluorescent product from 4-hydroxybenzaldehyde is shown to be 2_(4-hydroxyphenyl)_5,6-ethylenedioxybenzoxazole. The fluorescent derivatives of aromatic aldehydes can be separated by reversed-phase chromatography and their detection limits (S/N = 3) are 5-10 pmol on column.
๐ SIMILAR VOLUMES
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 compound