Enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography
Simultaneous enantioseparation of three chiral triazole fungicides i.e. penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography (CD-MEKC) under acidic condition was investigated with different HP-?-CD concentrations as chiral selector. The three tria...
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Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia
2008
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my.utm.77052010-10-08T09:46:57Z http://eprints.utm.my/id/eprint/7705/ Enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography Wan Ibrahim, Wan Aini Hermawan, Dadan Sanagi, Mohd. Marsin QD Chemistry Simultaneous enantioseparation of three chiral triazole fungicides i.e. penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography (CD-MEKC) under acidic condition was investigated with different HP-?-CD concentrations as chiral selector. The three triazole fungicides have an asymmetrically substituted carbon atom respectively, and they all contain two enantiomers. In order to achieve the best enantioresolution of these triazole fungicides, the HP-?-CD concentration range was optimized from 0 to 40 mM in 10 mM increment. The results indicate that separation of enantiomers was not achieved with concentration range of HP-?-CD from 0 to 20 mM. Simultaneous enantioseparation was successfully achived at 30 mM and 40 mM HP-?-CD concentration in 25 mM phosphate buffer (pH 3.0) solution that containing 50 mM SDS, 10% methanol and 5% acetonitrile. However, enantioresolution decreased for myclobutanil and triadimefon enantiomers with HP-?-CD concentration greater than 30 mM. In addition, an increase in the concentration of HP-?-CD caused a significant increase in the analysis time. In light of these aspects, the optimal concentration for HP-?-CD was decided to be 30 mM for the simultaneous chiral separation of the three triazole fungicides with resolutions (Rs) between enantiomers for penconazole, Rs = 0.81; myclobutanil, Rs = 1.14; triadimefon, Rs = 2.09; peak efficiencies (N) greater than 108 000 for all stereoisomers and analysis time of less than 15 min Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia 2008 Article PeerReviewed application/pdf en http://eprints.utm.my/id/eprint/7705/1/WanAinWan008_EnantioseparationofPenconazole.pdf Wan Ibrahim, Wan Aini and Hermawan, Dadan and Sanagi, Mohd. Marsin (2008) Enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography. Journal of Fundamental Sciences, 4 (2). pp. 445-450. ISSN 1823-626X http://jfs.ibnusina.utm.my/index.php/jfs/article/view/79 |
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QD Chemistry Wan Ibrahim, Wan Aini Hermawan, Dadan Sanagi, Mohd. Marsin Enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography |
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Simultaneous enantioseparation of three chiral triazole fungicides i.e. penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography (CD-MEKC) under acidic condition was investigated with different HP-?-CD concentrations as chiral selector. The three triazole fungicides have an asymmetrically substituted carbon atom respectively, and they all contain two enantiomers. In order to achieve the best enantioresolution of these triazole fungicides, the HP-?-CD concentration range was optimized from 0 to 40 mM in 10 mM increment. The results indicate that separation of enantiomers was not achieved with concentration range of HP-?-CD from 0 to 20 mM. Simultaneous enantioseparation was successfully achived at 30 mM and 40 mM HP-?-CD concentration in 25 mM phosphate buffer (pH 3.0) solution that containing 50 mM SDS, 10% methanol and 5% acetonitrile. However, enantioresolution decreased for myclobutanil and triadimefon enantiomers with HP-?-CD concentration greater than 30 mM. In addition, an increase in the concentration of HP-?-CD caused a significant increase in the analysis time. In light of these aspects, the optimal concentration for HP-?-CD was decided to be 30 mM for the simultaneous chiral separation of the three triazole fungicides with resolutions (Rs) between enantiomers for penconazole, Rs = 0.81; myclobutanil, Rs = 1.14; triadimefon, Rs = 2.09; peak efficiencies (N) greater than 108 000 for all stereoisomers and analysis time of less than 15 min |
format |
Article |
author |
Wan Ibrahim, Wan Aini Hermawan, Dadan Sanagi, Mohd. Marsin |
author_facet |
Wan Ibrahim, Wan Aini Hermawan, Dadan Sanagi, Mohd. Marsin |
author_sort |
Wan Ibrahim, Wan Aini |
title |
Enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography |
title_short |
Enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography |
title_full |
Enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography |
title_fullStr |
Enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography |
title_full_unstemmed |
Enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography |
title_sort |
enantioseparation of penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography |
publisher |
Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia |
publishDate |
2008 |
url |
http://eprints.utm.my/id/eprint/7705/1/WanAinWan008_EnantioseparationofPenconazole.pdf http://eprints.utm.my/id/eprint/7705/ http://jfs.ibnusina.utm.my/index.php/jfs/article/view/79 |
_version_ |
1643644834592849920 |
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13.211869 |