Literature DB >> 16957837

Facile and sensitive spectrophotometric determination of carbosulfan in formulations and environmental samples.

K Suresh Kumar1, K Suvardhan, D Rekha, K Kiran, G Chalapathi Rao, B Jayaraj, K Janardhanam, P Chiranjeevi.   

Abstract

Facile, selective and sensitive spectrophotometric method has been developed for the determination of carbosulfan in insecticidal formulations, fortified water, food grains, agriculture wastewater and soil samples with newly synthesized reagents. The method was based on acid and alkaline hydrolysis of the carbosulfan pesticide, and the resultant hydrolysis product of carbosulfan was coupled with 2,6-dibromo-4-methylaniline to give a yellow color product with lambda(max) of 464 nm or interaction with 2,6-dibromo-4-nitroaniline to produce yellow colored product with lambda(max) of 408 nm or coupling with 2,4,6-tribromoaniline to form red colored product has a lambda(max) of 471 nm. Under optimal conditions, Beer's law range for 2,6-dibromo-4-methylaniline (DBMA) was found to be 0.2-12.0 microg ml(-1), 0.6-16.0 microg ml(-1) for 2,6-dibromo-4-nitroaniline (DBNA) and 0.4-15.0 microg ml(-1) for 2,4,6-tribromoaniline (TBA). The molar absorptivity of the color systems were found to be 3.112 x 10(4) l mol(-1) cm(-1) for DBMA, 3.214 x 10(4) l mol(-1) cm(-1) for DBNA and 3.881 x 10(4) l mol(-1) cm(-1) for TBA. Sandell's of the color reactions are 0.013 microg cm(-2) (DBMA), 0.012 microg cm(-2) (DBNA) and 0.011 microg cm(-2) (TBA) respectively. The effect of the non-target species on the determination of carbosulfan was studied to enhance the selectivity of the proposed methods. The formation of colored derivatives with the coupling agents is instantaneous and stable for 28, 30, and 26 h. Performance of the proposed methods were compared statistically in terms Student's F and t-tests with the reported methods.

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Year:  2006        PMID: 16957837     DOI: 10.1007/s10661-006-9360-0

Source DB:  PubMed          Journal:  Environ Monit Assess        ISSN: 0167-6369            Impact factor:   2.513


  4 in total

1.  Monitoring of pesticides in drinking and related waters in NE Spain with a multiresidue SPE-GC-MS method including an estimation of the uncertainty of the analytical results.

Authors:  J Quintana; I Martí; F Ventura
Journal:  J Chromatogr A       Date:  2001-12-14       Impact factor: 4.759

2.  Liquid chromatographic determination of nine N-methylcarbamates in drinking water.

Authors:  Patrizia Morrica; Paola Fidente; Serenella Seccia
Journal:  Biomed Chromatogr       Date:  2005-01       Impact factor: 1.902

3.  [Simultaneous determinations of carbamate pesticides in cereal by high performance liquid chromatography with post-column fluorescence derivatization].

Authors:  W Yu; C Wang; X Chu
Journal:  Se Pu       Date:  1998-09

4.  High-performance liquid chromatography multiresidue method for the determination of N-methyl carbamates in fruit and vegetable juices.

Authors:  Consuelo Sánchez-Brunete; Beatriz Albero; José Luis Tadeo
Journal:  J Food Prot       Date:  2004-11       Impact factor: 2.077

  4 in total

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