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 | Acesso ao texto completo restrito à biblioteca da Biblioteca Rui Tendinha. Para informações adicionais entre em contato com biblioteca@incaper.es.gov.br. |
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Registro Completo |
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Biblioteca(s): |
Biblioteca Rui Tendinha. |
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Data corrente: |
29/04/2015 |
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Data da última atualização: |
23/10/2015 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 2 |
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Autoria: |
ABAKERLI, R. B; SPARRAPAN, R.; SAWAYA, A.C.H.F.; EBERLIN, M. N.; JARA, J.L.P.; RODRIGUES, N. R.; FAY, E. F.; LUIZ, A. J. B.; GALVÃO, T. D. L.; MARTINS, D. dos S.; YAMANISHI, O. K.; TOLEDO, H. H. B. |
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Afiliação: |
David dos Santos Martins, Incaper. |
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Título: |
Carbon disulfide formation in papaya under conditions of dithiocarbamate residue Analysis. |
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Ano de publicação: |
2015 |
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Fonte/Imprenta: |
Food Chemistry, v. 188, p. 71-76, december 2015. |
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DOI: |
http://dx.doi.org/10.1016/j.foodchem.2015.04.059 |
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Idioma: |
Inglês |
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Notas: |
In Press. |
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Conteúdo: |
Golden, Sunrise Solo and Tainung cultivars of papaya were found to release CS2 when submitted to experimental conditions of dithiocarbamate residue analysis. Three common analytical methods were used to quantitate CS2; one spectrophotometric method and two chromatographic methods. All three methods gave positive CS2 results for all three papaya varieties. Other endogenous compounds present in isooctane extracts of papaya fractions detected via gas chromatography (GC/ITD) using electron ionization (EI) were: carbonyl sulfide, dimethyl sulfide, carbon disulfide, 2-methylthiophene, 3-methylthiophene, 2-ethylthiophene, 3-ethylthiophene, benzylisothiocyanate, benzylthiocyanate and benzonitrile. Control samples were obtained from papaya plantations cultivated in experimental areas, in which no treatment with fungicides of the dithiocarbamate group was applied. Endogenous CS2 levels were compared with true dithiocarbamate residues measured in papaya samples from the field trials following applications of the mancozeb fungicide. Three days after application, true dithiocarbamate residues, measured by the procedure with isooctane partitioning and GC-ITD, were at the average level of 2 mg kg-1. |
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Palavras-Chave: |
Benzylisothiocyanate; Carbon disulfide; Dithiocarbamate residue analysis; Golden; Mamão; Papaya; Sunrise Solo; Tainung. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 02275naa a2200373 a 4500
001 1006341
005 2015-10-23
008 2015 bl uuuu u00u1 u #d
024 7 $ahttp://dx.doi.org/10.1016/j.foodchem.2015.04.059$2DOI
100 1 $aABAKERLI, R. B
245 $aCarbon disulfide formation in papaya under conditions of dithiocarbamate residue Analysis.$h[electronic resource]
260 $c2015
500 $aIn Press.
520 $aGolden, Sunrise Solo and Tainung cultivars of papaya were found to release CS2 when submitted to experimental conditions of dithiocarbamate residue analysis. Three common analytical methods were used to quantitate CS2; one spectrophotometric method and two chromatographic methods. All three methods gave positive CS2 results for all three papaya varieties. Other endogenous compounds present in isooctane extracts of papaya fractions detected via gas chromatography (GC/ITD) using electron ionization (EI) were: carbonyl sulfide, dimethyl sulfide, carbon disulfide, 2-methylthiophene, 3-methylthiophene, 2-ethylthiophene, 3-ethylthiophene, benzylisothiocyanate, benzylthiocyanate and benzonitrile. Control samples were obtained from papaya plantations cultivated in experimental areas, in which no treatment with fungicides of the dithiocarbamate group was applied. Endogenous CS2 levels were compared with true dithiocarbamate residues measured in papaya samples from the field trials following applications of the mancozeb fungicide. Three days after application, true dithiocarbamate residues, measured by the procedure with isooctane partitioning and GC-ITD, were at the average level of 2 mg kg-1.
653 $aBenzylisothiocyanate
653 $aCarbon disulfide
653 $aDithiocarbamate residue analysis
653 $aGolden
653 $aMamão
653 $aPapaya
653 $aSunrise Solo
653 $aTainung
700 1 $aSPARRAPAN, R.
700 1 $aSAWAYA, A.C.H.F.
700 1 $aEBERLIN, M. N.
700 1 $aJARA, J.L.P.
700 1 $aRODRIGUES, N. R.
700 1 $aFAY, E. F.
700 1 $aLUIZ, A. J. B.
700 1 $aGALVÃO, T. D. L.
700 1 $aMARTINS, D. dos S.
700 1 $aYAMANISHI, O. K.
700 1 $aTOLEDO, H. H. B.
773 $tFood Chemistry$gv. 188, p. 71-76, december 2015.
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