Attachment of neutrals during tandem mass spectrometry of sulfonic acid dyes and intermediates in an ion trap.
J Mass Spectrom
; 37(10): 1025-33, 2002 Oct.
Article
em En
| MEDLINE
| ID: mdl-12375276
ABSTRACT
Several positional isomers of 2-(2-quinolinyl)-1H-indene-1,3(2H)-dione mono- and disulfonic acids prepared as reference materials for development of analytical methods involved in FDA certification of D&C Yellow No. 10 (Quinoline Yellow) were found consistently to show [MH + 14](+) ions when their electrospray- or atmospheric pressure chemical ionization-prepared MH(+) ions were subjected to collisional activation. The source of these ions was found to be the methanol used as solvent in these procedures which combined with their [MH - H(2)O](+) ions under chemical ionization conditions. The reaction was found to be sensitive to their isomeric and chemical structures and other examples of this process are reviewed.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Ácidos Sulfônicos
/
Corantes
Idioma:
En
Revista:
J Mass Spectrom
Ano de publicação:
2002
Tipo de documento:
Article
País de afiliação:
Estados Unidos