Determination of the double bond position in functionalized monoenes by 
chemical ionization ion-trap mass spectrometry using acetonitrile as a reagent 
gas

Oldham, N. J.; Svatos, A.

doi:10.1002/(SICI)1097-0231(19990315)13:5<331::AID-RCM487>3.0.CO;2-A

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Determination of the double bond position in functionalized monoenes by chemical ionization ion-trap mass spectrometry using acetonitrile as a reagent gas

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Oldham, N. J.
Research Group Mass Spectrometry, MPI for Chemical Ecology, Max Planck Society;

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Svatos, A.
Research Group Mass Spectrometry, MPI for Chemical Ecology, Max Planck Society;

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Citation

Oldham, N. J., & Svatos, A. (1999). Determination of the double bond position in functionalized monoenes by chemical ionization ion-trap mass spectrometry using acetonitrile as a reagent gas. Rapid Communications in Mass Spectrometry, 13(5), 331-336. doi:10.1002/(SICI)1097-0231(19990315)13:5<331:AID-RCM487>3.0.CO;2-A.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-B383-4

Abstract

Acetonitrile may be used as a chemical ionization reagent gas in ion-trap mass spectrometry for the location of double bonds in functionalized long-chain monoenes, [C3H4N](+): derived from acetonitrile, reacts with carbon-carbon double bonds, generating