Mass spectrometry of onium compounds—II. Carnitine and O-acyl derivatives

✍ Scribed by Georg Hvistendahl; Kjell Undheim; Jon Bremer

• Publisher: John Wiley and Sons
• Year: 1970
• Tongue: English
• Weight: 273 KB
• Volume: 3
• Category: Article
• ISSN: 1076-5174
• DOI: 10.1002/oms.1210031112

✦ Synopsis

Abstract

Carnitine and its O‐acyl derivatives undergo two major pyrolytic reactions in the mass spectrometer. Firstly elimination of water from carnitine or acid from acylcarnitine takes place followed by intramolecular displacement and formation of crotonyl lactone and trimethylamine. Secondly intramolecular displacement occurs with formation of a substituted γ‐lactone and trimethylamine. For the lower acid derivatives only the elimination pathway is important. For carnitine and higher derivatives both processes are important.

The electron induced fragmentations of the major pyrolysis products are relatively simple. The most important pathways for the major components are discussed.

The pyrolytic composition and mode of fragmentation are characteristic and can be used for identification purposes.