Chemical Ionization Mass Spectrometry of Morphine Derivatives

    Volume 24, Issue 2 (April 1979)

    ISSN: 0022-1198

    CODEN: JFSOAD

    Published Online: 1 April 1979

    Page Count: 5


    Manura, J
    Chief forensic chemist, principal forensic chemist, and forensic chemist, New Jersey State Police, Forensic Science Bureau, West Trenton, N. J.

    Saferstein, R
    Chief forensic chemist, principal forensic chemist, and forensic chemist, New Jersey State Police, Forensic Science Bureau, West Trenton, N. J.

    Brettell, TA
    Chief forensic chemist, principal forensic chemist, and forensic chemist, New Jersey State Police, Forensic Science Bureau, West Trenton, N. J.

    (Received 27 July 1978; accepted 1 September 1978)

    Abstract

    Chemical ionization (CI) mass spectrometry is being used with increasing frequency for studying various classes of organic compounds. Molecular weight data and information relating to the loss of labile substituent groups have been obtained from organic compounds as diverse as biogenic amines [1], phenothiazines [2], polytertiary alkylamines [3], quaternary amines [4], esters of carboxylic acids [5], trinitroaromatics [6], and carbohydrates [7,8].


    Paper ID: JFS10836J

    DOI: 10.1520/JFS10836J

    ASTM International
    is a member of CrossRef.

    Author
    Title Chemical Ionization Mass Spectrometry of Morphine Derivatives
    Symposium , 0000-00-00
    Committee E30