The reagent gas is ionized before the analyte enters the reaction environment. Its ions then interact with analyte molecules through proton transfer, charge exchange, or adduct formation. These reactions produce detectable species such as [M+H]+, allowing the measured ion mass to provide information about the analyte’s molecular mass.
Limited fragmentation preserves more of the molecular-ion information than extensive fragmentation would. This makes the observed ion, including a protonated or adducted form, useful for estimating molecular mass and supporting compound identification. The resulting spectrum can therefore provide a complementary perspective when structural interpretation requires both mass information and fragment evidence.
These reaction pathways alter how the analyte appears in the mass spectrum. Proton transfer can generate a species such as [M+H]+, while charge exchange transfers charge between the reagent ion and analyte. Adduct formation attaches the analyte to another charged species. Recognizing these possibilities helps researchers interpret detected peaks without treating every peak as the neutral molecule itself.
First, the reagent gas is ionized to create reactive reagent ions. The analyte is then exposed to those ions, which react through proton transfer, charge exchange, or adduct formation. The resulting analyte-related ions are measured by mass spectrometry, and their masses are interpreted to support molecular-mass determination and compound characterization.
This mode is useful when researchers analyze biological compounds and want the molecular ion information to remain prominent. Supported applications include metabolites, lipids, drugs, and other biomolecules. Preserving that information can assist identification when a simpler molecular-mass signal is more informative than a spectrum dominated by extensive fragmentation.
Chemical ionization and electron ionization can contribute different evidence to compound characterization. Chemical ionization helps preserve molecular-ion information, whereas electron ionization data can provide complementary spectral information through its different ionization behavior. Comparing the two types of data can strengthen identification of metabolites, drugs, lipids, and related biological analytes.