. 2019 May 7;11(5):254. doi: 10.3390/toxins11050254

Table 7.

Optimized mass spectrometry conditions.

Compound	Precursor Ion (m/z)	Declustering Potential (V)	Product Ions (m/z) ^a	Collision Energy (V)	Cell Exit Potential (V)
Nivalenol	371.1 [M + CH₃COO]⁻	−40	281.0/59.0	−22/−40	−14/−5
Deoxyniwalenol	355.1 [M + CH₃COO]⁻	−35	264.8/58.9	−20/−38	−17/−1
13C-Deoxyniwalenol	370.2 [M + CH₃COO]⁻	−50	310.0	−14	−7
Diacetoxyscirpenol	384.1 [M + NH₄]⁺	51	307.0/247.0	17/19	20/16
T-2 toxin	484.1 [M + NH₄]⁺	61	215.0/185.0	29/25	12/14
13C-T-2 toxin	508.3 [M + NH₄]⁺	61	322.1	19	8
HT-2 toxin	442.2 [M + NH₄]⁺	51	215.0/263.0	19/17	14/18
13C-HT-2 toxin	464.1 [M + NH₄]⁺	51	278.1	17	18
Zearalenone	317.1 [M − H]⁻	−85	130.8/174.9	−40/−32	−7/−9
13C-Zearalenone	355.1 [M − H]⁻	−100	139.9	−42	−7

^a quantifier ions are given in bold.