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Submission id: EQ326509

Outputs for Genistein; LC-ESI-QFT; MS2; CE: 180; R=35000; [M+H]+


Database: Department of Environmental Chemistry, Eawag
Entry ID: EQ326509
Synonyms: Genistein, 5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one
Total mass: 270.2365
Formula: H10 C15 O5

Experimental information


MS type: MS2
Instrument: Q Exactive Plus Orbitrap Thermo Scientific
Instrument type: LC-ESI-QFT
Ionization: ESI
Ionization mode: POSITIVE

CAMP general report:

Acceptable mass threshold: 2.0158
Out of range queried mass peaks:
Replicated queried mass peaks: 51.023, 52.0308, 53.0386, 53.9975, 55.0179, 62.0151, 63.023, 65.0386, 66.0101, 66.0464, 67.9893, 68.0258, 68.9971, 75.0229, 76.0307, 78.0464, 79.0179, 79.0542, 88.0308, 89.0386, 90.0465, 91.018, 91.0543, 92.0257, 95.0492, 99.0229, 102.0465, 103.0543, 105.0448, 107.0491, 114.0464, 115.0543, 119.049, 126.0465, 127.0541, 129.0446, 132.0573, 139.0543, 140.0619, 151.0544, 169.0647,
Processing time: 0:00:04.589812

Results for the quried mass "98.0152"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C4O3 0.042 2 1 C12,C13,C14,C15,O18,O19,O20
C8 0.086 2 0 C1,C2,C3,C4,C7,C8,C9,C11
C8 0.086 2 0 C1,C5,C8,C10,C11,C12,C14,C15
C8 0.086 2 0 C1,C6,C8,C10,C11,C13,C14,C15
C8 0.086 2 0 C1,C2,C3,C4,C8,C9,C11,C15
C8 0.086 2 0 C1,C2,C4,C8,C11,C12,C14,C15
C8 0.086 2 0 C1,C2,C4,C8,C11,C13,C14,C15
C8 0.086 2 0 C1,C2,C4,C8,C9,C11,C14,C15
C8 0.086 2 0 C1,C2,C5,C8,C11,C12,C14,C15
C8 0.086 2 0 C1,C2,C6,C8,C11,C13,C14,C15
C8 0.086 2 0 C1,C3,C5,C8,C11,C12,C14,C15
C8 0.086 2 0 C1,C3,C6,C8,C11,C13,C14,C15
C8 0.086 2 0 C1,C3,C4,C8,C9,C11,C14,C15
C8 0.086 2 0 C1,C3,C8,C9,C11,C12,C14,C15
C8 0.086 2 0 C1,C3,C8,C9,C11,C13,C14,C15
C8 0.086 2 0 C1,C5,C7,C8,C11,C12,C14,C15
C8 0.086 2 0 C1,C5,C8,C11,C12,C13,C14,C15
C8 0.086 2 0 C1,C6,C7,C8,C11,C13,C14,C15
C8 0.086 2 0 C1,C6,C8,C11,C12,C13,C14,C15
C8 0.086 2 0 C1,C2,C3,C4,C8,C11,C14,C15
C8 0.086 2 0 C1,C2,C3,C8,C11,C12,C14,C15
C8 0.086 2 0 C1,C2,C3,C8,C11,C13,C14,C15
C8 0.086 2 0 C1,C2,C3,C8,C9,C11,C14,C15
C8 0.086 2 0 C1,C2,C7,C8,C11,C12,C14,C15
C8 0.086 2 0 C1,C2,C7,C8,C11,C13,C14,C15
C8 0.086 2 0 C1,C3,C7,C8,C11,C12,C14,C15
C8 0.086 2 0 C1,C3,C7,C8,C11,C13,C14,C15
C8 0.086 2 0 C1,C2,C4,C7,C8,C9,C11,C15
C8 0.086 2 0 C1,C3,C4,C7,C8,C9,C11,C15
C8 0.086 2 0 C2,C5,C8,C10,C11,C12,C14,C15
C8 0.086 2 0 C2,C6,C8,C10,C11,C13,C14,C15
C8 0.086 2 0 C2,C3,C4,C8,C9,C11,C14,C15
C8 0.086 2 0 C2,C4,C5,C8,C11,C12,C14,C15
C8 0.086 2 0 C2,C4,C6,C8,C11,C13,C14,C15
C8 0.086 2 0 C2,C4,C8,C9,C11,C12,C14,C15
C8 0.086 2 0 C2,C4,C8,C9,C11,C13,C14,C15
C8 0.086 2 0 C2,C5,C7,C8,C11,C12,C14,C15
C8 0.086 2 0 C2,C5,C8,C11,C12,C13,C14,C15
C8 0.086 2 0 C2,C6,C7,C8,C11,C13,C14,C15
C8 0.086 2 0 C2,C6,C8,C11,C12,C13,C14,C15
C8 0.086 2 0 C2,C4,C7,C8,C11,C12,C14,C15
C8 0.086 2 0 C2,C4,C7,C8,C11,C13,C14,C15
C8 0.086 2 0 C1,C2,C3,C7,C8,C9,C11,C15
C8 0.086 2 0 C2,C3,C4,C7,C8,C9,C11,C15
C8 0.086 2 0 C1,C3,C8,C11,C12,C13,C14,C15
C8 0.086 2 0 C2,C4,C8,C11,C12,C13,C14,C15
C8 0.086 2 0 C5,C6,C7,C10,C11,C13,C14,C15
C8 0.086 2 0 C5,C6,C8,C10,C11,C13,C14,C15
C8 0.086 2 0 C5,C6,C7,C10,C11,C12,C14,C15
C8 0.086 2 0 C5,C6,C8,C10,C11,C12,C14,C15
C8 0.086 2 0 C5,C6,C10,C11,C12,C13,C14,C15
C8 0.086 2 0 C5,C6,C7,C11,C12,C13,C14,C15
C8 0.086 2 0 C5,C6,C8,C11,C12,C13,C14,C15
C8 0.086 2 0 C5,C7,C10,C11,C12,C13,C14,C15
C8 0.086 2 1 C5,C8,C10,C11,C12,C13,C14,C15
C8 0.086 2 0 C6,C7,C10,C11,C12,C13,C14,C15
C8 0.086 2 1 C6,C8,C10,C11,C12,C13,C14,C15
C8 0.086 2 0 C1,C3,C7,C8,C9,C11,C14,C15
C8 0.086 2 0 C2,C4,C7,C8,C9,C11,C14,C15
C8 0.086 2 0 C5,C7,C8,C10,C11,C12,C14,C15
C8 0.086 2 0 C6,C7,C8,C10,C11,C13,C14,C15
C5O2 0.084 6 2 C5,C6,C7,C10,C13,O17,O20
C5O2 0.084 6 2 C5,C6,C10,C12,C13,O17,O18
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