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Submission id: BML01822

Outputs for 3,4-Dihydroxy-L-phenylalanine; LC-ESI-QTOF; MS2; CE 40 ev; [M+H]+


Database: Institute of Biological Chemistry, Washington State University
Entry ID: BML01822
Synonyms: 3,4-Dihydroxy-L-phenylalanine
Total mass: 197.1875
Formula: H11 C9 O4 N1

Experimental information


MS type: MS2
Instrument: Agilent 1200 RRLC; Agilent 6520 QTOF
Instrument type: LC-ESI-QTOF
Ionization mode: POSITIVE

CAMP general report:

Acceptable mass threshold: 2.0158
Out of range queried mass peaks:
Replicated queried mass peaks: 105.0359, 105.0588, 106.0669, 107.051, 107.0764, 107.0829, 107.0918, 107.1048, 107.1226, 107.1474, 107.6021, 108.0607, 110.0364, 111.0398, 117.0292, 117.0356, 117.0581, 117.0648, 134.0607, 135.0468, 136.0552,
Processing time: 0:00:01.135544

Results for the quried mass "104.0519"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C6O2 0.011 0 0 C1,C2,C4,C5,C7,C8,O11,O12
C5O2N1 0.009 2 0 C3,C4,C5,C6,C9,N10,O13,O14
C5O2N1 0.009 2 0 C1,C3,C5,C6,C9,N10,O13,O14
C6O1N1 0.034 2 0 C1,C2,C3,C5,C6,C7,N10,O11
C6O1N1 0.034 2 0 C3,C4,C5,C6,C7,C8,N10,O11
C6O1N1 0.034 2 0 C3,C4,C5,C6,C7,C8,N10,O12
C6O1N1 0.034 2 0 C3,C4,C5,C6,C8,C9,N10,O13
C6O1N1 0.034 2 0 C3,C4,C5,C6,C8,C9,N10,O14
C6O1N1 0.034 2 0 C3,C4,C5,C6,C8,C9,N10,O12
C6O1N1 0.034 2 0 C1,C3,C4,C5,C6,C8,N10,O12
C6O1N1 0.034 2 0 C1,C2,C3,C5,C6,C9,N10,O13
C6O1N1 0.034 2 0 C1,C2,C3,C5,C6,C9,N10,O14
C7N1 0.077 6 0 C1,C2,C3,C5,C6,C7,C8,N10
C7N1 0.077 6 0 C1,C2,C3,C5,C6,C7,C9,N10
C7N1 0.077 6 0 C3,C4,C5,C6,C7,C8,C9,N10
C7N1 0.077 6 0 C1,C3,C4,C5,C6,C7,C8,N10
C7N1 0.077 6 0 C2,C3,C4,C5,C6,C7,C8,N10
C7N1 0.077 6 0 C1,C2,C3,C4,C5,C6,C8,N10
C7N1 0.077 6 0 C1,C2,C3,C4,C5,C6,C7,N10
C7O1 0.054 4 0 C1,C2,C3,C5,C6,C7,C9,O13
C7O1 0.054 4 0 C1,C2,C3,C5,C6,C7,C9,O14
C7O1 0.054 4 0 C1,C2,C3,C5,C6,C7,C8,O12
C7O1 0.054 4 0 C1,C2,C3,C5,C6,C7,C9,O11
C7O1 0.054 4 0 C3,C4,C5,C6,C7,C8,C9,O11
C7O1 0.054 4 0 C3,C4,C5,C6,C7,C8,C9,O13
C7O1 0.054 4 0 C3,C4,C5,C6,C7,C8,C9,O14
C7O1 0.054 4 0 C1,C2,C3,C5,C6,C7,C8,O11
C7O1 0.054 4 0 C3,C4,C5,C6,C7,C8,C9,O12
C7O1 0.054 4 0 C1,C2,C3,C4,C5,C7,C8,O12
C7O1 0.054 4 0 C1,C2,C3,C4,C5,C7,C8,O11
C7O1 0.054 4 0 C1,C3,C4,C5,C6,C7,C8,O11
C7O1 0.054 4 0 C1,C3,C4,C5,C6,C8,C9,O12
C7O1 0.054 4 0 C1,C3,C4,C5,C6,C8,C9,O13
C7O1 0.054 4 0 C1,C3,C4,C5,C6,C8,C9,O14
C7O1 0.054 4 0 C1,C2,C3,C4,C5,C6,C8,O12
C7O1 0.054 4 0 C1,C2,C3,C4,C5,C6,C9,O13
C7O1 0.054 4 0 C1,C2,C3,C4,C5,C6,C9,O14
C7O1 0.054 4 0 C2,C3,C4,C5,C6,C7,C8,O12
C7O1 0.054 4 0 C2,C3,C4,C5,C6,C7,C8,O11
C7O1 0.054 4 0 C1,C2,C3,C4,C5,C6,C7,O11
C8 0.097 8 2 C1,C2,C3,C4,C5,C6,C7,C8
C8 0.097 8 2 C1,C2,C3,C4,C5,C6,C8,C9
C8 0.097 8 2 C1,C2,C3,C4,C5,C6,C7,C9
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