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Submission id: EA278112

Outputs for Metoclopramide; LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+


Database: Department of Environmental Chemistry, Eawag
Entry ID: EA278112
Synonyms: Metoclopramide, 4-amino-5-chloro-N-(2-diethylaminoethyl)-2-methoxy-benzamide
Total mass: 299.7955
Formula: H22 C14 N3 O2 Cl1

Experimental information


MS type: MS2
Instrument: LTQ Orbitrap XL Thermo Scientific
Instrument type: LC-ESI-ITFT
Ionization: ESI
Ionization mode: POSITIVE

CAMP general report:

Acceptable mass threshold: 2.0158
Out of range queried mass peaks:
Replicated queried mass peaks: 92.0494, 100.1121, 128.0262, 148.063, 156.0211, 168.9925, 170.0003, 183.032, 184.016, 212.0347,
Processing time: 0:00:03.326319

Results for the quried mass "102.0098"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C7N1 0.103 4 0 C6,C8,C9,C10,C11,C12,C14,N17
C7N1 0.103 4 1 C6,C9,C10,C11,C12,C13,C14,N17
C7N1 0.103 4 0 C6,C7,C8,C10,C11,C12,C14,N17
C7N1 0.103 4 0 C6,C7,C9,C10,C12,C13,C14,N17
C7N1 0.103 4 1 C6,C8,C10,C11,C12,C13,C14,N17
C7N1 0.103 4 0 C6,C8,C9,C10,C11,C13,C14,N17
C7N1 0.103 4 0 C6,C8,C9,C10,C12,C13,C14,N17
C7N1 0.103 4 0 C6,C7,C8,C9,C10,C13,C14,N17
C7N1 0.103 4 0 C6,C7,C8,C10,C11,C13,C14,N17
C7N1 0.103 4 2 C8,C9,C10,C11,C12,C13,C14,N17
C7N1 0.103 4 0 C8,C9,C10,C11,C12,C13,C14,N16
C4O1Cl1 0.499 2 1 C8,C10,C11,C13,Cl15,O20
C4O1Cl1 0.499 2 0 C8,C10,C11,C14,Cl15,O19
C4O1Cl1 0.499 2 1 C9,C11,C12,C13,Cl15,O20
C6N2 0.084 2 0 C4,C6,C7,C8,C10,C14,N17,N18
C6N2 0.084 2 0 C4,C6,C7,C10,C13,C14,N17,N18
C6N2 0.084 2 0 C1,C4,C6,C7,C10,C14,N17,N18
C6N2 0.084 2 0 C4,C5,C6,C7,C10,C14,N17,N18
C6N2 0.084 2 0 C1,C4,C5,C6,C7,C14,N17,N18
C6N2 0.084 2 0 C5,C6,C7,C8,C10,C14,N17,N18
C6N2 0.084 2 0 C5,C6,C7,C10,C13,C14,N17,N18
C6N2 0.084 2 0 C2,C5,C6,C7,C10,C14,N17,N18
C6N2 0.084 2 0 C6,C9,C10,C12,C13,C14,N16,N17
C6N2 0.084 2 0 C6,C8,C10,C11,C12,C14,N16,N17
C6N2 0.084 2 0 C6,C7,C8,C10,C11,C14,N17,N18
C6N2 0.084 2 0 C6,C7,C9,C10,C13,C14,N17,N18
C6N2 0.084 2 0 C6,C7,C8,C10,C13,C14,N17,N18
C6N2 0.084 2 0 C8,C9,C10,C12,C13,C14,N16,N17
C6N2 0.084 2 0 C8,C9,C10,C11,C12,C14,N16,N17
C6N2 0.084 2 0 C8,C10,C11,C12,C13,C14,N16,N17
C6N2 0.084 2 0 C9,C10,C11,C12,C13,C14,N16,N17
C6N1O1 0.060 0 0 C6,C8,C10,C11,C12,C14,N17,O19
C6N1O1 0.060 0 0 C6,C8,C10,C11,C13,C14,N17,O20
C6N1O1 0.060 0 0 C6,C9,C10,C12,C13,C14,N17,O20
C6N1O1 0.060 0 0 C6,C9,C10,C12,C13,C14,N17,O19
C6N1O1 0.060 0 0 C6,C7,C8,C10,C13,C14,N17,O20
C6N1O1 0.060 0 0 C6,C7,C8,C10,C11,C14,N17,O19
C6N1O1 0.060 0 0 C6,C7,C9,C10,C13,C14,N17,O19
C6N1O1 0.060 0 0 C6,C8,C9,C10,C13,C14,N17,O19
C6N1O1 0.060 0 0 C6,C8,C10,C11,C13,C14,N17,O19
C6N1O1 0.060 0 0 C6,C7,C9,C10,C13,C14,N17,O20
C6N1O1 0.060 0 0 C8,C9,C10,C11,C12,C13,N16,O20
C6N1O1 0.060 0 0 C8,C9,C10,C12,C13,C14,N16,O19
C6N1O1 0.060 0 0 C8,C9,C10,C12,C13,C14,N17,O20
C6N1O1 0.060 0 0 C8,C9,C10,C11,C12,C14,N16,O19
C6N1O1 0.060 0 0 C8,C10,C11,C12,C13,C14,N16,O19
C6N1O1 0.060 0 0 C8,C10,C11,C12,C13,C14,N17,O20
C6N1O1 0.060 0 0 C8,C10,C11,C12,C13,C14,N16,O20
C6N1O1 0.060 0 0 C8,C9,C10,C12,C13,C14,N16,O20
C6N1O1 0.060 0 0 C8,C9,C10,C12,C13,C14,N17,O19
C6N1O1 0.060 0 0 C8,C9,C10,C11,C12,C14,N17,O19
C6N1O1 0.060 0 0 C8,C9,C10,C11,C13,C14,N17,O20
C6N1O1 0.060 0 0 C8,C9,C10,C11,C13,C14,N17,O19
C6N1O1 0.060 0 0 C8,C10,C11,C12,C13,C14,N17,O19
C6N1O1 0.060 0 0 C9,C10,C11,C12,C13,C14,N17,O19
C6N1O1 0.060 0 0 C9,C10,C11,C12,C13,C14,N17,O20
C6N1O1 0.060 0 0 C9,C10,C11,C12,C13,C14,N16,O19
C6N1O1 0.060 0 0 C9,C10,C11,C12,C13,C14,N16,O20
C4N1Cl1 0.476 4 0 C8,C9,C11,C12,Cl15,N16
C4N1Cl1 0.476 4 1 C8,C10,C11,C12,Cl15,N16
C4N1Cl1 0.476 4 1 C9,C11,C12,C13,Cl15,N16
C7O1 0.080 2 0 C8,C9,C10,C11,C12,C13,C14,O19
C7O1 0.080 2 0 C8,C9,C10,C11,C12,C13,C14,O20
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