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Submission id: EA278105

Outputs for Metoclopramide; LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+


Database: Department of Environmental Chemistry, Eawag
Entry ID: EA278105
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: 168.9917, 184.016,
Processing time: 0:00:02.566789

Results for the quried mass "128.0266"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C8N1O1 0.081 2 0 C6,C8,C9,C10,C11,C12,C13,C14,N17,O20
C8N1O1 0.081 2 0 C6,C8,C9,C10,C11,C12,C13,C14,N17,O19
C8N1O1 0.081 2 0 C6,C7,C8,C9,C10,C11,C12,C14,N17,O19
C8N1O1 0.081 2 0 C6,C7,C8,C10,C11,C12,C13,C14,N17,O20
C8N1O1 0.081 2 0 C6,C7,C9,C10,C11,C12,C13,C14,N17,O20
C8N1O1 0.081 2 0 C6,C7,C9,C10,C11,C12,C13,C14,N17,O19
C8N1O1 0.081 2 0 C6,C7,C8,C9,C10,C11,C13,C14,N17,O20
C8N1O1 0.081 2 0 C6,C7,C8,C9,C10,C11,C13,C14,N17,O19
C8N1O1 0.081 2 0 C6,C7,C8,C9,C10,C12,C13,C14,N17,O20
C8N1O1 0.081 2 0 C6,C7,C8,C9,C10,C12,C13,C14,N17,O19
C8N1O1 0.081 2 0 C6,C7,C8,C10,C11,C12,C13,C14,N17,O19
C8N2 0.104 4 0 C4,C6,C7,C9,C10,C12,C13,C14,N17,N18
C8N2 0.104 4 0 C4,C6,C7,C8,C10,C11,C12,C14,N17,N18
C8N2 0.104 4 0 C1,C4,C6,C7,C8,C10,C11,C14,N17,N18
C8N2 0.104 4 0 C1,C4,C6,C7,C9,C10,C13,C14,N17,N18
C8N2 0.104 4 0 C4,C5,C6,C7,C8,C10,C11,C14,N17,N18
C8N2 0.104 4 0 C4,C5,C6,C7,C9,C10,C13,C14,N17,N18
C8N2 0.104 4 0 C4,C6,C7,C8,C10,C11,C13,C14,N17,N18
C8N2 0.104 4 0 C4,C6,C7,C8,C9,C10,C13,C14,N17,N18
C8N2 0.104 4 0 C1,C4,C5,C6,C7,C8,C10,C14,N17,N18
C8N2 0.104 4 0 C1,C4,C5,C6,C7,C10,C13,C14,N17,N18
C8N2 0.104 4 0 C1,C4,C6,C7,C8,C10,C13,C14,N17,N18
C8N2 0.104 4 0 C4,C5,C6,C7,C8,C10,C13,C14,N17,N18
C8N2 0.104 4 0 C5,C6,C7,C9,C10,C12,C13,C14,N17,N18
C8N2 0.104 4 0 C5,C6,C7,C8,C10,C11,C12,C14,N17,N18
C8N2 0.104 4 0 C2,C5,C6,C7,C8,C10,C11,C14,N17,N18
C8N2 0.104 4 0 C2,C5,C6,C7,C9,C10,C13,C14,N17,N18
C8N2 0.104 4 0 C5,C6,C7,C8,C10,C11,C13,C14,N17,N18
C8N2 0.104 4 0 C5,C6,C7,C8,C9,C10,C13,C14,N17,N18
C8N2 0.104 4 0 C2,C5,C6,C7,C8,C10,C13,C14,N17,N18
C8N2 0.104 4 0 C6,C7,C8,C9,C10,C11,C12,C14,N17,N18
C8N2 0.104 4 0 C6,C7,C9,C10,C11,C12,C13,C14,N17,N18
C8N2 0.104 4 0 C6,C8,C9,C10,C11,C12,C13,C14,N16,N17
C8N2 0.104 4 0 C6,C7,C8,C9,C10,C11,C12,C14,N16,N17
C8N2 0.104 4 0 C6,C7,C8,C10,C11,C12,C13,C14,N16,N17
C8N2 0.104 4 0 C6,C7,C8,C10,C11,C12,C13,C14,N17,N18
C8N2 0.104 4 0 C6,C7,C8,C9,C10,C11,C13,C14,N17,N18
C8N2 0.104 4 0 C6,C7,C8,C9,C10,C12,C13,C14,N16,N17
C8N2 0.104 4 0 C6,C7,C8,C9,C10,C12,C13,C14,N17,N18
C8N2 0.104 4 0 C6,C7,C9,C10,C11,C12,C13,C14,N16,N17
C6N1Cl1 0.455 6 1 C6,C7,C8,C10,C11,C14,Cl15,N17
C5O2Cl1 0.487 1 0 C8,C10,C11,C13,C14,Cl15,O19,O20
C7N3 0.084 2 0 C6,C7,C8,C10,C11,C12,C14,N16,N17,N18
C7N3 0.084 2 0 C6,C7,C9,C10,C12,C13,C14,N16,N17,N18
C5N2Cl1 0.475 4 1 C8,C10,C11,C12,C14,Cl15,N16,N17
C9N1 0.124 6 0 C6,C7,C8,C9,C10,C11,C12,C13,C14,N17
C5N1O1Cl1 0.498 2 0 C3,C9,C11,C12,C13,Cl15,N16,O20
C7N2O1 0.061 0 0 C1,C2,C4,C5,C6,C7,C14,N17,N18,O19
C6O1Cl1 0.478 4 1 C8,C9,C10,C11,C12,C14,Cl15,O19
C6O1Cl1 0.478 4 1 C8,C9,C10,C11,C13,C14,Cl15,O19
C6N2O1 0.145 12 0 C1,C4,C5,C6,C7,C14,N17,N18,O19
C6N2O1 0.145 12 2 C1,C4,C6,C7,C10,C14,N17,N18,O19
C6N2O1 0.145 12 2 C2,C5,C6,C7,C10,C14,N17,N18,O19
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