NMRFAM Logo Computational Annotation of MS Peaks (CAMP)
Home
Processed databases
Atom-Mass pairs
Submission id: EA278113

Outputs for Metoclopramide; LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M+H]+


Database: Department of Environmental Chemistry, Eawag
Entry ID: EA278113
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: 65.0385, 92.0494, 100.112, 128.0261, 148.063, 156.021, 168.9924, 170.0002, 182.024, 183.0319, 212.0346,
Processing time: 0:00:03.720680

Results for the quried mass "129.0101"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C8N1O1 0.105 3 0 C6,C8,C9,C10,C11,C12,C13,C14,N17,O20
C8N1O1 0.105 3 0 C6,C8,C9,C10,C11,C12,C13,C14,N17,O19
C8N1O1 0.105 3 0 C6,C7,C8,C9,C10,C11,C12,C14,N17,O19
C8N1O1 0.105 3 0 C6,C7,C9,C10,C11,C12,C13,C14,N17,O19
C8N1O1 0.105 3 0 C6,C7,C8,C10,C11,C12,C13,C14,N17,O20
C8N1O1 0.105 3 0 C6,C7,C9,C10,C11,C12,C13,C14,N17,O20
C8N2 0.128 5 0 C4,C6,C7,C9,C10,C12,C13,C14,N17,N18
C8N2 0.128 5 0 C4,C6,C7,C8,C10,C11,C12,C14,N17,N18
C8N2 0.128 5 0 C1,C4,C6,C7,C8,C10,C11,C14,N17,N18
C8N2 0.128 5 0 C1,C4,C6,C7,C9,C10,C13,C14,N17,N18
C8N2 0.128 5 0 C4,C5,C6,C7,C8,C10,C11,C14,N17,N18
C8N2 0.128 5 0 C4,C5,C6,C7,C9,C10,C13,C14,N17,N18
C8N2 0.128 5 0 C4,C6,C7,C8,C10,C11,C13,C14,N17,N18
C8N2 0.128 5 0 C4,C6,C7,C8,C9,C10,C13,C14,N17,N18
C8N2 0.128 5 0 C1,C4,C5,C6,C7,C8,C10,C14,N17,N18
C8N2 0.128 5 0 C1,C4,C5,C6,C7,C10,C13,C14,N17,N18
C8N2 0.128 5 0 C5,C6,C7,C9,C10,C12,C13,C14,N17,N18
C8N2 0.128 5 0 C5,C6,C7,C8,C10,C11,C12,C14,N17,N18
C8N2 0.128 5 0 C2,C5,C6,C7,C8,C10,C11,C14,N17,N18
C8N2 0.128 5 0 C2,C5,C6,C7,C9,C10,C13,C14,N17,N18
C8N2 0.128 5 0 C5,C6,C7,C8,C10,C11,C13,C14,N17,N18
C8N2 0.128 5 0 C5,C6,C7,C8,C9,C10,C13,C14,N17,N18
C8N2 0.128 5 0 C6,C7,C8,C9,C10,C11,C12,C14,N17,N18
C8N2 0.128 5 0 C6,C7,C9,C10,C11,C12,C13,C14,N17,N18
C8N2 0.128 5 0 C6,C8,C9,C10,C11,C12,C13,C14,N16,N17
C8N2 0.128 5 0 C6,C7,C8,C9,C10,C12,C13,C14,N16,N17
C8N2 0.128 5 0 C6,C7,C8,C10,C11,C12,C13,C14,N16,N17
C8N2 0.128 5 0 C6,C7,C8,C9,C10,C11,C12,C14,N16,N17
C8N2 0.128 5 0 C6,C7,C9,C10,C11,C12,C13,C14,N16,N17
C8N2 0.128 5 0 C6,C7,C8,C9,C10,C12,C13,C14,N17,N18
C8N2 0.128 5 0 C6,C7,C8,C9,C10,C11,C13,C14,N17,N18
C8N2 0.128 5 0 C6,C7,C8,C10,C11,C12,C13,C14,N17,N18
C5O2Cl1 0.497 1 0 C8,C10,C11,C13,C14,Cl15,O19,O20
C7N3 0.109 3 0 C6,C7,C8,C10,C11,C12,C14,N16,N17,N18
C7N3 0.109 3 0 C6,C7,C9,C10,C12,C13,C14,N16,N17,N18
C7N1O2 0.062 1 0 C8,C9,C10,C11,C12,C13,C14,N17,O19,O20
C7N1O2 0.062 1 0 C8,C9,C10,C11,C12,C13,C14,N16,O19,O20
C9N1 0.148 7 1 C6,C7,C8,C9,C10,C11,C12,C13,C14,N17
C5N1O1Cl1 0.474 3 0 C3,C9,C11,C12,C13,Cl15,N16,O20
C7N2O1 0.085 1 0 C1,C2,C4,C5,C6,C7,C14,N17,N18,O19
C6N2O1 0.170 13 1 C1,C4,C5,C6,C7,C14,N17,N18,O19


Flag Counter