Processed databases
Atom-Mass pairs
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: 2.0158Out 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 "120.0444"
| Formula | Mass differences | Num. used protons | Num. required extra protons | Atom names |
| C6N1Cl1 | 0.472 | 1 | 0 | C6,C7,C8,C10,C11,C14,Cl15,N17 |
| C6N1Cl1 | 0.472 | 1 | 0 | C6,C8,C10,C11,C12,C14,Cl15,N17 |
| C6N1Cl1 | 0.472 | 1 | 0 | C6,C8,C10,C11,C13,C14,Cl15,N17 |
| C6N1Cl1 | 0.472 | 1 | 0 | C8,C9,C10,C11,C12,C13,Cl15,N16 |
| C6N1Cl1 | 0.472 | 1 | 0 | C8,C9,C10,C11,C12,C14,Cl15,N17 |
| C6N1Cl1 | 0.472 | 1 | 0 | C8,C9,C10,C11,C13,C14,Cl15,N17 |
| C6N1Cl1 | 0.472 | 1 | 0 | C8,C9,C10,C11,C12,C14,Cl15,N16 |
| C6N1Cl1 | 0.472 | 1 | 0 | C8,C10,C11,C12,C13,C14,Cl15,N16 |
| C6N1Cl1 | 0.472 | 1 | 0 | C8,C10,C11,C12,C13,C14,Cl15,N17 |
| C6N1Cl1 | 0.472 | 1 | 0 | C9,C10,C11,C12,C13,C14,Cl15,N17 |
| C6N1Cl1 | 0.472 | 1 | 0 | C9,C10,C11,C12,C13,C14,Cl15,N16 |
| C5N2O2 | 0.021 | 0 | 0 | C6,C7,C10,C13,C14,N17,N18,O19,O20 |
| C5N2O2 | 0.021 | 0 | 0 | C9,C10,C12,C13,C14,N16,N17,O19,O20 |
| C7Cl1 | 0.491 | 1 | 0 | C8,C9,C10,C11,C12,C13,C14,Cl15 |
| C7O2 | 0.061 | 4 | 1 | C8,C9,C10,C11,C12,C13,C14,O19,O20 |
| C7N2 | 0.107 | 8 | 1 | C4,C6,C7,C9,C10,C13,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 1 | C4,C6,C7,C8,C10,C11,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 0 | C1,C4,C6,C7,C8,C10,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 0 | C1,C4,C6,C7,C10,C13,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 0 | C4,C5,C6,C7,C8,C10,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 0 | C4,C5,C6,C7,C10,C13,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 1 | C4,C6,C7,C8,C10,C13,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 0 | C1,C4,C5,C6,C7,C10,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 1 | C5,C6,C7,C9,C10,C13,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 1 | C5,C6,C7,C8,C10,C11,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 0 | C2,C5,C6,C7,C8,C10,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 0 | C2,C5,C6,C7,C10,C13,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 1 | C5,C6,C7,C8,C10,C13,C14,N17,N18 |
| C7N2 | 0.107 | 8 | 1 | C6,C7,C8,C10,C11,C12,C14,N16,N17 |
| C7N2 | 0.107 | 8 | 1 | C6,C7,C9,C10,C12,C13,C14,N16,N17 |
| C7N2 | 0.107 | 8 | 2 | C6,C8,C9,C10,C11,C12,C14,N16,N17 |
| C7N2 | 0.107 | 8 | 2 | C6,C8,C9,C10,C12,C13,C14,N16,N17 |
| C7N2 | 0.107 | 8 | 2 | C6,C7,C8,C9,C10,C13,C14,N17,N18 |
| C7N1O1 | 0.084 | 6 | 1 | C6,C8,C9,C10,C11,C12,C14,N17,O19 |
| C7N1O1 | 0.084 | 6 | 2 | C6,C9,C10,C11,C12,C13,C14,N17,O19 |
| C7N1O1 | 0.084 | 6 | 1 | C6,C7,C8,C10,C11,C13,C14,N17,O20 |
| C7N1O1 | 0.084 | 6 | 1 | C6,C7,C9,C10,C12,C13,C14,N17,O20 |
| C7N1O1 | 0.084 | 6 | 0 | C6,C7,C8,C10,C11,C12,C14,N17,O19 |
| C7N1O1 | 0.084 | 6 | 0 | C6,C7,C9,C10,C12,C13,C14,N17,O19 |
| C7N1O1 | 0.084 | 6 | 1 | C6,C8,C9,C10,C11,C13,C14,N17,O19 |
| C7N1O1 | 0.084 | 6 | 2 | C6,C8,C9,C10,C12,C13,C14,N17,O20 |
| C7N1O1 | 0.084 | 6 | 1 | C6,C8,C9,C10,C12,C13,C14,N17,O19 |
| C7N1O1 | 0.084 | 6 | 2 | C6,C8,C9,C10,C11,C13,C14,N17,O20 |
| C7N1O1 | 0.084 | 6 | 2 | C6,C8,C10,C11,C12,C13,C14,N17,O19 |
| C7N1O1 | 0.084 | 6 | 0 | C6,C7,C8,C9,C10,C13,C14,N17,O19 |
| C7N1O1 | 0.084 | 6 | 0 | C6,C7,C8,C10,C11,C13,C14,N17,O19 |
| C7N1O1 | 0.084 | 6 | 1 | C8,C9,C10,C11,C12,C13,C14,N16,O19 |
| C7N1O1 | 0.084 | 6 | 2 | C8,C9,C10,C11,C12,C13,C14,N16,O20 |
| C6N1O2 | 0.041 | 2 | 0 | C6,C8,C10,C11,C13,C14,N17,O19,O20 |
| C6N1O2 | 0.041 | 2 | 0 | C6,C7,C8,C10,C13,C14,N17,O19,O20 |
| C6N1O2 | 0.041 | 2 | 0 | C8,C9,C10,C12,C13,C14,N16,O19,O20 |
| C6N1O2 | 0.041 | 2 | 0 | C8,C10,C11,C12,C13,C14,N16,O19,O20 |
| C6N1O2 | 0.041 | 2 | 0 | C8,C10,C11,C12,C13,C14,N17,O19,O20 |
| C6N1O2 | 0.041 | 2 | 0 | C9,C10,C11,C12,C13,C14,N16,O19,O20 |
| C6N1O2 | 0.041 | 2 | 0 | C9,C10,C11,C12,C13,C14,N17,O19,O20 |
| C6N2O1 | 0.064 | 4 | 0 | C4,C6,C7,C10,C13,C14,N17,N18,O20 |
| C6N2O1 | 0.064 | 4 | 0 | C4,C6,C7,C8,C10,C14,N17,N18,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C4,C6,C7,C10,C13,C14,N17,N18,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C1,C4,C5,C6,C7,C14,N17,N18,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C5,C6,C7,C10,C13,C14,N17,N18,O20 |
| C6N2O1 | 0.064 | 4 | 0 | C5,C6,C7,C8,C10,C14,N17,N18,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C5,C6,C7,C10,C13,C14,N17,N18,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C6,C8,C10,C11,C12,C14,N16,N17,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C6,C9,C10,C12,C13,C14,N16,N17,O20 |
| C6N2O1 | 0.064 | 4 | 0 | C6,C9,C10,C12,C13,C14,N16,N17,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C6,C7,C8,C10,C13,C14,N17,N18,O20 |
| C6N2O1 | 0.064 | 4 | 0 | C6,C7,C8,C10,C11,C14,N17,N18,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C6,C7,C9,C10,C13,C14,N17,N18,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C6,C7,C9,C10,C13,C14,N17,N18,O20 |
| C6N2O1 | 0.064 | 4 | 0 | C6,C7,C8,C10,C13,C14,N17,N18,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C8,C9,C10,C12,C13,C14,N16,N17,O20 |
| C6N2O1 | 0.064 | 4 | 1 | C8,C10,C11,C12,C13,C14,N16,N17,O20 |
| C6N2O1 | 0.064 | 4 | 0 | C8,C9,C10,C12,C13,C14,N16,N17,O19 |
| C6N2O1 | 0.064 | 4 | 0 | C8,C10,C11,C12,C13,C14,N16,N17,O19 |
| C6N2O1 | 0.064 | 4 | 1 | C9,C10,C11,C12,C13,C14,N16,N17,O20 |