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Atom-Mass pairs
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Submission id: JP000940
Outputs for 1,1,1-TRICHLORO-2,2-BIS(PARA-CHLOROPHNYL)ETHANE; EI-B; MS
Database: UNIV. OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH, Tokyo
Entry ID: JP000940
Synonyms: 1,1,1-TRICHLORO-2,2-BIS(PARA-CHLOROPHNYL)ETHANE, 4,4'-DDT
Total mass: 354.4859
Formula: H9 C14 Cl5
Experimental information
MS type: MS
Instrument: JEOL JMS-01-SG
Instrument type: EI-B
Ionization: 70 eV
Ionization mode: POSITIVE
CAMP general report:
Acceptable mass threshold: 2.0158
Out of range queried mass peaks:
Replicated queried mass peaks: 51.0, 63.0, 74.0, 75.0, 86.0, 87.0, 89.0, 99.0, 100.0, 106.0, 111.0, 124.0, 136.0, 137.0, 139.0, 151.0, 164.0, 165.0, 173.0, 175.0, 176.0, 200.0, 201.0, 212.0, 214.0, 236.0, 237.0, 239.0, 247.0, 248.0, 284.0,
Processing time: 0:00:07.481905
Results for the quried mass "199.0"
Formula | Mass differences | Num. used protons | Num. required extra protons | Atom names |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C3,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,Cl16 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C3,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,Cl15 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C3,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl17 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C3,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl18 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C3,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl19 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl17 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl18 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl19 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C3,C4,C5,C6,C8,C9,C10,C11,C12,C13,C14,Cl16 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C2,C3,C4,C5,C6,C7,C9,C10,C11,C12,C13,C14,Cl16 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C3,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl17 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C3,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl18 |
C13Cl1 |
0.353 |
7 |
0 |
C1,C3,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl19 |
C13Cl1 |
0.353 |
7 |
0 |
C2,C3,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl17 |
C13Cl1 |
0.353 |
7 |
0 |
C2,C3,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl18 |
C13Cl1 |
0.353 |
7 |
0 |
C2,C3,C4,C5,C6,C7,C8,C9,C10,C11,C12,C13,C14,Cl19 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C2,C3,C6,C7,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C2,C4,C6,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C2,C3,C5,C7,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C2,C4,C5,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C3,C4,C5,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C2,C3,C4,C6,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C3,C4,C5,C7,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C2,C3,C4,C6,C7,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C2,C3,C5,C6,C7,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C2,C4,C5,C6,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C3,C5,C6,C7,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C4,C5,C6,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C4,C5,C7,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C2,C4,C6,C7,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C1,C3,C5,C7,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
C10Cl2 |
0.076 |
8 |
2 |
C2,C3,C6,C7,C8,C9,C10,C11,C12,C13,Cl15,Cl16 |
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