Name:
Adduct:
Polarity:
Z:
m/z:
±:
CCS: Å
±: %
SMI:

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ID Name Adduct Structure m/z RT CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_a454d5cec4030bcd5314308012192310 PK 11195 [M+K]+ 391.0974 1.01 191.54 CCC(C)N(C)C(=O)C1=CC2=CC=CC=C2C(=N1)C3=CC=CC=C3Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_6344373d12c7ee1669cdd0cc12706b0d PK 11195 [M+Na]+ 375.1234 0.99 190.59 CCC(C)N(C)C(=O)C1=CC2=CC=CC=C2C(=N1)C3=CC=CC=C3Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_bd541b7d8bbe2d3075842e4ddd90d91c Zearalenone [M-H]- 317.1394 0.88 177.8 CC1CCCC(=O)CCCC=CC2=C(C(=CC(=C2)O)O)C(=O)O1 Phenylpropanoids and polyketides -1 1 TW polyala
CCSBASE_028147a6e63200ba6048aa3afbbf0c1a Malic acid [M-H]- 133.0142 0.26 125.89 C(C(C(=O)O)O)C(=O)O Organic acids and derivatives -1 1 TW polyala
CCSBASE_cbd22f1b26fd752299340c553803397d Tetrac [M-H]- 746.6528 0.9 202.27 C1=C(C=C(C(=C1I)OC2=CC(=C(C(=C2)I)O)I)I)CC(=O)O Benzenoids -1 1 TW polyala
CCSBASE_2be8498adc818d5d0037e0414fe2a0bb 2,4,6-Trichlorophenol [M-H]- 194.9176 0.88 133.91 C1=C(C=C(C(=C1Cl)O)Cl)Cl Benzenoids -1 1 TW polyala
CCSBASE_bc011fc5b0ac9fd16666c436c182d769 Triethyl citrate [M+Na]+ 299.1101 0.84 167.09 CCOC(=O)CC(CC(=O)OCC)(C(=O)OCC)O Organic acids and derivatives 1 1 TW polyala
CCSBASE_fd4ce7f1287b770a41ba6a8cfc3dfbc5 Monuron [M+H]+ 199.0633 0.84 141.14 CN(C)C(=O)NC1=CC=C(C=C1)Cl Benzenoids 1 1 TW polyala
CCSBASE_9b6e2adeb2ce7c72bab61f2ab3c16a14 Monuron [M-H]- 197.0487 0.79 144.61 CN(C)C(=O)NC1=CC=C(C=C1)Cl Benzenoids -1 1 TW polyala
1 2 ... 50 51 52 53 54 55 56 ... 359 360