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

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ID Name Adduct Structure m/z RT CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_1f409a9938e18dfdac77d4cae81edade 9-Ethyl-3-nitro-9H-carbazole [M+H]+ 241.0972 0.93 150.8 CCN1C2=C(C=C(C=C2)[N+](=O)[O-])C3=CC=CC=C31 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_99f3e42eede6c15f8da852dee3845191 9-Ethyl-3-nitro-9H-carbazole [M+Na]+ 263.0791 0.89 155.69 CCN1C2=C(C=C(C=C2)[N+](=O)[O-])C3=CC=CC=C31 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_a08bffe558845b393d107e2ec087c0ff Diethofencarb [M+Na]+ 290.1363 0.83 176.14 CCOC1=C(C=C(C=C1)NC(=O)OC(C)C)OCC Benzenoids 1 1 TW polyala
CCSBASE_ff206d684861949f5e648c5090ef8d2e Rhodamine B [M]+ 443.2329 0.81 216.08 CCN(CC)C1=CC2=C(C=C1)C(=C3C=CC(=[N+](CC)CC)C=C3O2)C4=CC=CC=C4C(=O)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_7d5ab2d2201b7adea66ff114caa4ccb4 Nimesulide [M+H]+ 309.054 0.81 169.04 CS(=O)(=O)NC1=C(C=C(C=C1)[N+](=O)[O-])OC2=CC=CC=C2 Benzenoids 1 1 TW polyala
CCSBASE_7434fc3688cd318a4cc5eeee74a00fde N-(3-Aminophenyl)propanamide [M+H]+ 165.1022 0.67 135.83 CCC(=O)NC1=CC=CC(=C1)N Benzenoids 1 1 TW polyala
CCSBASE_00d9f70de5d638d3c1249a70db1d15ad Coumaphos [M+H]+ 363.0217 0.91 179.04 CCOP(=S)(OCC)OC1=CC2=C(C=C1)C(=C(C(=O)O2)Cl)C Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_53211294de3779f9a0c8552446748c22 Coumaphos [M+Na]+ 385.0037 0.91 198.33 CCOP(=S)(OCC)OC1=CC2=C(C=C1)C(=C(C(=O)O2)Cl)C Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_fd0716f0dc72349dffd37ea0647ed634 4'-Acetylbiphenyl [M+H]+ 197.0961 0.88 143.21 CC(=O)C1=CC=C(C=C1)C2=CC=CC=C2 Organic oxygen compounds 1 1 TW polyala
CCSBASE_49167075047399b2ecebb8a97bea23df 2,2'-(Oxydimethanediyl)bis(2-ethylpropane-1,3-diol) [M+H]+ 251.1853 0.71 155.44 CCC(CO)(CO)COCC(CC)(CO)CO Organic oxygen compounds 1 1 TW polyala
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