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_aff57e322ff8db7dab140b2fbb142fd3 CP-634384 [M-H]- 340.119 0.94 197.83 CC1=CC(=CC(=C1OC2=C3CCCC3=C(C=C2)O)C)NC(=O)C(=O)O Organic oxygen compounds -1 1 TW polyala
CCSBASE_dcfc0545592ff23d1d5dea9227317a63 CP-409092 [M+Na]+ 320.1369 0.77 183.02 CNCC1=CC=C(C=C1)NC(=O)C2=CNC3=C2C(=O)CCC3 Benzenoids 1 1 TW polyala
CCSBASE_ad614c2b5e747e07b11fe4c987f1c2af CP-409092 [M-H]- 296.1404 0.72 177.51 CNCC1=CC=C(C=C1)NC(=O)C2=CNC3=C2C(=O)CCC3 Benzenoids -1 1 TW polyala
CCSBASE_720871d0cb3245da971720971b7558dd Rosiglitazone maleate [M+H]+ 358.122 0.77 174.49 CN(CCOC1=CC=C(C=C1)CC2C(=O)NC(=O)S2)C3=CC=CC=N3 Benzenoids 1 1 TW polyala
CCSBASE_0c2b02fef97447c973fac8f54743f591 Rosiglitazone maleate [M+Na]+ 380.1039 0.76 181.9 CN(CCOC1=CC=C(C=C1)CC2C(=O)NC(=O)S2)C3=CC=CC=N3 Benzenoids 1 1 TW polyala
CCSBASE_ed7c3560e922277daf1f120a4fb0d23e Rosiglitazone maleate [M-H]- 356.1074 0.71 177.56 CN(CCOC1=CC=C(C=C1)CC2C(=O)NC(=O)S2)C3=CC=CC=N3 Benzenoids -1 1 TW polyala
CCSBASE_c07387f68b506893d8e4b51ee839c712 Colchicine [M+H]+ 400.1755 0.82 193.87 CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC Hydrocarbon derivatives 1 1 TW polyala
CCSBASE_4d1cc774f91a3c2515d5ab170b023d30 Colchicine [M+H-H2O]+ 382.165 0.82 188.05 CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC Hydrocarbon derivatives 1 1 TW polyala
CCSBASE_8a8c2c7d3fdac7a8fb11804aebcd04be Colchicine [M+Na]+ 422.1574 0.85 199.41 CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC Hydrocarbon derivatives 1 1 TW polyala
CCSBASE_463c53be7026b65e106c117f8f4043b0 Isoniazid [M-H]- 136.0516 0.81 131.39 C1=CN=CC=C1C(=O)NN Organoheterocyclic compounds -1 1 TW polyala
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