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_1f8ad3cc9147f262f4a146e0d257f906 Sulfosuccinic acid [M-H]- 196.9761 0.26 129.94 C(C(C(=O)O)S(=O)(=O)O)C(=O)O Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_ce5d16fb2725beed7978836292592832 Atorvastatin [M+H]+ 559.2603 0.88 232.1 CC(C)C1=C(C(=C(N1CCC(CC(CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_457f31b0e72aec085a9bf3906b7776bf Atorvastatin [M+H-H2O]+ 541.2498 0.88 222.79 CC(C)C1=C(C(=C(N1CCC(CC(CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_52e86df848e0d7bfbcf4356460440257 Atorvastatin [M+Na]+ 581.2422 0.87 228.37 CC(C)C1=C(C(=C(N1CCC(CC(CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_f79c180fac3287d2c7db0693146133e7 Atorvastatin [M-H]- 557.2457 0.85 228.73 CC(C)C1=C(C(=C(N1CCC(CC(CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4 Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_c0b4f128c3303a30d71d57e03525c101 Atorvastatin [M-H-H2O]- 539.2346 0.85 227.2 CC(C)C1=C(C(=C(N1CCC(CC(CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4 Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_0c09e69c7ac2f56ae657ea5f1acc1d82 Phenyl dihydrogen phosphate [M-H-H2O]- 154.9898 0.81 120.09 C1=CC=C(C=C1)OP(=O)(O)O Organic acids and derivatives -1 1 TW polyala
CCSBASE_43038397f466f5b3408799eff51fb9dc Octyl beta-D-glucopyranoside [M+FA-H]- 337.1868 0.81 189.77 CCCCCCCCOC1C(C(C(C(O1)CO)O)O)O Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_3a2f2484f898426d4b5179141c81039b Octyl beta-D-glucopyranoside [M+K]+ 331.1517 0.84 171.82 CCCCCCCCOC1C(C(C(C(O1)CO)O)O)O Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_607208e0761d281a6b06bd62834b3a6a Octyl beta-D-glucopyranoside [M+Na]+ 315.1778 0.84 179.52 CCCCCCCCOC1C(C(C(C(O1)CO)O)O)O Lipids and lipid-like molecules 1 1 TW polyala
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