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_5413911234ccef48f7118295a55fcd94 Tetradifon [M+H]+ 356.8886 1.02 166.52 C1=CC(=CC=C1S(=O)(=O)C2=CC(=C(C=C2Cl)Cl)Cl)Cl  Benzenoids 1 1 TW polyala
CCSBASE_6fc06f9979556a7fe2cc80a29e78de26 Trilostane [M+H]+ 330.2064 0.87 182.34 CC12CCC3C(C1CCC2O)CCC45C3(CC(=C(C4O5)O)C#N)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_e70d564c55faaf5ff1de4f4f8fa4936a Trilostane [M+H-H2O]+ 312.1959 0.87 176.18 CC12CCC3C(C1CCC2O)CCC45C3(CC(=C(C4O5)O)C#N)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_a48fb73b774bd9267aa54b5430d5f202 Trilostane [M+Na]+ 352.1883 0.88 205.85 CC12CCC3C(C1CCC2O)CCC45C3(CC(=C(C4O5)O)C#N)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_71433ace35078cecb5168aa5185705d5 Trilostane [M+Na]+ 352.1883 0.88 193.86 CC12CCC3C(C1CCC2O)CCC45C3(CC(=C(C4O5)O)C#N)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_6a6134f8d7ce83165f2353161222d400 Trilostane [M+Na]+ 352.1883 0.88 176.94 CC12CCC3C(C1CCC2O)CCC45C3(CC(=C(C4O5)O)C#N)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_7d04d54b83b5fbb3fc13ec67803cce0b Trilostane [M-H]- 328.1918 0.83 184.87 CC12CCC3C(C1CCC2O)CCC45C3(CC(=C(C4O5)O)C#N)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_5b177f7833ff0ad268e3d24cbfbbab9c Trilostane [M-H-H2O]- 310.1807 0.84 180.56 CC12CCC3C(C1CCC2O)CCC45C3(CC(=C(C4O5)O)C#N)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_4ab692e368a8a4e724ab7bd341b0818a Fenchlorazole-ethyl [M+H]+ 403.9102 0.98 179.12 CCOC(=O)C1=NN(C(=N1)C(Cl)(Cl)Cl)C2=C(C=C(C=C2)Cl)Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_3bf357d32facf9415118e31799f2694d Fenchlorazole-ethyl [M+K]+ 441.8661 0.99 187.07 CCOC(=O)C1=NN(C(=N1)C(Cl)(Cl)Cl)C2=C(C=C(C=C2)Cl)Cl Organoheterocyclic compounds 1 1 TW polyala
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