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_f731e4e8fd6a27431479add5bbc5ef71 Phosalone [M+Na]+ 389.9761 0.97 179.49 CCOP(=S)(OCC)SCN1C2=C(C=C(C=C2)Cl)OC1=O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_39ad2ec5478100efe37fae8673f625d8 5-Amino-2-methylbenzenesulfonic acid [M-H]- 186.023 0.67 140.35 CC1=C(C=C(C=C1)N)S(=O)(=O)O Benzenoids -1 1 TW polyala
CCSBASE_be6cc27b9065aa97d35179e2159c17e6 Cladribine [M+FA-H]- 330.0611 0.73 174.03 C1C(C(OC1N2C=NC3=C(N=C(N=C32)Cl)N)CO)O Nucleosides, nucleotides, and analogues -1 1 TW polyala
CCSBASE_c47bc91a8cbe92ef58440880713ece7b Cladribine [M+H]+ 286.0701 0.77 155.73 C1C(C(OC1N2C=NC3=C(N=C(N=C32)Cl)N)CO)O Nucleosides, nucleotides, and analogues 1 1 TW polyala
CCSBASE_b9bace68dee316c3ebf1095986fc1506 Cladribine [M+Na]+ 308.0521 0.77 162.04 C1C(C(OC1N2C=NC3=C(N=C(N=C32)Cl)N)CO)O Nucleosides, nucleotides, and analogues 1 1 TW polyala
CCSBASE_9b369529b2f596346c7eba279ce31395 Cladribine [M-H]- 284.0556 0.73 160.62 C1C(C(OC1N2C=NC3=C(N=C(N=C32)Cl)N)CO)O Nucleosides, nucleotides, and analogues -1 1 TW polyala
CCSBASE_f12b5816799955a33f3b898d491f4ee9 Ethyl 3-acetyl-4-oxopentanoate [M-H]- 185.0819 0.78 144.02 CCOC(=O)CC(C(=O)C)C(=O)C Organic acids and derivatives -1 1 TW polyala
CCSBASE_12a2ceb1ae56108f6472acd92d6a1f38 Isoxaben [M+H]+ 333.1809 0.9 183.59 CCC(C)(CC)C1=NOC(=C1)NC(=O)C2=C(C=CC=C2OC)OC Benzenoids 1 1 TW polyala
CCSBASE_92d57b6e4bce14627553085f56c8396b Isoxaben [M-H]- 331.1663 0.85 186.58 CCC(C)(CC)C1=NOC(=C1)NC(=O)C2=C(C=CC=C2OC)OC Benzenoids -1 1 TW polyala
CCSBASE_caaaf20311117530b9cf1878bf5b9428 Lenacil [M+H]+ 235.1441 0.88 154.57 C1CCC(CC1)N2C(=O)C3=C(CCC3)NC2=O Organoheterocyclic compounds 1 1 TW polyala
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