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_ce80506999514f180addc1213df79b78 MK-968 [M+Na]+ 396.1606 0.84 189.38 C1CC(CCC1NC2=NC=NC3=C2C=NN3)OCC(C4=CC=CC=C4F)F Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_9f0865beed5a9db43dc6904f712e79d6 MK-968 [M+Na]+ 396.1606 0.84 206.81 C1CC(CCC1NC2=NC=NC3=C2C=NN3)OCC(C4=CC=CC=C4F)F Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_a3f73c5d9e192c7b18d50f3ab2ca442f MK-968 [M-H]- 372.1641 0.79 199.8 C1CC(CCC1NC2=NC=NC3=C2C=NN3)OCC(C4=CC=CC=C4F)F Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_c5fe71625f394ee1215ecaf694e28d94 Triglycidyl isocyanurate [M+H]+ 298.1034 0.76 157.91 C1C(O1)CN2C(=O)N(C(=O)N(C2=O)CC3CO3)CC4CO4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_ddb370842c7e03477de81a8237dde7b1 Triglycidyl isocyanurate [M+K]+ 336.0593 0.74 164.49 C1C(O1)CN2C(=O)N(C(=O)N(C2=O)CC3CO3)CC4CO4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_e982a130ab07e13d5837c45fd4c69d13 Triglycidyl isocyanurate [M+Na]+ 320.0853 0.75 161.39 C1C(O1)CN2C(=O)N(C(=O)N(C2=O)CC3CO3)CC4CO4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_ed807c30b75528405bc0d9e581c15150 Diethyl butanedioate [M+Na]+ 197.0784 0.81 141.09 CCOC(=O)CCC(=O)OCC Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_0f17730af02fa392a6ed7756af05e644 4,4'-Bipyridine [M+H]+ 157.076 0.73 133.04 C1=CN=CC=C1C2=CC=NC=C2 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_1809cee46614a081ee1e572d28575f9a Sulfasalazine [M+H]+ 399.0758 0.87 198.68 C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC(=C(C=C3)O)C(=O)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_9d9734afe135147d9f68219b49a268b4 Sulfasalazine [M+H-H2O]+ 381.0653 0.87 193.39 C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC(=C(C=C3)O)C(=O)O Organoheterocyclic compounds 1 1 TW polyala
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