Name:
Adduct:
Polarity:
Z:
m/z:
±:
CCS: Å
±: %
SMI:

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ID Name Adduct Structure m/z RT CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_b76f7a05f81abbe6468345fa51c65bd8 Etoposide [M-H]- 587.177 0.76 221.25 CC1OCC2C(O1)C(C(C(O2)OC3C4COC(=O)C4C(C5=CC6=C(C=C35)OCO6)C7=CC(=C(C(=C7)OC)O)OC)O)O Lignans, neolignans and related compounds -1 1 TW polyala
CCSBASE_27715ff0629f7e4aba8380c397bbec6b Fenbendazole [M+H]+ 300.0801 0.88 171.5 COC(=O)NC1=NC2=C(N1)C=C(C=C2)SC3=CC=CC=C3   Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_3825bf9120c5edc8dd4b24417abbca93 Fenpropathrin [M+H]+ 350.1751 1.08 185.09 CC1(C(C1(C)C)C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3)C Benzenoids 1 1 TW polyala
CCSBASE_5ad64ef7c3b266c076ef984fa717df96 Fenpropathrin [M+Na]+ 372.157 1.07 186.0 CC1(C(C1(C)C)C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3)C Benzenoids 1 1 TW polyala
CCSBASE_7873d5c17f48ba5f99b228f0c95fe7f1 Fenthion [M+H]+ 279.0273 0.9 158.72 CC1=C(C=CC(=C1)OP(=S)(OC)OC)SC Organic acids and derivatives 1 1 TW polyala
CCSBASE_ddca4d1b77cbceb54ac0069ace10ff97 Fenthion [M+Na]+ 301.0092 0.9 165.73 CC1=C(C=CC(=C1)OP(=S)(OC)OC)SC Organic acids and derivatives 1 1 TW polyala
CCSBASE_2f72f6092fcd85bcd605464b618d4429 Florasulam [M+H]+ 360.0373 0.8 169.98 COC1=NC=C(C2=NC(=NN21)S(=O)(=O)NC3=C(C=CC=C3F)F)F  Benzenoids 1 1 TW polyala
CCSBASE_b3eb3e5dd2e9b5d882b81fd78e8d0e81 Florasulam [M+K]+ 397.9932 0.79 184.92 COC1=NC=C(C2=NC(=NN21)S(=O)(=O)NC3=C(C=CC=C3F)F)F Benzenoids 1 1 TW polyala
CCSBASE_580053a2ff688df34bab498727e56ae9 Florasulam [M+Na]+ 382.0192 0.79 179.09 COC1=NC=C(C2=NC(=NN21)S(=O)(=O)NC3=C(C=CC=C3F)F)F  Benzenoids 1 1 TW polyala
CCSBASE_feaf7b9293cc5b396bdaa684b7c5826b Florasulam [M-H]- 358.0227 0.76 174.49 COC1=NC=C(C2=NC(=NN21)S(=O)(=O)NC3=C(C=CC=C3F)F)F Benzenoids -1 1 TW polyala
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