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_d049d7e1541e6dbffc094dbc1af328ee Cytembena [M+H-H2O]+ 266.9652 0.86 140.73 COC1=CC=C(C=C1)C(=O)C(=CC(=O)[O-])Br Benzenoids 1 1 TW polyala
CCSBASE_4bea30fba7623408b87f51bff1d508b0 4-Chlorobenzenesulfonic acid [M-H]- 190.9575 0.74 136.51 C1=CC(=CC=C1S(=O)(=O)O)Cl Benzenoids -1 1 TW polyala
CCSBASE_99f2ab15d4982dd84320aa80bfed8924 (2,2-Dimethoxyethyl)benzene [M+FA-H]- 211.0976 0.77 151.35 COC(CC1=CC=CC=C1)OC Benzenoids -1 1 TW polyala
CCSBASE_9266dfea746856fbbd995bb3ce537f2c Ethionamide [M+H]+ 167.0638 0.75 136.59 CCC1=NC=CC(=C1)C(=S)N Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_a37bf5c5dc2c9e52392d7b8ed67a58db Ethionamide [M-H]- 165.0492 0.69 139.91 CCC1=NC=CC(=C1)C(=S)N Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_38ec3a8dfd0283a49916e6696c442249 gamma-Nonanolactone [M+FA-H]- 201.1132 0.78 148.2 CCCCCC1CCC(=O)O1 Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_a0a9aaf1fbc9bf963a64610529cc9344 4-Hydroxybenzoic acid [M-H]- 137.0244 0.72 131.53 C1=CC(=CC=C1C(=O)O)O Benzenoids -1 1 TW polyala
CCSBASE_76fb06b45fb5d314d70b4d54a0474d70 UK-333747 [M+H]+ 435.037 0.8 189.74 COCC1=NN=C(N1C2=C3C(=CC(=C2Cl)Cl)NC(=O)C(=O)N3)C4=C[N+](=CC=C4)[O-] Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_65e77d135f10b216453842c8082bf58e UK-333747 [M-H]- 433.0224 0.74 189.81 COCC1=NN=C(N1C2=C3C(=CC(=C2Cl)Cl)NC(=O)C(=O)N3)C4=C[N+](=CC=C4)[O-] Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_5ea845752f4dd0c4541943a628060d25 E-Cinnamic acid [M-H]- 147.0451 0.79 139.77 C1=CC=C(C=C1)C=CC(=O)O Phenylpropanoids and polyketides -1 1 TW polyala
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