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_e3dda273e650d29f038aa0d332e0749a 2,4-D-Butotyl [M+Na]+ 343.0474 0.93 174.31 CCCCOCCOC(=O)COC1=C(C=C(C=C1)Cl)Cl  None 1 1 TW polyala
CCSBASE_aab6121c234afdbb8f4bd7b5a9f51e8e Decanedioic acid [M+Na]+ 225.1097 0.78 150.13 C(CCCCC(=O)O)CCCC(=O)O   Benzenoids 1 1 TW polyala
CCSBASE_ab658a01f36ae42b4f345c910c69e67a Decanedioic acid [M-H]- 201.1132 0.81 146.36 C(CCCCC(=O)O)CCCC(=O)O Benzenoids -1 1 TW polyala
CCSBASE_9df93170fa1ed2b210793f0b6237fb08 Terbutryn [M+H]+ 242.1434 0.81 160.16 CCNC1=NC(=NC(=N1)SC)NC(C)(C)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_ccf98520126fc9e0ec188461d9c3cdea PharmaGSID_48510 [M+H-H2O]+ 419.1014 0.79 190.74 C1=CC(=CC(=C1)N(CC2=CN=CC=C2)C3=CC(=C(C=C3)OC(F)F)OC(F)F)C(=O)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_61492ba6ce2b401e2578441e340f170e PharmaGSID_48510 [M-H]- 435.0973 0.82 203.94 C1=CC(=CC(=C1)N(CC2=CN=CC=C2)C3=CC(=C(C=C3)OC(F)F)OC(F)F)C(=O)O Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_349843fe899bfb5386739f33b56c3a45 N,N-Dimethyldodecan-1-amine [M+H]+ 214.2529 0.83 169.53 CCCCCCCCCCCCN(C)C   None 1 1 TW polyala
CCSBASE_b85646028e9df5c99dac12a6cacc1e29 Kinetin [M+H]+ 216.088 0.73 144.79 C1=COC(=C1)CNC2=NC=NC3=C2NC=N3   Organic nitrogen compounds 1 1 TW polyala
CCSBASE_e7744fcfb128cf678fe54bb63e6138dd Kinetin [M+H-H2O]+ 198.0775 0.73 136.94 C1=COC(=C1)CNC2=NC=NC3=C2NC=N3   Organic nitrogen compounds 1 1 TW polyala
CCSBASE_eaf62e9dc74fa2934184a26451f840b3 Kinetin [M-H]- 214.0734 0.75 149.79 C1=COC(=C1)CNC2=NC=NC3=C2NC=N3 Organic nitrogen compounds -1 1 TW polyala
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