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_757c13833ddc3941019407eea3a83e10 Trelanserin [M+K]+ 504.1267 0.71 207.02 C1CN(CCN1CCC2=CC(=O)N(C3=C2C=CC(=C3)F)CC(=O)N)C4=NC=CC5=C4C=CS5 Organic acids and derivatives 1 1 TW polyala
CCSBASE_00675793f5465fffce5bc248f5e5e289 Aldoxycarb [M+K]+ 261.0306 0.69 150.31 CC(C)(C=NOC(=O)NC)S(=O)(=O)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_0ef5923f87476c2274ba0ca4aea26468 Aldoxycarb [M+Na]+ 245.0566 0.68 148.4 CC(C)(C=NOC(=O)NC)S(=O)(=O)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_63b20e119a9f9aa25e1f74d165faee90 Trelanserin [M+Na]+ 488.1527 0.71 204.71 C1CN(CCN1CCC2=CC(=O)N(C3=C2C=CC(=C3)F)CC(=O)N)C4=NC=CC5=C4C=CS5 Organic acids and derivatives 1 1 TW polyala
CCSBASE_86e4d840c41fff93c80024bceb5782a6 Trelanserin [M+Na]+ 488.1527 0.71 169.87 C1CN(CCN1CCC2=CC(=O)N(C3=C2C=CC(=C3)F)CC(=O)N)C4=NC=CC5=C4C=CS5 Organic acids and derivatives 1 1 TW polyala
CCSBASE_c96e1df5f082ee647b324004a8ad9a22 2-Ethylbutyric acid [M-H]- 115.0764 0.75 134.55 CCC(CC)C(=O)O None -1 1 TW polyala
CCSBASE_aff7328080a8be8826ff4c19f9ff81cb 1,2-Diethoxybenzene [M+FA-H]- 211.0976 0.78 151.81 CCOC1=CC=CC=C1OCC None -1 1 TW polyala
CCSBASE_373954ccb4d0b7297877485954fa5d5c N-(4-Methylpentan-2-yl)-N-phenylbenzene-1,4-diamine [M+H]+ 269.2012 0.79 173.5 CC(C)CC(C)N(C1=CC=CC=C1)C2=CC=C(C=C2)N  None 1 1 TW polyala
CCSBASE_28b6100057345dd036af3c5b3f5b9aca Zileuton [M+Na]+ 259.0511 0.79 154.11 CC(C1=CC2=CC=CC=C2S1)N(C(=O)N)O Organic nitrogen compounds 1 1 TW polyala
CCSBASE_44de5dca1d210923531a31753a188dab Neopentyl glycol diglycidyl ether [M+Na]+ 239.1254 0.78 149.49 CC(C)(COCC1CO1)COCC2CO2 Organoheterocyclic compounds 1 1 TW polyala
1 2 ... 150 151 152 153 154 155 156 ... 359 360