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_b80bfaeded7c1ff33136b416a6a8bf4f Bithionol [M-H]- 354.874 0.97 170.35 C1=C(C=C(C(=C1SC2=C(C(=CC(=C2)Cl)Cl)O)O)Cl)Cl Organosulfur compounds -1 1 TW polyala
CCSBASE_f9ad15bf164cdef1a52e6faab819d24f Budesonide [M+Cl]- 465.2049 0.9 210.71 CCCC1OC2CC3C4CCC5=CC(=O)C=CC5(C4C(CC3(C2(O1)C(=O)CO)C)O)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_22cb0525fbf0872cdf3ae236983ae7c0 Budesonide [M+FA-H]- 475.2337 0.9 212.31 CCCC1OC2CC3C4CCC5=CC(=O)C=CC5(C4C(CC3(C2(O1)C(=O)CO)C)O)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_08ea28b51dcd04a67afec0a541bc8a53 Budesonide [M+H]+ 431.2428 0.97 203.98 CCCC1OC2CC3C4CCC5=CC(=O)C=CC5(C4C(CC3(C2(O1)C(=O)CO)C)O)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_07beff2488ad662ac141828f10c78c83 Budesonide [M+H-H2O]+ 413.2323 0.95 200.12 CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@@]5([C@H]4[C@H](C[C@@]3([C@@]2(O1)C(=O)CO)C)O)C  Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_75096a8b397e90c5c7ea48ce1e2ddeac Budesonide [M+Na]+ 453.2248 0.96 227.0 CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@@]5([C@H]4[C@H](C[C@@]3([C@@]2(O1)C(=O)CO)C)O)C  Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_49898f6d07b3af1badc07b26ec47301d Butachlor [M+H]+ 312.1725 1.02 172.33 CCCCOCN(C1=C(C=CC=C1CC)CC)C(=O)CCl Benzenoids 1 1 TW polyala
CCSBASE_1d74f7e952abb9b4aa3db150ddd5d225 Butachlor [M+Na]+ 334.1544 1.05 181.97 CCCCOCN(C1=C(C=CC=C1CC)CC)C(=O)CCl Benzenoids 1 1 TW polyala
CCSBASE_6d018f38a1afb531342a6ac4d54d63a1 Butyl benzoate [M+FA-H]- 223.0976 0.81 151.68 CCCCOC(=O)C1=CC=CC=C1 Benzenoids -1 1 TW polyala
CCSBASE_9ded00e143f9d68d7ed574d2ff62926a Butyl methacrylate [M+FA-H]- 187.0976 0.76 143.87 CCCCOC(=O)C(=C)C Organic acids and derivatives -1 1 TW polyala
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