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_810dbd9f4d93db53351550839a393f49 N-(2-Fluorenyl)-2,2,2-trifluoroacetamide [M+H]+ 278.0787 0.92 158.54 C1C2=CC=CC=C2C3=C1C=C(C=C3)NC(=O)C(F)(F)F Benzenoids 1 1 TW polyala
CCSBASE_e46efd7d4ca6cbcdfbc68a3fdeb5cbd6 N-(2-Fluorenyl)-2,2,2-trifluoroacetamide [M-H]- 276.0642 0.89 160.93 C1C2=CC=CC=C2C3=C1C=C(C=C3)NC(=O)C(F)(F)F Benzenoids -1 1 TW polyala
CCSBASE_58d97e349a5ee4f95bc25ceb1e4dec46 Ethisterone [M+H]+ 313.2162 0.9 177.96 CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_e9be55c873999b80191ce0b7d99f6740 Ethisterone [M+H-H2O]+ 295.2057 0.9 172.08 CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_3664a5c71cc92f7e1ee70c507953cdfb Ethisterone [M+Na]+ 335.1981 0.9 201.08 CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_df16f7976e6f2e5f29d86f1b89b154b4 Ethisterone [M+Na]+ 335.1981 0.9 176.88 CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_4e652d594302fe8b9f0191d6cdf1724a Ethisterone [M-H]- 311.2017 0.91 181.65 CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_f0ceda1df8d122a48956926f67a2b1c6 Benzyl salicylate [M-H]- 227.0714 0.89 155.85 C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2O Benzenoids -1 1 TW polyala
CCSBASE_2b6edb6b75af85361cca8ace729b28b7 3-Octanone [M+FA-H]- 173.1183 0.81 146.27 CCCCCC(=O)CC Organic oxygen compounds -1 1 TW polyala
CCSBASE_255c6b71575c89b58020fb5a4aa95612 N,N-Diisopropylaniline [M+H]+ 178.159 0.73 142.21 CC(C)N(C1=CC=CC=C1)C(C)C Organic nitrogen compounds 1 1 TW polyala
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