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_1a628ea32f83bda94dd8fadec2f22054 Labetalol hydrochloride [M+H]+ 329.186 0.74 177.84 CC(CCC1=CC=CC=C1)NCC(C2=CC(=C(C=C2)O)C(=O)N)O Benzenoids 1 1 TW polyala
CCSBASE_0200bf83510709a0df9d8bbc6ba5f4bd Labetalol hydrochloride [M+H-H2O]+ 311.1755 0.76 174.38 CC(CCC1=CC=CC=C1)NCC(C2=CC(=C(C=C2)O)C(=O)N)O Benzenoids 1 1 TW polyala
CCSBASE_f7970919ee68ea61c9a9c9f8c0d9e7d3 Labetalol hydrochloride [M-H]- 327.1714 0.73 183.72 CC(CCC1=CC=CC=C1)NCC(C2=CC(=C(C=C2)O)C(=O)N)O Benzenoids -1 1 TW polyala
CCSBASE_fd5529be601f22a495e8fa9cd2143ddb Lamivudine [M+Na]+ 252.0413 0.71 149.84 C1[C@H](O[C@H](S1)CO)N2C=CC(=NC2=O)N   Nucleosides, nucleotides, and analogues 1 1 TW polyala
CCSBASE_7036d480fbe36725d4a1ab41a0003466 Leflunomide [M+H]+ 271.0689 0.9 156.99 CC1=C(C=NO1)C(=O)NC2=CC=C(C=C2)C(F)(F)F Benzenoids 1 1 TW polyala
CCSBASE_46e11a417393bb0c770f03de278890c1 Leucomalachite green [M+H]+ 331.2169 0.89 194.16 CN(C)C1=CC=C(C=C1)C(C2=CC=CC=C2)C3=CC=C(C=C3)N(C)C   Benzenoids 1 1 TW polyala
CCSBASE_758082724eac57a2402e81bec4c33975 Losartan potassium [M+H-H2O]+ 405.159 0.85 195.04 CCCCC1=NC(=C(N1CC2=CC=C(C=C2)C3=CC=CC=C3C4=NN=N[N-]4)CO)Cl Benzenoids 1 1 TW polyala
CCSBASE_ef6dec08297da79ca3334551dc971356 Losartan potassium [M-H]- 421.1549 0.81 204.53 CCCCC1=NC(=C(N1CC2=CC=C(C=C2)C3=CC=CC=C3C4=NN=N[N-]4)CO)Cl Benzenoids -1 1 TW polyala
CCSBASE_3ba3a37c39d8dc926c38357f3dfc00a4 Malaoxon [M+H]+ 315.0662 0.83 161.37 CCOC(=O)CC(C(=O)OCC)SP(=O)(OC)OC Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_23c34723d20dd364f874aaff27eec88a Malaoxon [M+Na]+ 337.0481 0.83 165.16 CCOC(=O)CC(C(=O)OCC)SP(=O)(OC)OC Lipids and lipid-like molecules 1 1 TW polyala
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