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_0707cc0ea04244971db6bda51b7ba2e4 4-Dimethylaminoantipyrine [M+H]+ 232.1444 0.74 152.17 CC1=C(C(=O)N(N1C)C2=CC=CC=C2)N(C)C   Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_0b15e07d952abb6c20ae7291987f0539 4-Dimethylaminoantipyrine [M+Na]+ 254.1264 0.73 164.14 CC1=C(C(=O)N(N1C)C2=CC=CC=C2)N(C)C   Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_ef73d3aba8ad499cbc9584a44607a123 4-Hydroxy-3-nitrophenylarsonic acid [M+H]+ 263.9484 0.74 144.87 C1=CC(=C(C=C1[As](=O)(O)O)[N+](=O)[O-])O Benzenoids 1 1 TW polyala
CCSBASE_5d50f3d6075231dd6212fe597fef15df 4-Hydroxy-3-nitrophenylarsonic acid [M+H-H2O]+ 245.9379 0.73 138.1 C1=CC(=C(C=C1[As](=O)(O)O)[N+](=O)[O-])O Benzenoids 1 1 TW polyala
CCSBASE_adece5dfc7b1386502068454ba6f7bf1 4-Hydroxy-3-nitrophenylarsonic acid [M+K]+ 301.9043 0.73 174.05 C1=CC(=C(C=C1[As](=O)(O)O)[N+](=O)[O-])O Benzenoids 1 1 TW polyala
CCSBASE_b9637acc070549cc71ad696138b7ab71 4-Hydroxy-3-nitrophenylarsonic acid [M-H]- 261.9338 0.69 143.73 C1=CC(=C(C=C1[As](=O)(O)O)[N+](=O)[O-])O Benzenoids -1 1 TW polyala
CCSBASE_bd3bec5dda6bfa4ab726214dff10bbba 4-Hydroxy-3-nitrophenylarsonic acid [M-H-H2O]- 243.9227 0.69 135.36 C1=CC(=C(C=C1[As](=O)(O)O)[N+](=O)[O-])O Benzenoids -1 1 TW polyala
CCSBASE_c66a17c17eba4100042ec5e1eac87491 4-Hydroxybenzophenone [M+H]+ 199.0754 0.85 140.94 C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)O   Benzenoids 1 1 TW polyala
CCSBASE_b830f459ba3d90506d6db53ddb8bc41c 4-Hydroxybenzophenone [M-H]- 197.0608 0.8 147.77 C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)O Benzenoids -1 1 TW polyala
CCSBASE_922eb64942d080ddac81ea47f36a0e26 4-Methylumbelliferone [M+H]+ 177.0546 0.79 131.35 CC1=CC(=O)OC2=C1C=CC(=C2)O  Phenylpropanoids and polyketides 1 1 TW polyala
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