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_89050f080cfcbca59dd15eb0313ed9d2 1,3-Butylene diacrylate [M+FA-H]- 243.0874 0.72 154.6 CC(CCOC(=O)C=C)OC(=O)C=C Organic acids and derivatives -1 1 TW polyala
CCSBASE_c8832993dae90aaf3bc180e6f0e368be 1,3-Butylene diacrylate [M-H]- 197.0819 0.73 146.65 CC(CCOC(=O)C=C)OC(=O)C=C Organic acids and derivatives -1 1 TW polyala
CCSBASE_987ea4d5a4f7e4bd904432830d96c30b Hexahydro-1,3,5-tris(1-oxoallyl)-1,3,5-triazine [M+Cl]- 284.0807 0.72 161.7 C=CC(=O)N1CN(CN(C1)C(=O)C=C)C(=O)C=C Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_65b3d391b36bcc7643ce9c69718aaab5 Hexahydro-1,3,5-tris(1-oxoallyl)-1,3,5-triazine [M+Na]+ 272.1006 0.73 157.93 C=CC(=O)N1CN(CN(C1)C(=O)C=C)C(=O)C=C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_078718f509795bde3d7dffc7b6286036 2,4,5-Trimethylaniline [M+H]+ 136.1121 0.77 135.97 CC1=CC(=C(C=C1C)N)C Benzenoids 1 1 TW polyala
CCSBASE_84ebc32f6efb9dc69acc8201856d1b35 Chlorthiamid [M+H]+ 205.9593 0.79 135.77 C1=CC(=C(C(=C1)Cl)C(=S)N)Cl Benzenoids 1 1 TW polyala
CCSBASE_7e722b8473358d61f931bf6e25b4fa48 1,3-Dihydro-1,3,3-trimethyl-2H-indol-2-ylidene acetaldehyde [M+H]+ 202.1226 0.86 145.61 CC1(C2=CC=CC=C2N(C1=CC=O)C)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_93c13995707ea29200d157fe7ae6a6c1 Furalaxyl [M+Na]+ 324.1206 0.9 174.4 CC1=C(C(=CC=C1)C)N(C(C)C(=O)OC)C(=O)C2=CC=CO2 Benzenoids 1 1 TW polyala
CCSBASE_a38279c61d9ad6905529557d2c195ac4 Hexanedihydrazide [M+Cl]- 209.0811 0.76 145.44 C(CCC(=O)NN)CC(=O)NN Organic acids and derivatives -1 1 TW polyala
CCSBASE_21e2f98e8aeeb15e22562307e4618119 Tetraisopropyl methylenediphosphonate [M+K]+ 383.1149 0.9 184.94 CC(C)OP(=O)(CP(=O)(OC(C)C)OC(C)C)OC(C)C Organic acids and derivatives 1 1 TW polyala
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