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_b65025207a87163e40f95a96a114160f Chloropropylate [M+H-H2O]+ 321.0444 1.02 171.0 CC1=NC=C(N1CC(CCl)O)[N+](=O)[O-]  Benzenoids 1 1 TW polyala
CCSBASE_c0bf15f95f19be29af636d009c116380 Chlorotrianisene [M+H]+ 381.1252 1.08 188.67 COC1=CC=C(C=C1)C(=C(C2=CC=C(C=C2)OC)Cl)C3=CC=C(C=C3)OC Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_7cb5e06585c97c9da8be545abf28d72c Chloroxuron [M+H]+ 291.0895 0.91 171.51 CN(C)C(=O)NC1=CC=C(C=C1)OC2=CC=C(C=C2)Cl   Benzenoids 1 1 TW polyala
CCSBASE_ec6e940c1f87d283ef0cac8a22caf9fa Chloroxuron [M+Na]+ 313.0714 0.91 180.08 CN(C)C(=O)NC1=CC=C(C=C1)OC2=CC=C(C=C2)Cl   Benzenoids 1 1 TW polyala
CCSBASE_9b59eecec92d1cd3a8bf5beaffdc1cf9 Chlorpheniramine maleate [M+H]+ 275.131 0.73 163.73 CN(C)CCC(C1=CC=C(C=C1)Cl)C2=CC=CC=N2 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_26012d49677b0f684f8b478c65c703cf Chlorpropamide [M+H]+ 277.0408 0.83 158.53 CCCNC(=O)NS(=O)(=O)C1=CC=C(C=C1)Cl  Benzenoids 1 1 TW polyala
CCSBASE_fa42ed09f3eaa0269c1a0aa761cea512 Chlorpropamide [M+Na]+ 299.0228 0.83 169.47 CCCNC(=O)NS(=O)(=O)C1=CC=C(C=C1)Cl  Benzenoids 1 1 TW polyala
CCSBASE_4e8faa0f2286caac2cedfd7fdd9a71ac Chlorpropamide [M-H]- 275.0262 0.79 162.41 CCCNC(=O)NS(=O)(=O)C1=CC=C(C=C1)Cl Benzenoids -1 1 TW polyala
CCSBASE_272b94f02e1c356fa5275ca4e549936d CI-1044 [M+H]+ 398.1612 0.78 196.47 C1CN2C(=O)[C@@H](N=C(C3=CC(=CC1=C32)N)C4=CC=CC=C4)NC(=O)C5=CN=CC=C5   Organic acids and derivatives 1 1 TW polyala
CCSBASE_cfda54e75d63a33ff99b5f1874237a25 CI-1044 [M+Na]+ 420.1431 0.75 205.42 C1CN2C(=O)[C@@H](N=C(C3=CC(=CC1=C32)N)C4=CC=CC=C4)NC(=O)C5=CN=CC=C5   Organic acids and derivatives 1 1 TW polyala
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