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_214d2fbbdbbb04325f55046ba2846806 Tolnaftate [M+Na]+ 330.0923 0.97 182.43 CC1=CC(=CC=C1)N(C)C(=S)OC2=CC3=CC=CC=C3C=C2   Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_7c643c6f487b87c5f7175e7e89dcda63 3-Phenoxybenzenemethanol [M+H-H2O]+ 183.0805 0.83 136.28 C1=CC=C(C=C1)OC2=CC=CC(=C2)CO   None 1 1 TW polyala
CCSBASE_ae51762fc764d44d1be07df2ee0737d0 Fenuron [M+H]+ 165.1023 0.73 133.74 CN(C)C(=O)NC1=CC=CC=C1   Benzenoids 1 1 TW polyala
CCSBASE_5001fb5944d7ea83b374a03dc26b0fee Betamethasone 21-phosphate disodium [M+H]+ 473.1735 0.82 197.05 C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@@]4([C@]3([C@H](C[C@@]2([C@]1(C(=O)COP(=O)([O-])[O-])O)C)O)F)C Benzenoids 1 1 TW polyala
CCSBASE_5f7b948dfc3a0a79f79ffaf018cff126 Betamethasone 21-phosphate disodium [M+K]+ 511.1294 0.83 212.63 C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@@]4([C@]3([C@H](C[C@@]2([C@]1(C(=O)COP(=O)([O-])[O-])O)C)O)F)C Benzenoids 1 1 TW polyala
CCSBASE_a7481f95c6760c26e12ba23212614702 Betamethasone 21-phosphate disodium [M+Na]+ 495.1554 0.82 206.53 C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@@]4([C@]3([C@H](C[C@@]2([C@]1(C(=O)COP(=O)([O-])[O-])O)C)O)F)C Benzenoids 1 1 TW polyala
CCSBASE_3be78a8ff0b85170355b15ea57e34015 Betamethasone 21-phosphate disodium [M-H]- 471.1589 0.91 201.13 CC1CC2C3CCC4=CC(=O)C=CC4(C3(C(CC2(C1(C(=O)COP(=O)([O-])[O-])O)C)O)F)C Benzenoids -1 1 TW polyala
CCSBASE_591ed7aeb62b7849ca85222ff5f5820d Methiuron [M+H]+ 195.0951 0.76 143.06 CC1=CC(=CC=C1)NC(=S)N(C)C  Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_42bc6d60feaec1a0e7a886a01029bfe1 Guaifenesin [M+Na]+ 221.0784 0.73 145.25 COC1=CC=CC=C1OCC(CO)O   Benzenoids 1 1 TW polyala
CCSBASE_44ee002f29fa4ab4b53f5d012ff9041a Methiuron [M-H]- 193.0805 0.78 149.09 CC1=CC(=CC=C1)NC(=S)N(C)C Lipids and lipid-like molecules -1 1 TW polyala
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