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_4ee3e451bf4c9901b661582157953f1c 2,4-Di-tert-pentylphenol [M+K]+ 273.1616 0.8 159.79 CCC(C)(C)C1=CC(=C(C=C1)O)C(C)(C)CC Benzenoids 1 1 TW polyala
CCSBASE_c81f12bae1bc65f5dbf04bac0ae0b796 Tolcapone [M+H]+ 274.071 0.9 158.17 CC1=CC=C(C=C1)C(=O)C2=CC(=C(C(=C2)O)O)[N+](=O)[O-] Benzenoids 1 1 TW polyala
CCSBASE_58fcc881b56dcbaeed8d1896ad23cf87 Tolcapone [M-H]- 272.0564 0.85 163.41 CC1=CC=C(C=C1)C(=O)C2=CC(=C(C(=C2)O)O)[N+](=O)[O-] Benzenoids -1 1 TW polyala
CCSBASE_5636b0734e42d0c8e442ac37197e60d7 SB281832 [M+H]+ 407.1514 0.82 195.5 C1=CC=C(C=C1)OC2=NC=CC(=N2)C3=C(N=CN3C(CO)CO)C4=CC=C(C=C4)F Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_f0b2d661aabce11d29ab0cbcdd26e357 Pirinixic acid [M+H]+ 324.0568 0.92 174.41 CC1=C(C(=CC=C1)NC2=CC(=NC(=N2)SCC(=O)O)Cl)C Organosulfur compounds 1 1 TW polyala
CCSBASE_e63085b89aa085099f1ea71aa940c263 Pirinixic acid [M+H-H2O]+ 306.0463 0.92 167.97 CC1=C(C(=CC=C1)NC2=CC(=NC(=N2)SCC(=O)O)Cl)C Organosulfur compounds 1 1 TW polyala
CCSBASE_8da083d8d3bb356430a8adbbfae88d51 Pirinixic acid [M+Na]+ 346.0387 0.92 180.38 CC1=C(C(=CC=C1)NC2=CC(=NC(=N2)SCC(=O)O)Cl)C Organosulfur compounds 1 1 TW polyala
CCSBASE_0343985472310926f040b6e4de393f10 Pirinixic acid [M-H-H2O]- 304.0311 0.89 171.58 CC1=C(C(=CC=C1)NC2=CC(=NC(=N2)SCC(=O)O)Cl)C Organosulfur compounds -1 1 TW polyala
CCSBASE_80d5f52bb5c4aaf21bf25f840fef0afc 2-[2-(2-Ethoxyethoxy)ethoxy]ethanol [M+Na]+ 201.1097 0.77 139.53 CCOCCOCCOCCO Organic oxygen compounds 1 1 TW polyala
CCSBASE_9114d5c895a0c69f1a0c8abd4fe9ea3c Benzyl butyl phthalate [M+Na]+ 335.1254 1.01 177.3 CCCCOC(=O)C1=CC=CC=C1C(=O)OCC2=CC=CC=C2 Benzenoids 1 1 TW polyala
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