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_8bed0d36a6b941b349315b44b50520fb Isobornyl propanoate [M-H]- 209.1547 0.83 159.02 CCC(=O)OC1CC2CCC1(C2(C)C)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_d8b2f48ef9964b1ad35fce3f5dd4be95 N-Butyl-p-toluenesulfonamide [M+H]+ 228.1053 0.85 151.24 CCCCNS(=O)(=O)C1=CC=C(C=C1)C Benzenoids 1 1 TW polyala
CCSBASE_64d3126aa180b2e8b9136b5fc07d18b9 N-Butyl-p-toluenesulfonamide [M+Na]+ 250.0872 0.85 168.0 CCCCNS(=O)(=O)C1=CC=C(C=C1)C Benzenoids 1 1 TW polyala
CCSBASE_0440e0426d2bd85cf5b428f197a54927 Tris(2-chloroisopropyl)phosphate [M+H]+ 327.0081 0.87 162.12 CC(CCl)OP(=O)(OC(C)CCl)OC(C)CCl Organic acids and derivatives 1 1 TW polyala
CCSBASE_45d5e216e205fb2afb6a32e6095e1dbf Tris(2-chloroisopropyl)phosphate [M+Na]+ 348.99 0.87 169.73 CC(CCl)OP(=O)(OC(C)CCl)OC(C)CCl Organic acids and derivatives 1 1 TW polyala
CCSBASE_b08f375da71874d776dd79a224b93eb8 Tolbutamide [M+H]+ 271.1111 0.82 162.21 CCCCNC(=O)NS(=O)(=O)C1=CC=C(C=C1)C Benzenoids 1 1 TW polyala
CCSBASE_85eae138e57519e56526f78d29e205be Tolbutamide [M+Na]+ 293.093 0.82 173.15 CCCCNC(=O)NS(=O)(=O)C1=CC=C(C=C1)C Benzenoids 1 1 TW polyala
CCSBASE_42f16219a9e4499b6046b524d2bb408e Tolbutamide [M-H]- 269.0965 0.79 167.26 CCCCNC(=O)NS(=O)(=O)C1=CC=C(C=C1)C Benzenoids -1 1 TW polyala
CCSBASE_b114de0dbe1b5b3703bfc32324dbca96 Chlorfenvinphos [M+H]+ 358.9768 0.93 166.25 CCOP(=O)(OCC)OC(=CCl)C1=C(C=C(C=C1)Cl)Cl Benzenoids 1 1 TW polyala
CCSBASE_6d0cd8a93123551ada4003829faa3f13 Chlorfenvinphos [M+Na]+ 380.9587 0.93 177.56 CCOP(=O)(OCC)OC(=CCl)C1=C(C=C(C=C1)Cl)Cl Benzenoids 1 1 TW polyala
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