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_20ce467d906992088302417b48e23eee 4-(2-Methylbutan-2-yl)cyclohexanol [M+FA-H]- 215.1653 0.93 157.23 CCC(C)(C)C1CCC(CC1)O None -1 1 TW polyala
CCSBASE_cda3fdc23c745d2b7768ff390915c19d 4-(2-Methylbutan-2-yl)cyclohexanol [M-H]- 169.1598 0.93 149.3 CCC(C)(C)C1CCC(CC1)O None -1 1 TW polyala
CCSBASE_bddf0c9c0db54eda3c9e79aac4aa64cd 4,4'-Diaminobiphenyl methane [M+H]+ 199.123 0.67 157.82 C1=CC(=CC=C1CC2=CC=C(C=C2)N)N None 1 1 TW polyala
CCSBASE_01fbc25573db228acc59bde329493f3b Ethylene acrylate [M+H-H2O]+ 153.0547 0.74 127.48 C=CC(=O)OCCOC(=O)C=C Benzenoids 1 1 TW polyala
CCSBASE_771624e550e022aefb1bb41f1c7a79a5 Ethylene acrylate [M+FA-H]- 215.0561 0.72 144.71 C=CC(=O)OCCOC(=O)C=C Benzenoids -1 1 TW polyala
CCSBASE_d0b5c824081d48b1e38c5fe54eb022be Tomelukast [M+H]+ 319.1765 0.85 173.27 CCCC1=C(C=CC(=C1O)C(=O)C)OCCCCC2=NNN=N2 Organic acids and derivatives 1 1 TW polyala
CCSBASE_759738d52cae23317507c0d169431483 Tomelukast [M+Na]+ 341.1584 0.85 174.22 CCCC1=C(C=CC(=C1O)C(=O)C)OCCCCC2=NNN=N2 Organic acids and derivatives 1 1 TW polyala
CCSBASE_27162570f5156853cd6334b4cf074bea Tomelukast [M-H]- 317.1619 0.87 183.81 CCCC1=C(C=CC(=C1O)C(=O)C)OCCCCC2=NNN=N2 Organic acids and derivatives -1 1 TW polyala
CCSBASE_a449c926f6c223657c0c2d9993d60557 Mizolastine [M+H]+ 433.2147 0.74 200.18 CN(C1CCN(CC1)C2=NC3=CC=CC=C3N2CC4=CC=C(C=C4)F)C5=NC=CC(=O)N5 Organic oxygen compounds 1 1 TW polyala
CCSBASE_e38681e48687e5bcbc02f4b1c90db7f9 Mizolastine [M+K]+ 471.1706 0.74 194.47 CN(C1CCN(CC1)C2=NC3=CC=CC=C3N2CC4=CC=C(C=C4)F)C5=NC=CC(=O)N5 Organic oxygen compounds 1 1 TW polyala
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