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_1e03b9b09aad6568158facf670e58562 Gemfibrozil [M+Na]+ 273.1461 1.04 166.94 CC1=CC(=C(C=C1)C)OCCCC(C)(C)C(=O)O Benzenoids 1 1 TW polyala
CCSBASE_a5c0bcdbc1ac8beb8a0d8c7d54d9c6e1 Thiamine nitrate [M]+ 265.1118 0.77 156.39 CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCO Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_2f76468f31ab2733446add0407a1dc91 3-(Trifluoromethyl)aniline [M+H]+ 162.0525 0.85 134.6 C1=CC(=CC(=C1)N)C(F)(F)F Benzenoids 1 1 TW polyala
CCSBASE_81c4dfc9935dc5a43ff1be8307345cce Citronellic acid [M-H]- 169.1234 0.93 152.32 CC(CCC=C(C)C)CC(=O)O Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_d292d6080153f8ad2286735464b1a9f2 Bismaleimide [M+H]+ 359.1027 0.87 187.61 C1=CC(=CC=C1CC2=CC=C(C=C2)N3C(=O)C=CC3=O)N4C(=O)C=CC4=O Benzenoids 1 1 TW polyala
CCSBASE_246ce3e7742b3a7899c1306fcc7b4c8d Bismaleimide [M+Na]+ 381.0846 0.87 180.28 C1=CC(=CC=C1CC2=CC=C(C=C2)N3C(=O)C=CC3=O)N4C(=O)C=CC4=O Benzenoids 1 1 TW polyala
CCSBASE_bc7e52651afa045050e351eae8aa4a07 Doxylamine succinate [M+H]+ 271.1805 0.75 162.87 CC(C1=CC=CC=C1)(C2=CC=CC=N2)OCCN(C)C Benzenoids 1 1 TW polyala
CCSBASE_88173759c93fbd6f9a26693d281297d9 Doxylamine succinate [M+Na]+ 293.1624 0.75 168.35 CC(C1=CC=CC=C1)(C2=CC=CC=N2)OCCN(C)C Benzenoids 1 1 TW polyala
CCSBASE_f03913257638a59a94327af659f09352 Cytembena [M+H]+ 284.9757 0.86 148.13 COC1=CC=C(C=C1)C(=O)C(=CC(=O)[O-])Br Benzenoids 1 1 TW polyala
CCSBASE_194df8c0c9c501957f938f4f2a664af8 Cytembena [M+H]+ 284.9757 0.86 162.01 COC1=CC=C(C=C1)C(=O)C(=CC(=O)[O-])Br Benzenoids 1 1 TW polyala
1 2 ... 252 253 254 255 256 257 258 ... 359 360