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_45f991ecf2048b79cfd06126d687a903 Carabersat [M-H-H2O]- 338.1192 0.79 184.93 CC(=O)C1=CC2=C(C=C1)OC(C(C2NC(=O)C3=CC=C(C=C3)F)O)(C)C Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_b21d600cc4fa2cc2f50f82a537160a03 1,3,6-Hexanetricarbonitrile [M+H]+ 162.1026 0.72 136.62 C(CC#N)CC(CCC#N)C#N Organic nitrogen compounds 1 1 TW polyala
CCSBASE_c457a76ca4d995b2833bdb34a05a0ee7 Sodium ethasulfate [M-H]- 209.0853 0.89 153.74 CCCCC(CC)COS(=O)(=O)[O-] Organic acids and derivatives -1 1 TW polyala
CCSBASE_4c8293cb8c3a7bddf0cc1b96ccfd5752 Crufomate [M+H]+ 292.0864 0.92 164.81 CC(C)(C)C1=CC(=C(C=C1)OP(=O)(NC)OC)Cl Benzenoids 1 1 TW polyala
CCSBASE_c35286da929b911dd314577d0414bda6 Crufomate [M+Na]+ 314.0683 0.92 175.29 CC(C)(C)C1=CC(=C(C=C1)OP(=O)(NC)OC)Cl Benzenoids 1 1 TW polyala
CCSBASE_73d648f8d6b553043e986259f0fa31e5 Ethyltriethoxysilane [M-H]- 191.1109 0.85 149.06 CCO[Si](CC)(OCC)OCC Organometallic compounds -1 1 TW polyala
CCSBASE_83739e9e9003a4ad90bbf94f17865ce3 Dehydroepiandrosterone [M+H-H2O]+ 271.2057 0.92 165.4 CC12CCC3C(C1CCC2=O)CC=C4C3(CCC(C4)O)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_283d355190afaf9886375bec50a136dd 2-Amino-6-nitrobenzothiazole [M+FA-H]- 240.0084 0.78 147.72 C1=CC2=C(C=C1[N+](=O)[O-])SC(=N2)N Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_340719e916fea573385bdbf0fd0d78e8 2-Amino-6-nitrobenzothiazole [M+H]+ 196.0175 0.8 138.28 C1=CC2=C(C=C1[N+](=O)[O-])SC(=N2)N Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_e01c6cf2f94ee85e16e31aa45fbe97e6 2-Amino-6-nitrobenzothiazole [M-H]- 194.0029 0.77 135.43 C1=CC2=C(C=C1[N+](=O)[O-])SC(=N2)N Organoheterocyclic compounds -1 1 TW polyala
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