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_115f286ca5316027b2e7c572be6213f2 Prothioconazole [M+H]+ 344.0386 1.0 169.48 C1CC1(C(CC2=CC=CC=C2Cl)(CN3C(=S)N=CN3)O)Cl Benzenoids 1 1 TW polyala
CCSBASE_657f983ad3a277fb839bae66c5a134d6 Prothioconazole [M+H-H2O]+ 326.0281 1.0 164.79 C1CC1(C(CC2=CC=CC=C2Cl)(CN3C(=S)N=CN3)O)Cl Benzenoids 1 1 TW polyala
CCSBASE_d05c816dc405a62cd517b506b605da07 Prothioconazole [M+Na]+ 366.0205 1.0 173.0 C1CC1(C(CC2=CC=CC=C2Cl)(CN3C(=S)N=CN3)O)Cl Benzenoids 1 1 TW polyala
CCSBASE_8fc968a7436ee0ce6f1ef6a463f1ce97 Tetrabutylphosphonium chloride [M]+ 259.2549 0.83 173.84 CCCC[P+](CCCC)(CCCC)CCCC Organophosphorus compounds 1 1 TW polyala
CCSBASE_30654088b5b7d19fa602fa1e893275b6 L-Verbenone [M-H]- 149.0972 0.74 140.27 CC1=CC(=O)C2CC1C2(C)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_c2aa3ccee9c0fc21920cd576306b5bb1 BPS-MPE4 [M+H]+ 341.0842 0.93 182.13 C1=CC=C(C=C1)COC2=CC=C(C=C2)S(=O)(=O)C3=CC=C(C=C3)O Benzenoids 1 1 TW polyala
CCSBASE_2a33d0ceac32bf1168bd1ea46b3de6d3 BPS-MPE4 [M-H]- 339.0696 0.85 184.56 C1=CC=C(C=C1)COC2=CC=C(C=C2)S(=O)(=O)C3=CC=C(C=C3)O Benzenoids -1 1 TW polyala
CCSBASE_ea891619bd5c49965453d95c011ad81c Tetrabutyl ethylidenebisphenol [M+FA-H]- 483.348 1.0 215.17 CC(C1=C(C(=CC(=C1)C(C)(C)C)C(C)(C)C)O)C2=C(C(=CC(=C2)C(C)(C)C)C(C)(C)C)O Benzenoids -1 1 TW polyala
CCSBASE_05b4413fb20e268bec8ad05f8f5fb961 4-Chlorobenzoic acid [M-H]- 154.9905 0.81 132.84 C1=CC(=CC=C1C(=O)O)Cl Benzenoids -1 1 TW polyala
CCSBASE_9d185827f65a9a9b6214c68aa17683f6 Erythrosin B [M-H]- 834.6478 1.04 215.56 C1=CC=C2C(=C1)C(=O)OC23C4=CC(=C(C(=C4OC5=C(C(=C(C=C35)I)O)I)I)O)I Organoheterocyclic compounds -1 1 TW polyala
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