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_844f24c06aa22397727a6f8a0a5e2d2c Fenhexamid [M+H]+ 302.0709 0.92 165.25 CC1(CCCCC1)C(=O)NC2=C(C(=C(C=C2)O)Cl)Cl Benzenoids 1 1 TW polyala
CCSBASE_63bd78dba57d7310f380757a9401f219 Fenhexamid [M-H]- 300.0563 0.86 172.12 CC1(CCCCC1)C(=O)NC2=C(C(=C(C=C2)O)Cl)Cl Benzenoids -1 1 TW polyala
CCSBASE_bf509eb1e939dd70b2674db774e0e392 N,N'-Methylenebisacrylamide [M+Na]+ 177.0634 0.73 135.48 C=CC(=O)NCNC(=O)C=C Organic acids and derivatives 1 1 TW polyala
CCSBASE_faaa5e5eac4f67a72a4a52112141d4c9 Isopropalin [M+H]+ 310.1762 1.11 170.99 CCCN(CCC)C1=C(C=C(C=C1[N+](=O)[O-])C(C)C)[N+](=O)[O-] Benzenoids 1 1 TW polyala
CCSBASE_d96e286beb12d97233d43b35e1cbb965 Mefenamic acid [M+H]+ 242.1176 1.02 154.46 CC1=C(C(=CC=C1)NC2=CC=CC=C2C(=O)O)C Benzenoids 1 1 TW polyala
CCSBASE_31030196cfc030cbe99ce0ca8f6ba019 Mefenamic acid [M+H-H2O]+ 224.1071 1.01 147.5 CC1=C(C(=CC=C1)NC2=CC=CC=C2C(=O)O)C Benzenoids 1 1 TW polyala
CCSBASE_4b7506f168f15db13f72950fe9d96609 Mefenamic acid [M-H]- 240.103 0.95 161.52 CC1=C(C(=CC=C1)NC2=CC=CC=C2C(=O)O)C Benzenoids -1 1 TW polyala
CCSBASE_a7bada9b9abdef84f695744fba218c84 Endothal [M+FA-H]- 231.051 0.69 148.33 C1CC2C(C(C1O2)C(=O)O)C(=O)O Organic acids and derivatives -1 1 TW polyala
CCSBASE_07b7c13c804548af5a2ba308e30f3487 Endothal [M+Na]+ 209.042 0.73 137.94 C1CC2C(C(C1O2)C(=O)O)C(=O)O Organic acids and derivatives 1 1 TW polyala
CCSBASE_e6df915f953783d0bfba3a4a9390befc Endothal [M-H]- 185.0455 0.69 139.83 C1CC2C(C(C1O2)C(=O)O)C(=O)O Organic acids and derivatives -1 1 TW polyala
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