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_4ce9a08680f3930348dfcdb14f4954d6 1-(2,6-Dichlorophenyl)-2-indolinone [M+Na]+ 299.9953 0.85 136.85 C1C2=CC=CC=C2N(C1=O)C3=C(C=CC=C3Cl)Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_c01c35afbc3d0a088305ab75ef6583c0 1-(2,6-Dichlorophenyl)-2-indolinone [M+Na]+ 299.9953 0.85 167.82 C1C2=CC=CC=C2N(C1=O)C3=C(C=CC=C3Cl)Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_bedc3f021c397b8d2d2fe8b05b966fbe 1,4-Dioxacycloheptadecane-5,17-dione [M+H]+ 271.1904 0.97 164.5 C1CCCCCC(=O)OCCOC(=O)CCCCC1 Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_2e0767e593024d05275f7f3ab4f1bca1 1,4-Dioxacycloheptadecane-5,17-dione [M+K]+ 309.1463 0.97 169.86 C1CCCCCC(=O)OCCOC(=O)CCCCC1 Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_3b1c768f2c710e731023f56265feeece 1,4-Dioxacycloheptadecane-5,17-dione [M+Na]+ 293.1723 0.98 168.76 C1CCCCCC(=O)OCCOC(=O)CCCCC1 Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_2d8f13203d812c070b4ed7ca7d8372d1 1-Phenyl-3-methyl-5-pyrazolone [M+H]+ 175.0866 0.74 136.62 CC1=NN(C(=O)C1)C2=CC=CC=C2 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_c7f5d4b6d98636233e34c8bb5ed06e41 Nizatidine [M+Cl]- 366.0831 0.67 191.9 CNC(=C[N+](=O)[O-])NCCSCC1=CSC(=N1)CN(C)C Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_9884bc4445dd2e63cd1e17f1f87a867f Nizatidine [M+H]+ 332.1209 0.68 169.06 CNC(=C[N+](=O)[O-])NCCSCC1=CSC(=N1)CN(C)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_7c84763f265065c25c84f67010a35dd0 Nizatidine [M+H-H2O]+ 314.1104 0.69 170.59 CNC(=C[N+](=O)[O-])NCCSCC1=CSC(=N1)CN(C)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_86b4e892e4890764e6ffcfec39748a3d Nizatidine [M+K]+ 370.0768 0.69 177.8 CNC(=C[N+](=O)[O-])NCCSCC1=CSC(=N1)CN(C)C Organoheterocyclic compounds 1 1 TW polyala
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