Name:
Adduct:
Polarity:
Z:
m/z:
±:
CCS: Å
±: %
SMI:

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ID Name Adduct Structure m/z RT CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_4b65ac43913d37d799c08fb14813c052 Flumetsulam [M+H]+ 326.0518 0.78 165.04 CC1=NC2=NC(=NN2C=C1)S(=O)(=O)NC3=C(C=CC=C3F)F Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_fc79be7af474fbc0d189ae10694b731a Flumetsulam [M+K]+ 364.0077 0.78 180.34 CC1=NC2=NC(=NN2C=C1)S(=O)(=O)NC3=C(C=CC=C3F)F Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_5a9b2720907b4e7af34b54dee8c5427e Flumetsulam [M+Na]+ 348.0337 0.78 174.06 CC1=NC2=NC(=NN2C=C1)S(=O)(=O)NC3=C(C=CC=C3F)F Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_ace67bb78c07e9f50af0ea8483858b7e Flumetsulam [M-H]- 324.0372 0.73 171.38 CC1=NC2=NC(=NN2C=C1)S(=O)(=O)NC3=C(C=CC=C3F)F Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_0612d90ddfd3c5476d1c20d443bfb380 PD 0343701 [M+H]+ 435.2213 0.78 203.62 CC1=CC(=CC2=C1NC(=O)CC2(C)C)CCN3CCN(CC3)C4=NSC5=CC=CC=C54 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_2677d1917badfcf0276d0df8fc760406 Thiamethoxam [M+H]+ 292.0266 0.74 157.61 CN\1COCN(/C1=N/[N+](=O)[O-])CC2=CN=C(S2)Cl   Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_cd8784a19b2cffe0c3ffc352deef2e3f Thiamethoxam [M+Na]+ 314.0085 0.74 158.55 CN\1COCN(/C1=N/[N+](=O)[O-])CC2=CN=C(S2)Cl   Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_f26692a91a3af29a594023029f857bdc (E)-11-Tetradecen-1-ol acetate [M+FA-H]- 299.2228 0.95 175.38 CCC=CCCCCCCCCCCOC(=O)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_ed79842bf21c9c6649661d47d6a5c211 Icaridin [M+Na]+ 252.157 0.88 164.2 CCC(C)OC(=O)N1CCCCC1CCO Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_03516a349f1a36d7634f8375ae122a30 Icaridin [M-H]- 228.1605 0.81 158.15 CCC(C)OC(=O)N1CCCCC1CCO Organoheterocyclic compounds -1 1 TW polyala
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