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_efe217eccc629d6a81753db836d72606 Tebufenpyrad [M+Na]+ 356.15 1.07 191.52 CCC1=NN(C(=C1Cl)C(=O)NCC2=CC=C(C=C2)C(C)(C)C)C Benzenoids 1 1 TW polyala
CCSBASE_0528fffc9f9820ef882422eb10a2df14 Pencycuron [M+H]+ 329.1415 0.98 179.1 C1CCC(C1)N(CC2=CC=C(C=C2)Cl)C(=O)NC3=CC=CC=C3 Benzenoids 1 1 TW polyala
CCSBASE_8ef0e2dd4510fd7e03e7c3abe9e5d90b Pencycuron [M+Na]+ 351.1235 0.98 189.86 C1CCC(C1)N(CC2=CC=C(C=C2)Cl)C(=O)NC3=CC=CC=C3 Benzenoids 1 1 TW polyala
CCSBASE_1a174a1d08172049fadf66a8e7511ffc Indoxacarb [M+H]+ 528.078 0.98 203.13 COC(=O)C12CC3=C(C1=NN(CO2)C(=O)N(C4=CC=C(C=C4)OC(F)(F)F)C(=O)OC)C=CC(=C3)Cl Benzenoids 1 1 TW polyala
CCSBASE_0f14dbb0d087bc1e8be8fb542b7a4851 Indoxacarb [M+H]+ 528.078 0.98 215.72 COC(=O)C12CC3=C(C1=NN(CO2)C(=O)N(C4=CC=C(C=C4)OC(F)(F)F)C(=O)OC)C=CC(=C3)Cl Benzenoids 1 1 TW polyala
CCSBASE_4ac055aa621a900fd65d5838c725d815 Indoxacarb [M+Na]+ 550.0599 0.98 216.74 COC(=O)C12CC3=C(C1=NN(CO2)C(=O)N(C4=CC=C(C=C4)OC(F)(F)F)C(=O)OC)C=CC(=C3)Cl Benzenoids 1 1 TW polyala
CCSBASE_5dc94879a67e06d871bf4303567ca648 AVE3247 [M+H]+ 526.131 0.81 225.66 C1CC1N2CCC(CC2)NC(=O)C3=NC4=C(N3CC5=NOC(=C5)C6=CC=C(S6)Cl)C=CC(=C4)C(=O)[O-] Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_0e672b3d60336078efa4834c86d85306 AVE3247 [M+Na]+ 548.113 0.81 243.79 C1CC1N2CCC(CC2)NC(=O)C3=NC4=C(N3CC5=NOC(=C5)C6=CC=C(S6)Cl)C=CC(=C4)C(=O)[O-] Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_c02eb3cfb07e14ea437983193af3f1fd AVE3247 [M-H]- 524.1165 0.77 233.93 C1CC1N2CCC(CC2)NC(=O)C3=NC4=C(N3CC5=NOC(=C5)C6=CC=C(S6)Cl)C=CC(=C4)C(=O)[O-] Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_c63ba8c931b4a27de2cf9ffc5ba92380 AVE3247 [M-H]- 524.1165 0.77 248.04 C1CC1N2CCC(CC2)NC(=O)C3=NC4=C(N3CC5=NOC(=C5)C6=CC=C(S6)Cl)C=CC(=C4)C(=O)[O-] Organoheterocyclic compounds -1 1 TW polyala
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