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_868d87a6d2600cffd6178bf0e94bb318 SSR161421 [M-H]- 407.1513 0.83 208.2 COC1=CC=C(C=C1)C(=O)NC2=NC3=CC=CC=C3C(=C2C#N)NCC4=CC=CC=C4 Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_b57790adeebaefa7a49f36f786c50cf3 CI-1018 [M+H]+ 397.1659 0.91 199.42 CC1=CC2=C3C(=C1)C(=NC(C(=O)N3CC2)NC(=O)C4=CC=NC=C4)C5=CC=CC=C5 Organic acids and derivatives 1 1 TW polyala
CCSBASE_93572a0b5b95b48acdf2d8ba94cf21bb CI-1018 [M+H-H2O]+ 379.1554 0.91 192.45 CC1=CC2=C3C(=C1)C(=NC(C(=O)N3CC2)NC(=O)C4=CC=NC=C4)C5=CC=CC=C5 Organic acids and derivatives 1 1 TW polyala
CCSBASE_37d4fec21c1e5319aa19eb4331dd2101 CI-1018 [M+Na]+ 419.1478 0.93 207.06 CC1=CC2=C3C(=C1)C(=NC(C(=O)N3CC2)NC(=O)C4=CC=NC=C4)C5=CC=CC=C5 Organic acids and derivatives 1 1 TW polyala
CCSBASE_ff1fcf1452bc75b03356d2480456792d CI-1018 [M-H]- 395.1513 0.85 195.0 CC1=CC2=C3C(=C1)C(=NC(C(=O)N3CC2)NC(=O)C4=CC=NC=C4)C5=CC=CC=C5 Organic acids and derivatives -1 1 TW polyala
CCSBASE_23131f8c53b16a93620ee97c84c0d407 Ethylhexadecyldimethylammonium bromide [M]+ 298.3468 0.98 200.37 CCCCCCCCCCCCCCCC[N+](C)(C)CC Organic nitrogen compounds 1 1 TW polyala
CCSBASE_d99c8453bf6dd5b54946cf304bc13ef0 CP-863187 [M+H]+ 341.1209 0.87 175.5 CC(C)C1=NN=C2N1C=C(C=C2)C3=C(N=CO3)C4=C(C=CC(=C4)F)F Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_9afc9131f1c0ad56315457b95a3712a4 CP-863187 [M+Na]+ 363.1028 0.87 193.12 CC(C)C1=NN=C2N1C=C(C=C2)C3=C(N=CO3)C4=C(C=CC(=C4)F)F Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_722c57b6e17429e3ac592382d16261e3 4-Cyclohexylcyclohexanone [M+FA-H]- 225.1496 0.85 160.38 C1CCC(CC1)C2CCC(=O)CC2 Organic oxygen compounds -1 1 TW polyala
CCSBASE_55d831ca3b6461ff417c270116a65599 Flucarbazone-sodium [M+H]+ 397.0424 0.84 174.05 CN1C(=NN(C1=O)C(=O)[N-]S(=O)(=O)C2=CC=CC=C2OC(F)(F)F)OC Benzenoids 1 1 TW polyala
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