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_e1dfdfca62b7f1f51a7fd4433b25336f Kadethrin [M+H]+ 397.1468 0.96 191.76 CC1(C(C1C(=O)OCC2=COC(=C2)CC3=CC=CC=C3)C=C4CCSC4=O)C Benzenoids 1 1 TW polyala
CCSBASE_de335ad2647ea8680a644f866190d251 Kadethrin [M+H-H2O]+ 379.1363 0.95 187.44 CC1(C(C1C(=O)OCC2=COC(=C2)CC3=CC=CC=C3)C=C4CCSC4=O)C Benzenoids 1 1 TW polyala
CCSBASE_24c88c8b76674591b99ab36660cf42cb Kadethrin [M+K]+ 435.1027 0.96 192.99 CC1(C(C1C(=O)OCC2=COC(=C2)CC3=CC=CC=C3)C=C4CCSC4=O)C Benzenoids 1 1 TW polyala
CCSBASE_1593c4d028ff4ac3c060b4a0bb191148 Kadethrin [M+Na]+ 419.1287 0.95 190.18 CC1(C(C1C(=O)OCC2=COC(=C2)CC3=CC=CC=C3)C=C4CCSC4=O)C Benzenoids 1 1 TW polyala
CCSBASE_8b393ae0b64e56c41fe84f535b473594 Benalaxyl [M+H]+ 326.1751 0.97 172.68 CC1=C(C(=CC=C1)C)N(C(C)C(=O)OC)C(=O)CC2=CC=CC=C2 Organic acids and derivatives 1 1 TW polyala
CCSBASE_a55b4a21d8003b54220d9ea3e3908b02 PD-0333941 [M+H]+ 391.1652 0.91 188.99 CC1=C(N=C(O1)C2=CC=CC=C2)CCOC3=CC=CC4=C3C=CN4CCC(=O)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_957a2bad2c59a3a77d876ecff1455785 N,N-Dibutyl-N-methylbutan-1-aminium chloride [M]+ 200.2373 0.73 156.54 CCCC[N+](C)(CCCC)CCCC Organic nitrogen compounds 1 1 TW polyala
CCSBASE_778fa547d9461d30f1761b89175f80c5 Dimethyl 2,6-naphthalenedicarboxylate [M+H]+ 245.0808 0.9 153.83 COC(=O)C1=CC2=C(C=C1)C=C(C=C2)C(=O)OC Benzenoids 1 1 TW polyala
CCSBASE_199eb09e984f2d2052ca3b43a9c7ee21 Nefiracetam [M+H]+ 247.1441 0.73 156.11 CC1=C(C(=CC=C1)C)NC(=O)CN2CCCC2=O Organic acids and derivatives 1 1 TW polyala
CCSBASE_1c882d1cf40c7b78ef0a3dcd0f151490 Nefiracetam [M+K]+ 285.1 0.74 165.59 CC1=C(C(=CC=C1)C)NC(=O)CN2CCCC2=O Organic acids and derivatives 1 1 TW polyala
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