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_57faa68242cd311b9b3d72f63af797ec Fosthiazate [M+Na]+ 306.0358 0.85 165.15 CCC(C)SP(=O)(N1CCSC1=O)OCC Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_cf0b0890d481a92044b5718a87aace4e Carbofuran [M+Na]+ 244.0944 0.83 156.44 CC1(CC2=C(O1)C(=CC=C2)OC(=O)NC)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_2da5e07dece575ae8af9b5eb115aa54e Terbacil [M-H]- 215.0593 0.8 148.45 CC1=C(C(=O)N(C(=O)N1)C(C)(C)C)Cl Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_bf10e4c9ca6a57a0696ccccf9052107f Butylate [M+H]+ 218.1573 1.03 151.48 CCSC(=O)N(CC(C)C)CC(C)C Organosulfur compounds 1 1 TW polyala
CCSBASE_1e9bbe0fd8b413476be4eac9a2bd1e4e CP-457677 [M+H-H2O]+ 363.1504 0.87 190.97 CC(C)(C1=CC=C(C=C1)CNC(=O)C2=C(N=CC=C2)OC3=CC=C(C=C3)F)O Organic oxygen compounds 1 1 TW polyala
CCSBASE_4b09d07500827605dea8b1780dac785b CP-457677 [M+Na]+ 403.1428 0.87 189.2 CC(C)(C1=CC=C(C=C1)CNC(=O)C2=C(N=CC=C2)OC3=CC=C(C=C3)F)O Organic oxygen compounds 1 1 TW polyala
CCSBASE_1c73976f9c2b72a741ed4b79982be798 Spiroxamine [M+H]+ 298.2741 0.83 180.85 CCCN(CC)CC1COC2(O1)CCC(CC2)C(C)(C)C  Organic oxygen compounds 1 1 TW polyala
CCSBASE_9132e0de404ff0594051c1d8aa78ebdb Dimethyl phthalate [M-H]- 193.0506 0.73 143.21 COC(=O)C1=CC=CC=C1C(=O)OC Benzenoids -1 1 TW polyala
CCSBASE_497f8490eb77bed7aa25a1ec5d873612 Ketoconazole [M+H]+ 531.156 0.81 213.59 CC(=O)N1CCN(CC1)C2=CC=C(C=C2)OC[C@H]3CO[C@](O3)(CN4C=CN=C4)C5=C(C=C(C=C5)Cl)Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_b461d473a3c45f6120e2c96c5d46bd2e Isoproterenol hydrochloride [M+H]+ 212.1281 0.71 149.67 CC(C)NCC(C1=CC(=C(C=C1)O)O)O Benzenoids 1 1 TW polyala
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