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_fea097f9e025ba734fdee86bc2789d3b Benzyldimethyloctylammonium chloride [M]+ 248.2373 0.82 171.26 CCCCCCCC[N+](C)(C)CC1=CC=CC=C1 Benzenoids 1 1 TW polyala
CCSBASE_76353b3b2af95bef39804aea89eb1bb8 Pentamidine [M+H]+ 341.1972 0.76 174.26 C1=CC(=CC=C1C(=N)N)OCCCCCOC2=CC=C(C=C2)C(=N)N Benzenoids 1 1 TW polyala
CCSBASE_36deab7789ceae2f57e1c8d1dd33371c Isoprocarb [M+Na]+ 216.0995 0.86 149.52 CC(C)C1=CC=CC=C1OC(=O)NC Benzenoids 1 1 TW polyala
CCSBASE_c58b47e8f26d7b0cb4339769b44c3a9f trans-2-Methoxycinnamaldehyde [M+H]+ 163.0754 0.86 131.49 COC1=CC=CC=C1C=CC=O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_ff2e46e6eeea5016644a00ff53c33bec 2-Amino-5-chlorobenzophenone [M+H]+ 232.0524 0.93 151.65 C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)Cl)N Benzenoids 1 1 TW polyala
CCSBASE_f3ad65adc30932ab4eff954308222ad1 Chlorobenzilate [M+H-H2O]+ 307.0288 0.98 166.05 CCOC(=O)C(C1=CC=C(C=C1)Cl)(C2=CC=C(C=C2)Cl)O Benzenoids 1 1 TW polyala
CCSBASE_d04441a9fb64aa919e19573d4275b8a9 Indomethacin [M+H]+ 358.0841 0.95 179.3 CC1=C(C2=C(N1C(=O)C3=CC=C(C=C3)Cl)C=CC(=C2)OC)CC(=O)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_d2185783ba5a6eccc53a9e812a1e9bfd Indomethacin [M+Na]+ 380.066 0.95 187.2 CC1=C(C2=C(N1C(=O)C3=CC=C(C=C3)Cl)C=CC(=C2)OC)CC(=O)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_370d10f6dfbede21c5211417bb8b7e36 2-[Methacryloyloxy]ethyl acetoacetate [M+Na]+ 237.0733 0.81 147.76 CC(=C)C(=O)OCCOC(=O)CC(=O)C Organic acids and derivatives 1 1 TW polyala
CCSBASE_1efd66e94ec8e4de5c6b1ed36dedfed2 Flusilazole [M+H]+ 316.1076 0.94 172.57 C[Si](CN1C=NC=N1)(C2=CC=C(C=C2)F)C3=CC=C(C=C3)F Benzenoids 1 1 TW polyala
1 2 ... 186 187 188 189 190 191 192 ... 359 360