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_c88ba7f8267f56ab24ab5d16f3e5b769 Diphenyl phosphate [M-H]- 249.0322 0.84 155.82 C1=CC=C(C=C1)OP(=O)(O)OC2=CC=CC=C2 Benzenoids -1 1 TW polyala
CCSBASE_16dfdfae781522721760007d372c3f4c L-Phenylalanine [M-H]- 164.0717 0.68 142.49 C1=CC=C(C=C1)CC(C(=O)O)N None -1 1 TW polyala
CCSBASE_ae71d489f958db29e713d51709021abc Clofibric acid [M-H]- 213.0324 0.87 150.75 CC(C)(C(=O)O)OC1=CC=C(C=C1)Cl Organic acids and derivatives -1 1 TW polyala
CCSBASE_e1bf43e5c7a5ed7b6c82ec156196d4f7 Sulindac [M+H]+ 357.0955 0.83 189.25 CC1=C(C2=C(C1=CC3=CC=C(C=C3)S(=O)C)C=CC(=C2)F)CC(=O)O Benzenoids 1 1 TW polyala
CCSBASE_90c98e1c6d9a0eb3bd6fcf396c9b2b58 Ethyl 3-(N-butylacetamido)propionate [M+Na]+ 238.1413 0.79 159.83 CCCCN(CCC(=O)OCC)C(=O)C Benzenoids 1 1 TW polyala
CCSBASE_44a0c7209e98a90a7359ea286bf90c9a Sulindac [M+Na]+ 379.0774 0.83 206.4 CC1=C(C2=C(C1=CC3=CC=C(C=C3)S(=O)C)C=CC(=C2)F)CC(=O)O Benzenoids 1 1 TW polyala
CCSBASE_30d32eca978d991d0a07f3025af7f4ed Sulindac [M+Na]+ 379.0774 0.83 182.14 CC1=C(C2=C(C1=CC3=CC=C(C=C3)S(=O)C)C=CC(=C2)F)CC(=O)O Benzenoids 1 1 TW polyala
CCSBASE_15b72c7a4c5e3d707b5a0a3f2b1038ea Ethyl 3-(N-butylacetamido)propionate [M+K]+ 254.1153 0.8 160.45 CCCCN(CCC(=O)OCC)C(=O)C Benzenoids 1 1 TW polyala
CCSBASE_7813768e14ad8ed3a70b81c00ec21cda Ethyl 3-(N-butylacetamido)propionate [M-H]- 214.1448 0.81 153.91 CCCCN(CCC(=O)OCC)C(=O)C Benzenoids -1 1 TW polyala
CCSBASE_093ff0d9adc5dc8fd9dda9a2d2b50716 Trelanserin [M+H]+ 466.1708 0.71 195.45 C1CN(CCN1CCC2=CC(=O)N(C3=C2C=CC(=C3)F)CC(=O)N)C4=NC=CC5=C4C=CS5 Organic acids and derivatives 1 1 TW polyala
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