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_e78af6188f76e0882ddffbbf55de702c CP-105696 [M+K]+ 467.162 1.06 208.29 C1CCC(C1)(C2=CC3=C(C=C2)C(C(CO3)CC4=CC=C(C=C4)C5=CC=CC=C5)O)C(=O)O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_2fb795577a70efcd0bc6d507f5c117ee Glybenclamide [M+H]+ 494.1511 0.93 204.36 COC1=C(C=C(C=C1)Cl)C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC3CCCCC3 Benzenoids 1 1 TW polyala
CCSBASE_10d57068abccc14ca1ef35b1b3d89666 Glybenclamide [M+K]+ 532.107 0.93 221.61 COC1=C(C=C(C=C1)Cl)C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC3CCCCC3 Benzenoids 1 1 TW polyala
CCSBASE_630f38159d8731fdeefecc28ffec20b2 4-tert-Butylphenol [M+FA-H]- 195.1027 0.75 149.63 CC(C)(C)C1=CC=C(C=C1)O Benzenoids -1 1 TW polyala
CCSBASE_b4439ade776a0aeb70ccfe53b984f037 Dihexyl phthalate [M+H]+ 335.2217 1.01 178.51 CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC Benzenoids 1 1 TW polyala
CCSBASE_9a2a53585448805bbebd962e8b0a1b56 FR130739 [M+H]+ 410.2088 0.88 195.45 CCCCC1=NC2=C(N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NN=N[N-]5)N=CC=C2 Benzenoids 1 1 TW polyala
CCSBASE_a3be25d23d97cb33ad64ed266596f529 Thimerosal [M+H-H2O]+ 367.0076 0.88 137.23 CC[Hg]SC1=CC=CC=C1C(=O)[O-] Benzenoids 1 1 TW polyala
CCSBASE_ff418bfc704c438c2759232d535f6502 2-Ethyl-3-hydroxy-4H-pyran-4-one [M-H]- 139.04 0.73 133.48 CCC1=C(C(=O)C=CO1)O Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_9b7e44c57e36e93f46f50db303c3dfdd 2,6-Dimethylaniline [M+H]+ 122.0964 0.71 130.3 CC1=C(C(=CC=C1)C)N Benzenoids 1 1 TW polyala
CCSBASE_b2eafca2cd76237398849c680661a8fb 4-Pentylaniline [M+H]+ 164.1434 0.78 152.48 CCCCCC1=CC=C(C=C1)N Benzenoids 1 1 TW polyala
1 2 ... 77 78 79 80 81 82 83 ... 359 360