Name:
Adduct:
Polarity:
Z:
m/z:
±:
CCS: Å
±: %
SMI:

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ID Name Adduct Structure m/z RT CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_3125825e000f9f8026a20fa8bc317bb8 Sulfamethazine [M+Na]+ 301.073 0.74 169.65 CC1=CC(=NC(=N1)NS(=O)(=O)C2=CC=C(C=C2)N)C  Benzenoids 1 1 TW polyala
CCSBASE_00495a59d2db1266e0b2a6370495af44 Sulpiride [M+H]+ 342.1482 0.73 182.12 CCN1CCCC1CNC(=O)C2=C(C=CC(=C2)S(=O)(=O)N)OC   Benzenoids 1 1 TW polyala
CCSBASE_89d134dc4242c78b4bd80f88c9bd43f2 Sulpiride [M+Na]+ 364.1301 0.73 189.09 CCN1CCCC1CNC(=O)C2=C(C=CC(=C2)S(=O)(=O)N)OC   Benzenoids 1 1 TW polyala
CCSBASE_d4eb6cf38b415bc09ce37bf9f5b24626 Sulpiride [M-H]- 340.1336 0.69 187.41 CCN1CCCC1CNC(=O)C2=C(C=CC(=C2)S(=O)(=O)N)OC Benzenoids -1 1 TW polyala
CCSBASE_80cee985e68d6322893bf73e32a8d5a8 Tamoxifen [M+H]+ 372.2322 0.88 195.93 CC/C(=C(\C1=CC=CC=C1)/C2=CC=C(C=C2)OCCN(C)C)/C3=CC=CC=C3  Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_9e0155cc9df16b1c926ee1f14e2c8040 Tembotrione [M+Na]+ 463.02 0.86 183.37 CS(=O)(=O)C1=C(C(=C(C=C1)C(=O)C2C(=O)CCCC2=O)Cl)COCC(F)(F)F   Organic oxygen compounds 1 1 TW polyala
CCSBASE_261aafcdb69ebb950fb027201c6c8ae9 Tembotrione [M-H]- 439.0235 0.84 191.19 CS(=O)(=O)C1=C(C(=C(C=C1)C(=O)C2C(=O)CCCC2=O)Cl)COCC(F)(F)F Organic oxygen compounds -1 1 TW polyala
CCSBASE_46871c43885c12a513a5864aa9a494d4 Terbufos sulfone [M+Na]+ 343.0232 0.88 169.62 CCOP(=S)(OCC)SCS(=O)(=O)C(C)(C)C Organic acids and derivatives 1 1 TW polyala
CCSBASE_c6794d59cb02927394515d05010a1851 tert-Butyl 4-hydroxybenzoate [M-H]- 193.087 0.83 150.49 CC(C)(C)OC(=O)C1=CC=C(C=C1)O Benzenoids -1 1 TW polyala
CCSBASE_06b1bd1bc2ff390504f747603cdf6a59 tert-Butylperoxy 2-ethylhexyl carbonate [M-H-H2O]- 227.1647 0.86 160.01 CCCCC(CC)COC(=O)OOC(C)(C)C Organic acids and derivatives -1 1 TW polyala
1 2 ... 240 241 242 243 244 245 246 ... 359 360