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_42542fa87a9d2fff27e50a7571e665dc Indinavir sulfate [M-H-H2O]- 594.3444 0.76 253.36 CC(C)(C)NC(=O)C1CN(CCN1CC(CC(CC2=CC=CC=C2)C(=O)NC3C(CC4=CC=CC=C34)O)O)CC5=CN=CC=C5 Organic acids and derivatives -1 1 TW polyala
CCSBASE_033be9d8a0e92b2386b5a58cc31362c4 Isobutyl 3-phenylacrylate [M+FA-H]- 249.1132 0.82 144.34 CC(C)COC(=O)C=CC1=CC=CC=C1 Phenylpropanoids and polyketides -1 1 TW polyala
CCSBASE_f911ebcd990e2ea3920bdf12837466f6 Isocarbophos [M+Na]+ 312.043 0.86 166.39 CC(C)OC(=O)C1=CC=CC=C1OP(=S)(N)OC Benzenoids 1 1 TW polyala
CCSBASE_0a9c386910a199466724da0a28cd04a1 Isofenphos [M+K]+ 384.0795 0.98 184.09 CCOP(=S)(NC(C)C)OC1=CC=CC=C1C(=O)OC(C)C   Benzenoids 1 1 TW polyala
CCSBASE_f996d5a0043225d2c43e7b2a866bc43c Isofenphos [M+Na]+ 368.1056 0.98 181.82 CCOP(=S)(NC(C)C)OC1=CC=CC=C1C(=O)OC(C)C Benzenoids 1 1 TW polyala
CCSBASE_5d26effdb418dd1a5907970b9cd84209 Isoxathion [M+H]+ 314.061 0.97 167.04 CCOP(=S)(OCC)OC1=NOC(=C1)C2=CC=CC=C2  Organic acids and derivatives 1 1 TW polyala
CCSBASE_ffd0979ee922421596a13183cefbfacf Isoxathion [M+Na]+ 336.043 0.97 178.96 CCOP(=S)(OCC)OC1=NOC(=C1)C2=CC=CC=C2  Organic acids and derivatives 1 1 TW polyala
CCSBASE_609c33c92440361a01b01c3db4e64e1c Karbutilate [M+H]+ 280.1656 0.82 170.73 CC(C)(C)NC(=O)OC1=CC=CC(=C1)NC(=O)N(C)C Benzenoids 1 1 TW polyala
CCSBASE_d7fb50f3ffd68a431f3fa686bfe04162 Karbutilate [M+K]+ 318.1214 0.82 175.78 CC(C)(C)NC(=O)OC1=CC=CC(=C1)NC(=O)N(C)C Benzenoids 1 1 TW polyala
CCSBASE_6bd31e2f6f5418679a1f6925821bda11 Karbutilate [M+Na]+ 302.1475 0.83 173.49 CC(C)(C)NC(=O)OC1=CC=CC(=C1)NC(=O)N(C)C Benzenoids 1 1 TW polyala
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