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_9e996be9d3afbd3b40223c000a10169d Pyraflufen-ethyl [M+H]+ 413.0277 0.9 185.14 CCOC(=O)COC1=C(C=C(C(=C1)C2=NN(C(=C2Cl)OC(F)F)C)F)Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_b744bfdf808f78996d46996aeed481ea Pyraflufen-ethyl [M+Na]+ 435.0097 0.9 195.48 CCOC(=O)COC1=C(C=C(C(=C1)C2=NN(C(=C2Cl)OC(F)F)C)F)Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_5ba954be8223d4878bab612a57c2f068 C.I. Acid Orange 10 [M-H]- 407.0013 0.73 191.27 C1=CC=C(C=C1)N=NC2=C(C=CC3=CC(=CC(=C32)S(=O)(=O)[O-])S(=O)(=O)[O-])O Benzenoids -1 1 TW polyala
CCSBASE_a92f51efd59dc1c12eed46cb9843601f Loratadine [M+H]+ 383.1521 0.85 187.49 CCOC(=O)N1CCC(=C2C3=C(CCC4=C2N=CC=C4)C=C(C=C3)Cl)CC1 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_1f74363135664460ff4de57ab70448c3 Loratadine [M+Na]+ 405.134 0.84 194.34 CCOC(=O)N1CCC(=C2C3=C(CCC4=C2N=CC=C4)C=C(C=C3)Cl)CC1 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_ebd78268eb7564612db2fa55c9035433 Hexyl methacrylate [M+FA-H]- 215.1289 0.8 152.37 CCCCCCOC(=O)C(=C)C Organic acids and derivatives -1 1 TW polyala
CCSBASE_39f32182b4326d799d0c2b67259ad6cf Fumaric acid [M+Na]+ 139.0002 0.78 146.53 C(=CC(=O)O)C(=O)O Organic acids and derivatives 1 1 TW polyala
CCSBASE_1cd731025b2d6666ff956e1c4ddfd4fa Vatalanib dihydrochloride [M+H]+ 347.1058 0.71 184.12 C1=CC=C2C(=C1)C(=NN=C2NC3=CC=C(C=C3)Cl)CC4=CC=NC=C4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_5d0e9c76e1fc527d22c2f01e4e79bdc7 Vatalanib dihydrochloride [M+Na]+ 369.0877 0.71 189.3 C1=CC=C2C(=C1)C(=NN=C2NC3=CC=C(C=C3)Cl)CC4=CC=NC=C4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_71d1e647a0365e890daff8fadb2bd64f Vatalanib dihydrochloride [M-H]- 345.0912 0.71 187.4 C1=CC=C2C(=C1)C(=NN=C2NC3=CC=C(C=C3)Cl)CC4=CC=NC=C4 Organoheterocyclic compounds -1 1 TW polyala
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