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_7934b8581045c1a912ac36f7e296cde9 Monoethyl phthalate [M+Na]+ 217.0471 0.81 149.55 CCOC(=O)C1=CC=CC=C1C(=O)O Benzenoids 1 1 TW polyala
CCSBASE_e7b025024ee75e387bc37ddf0d330536 Mestranol [M-H]- 309.186 0.85 175.8 CC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)OC Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_ae9573eec0fd5192246f77fed37ad66d Norethindrone [M+H]+ 299.2006 0.91 174.45 CC12CCC3C(C1CCC2(C#C)O)CCC4=CC(=O)CCC34 Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_50e250e6bbda56916b783d37b0c6042b Norethindrone [M+H-H2O]+ 281.1901 0.91 168.58 CC12CCC3C(C1CCC2(C#C)O)CCC4=CC(=O)CCC34 Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_35a75730f372f6cd8f7abd46da312ee6 Cromolyn sodium [M+H]+ 469.0765 0.8 203.66 C1=CC2=C(C(=C1)OCC(COC3=CC=CC4=C3C(=O)C=C(O4)C(=O)[O-])O)C(=O)C=C(O2)C(=O)[O-] Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_162c95aab578c8679cbdf58bf643aa4b Cromolyn sodium [M+H-H2O]+ 451.066 0.8 193.2 C1=CC2=C(C(=C1)OCC(COC3=CC=CC4=C3C(=O)C=C(O4)C(=O)[O-])O)C(=O)C=C(O2)C(=O)[O-] Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_917797e9fa2ac07d6b9b51b88aef713b Cromolyn sodium [M+K]+ 507.0324 0.79 210.66 C1=CC2=C(C(=C1)OCC(COC3=CC=CC4=C3C(=O)C=C(O4)C(=O)[O-])O)C(=O)C=C(O2)C(=O)[O-] Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_c891fe3316759131c06c2375bba1445f Cromolyn sodium [M+Na]+ 491.0585 0.8 207.05 C1=CC2=C(C(=C1)OCC(COC3=CC=CC4=C3C(=O)C=C(O4)C(=O)[O-])O)C(=O)C=C(O2)C(=O)[O-] Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_ef918c8a6cfcf9f47012f04242416c53 Cromolyn sodium [M-H]- 467.062 0.79 184.99 C1=CC2=C(C(=C1)OCC(COC3=CC=CC4=C3C(=O)C=C(O4)C(=O)[O-])O)C(=O)C=C(O2)C(=O)[O-] Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_01dc937838c477d9a25e820946e70d93 Oct-1-en-3-yl acetate [M+FA-H]- 215.1289 0.81 151.44 CCCCCC(C=C)OC(=O)C Organic acids and derivatives -1 1 TW polyala
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