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_ded974f6f3368349ec0e709c9696819a Chlortetracycline hydrochloride [M-H]- 477.107 0.71 202.39 CC1(C2CC3C(C(=O)C(=C(C3(C(=O)C2=C(C4=C(C=CC(=C41)Cl)O)O)O)O)C(=O)N)N(C)C)O Phenylpropanoids and polyketides -1 1 TW polyala
CCSBASE_77e61d19d0b60d9046e57ecd279d8262 Diethyl L-tartrate [M+Na]+ 229.0683 0.71 151.32 CCOC(=O)C(C(C(=O)OCC)O)O Organic acids and derivatives 1 1 TW polyala
CCSBASE_59fd289b436750d1b0fb402fdf938be1 Diethyl L-tartrate [M-H-H2O]- 187.0606 0.71 139.98 CCOC(=O)C(C(C(=O)OCC)O)O Organic acids and derivatives -1 1 TW polyala
CCSBASE_036ef4625aa256d5eca2e87ef24aa3f6 (-)Carophyllene oxide [M+H-H2O]+ 203.1795 0.99 148.28 CC1(CC2C1CCC3(C(O3)CCC2=C)C)C Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_fcd89f3d209b29529fca8c7f727884a5 (7S)-Hydroprene [M+FA-H]- 311.2228 0.91 178.54 CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_4c0dc54f3fbfa41a0757a4d72bc95e99 2-(Dodecyloxy)ethanol [M-H-H2O]- 211.2062 0.98 160.24 CCCCCCCCCCCCOCCO Organic oxygen compounds -1 1 TW polyala
CCSBASE_7b5e3c223295b045516150d171f20f15 4-Propylcyclohexanone [M+FA-H]- 185.1183 0.79 147.78 CCCC1CCC(=O)CC1 Organic oxygen compounds -1 1 TW polyala
CCSBASE_82f040c87eb0cdfa8f484d8392e3b36c 4-Propylcyclohexanone [M-H]- 139.1128 0.78 139.56 CCCC1CCC(=O)CC1 Organic oxygen compounds -1 1 TW polyala
CCSBASE_534c4f0f6f137d720747a09a507da4d7 2-Cyclohexylethyl acetate [M+FA-H]- 215.1289 0.81 151.14 CC(=O)OCCC1CCCCC1 Organic acids and derivatives -1 1 TW polyala
CCSBASE_927cbb91b15f381c635f6c6dcc22b37c 2-Cyclohexylethyl acetate [M+H]+ 171.138 0.72 141.64 CC(=O)OCCC1CCCCC1 Organic acids and derivatives 1 1 TW polyala
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