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_1f0ea58f7c1b9d97b772577f8f9f7fe7 Lenacil [M-H]- 233.1295 0.83 160.17 C1CCC(CC1)N2C(=O)C3=C(CCC3)NC2=O Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_71f52682aed65be62188f1a1b493645e 2,4-Xylenesulfonic acid monohydrate [M-H]- 185.0278 0.76 141.31 CC1=CC(=C(C=C1)S(=O)(=O)O)C Benzenoids -1 1 TW polyala
CCSBASE_9adf67028826875f1b757176a1e095ed Cycloheximide [M+H]+ 282.17 0.81 167.5 CC1CC(C(=O)C(C1)C(CC2CC(=O)NC(=O)C2)O)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_6c80424e96a45b39b80c203e8284b872 Cycloheximide [M+H-H2O]+ 264.1595 0.81 165.59 CC1CC(C(=O)C(C1)C(CC2CC(=O)NC(=O)C2)O)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_1016a77d1094fe96eda2cc8486cddb00 Cycloheximide [M+Na]+ 304.1519 0.81 172.19 CC1CC(C(=O)C(C1)C(CC2CC(=O)NC(=O)C2)O)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_56bb923c5a58ba4713c540068bb43a96 Cycloheximide [M-H]- 280.1554 0.76 170.95 CC1CC(C(=O)C(C1)C(CC2CC(=O)NC(=O)C2)O)C Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_785c7966c1d433a9d5c3ee13ed165bc0 3,4,5,6-Tetrachloropyridine-2-carboxylic acid [M-H]- 259.8659 0.86 147.44 C1(=C(C(=NC(=C1Cl)Cl)C(=O)O)Cl)Cl Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_c133c8c73e2d450a5ac3c2f2743e52fc UK-373911 [M+H]+ 385.0539 0.79 187.58 CNC1CCC(C2=C1C=C(C=C2)S(=O)(=O)N)C3=CC(=C(C=C3)Cl)Cl Benzenoids 1 1 TW polyala
CCSBASE_50a2aa888dcf2612d415a0f26fb7ac1a Octyl gallate [M-H]- 281.1394 0.89 174.82 CCCCCCCCOC(=O)C1=CC(=C(C(=C1)O)O)O Benzenoids -1 1 TW polyala
CCSBASE_ae25f9d7649ee1d41df01dfe37701468 alpha-Terpineol [M+FA-H]- 199.134 0.81 152.23 CC1=CCC(CC1)C(C)(C)O Lipids and lipid-like molecules -1 1 TW polyala
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