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_cb4d9304887434619c7e0c3517b4ed68 Pyraclostrobin [M+Na]+ 410.0878 0.97 191.59 COC(=O)N(C1=CC=CC=C1COC2=NN(C=C2)C3=CC=C(C=C3)Cl)OC   Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_5d15e71f4ee505ccd7443a15b9429d62 Pyrazophos [M+H]+ 374.0934 1.0 187.54 CCOC(=O)C1=CN2C(=CC(=N2)OP(=S)(OCC)OCC)N=C1C  Organic acids and derivatives 1 1 TW polyala
CCSBASE_f82467c5c1a5106eabbebb88461aaf98 Pyrazophos [M+Na]+ 396.0753 1.0 193.26 CCOC(=O)C1=CN2C(=CC(=N2)OP(=S)(OCC)OCC)N=C1C  Organic acids and derivatives 1 1 TW polyala
CCSBASE_34c3f698d50998e5f07f289b1d0c0790 Pyrazophos [M-H]- 372.0788 0.93 188.68 CCOC(=O)C1=CN2C(=CC(=N2)OP(=S)(OCC)OCC)N=C1C Organic acids and derivatives -1 1 TW polyala
CCSBASE_53789af882a976c11bb06985cc4c565a Pyrithiobac [M+H]+ 327.0201 0.9 166.06 COC1=CC(=NC(=N1)SC2=C(C(=CC=C2)Cl)C(=O)O)OC  Benzenoids 1 1 TW polyala
CCSBASE_0f89aae6eac5cc16b1a2ed01f04bd86d Pyrithiobac [M+H-H2O]+ 309.0096 0.9 159.17 COC1=CC(=NC(=N1)SC2=C(C(=CC=C2)Cl)C(=O)O)OC  Benzenoids 1 1 TW polyala
CCSBASE_bfa6f891e368c455835f81635db1610b Pyrithiobac [M+Na]+ 349.002 0.9 172.44 COC1=CC(=NC(=N1)SC2=C(C(=CC=C2)Cl)C(=O)O)OC Benzenoids 1 1 TW polyala
CCSBASE_e6ddc20cd4e3666792197b85175c658d Pyrithiobac-sodium [M+H]+ 327.0201 0.91 166.06 COC1=CC(=NC(=N1)SC2=C(C(=CC=C2)Cl)C(=O)[O-])OC Benzenoids 1 1 TW polyala
CCSBASE_cc2683ad94e9911affb04e57d5808bb3 Pyrithiobac-sodium [M+H-H2O]+ 309.0096 0.9 159.05 COC1=CC(=NC(=N1)SC2=C(C(=CC=C2)Cl)C(=O)[O-])OC Benzenoids 1 1 TW polyala
CCSBASE_ff1bb0c6e7c8e8c9690fd326439c304d Pyrithiobac-sodium [M+Na]+ 349.002 0.9 172.44 COC1=CC(=NC(=N1)SC2=C(C(=CC=C2)Cl)C(=O)[O-])OC Benzenoids 1 1 TW polyala
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