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_216a74c04b573bc396de64902d6ba764 5,5-Diphenylhydantoin [M+H]+ 253.0972 0.84 159.3 C1=CC=C(C=C1)C2(C(=O)NC(=O)N2)C3=CC=CC=C3 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_19873f6327321e165e8a495ef8cf1eb0 5,5-Diphenylhydantoin [M-H]- 251.0826 0.78 161.36 C1=CC=C(C=C1)C2(C(=O)NC(=O)N2)C3=CC=CC=C3 Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_261724ec361868f3defb9cb85405f8b1 Spirodiclofen [M+H]+ 411.1125 1.02 189.14 CCC(C)(C)C(=O)OC1=C(C(=O)OC12CCCCC2)C3=C(C=C(C=C3)Cl)Cl Benzenoids 1 1 TW polyala
CCSBASE_d77f088cca00eb07bea4d047c09cb5c6 PharmaGSID_48516 [M+H]+ 340.0205 0.87 171.58 C1=CC=C(C=C1)C=CS(=O)(=O)NC(=O)C2=C(C=C(C=C2)F)Cl Benzenoids 1 1 TW polyala
CCSBASE_2c7e46d22cffdc77ac5e7ef787360ee0 PharmaGSID_48516 [M+Na]+ 362.0024 0.87 185.03 C1=CC=C(C=C1)C=CS(=O)(=O)NC(=O)C2=C(C=C(C=C2)F)Cl Benzenoids 1 1 TW polyala
CCSBASE_e280c844ed092cf9625e6f2c7cd3a6b6 PharmaGSID_48516 [M-H]- 338.0059 0.82 177.92 C1=CC=C(C=C1)C=CS(=O)(=O)NC(=O)C2=C(C=C(C=C2)F)Cl Benzenoids -1 1 TW polyala
CCSBASE_851b2feeac0d93440873a118cd6f86b4 Acetochlor [M+H]+ 270.1256 0.92 157.8 CCC1=CC=CC(=C1N(COCC)C(=O)CCl)C Benzenoids 1 1 TW polyala
CCSBASE_66cbfffe80f89efdf16582f4d17e6a58 Acetochlor [M+Na]+ 292.1075 0.94 169.6 CCC1=CC=CC(=C1N(COCC)C(=O)CCl)C Benzenoids 1 1 TW polyala
CCSBASE_488c203fe119f2de90a74d1cf7b8d393 AVE2865 [M+H]+ 456.0933 0.96 199.41 C1CN(CCC1C(=O)O)C2=C(C=C(C=C2)F)NC(=O)NC(=O)C3=CC(=C(C=C3Cl)F)F Benzenoids 1 1 TW polyala
CCSBASE_2ed7f7429f49eaa2f5aaa7798b120928 AVE2865 [M+Na]+ 478.0752 0.96 191.23 C1CN(CCC1C(=O)O)C2=C(C=C(C=C2)F)NC(=O)NC(=O)C3=CC(=C(C=C3Cl)F)F Benzenoids 1 1 TW polyala
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