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_8e50fb735be32060dad070c598ccc536 Sulprofos [M+H]+ 323.0358 0.99 169.37 CCCSP(=S)(OCC)OC1=CC=C(C=C1)SC Benzenoids 1 1 TW polyala
CCSBASE_771a07653e0f2d7e712bf0bc7bf373d1 Tribufos [M+H]+ 315.1034 1.07 175.59 CCCCSP(=O)(SCCCC)SCCCC Organophosphorus compounds 1 1 TW polyala
CCSBASE_5b9dfa7538578ebf03f50319bdfd3a86 Tribufos [M+Na]+ 337.0854 1.08 190.89 CCCCSP(=O)(SCCCC)SCCCC Organophosphorus compounds 1 1 TW polyala
CCSBASE_e90c94b5be7843de553a8f0aad561090 4-Chloro-2-methylaniline hydrochloride [M+H]+ 142.0418 0.74 133.11 CC1=C(C=CC(=C1)Cl)N Benzenoids 1 1 TW polyala
CCSBASE_b6e4684d6787b19070b95b542a21056b 2,5,8,11,14-Pentaoxahexadecan-16-ol [M+H]+ 253.1646 0.69 151.56 COCCOCCOCCOCCOCCO Organic oxygen compounds 1 1 TW polyala
CCSBASE_91a50f045a2a6eb7ea507d31f32dc98a Formononetin [M+H]+ 269.0808 0.83 158.34 COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_b8cbf6872fabc076087325e6c7f070ea Formononetin [M+Na]+ 291.0628 0.82 168.55 COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_e7dbae38ddc4a6eda709a01be3229884 (Phenylphosphoryl)bis[(2,4,6-trimethylphenyl)methanone] [M+H]+ 419.1771 0.96 194.34 CC1=CC(=C(C(=C1)C)C(=O)P(=O)(C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3C)C)C)C Benzenoids 1 1 TW polyala
CCSBASE_523d40501c67cea4e4a133ee7b86d421 Dodecane-1-sulfonyl chloride [M+H-H2O]+ 251.1232 0.74 153.65 CCCCCCCCCCCCS(=O)(=O)Cl Organohalogen compounds 1 1 TW polyala
CCSBASE_2f8b398d682800659be38e9317e874c4 Dodecane-1-sulfonyl chloride [M+Na]+ 291.1156 0.74 162.12 CCCCCCCCCCCCS(=O)(=O)Cl Organohalogen compounds 1 1 TW polyala
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