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_2a09f8b26b1336179c0d37d59a9db967 Tetrabromobisphenol A bis(2-hydroxyethyl) ether [M+Na]+ 654.7946 0.98 198.63 CC(C)(C1=CC(=C(C(=C1)Br)OCCO)Br)C2=CC(=C(C(=C2)Br)OCCO)Br   Benzenoids 1 1 TW polyala
CCSBASE_eb02658fa920d235b9d3c247518881f5 Tetradonium bromide [M]+ 256.2999 0.91 187.13 CCCCCCCCCCCCCC[N+](C)(C)C Organic nitrogen compounds 1 1 TW polyala
CCSBASE_dee5424fd13d235912d914b6b2f1cb86 Thiamine thiozole [M+H]+ 144.0478 0.71 125.34 CC1=C(SC=N1)CCO Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_661e219eace31f2fbbcf3d272b35b7f7 Thiofanox [M+Na]+ 241.0981 0.85 158.08 CC(C)(C)C(=NOC(=O)NC)CSC   Organic acids and derivatives 1 1 TW polyala
CCSBASE_605a9bce61bfe8a2a99286b84c2d7f6d Todralazine hydrochloride [M+H]+ 233.1033 0.74 150.48 CCOC(=O)NNC1=NN=CC2=CC=CC=C21 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_4e172e35f944de3e796e3440c5c1f893 Todralazine hydrochloride [M+Na]+ 255.0852 0.73 157.97 CCOC(=O)NNC1=NN=CC2=CC=CC=C21 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_fb3811e481c4de408bf56842b7cf4847 Tolazamide [M+H]+ 312.1376 0.86 173.35 CC1=CC=C(C=C1)S(=O)(=O)NC(=O)NN2CCCCCC2 Benzenoids 1 1 TW polyala
CCSBASE_7afe2c53bfe20fec78cf1d21ddd0c0fa Tolazamide [M+K]+ 350.0935 0.86 199.47 CC1=CC=C(C=C1)S(=O)(=O)NC(=O)NN2CCCCCC2 Benzenoids 1 1 TW polyala
CCSBASE_4377d7e3c9c0b2bc7dead2bb4628dee5 Tolazamide [M+K]+ 350.0935 0.86 180.11 CC1=CC=C(C=C1)S(=O)(=O)NC(=O)NN2CCCCCC2 Benzenoids 1 1 TW polyala
CCSBASE_834fc3c4aa7398692a1f6fb58c71a8d4 Tolazamide [M+Na]+ 334.1196 0.86 181.0 CC1=CC=C(C=C1)S(=O)(=O)NC(=O)NN2CCCCCC2 Benzenoids 1 1 TW polyala
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