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_d73a0e77a8ab260bd6a7b6cc094968dd Monocrotaline [M+H]+ 326.1598 0.7 172.12 CC1C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C1(C)O)(C)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_90da148a6215eb89157422fb694cad9e Cetylpyridinium chloride [M]+ 304.2999 0.96 196.99 CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_4b22c5acd1adabc1343f4bbbab74605b 4'-(Chloroacetyl)acetanilide [M-H]- 210.0327 0.75 146.78 CC(=O)NC1=CC=C(C=C1)C(=O)CCl Organic oxygen compounds -1 1 TW polyala
CCSBASE_eb601599b530d3d0c20a614b43a06b06 4-(Diglycidylamino)phenyl glycidyl ether [M+H]+ 278.1387 0.79 166.59 C1C(O1)CN(CC2CO2)C3=CC=C(C=C3)OCC4CO4 Benzenoids 1 1 TW polyala
CCSBASE_711e32f42a55bc033f68698bf4e59141 4-(Diglycidylamino)phenyl glycidyl ether [M+H-H2O]+ 260.1282 0.78 161.47 C1C(O1)CN(CC2CO2)C3=CC=C(C=C3)OCC4CO4 Benzenoids 1 1 TW polyala
CCSBASE_005f6b5ac21b9ea6a66710a41b472354 Alachlor sec-oxanilic acid sodium salt [M-H]- 220.0979 0.81 157.01 CCC1=C(C(=CC=C1)CC)NC(=O)C(=O)[O-] Organic acids and derivatives -1 1 TW polyala
CCSBASE_7587a1a16354d3ae7a407d5144a6e005 Citronellyl propionate [M-H-H2O]- 193.1592 0.88 152.36 CCC(=O)OCCC(C)CCC=C(C)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_842e947307b9e8a3a16a0ffafd3dc9cb 2-Amino-5-nitrophenol [M-H]- 153.0306 0.72 129.56 C1=CC(=C(C=C1[N+](=O)[O-])O)N Benzenoids -1 1 TW polyala
CCSBASE_6ca8ece7dfb140b2670c5f7286d3791c 4-Hydroxybenzonitrile [M-H]- 118.0298 0.74 127.97 C1=CC(=CC=C1C#N)O Benzenoids -1 1 TW polyala
CCSBASE_e23c5bbec4d363efb7705f75ea9fe00d Benzethonium chloride [M]+ 412.321 0.89 209.11 CC(C)(C)CC(C)(C)C1=CC=C(C=C1)OCCOCC[N+](C)(C)CC2=CC=CC=C2 Benzenoids 1 1 TW polyala
1 2 ... 112 113 114 115 116 117 118 ... 359 360