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_e2e85737ec4527ed81e1c3b06b389fae Diphenyl isophthalate [M+H]+ 319.0965 1.02 179.61 C1=CC=C(C=C1)OC(=O)C2=CC(=CC=C2)C(=O)OC3=CC=CC=C3 Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_67c222702e676f62f822bdd66c686dd3 Diphenyl isophthalate [M+Na]+ 341.0784 1.02 192.9 C1=CC=C(C=C1)OC(=O)C2=CC(=CC=C2)C(=O)OC3=CC=CC=C3 Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_d6aec40b4b12428e2a884349681f33ac Diphenyl phthalate [M+Na]+ 341.0784 0.97 179.22 C1=CC=C(C=C1)OC(=O)C2=CC=CC=C2C(=O)OC3=CC=CC=C3   Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_4753d78a3bd0648fd7996461b1cd9fcc Disulfiram [M+Na]+ 319.0402 0.93 169.68 CCN(CC)C(=S)SSC(=S)N(CC)CC   Organic nitrogen compounds 1 1 TW polyala
CCSBASE_d8803b61cfd4b587e15eb97c8b502c8c Dithiopyr [M+H]+ 402.0615 1.0 176.81 CC(C)CC1=C(C(=NC(=C1C(=O)SC)C(F)(F)F)C(F)F)C(=O)SC   Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_1b5b07954970702b889ff8dcd6c005e7 Dithiopyr [M+H-H2O]+ 384.051 1.0 175.24 CC(C)CC1=C(C(=NC(=C1C(=O)SC)C(F)(F)F)C(F)F)C(=O)SC  Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_acf893a93602b8e3bf8ddecb2755a788 dl-Menthol [M+FA-H]- 201.1496 0.87 155.73 CC1CCC(C(C1)O)C(C)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_d926bca057a51e351ca38712a6d0a4b2 Dodecanedioic acid [M+Na]+ 253.141 0.89 159.62 C(CCCCCC(=O)O)CCCCC(=O)O  Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_aec224bcfdbf0b5d36b7079cc8d56b2f Dodecanedioic acid [M-H]- 229.1445 0.84 155.91 C(CCCCCC(=O)O)CCCCC(=O)O Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_c2472055ff7f702898c11a8fde24ce2b Dodecanedioic acid [M-H-H2O]- 211.1334 0.84 157.24 C(CCCCCC(=O)O)CCCCC(=O)O Lipids and lipid-like molecules -1 1 TW polyala
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