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_7926cec3f0b00fbd848e8ae0633faae7 Tolazamide [M-H]- 310.1231 0.81 178.86 CC1=CC=C(C=C1)S(=O)(=O)NC(=O)NN2CCCCCC2 Benzenoids -1 1 TW polyala
CCSBASE_136849d050d5889843ff497c4e9975ad trans,trans-Farnesyl acetate [M+FA-H]- 309.2071 0.89 176.88 CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_a1ecb25781fc954de5c19337964a9a5d Tri-allate [M+H]+ 304.0091 1.07 160.72 CC(C)N(C(C)C)C(=O)SCC(=C(Cl)Cl)Cl  Organosulfur compounds 1 1 TW polyala
CCSBASE_cf02f0f0d137b7286ebd511a604109d3 Triamcinolone acetonide [M+FA-H]- 479.2087 0.83 206.43 CC1(OC2CC3C4CCC5=CC(=O)C=CC5(C4(C(CC3(C2(O1)C(=O)CO)C)O)F)C)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_ffcaeda00c91c0fcf5c04e73b1258cfa Triamcinolone acetonide [M+H]+ 435.2177 0.88 196.99 C[C@]12C[C@@H]([C@]3([C@H]([C@@H]1C[C@@H]4[C@]2(OC(O4)(C)C)C(=O)CO)CCC5=CC(=O)C=C[C@@]53C)F)O Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_0a36c51ac1eea2b557a6f02091a3cb01 Triamcinolone acetonide [M+Na]+ 457.1997 0.88 221.11 C[C@]12C[C@@H]([C@]3([C@H]([C@@H]1C[C@@H]4[C@]2(OC(O4)(C)C)C(=O)CO)CCC5=CC(=O)C=C[C@@]53C)F)O Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_3db46ab4711f9414530b2df797a29081 Triamcinolone acetonide [M-H-H2O]- 415.1921 0.83 197.99 CC1(OC2CC3C4CCC5=CC(=O)C=CC5(C4(C(CC3(C2(O1)C(=O)CO)C)O)F)C)C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_e15b59fb5e74fcd537fe7c9a83428f3a Trichlorfon [M+H]+ 256.9299 0.74 137.38 COP(=O)(C(C(Cl)(Cl)Cl)O)OC   Organic acids and derivatives 1 1 TW polyala
CCSBASE_c1de3ded5f627121c2c23caf18ff9f94 Triethylene glycol diacetate [M+Na]+ 257.0996 0.78 151.58 CC(=O)OCCOCCOCCOC(=O)C Organic acids and derivatives 1 1 TW polyala
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