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_50a21849fa57aed57d9de4c682041e4f Cloransulam-methyl [M-H]- 428.0237 0.78 189.33 CCOC1=NC(=CC2=NC(=NN21)S(=O)(=O)NC3=C(C=CC=C3Cl)C(=O)OC)F Benzenoids -1 1 TW polyala
CCSBASE_5058c383c89fec8c79748950d094d5e3 Bromadiolone [M+H-H2O]+ 509.0747 0.97 218.95 C1=CC=C(C=C1)C(CC(C2=CC=C(C=C2)C3=CC=C(C=C3)Br)O)C4=C(C5=CC=CC=C5OC4=O)O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_6b05f61401231787a16a5bf0f99c8a70 Bromadiolone [M+K]+ 565.0411 0.96 229.5 C1=CC=C(C=C1)C(CC(C2=CC=C(C=C2)C3=CC=C(C=C3)Br)O)C4=C(C5=CC=CC=C5OC4=O)O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_d871b70208693b633a81a609ef9bf6ec Bromadiolone [M+Na]+ 549.0672 0.97 233.39 C1=CC=C(C=C1)C(CC(C2=CC=C(C=C2)C3=CC=C(C=C3)Br)O)C4=C(C5=CC=CC=C5OC4=O)O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_26290ff129dbbe48cb75f863b49ff74e Dihexylamine [M+H]+ 186.2216 0.76 158.09 CCCCCCNCCCCCC Organic nitrogen compounds 1 1 TW polyala
CCSBASE_7d4fc3e6d3e8c121e0dcccb799a80ad1 Acetoacetanilide [M+H-H2O]+ 160.0758 0.76 133.21 CC(=O)CC(=O)NC1=CC=CC=C1 Benzenoids 1 1 TW polyala
CCSBASE_ce684dec0b46d1fc6ed347c07a9670fa Acetoacetanilide [M-H]- 176.0717 0.79 140.69 CC(=O)CC(=O)NC1=CC=CC=C1 Benzenoids -1 1 TW polyala
CCSBASE_cba20dfebaad155b5b64929289c9a723 Tetraethyleneglycol dimethacrylate [M+K]+ 369.131 0.84 181.14 CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(=C)C Organic acids and derivatives 1 1 TW polyala
CCSBASE_73f774f913b5cb3b9e9e79e2d3eb2a3d Tetraethyleneglycol dimethacrylate [M+Na]+ 353.1571 0.83 176.28 CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(=C)C Organic acids and derivatives 1 1 TW polyala
CCSBASE_63fe6e63abfbeb1ffc95fab818a0e4ab 4-Hexylresorcinol [M-H]- 193.1234 0.85 153.32 CCCCCCC1=C(C=C(C=C1)O)O Benzenoids -1 1 TW polyala
1 2 ... 287 288 289 290 291 292 293 ... 359 360