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_d0eac3d57486e16c82fc6039a6545689 Fenchlorazole-ethyl [M+Na]+ 425.8922 0.98 189.47 CCOC(=O)C1=NN(C(=N1)C(Cl)(Cl)Cl)C2=C(C=C(C=C2)Cl)Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_98e6d779ece5eaaff2f7b5d2566731be 2-(Diethylamino)ethyl acrylate [M+H]+ 172.1332 0.71 134.69 CCN(CC)CCOC(=O)C=C Organic acids and derivatives 1 1 TW polyala
CCSBASE_7b69c933673106ba4530a12021e86646 2-(Diethylamino)ethyl acrylate [M+Na]+ 194.1151 0.71 144.26 CCN(CC)CCOC(=O)C=C Organic acids and derivatives 1 1 TW polyala
CCSBASE_aa2c230557faa717aba7e91adf1b0632 C.I. Acid Orange 3 [M+H]+ 431.0656 0.97 198.84 C1=CC=C(C=C1)NC2=C(C=C(C=C2)NC3=C(C=C(C=C3)[N+](=O)[O-])[N+](=O)[O-])S(=O)(=O)[O-] Benzenoids 1 1 TW polyala
CCSBASE_74fbc8a6b195aee6dfa6e0c72bdb1b6d C.I. Acid Orange 3 [M+H-H2O]+ 413.0551 0.97 192.45 C1=CC=C(C=C1)NC2=C(C=C(C=C2)NC3=C(C=C(C=C3)[N+](=O)[O-])[N+](=O)[O-])S(=O)(=O)[O-] Benzenoids 1 1 TW polyala
CCSBASE_4672e3f5a8dca563a8be6bbc926069fd C.I. Acid Orange 3 [M+K]+ 469.0215 0.98 213.03 C1=CC=C(C=C1)NC2=C(C=C(C=C2)NC3=C(C=C(C=C3)[N+](=O)[O-])[N+](=O)[O-])S(=O)(=O)[O-] Benzenoids 1 1 TW polyala
CCSBASE_3a902954230e081c448c65e4b3d9fed5 C.I. Acid Orange 3 [M+Na]+ 453.0475 0.97 201.8 C1=CC=C(C=C1)NC2=C(C=C(C=C2)NC3=C(C=C(C=C3)[N+](=O)[O-])[N+](=O)[O-])S(=O)(=O)[O-] Benzenoids 1 1 TW polyala
CCSBASE_efd4480ecc67d1d7cd9fd5db438570d0 C.I. Acid Orange 3 [M-H-H2O]- 411.0399 0.98 191.59 C1=CC=C(C=C1)NC2=C(C=C(C=C2)NC3=C(C=C(C=C3)[N+](=O)[O-])[N+](=O)[O-])S(=O)(=O)[O-] Benzenoids -1 1 TW polyala
CCSBASE_9b65e1e066b5fb8beedae69fda00aa68 12-Oxahexadecanolide [M+Na]+ 279.1931 1.07 162.77 C1CCCCCOCCCCOC(=O)CCCC1 Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_da524a67967d7994e70e9d42582a4d47 2-Heptylcyclopentanone [M+FA-H]- 227.1653 0.86 159.93 CCCCCCCC1CCCC1=O Organic oxygen compounds -1 1 TW polyala
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