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_96eef3c278e437e1f440026bd7628c47 Bis[2-(2-butoxyethoxy)ethyl] adipate [M-H]- 433.2807 1.0 206.89 CCCCOCCOCCOC(=O)CCCCC(=O)OCCOCCOCCCC Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_bcf0e4a5a1546ccaa4722e26b1d0b176 Apomorphine hydrochloride hydrate [M-H]- 266.1187 0.7 162.96 CN1CCC2=C3C1CC4=C(C3=CC=C2)C(=C(C=C4)O)O Alkaloids and derivatives -1 1 TW polyala
CCSBASE_8dd56da1373294fa5776fd94673036a3 sec-Butylparaben [M-H]- 193.087 0.85 149.85 CCC(C)OC(=O)C1=CC=C(C=C1)O Benzenoids -1 1 TW polyala
CCSBASE_af01872bef02d4fd37c9b889ba8e93e7 CP-671305 [M-H]- 453.1104 0.82 201.57 CC(C(=O)O)OC1=CC(=C(C=C1)CNC(=O)C2=C(N=CC=C2)OC3=CC4=C(C=C3)OCO4)F Benzenoids -1 1 TW polyala
CCSBASE_469803548ecf0eefbe493608a1733693 Hydroxycitronellal [M-H]- 171.1391 0.97 146.79 CC(CCCC(C)(C)O)CC=O Organic oxygen compounds -1 1 TW polyala
CCSBASE_f3931346121469e35cce804922e128b6 alpha-Hexyl-gamma-butyrolactone [M-H]- 169.1234 0.82 149.78 CCCCCCC1CCOC1=O Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_f17b04c339ed6f25167b8f607f6b970d Benfuracarb [M-H]- 409.1803 0.8 192.61 CCOC(=O)CCN(C(C)C)SN(C)C(=O)OC1=CC=CC2=C1OC(C2)(C)C Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_98e450ff71ccfb9d0af52964ff30a0c1 2,4,4'-Trihydroxybenzophenone [M-H]- 229.0506 0.78 153.94 C1=CC(=CC=C1C(=O)C2=C(C=C(C=C2)O)O)O Benzenoids -1 1 TW polyala
CCSBASE_b8a5462ab8cf01e2cc19ea58252c102d (-)-Epigallocatechin gallate [M-H]- 457.0777 0.71 199.24 C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O Phenylpropanoids and polyketides -1 1 TW polyala
CCSBASE_e105d98e3c640f0ca8c73576e0d8886e 2,4-Hexadienyl isobutyrate [M-H]- 167.1078 0.77 145.61 CC=CC=CCOC(=O)C(C)C Organic acids and derivatives -1 1 TW polyala
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