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_fc6ab222c03d0bec7d6b8f84e0f2ca31 Nitralin [M-H]- 344.0922 0.78 177.24 CCCN(CCC)C1=C(C=C(C=C1[N+](=O)[O-])S(=O)(=O)C)[N+](=O)[O-] Benzenoids -1 1 TW polyala
CCSBASE_6e8003a137b2a1d46eab98775c0bb086 Ximelagatran [M-H]- 472.2565 0.69 218.35 CCOC(=O)CNC(C1CCCCC1)C(=O)N2CCC2C(=O)NCC3=CC=C(C=C3)C(=NO)N Organic acids and derivatives -1 1 TW polyala
CCSBASE_224134cc23da353e45d2667a007d4dd1 Metolachlor OA [M-H]- 278.1398 0.87 168.99 CCC1=CC=CC(=C1N(C(C)COC)C(=O)C(=O)O)C Organic acids and derivatives -1 1 TW polyala
CCSBASE_11f74bfae3f8990190586d8a4b3d59f6 4-Chlorobenzenesulphonamide [M-H]- 189.9735 0.74 139.36 C1=CC(=CC=C1S(=O)(=O)N)Cl Benzenoids -1 1 TW polyala
CCSBASE_1d0589c7a929899b38488a82d9d8c379 C.I. Acid Orange 8, monosodium salt [M-H]- 341.0601 0.97 185.64 CC1=C(C=CC(=C1)S(=O)(=O)[O-])N=NC2=C(C=CC3=CC=CC=C32)O Benzenoids -1 1 TW polyala
CCSBASE_b567f7dfa60d3176e55c3480dc62d5d4 Propylparaben [M-H]- 179.0713 0.81 145.75 CCCOC(=O)C1=CC=C(C=C1)O Benzenoids -1 1 TW polyala
CCSBASE_fcd5c5e7c99ceca8810943373ffd7527 Imidacloprid [M-H]- 254.045 0.73 158.39 C1CN(C(=N[N+](=O)[O-])N1)CC2=CN=C(C=C2)Cl Organic nitrogen compounds -1 1 TW polyala
CCSBASE_48e1fbade7838597b06764ca7bd1e00a Tetrahydrofurfuryl acrylate [M-H]- 155.0713 0.77 137.96 C=CC(=O)OCC1CCCO1 Organic acids and derivatives -1 1 TW polyala
CCSBASE_db6f3903ee3aae2745667ca9fee25e52 PharmaGSID_48514 [M]- 365.0415 0.85 190.71 CC1=CC(=C(C=C1)C(=O)NS(=O)(=O)C=CC2=CC=C(C=C2)OC)Cl Benzenoids -1 1 TW polyala
CCSBASE_9f1f1fb2dcd554817df48c36a45577b3 Oleyl sarcosine [M-H]- 352.2857 1.12 196.52 CCCCCCCCC=CCCCCCCCC(=O)N(C)CC(=O)O Organic acids and derivatives -1 1 TW polyala
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