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_1e40dccaad52188a0c8ab820193a28d2 C.I. Solvent Orange 7 [M-H-H2O]- 257.1079 0.74 158.08 CC1=CC(=C(C=C1)N=NC2=C(C=CC3=CC=CC=C32)O)C Benzenoids -1 1 TW polyala
CCSBASE_af97a4b576b8aee86743790ef4670def Formetanate hydrochloride [M+H]+ 222.1237 0.73 154.76 CNC(=O)OC1=CC=CC(=C1)N=CN(C)C Benzenoids 1 1 TW polyala
CCSBASE_e544089f76cc2c6b2e98f543578a5513 Atrazine [M+H]+ 216.101 0.87 150.02 CCNC1=NC(=NC(=N1)Cl)NC(C)C Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_7d3688a740e3e30569f69155a3eb573b Coumatetralyl [M+H]+ 293.1172 0.93 164.29 C1CC(C2=CC=CC=C2C1)C3=C(C4=CC=CC=C4OC3=O)O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_fb0bf51cf3355b7cb0e79a7eeb16d435 Coumatetralyl [M+Na]+ 315.0992 0.93 171.28 C1CC(C2=CC=CC=C2C1)C3=C(C4=CC=CC=C4OC3=O)O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_96cc180bbe7bad1d8bd1f66784e22099 Coumatetralyl [M-H]- 291.1026 0.9 169.19 C1CC(C2=CC=CC=C2C1)C3=C(C4=CC=CC=C4OC3=O)O Phenylpropanoids and polyketides -1 1 TW polyala
CCSBASE_0a5e15c602a1e769c34cab5501726770 Oxamyl [M+Na]+ 242.057 0.71 149.31 CNC(=O)O/N=C(/C(=O)N(C)C)\SC Organic acids and derivatives 1 1 TW polyala
CCSBASE_a3f32130e45b36ad7a06fe6d7a621b74 Fluoxastrobin [M+H]+ 459.0866 0.91 202.5 CO/N=C(\C1=CC=CC=C1OC2=C(C(=NC=N2)OC3=CC=CC=C3Cl)F)/C4=NOCCO4 Organic oxygen compounds 1 1 TW polyala
CCSBASE_268fe3312eb51c7ece60cb2d7593c9a9 Fluoxastrobin [M+Na]+ 481.0685 0.91 206.49 CO/N=C(\C1=CC=CC=C1OC2=C(C(=NC=N2)OC3=CC=CC=C3Cl)F)/C4=NOCCO4 Organic oxygen compounds 1 1 TW polyala
CCSBASE_3b49c2272bcc00667cfd0a79ac0d0dd2 Besonprodil [M+H]+ 403.1486 0.76 199.19 C1CN(CCC1CC2=CC=C(C=C2)F)CCS(=O)C3=CC4=C(C=C3)NC(=O)O4 Organoheterocyclic compounds 1 1 TW polyala
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