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_00250ed526b0d5e801d3ec5bd44ab043 3-Hydroxyfluorene [M-H]- 181.0659 0.73 143.61 C1C2=C(C=C(C=C2)O)C3=CC=CC=C31 Benzenoids -1 1 TW polyala
CCSBASE_0f669c1be62db29755bcf47482562e09 4-Aminobenzoic acid [M+H]+ 138.055 0.73 133.72 C1=CC(=CC=C1C(=O)O)N Benzenoids 1 1 TW polyala
CCSBASE_c46bc4ec7a1a88643840eaa1af2da2e6 Methomyl [M+H]+ 163.0536 1.02 123.57 CC(=NOC(=O)NC)SC Organic acids and derivatives 1 1 TW polyala
CCSBASE_638ba9add769906fceb3b206d15c8ea3 DEET [M+H]+ 192.1383 0.89 144.48 CCN(CC)C(=O)C1=CC=CC(=C1)C Benzenoids 1 1 TW polyala
CCSBASE_e558a06da9a99fb6b80ae5d72dd097ec Triclosan [M-H]- 286.9439 0.95 160.17 C1=CC(=C(C=C1Cl)O)OC2=C(C=C(C=C2)Cl)Cl Benzenoids -1 1 TW polyala
CCSBASE_9ed4cdb3c8e2b73eb37b9fdd1c41d4b5 2-(Phenylmethylene)octanal [M+H]+ 217.1587 0.87 152.02 CCCCCC/C(=C\C1=CC=CC=C1)/C=O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_d1bed0ee2c3065412b90bbd8688e30d2 4-Hydroxytamoxifen [M+H]+ 388.2271 0.84 203.38 CCC(=C(C1=CC=C(C=C1)O)C2=CC=C(C=C2)OCCN(C)C)C3=CC=CC=C3 Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_48d3e5136fcada4c3ec43d7e40220a5b PharmaGSID_48172 [M+H]+ 437.1642 0.78 210.75 C1CCCN(CC1)CC2=CC=C(S2)C3=NC(=NO3)CCN4C(=O)C5=CC=CC=C5C4=O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_08a88381fc6f33c0e8809ae98ff2db12 PharmaGSID_48172 [M+Na]+ 459.1461 0.78 212.63 C1CCCN(CC1)CC2=CC=C(S2)C3=NC(=NO3)CCN4C(=O)C5=CC=CC=C5C4=O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_999b5840ae59fa927f3a9885a7941f55 Didecyldimethylammonium chloride [M]+ 326.3781 0.96 210.57 CCCCCCCCCC[N+](C)(C)CCCCCCCCCC Organic nitrogen compounds 1 1 TW polyala
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