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_502e037747a02d9b8d5e3b9e306edee5 N-Methylphthalimide [M+H]+ 162.055 0.77 127.51 CN1C(=O)C2=CC=CC=C2C1=O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_b7f48d5a8b40940019ba778f78d24746 Benzalkonium chloride C14 [M]+ 332.3312 0.91 203.46 CCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_e438df6fd2652f75bad0732a4068a947 Ampicillin [M-H]- 348.1023 0.74 182.89 CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)C Organic acids and derivatives -1 1 TW polyala
CCSBASE_745f390d1f3300399d681734cff41215 4-(Diethylamino)benzaldehyde [M+H]+ 178.1226 0.83 139.93 CCN(CC)C1=CC=C(C=C1)C=O Benzenoids 1 1 TW polyala
CCSBASE_79987e0662887cdf2a94332e78edfac1 2-Isopropylaniline [M+H]+ 136.1121 0.72 135.32 CC(C)C1=CC=CC=C1N Benzenoids 1 1 TW polyala
CCSBASE_0769994f0c7ffa0b49a65061bc05c3b2 Diketometribuzin [M+H]+ 185.1033 0.75 140.52 CC(C)(C)C1=NNC(=O)N(C1=O)N Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_58b8a35dd429cfc6e79b685ad0df1f75 Diketometribuzin [M-H]- 183.0887 0.75 143.06 CC(C)(C)C1=NNC(=O)N(C1=O)N Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_5630561475ab844c347aed4b8f5d23b3 4-Octanolide [M+FA-H]- 187.0976 0.76 144.04 CCCCC1CCC(=O)O1 Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_24eddd43750f5ae61b98ef3da5280c7b 4,5-Dichloro-2-octyl-3(2H)-isothiazolone [M+H]+ 282.0481 0.99 164.48 CCCCCCCCN1C(=O)C(=C(S1)Cl)Cl Organohalogen compounds 1 1 TW polyala
CCSBASE_bbb7a00ac046343a02f4cedf799183a2 4,5-Dichloro-2-octyl-3(2H)-isothiazolone [M+Na]+ 304.03 0.99 176.63 CCCCCCCCN1C(=O)C(=C(S1)Cl)Cl Organohalogen compounds 1 1 TW polyala
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