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_cb87e7463c3426c41ca3f611043a53fd Nalidixic acid [M+H]+ 233.0921 0.88 145.87 CCN1C=C(C(=O)C2=C1N=C(C=C2)C)C(=O)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_009d8fc29f90560028e6b8d478347fde Nalidixic acid [M+H-H2O]+ 215.0816 0.88 143.49 CCN1C=C(C(=O)C2=C1N=C(C=C2)C)C(=O)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_cc4af1b981944bcc2c3de07c41b9c8bf Nalidixic acid [M+Na]+ 255.074 0.87 159.15 CCN1C=C(C(=O)C2=C1N=C(C=C2)C)C(=O)O Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_caca03d0cc7eba5f32eae58f7892cf51 Benzylhexadecyldimethylammonium chloride [M]+ 360.3625 1.02 213.74 CCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 Benzenoids 1 1 TW polyala
CCSBASE_3892b28945036455a82cc821f3f0acbe Allyl isovalerate [M+FA-H]- 187.0976 0.76 143.94 CC(C)CC(=O)OCC=C Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_cb8721837408569544887864853d0e6e 1,2,4-Benzenetricarboxylic acid [M+H-H2O]+ 193.0132 0.77 133.36 C1=CC(=C(C=C1C(=O)O)C(=O)O)C(=O)O Organic acids and derivatives 1 1 TW polyala
CCSBASE_7c4d3995228413d9934c4e747390e668 1,2,4-Benzenetricarboxylic acid [M-H]- 209.0091 0.72 140.0 C1=CC(=C(C=C1C(=O)O)C(=O)O)C(=O)O Organic acids and derivatives -1 1 TW polyala
CCSBASE_6ffdb18806de64e0691deb027a661282 1,2,4-Benzenetricarboxylic acid [M-H-H2O]- 190.998 0.73 137.12 C1=CC(=C(C=C1C(=O)O)C(=O)O)C(=O)O Organic acids and derivatives -1 1 TW polyala
CCSBASE_6be3f3ee1091b8f0eafae7a34e976a5a BisOPP-A [M-H]- 379.1703 0.95 204.03 CC(C)(C1=CC(=C(C=C1)O)C2=CC=CC=C2)C3=CC(=C(C=C3)O)C4=CC=CC=C4 Phenylpropanoids and polyketides -1 1 TW polyala
CCSBASE_6a3f7fcbaac1757cf066b91a2aeeb614 7-Methoxy-3,7-dimethyloctanal [M+Na]+ 209.1512 0.97 153.2 CC(CCCC(C)(C)OC)CC=O Organic oxygen compounds 1 1 TW polyala
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