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_1fc75f3f3d5ddb0ee6e26dc30bf25d62 Fluorosalan [M+H]+ 439.8926 1.03 175.77 C1=CC(=CC(=C1)NC(=O)C2=C(C(=CC(=C2)Br)Br)O)C(F)(F)F Benzenoids 1 1 TW polyala
CCSBASE_640ec7815720ad98743099a34a3f2807 Fluorosalan [M-H]- 437.878 1.01 175.67 C1=CC(=CC(=C1)NC(=O)C2=C(C(=CC(=C2)Br)Br)O)C(F)(F)F Benzenoids -1 1 TW polyala
CCSBASE_da688d25e2c60c6e341e629c937e0d4c Phenylphosphonic acid [M+H]+ 159.0206 0.36 130.88 C1=CC=C(C=C1)P(=O)(O)O Benzenoids 1 1 TW polyala
CCSBASE_599be18400a8c35ca3f2979d7328386a Phenylphosphonic acid [M-H]- 157.006 0.35 133.84 C1=CC=C(C=C1)P(=O)(O)O Benzenoids -1 1 TW polyala
CCSBASE_67f07b7a460c9b48e31f496cb81a6340 Ethylphenylacetylurea [M+K]+ 245.0687 0.79 158.19 CCC(C1=CC=CC=C1)C(=O)NC(=O)N Benzenoids 1 1 TW polyala
CCSBASE_6c10bf7218140b849ce285644281c577 Ethylphenylacetylurea [M+Na]+ 229.0947 0.79 155.45 CCC(C1=CC=CC=C1)C(=O)NC(=O)N Benzenoids 1 1 TW polyala
CCSBASE_cc609106d7992b3d8943dd9a85b8f97c 2-Amino-5-nitrobenzonitrile [M-H]- 162.0309 0.76 129.68 C1=CC(=C(C=C1[N+](=O)[O-])C#N)N Benzenoids -1 1 TW polyala
CCSBASE_fb5f5b043e2871b77ef587539a9c6b89 N-(3,4-Dichlorophenyl)-N'-methylurea [M+H]+ 219.0086 0.81 145.02 CNC(=O)NC1=CC(=C(C=C1)Cl)Cl Benzenoids 1 1 TW polyala
CCSBASE_ebc5770825b651cd584786c3951661d8 N-(3,4-Dichlorophenyl)-N'-methylurea [M-H]- 216.9941 0.8 144.54 CNC(=O)NC1=CC(=C(C=C1)Cl)Cl Benzenoids -1 1 TW polyala
CCSBASE_232689083e5b55e596288b57a72544c6 1,4-Butanediol diacrylate [M+FA-H]- 243.0874 0.73 155.4 C=CC(=O)OCCCCOC(=O)C=C Organic acids and derivatives -1 1 TW polyala
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