Name:
Adduct:
Polarity:
Z:
m/z:
±:
CCS: Å
±: %
SMI:

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ID Name Adduct Structure m/z RT CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_46f2d972b8899bc590b8ed59523b3cdc Indole-3-acetic acid [M-H]- 174.056 0.77 145.16 C1=CC=C2C(=C1)C(=CN2)CC(=O)O Benzenoids -1 1 TW polyala
CCSBASE_cc82713b1d6780ee749c673d35caf310 Indole-3-acetic acid [M-H]- 174.056 0.77 137.53 C1=CC=C2C(=C1)C(=CN2)CC(=O)O Benzenoids -1 1 TW polyala
CCSBASE_f91caf0bd29d01725bdc01c545d917bb Tetradecylpyridinium bromide [M]+ 276.2686 0.88 186.79 CCCCCCCCCCCCCC[N+]1=CC=CC=C1 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_2988a691fa798bcc6b2f2b2c404d1732 4-Chlorophenol [M-H]- 126.9956 0.82 126.36 C1=CC(=CC=C1O)Cl None -1 1 TW polyala
CCSBASE_48c3fd1fba1b088816d01df542b21b10 CP-607366 [M+H]+ 300.0353 0.76 168.45 CNCC1=C(C=CC(=C1)F)OC2=CC(=C(C=C2)Cl)Cl   Benzenoids 1 1 TW polyala
CCSBASE_1d2a347071f2dcd2fd0c225ee4143ce2 2,4-Dihydroxybenzophenone [M+H]+ 215.0703 0.83 144.17 C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2)O)O  None 1 1 TW polyala
CCSBASE_88af04f7427523f3b1a15ec19f25f2e6 2,4-Dihydroxybenzophenone [M-H]- 213.0557 0.85 149.25 C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2)O)O None -1 1 TW polyala
CCSBASE_966058484d305181c7bd7d00d5f37766 4-Chloro-2-methylaniline [M+H]+ 142.0418 0.74 132.74 CC1=C(C=CC(=C1)Cl)N   None 1 1 TW polyala
CCSBASE_0c071dbeed183e65d759efc91dff6e8c Tridemorph [M+H]+ 298.3105 0.83 185.16 CCCCCCCCCCCCCN1CC(OC(C1)C)C Benzenoids 1 1 TW polyala
CCSBASE_4b46d5d11bd8bd7ca2e1cbd865d11384 Fenarimol [M+H]+ 331.04 0.88 172.89 C1=CC=C(C(=C1)C(C2=CC=C(C=C2)Cl)(C3=CN=CN=C3)O)Cl   Organoheterocyclic compounds 1 1 TW polyala
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