| Identification | Back Directory | [Name]
2,4,6-TRIPHENYLANILINE | [CAS]
6864-20-6 | [Synonyms]
2,4,6-TRIPHENYLANILINE
2,4,6-Triphenylaniline b
2,4,6-Triphenylaniline 97%
5'-Phenyl-[1,1':3',1''-terphenyl]-2'-amine
5'-Phenyl-[1,1':3',1''-terphenyl]-2'-amine
[1,1':3',1''-Terphenyl]-2'-amine, 5'-phenyl- | [Molecular Formula]
C24H19N | [MDL Number]
MFCD00012371 | [MOL File]
6864-20-6.mol | [Molecular Weight]
321.41 |
| Chemical Properties | Back Directory | [Melting point ]
122-125 °C(lit.)
| [Boiling point ]
465.4±14.0 °C(Predicted) | [density ]
1.117±0.06 g/cm3(Predicted) | [form ]
powder | [pka]
2.69±0.10(Predicted) | [color ]
White to yellow | [InChI]
1S/C24H19N/c25-24-22(19-12-6-2-7-13-19)16-21(18-10-4-1-5-11-18)17-23(24)20-14-8-3-9-15-20/h1-17H,25H2 | [InChIKey]
AGWKGKUGJDMKMT-UHFFFAOYSA-N | [SMILES]
Nc1c(cc(cc1-c2ccccc2)-c3ccccc3)-c4ccccc4 |
| Hazard Information | Back Directory | [Uses]
2,4,6-Triphenylaniline has anti-diabetic activity and can be encapsulated in nano-emulsions (NE) to enhance stability and permeability. The NE loaded with 2,4,6-Triphenylaniline inhibits α-glucosidase and α-amylase[1]. | [General Description]
2,4,6-Triphenylaniline was oxidized to azo(2,4,6-triphenylbenzene) in acetonitrile containing pyridine. | [IC 50]
α-glucosidase; α-amylase | [References]
[1] Nathiya Ranganathan, et al. 2,4,6-Triphenylaniline nanoemulsion formulation, optimization, and its application in type 2 diabetes mellitus. J Cell Physiol. 2019 Dec;234(12):22505-22516. DOI:10.1002/jcp.28814 |
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