![4,4′,4′′-Tris[phenyl(m-tolyl)amino]triphenylamine molecular structure](/images/molecules/4-4-4--tris-phenyl-m-tolyl-amino-triphenylamine-124729-98-2.png)
Ordering
Available Variants1 g
CHA.53941-1g
Price
€66.48
Available – Dispatch in 14 days
5 g
CHA.53941-5g
Price
€260.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.53941-1g | €66.48 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.53941-5g | €260.00 |
98.0%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C57H48N4 |
|---|---|
| CAS Number | 124729-98-2 |
| Molecular Weight | 789.02 |
| NACRES | NA.23 |
| PubChem Substance ID | 329767830 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD00799401 |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
4,4′,4′′-Tris[phenyl(m-tolyl)amino]triphenylamine, with a CAS number of 124729-98-2, is a complex organic compound that exhibits notable properties. This material is characterized by its unique molecular structure, which consists of a triphenylamine core substituted with phenyl and m-tolyl groups. The presence of these substituents imparts the compound with distinct electronic and optical characteristics, making it suitable for various applications. Research has shown that this compound can be utilized in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices, where its ability to facilitate charge transport and emission is highly valued. Further studies are ongoing to explore the full potential of this compound and its derivatives in advancing the field of organic electronics. Its synthesis and properties have been the subject of scientific investigation, aiming to optimize its performance.
