Catalog Number | ACM217594-3 |
CAS Number | 217-59-4 |
Structure | ![]() |
Synonyms | 9,10-Benzophenanthrene |
IUPAC Name | Triphenylene |
Molecular Weight | 228.3 |
Molecular Formula | C18H12 |
Canonical SMILES | C1=CC=C2C(=C1)C3=CC=CC=C3C4=CC=CC=C24 |
InChI | InChI=1S/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H |
InChI Key | SLGBZMMZGDRARJ-UHFFFAOYSA-N |
Boiling Point | 438 ºC |
Melting Point | 195-198 ºC |
Purity | 99%+ |
Density | 1.302 g/ml |
Solubility | 1.80e-07 M |
Appearance | White to beige crystalline |
Application | Triphenylene is a versatile polycyclic aromatic hydrocarbon characterized by its white to beige crystalline needle-like appearance. It serves multiple purposes across various fields due to its unique properties. Primarily, triphenylene is instrumental in the development of semiconductor devices, owing to its ability to emit fluorescence in the ultraviolet region. As an ortho-fused polycyclic arene, consisting of four linked benzene rings, it acts as a fundamental building block for synthesizing macromolecular compounds with extensive conjugated structures. This makes it invaluable in the research of organic supramolecular materials, where it is used to explore advanced optics and electronics applications. Furthermore, triphenylene functions as a discotic mesogen in liquid crystalline materials, and plays a role in the creation of specific compounds such as triphenylene-2-carbaldehyde, showcasing its adaptability and significance in scientific research and industrial applications. |
Storage | room temp |
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