217-59-4
217-59-4
Chemical Structure
Triphenylene
- CAS No.: 217-59-4
- Formula:C18H12
- Molecular Weight:228.29
IUPAC Name: triphenylene
InChIKey: SLGBZMMZGDRARJ-UHFFFAOYSA-N
SMILES: C=1C=CC=2C(C1)=C3C=CC=CC3=C4C=CC=CC24
Biological Activity: Triphenylene is a π−π* type UV-B absorbing Photosensitizer. Triphenylene targets the Aryl hydrocarbon receptor. Triphenylene directly triplet-photosensitizes adjacent thymines, thereby inducing cyclobutane pyrimidine dimer formation. Triphenylene can intercalate into tissue and transmit phosphorescence through biological tissue, indicating its potential use in biosensing and deep-tissue optical delivery[1][2][3][4][5][6].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Triphenylene | Triphenylene is a π−π* type UV-B absorbing Photosensitizer. Triphenylene targets the Aryl hydrocarbon receptor. Triphenylene directly triplet-photosensitizes adjacent thymines, thereby inducing cyclobutane pyrimidine dimer formation. Triphenylene can intercalate into tissue and transmit phosphorescence through biological tissue, indicating its potential use in biosensing and deep-tissue optical delivery. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Triphenylene-d12 | 98% | Triphenylene-d12 is the d12-labeled Triphenylene (HY-W017708). Triphenylene is a π−π* type UV-B absorbing Photosensitizer. Triphenylene targets the Aryl hydrocarbon receptor. Triphenylene directly triplet-photosensitizes adjacent thymines, thereby inducing cyclobutane pyrimidine dimer formation. Triphenylene can intercalate into tissue and transmit phosphorescence through biological tissue, indicating its potential use in biosensing and deep-tissue optical delivery. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Matsuoka R, et al. Expansion of the Graphdiyne Family: A Triphenylene-Cored Analogue. ACS applied materials & interfaces. 2019 Jan 23;11(3):2730-2733. [Content Brief]
- [2]. Yang X, et al. Cryogenically Flexible Phosphorescent Organic Crystals that Transmit Self-Sustained Persistent Luminescence with Spatiotemporal Control. Journal of the American Chemical Society. 2025 Jul 02;147(26):22961-22971. [Content Brief]
- [3]. Komprda J, et al. Methodological Challenges in the Application of QSAR Models for Chemical Prioritization and Toxicity Assessment: A Case Study on Aryl Hydrocarbon Receptor Activity in Environmental Pollutant Mixtures. ACS environmental Au. 2026 Mar 18;6(2):295-309.
- [4]. Häcker S, et al. Probing of DNA Photochemistry with C‑Nucleosides of Xanthones and Triphenylene as Photosensitizers To Study the Formation of Cyclobutane Pyrimidine Dimers. JACS Au. 2023 Jul 24;3(7):1843-50. [Content Brief]
- [5]. Kadhim NH, et al. Synergistic light-metal activation in Aza-triphenylene covalent organic frameworks for reversible hydrogen uptake. Surfaces and Interfaces. 2026 Sep 16:110641.
- [6]. Ashy, et al. Enhancing Solar Thermal Fuel Efficiency through Dopant-Mediated Structural Modifications in Triphenylene-Based Mesogenic Matrices. ACS Applied Energy Materials. 2025 Jan 13;8(1):259-66.
