Triphenylene - ≥98% , CAS No.217-59-4

CAS: 217-59-4 Cat. No.: T124123 Fórmula: C₁₈H₁₂ Peso molecular: 228.29 Beilstein Registry Number: 1342908 Número CE: 205-922-9 PubChem CID: 9170

GRADE & PURITY ≥98%

Synonyms

NSC 57455 | OL10154 | TRIPHENYLENE [MI] | T0513 | 18WX3373I0 | BBL100122 | Benzo[l]phenanthrene | C19541 | EINECS 205-922-9 | AKOS004908298 | Benzo(l)phenanthrene | Isochrysene | Q2975866 | UNII-18WX3373I0 | CCRIS 1301 | 1,2:3,4-Dibenznaphthalene | SB6686

Storage

Room temperature

Shipped In

Normal

Visão geral

A compound that fluoresces in the ultraviolet region.

Specifications

Sinónimos

NSC 57455 | OL10154 | TRIPHENYLENE [MI] | T0513 | 18WX3373I0 | BBL100122 | Benzo[l]phenanthrene | C19541 | EINECS 205-922-9 | AKOS004908298 | Benzo(l)phenanthrene | Isochrysene | Q2975866 | UNII-18WX3373I0 | CCRIS 1301 | 1,2:3,4-Dibenznaphthalene | SB6686

Especificações e pureza

≥98%

Mecanismos bioquímicos e fisiológicos

Separation of Aromatic Compounds Using Ascentis RP-Amide Separation of Aromatic Compounds Using Ascentis C18

Condições de armazenamento de armazenamento

Room temperature

Enviado em

Normal

Pureza

≥98%

Nomes e identificadores

• Pubchem Sid: 504751795
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751795
• Sorrisos canónicos: C1=CC=C2C(=C1)C3=CC=CC=C3C4=CC=CC=C24
• IUPAC Name: triphenylene
• InChIKey: SLGBZMMZGDRARJ-UHFFFAOYSA-N
• 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
• SMILES isoméricas: C1=CC=C2C(=C1)C3=CC=CC=C3C4=CC=CC=C24
• WGK Alemanha: 3
• RTECS: YK2925000
• PubChem CID: 9170
• Peso molecular: 228.29
• Beilstein: 1342908
• Reaxy-Rn: 1342908

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Phenanthrenes and derivatives
      • Subclass Triphenylenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Phenanthrenes and derivatives
• Subclass: Triphenylenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Triphenylenes
• Alternative Parents: Naphthalenes Aromatic hydrocarbons Polycyclic hydrocarbons Unsaturated hydrocarbons
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Triphenylene - Naphthalene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
• Descrição: This compound belongs to the class of organic compounds known as triphenylenes. These are compounds containing a triphenylene moiety, which consists of four fused benzene rings forming a 9,10-benzo[l]phenanthrene.
• External Descriptors: ortho-fused polycyclic arene

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mecanismos de ação

Propriedades químicas e físicas

• Ponto de ebulição (°C): 438°C
• Ponto de fusão (°C): 196.0-200.0°C
• Peso molecular: 228.300 g/mol
• XLogP3: 4.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 228.094 Da
• Monoisotopic Mass: 228.094 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 217.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referências

1. Houmei Liu, Zhan Li, Makoto Takafuji, Hirotaka Ihara, Hongdeng Qiu.  (2017)  Octadecylimidazolium ionic liquid-modified magnetic materials: Preparation, adsorption evaluation and their excellent application for honey and cinnamon.  FOOD CHEMISTRY,      [PMID:28372166] [10.1016/j.foodchem.2017.02.080]

2. Fafu Yang, Jianwei Xie, Hongyu Guo, Bingting Xu, Congcong Li.  (2012)  Novel discotic liquid crystal oligomers: 1,3,5-triazine-based triphenylene dimer and trimer with wide mesophase.  LIQUID CRYSTALS,      [PMID:] [10.1080/02678292.2012.717112]

3. Yali Yang, Jia Chen, Xiaojing Liang, Bei Liu, Kaijun Quan, Xiuhui Liu, Hongdeng Qiu.  (2024)  Adjustable chromatographic performance of silica-based mixed-mode stationary phase through the control of co-grafting amounts of imidazole and C18 chain.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:38598894] [10.1016/j.chroma.2024.464889]

4. Jia-Xu Shuang, Jie Sheng, Yunzhong Wu, Manyu Liu, Changsheng Xing, Rui Liu, Tong Zhang, Bin Liu, Yekang Guan, Lidong Wang, Weidong Fei.  (2025)  In-situ synthesis of graphene/Cu powder and composite through mechanochemical route.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2025.178940]

5. Ruting Xiao, Aijin Shen, Gaowa Jin, Wenyi Yu, Zhimou Guo, Jing Zeng.  (2019)  Synthesis and chromatographic evaluation of a new stationary phase based on mild thiol-Michael addition reaction.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:31889519] [10.1016/j.chroma.2019.460807]

6. Weiting Gao, Jiajun Li, Xuelang Gao, Qinglin Liu.  (2025)  Planar-conjugated hyperbranched poly(aryl piperidinium) anion exchange membranes for sustainable energy devices.  Journal of Energy Chemistry,      [PMID:] [10.1016/j.jechem.2025.10.044]

7. Le Wang, Xiaoyu Li, Jiejun Zeng, Yunji Xie, Di Liu, Jiaran Song, Yuanlong Wu, Zhe Wang.  (2025)  Branching-induced dimensional stability and conductivity balance in anion exchange membranes for fuel cells.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2025.125112]

8. Yali Yang, Hui Ding, Kaijun Quan, Hongwei Zhao, Mingxia Sun, Zhimin Yang, Xiuhui Liu, Hongdeng Qiu, Jia Chen.  (2026)  Pyrene trisulfonic acid-functionalized silica-based multi-mode stationary phase for separation of hydrophilic, hydrophobic compounds and rare earth ions.  ANALYTICA CHIMICA ACTA,      [PMID:41813355] [10.1016/j.aca.2026.345267]

9. Chuyue Zhang, Le Duan, Xu Wang, Lanlan Qiu, Deli Xiao.  (2026)  Preparation of Polyamine-Silica Macrocyclic Chromatographic Stationary Phase for the Separation of Aromatic Compounds.  Separations,  13  (8): (232).  [PMID:] [10.3390/separations13080232]

Perguntas frequentes

What is the purity of this product?

This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 217-59-4, the molecular formula is C18H12, and the molecular weight is 228.29 g/mol. InChIKey SLGBZMMZGDRARJ-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.