Determine the necessary mass, volume, or concentration for preparing a solution.
≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Desiccated Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488180151 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488180151 |
| Kanonisches Lächeln | C1=CC=C(C=C1)C2=CC=CC=C2C3=CC=CC=C3 |
| IUPAC Name | 1,2-diphenylbenzene |
| InChIKey | OIAQMFOKAXHPNH-UHFFFAOYSA-N |
| INCHI | 1S/C18H14/c1-3-9-15(10-4-1)17-13-7-8-14-18(17)16-11-5-2-6-12-16/h1-14H |
| Isomere SMILES | C1=CC=C(C=C1)C2=CC=CC=C2C3=CC=CC=C3 |
| WGK Deutschland | 3 |
| RTECS | WZ6472000 |
| PubChem CID | 6766 |
| Molekulargewicht | 230.3 |
| Beilstein | 1908446 |
| Reaxy-Rn | 1908446 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Klasse | Benzene and substituted derivatives |
| Subclass | Terphenyls |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Terphenyls |
| Alternative Parents | Biphenyls and derivatives Aromatic hydrocarbons Unsaturated hydrocarbons |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Terphenyl - Biphenyl - Aromatic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homomonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as terphenyls. These are polycyclic aromatic compounds containing a terphenyl skeleton, which consists of a benzene ring substituted with two phenyl groups. Isomers of terphenyl include m-terphenyls (1,3-diphenylbenzenes), o-terphenyls (1,2-diphenylbenzenes), p-terphenyls (1,4-diphenylbenzenes). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
| Certificate of Analysis | Jun 16, 2026 | T113760 | |
| Certificate of Analysis | Dec 12, 2025 | T113760 | |
| Certificate of Analysis | Oct 21, 2024 | T113760 | |
| Certificate of Analysis | Oct 21, 2024 | T113760 | |
| Certificate of Analysis | Aug 09, 2023 | T113760 | |
| Certificate of Analysis | Jun 05, 2023 | T113760 | |
| Certificate of Analysis | May 15, 2023 | T113760 | |
| Certificate of Analysis | Feb 07, 2023 | T113760 | |
| Certificate of Analysis | Mar 08, 2022 | T113760 | |
| Certificate of Analysis | Mar 08, 2022 | T113760 | |
| Certificate of Analysis | Mar 08, 2022 | T113760 | |
| Certificate of Analysis | Mar 08, 2022 | T113760 | |
| Certificate of Analysis | Mar 08, 2022 | T113760 |
| Löslichkeit | Insoluble in water; Degree of Solubility in water: 1.24 mg/l 25 °C; Soluble in Methanol,Toluene,Benzene,Chloroform,Acetone; Very slightly soluble in Ethanol |
|---|---|
| Flammpunkt (°F) | 235.4 °F |
| Flammpunkt (°C) | 113 °C |
| Siedepunkt (°C) | 332°C |
| Schmelzpunkt (°C) | 58°C |
| Molekulargewicht | 230.300 g/mol |
| XLogP3 | 6.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 2 |
| Exact Mass | 230.11 Da |
| Monoisotopic Mass | 230.11 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 206.000 |
| 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 |
| 1. Weiting Gao, Xuelang Gao, Qiugen Zhang, Aimei Zhu, Qinglin Liu. (2023) Durable poly(binaphthyl-co-p-terphenyl piperidinium)-based anion exchange membranes with dual side chains. Journal of Energy Chemistry, [PMID:] [10.1016/j.jechem.2023.11.008] |
| 2. Yaming Sun, Wenjie Sun, Junnan Li, Tao Zhang, Wenjie Zhao, Guoqiang Xiang, Tiantian Yang, Lijun He. (2023) Highly graphitized porous carbon/reduced graphene oxide for ultrahigh enrichment and ultrasensitive determination of polycyclic aromatic hydrocarbons. JOURNAL OF HAZARDOUS MATERIALS, [PMID:37827103] [10.1016/j.jhazmat.2023.132699] |
| 3. Wen-Bo Xie, Hao Li, Lei Zeng, Li-Juan Jiang, Wen Li, Lu Xia, Fu-Hou Lei. (2022) Separation of Panax notoginseng saponins on modified rosin ester-bonded silica stationary phase and its mechanism. ANALYTICA CHIMICA ACTA, [PMID:36628701] [10.1016/j.aca.2022.340661] |
| 4. 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] |
| 5. Lina Li, Kun Cai, Pengyuan Wang, Hao Ren, Guangshan Zhu. (2014) Construction of Sole Benzene Ring Porous Aromatic Frameworks and Their High Adsorption Properties. ACS Applied Materials & Interfaces, [PMID:25495481] [10.1021/am505697f] |
| 6. 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] |
| 7. Min Sun, Jiaqing Feng, Yang Feng, Xubo Xin, Yali Ding, Juanjuan Feng. (2024) Core-shell silica@pyridyl conjugated microporous polymer as a stationary phase for high performance liquid chromatography. ANALYTICA CHIMICA ACTA, [PMID:38309855] [10.1016/j.aca.2024.342258] |
| 8. Jing Li, Li Xu, Zhi-guo Shi. (2018) Waxberry-like hierarchically porous ethyl-bridged hybrid silica microsphere: A substrate for enzyme catalysis and high-performance liquid chromatography. JOURNAL OF CHROMATOGRAPHY A, [PMID:30527847] [10.1016/j.chroma.2018.11.073] |
| 9. 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] |