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m-Terphenyl - 98%, high purity , CAS No.92-06-8
Basic Description
Synonyms
InChI=1/C18H14/c1-3-8-15(9-4-1)17-12-7-13-18(14-17)16-10-5-2-6-11-16/h1-14 | 1,3-Diphenylbenzene | 1,3-Diphenyl-benzene | NCGC00259128-01 | m-Diphenylbenzene | EINECS 202-122-1 | Q20965190 | 1,3-Terphenyl | AKOS002386404 | Benzene, m-diphenyl- | NCGC00249
Specifications & Purity
≥98%
Shipped In
Normal
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Terphenyls
Intermediate Tree Nodes
Not available
Direct Parent
M-terphenyls
Alternative Parents
Biphenyls and derivatives Aromatic hydrocarbons Unsaturated hydrocarbons
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Meta-terphenyl - Biphenyl - Aromatic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as m-terphenyls. These are terphenyls with a structure containing the 1,3-diphenylbenzene skeleton.
External Descriptors
Not available
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.
Names and Identifiers
Pubchem Sid
488180274
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488180274
IUPAC Name
1,3-diphenylbenzene
INCHI
InChI=1S/C18H14/c1-3-8-15(9-4-1)17-12-7-13-18(14-17)16-10-5-2-6-11-16/h1-14H
InChIKey
YJTKZCDBKVTVBY-UHFFFAOYSA-N
Smiles
C1=CC=C(C=C1)C2=CC(=CC=C2)C3=CC=CC=C3
Isomeric SMILES
C1=CC=C(C=C1)C2=CC(=CC=C2)C3=CC=CC=C3
WGK Germany
2
RTECS
WZ6470000
PubChem CID
7076
Molecular Weight
230.3
Beilstein
1864778
Reaxy-Rn
1864778
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in benzene, alcohol, toluene, ether
Boil Point(°C)
379°C
Melt Point(°C)
84-88°C
Molecular Weight
230.300 g/mol
XLogP3
5.600
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
208.000
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
Citations of This Product
1.
Jiaqiang Huang, Zongxue Yu, Junlei Tang, Pingquan Wang, Xiuzhu Zhang, Juan Wang, Xianzhang Lei.
(2024)
High-performance anion exchange membranes based on poly(aryl piperidinium): With interpenetrating ion transport channels induced by fluorinated crosslinking and side chains.
FUEL,
357
(129686).
2.
Chenyang Zheng, Di Xiao, Junfeng Zhang, Yabiao Pei, Lianqin Wang, Xin Liu, Yan Yin, Michael D. Guiver, Xianguo Li.
(2023)
Conformational distortion of the ionomer backbone for reinforcing the catalyst layer under dynamic operation.
Journal of Materials Chemistry A,
11
(33):
(17542-17549).
3.
Song Wanjie, Peng Kang, Xu Wei, Liu Xiang, Zhang Huaqing, Liang Xian, Ye Bangjiao, Zhang Hongjun, Yang Zhengjin, Wu Liang, Ge Xiaolin, Xu Tongwen.
(2023)
Upscaled production of an ultramicroporous anion-exchange membrane enables long-term operation in electrochemical energy devices.
Nature Communications,
14
(1):
(1-11).
4.
Chunming Chen, Xingrong Zeng, Zhenlun Peng, Zhonghua Chen.
(2023)
Polyaromatic anion exchange membranes for alkaline fuel cells with high hydroxide conductivity and alkaline stability.
JOURNAL OF APPLIED POLYMER SCIENCE,
140
(20):
(e53795).
5.
Nan Li, Lanlan Huo, Wenjing Shen, Chenghong Qiang, Mianmian Wu, Guifang Sun, Qingfei Li, Minghao Shi, Jiangquan Ma.
(2023)
Porous organic polymers for superefficient removal of pollutants from water: Design, synthesis and adsorption performance.
Journal of Cleaner Production,
396
(136558).
6.
Chuan Long, Zhihua Wang, Hong Zhu.
(2021)
High chemical stability anion exchange membrane based on poly(aryl piperidinium): Effect of monomer configuration on membrane properties.
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,
46
(18524).
7.
Chuanrui Lu, Chuan Long, Yunxi Li, Ziming Li, Hong Zhu.
(2020)
Chemically stable poly(meta-terphenyl piperidinium) with highly conductive side chain for alkaline fuel cell membranes.
JOURNAL OF MEMBRANE SCIENCE,
598
(117797).
8.
Shuangshuang Hou, Shumaila Razzaque, Bien Tan.
(2019)
Effects of synthesis methodology on microporous organic hyper-cross-linked polymers with respect to structural porosity, gas uptake performance and fluorescence properties.
Polymer Chemistry,
10
(11):
(1299-1311).
9.
Lina Li, Kun Cai, Pengyuan Wang, Hao Ren, Guangshan Zhu.
(2015)
Construction of Sole Benzene Ring Porous Aromatic Frameworks and Their High Adsorption Properties.
ACS Applied Materials & Interfaces,
7
(1):
(201–208).
10.
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,
1722
(464889).
11.
Xueqing You, Qing Ju, Yichang Ma, Guiqin Yi, Zhangtang Jiang, Nanwen Li, Qiugen Zhang.
(2024)
High conductivity poly(meta-terphenyl alkylene)s proton exchange membranes for high temperature fuel cell.
CHEMICAL ENGINEERING JOURNAL,
487
(150535).
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