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1,2,4,5-Tetramethylbenzene - Standard for quantitative NMR,99.8%(GC), high purity , CAS No.95-93-2
Basic Description
Synonyms
1,2,4,5-TETRAMETHYLBENZENE | 95-93-2 | Durene | Durol | Benzene, 1,2,4,5-tetramethyl- | p-Xylene, 2,5-dimethyl- | 1,2,4,5-tetramethyl-benzene | DTXSID1029124 | CHEBI:38978 | 181426CFYB | NSC-6770 | DTXCID309124 | CAS-95-93-2 | NSC 6770 | EINECS 202-465-7 | Duren | UNII-181426CFYB | AI3-25
Specifications & Purity
Standard for quantitative NMR, ≥99.8%(GC)
Shipped In
Normal
Grade
Standard for quantitative NMR
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Benzene and substituted derivatives
Alternative Parents
Aromatic hydrocarbons Unsaturated hydrocarbons
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Monocyclic benzene moiety - Aromatic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors
tetramethylbenzene
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.
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
1,2,4,5-tetramethylbenzene
INCHI
InChI=1S/C10H14/c1-7-5-9(3)10(4)6-8(7)2/h5-6H,1-4H3
InChIKey
SQNZJJAZBFDUTD-UHFFFAOYSA-N
Smiles
CC1=CC(=C(C=C1C)C)C
Isomeric SMILES
CC1=CC(=C(C=C1C)C)C
WGK Germany
1
RTECS
DC0500000
UN Number
1325
Packing Group
II
Molecular Weight
134.22
Beilstein
1903393
Reaxy-Rn
1903393
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Moisture sensitive.
Flash Point(°F)
165.2 °F
Flash Point(°C)
73℃
Boil Point(°C)
191-193°C
Melt Point(°C)
80°C
Molecular Weight
134.220 g/mol
XLogP3
4.000
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
0
Exact Mass
134.11 Da
Monoisotopic Mass
134.11 Da
Topological Polar Surface Area
0.000 Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
80.600
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.
Yewei Xu, Chunyan Yang, Hongyang Deng, Chi Zhong, Peiyu He, Tinghong Zhang, Yi Sun, Rui Yuan, Shuen Liang, Biao Kang, Guanjun Chang.
(2023)
Efficient adsorption of trinitrotoluene by isoxazoline-based porous polymers prepared from room-temperature stable bis(nitrile oxide).
JOURNAL OF APPLIED POLYMER SCIENCE,
140
(13):
(e53678).
2.
Qian Zhou, Bingxiao Feng, Lining Hao, Chao Pan, Hongbing Song, Hengjun Gai, Quanhong Zhu, Meng Xiao, Tingting Huang.
(2023)
Preparation and application of low-cost fibers for efficient adsorption of oil from coal pyrolysis wastewater and establishment of quantitative equation for calculating oil contact angle under water.
Journal of Water Process Engineering,
51
(103461).
3.
Liu Huijun, Li Caixia, Wang Hong, Huang Zhongping, Zhang Peipei, Pan Zaifa, Wang Lili.
(2014)
Characterization of Volatile Organic Metabolites in Lung Cancer Pleural Effusions by SPME–GC/MS Combined with an Untargeted Metabolomic Method.
CHROMATOGRAPHIA,
77
(19):
(1379-1386).
4.
Xinlai Wei, Zhi Wang, Yang Wu, Zhimin Yu, Jie Jin, Ke Wu.
(2014)
Fast pyrolysis of cellulose with solid acid catalysts for levoglucosenone.
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS,
107
(150).
5.
Huijun Liu, Hong Wang, Caixia Li, Lichao Wang, Zaifa Pan, Lili Wang.
(2014)
Investigation of volatile organic metabolites in lung cancer pleural effusions by solid-phase microextraction and gas chromatography/mass spectrometry.
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,
945-946
(53).
6.
Xian-wei Sui, Zhi Wang, Bing Liao, Ying Zhang, Qing-xiang Guo.
(2012)
Preparation of levoglucosenone through sulfuric acid promoted pyrolysis of bagasse at low temperature.
BIORESOURCE TECHNOLOGY,
103
(466).
7.
Ganshang Si, Yanchun Wang, Xu Liu, Changwei Sun, Junfang Miao, Zhengang Li.
(2024)
Detection of powder samples based on UV Raman-fluorescence spectroscopy.
OPTICS COMMUNICATIONS,
571
(130950).
8.
Yafei Sang, Xiaolong Jia, Pengpeng Wu, Xiangquan Yan, Xiaotao Kuang, Quan Feng, Jiahao Qiao, Min Chen, Jian Zhang, Xiuli Yan, Tao Chang.
(2025)
One pot synthesis rich in bromine anion ionic porous organic polymer for CO2 catalytic conversion.
NEW JOURNAL OF CHEMISTRY,
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