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2-Ethylanthraquinone - 97%, high purity , CAS No.84-51-5
Basic Description
Synonyms
2-Ethyl-9,10-anthraquinone | CAS-84-51-5 | SMR000203366 | .BETA.-ETHYLANTHRAQUINONE | beta-Ethylanthraquinone | EU-0034302 | 2-ethyl-9,10-dihydroanthracene-9,10-dione | 2-Ethylanthraquinone, 97% | InChI=1/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-1
Specifications & Purity
≥97%
Shipped In
Normal
Product Description
Product Application:
2-Ethylanthraquinone can be used as a photoinitiator of crosslinking or degradation of polyethylene. It is used to produce hydrogen peroxide by hydrogenation with the help of Pd/polyaniline as the catalysts.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Anthracenes
Subclass
Anthraquinones
Intermediate Tree Nodes
Not available
Direct Parent
Anthraquinones
Alternative Parents
Aryl ketones Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Anthraquinone - 9,10-anthraquinone - Aryl ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.
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.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
504751168
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504751168
IUPAC Name
2-ethylanthracene-9,10-dione
INCHI
InChI=1S/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3
InChIKey
SJEBAWHUJDUKQK-UHFFFAOYSA-N
Smiles
CCC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O
Isomeric SMILES
CCC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O
WGK Germany
1
RTECS
CB0525000
Molecular Weight
236.27
Beilstein
7(1)425
Reaxy-Rn
1969873
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1969873&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Insoluble in water.
Flash Point(°F)
168℃
Flash Point(°C)
168℃
Boil Point(°C)
190 °C
Melt Point(°C)
108°C
Molecular Weight
236.260 g/mol
XLogP3
4.400
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
1
Exact Mass
236.084 Da
Monoisotopic Mass
236.084 Da
Topological Polar Surface Area
34.100 Ų
Heavy Atom Count
18
Formal Charge
0
Complexity
360.000
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.
Yuanyuan Song, Ziqi Wang, Yijing Long, Yang Mao, Feng Jiang, Yuanyuan Lu.
(2022)
2-Alkyl-anthraquinones inhibit Candida albicans biofilm via inhibiting the formation of matrix and hyphae.
RESEARCH IN MICROBIOLOGY,
173
(103955).
2.
Zhichao Yang, Weiquan Cai, Jinpeng Zhou, Qing Xia, Tielin Wang.
(2020)
Fast, Large-Scale, and Stable Preparation of η-Al2O3 Microspheres by Fully Utilizing N,N-Dimethylformamide at Room Temperature.
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,
59
(10):
(4203–4209).
3.
Weiquan Cai, Junlin Zhuo, Jimin Fang, Zhichao Yang.
(2019)
2-Ethyl-9,10-anthraquinone assisted sol–gel synthesis of Pd/γ-Al2O3 nanorods with enhanced catalytic performance in 2-ethyl-9,10-anthraquinone hydrogenation.
CHINESE JOURNAL OF CHEMICAL ENGINEERING,
27
(1863).
4.
Zhigang Lei, Yaru Guo, Yanyan Guo, Xinxin Li, Chengna Dai.
(2017)
H2 solubility and mass transfer in anthraquinone working solution: Experimental and modeling study.
CHINESE JOURNAL OF CHEMICAL ENGINEERING,
25
(143).
5.
Haoying Zhang, Qi Zhang, Ting Zuo, Ziqi Wang, Jianmin Liao, Yuanyuan Lu.
(2025)
2-Chloromethyl Anthraquinone Inhibits Candida Albicans Biofilm Formation by Inhibiting the Ras1-cAMP-Efg1 Pathway.
RESEARCH IN MICROBIOLOGY,
(104280).
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