Determine the necessary mass, volume, or concentration for preparing a solution.
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≥99%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Ethoxybenzene (Phenetole) was used as an analyte in assaying the performance of the porous graphitic carbon (PGC) particles.
| Pubchem Sid | 504751426 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751426 |
| Sonrisas canónicas | CCOC1=CC=CC=C1 |
| IUPAC Name | ethoxybenzene |
| InChIKey | DLRJIFUOBPOJNS-UHFFFAOYSA-N |
| INCHI | 1S/C8H10O/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3 |
| Isómeros SMILES | CCOC1=CC=CC=C1 |
| WGK Alemania | 2 |
| RTECS | SI7700000 |
| Número ONU | 3271 |
| Grupo de embalaje | III |
| Peso molecular | 122.16 |
| Beilstein | 636270 |
| Reaxy-Rn | 636270 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636270&ln= |
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 |
| Clase | Phenol ethers |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenol ethers |
| Alternative Parents | Phenoxy compounds Alkyl aryl ethers Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. |
| External Descriptors | aromatic ether |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Sep 17, 2025 | E108655 | |
| Certificate of Analysis | Sep 17, 2025 | E108655 | |
| Certificate of Analysis | Jun 09, 2025 | E108655 | |
| Certificate of Analysis | Jun 09, 2025 | E108655 | |
| Certificate of Analysis | Dec 10, 2022 | E108655 | |
| Certificate of Analysis | Dec 10, 2022 | E108655 | |
| Certificate of Analysis | Oct 31, 2022 | E108655 | |
| Certificate of Analysis | Oct 31, 2022 | E108655 |
| Solubilidad | Insoluble in water, soluble in alcohol and ether. |
|---|---|
| Sensibilidad | Light Sensitive |
| Índice de refracción | 1.505 |
| Punto de inflamación (°F) | 134°F |
| Punto de inflamación (°C) | 57℃ |
| Punto de ebullición (°C) | 172°C |
| Punto de fusión (°C) | -30°C |
| Peso molecular | 122.160 g/mol |
| XLogP3 | 2.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 122.073 Da |
| Monoisotopic Mass | 122.073 Da |
| Topological Polar Surface Area | 9.200 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 65.000 |
| 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. Kang Yuan, Hao Li, Rui Zuo, Baiqin Gan, Chengjia Xiong. (2023) Highly Sensitive Detection of Isomers through Dynamic Reflection Spectroscopy Based on Simple Amorphous Photonic Crystals. Journal of Physical Chemistry C, [PMID:] [10.1021/acs.jpcc.3c04812] |
| 2. Tao Xie, Jing-Pei Cao, Chen Zhu, Xiao-Yan Zhao, Ming Zhao, Yun-Peng Zhao, Xian-Yong Wei. (2019) Selective cleavage of CO bond in benzyl phenyl ether over Pd/AC at room temperature. FUEL PROCESSING TECHNOLOGY, [PMID:] [10.1016/j.fuproc.2019.02.022] |
| 3. Bao Zhang, Jun Li, Yuying Gao, Ruifeng Chong, Zhiliang Wang, Lin Guo, Xianwen Zhang, Can Li. (2016) To boost photocatalytic activity in selective oxidation of alcohols on ultrathin Bi2MoO6 nanoplates with Pt nanoparticles as cocatalyst. JOURNAL OF CATALYSIS, [PMID:] [10.1016/j.jcat.2016.11.023] |
| 4. Zhenyu Bao, Weijiang Zhang, Yinglai Chen, Jiao Xu, Xianbao Cui. (2014) Densities, viscosities and volumetric properties of BF3·anisole and BF3·phenetole complexes at T = (283.15 to 303.15)K. JOURNAL OF MOLECULAR LIQUIDS, [PMID:] [10.1016/j.molliq.2014.06.011] |
| 5. Zhao Chang-Xin, Li Zheng, Chen Bin, Chen Fu, Wang Chunsheng. (2025) Self-adaptive electrolytes for fast-charging batteries. Nature Energy, [PMID:] [10.1038/s41560-025-01801-0] |