≥97%(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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application：
1,3,5-Triethylbenzene was used as a supramoelcular template to organize molecular-recognition elements. It was also used to synthesize a series of di- and trinucleating ligands.
| Sonrisas canónicas | CCC1=CC(=CC(=C1)CC)CC |
|---|---|
| IUPAC Name | 1,3,5-triethylbenzene |
| InChIKey | WJYMPXJVHNDZHD-UHFFFAOYSA-N |
| INCHI | 1S/C12H18/c1-4-10-7-11(5-2)9-12(6-3)8-10/h7-9H,4-6H2,1-3H3 |
| Isómeros SMILES | CCC1=CC(=CC(=C1)CC)CC |
| PubChem CID | 7602 |
| Peso molecular | 162.28 |
| Beilstein | 5(4)1133 |
| Reaxy-Rn | 2039481 |
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 | 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 |
| Descripción | 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 | Not available |
| Solubilidad | Insoluble in water; Soluble in Ether,Alcohol |
|---|---|
| Índice de refracción | 1.5 |
| Punto de inflamación (°F) | 76°C(lit.) |
| Punto de inflamación (°C) | 76°C(lit.) |
| Punto de ebullición (°C) | 218°C |
| Punto de fusión (°C) | -66°C(lit.) |
| Peso molecular | 162.270 g/mol |
| XLogP3 | 4.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 3 |
| Exact Mass | 162.141 Da |
| Monoisotopic Mass | 162.141 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 81.400 |
| 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. Fang Lan, Qin Wang, Hui Chen, Yi Chen, Yuanyuan Zhang, Bowen Huang, Hongbo Liu, Jian Liu, Run Li. (2020) Preparation of Hydrophilic Conjugated Microporous Polymers for Efficient Visible Light-Driven Nicotinamide Adenine Dinucleotide Regeneration and Photobiocatalytic Formaldehyde Reduction. ACS Catalysis, [PMID:] [10.1021/acscatal.0c03652] |
| 2. Ye He, Mengyang Wang, Haotian Zhang, Youxi Zhang, Yikun Gao, Siling Wang. (2019) Protective properties of mesocellular silica foams against aggregation and enzymatic hydrolysis of loaded proteins for oral protein delivery. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:31706652] [10.1016/j.jcis.2019.10.118] |
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