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| | CORONENE Basic information |
| Product Name: | CORONENE | | Synonyms: | Coronene (purity);45070, Coronene (purity);CORONENE, SUBLIMED, 99%;Coronene solution;Coronene (refined product of C0386);1,12:4,5:8,9-Triethenotriphenylene;1,4,7,10,13,16-(1,2,3,4,5,6-Benzenehexyl)-1,3,5,7,9,11,13,15,17-cyclooctadecanonene;Coronene,95% | | CAS: | 191-07-1 | | MF: | C24H12 | | MW: | 300.35 | | EINECS: | 205-881-7 | | Product Categories: | OLED materials,pharm chemical,electronic;strong recommend;Active Pharmaceutical Ingredients;Organic Semiconductors;p-Type Oligomers;Pyrrolidines ,Pyrroles;Electroluminescence;Functional Materials;Alphabetic;C;CO - CZ;Arenes;Building Blocks;Organic Building Blocks;Charge Transport and Photosensitizing MaterialsOrganic Conductors and Photovoltaics: OFET and OPV Materials;ArenesOrganic Electronics and Photonics;OLED and PLED Materials | | Mol File: | 191-07-1.mol |  |
| | CORONENE Chemical Properties |
| Melting point | 428 °C (lit.) | | Boiling point | 525 °C (lit.) | | density | 1.39 | | refractive index | 1.4800 (estimate) | | Fp | 6 °C | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Crystalline Powder | | color | Yellow to greenish | | Water Solubility | 0.1ug/L(25 ºC) | | Merck | 14,2536 | | BRN | 658468 | | Stability: | Stable. Combustible. Incompatible with strong oxidizing agents. | | CAS DataBase Reference | 191-07-1(CAS DataBase Reference) | | IARC | 3 (Vol. 32, Sup 7, 92) 1987 | | EPA Substance Registry System | Coronene (191-07-1) |
| | CORONENE Usage And Synthesis |
| Chemical Properties | yellow to gold fibrous powder | | Uses | Coronene is a polycyclic aromatic hydrocarbon found in smoked fish and was examined for potential toxic and carcinogenic effects. | | Uses | Ultraviolet phosphor for charge-coupled devices. | | Uses | Used to synthesize MBE-grown layered superconductors. | | Definition | ChEBI: A ortho- and peri-fused polycyclic arene that consists of six peri-fused benzene rings. | | Carcinogenicity | An initiation–promotion assay
in mice gave positive results; a repeated application gave
negative results. On the basis of these studies, the working
group concluded that these data were inadequate to permit an
evaluation of the carcinogenicity of coronene to experimental
animals. | | Purification Methods | Crystallise coronene from *benzene or toluene, then sublime it in a vacuum. [Beilstein 5 III 2651.] |
| | CORONENE Preparation Products And Raw materials |
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