Tetrasodium 1,3,6,8-pyrenetetrasulfonate is a highly water-soluble derivative of pyrene, a polycyclic aromatic hydrocarbon
| Names | |
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| IUPAC name
Tetrasodium 1,3,6,8-pyrenetetrasulfonate | |
Other names
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| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.154.826 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C16H6Na4O12S4 | |
| Molar mass | 610.41 g·mol−1 |
| Appearance | Green crystalline powder[1] |
| Melting point | 102-104 °C[2] |
| Soluble | |
| Hazards | |
| GHS labelling:[3] | |
| Warning | |
| H315, H319, H335 | |
| P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501 | |
| Related compounds | |
Related compounds |
Pyranine |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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The compound can be synthesized in one step by treating pyrene with 50% oleum and sodium sulfate. A traditional two-step method was treating the pyrene with sulfuric acid and sodium sulfate and then treating it with 60% oleum and sodium sulfate.[4]
References
edit- ↑ https://www.fishersci.com/store/msds?partNumber=AC325560010&productDescription=1%2C3%2C6%2C8-PYRENETETRASULFONIC+1G&vendorId=VN00032119&countryCode=US&language=en
- ↑ https://www.echemi.com/sds/1368-pyrenetetrasulfonic-acid-tetra-temppid160705011940.html
- ↑ "Tetrasodium 1,3,6,8-pyrenetetrasulfonate". PubChem. National Center for Biotechnology Information.
- ↑ Chen, Liangzhe; Hu, Biao; Zhang, Jieyu; Zhang, Jinmei; Huang, Shuting; Ren, Ping; Zou, Yang; Ding, Fuyuan; Liu, Xinghai; Li, Houbin (2018-12-19). "A facile synthesis of 1,3,6,8-pyrenesulfonic acid tetrasodium salt as a hydrosoluble fluorescent ink for anti-counterfeiting applications". RSC Advances. 9 (1): 476–481. doi:10.1039/C8RA09106D. ISSN 2046-2069. PMC 9059271. PMID 35521570.
