3564-70-3
disodium dibenzo[b,def]chrysene-7,14-diyl bis(sulphate)
CAS: 3564-70-3
Molecular Formula: C24H12Na2O8S2
3564-70-3 - Names and Identifiers
3564-70-3 - Physico-chemical Properties
| Molecular Formula | C24H12Na2O8S2 |
| Molar Mass | 538.45682 |
| Physical and Chemical Properties | EPA Chemical Information Dibenzo [B, def]chrysene-7,14-diol, bis(hydrogen sulfate), disodium salt (3564-70-3) |
3564-70-3 - Upstream Downstream Industry
| Raw Materials | Vat Yellow 4 Pyridine |
3564-70-3 - Introduction
disodium dibenzo [B, def]chrysene-7,14-diyl bis(sulphate) is an organic compound. Its chemical formula is C22H12O8S2Na2, and its structure contains two benzene rings and connects the pyrene groups at positions 7 and 14. This compound is a compound having a high degree of structural stability.
The main use of this compound is as an organic photoelectric material. Because of its good photoelectric conversion efficiency and stability, it can be used in solar cells, light-emitting diodes and organic field effect transistors.
The method of preparing disodium dibenzo [B, def]chrysene-7,14-diyl bis(sulphate) is more complicated. A common preparation method is to synthesize a pyrene compound with a benzene ring and react with sulfuric acid to generate the target compound.
Regarding the safety information of this compound, due to its strong photoelectric conversion function, care should be taken to avoid prolonged exposure to strong light to avoid undesirable photogenerated chemical reactions. In addition, protective measures should be taken in the working environment to avoid skin contact and inhalation. For these specific safety information, it is recommended to refer to the relevant safety data table when using it.
The main use of this compound is as an organic photoelectric material. Because of its good photoelectric conversion efficiency and stability, it can be used in solar cells, light-emitting diodes and organic field effect transistors.
The method of preparing disodium dibenzo [B, def]chrysene-7,14-diyl bis(sulphate) is more complicated. A common preparation method is to synthesize a pyrene compound with a benzene ring and react with sulfuric acid to generate the target compound.
Regarding the safety information of this compound, due to its strong photoelectric conversion function, care should be taken to avoid prolonged exposure to strong light to avoid undesirable photogenerated chemical reactions. In addition, protective measures should be taken in the working environment to avoid skin contact and inhalation. For these specific safety information, it is recommended to refer to the relevant safety data table when using it.
Last Update：2024-04-10 22:29:15
