Methylene green
Names | |
---|---|
IUPAC name
[7-(dimethylamino)-4-nitrophenothiazin-3-ylidene]-dimethylazanium
chloride
| |
Other names
Basic Green 5; CI 52020
| |
Identifiers | |
3D model (JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.018.392 |
MeSH | C028673 |
PubChem CID
|
|
UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C16H17ClN4O2S | |
Molar mass | 364.85 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
what is ?) | (|
Infobox references | |
Methylene green is a heterocyclic aromatic chemical compound similar to methylene blue. It is used as a dye.[1] It functions as a visible light-activated photocatalyst in organic synthesis.[2]
References[]
- ^ Senior W (November 1969). "Staining of animal tissues with the dye base of methylene green in benzene to facilitate identification and selection of material". Stain Technol. 44 (6): 269–71. doi:10.3109/10520296909063364. PMID 4187577.
- ^ Rogers, David A.; Gallegos, Jillian M.; Hopkins, Megan D.; Lignieres, Austin A.; Pitzel, Amy K.; Lamar, Angus A. (September 2019). "Visible-light photocatalytic activation of N-chlorosuccinimide by organic dyes for the chlorination of arenes and heteroarenes". Tetrahedron. 75 (36): 130498. doi:10.1016/j.tet.2019.130498.
External links[]
- methylene green (at stainsfile)
Categories:
- Histology
- Thiazine dyes
- Phenothiazines
- Chlorides
- Heterocyclic compound stubs