Methyl violet 2B

Methyl violet 2B
	Methyl violet 2B
Names
	IUPAC name 4,4′-[(4-Imino-2,5-cyclohexadien-1-yliden)methylen]bis(N,N-dimethylaniline)hydrochloride
	Other names Tetraamethylparosanilinium chloride;
Identifiers
CAS Number	8004-87-3 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:90108;
ChemSpider	21164086 ;
ECHA InfoCard	100.074.935
EC Number	610-776-8;
PubChem CID	91997555;
UNII	9691711H0F ;
	InChI Key: WWKGVZASJYXZKN-UHFFFAOYSA-N ;
	SMILES CN(C)C1=CC=C(C=C1)C(=C2C=CC(=N)C=C2)C3=CC=C(C=C3)N(C)C.Cl;
Properties
Chemical formula	C23H26N3Cl
Appearance	Green to dark-green powder
Melting point	decomposes
Solubility in water	Soluble in water, ethanol, insoluble in xylene
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Methyl violet 2B (Tetramethylparosanilinium chloride, 4,4′-[(4-imino-2,5-cyclohexadien-1-ylidene)methylen]bis(N,N-dimethylaniline)hydrochloride) is a violet triarylmethane dye from the group of cationic dyes and an essential component of C.I. Basic Violet 1 (trivial name methyl violet). Methyl violets are mixtures of tetramethyl (2B), pentamethyl (6B) and hexamethyl (10B) pararosanilins.

References

1 2 3 R. W. Sabnis (29 March 2010). Handbook of Biological Dyes and Stains: Synthesis and Industrial Applications. John Wiley and Sons. pp. 309–. ISBN 978-0-470-40753-0. Retrieved 27 June 2011.
↑ Bouasla, C.; Samar, M. E. H.; Ismail, F. (2010). "Degradation of methyl violet 6B dye by the Fenton process". Desalination. 254 (1–3): 35–41. doi:10.1016/j.desal.2009.12.017.

[b1-1] 1 2 3 R. W. Sabnis (29 March 2010). Handbook of Biological Dyes and Stains: Synthesis and Industrial Applications. John Wiley and Sons. pp. 309–. ISBN 978-0-470-40753-0. Retrieved 27 June 2011.

[2] Bouasla, C.; Samar, M. E. H.; Ismail, F. (2010). "Degradation of methyl violet 6B dye by the Fenton process". Desalination. 254 (1–3): 35–41. doi:10.1016/j.desal.2009.12.017.