Methyl violet is a family of organic compounds that are mainly used as dyes. Depending on the number of attached methyl groups, the color of the dye can be altered. Its main use is as a purple dye for textiles and to give deep violet colors in paint and ink. It is also used as a hydration indicator for silica gel. Methyl violet 10B is also known as crystal violet (and many other names) and has medical uses.[1]
The term methyl violet encompasses three compounds that differ in the number of methyl groups attached to the aminefunctional group. Methyl violets are mixtures of tetramethyl (2B), pentamethyl (6B) and hexamethyl (10B) pararosanilins.[2]
Methyl violet 2B (IUPAC name: '4,4'-((4-Iminocyclohexa-2,5-dien-1-ylidene)methylene)bis(N,N-dimethylaniline) monohydrochloride) is a green powder which is soluble in water and ethanol but not in xylene. It appears yellow in solution of low pH (~0.15) and changes to violet with pH increasing toward 3.2.[3]
Methyl violet 10B has six methyl groups. It is known in medicine as Gentian violet (or crystal violet or pyoctanin(e)[1]) and is the active ingredient in a Gram stain, used to classify bacteria. It is used as a pH indicator, with a range between 0 and 1.6. The protonated form (found in acidic conditions) is yellow, turning blue-violet above pH levels of 1.6.[4]
Methyl violet 10B inhibits the growth of many Gram positive bacteria, except streptococci.[citation needed] When used in conjunction with nalidixic acid (which destroys gram-negative bacteria), it can be used to isolate the streptococci bacteria for the diagnosis of an infection.[citation needed]
Methyl violet is a mutagen and mitotic poison, therefore concerns exist regarding the ecological impact of the release of methyl violet into the environment. Methyl violet has been used in vast quantities for textile and paper dyeing, and 15% of such dyes produced worldwide are released to environment in wastewater. Numerous methods have been developed to treat methyl violet pollution. The three most prominent are chemical bleaching, biodegradation, and photodegradation.
Biodegradation has been well investigated because of its relevance to sewage plants with specialized microorganisms. Two microorganisms that have been studied in depth are the white rot fungus and the bacterium Nocardia Corallina.[7][8]
Light alone does not rapidly degrade methyl violet,[9] but the process is accelerated upon the addition of large band-gap semiconductors, TiO2orZnO.[10][11]
Many other methods have been developed to treat the contamination of dyes in a solution, including electrochemical degradation,[12] ion exchange,[13] laser degradation, and absorption onto various solids such as activated charcoal.
^Pizzolato, T (2002). "Colour removal with NaClO of dye wastewater from an agate-processing plant in Rio Grande do Sul, Brazil". International Journal of Mineral Processing. 65 (3–4): 203–211. Bibcode:2002IJMP...65..203P. doi:10.1016/S0301-7516(01)00082-5.
^Yatome, Chizuko; Yamada, Shigeyuki; Ogawa, Toshihiko; Matsui, Masaki (1993). "Degradation of Crystal violet by Nocardia corallina". Applied Microbiology and Biotechnology. 38 (4). doi:10.1007/BF00242956. S2CID43686541.
^Bhasikuttan, A; Sapre, A.V.; Shastri, L.V. (1995). "Oxidation of crystal violet and malachite green in aqueous solutions — a kinetic spectrophotometric study". Journal of Photochemistry and Photobiology A: Chemistry. 90 (2–3): 177–182. Bibcode:2018JPPA..364...59D. doi:10.1016/1010-6030(95)04094-V.
^Senthilkumaar, S; Porkodi, K (2005). "Heterogeneous photocatalytic decomposition of Crystal Violet in UV-illuminated sol-gel derived nanocrystalline TiO2 suspensions". Journal of Colloid and Interface Science. 288 (1): 184–9. Bibcode:2005JCIS..288..184S. doi:10.1016/j.jcis.2005.02.066. PMID15927578.
^Sahoo, C; Gupta, A; Pal, A (2005). "Photocatalytic degradation of Crystal Violet (C.I. Basic Violet 3) on silver ion doped TiO". Dyes and Pigments. 66 (3): 189–196. doi:10.1016/j.dyepig.2004.09.003.
^Wu, J; Liu, C; Chu, K; Suen, S (2008). "Removal of cationic dye methyl violet 2B from water by cation exchange membranes". Journal of Membrane Science. 309 (1–2): 239–245. doi:10.1016/j.memsci.2007.10.035.
