Methyl violet structure

N-Alkylhydroxamic acid hydrolysis Methyl Violet + OH" Cl C12H25S03Na + H30+, CTABr + OH". An attempt made to separate electronic and hydrophobic effects on the micellar reaction Anionic and cationic micelles. Effect of surfactant structure examined Berndt el at., 1984 Malaviya and Katiyar, 1984... 

Methyl Violet consists of the basic structure of Pigment Violet 3 (126). 

Methyl Violet -E OH Cl Anionic and cationic micelles. Effect of surfactant structure examined Malaviya and Katiyar, 1984... 

Figure 5 Structure of the dendritic box containing two encapsulated methyl violet residues synthesized by Meijer and coworkers (R = Ph)22...

Figure 3.62 Structure of a cationic dye, methyl violet, used to sensitise CuSCN...

To the conditions enunciated by Mehrling and Welde might be added that the side chain must be unsaturated since di-hydroionone only has a faint odour, and also that the violet odour is occasiopally present with bodies of quite different structure from the ionones, for instance A 2 2 4 tri-methyl-tetra-hydro-benzaldehyde. 

These compounds are triphenylmethane pigments. Strictly speaking, they should be referred to as triaminophenylmethane derivatives. The parent structure is known as reddish violet parafuchsin (118) or its anhydro base pararosaniline (119). The parent compound may bear between one and three methyl substituents (fuchsin, new fuchsin). 

Mesoionic 4-amino-l,2,3,5-thiatriazoles constitute the only class of mesoionic 1,2,3,5-thiatriazoles known. They are prepared by the reaction of l-amino-l-methyl-3-phenylguanidine with approximately 2 equivalents of thionyl chloride with pyridine as solvent (88ACS(B)63>. They are obtained as the yellow 1 1 pyridine complexes (17). The dark-violet mesoionic 1,2,3,5-thiatriazole (18) was liberated on treatment with aqueous potassium carbonate (Scheme 3). The structure is established on the basis of elemental analysis and spectroscopic data. In particular, the IR spectrum is devoid of NH absorptions. Compound (18) exhibits a long-wavelength absorption at 463 nm in methanol. When mixed with an equivalent amount of pyridinium chloride, complex (17) is formed and the absorption shifts to 350 mn. The mesoionic thiatriazoles are sensitive towards mineral acids and aqueous base and although reaction takes place with 1,3-dipolarophiles such as dimethyl acetylene-dicarboxylate, a mixture of products were obtained which were not identified. 

Whereas in L Air du Temps it is the woody-iris character of the methyl ionone that develops in combination with the vetiveryl acetate, in Paris it forms the basis of a violet accord, with Iso E Super as the woody note. Iso E Super, one of the most important of the newer synthetics, is another chameleon-type product combining woody and amber aspects with some of the character of methyl ionone. Used in Paris as part of the L Air du Temps structure, it forms a natural link between the other materials and the violet accord. 

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