Acid violet 43
Solid powder
Catalysts and Ligands
Acid Violet 43 is a synthetic dye that belongs to the class of triarylmethane dyes. It is commonly used in the textile, paper, and leather industries as a colorant. Acid Violet 43 has also been studied for its potential therapeutic and environmental applications.
432.4 g/mol
432.4 g/mol
Formulation:
432.4 g/mol
Source:
Usage:
Acid violet 43
The product is for non-human research only. Not for therapeutic or veterinary use.
Catalog Number: BT-257390
CAS Number: 4430-18-6
Molecular Formula: C21H15NNaO6S+
Molecular Weight: 432.4 g/mol
| CAS Number | 4430-18-6 |
|---|---|
| Product Name | Acid violet 43 |
| Molecular Formula | C21H15NNaO6S+ |
| Molecular Weight | 432.4 g/mol |
| Appearance | Solid powder |
| InChI | InChI=1S/C21H15NO6S.Na/c1-11-6-7-14(17(10-11)29(26,27)28)22-15-8-9-16(23)19-18(15)20(24)12-4-2-3-5-13(12)21(19)25;/h2-10,22-23H,1H3,(H,26,27,28);/q;+1/p-1 |
| InChI Key | GTKIEPUIFBBXJQ-UHFFFAOYSA-M |
| Isomeric SMILES | CC1=CC(=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O)S(=O)(=O)[O-].[Na+] |
| IUPAC Name | sodium;2-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]-5-methylbenzenesulfonate |
| Canonical SMILES | CC1=CC(=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O)S(=O)(=O)[O-].[Na+] |
| Description | Acid Violet 43 is a synthetic dye that belongs to the class of triarylmethane dyes. It is commonly used in the textile, paper, and leather industries as a colorant. Acid Violet 43 has also been studied for its potential therapeutic and environmental applications. |
| Method of Synthesis or Extraction | Acid Violet 43 can be synthesized by several methods, including the condensation of dimethyl aniline with benzaldehyde, the reaction of benzaldehyde with dimethyl-p-phenylenediamine, and the reaction of benzaldehyde with N,N-dimethylaniline in the presence of sulfuric acid. The efficiency and yield of each method vary depending on the reaction conditions and the purity of the starting materials. However, the synthesis of Acid Violet 43 can be hazardous to the environment and human health due to the use of toxic chemicals and the generation of waste products. Therefore, it is essential to consider environmental and safety considerations when choosing a method of synthesis or extraction. |
| Chemical Structure and Biological Activity | The chemical structure of Acid Violet 43 consists of a triarylmethane core with two methyl groups and a sulfonic acid group attached to the central carbon atom. Acid Violet 43 has been shown to exhibit biological activity, including antimicrobial, antitumor, and antioxidant properties. The mechanism of action of Acid Violet 43 is not fully understood, but it is believed to involve the inhibition of enzymes and the disruption of cellular processes. |
| Biological Effects | Acid Violet 43 has been shown to affect cell function and signal transduction in various cell types. It has been reported to induce apoptosis in cancer cells and to inhibit the growth of bacteria and fungi. However, Acid Violet 43 can also have potential toxic effects on cells and organisms, including genotoxicity and cytotoxicity. Therefore, it is important to consider the potential therapeutic and toxic effects of Acid Violet 43 when evaluating its applications. |
| Applications | Acid Violet 43 has been studied for its potential applications in medical research, environmental research, and industrial research. In medical research, Acid Violet 43 has been investigated for its role in drug development, including its potential as an anticancer agent. Clinical trials have shown promising results in the treatment of certain types of cancer. However, further research is needed to evaluate its safety and efficacy. In environmental research, Acid Violet 43 has been studied for its effects on ecosystems and its role in pollution management. It has been shown to have toxic effects on aquatic organisms and to be persistent in the environment. Therefore, it is important to consider the sustainability and environmental impact of Acid Violet 43 when evaluating its applications. In industrial research, Acid Violet 43 has been used in manufacturing processes to improve product quality and efficiency. However, health and safety considerations must be taken into account when using Acid Violet 43 in industrial applications. |
| Future Perspectives and Challenges | The use and study of Acid Violet 43 face several limitations and challenges, including its potential toxicity, environmental impact, and limited understanding of its mechanism of action. Possible solutions and improvements include the development of safer and more efficient methods of synthesis or extraction, the evaluation of its safety and efficacy in clinical trials, and the investigation of its potential applications in environmental and industrial research. Future trends and prospects in the application of Acid Violet 43 in scientific research include the development of new therapeutic agents and the exploration of its potential as a tool for studying cellular processes. Conclusion: Acid Violet 43 is a synthetic dye that has been studied for its potential therapeutic and environmental applications. The methods of synthesis or extraction, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges of Acid Violet 43 have been discussed in this paper. Further research is needed to evaluate its safety and efficacy in clinical trials and to investigate its potential applications in environmental and industrial research. |
| Other CAS Number | 4430-18-6 |
| Pictograms | Corrosive |
| Shelf Life | >2 years if stored properly |
| SMILES | CC1=CC(=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O)S(=O)(=O)[O-].[Na+] |
| Solubility | Soluble in DMSO |
| Storage | Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
| Synonyms | CI 60730;Violet 43;CI NO 60730;MURASAKI401;SOLWAY PURPLE;EXT. VIOLET 2;ACID VIOLET 43;Acid Violet 3B;EXT.D&CVIOLET2;SOLWAY PURPLE R |
| Reference | 1. Fiume MZ. Final report on the safety assessment of Acid Violet 43. Int J Toxicol. 2001;20 Suppl 3:1-6. PMID: 11766130. 2. Thorén S, Yazar K. Contact allergens in 'natural' hair dyes. Contact Dermatitis. 2016 May;74(5):302-4. doi: 10.1111/cod.12519. PMID: 27040875. 3. Volná K, Holcapek M, Kolárová L, Lemr K, Cáslavský J, Kacer P, Poustka J, Hubálek M. Comparison of negative ion electrospray mass spectra measured by seven tandem mass analyzers towards library formation. Rapid Commun Mass Spectrom. 2008;22(2):101-8. doi: 10.1002/rcm.3334. PMID: 18058959. |
| PubChem Compound | Acid violet 43 |
| Last Modified | May 30 2023 |