Triphenylmethane (CAS 519-73-3)
QUICK LINKS
Triphenylmethane, a versatile chemical compound, finds application in synthesizing various organic compounds. Notably, it has proven effective in treating biological wastewater, serving as a means to eliminate metal ions from water sources. This compound′s bactericidal properties are significant, and it displays an intriguing ability to interact with metal ions, like copper and zinc, resulting in the formation of metal chelates. Investigating its interaction with metal hydroxides, scientists have delved into the subject, employing Langmuir and Freundlich adsorption models. Impressively, triphenylmethane showcases reactivity across a spectrum of metals, encompassing copper, zinc, lead, mercury, silver, gold, and platinum. It′s worth noting that this compound bears some degree of toxicity for both animals and humans upon oral ingestion or inhalation. In addition to its direct applications, triphenylmethane plays a pivotal role in the synthesis of diverse organic compounds. Its significance extends to serving as a biological solution for wastewater treatment, thanks to its metal ion extraction prowess.
Triphenylmethane (CAS 519-73-3) References
- Glucocorticoid receptor antagonists. | Clark, RD. 2008. Curr Top Med Chem. 8: 813-38. PMID: 18537690
- Triphenylmethane dye activation of beta-arrestin. | Barak, LS., et al. 2013. Biochemistry. 52: 5403-14. PMID: 23865508
- Mechanism of triphenylmethane Cresol Red degradation by Trichoderma harzianum M06. | Nor, NM., et al. 2015. Bioprocess Biosyst Eng. 38: 2167-75. PMID: 26275435
- Biodegradation of triphenylmethane dye crystal violet by Cedecea davisae. | Cao, DJ., et al. 2019. Spectrochim Acta A Mol Biomol Spectrosc. 210: 9-13. PMID: 30419454
- The triphenylmethane dye brilliant blue G is only moderately effective at inhibiting amyloid formation by human amylin or at disaggregating amylin amyloid fibrils, but interferes with amyloid assays; Implications for inhibitor design. | Akter, R., et al. 2019. PLoS One. 14: e0219130. PMID: 31404073
- Preparation of MgTi2O5 nanoparticles for sonophotocatalytic degradation of triphenylmethane dyes. | Selvamani, T., et al. 2021. Ultrason Sonochem. 75: 105585. PMID: 34087757
- Ultrafast Excited State Relaxation Dynamics of New Fuchsine- a Triphenylmethane Derivative Dye. | Biswas, C., et al. 2021. Chemphyschem. 22: 2562-2572. PMID: 34528749
- A novel co-catalyzed system between persulfate and chlorite by sonolysis for removing triphenylmethane derivative. | Xu, Q., et al. 2022. J Environ Sci (China). 112: 291-306. PMID: 34955213
- Light-driven bio-decolorization of triphenylmethane dyes by a Clostridium thermocellum-CdS biohybrid. | Wang, H., et al. 2022. J Hazard Mater. 431: 128596. PMID: 35248959
- Removal of triphenylmethane dyes by Streptomyces bacillaris: A study on decolorization, enzymatic reactions and toxicity of treated dye solutions. | Adenan, NH., et al. 2022. J Environ Manage. 318: 115520. PMID: 35717698
- Triphenylmethane dye (C52H54N4O12) is potentially a hazardous substance in edible freshwater fish at trace level: toxicity, hematology, biochemistry, antioxidants, and molecular docking evaluation study. | Poopal, RK., et al. 2023. Environ Sci Pollut Res Int. 30: 28759-28779. PMID: 36401692
- A review of the genotoxicity of food, drug and cosmetic colours and other azo, triphenylmethane and xanthene dyes. | Combes, RD. and Haveland-Smith, RB. 1982. Mutat Res. 98: 101-248. PMID: 7043261
- Biodegradation of triphenylmethane dyes. | Azmi, W., et al. 1998. Enzyme Microb Technol. 22: 185-91. PMID: 9463944
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Triphenylmethane, 25 g | sc-251378 | 25 g | $24.00 |