6333-33-1

Usage

Uses

Used in Personal Care Products:
Triclosan is used as an antimicrobial agent in personal care products for its ability to inhibit the growth of bacteria and fungi, thereby promoting hygiene and preventing infections.
Used in Household Products:
In household products, triclosan is utilized as a preservative and sanitizing agent to maintain cleanliness and prevent the spread of harmful microorganisms.
Used in Medical Devices:
Triclosan is also employed in the manufacturing of certain medical devices to ensure sterility and reduce the risk of infection during medical procedures.
However, due to concerns regarding its potential negative impact on human health and the environment, there is an ongoing debate about the safety and necessity of triclosan in various products. Regulatory restrictions have been imposed in some regions to mitigate the risks associated with its use.

Upstream product

• 50-00-0 formaldehyd 
• 120-83-2 2,4-dichlorophenol 
• 7647-01-0 hydrogenchloride 
• 6641-02-7 3,5-dichloro-2-hydroxybenzyl alcohol 
• 90-60-8 3,5-dichlorosalicyclaldehyde 

Downstream Products

• 17387-53-0 4,4',6'-trichloro-3,5-dimethyl-2,2'-methanediyl-di-phenol 
• 6641-02-7 3,5-dichloro-2-hydroxybenzyl alcohol 
• 90-60-8 3,5-dichlorosalicyclaldehyde 
• 5419-53-4 4,6,4'-trichloro-2,2'-methanediyl-di-phenol 
• 24299-63-6 <3.5-Dichlor-2-hydroxy-benzyl>-<2-(3-methyl-benzyl)-4.6-dimethyl-phenyl>-sulfon 
• 101792-45-4 1,4-bis-(3,5-dichloro-2-hydroxy-phenylmethanesulfonyl)-butane 
• 51866-26-3 4-chloro-2-(5-chloro-2-hydroxy-benzyl)-6-(3,5-dichloro-2-hydroxy-benzyl)-phenol 
• 108122-97-0 3,5-dimethyl-2,2'-methanediyl-di-phenol 
• 89101-37-1 4,6,4'-trichloro-6'-chloromethyl-2,2'-methanediyl-di-phenol 
• 873414-20-1 6,8-dichloro-2-phenyl-4H-benzo[1,3]dioxin 

Relevant academic research and scientific papers

Modulation of electronic and redox properties in phenolate-rich cobalt(iii) complexes and their implications for catalytic proton reduction

We investigate the redox, spectroscopy and catalytic reactivity of new cobalt(iii) complexes based on phenolate-rich [N2O3] ligands. These complexes are described as [CoIII(LX)MeOH], where X indicates the presence of chloro (1), bromo (2), iodo (3), or tert-butyl (4) substituents in the 3rd and 5th positions of each phenolate ring. These substituents modulate the Co(iii) ← PheO- LMCT bands of the parent complexes with 1 (451) > 2 (453) > 3 (456) > 4 (468 nm) and the redox potentials involved with the Co(iii)/Co(ii) and ligand reduction and with the phenolate/phenoxyl oxidation processes. The influence of the substituents on the phenolate pendant arms was also observed on the kinetic parameters; 1 presented a rate constant of 1.0 × 10-3 s-1 whereas 4 showed a considerably slower rate (5.3 × 10-5 s-1). Species 1 and 4 are electrocatalysts towards proton reduction in the presence of weak acid in acetonitrile. A TON of 10.8 was observed for 1 after 3 h of bulk electrolysis at -2.20 VFc/Fc+ using a mercury pool as the working electrode. This journal is