60834-77-7 Usage
Uses
Used in Personal Care Products:
2,6-diisopropyl-3,5-xylenol is used as an antibacterial agent in personal care products such as soaps, toothpaste, and cosmetics. Its antimicrobial properties help to reduce the growth of bacteria and prevent infections.
Used in Household Products:
Triclosan is used as a preservative and antibacterial agent in household products, including cutting boards and kitchen utensils. It helps to maintain cleanliness and prevent the spread of bacteria in these items.
Used in Healthcare Settings:
Historically, 2,6-diisopropyl-3,5-xylenol has been used as an antimicrobial agent in healthcare settings to prevent the spread of infections and maintain a hygienic environment. However, due to concerns about its potential negative effects, its use in healthcare is being reevaluated.
Despite its antimicrobial properties, the potential risks associated with triclosan have prompted efforts to find safer alternatives in consumer products. Studies have linked triclosan to hormone disruption, antibiotic resistance, and environmental toxicity, which has led to its ban in some countries and a push for reduced use in others. As a result, there is a growing demand for safer and more eco-friendly alternatives to triclosan in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 60834-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,3 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60834-77:
(7*6)+(6*0)+(5*8)+(4*3)+(3*4)+(2*7)+(1*7)=127
127 % 10 = 7
So 60834-77-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O/c1-8(2)12-10(5)7-11(6)13(9(3)4)14(12)15/h7-9,15H,1-6H3
60834-77-7Relevant academic research and scientific papers
Synthesis, Biological Evaluation, and Preliminary Structure-Activity Considerations of a Series of Alkylphenols as Intravenous Anesthetic Agents
James, Roger,Glen, John B.
, p. 1350 - 1357 (2007/10/02)
Following our discovery of the intravenous (iv) anesthetic activity of 2,6-diethylphenol in mice, a series of alkylphenols was examined in this species and the most active analogues were further evaluated in rabbits.The synthesis of compounds which were not commercially available was accomplished by adaptations of standard ortho-alkylation procedures for phenols.Structure-activity relationships were found to be complex, but, in general, potency and kinetics appeared to be a function of both the lipophilic character and the degree of steric hindrance exerted by ortho substituents.The most interesting compounds were found in the 2,6-dialkyl series, and the greatest potency was associated with 2,6-di-sec-alkyl substitution.In particular, 2,6-diisopropylphenol (ICI 35868) emerged as a candidate for further development and has subsequently been shown to be an effective iv anesthetic agent in man.
