19614-80-3 Usage
Uses
Used in Polymer Industry:
2,2'-dithiobis[4-tert-butylphenol] is used as an antioxidant and stabilizer for polymers to prevent degradation caused by heat, light, and oxygen exposure. Its strong antioxidant properties help maintain the polymer's integrity and extend its shelf life.
Used in Rubber Industry:
In the rubber industry, 2,2'-dithiobis[4-tert-butylphenol] serves as an essential additive to enhance the stability and durability of rubber products. It protects rubber from oxidative degradation, ensuring a longer-lasting and more reliable performance.
Used in Adhesives Industry:
2,2'-dithiobis[4-tert-butylphenol] is used as an antioxidant in adhesive formulations to improve their resistance to degradation and prolong their usability. Its ability to scavenge free radicals helps maintain the adhesive's bonding strength and performance over time.
Used in Lubricants Industry:
As an antioxidant in lubricants, 2,2'-dithiobis[4-tert-butylphenol] plays a crucial role in preventing the oxidation of lubricating oils, which can lead to the formation of sludge and deposits. This helps in maintaining the lubricants' efficiency and extending the life of machinery and equipment.
Check Digit Verification of cas no
The CAS Registry Mumber 19614-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,1 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19614-80:
(7*1)+(6*9)+(5*6)+(4*1)+(3*4)+(2*8)+(1*0)=123
123 % 10 = 3
So 19614-80-3 is a valid CAS Registry Number.
19614-80-3Relevant academic research and scientific papers
REACTION OF p-tert-BUTYLPHENOL AND 2-METHYL-4-tert-BUTYLPHENOL WITH SULFUR MONO- AND DICHLORIDE
Brezhneva, L. I.,Vasilevskaya, T. N.,Andrievskii, V. N.,Maksimov, I. E.
, p. 1723 - 1726 (2007/10/02)
The reaction of p-tert-butylphenol and 2-methyl-4-tert-butylphenol with sulfur monochloride and dichloride leads to the formation of complex mixtures of products, among which bis(2-hydroxy-5-tert-butylphenyl) and bis(2-hydroxy-3-methyl-5-tert-butylphenyl) sulfides and disulfides were identified by liquid chromatography.It was shown that only the reaction of 2-methyl-4-tert-butylphenol with sulfur dichloride leads to the preferential formation of the corresponding phenol sulfide.
