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4,4''-THIODI(2,6-DI-TERT-BUTYLPHENOL), also known as 3,3'-Thiodi(2,6-di-tert-butylphenol), is a chemical compound with the molecular formula C28H42OS. It is a white crystalline solid that is widely used as an antioxidant in various industrial applications, particularly in the rubber and plastics industries. 4,4''-THIODI(2,6-DI-TERT-BUTYLPHENOL) is effective in preventing the oxidation of rubber and plastics, thereby extending their lifespan and maintaining their physical properties. It is also known for its thermal stability and low volatility, which makes it suitable for use in high-temperature applications. The compound is characterized by its ability to scavenge free radicals, which are responsible for the degradation of materials over time. Due to its chemical structure, 4,4''-THIODI(2,6-DI-TERT-BUTYLPHENOL) is a powerful antioxidant that helps protect materials from the damaging effects of oxygen and heat.

4673-51-2

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4673-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4673-51-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4673-51:
(6*4)+(5*6)+(4*7)+(3*3)+(2*5)+(1*1)=102
102 % 10 = 2
So 4673-51-2 is a valid CAS Registry Number.

4673-51-2Relevant academic research and scientific papers

Electronic and hydrogen bonding effects on the chain-breaking activity of sulfur-containing phenolic antioxidants

Amorati, Riccardo,Fumo, Maria Grazia,Menichetti, Stefano,Mugnaini, Veronica,Pedulli, Gian Franco

, p. 6325 - 6332 (2007/10/03)

A kinetic and thermodynamic investigation of phenols para-substituted with thiyl (SR), sulfinyl (SOR), and sulfonyl (SO2R) groups and ortho-substituted with thiyl groups is reported. The effect of the sulfur substituents on the O-H bond dissoci

Mechanism of the antioxidative effect of bis(4-hydroxy-3,5-di-tert-butylphenyl) sulfide and polysulfides in cumene oxidation

Farzaliev,Allakhverdiev,Sattar-zade,Rzaeva

, p. 2083 - 2086 (2007/10/03)

Bis(4-hydroxy-3,5-di-tert-butylphenyl) sulfide and polysulfides were prepared, and their inhibiting power was studied in relation to the number of sulfur atoms.

Reaction of Sulfur with 2,6-Di-tert-butylphenol in Dipolar Aprotic Solvenys

Bukharov, S. V.,Konoshenko, L. V.,Solov'eva, S E.,Gainullin, V. I.,Syakaev, V. V.,Mannanov, T. G.,Chugunov, Yu. V.,Samuilov, Ya. D.

, p. 126 - 129 (2007/10/03)

In dipolar aprotic solvents 2,6-di-tert-butylphenol reversibly reacts with elemental sulfur to form a mixture of bis(3,5-di-tert-butyl-4-hydroxyphenyl) polysulfides. The reverse process is initiated by hydrogen sulfide, and removal of the latter from the reaction mixture makes possible the polysulfides to be obtained in nearly quantitative yield.

Oxidative Dehydrogenation of Sterically Hindered para-Substituted Phenols with 3,3′,5,5′-Tetra-tert-butyl-4,4′-diphenoquinone

Mukmeneva,Bukharov,Kadyrova,Zharkova,Gorshunova,Fazlieva

, p. 1486 - 1489 (2007/10/03)

The reactivity of 4-methyl-, 4-mercapto-, and 4-methoxymethyl-2,6-di-tert-butylphenols in oxidative dehydrogenation with 3,3′,5,5′-tetra-tert-butyl-4,4′-diphenoquinone was studied, and the structure of products was determined.

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