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3,5-di-tert-butyl-6-methylcatechol is an organic compound characterized by its molecular formula C14H22O2. It is a derivative of catechol, which is a type of phenol with two hydroxyl groups on adjacent carbon atoms. In this specific compound, the 3 and 5 positions on the benzene ring are substituted with tert-butyl groups, and the 6 position is substituted with a methyl group. This structure endows the compound with antioxidant properties, making it useful in stabilizing materials against oxidative degradation. It is commonly used as an antioxidant in industrial applications, particularly in the rubber and plastics industries, to prevent the breakdown of polymers due to exposure to oxygen and heat. The compound's stability and effectiveness in these applications are attributed to its ability to donate hydrogen atoms to reactive oxygen species, thereby neutralizing them and protecting the material from degradation.

2563-11-3

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2563-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2563-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2563-11:
(6*2)+(5*5)+(4*6)+(3*3)+(2*1)+(1*1)=73
73 % 10 = 3
So 2563-11-3 is a valid CAS Registry Number.

2563-11-3Downstream Products

2563-11-3Relevant academic research and scientific papers

New sterically-hindered catechols/o-benzoquinones. Reduction of 4,6-di-tert-butyl-2,3-dihydroxybenzaldehyde

Arsenyev, Maxim V.,Baranov, Eugene V.,Shurygina, Margarita P.,Chesnokov, Sergey A.,Abakumov, Gleb A.

, p. 552 - 554 (2016)

Reduction of aldehyde group in 4,6-di-tert-butyl-2,3-dihydroxybenzaldehyde leads to methoxymethyl (NaBH4, MeOH) or methyl (Zn, MeOH) analogues, which were further oxidized into the corresponding o-benzoquinones. Their photostability in benzene

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