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2-(3,5-di-tert-butyl-4-hydroxybenzylamino)ethanol is a complex organic compound with the molecular formula C18H31NO2. It is a derivative of ethanol, featuring a hydroxyl group (-OH) and an amino group (-NH2) attached to a benzene ring. The benzene ring is substituted with two tert-butyl groups (C4H9) at the 3rd and 5th positions, and a hydroxyl group at the 4th position. 2-(3,5-di-tert-butyl-4-hydroxybenzylamino)ethanol is known for its antioxidant properties and is commonly used as a stabilizer in various industrial applications, such as in the production of polymers and plastics, to prevent degradation caused by oxidation. Its unique structure provides it with the ability to scavenge free radicals, thereby protecting materials from oxidative damage.

792-40-5

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792-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 792-40-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 792-40:
(5*7)+(4*9)+(3*2)+(2*4)+(1*0)=85
85 % 10 = 5
So 792-40-5 is a valid CAS Registry Number.

792-40-5Downstream Products

792-40-5Relevant academic research and scientific papers

Synthesis of nitrogen-containing metal dithiophosphates

Markova,Mamedov,Rafieva,Dzhanibekov

body text, p. 256 - 260 (2012/08/08)

Problems associated with synthesis of metal complexes and salts of dithiophosphates containing phosphorus, sulfur, and nitrogen heteroatoms and a sterically hindered hydroxy group in their molecule are considered. Pleiades Publishing, Ltd., 2012.

Reaction of 3,5-Di-tert-butyl-4-hydroxybenzyl Acetate with Amines

Bukharov,Nugumanova,Mukmeneva

, p. 1605 - 1608 (2007/10/03)

3,5-Di-tert-butyl-4-hydroxybenzyl acetate reacts with primary and secondary amines to give mainly the corresponding benzylamines. Base-catalyzed transformation of 3,5-di-tert-butyl-4-hydroxybenzyl acetate into 2,6-di-tert-butyl-4-methylene-2,5-cyclohexadienone occurs to a small extent. The major product of the reaction of 3,5-di-tert-butyl-4-hydroxybenzyl acetate with aqueous ammonia is bis(3,5-di-tert-butyl-4-hydroxybenzyl) ether which is formed by the action of ammonium acetate liberated during the process.

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