251920-20-4

Basic information

• Product Name: 2,6-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-tert-butylphenol
• Synonyms: 2,6-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-tert-butylphenol
• CAS NO: 251920-20-4
• Molecular Weight: 502.737
• Mol File: 251920-20-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,6-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-tert-butylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-tert-butylphenol(251920-20-4)
• EPA Substance Registry System: 2,6-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-tert-butylphenol(251920-20-4)

Safety Data

• Hazardous Substances Data: 251920-20-4(Hazardous Substances Data)

Upstream product

• 2409-55-4 2-tert-Butyl-4-methylphenol 
• 2203-14-7 4-tert-butyl-2,5-bis(hydroxymethyl)phenol 

Downstream Products

• 251920-08-8 4-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-2,8-di-tert-butyl-6-diethylamino-10-methyldibenzo[d.g][1.3.2]dioxaphosphocin 
• 478367-23-6 (Nb((CH₃)3CC₆H₂OH(CH₂C₆H₂(CH₃)(C(CH₃)3)O)2)(CH₃CN)Cl₃) 
• 478658-96-7 (Nb((CH₃)3CC₆H₂O(CH₂C₆H₂(CH₃)(C(CH₃)3)O)2)Cl₂)2*C₇H₈ 
• 38916-74-4 2,6-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-tert-butyl-anisole 

Relevant articles and documents

Structure, thermal stability, antioxidant activity and DFT studies of trisphenols and related phenols

Two kinds of trisphenols have been successfully synthesized and their structures were confirmed by IR spectra, 1HNMR, 13CNMR, mass spectra and X-ray diffraction. They exhibited better thermal stability than both monophenol and bisphenols due to their higher molecular weight. Moreover, their antioxidant activities have been investigated in lubricant oil using PDSC and RBOT. The results showed that the o-trisphenol 3b exhibited the best antioxidant activity while the p-trisphenol 3a was the worst. In addition, their relationship between structures and properties has been further explored by a series of DFT calculations including the BDE values, the IP values and the Gibbs free energy barriers for the reaction between phenols and methylperoxyl radicals.