22247-58-1

Usage

Uses

Used in Coatings Industry:
2,2'-Methylenebis[4-methyl-6-(hydroxymethyl)phenol] is used as a key component in the formulation of coatings for its ability to enhance the chemical and heat resistance of the final product, ensuring durability and performance in various applications.
Used in Adhesives Industry:
In the adhesives industry, 2,2'-Methylenebis[4-methyl-6-(hydroxymethyl)phenol] serves as a critical ingredient for developing high-strength adhesives that can withstand harsh conditions, making them suitable for a wide range of bonding applications.
Used in Composites Industry:
2,2'-Methylenebis[4-methyl-6-(hydroxymethyl)phenol] is utilized as a building block in the production of composite materials, contributing to their exceptional strength and resistance to chemical and thermal stress, which is vital for applications in aerospace, automotive, and construction sectors.
However, it is important to note that there are concerns regarding the potential toxicity and environmental impact of 2,2'-Methylenebis[4-methyl-6-(hydroxymethyl)phenol]. As a result, its use is subject to increased scrutiny and regulation to ensure safety and sustainability.

Upstream product

• 50-00-0 formaldehyd 
• 3236-63-3 2,2'-methylenebis(4-methylphenol) 
• 106-44-5 p-cresol 
• 56-23-5 tetrachloromethane 
• 7726-95-6 bromine 
• 64-19-7 acetic acid 
• 613-84-3 2-hydroxy-5-methylbenzaldehyde 
• 4383-07-7 2-hydroxymethyl-4-methylphenol 
• 80678-92-8 3-(5-methylsalicyl)-5-methylsalicyl alcohol 
• 56418-90-7 2,2'-dihydroxy-5,5'-dimethyl-3,3'-methanediyl-di-benzoic acid 
• 91-04-3 2,6-bis(hydroxymethyl)-4-methylphenol 

Downstream Products

• 20837-68-7 6,6′-methylenebis(2-(2-hydroxy-5-methylbenzyl)-4-methylphenol) 
• 53589-22-3 bis-[2-hydroxy-3-(2-hydroxy-3,5-dimethyl-benzyl)-5-methyl-phenyl]-methane 
• 252062-98-9 2-(chloromethyl)-6-[[3-(chloromethyl)-2-hydroxy-5-methyl-phenyl]methyl]-4-methylphenol 
• 129758-73-2 6,6'-bis(bromomethyl)-4,4'-dimethyl-2,2'-methanediyldiphenol 
• 65909-98-0 methylenebis-2,2'-(6-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-4-methyl)phenol 
• 502545-54-2 2,2′-methylenebis(4-methyl-6-formylphenol) 
• 332417-55-7 p-methyl-N-benzyl-tetrahomodiazacalix[4]arene 
• 50-00-0 formaldehyd 
• 7732-18-5 water 
• 1234880-15-9 C₁₉H₂₄O₄ 
• 53666-97-0 bis-[2-acetoxy-3-(2-acetoxy-3,5-dimethyl-benzyl)-5-methyl-phenyl]-methane 
• 250352-83-1 bis{3-[2-(5,5-dimethyl-1,3,2-dioxaphosphorinan-2-yloxy)-5-methylbenzyl]-2-(5,5-dimethyl-1,3,2-dioxaphosphorinan-2-yloxy)-5-methylphenyl}methane 
• 250352-76-2 bis{3-[2-(4-methyl-1,3,2-dioxaphosphorinan-2-yloxy)-5-methylbenzyl]-2-(4-methyl-1,3,2-dioxaphosphorinan-2-yloxy)-5-methylphenyl}methane 

Relevant academic research and scientific papers

Synthesis of Monofunctionalized Calix[5]arenes

Seven OH-free and O -permethylated monofunctionalized calix[5]arenes carrying either additional methyl or tert -butyl groups are prepared following fragment condensation protocols. This strategy proves to be superior to previous approaches. Calix[5]arenes with free OH groups all adopt a cone conformation stabilized by a seam of hydrogen bonds at the lower rim. Post-condensation modifications, i.e., methylation of phenolic OH groups or functional group interconversions can also be achieved. Bulky tert -butyl groups are also found to stabilize the cone conformations of O -methylated compounds. These compounds offer versatile functional groups that make these concave molecules interesting building blocks for the synthesis of more sophisticated molecular architectures.

Amino group containing phenol derivative

An object of the present invention is to provide a material which resolves the drawbacks associated with polyimide polymers, and yet retains the advantages offered by conventional polyimide polymers. ???An amino group containing phenol derivative of the p

Positive resist composition and photosensitizers

A positive photoresist compositions comprising, as a photosensitizer, a quinonediazide sulfonic acid ester of a phenol compound represented by the following formula (I): STR1 wherein Q1, Q2, Q3, Q4, Q5/sup

Synthesis and binding behavior of an artificial receptor based on 'upper rim' functionalized calix[5]arene

A new calix[5]arene possessing two benzoic acid moieties was synthesized as an artificial receptor and its ability of binding to a variety of amine guests was investigated. The structures of the complexes with the mines were proposed by the molecular mechanics calculation using MacroModel V. 4.0.