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CAS:2219-82-1 | 2-tert-Butyl-6-methylphenol

CAS:2219-82-1 | 2-tert-Butyl-6-methylphenol

Molecular Formula:C11H16O
Molecular Weight:164.24
EINECS:218-734-7
Package:500g 5kg 10kg
Worldwide Delivery
Made in China

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Product Introduction

Introduction of CAS:2219-82-1 | 2-tert-Butyl-6-methylphenol

 

2-tert-Butyl-6-methylphenol (2-TBM) is a phenolic compound found in many commercial products, including paints, coatings, and adhesives. It is a highly versatile compound with a wide range of applications in the scientific community. In the laboratory, 2-TBM can be used as a reagent, catalyst, or intermediate in organic synthesis.It can be used in organic chemical and pharmaceutical intermediates, natural and synthetic rubber, polyolefin plastics, adhesives, petroleum lubricants and carbon black have a synergistic effect on the production of antioxidants and ultraviolet absorbers.

 

Specification of CAS:2219-82-1 | 2-tert-Butyl-6-methylphenol

 

ITEMS

SPECIFICATION

Boiling point

230 °C (lit.)

Melt point

24-27 °C (lit.)

Density

0.967 g/mL at 25 °C (lit.)

Refractive index

n20/D 1.519(lit.)

PSA

20.23000

LogP

2.99810

Form

Powder to block to clear liquid

Color

White to yellow to orange

Storage condition

Keep in dark place,Inert atmosphere,Room temperature

 

Research Application of CAS:2219-82-1 | 2-tert-Butyl-6-methylphenol

 

Industrial Applications

In addition to its scientific research applications, it's important to note that related compounds, such as 2,6-di-tert-butyl-4-methylphenol, are used as antioxidants in various industrial applications. These include usage in cosmetics, vitamins, pharmaceuticals, rubber, oils, and fats, as well as a fuel additive in the petroleum industry and in hydraulic fluids, turbine and gear oils, and jet fuels​​.

 

Synthesis of Biologically Active Compounds

2-tert-Butyl-6-methylphenol serves as an intermediate in the synthesis of biologically active compounds. This is achieved through specific synthesis methods, such as the methylation of 2-tert-butylphenol in alkaline mediums, leading to the formation of compounds with biological activity​.

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