4-tert-butyl-2,6-xylenol

  • Name:4-tert-butyl-2,6-xylenol
  • CAS:879-97-0
  • Purity:99%
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Details

Manufacturer Sells Best Quality 4-tert-butyl-2,6-xylenol 879-97-0 with stock

  • Molecular Formula:C12H18 O
  • Molecular Weight:178.274
  • Vapor Pressure:0.0158mmHg at 25°C 
  • Melting Point:82.4°C 
  • Refractive Index:1.5091 (estimate) 
  • Boiling Point:248°C at 760 mmHg 
  • Flash Point:114.7°C 
  • PSA：20.23000 
  • Density:0.952g/cm3 
  • LogP:3.30650 

4-tert-butyl-2,6-xylenol(Cas 879-97-0) Usage

General Description

4-tert-butyl-2,6-xylenol, also known as TBX, is a chemical compound that is commonly used as an antioxidant and preservative in various personal care and cosmetic products. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. TBX is known for its ability to inhibit the growth of bacteria and fungi, making it a popular ingredient in soaps, lotions, and other skincare products. It is also used in the manufacturing of plastics, rubbers, and adhesives as a stabilizer and antioxidant. However, there have been concerns about its potential harmful effects on human health and the environment, leading to regulatory restrictions in some countries.

InChI:InChI=1/C12H18O/c1-8-6-10(12(3,4)5)7-9(2)11(8)13/h6-7,13H,1-5H3

879-97-0 Relevant articles

Catalytic Activation of Unstrained C(Aryl)-C(Alkyl) Bonds in 2,2′-Methylenediphenols

Dong, Guangbin,Ratchford, Benjamin L.,Xue, Yibin,Zhang, Rui,Zhu, Jun

supporting information, p. 3242 - 3249 (2022/02/23)

Catalytic activation of unstrained and n...

Process preparation method of 4-substituted-2, 6-dimethylphenol

-

Paragraph 0122-0123; 0125, (2019/07/11)

The present invention discloses a proces...

Site-selective Oxidative Dearomatization of Phenols and Naphthols into ortho-Quinols or Epoxy ortho-Quinols using Oxone as the Source of Dimethyldioxirane

Cabrera-Afonso, María J.,Carre?o, M. Carmen,Urbano, Antonio

supporting information, (2019/08/21)

A novel reactivity of dimethyldioxirane,...

Synthesis of phenols and aryl silyl ethers via arylation of complementary hydroxide surrogates

Reitti, Marcus,Gurubrahamam, Ramani,Walther, Melanie,Lindstedt, Erik,Olofsson, Berit

supporting information, p. 1785 - 1788 (2018/04/14)

Two transition-metal-free methods to acc...

879-97-0 Process route

4-tert-butyl-2,5-bis(hydroxymethyl)phenol
2203-14-7

4-tert-butyl-2,5-bis(hydroxymethyl)phenol

2,6-dimethyl-4-tert-butylphenol
879-97-0

2,6-dimethyl-4-tert-butylphenol

Conditions
Conditions Yield
With palladium on activated charcoal; hydrogen; In methanol; water; at 20 ℃; for 48h; Large scale;
96%
tert-butyl(4-(tert-butyl)-2,6-dimethylphenoxy)dimethylsilane

tert-butyl(4-(tert-butyl)-2,6-dimethylphenoxy)dimethylsilane

2,6-dimethyl-4-tert-butylphenol
879-97-0

2,6-dimethyl-4-tert-butylphenol

Conditions
Conditions Yield
With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 - 25 ℃; for 3h;
73%

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