Home >Organic Chemicals > 2,6-di-tert-butyl-4-(methoxymethyl)phenol

2,6-di-tert-butyl-4-(methoxymethyl)phenol
  • Chemical Name: 2,6-di-tert-butyl-4-(methoxymethyl)phenol
  • CAS No.: 87-97-8

Good factory exports good 2,6-di-tert-butyl-4-(methoxymethyl)phenol 87-97-8

  • Molecular Formula: C16H26 O2
  • Molecular Weight: 250.381
  • Vapor Pressure: 0.00154mmHg at 25°C 
  • Melting Point: 101 °C 
  • Refractive Index: 1.6000 (estimate) 
  • Boiling Point: 286.3°C at 760 mmHg 
  • PKA: 11.17±0.70(Predicted) 
  • Flash Point: 90.9°C 
  • PSA: 29.46000 
  • Density: 0.961g/cm3 
  • LogP: 4.13360 

2,6-di-tert-butyl-4-(methoxymethyl)phenol(Cas 87-97-8) Usage

General Description

2,6-di-tert-butyl-4-(methoxymethyl)phenol is a type of organic compound having intricate chemical structure that falls under the category of phenolic antioxidants. These are widely used to prevent oxidation in substances such as plastics, rubber, and petroleum products. The general constitutional formula of this chemical consists of aromatic phenol unit which is modified by 2,6-di-tert-butyl groups and a methoxymethyl substituted at the 4th position. Although it's less common than some similar chemicals, its primary usage lies in the protection of industrial materials from oxidative damage. This chemical is not usually encountered outside of industrial settings and should be handled with care. Its properties, nomenclature and usage may significantly vary between scientific disciplines and commercial applications.

InChI:InChI=1/C16H26O2/c1-15(2,3)12-8-11(10-18-7)9-13(14(12)17)16(4,5)6/h8-9,17H,10H2,1-7H3

87-97-8 Relevant articles

Bifunctional compound and synthesis method thereof, and applications of bifunctional compound as antioxidant

-

Page/Page column 10-16, (2020/02/14)

The invention discloses a bifunctional c...

Highly selective conversion of guaiacol to: Tert -butylphenols in supercritical ethanol over a H2WO4 catalyst

Mai, Fuhang,Cui, Kai,Wen, Zhe,Wu, Kai,Yan, Fei,Chen, Mengmeng,Chen, Hong,Li, Yongdan

, p. 2764 - 2771 (2019/02/01)

The conversion of guaiacol is examined a...

Novel method for synthesizing antioxidant 330 by catalyst

-

Page/Page column 8-11; 17, (2018/09/28)

The invention aims at providing a method...

Antiradical activity of benzazole-2-thiones

Gataullina,Mogilevtseva,Nugumanova,Bukharov,Tagasheva,Deberdeev, R. Ya.

, p. 1919 - 1923 (2017/10/27)

Reaction of benzoxazole-2-thione with 3,...

87-97-8 Process route

3,3',5,5'-tetra-tert-butyl-1,1'-dimethyl-[1,1'-bi(cyclohexane)]-2,2',5,5'-tetraene-4,4'-dione
131544-10-0

3,3',5,5'-tetra-tert-butyl-1,1'-dimethyl-[1,1'-bi(cyclohexane)]-2,2',5,5'-tetraene-4,4'-dione

2,6-di-tert-butyl-4-methoxymethylene-phenol
87-97-8

2,6-di-tert-butyl-4-methoxymethylene-phenol

2,6-di-tert-butyl-4-methyl-phenol
128-37-0

2,6-di-tert-butyl-4-methyl-phenol

2,6-di-tert-butyl-4-methylene-2,5-cyclohexadien-1-one
2607-52-5

2,6-di-tert-butyl-4-methylene-2,5-cyclohexadien-1-one

4-methoxy-4-methyl-2,6-ditert-butylcyclohexa-2,5-dienone
2411-18-9

4-methoxy-4-methyl-2,6-ditert-butylcyclohexa-2,5-dienone

Conditions
Conditions Yield
With methanol; trifluorormethanesulfonic acid; at 30 ℃; for 0.35h;
methanol
67-56-1

methanol

formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

2,6-di-tert-butylphenol
128-39-2

2,6-di-tert-butylphenol

2,6-di-tert-butyl-4-methoxymethylene-phenol
87-97-8

2,6-di-tert-butyl-4-methoxymethylene-phenol

Conditions
Conditions Yield
With potassium hydroxide;
95%
With potassium hydroxide;
95%
With piperazine; ethylenediamine; at 135 ℃; for 3h;
84%
With potassium hydroxide; In water; for 0.5h; Inert atmosphere; Reflux;
5.01 g

87-97-8 Upstream products

  • 50-00-0
    50-00-0

    formaldehyd

  • 128-39-2
    128-39-2

    2,6-di-tert-butylphenol

  • 2091-51-2
    2091-51-2

    4-(bromomethyl)-2,6-di-tert-butylphenol

  • 1620-98-0
    1620-98-0

    3,5-di-t-butyl-4-hydroxybenzaldehyde

87-97-8 Downstream products

  • 1620-98-0
    1620-98-0

    3,5-di-t-butyl-4-hydroxybenzaldehyde

  • 1070-83-3
    1070-83-3

    tert-Butylacetic acid

  • 20357-48-6
    20357-48-6

    2,6-di-tert-butyl-4-(methoxymethylene)cyclohexa-2,5-dienone

  • 980-17-6
    980-17-6

    diisopropyl (3,5-di-tert-butyl-4-hydroxybenzyl)phosphonate