Home >Organic Chemicals > 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
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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
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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
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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
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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
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87-97-8
2,6-di-tert-butyl-4-methoxymethylene-phenol
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128-37-0
2,6-di-tert-butyl-4-methyl-phenol
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2607-52-5
2,6-di-tert-butyl-4-methylene-2,5-cyclohexadien-1-one
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2411-18-9
4-methoxy-4-methyl-2,6-ditert-butylcyclohexa-2,5-dienone
| Conditions | Yield |
|---|---|
|
With
methanol; trifluorormethanesulfonic acid;
at 30 ℃;
for 0.35h;
|
-
-
67-56-1
methanol
-
-
50-00-0,30525-89-4,61233-19-0
formaldehyd
-
-
128-39-2
2,6-di-tert-butylphenol
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-
87-97-8
2,6-di-tert-butyl-4-methoxymethylene-phenol
| 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
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50-00-0
formaldehyd
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128-39-2
2,6-di-tert-butylphenol
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2091-51-2
4-(bromomethyl)-2,6-di-tert-butylphenol
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1620-98-0
3,5-di-t-butyl-4-hydroxybenzaldehyde
87-97-8 Downstream products
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1620-98-0
3,5-di-t-butyl-4-hydroxybenzaldehyde
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1070-83-3
tert-Butylacetic acid
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20357-48-6
2,6-di-tert-butyl-4-(methoxymethylene)cyclohexa-2,5-dienone
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980-17-6
diisopropyl (3,5-di-tert-butyl-4-hydroxybenzyl)phosphonate