Product Details
Factory Supply Industrial Grade 4-octylpyrocatechol 7580-46-3 with Best Price
- Molecular Formula: C14H22 O2
- Molecular Weight: 222.327
- Vapor Pressure: 1.28E-05mmHg at 25°C
- Melting Point: 40 °C
- Boiling Point: 357.9°C at 760 mmHg
- PKA: 9.91±0.10(Predicted)
- Flash Point: 165.4°C
- PSA： 40.46000
- Density: 1.019g/cm3
- LogP: 4.00080
4-octylpyrocatechol(Cas 7580-46-3) Usage
|
General Description |
4-octylpyrocatechol, also known as 4-OPC, is a chemical compound that belongs to the family of pyrocatechols. It is a phenolic antioxidant that is commonly used in the rubber industry as a stabilizer against degradation from heat, oxygen, and flexing. 4-OPC is also used as a stabilizer for adhesives, coatings, and plastics to prevent color change and degradation. In addition, it has been found to have potential applications in the medical field, such as in anti-inflammatory and anti-cancer treatments. The chemical structure of 4-octylpyrocatechol allows for its highly efficient free-radical scavenging properties, making it an important compound for various industrial and medical applications. |
InChI:InChI=1/C14H22O2/c1-2-3-4-5-6-7-8-12-9-10-13(15)14(16)11-12/h9-11,15-16H,2-8H2,1H3
7580-46-3 Relevant articles
A template-free approach to nanotube-decorated polymer surfaces using 3,4-phenylenedioxythiophene (PhEDOT) monomers
Szczepanski, Caroline R.,M'Jid, Inès,Darmanin, Thierry,Godeau, Guilhem,Guittard, Frédéric
, p. 17308 - 17323 (2016/11/18)
In this work, novel 3,4-phenylenedioxyth...
The synthesis, structure and activity evaluation of pyrogallol and catechol derivatives as Helicobacter pylori urease inhibitors
Xiao, Zhu-Ping,Ma, Tao-Wu,Fu, Wei-Chang,Peng, Xiao-Chun,Zhang, Ai-Hua,Zhu, Hai-Liang
experimental part, p. 5064 - 5070 (2010/12/24)
Some pyrogallol and catechol derivatives...
Conception, characterization and correlation of new marine odorants
Kraft, Philip,Eichenberger, Walter
, p. 3735 - 3743 (2007/10/03)
Via a synthetic sequence consisting of P...
Quantitative structure-activity relationship of catechol derivatives inhibiting 5-lipoxygenase
Naito,Sugiura,Yamaura,Fukaya,Yokoyama,Nakagawa,Ikeda,Senda,Fujita
, p. 1736 - 1745 (2007/10/02)
Various catechol derivatives (β-substitu...
7580-46-3 Process route
-
-
93154-30-4
1,2-dimethoxy-4-octyl-benzene
-
-
7580-46-3
4-n-Octylcatechol
| Conditions | Yield |
|---|---|
|
With
boron tribromide;
In
dichloromethane;
at 20 ℃;
for 3h;
|
83%
|
|
With
trimethylsilyl iodide;
In
acetonitrile;
at 20 ℃;
for 60h;
|
68%
|
-
-
118198-70-2
1-(3,4-Dihydroxyphenyl)-n-octanol
-
-
7580-46-3
4-n-Octylcatechol
| Conditions | Yield |
|---|---|
|
With
hydrogen;
palladium on activated charcoal;
In
ethanol;
for 2h;
Ambient temperature;
five drops 12N HCl;
|
80%
|
7580-46-3 Upstream products
-
118198-70-2
1-(3,4-Dihydroxyphenyl)-n-octanol
-
93154-30-4
1,2-dimethoxy-4-octyl-benzene
-
91-16-7
1,2-dimethoxybenzene
-
124-07-2
Octanoic acid