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Octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate
[CAS# 125643-61-0]

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Complete supplier list of Octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate
Identification
Classification Food additive >> Antioxidants
Name Octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate
Synonyms 3,5-Bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoic acid C7-9-branched alkyl esters; Antioxidant 1135; Evernox 1135
Molecular Structure CAS # 125643-61-0, Octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate, 3,5-Bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoic acid C7-9-branched alkyl esters, Antioxidant 1135, Evernox 1135
Molecular Formula C25H42O3
Molecular Weight 390.60
CAS Registry Number 125643-61-0
EC Number 406-040-9
SMILES CCCCCCCCOC(=O)CCC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C
Properties
Solubility 0.0007351 mg/L (25 ºC water)
Density 1.0±0.1 g/cm3, Calc.*
Index of Refraction 1.493, Calc.*
Melting point 178.58 ºC
Boiling Point 444.4±40.0 ºC (760 mmHg), Calc.*, 444.78 ºC
Flash Point 159.2±20.1 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Statements H413    Details
Precautionary Statements P273-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
SDS Available
up Discovory and Applicatios
Octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate, commonly known as Irganox 1076, is a phenolic antioxidant widely used in the polymer industry to prevent the oxidative degradation of plastics and other materials. The discovery of this compound was driven by the need for more effective stabilizers that could extend the lifespan and maintain the properties of polymers exposed to environmental factors such as heat, light, and oxygen.

The synthesis of octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate involves the esterification of 3,5-di-tert-butyl-4-hydroxyhydrocinnamic acid with 2-ethylhexanol. The presence of the bulky tert-butyl groups in the molecule provides steric hindrance, which protects the phenolic hydroxyl group from reacting with free radicals, thus enhancing the compound’s antioxidant properties. The octyl group, derived from 2-ethylhexanol, increases the lipophilicity of the molecule, improving its compatibility with various polymer matrices and ensuring its uniform distribution within the material.

One of the primary applications of octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate is in the stabilization of polyolefins such as polyethylene and polypropylene. These polymers are prone to oxidative degradation, which can lead to discoloration, brittleness, and loss of mechanical properties. By incorporating this antioxidant into the polymer matrix, manufacturers can significantly improve the material's resistance to oxidation, thereby extending its service life and maintaining its aesthetic and mechanical properties over time.

The use of octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate is not limited to polyolefins; it is also effective in other polymers such as polyurethanes, polyamides, and polyesters. In these materials, the antioxidant helps to prevent the degradation that can occur during processing at high temperatures, as well as during the material’s use in end applications. The effectiveness of this compound in various polymer systems makes it a versatile and widely used additive in the plastics industry.

Another significant application of octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate is in the stabilization of lubricants and oils. The compound is used in automotive and industrial lubricants to prevent the oxidation of the base oil, which can lead to the formation of sludge, varnish, and acidic by-products that degrade the performance of the lubricant. By preventing oxidative degradation, this antioxidant helps to maintain the viscosity, color, and overall performance of the lubricant over extended periods of use.

In addition to its antioxidant properties, octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate also provides light stabilization, making it useful in applications where materials are exposed to UV radiation. The combination of light and thermal stability makes this compound particularly valuable in outdoor applications, where materials are subjected to harsh environmental conditions.

Research into octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate continues as scientists explore its potential in new applications and improve its performance in existing ones. The compound’s ability to stabilize a wide range of materials makes it an essential component in the production of high-performance polymers, lubricants, and other materials that require long-term stability and durability.
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