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2,6-Di-tert-butyl-4-ethoxymethyl-phenol, also known as Ethyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate or Ionol, is a synthetic organic compound that belongs to the class of phenolic antioxidants. It is widely used as an antioxidant and stabilizer in various industrial applications, including the stabilization of polymers, lubricants, and fuels. 2,6-DI-TERT-BUTYL-4-ETHOXYMETHYL-PHENOL is characterized by its ability to prevent the oxidation of materials, thereby extending their shelf life and improving their performance. It is particularly effective in protecting against the harmful effects of heat, light, and oxygen, which can cause degradation in materials over time. The chemical structure of 2,6-Di-tert-butyl-4-ethoxymethyl-phenol features a phenol core with two tert-butyl groups at the 2 and 6 positions, an ethoxymethyl group at the 4 position, and an ester linkage, which contributes to its antioxidant properties.

3080-84-0

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3080-84-0 Usage

Molecular weight

278.43 g/mol The mass of one mole of 2,6-Di-tert-butyl-4-ethoxymethyl-phenol.

Organic compound

A compound containing carbon atoms In this case, 2,6-Di-tert-butyl-4-ethoxymethyl-phenol is an organic compound.

Phenolic antioxidant

A type of antioxidant that contains a phenol group This chemical is a phenolic antioxidant, which helps prevent the degradation of materials.

Stabilizer in polymers and plastics

Prevents degradation from heat, oxygen, and light It is used to maintain the integrity and performance of polymer-based materials.

Inhibits oxidation of polymer

Helps to extend the usable lifespan of materials By inhibiting oxidation, it improves the durability and resistance of the materials.

Used in production of rubber, adhesives, and coatings

Enhances durability and resistance to environmental conditions The chemical is utilized in various industrial applications to improve the performance of materials.

Important additive

Preserves the integrity and performance of polymer-based materials 2,6-Di-tert-butyl-4-ethoxymethyl-phenol is a crucial component in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3080-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3080-84:
(6*3)+(5*0)+(4*8)+(3*0)+(2*8)+(1*4)=70
70 % 10 = 0
So 3080-84-0 is a valid CAS Registry Number.

3080-84-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-(ethoxymethyl)phenol

1.2 Other means of identification

Product number -
Other names Phenol,2,6-bis(1,1-dimethylethyl)-4-(ethoxymethyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3080-84-0 SDS

3080-84-0Relevant academic research and scientific papers

Reaction of 2,6-di-tert-butyl-4-hydroxymethylphenol with dodecaneselenolate and sodium selenide

Yagunov,Kholshin,Kandalintseva,Prosenko

, (2021)

Synthesis of 2,6-di-tert-butyl-4-(dodecylselanylmethyl)phenol and bis(3,5-di-tert-butyl-4-hydroxybenzyl) selenide by the reaction of 2,6-di-tert-butyl-4-hydroxymethylphenol with dodecaneselenolate and sodium selenide was developed.

The Oxidation of 2,4,6-Trimethylphenol with Molecular Oxygen Catalyzed by a Copper(II)-Oxime or Copper(II)-Amine System

Shimizu, Masao,Watanabe, Yoshihito,Orita, Hideo,Hayakawa, Takashi,Takehira, Katsuomi

, p. 251 - 257 (2007/10/02)

2,4,6-Trimethylphenol (1a) was selectively oxidized to 3,5-dimethyl-4-hydroxybenzaldehyde (2a) by molecular oxygen in the presence of a copper(II) chloride-oxime or copper(II) chloride-amine catalyst in alcohol at ambient temperature.When an acid was present in the catalyst system, the formation of both 2,6-dimethyl-p-benzoquinone (3) and a formaldehyde dialkyl acetal was accelerated.It is likely that 2a is produced by way of the formation of a quinonemethide intermediate, followed by a repeated 1,6-addition of alcohol on the intermediate to form a 4-(alkoxymethyl)-2,6-dimethylphenol (5a), and then 3,5-dimethyl-4-hydroxybenzaldehyde dialkyl acetal, which would be hydrolyzed to 2a.When the reaction time was shortened, 5a was isolated in good yield.Oxidations of the other p-methyl-substituted phenols were also examined using the present oxidation system.

A Facile Synthesis of 4-Alkoxymethylphenols by a Copper(II)-Acetoxime Catalyst/O2 System

Shimizu, Masao,Watanabe, Yoshihito,Orita, Hideo,Hayakawa, Takashi,Takehira, Katsuomi

, p. 2053 - 2056 (2007/10/02)

4-Alkoxymethyl-2,6-dimethylphenols were synthesized from 2,4,6-trimethylphenol in good yields by a copper(II) chloride-acetoxime catalyst/molecular oxygen system in alcohols at ambient temperature.The oxidation of the other p-methylsubstituted phenols were also examined.

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