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Phenol, 2,4,6-tris(1,1-dimethylethyl)-, acetate, also known as 2,4,6-tris(tert-butyl)phenol acetate, is a chemical compound derived from phenol. It is characterized by the presence of three tert-butyl groups (1,1-dimethylethyl) attached to the phenol molecule at the 2, 4, and 6 positions. The acetate group is attached to the hydroxyl group of the phenol, forming an ester. Phenol, 2,4,6-tris(1,1-dimethylethyl)-, acetate is often used as an antioxidant and stabilizer in various industrial applications, such as in the production of plastics, rubber, and adhesives, to prevent oxidation and degradation. It is also known for its ability to protect materials from the effects of heat, light, and oxygen, thereby extending their shelf life and performance.

5180-48-3

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5180-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5180-48-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5180-48:
(6*5)+(5*1)+(4*8)+(3*0)+(2*4)+(1*8)=83
83 % 10 = 3
So 5180-48-3 is a valid CAS Registry Number.

5180-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,2,4,6-tritert-butylphenol

1.2 Other means of identification

Product number -
Other names Phenol,2,4,6-tris(1,1-dimethylethyl)-,acetate

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:5180-48-3 SDS

5180-48-3Downstream Products

5180-48-3Relevant academic research and scientific papers

Silica gel-supported phosphotungstic acid (PTA) catalysed acylation of alcohols and phenols with acetic anhydride under mild reaction conditionst

Jin, Tong-Shou,Xiao, Jin-Chong,Wang, Zhen-Hua,Li, Tong-Shuang

, p. 412 - 414 (2007/10/03)

Phosphotungstic acid, which is commercially available, practically and efficiently catalyses the acylation of a series of alcohols and phenols with acetic anhydride at room temperature of at refluxing temperature.

Sterically hindered aromatic compounds. XI. Spectral and product studies of the decomposition of N-nitrosoacetanilides

Barclay, L. Ross C.,Dust, Julian M.

, p. 607 - 615 (2007/10/02)

Decomposition of N-nitroso-2,4,6-tri-tert-butylacetanilide (1) in benzene forms products 2,4,6-tri-tert-butylphenyl acetate (3), 3-(3,5-di-tert-butylphenyl)-2-acetoxy-2-methylpropane (4), and hydrocarbons 3-(3,5-di-tert-butylphenyl)-and 1-(3,5-di-tert-butylphenyl)-2-methylpropene (5 and 6) explained by a reactive aryl cation (2), the rearranged products (4, 5, 6) originating from a 1,5-hydride shift from an ortho tert-butyl group in 2.In contrast, decomposition of 1 in triethylamine forms products 1,3,5-tri-tert-butylbenzene (10), 2,4,6-tri-tert-butylacetanilide (15), and 2-(3,5-di-tert-butylphenyl)-2-methylpropanal oxime (13), expected of a free radical pathway.Electron spin resonance evidence is given for intermediates formed by rearrangement of the 2,4,6-tri-tert-butylphenyl radical and spin trapped by the nitroso group of 1.CIDNP and esr studies on the dediazoniation of N-nitrosoacetanilide and aniline in the presence of tertiary amines support the proposed electron transfer mechanism.The results are briefly discussed in terms of the role of steric effects and electron transfer in the dediazoniation of nitrosoacetanilides and diazonium salts.

SYNTHESIS OF 4-ALKOXY- AND 4-ACYLOXY-2,6-DI-tert-BUTYLPHENOLS AND QUINOL ETHERS BASED ON THEM

Dobronravova, Z. A.,Meshcheryakov, V. I.,Prishchenko, Yu. E.,Gavrilov, L. D.,Vereshchagin, L. I.

, p. 910 - 914 (2007/10/02)

4-Alkoxy- and 4-acyloxy-2,6-di-tert-butylphenols were obtained by the alkylation and acylation of 2,6-di-tert-butyl-p-dihydroxybenzene.With quinone dioximes under oxidizing conditions the products form quinol ethers.

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