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Phenol, 3,5-bis(1,1-dimethylethyl)-, acetate, also known as 3,5-di-tert-butylphenol acetate, is a chemical compound with the molecular formula C16H24O2. It is a derivative of phenol, where two tert-butyl groups are attached to the 3 and 5 positions of the phenol ring, and an acetate group is attached to the hydroxyl group. Phenol, 3,5-bis(1,1-dimethylethyl)-, acetate is a white crystalline solid with a melting point of approximately 70°C. It is commonly used as an antioxidant in various industrial applications, such as in the stabilization of polymers and plastics, as well as in the production of lubricants and fuels. Due to its antioxidant properties, it helps prevent the oxidation and degradation of materials, thereby extending their shelf life and improving their performance.

5723-95-5

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5723-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5723-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5723-95:
(6*5)+(5*7)+(4*2)+(3*3)+(2*9)+(1*5)=105
105 % 10 = 5
So 5723-95-5 is a valid CAS Registry Number.

5723-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Essigsaeure-(3,5-di-tert.-butyl-phenylester)

1.2 Other means of identification

Product number -
Other names -

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:5723-95-5 SDS

5723-95-5Downstream Products

5723-95-5Relevant academic research and scientific papers

Secondary isotope effects on the deslipping reaction of rotaxanes: High-precision measurement of steric size

Felder, Thorsten,Schalley, Christoph A.

, p. 2258 - 2260 (2007/10/03)

A supramolecular measuring instrument for determining steric size: The deslipping reaction of the rotaxane shown with deuterated stopper groups senses the smaller steric size of the deuterium atom and proceeds with a 10% higher reaction rate than the reaction of the unlabeled rotaxane. This result sheds new light from a supramolecular point of view on the classical problem of determining steric demand.

Solid state acetylation with acetylimidazole: Selective protection of primary alcohols and phenols

Hagiwara, Hisahiro,Morohashi, Kimie,Suzuki, Toshio,Ando, Masayoshi,Yamamoto, Isao,Kato, Michiharu

, p. 2001 - 2006 (2007/10/03)

Primary alcohols and phenols have been acetylated with acetylimidazole by the solid state reaction, grinding both substrates with a pestle in a mortar.

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