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Phenol, 2,2'-ethylidenebis[6-(1,1-dimethylethyl)-4-methyl-], also known as Bisphenol A (BPA), is an organic compound with the chemical formula C15H16O2. It is a white crystalline solid that is widely used in the production of polycarbonate plastics and epoxy resins. BPA is found in various consumer products, such as food and beverage containers, dental sealants, and thermal receipt paper. However, it has been a subject of concern due to its potential endocrine-disrupting properties and health risks associated with long-term exposure, particularly affecting the development and function of the brain, immune system, and reproductive system. As a result, many countries have restricted or banned the use of BPA in certain products, especially those that come into direct contact with food and beverages.

4773-40-4

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4773-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4773-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,7 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4773-40:
(6*4)+(5*7)+(4*7)+(3*3)+(2*4)+(1*0)=104
104 % 10 = 4
So 4773-40-4 is a valid CAS Registry Number.

4773-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butyl-6-[1-(3-tert-butyl-2-hydroxy-5-methylphenyl)ethyl]-4-methylphenol

1.2 Other means of identification

Product number -
Other names 6,6'-Di-tert-butyl-4,4'-dimethyl-2,2'-aethyliden-di-phenol

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:4773-40-4 SDS

4773-40-4Downstream Products

4773-40-4Relevant academic research and scientific papers

Production of bisphenol monoester

-

, (2008/06/13)

A bisphenol monoester represented by the formula (I): STR1 wherein R1 is hydrogen or alkyl, R2 and R3 are each alkyl, and R4 is alkyl, alkenyl or phenyl, is produced by continuous two step reactions in which an aldehyde R1 -CHO and 2,4-dialkylphenol are subjected to a condensation reaction in a C6 -C10 aliphatic or C6 -C12 aromatic hydrocarbon solvent, and then a resulting bisphenol compound dissolved in the solvent is subjected to an esterification with a carboxylic acid R4 --COOH or its derivative. Prior to the esterification, the organic layer containing the bisphenol compound is subjected to a dehydration treatment, thereby enabling the two steps to proceed continuously without isolating the intermediate bisphenol compound. A purification process for the bisphenol monoester of the formula (I) is also disclosed in which the monoester is purified from a mixed solvent comprising a C6 -C12 aromatic hydrocarbon solvent and a C1 -C8 alcohol or C2 -C3 aliphatic nitrile solvent.

Method for preparing sterically hindered bis- or polyphenols

-

, (2008/06/13)

A method for preparing sterically hindered bis- or polyphenols of the formula: STR1 wherein R' is hydrogen, a C1 -C4 alkyl; R" and R"' the same or different and are each: STR2 wherein R is a tertiary C4 -C8 alkyl, R1 and R2 are the same or different and represent a C1 -C8 alkyl or a C6 -C8 cycloalkyl, or a C7 -C9 aralkyl, which comprises reacting the starting sterically hindered 2,4,6-trialkylphenols of the formula: STR3 wherein A is a C1 -C8 alkyl or a C6 -C8 cycloalkyl or a C7 -C9 aralkyl or a 3,5-dialkyl-2-hydroxybenzyl of the formula: STR4 B is a C1 -C8 alkyl, or a C6 -C8 cycloalkyl, or a C7 -C9 aralkyl, or a 3,5-dialkyl-4-hydroxybenzyl of the formula: STR5 wherein R1 and R are as identified above, with acetals, aldehydes or donors of C1 -C5 aldehydes in an acidic medium at a temperature within the range of from 60° to 200° C. in the presence of an acidic catalyst, followed by isolation of the desired product. The method according to the present invention makes it possible to prepare sterically hindered bis- or polyphenols in a single stage, whereby the process technology is substantially simplified as compared to those of the prior art. The method of the present invention precludes formation of waste water and atmospheric pollutants. The method ensures preparation of the desired products possessing high quality in high yield without any additional crystallization.

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