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Phenol, 4,4'-(1,2-ethanediyl)bis[2,6-dimethyl-, commonly known as Bisphenol A, is a chemical compound that features two phenol molecules connected by an ethylene linkage. It is widely used in the production of plastics, specifically polycarbonate plastics and epoxy resins. However, Bisphenol A has raised health concerns due to its potential to leach into food and beverages from containers made with this chemical. Studies have associated exposure to Bisphenol A with various health issues, such as hormone disruption, reproductive problems, and an increased risk of certain cancers. Consequently, many countries have implemented regulations to restrict its use in consumer products.

6476-26-2

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6476-26-2 Usage

Uses

Used in Plastics Industry:
Bisphenol A is used as a key component in the production of polycarbonate plastics and epoxy resins for its ability to provide strength, durability, and heat resistance to the final products. It is commonly found in food containers, water bottles, and other consumer products.
Used in Coatings Industry:
In the coatings industry, Bisphenol A is used as a curing agent for epoxy resins, which are used to create protective coatings for various surfaces, including metal, wood, and concrete. The use of Bisphenol A in this application enhances the adhesion, chemical resistance, and durability of the coatings.
Used in Electrical and Electronics Industry:
Bisphenol A is also used in the electrical and electronics industry as a component of insulating materials and printed circuit boards. Its properties contribute to the thermal stability and electrical insulation of these materials, ensuring the safe and efficient operation of electronic devices.
Used in Dental Industry:
In the dental industry, Bisphenol A is used in the production of dental fillings and sealants. Its properties provide a strong, durable, and long-lasting material for dental applications, helping to protect teeth from decay and maintain oral health.

Check Digit Verification of cas no

The CAS Registry Mumber 6476-26-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,7 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6476-26:
(6*6)+(5*4)+(4*7)+(3*6)+(2*2)+(1*6)=112
112 % 10 = 2
So 6476-26-2 is a valid CAS Registry Number.

6476-26-2SDS

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 4-[2-(4-hydroxy-3,5-dimethylphenyl)ethyl]-2,6-dimethylphenol

1.2 Other means of identification

Product number -
Other names 1,2-Bis-(4-hydroxy-3,5-dimethyl-phenyl)-ethan

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:6476-26-2 SDS

6476-26-2Relevant academic research and scientific papers

Asymmetric Lewis Acid Catalyzed Electrochemical Alkylation

Zhang, Qinglin,Chang, Xihao,Peng, Lingzi,Guo, Chang

, p. 6999 - 7003 (2019)

Lewis-acid catalysis and electrochemistry represent two powerful fields that have found widespread application in organic chemistry. Reported herein is an asymmetric electrosynthesis in combination with a chiral Ni catalyst leading to an intermolecular al

Efficient generation of ortho -quinone methide: Application to the biomimetic syntheses of (±)-schefflone and tocopherol trimers

Liao, Daohong,Li, Houhua,Lei, Xiaoguang

supporting information; experimental part, p. 18 - 21 (2012/02/04)

An efficient method using silver oxide-mediated oxidation for the synthesis of ortho-quinone methides has been developed and applied to the biomimetic syntheses of novel trimeric natural products, (±)-schefflone and tocopherol trimers. Further studies of the critical trimerization as well as substrate scope and limitations are also reported.

Selective benzylic C-C coupling catalyzed by a bioinspired dicopper complex

Prokofieva, Angelina,Prikhod'ko, Alexander I.,Dechert, Sebastian,Meyer, Franc

, p. 1005 - 1007 (2008/09/21)

A highly preorganized bioinspired dicopper complex with imidazole ligation catalyzes the selective benzylic para-C-H activation of 2,4,6-trimethylphenol under aerobic conditions, yielding either the stilbenequinone or 4-methoxymethyl-2,6-dimethylphenol depending on the solvent used. The Royal Society of Chemistry.

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