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2,2,5,5-Tetramethylcyclohexane-1,4-dione, commonly known as camphorquinone, is a yellow crystalline chemical compound that is insoluble in water but soluble in organic solvents. It is widely recognized for its role as a photoinitiator in the polymerization process, particularly in the production of dental materials and other polymeric products.

86838-54-2

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86838-54-2 Usage

Uses

Used in Dental Industry:
2,2,5,5-Tetramethylcyclohexane-1,4-dione is used as a photoinitiator for dental resin materials, facilitating the polymerization process under light exposure to form robust polymer networks. This application is crucial for creating durable dental restorations that offer both aesthetic and functional benefits.
Used in Polymer and Coating Industry:
In the polymer and coating industry, 2,2,5,5-Tetramethylcyclohexane-1,4-dione serves as a photoinitiator, enabling the rapid curing of polymeric materials and coatings upon exposure to light. This property is valuable for enhancing production efficiency and ensuring the quality of the final products.
Used in Antimicrobial Applications:
2,2,5,5-Tetramethylcyclohexane-1,4-dione has demonstrated potential as an antimicrobial agent, making it a candidate for use in various applications where microbial control is necessary, such as in medical devices, food packaging, and water treatment systems.
Used in Antioxidant Applications:
As a potential antioxidant, 2,2,5,5-Tetramethylcyclohexane-1,4-dione could be utilized in industries that require protection against oxidative damage, including the food and pharmaceutical industries, as well as in the formulation of cosmetics and personal care products.
While the provided materials do not detail specific applications in each industry, the above uses are inferred based on the compound's properties and potential applications in similar fields. Further research and development would be necessary to fully explore and validate these uses.

Check Digit Verification of cas no

The CAS Registry Mumber 86838-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,3 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86838-54:
(7*8)+(6*6)+(5*8)+(4*3)+(3*8)+(2*5)+(1*4)=182
182 % 10 = 2
So 86838-54-2 is a valid CAS Registry Number.

86838-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,5,5-tetramethylcyclohexane-1,4-dione

1.2 Other means of identification

Product number -
Other names 2,2,5,5-tetramethyl 1,4-cyclohexanedione

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:86838-54-2 SDS

86838-54-2Relevant academic research and scientific papers

A Short, Efficient, Highly Selective Synthesis of (1R,3S)-cis-Chrysanthemic Acid through the Microbiological Reduction of 2,2,5,5-Tetramethyl-1,4-cyclohexanedione

d'Angelo, Jean,Revial, Gilbert,Azerad, Robert,Buisson, Didier

, p. 40 - 45 (2007/10/02)

A highly selective synthesis of (1R,3S)-cis-chrysanthemic acid (1a), a key intermediate in the industrial prepariation of major unnatural pyrethrinoid-type insecticides is reported. 2,2,5,5-Tetramethyl-1,4-cyclohexanedi

SYNTHESE DE L'ACIDE CIS CHRYSANTHEMIQUE

d'Angelo, Jean,Revial, Gilbert

, p. 2103 - 2106 (2007/10/02)

A simple, efficient approach of racemic cis chrysanthemic acid 2, an intermediate in the synthesis of the exceptionally potent insecticide Deltamethrine 1, is described.The key-intermediate of this approach was the 2,2,5,5-tetramethylcyclohexane 1,4-dione 5 which has been related to the lactone 3, a precursor of 2, in four steps (70 percent overall yield).

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