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4-SEC-BUTYL-2-TERT-BUTYLPHENOL, also known as 2-tert-butyl-4-sec-butylphenol, is an aromatic compound that serves as an essential antioxidant and ultraviolet stabilizer in a variety of industrial applications. It is synthesized through the reaction of phenol and isobutene, which results in a molecule with a tert-butyl group and a sec-butyl group attached to the benzene ring. This structure endows it with the capability to prevent the degradation of materials and extend their shelf life by inhibiting the formation of free radicals and other reactive species that can cause oxidative damage. However, due to its potential for skin and eye irritation, as well as its flammability, 4-SEC-BUTYL-2-TERT-BUTYLPHENOL requires careful handling and adherence to proper safety precautions.

52184-13-1

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52184-13-1 Usage

Uses

Used in Lubricant Industry:
4-SEC-BUTYL-2-TERT-BUTYLPHENOL is used as an antioxidant and UV stabilizer for enhancing the performance and longevity of lubricants. It helps in preventing the oxidation of lubricants, which can lead to the formation of sludge and varnish, thereby extending the service life of the lubricants and the machinery they protect.
Used in Plastics Industry:
In the plastics industry, 4-SEC-BUTYL-2-TERT-BUTYLPHENOL is used as a stabilizing agent to protect plastics from degradation caused by exposure to heat, light, and oxygen. This helps in maintaining the physical properties and appearance of the plastics, ensuring their durability and resistance to environmental stress cracking.
Used in Polymer Industry:
4-SEC-BUTYL-2-TERT-BUTYLPHENOL is utilized as an additive in the production of polymers to improve their stability and resistance to degradation. It aids in preserving the structural integrity and performance of polymers over time, particularly in applications where they are exposed to harsh conditions or UV radiation.
Used in Coatings Industry:
4-SEC-BUTYL-2-TERT-BUTYLPHENOL is employed as a component in coatings to provide protection against UV-induced degradation, which can cause discoloration, chalking, and loss of adhesion. Its inclusion in coatings helps in maintaining the aesthetic appeal and functional performance of coated surfaces, particularly in exterior applications.
Used in Adhesives Industry:
In the adhesives industry, 4-SEC-BUTYL-2-TERT-BUTYLPHENOL is used as a stabilizing agent to enhance the durability and performance of adhesive formulations. It helps in preventing the oxidative degradation of adhesives, ensuring their long-term bonding strength and resistance to environmental factors.

Check Digit Verification of cas no

The CAS Registry Mumber 52184-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,8 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52184-13:
(7*5)+(6*2)+(5*1)+(4*8)+(3*4)+(2*1)+(1*3)=101
101 % 10 = 1
So 52184-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O/c1-6-10(2)11-7-8-13(15)12(9-11)14(3,4)5/h7-10,15H,6H2,1-5H3

52184-13-1SDS

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 4-sec-Butyl-2-tert-butyl-phenol

1.2 Other means of identification

Product number -
Other names Phenol, 2-(1,1-dimethylethyl)-4-(1-methylpropyl)-

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:52184-13-1 SDS

52184-13-1Upstream product

52184-13-1Downstream Products

52184-13-1Relevant academic research and scientific papers

Process for the production of 2-aryl-2H-benzotriazoles

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, (2008/06/13)

A process for the production of 2-aryl-2H-benzotriazoles comprises reducing and cyclizing the corresponding o-nitroazobenzenes with hydrogen at a temperature in the range of about 20° C. to about 100° C. and at a pressure in the range of about 15 psia (1 atmosphere) to about 1000 psia (66 atmospheres) in an alkaline medium at a pH over 10 in the presence of a nickel catalyst, preferably molybdenum-promoted Raney nickel. High yields of pure product are obtained directly with a concomitant reduction of undesired by-product and a reduction in effluent pollution problems.

Process for the production of 2-aryl-2H-benzotriazoles

-

, (2008/06/13)

A process for the production of 2-aryl-2H-benzotriazoles comprises reducing and cyclizing the corresponding o-nitroazobenzenes with carbon monoxide at a temperature in the range of about 20° C. to about 150° C. and at a pressure in the range of about 15 psia (1 atmosphere) to about 1000 psia (66 atmospheres) in an alkaline medium at a pH over 10 in the presence of a copper-amine complex catalyst. High yields of pure product are obtained with a concomitant reduction of undesired by-products and a reduction in effluent pollution problems.

Process for the production of 2-aryl-2H-benzotriazoles

-

, (2008/06/13)

An improved process for the production of 2-aryl-2H-benzotriazoles by the reduction of o-nitroazobenzene intermediates with zinc in alkaline medium comprises employing a ratio of moles of alkali to moles of o-nitroazobenzene intermediate in the range of 0.2-1.7/1 in the presence of less than 150 ppm of iron based on zinc used. The improved process results in higher yields of high purity products with a concomitant reduction in the amount of undesired cleavage amine by-products and a reduction in effluent pollution problems. The process is carried out in a polar/non-polar solvent mixture.

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