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4-(1,1,3,3-tetramethylbutyl)pyrocatechol, also known as 4-tert-butylpyrocatechol, is a chemical compound that belongs to the class of alkylated pyrocatechols. It is derived from pyrocatechol, an organic compound, and is widely recognized for its antioxidant properties. 4-(1,1,3,3-tetramethylbutyl)pyrocatechol is highly valued for its capacity to prevent oxidative degradation in a variety of materials such as polymers, plastics, and rubbers. It functions by inhibiting the formation of free radicals, which are known to cause material degradation and deterioration, thereby enhancing the stability and longevity of products in which it is used.

1139-46-4

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1139-46-4 Usage

Uses

Used in Polymer Industry:
4-(1,1,3,3-tetramethylbutyl)pyrocatechol is used as an antioxidant for enhancing the stability and longevity of polymers. It helps in preventing oxidative degradation, thereby improving the overall performance and durability of the polymer products.
Used in Plastics Industry:
In the plastics industry, 4-(1,1,3,3-tetramethylbutyl)pyrocatechol is utilized as an additive to prevent the oxidative degradation of plastics. Its incorporation into plastic materials ensures a longer shelf life and improved resistance to environmental stressors, such as heat and UV radiation.
Used in Rubber Industry:
4-(1,1,3,3-tetramethylbutyl)pyrocatechol is used as a stabilizing agent in the rubber industry. It protects rubber products from oxidative degradation, which can lead to hardening and loss of elasticity, thus maintaining the rubber's flexibility and performance over time.
It is important to handle and use 4-(1,1,3,3-tetramethylbutyl)pyrocatechol with care, as it can be hazardous if not properly managed. Its careful application ensures that it serves its purpose effectively while minimizing any potential risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 1139-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1139-46:
(6*1)+(5*1)+(4*3)+(3*9)+(2*4)+(1*6)=64
64 % 10 = 4
So 1139-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O2/c1-13(2,3)9-14(4,5)10-6-7-11(15)12(16)8-10/h6-8,15-16H,9H2,1-5H3

1139-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,4,4-trimethylpentan-2-yl)benzene-1,2-diol

1.2 Other means of identification

Product number -
Other names 4-(1,1,3,3-tetramethyl-butyl)-pyrocatechol

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:1139-46-4 SDS

1139-46-4Relevant academic research and scientific papers

Chloroindate(iii) ionic liquids as catalysts for alkylation of phenols and catechol with alkenes

Gunaratne, H. Q. Nimal,Lotz, Tobias J.,Seddon, Kenneth R.

scheme or table, p. 1821 - 1824 (2011/01/07)

Chloroindate(iii) ionic liquids are shown to be versatile catalysts for the alkylation of phenols with alkenes, giving high conversions to alkylated phenols with high selectivities.

ALKYLATION OF HYDROXYARENES WITH OLEFINS, ALCOHOLS AND ETHERS IN IONIC LIQUIDS

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Page/Page column 26, (2008/06/13)

Hydroxyarenes are alkylated using an ionic liquid catalyst system with olefins, alcohols, or ethers as alkylating agents. The ionic liquid catalyst system comprises chloroindate (III) anions. The reactions may be conducted at moderate temperatures and pressures to yield commercially relevant alkylated hydroxyarene compounds.

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