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P-Isopropyl-phenyl-p-tolyl-amine, with the molecular formula C18H23N, is an aromatic amine that features isopropyl, phenyl, and p-tolyl groups. It is a versatile chemical compound known for its applications across various industries due to its unique structural properties.

494834-22-9

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494834-22-9 Usage

Uses

Used in Chemical Industry:
P-Isopropyl-phenyl-p-tolyl-amine is used as an intermediate in the synthesis of various industrial chemicals, playing a crucial role in the production process due to its reactive amine group and aromatic structure.
Used as a Stabilizer and Antioxidant in Polymers and Rubbers:
In the polymer and rubber industry, P-Isopropyl-phenyl-p-tolyl-amine serves as a stabilizer and antioxidant, helping to prevent degradation and maintain the stability and performance of these materials over time.
Used as a Chemical Additive in Lubricant Manufacturing:
P-Isopropyl-phenyl-p-tolyl-amine is utilized as a chemical additive in the manufacturing of lubricants, enhancing their properties and ensuring their effectiveness in various applications.
Used as an Antioxidant in Fuels:
P-ISOPROPYL-PHENYL-P-TOLYL-AMINE is also employed as an antioxidant in fuels to prevent degradation, thereby maintaining the fuel's stability and extending its shelf life.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, P-Isopropyl-phenyl-p-tolyl-amine finds use in the synthesis of various organic compounds, contributing to the development of new drugs and medicinal agents.
Used in Agricultural Industry:
Furthermore, P-Isopropyl-phenyl-p-tolyl-amine has applications in the agricultural industry, where it is used as a component in the formulation of pesticides and herbicides, aiding in the protection and enhancement of crop yields.

Check Digit Verification of cas no

The CAS Registry Mumber 494834-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,4,8,3 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 494834-22:
(8*4)+(7*9)+(6*4)+(5*8)+(4*3)+(3*4)+(2*2)+(1*2)=189
189 % 10 = 9
So 494834-22-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H19N/c1-12(2)14-6-10-16(11-7-14)17-15-8-4-13(3)5-9-15/h4-12,17H,1-3H3

494834-22-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name p-Isopropylphenyl-p-tolyl-amine

1.2 Other means of identification

Product number -
Other names 4-methyl-N-(4-propan-2-ylphenyl)aniline

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:494834-22-9 SDS

494834-22-9Downstream Products

494834-22-9Relevant academic research and scientific papers

Aromatic amine derivatives having fluorenyl moiety and organic light-emitting diode including the same

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Paragraph 0268-0270; 0295; 0300; 0301, (2020/03/24)

The present invention relates to aromatic amine derivatives with a fluorene structure and a light-emitting element including the same, and more specifically, to an organic light-emitting compound expressed as [Formula A] and a light-emitting element containing the same. [Formula A] In [Formula A], X1 or X8 and Ar1, Ar2 are specifically defined in the description of the invention.

One-pot synthesis of diarylamines from two aromatic amines via oxidative dearomatization-imino exchange-reductive aromatization

Zhang, Li,Wang, Weibin,Fan, Renhua

supporting information, p. 2018 - 2021 (2013/05/23)

A one-pot synthetic strategy for diarylamines using only aromatic amines as starting materials has been developed. This method involved a PhI(OAc) 2-induced oxidative dearomatization of N-sulfonyl protected para-substituted anilines, a Bi(OTf)3-catalyzed imino exchange reaction between N-sulfonyl cyclohexadienimines and aromatic amines, and a CF3COOH/Zn mediated reductive aromatization of the resulting N-aryl cyclohexadienimines.

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