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P-tert-amyl aniline, also known as 4-(tert-pentyl)aniline, is an organic chemical compound with the molecular formula C11H17N. It is a substituted aniline, characterized as an aromatic secondary amine with a tert-amyl group attached to the para position of the phenyl ring. p-tert-amyl aniline is recognized for its role as an intermediate in the synthesis of various organic compounds and is known for its potential toxicity and irritant properties, necessitating careful handling and safety measures.

2049-92-5

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2049-92-5 Usage

Uses

Used in Chemical Synthesis:
P-tert-amyl aniline is used as an intermediate in the synthesis of dyes, pigments, and pharmaceuticals, contributing to the development of a wide range of colorants and medicinal agents.
Used in Plastics and Polymers Industry:
In the plastics and polymers industry, p-tert-amyl aniline serves as a stabilizer, enhancing the durability and performance of these materials by preventing degradation and maintaining their structural integrity over time.
Used in Organic Peroxides Production:
P-tert-amyl aniline is also utilized in the production of organic peroxides, which are essential in various industrial processes, including the manufacture of polymers and the curing of resins.
Given the toxic nature of p-tert-amyl aniline when ingested or inhaled, and its potential to cause skin and eye irritation, it is crucial to implement proper handling procedures and safety precautions in all applications of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 2049-92-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2049-92:
(6*2)+(5*0)+(4*4)+(3*9)+(2*9)+(1*2)=75
75 % 10 = 5
So 2049-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N/c1-4-11(2,3)9-5-7-10(12)8-6-9/h5-8H,4,12H2,1-3H3

2049-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-methylbutan-2-yl)aniline

1.2 Other means of identification

Product number -
Other names 4-(tert-Pentyl)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:2049-92-5 SDS

2049-92-5Relevant academic research and scientific papers

Selective Acid-Catalyzed Hydroarylation of Nonactivated Alkenes with Aniline Assisted by Hexafluoroisopropanol

De Oliveira Vigier, Karine,Humblot, Anaelle,Jér?me, Fran?ois,Jiang, Fan,Peng, Gongming,Pera-Titus, Marc,Wischert, Raphael

, p. 17896 - 17905 (2021/12/13)

The catalytic hydroarylation of nonactivated alkenes with aniline is a reaction of high interest, aiming at providing C-functionalized aniline derivatives that are important precursors for the fabrication of polyurethanes. However, this reaction remains a

BENZIIMIDAZOLE AND IMIDAZOPYRIDINE DERIVATIVES AS SODIUM CHANNEL MODULATORS

-

Page/Page column 179, (2013/08/15)

The invention relates to benzimidazole and imidazopyridine derivatives, to their use in medicine, to compositions containing them, to processes for their preparation and to intermediates used in such processes. More particularly the invention relates to new Nav1.8 modulators of formula (I) or pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, R7. X and Y are as defined in the description. Nav1.8 modulators are potentially useful in the treatment of a wide range of disorders, particularly pain.

Preparation of p-substituted, aromatic amines

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, (2008/06/13)

p-Substituted aromatic amines are prepared by reacting a p-substituted, aromatic carbamic acid ester with an aromatic amine in the presence of an aliphatic or cycloaliphatic alcohol. The aromatic amines obtainable by the process according to the invention are antiseptics and valuable starting materials for the preparation of dyes, resins, finishes, plastics, pesticides and drugs.

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