2049-92-5

Basic information

• Product Name: p-tert-amyl aniline
• Synonyms: p-tert-amyl aniline;4-(1,1-Dimethylpropyl)aniline;4-(1,1-Dimethylpropyl)benzenamine;4-Aminophenyl-t-pentane;p-tert-Pentylaniline;4-(tert-Pentyl)aniline;4-tert-Amylaniline
• CAS NO: 2049-92-5
• Molecular Formula: C₁₁H₁₇N
• Molecular Weight: 163.2594
• Mol File: 2049-92-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 46.25°C (estimate)
• Boiling Point: 253.03°C (estimate)
• Flash Point: 108.8°C
• Appearance: /
• Density: 0.9137 (estimate)
• Vapor Pressure: 0.0152mmHg at 25°C
• Refractive Index: 1.5112 (estimate)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: p-tert-amyl aniline(CAS DataBase Reference)
• NIST Chemistry Reference: p-tert-amyl aniline(2049-92-5)
• EPA Substance Registry System: p-tert-amyl aniline(2049-92-5)

Safety Data

• Hazardous Substances Data: 2049-92-5(Hazardous Substances Data)

Usage

General Description

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, meaning it is an aromatic secondary amine with a tert-amyl group attached to the para position of the phenyl ring. P-tert-amyl aniline is commonly used as an intermediate in the synthesis of dyes, pigments, and pharmaceuticals. It is also used as a stabilizer for plastics and polymers, as well as in the production of organic peroxides. This chemical is known to be toxic if ingested or inhaled and can cause skin and eye irritation, so proper handling and safety precautions are necessary when working with it.

InChI:InChI=1/C11H17N/c1-4-11(2,3)9-5-7-10(12)8-6-9/h5-8H,4,12H2,1-3H3

Upstream product

• 80-46-6 4-t-amylphenol 
• 2049-95-8 tery-amylbenzene 
• 6284-98-6 1-(1,1-dimethylpropyl)-4-nitrobenzene 
• 75-85-4 tert-Amyl alcohol 
• 62-53-3 aniline 
• 513-35-9 2-methyl-but-2-ene 
• 142-04-1 aniline hydrochloride 
• 542-11-0 aniline hydrobromide 
• 594-36-5 2-methyl-2-butylchloride 
• 507-36-8 2-bromo-2-methylbutane 
• 71-43-2 benzene 
• 78649-49-7 methyl N-(4-tert.-pentyl-phenyl)-carbamate 
• 563-46-2 2-Methyl-1-butene 

Downstream Products

• 101275-86-9 (4,5-dimethyl-thiazol-2-yl)-(4-tert-pentyl-phenyl)-amine 
• 102177-77-5 3-[4-(1,1-dimethyl-propyl)-anilino]-phthalide 
• 114833-64-6 N-[4-(1,1-dimethylpropyl)phenyl]-5-methylisoxazol-4-yl-carboxamide 
• 5414-81-3 sulfanilic acid-(2,6-dibromo-4-tert-pentyl-anilide) 
• 858241-50-6 4-(1,1-dimethylpropyl)benzene-1,2-diamine 
• 132180-27-9 N-[4-(1,1-dimethylpropyl)-2-nitrophenyl]acetamide 
• 2049-95-8 tery-amylbenzene 
• 80-46-6 4-t-amylphenol 
• 7463-20-9 N-[4-(1,1-dimethylpropyl)phenyl]acetamide 
• 79105-82-1 1-[2-Amino-5-(1,1-dimethyl-propyl)-phenyl]-2,2-dimethoxy-ethanol 
• 79097-96-4 1-[2-Amino-5-(1,1-dimethyl-propyl)-phenyl]-2,2-dimethoxy-ethanone 
• 235101-29-8 6-(tert-pentyl)benzo[d]thiazol-2-amine 

Relevant articles and documents

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

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

Preparation of p-substituted, aromatic amines

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.