767-77-1

Basic information

• Product Name: Benzenamine, 2,3,5-trimethyl-
• Synonyms: Benzenamine, 2,3,5-trimethyl-;2,3,5-trimethylaniline
• CAS NO: 767-77-1
• Molecular Formula: C₉H₁₃N
• Molecular Weight: 135.20622
• Mol File: 767-77-1.mol

Chemical Properties

• Melting Point: 39 °C
• Boiling Point: 239.2±9.0 °C(Predicted)
• Appearance: /
• Density: 0.962±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 4.70±0.10(Predicted)
• CAS DataBase Reference: Benzenamine, 2,3,5-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2,3,5-trimethyl-(767-77-1)
• EPA Substance Registry System: Benzenamine, 2,3,5-trimethyl-(767-77-1)

Safety Data

• Hazardous Substances Data: 767-77-1(Hazardous Substances Data)

Usage

Uses

Used in Dye Production:
Benzenamine, 2,3,5-trimethylis used as a chemical intermediate for the production of dyes. Its unique chemical structure allows for the creation of a range of colored compounds, making it valuable in the dye industry.
Used in Pharmaceutical Synthesis:
Benzenamine, 2,3,5-trimethylis also utilized as an intermediate in the synthesis of pharmaceuticals. Its reactivity and ability to form various chemical bonds make it a key component in the development of new drugs.
Used in Antioxidant Production:
Benzenamine, 2,3,5-trimethylis used as a precursor in the production of antioxidants. Its presence in these compounds helps to prevent oxidation, which is essential in various industrial applications to extend the shelf life of products.
Used in Rubber Accelerator Synthesis:
In the rubber industry, this compound is used as a chemical intermediate in the synthesis of rubber accelerators. These accelerators are vital in the vulcanization process, enhancing the strength and durability of rubber products.

Upstream product

• 609-88-1 1,2,4-trimethyl-6-nitrobenzene 
• 154152-57-5 4-bromo-3-nitro-1,2,5-trimethylbenzene 
• 7647-01-0 hydrogenchloride 
• 60-29-7 diethyl ether 
• 95-63-6 1,2,4-Trimethylbenzene 
• 5469-19-2 1-bromo-2,4,5-trimethylbenzene 
• 20794-17-6 6-Acetoxy-3,5,6-trimethyl-2,4-cyclohexadien-1-on 

Downstream Products

• 4734-73-0 2,3,5-trimethyl-p-phenylenediamine 
• 935-92-2 2,3,5-Trimethyl-1,4-benzoquinone 
• 697-82-5 2,3,5-trimethylphenol 
• 120393-53-5 4-iodo-2,3,5-trimethyl-aniline 
• 861785-98-0 N,N-dichloro-2,3,5-trimethyl-aniline 
• 83341-35-9 4-(2,2,3,3-Tetramethylbutyl)-2-(2,3,5-trimethylphenylazo)phenol 
• 861347-78-6 2,3,5-trimethyl-N⁴-(2,3,5-trimethyl-phenyl)-p-phenylenediamine 

Relevant articles and documents

STEREOSELECTIVE SYNTHESIS OF 5-ARYL-3-METHYL-2E,4E-PENTADIENALS

A series of 5-aryl-3-methyl-2E,4E-pentadienals were synthesized stereoselectively from 4-aryl-3E-buten-2-ones and methylmagnesium iodide followed by formylation of the obtained tertiary dimethylstyrylcarbinols by the formylating complex produced from dimethylformamide and phosphorus oxychloride.A synthesis of 2,3,6-trimethyl-4-methoxybenzaldehyde, starting from pseudocumene, is proposed.

Manufacture of aromatic amino compounds

A process for producing an aromatic amine comprises heating an aromatic sulfonate and a metal amide in liquid ammonia in a closed reactor at a temperature of at least 40° C to produce a metal arylamide and reacting the resultant metal arylamide with water or lower aliphatic alcohol to produce an aromatic amine.