4534-11-6

Basic information

• Product Name: 3-METHYL-4-ISOPROPYLANILINE HYDROCHLORIDE
• Synonyms: 3-METHYL-4-ISOPROPYLANILINE HYDROCHLORIDE;4-ISOPROPYL-3-METHYLANILINE HYDROCHLORIDE;4-isopropyl-m-toluidinium chloride;3-Methyl-4-isopropylanilineHCl;3-Methyl-4-(propan-2-yl)aniline hydrochloride
• CAS NO: 4534-11-6
• Molecular Formula: C₁₀H₁₅N*ClH
• Molecular Weight: 185.69
• EINECS: 224-876-0
• Mol File: 4534-11-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 223 °C
• Boiling Point: 247°Cat760mmHg
• Flash Point: 106°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.0263mmHg at 25°C
• Refractive Index: 1.538
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility: Slightly soluble in water (9.9 g/L)
• CAS DataBase Reference: 3-METHYL-4-ISOPROPYLANILINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHYL-4-ISOPROPYLANILINE HYDROCHLORIDE(4534-11-6)
• EPA Substance Registry System: 3-METHYL-4-ISOPROPYLANILINE HYDROCHLORIDE(4534-11-6)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 20/21/22-36/37/38-22
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 4534-11-6(Hazardous Substances Data)

Usage

Uses

4-Isopropyl-3-methylaniline hydrochloride is used to synthesis of fine chemical, organic intermediates.

InChI:InChI=1/C10H15N/c1-7(2)10-5-4-9(11)6-8(10)3/h4-7H,11H2,1-3H3

Upstream product

• 4514-88-9 E-verbanone oxime 
• 64123-64-4 2-isopropyl-5-nitro-benzyl chloride 

Downstream Products

• 64123-34-8 N-Isopropyl-4,6-dinitro-o-Cymen-5-amine 
• 1425782-74-6 2-chloro-N-(4-isopropyl-3-methylphenyl)nicotinamide 
• 4534-10-5 4-Isopropyl-3-methylaniline 

Relevant articles and documents

BECKMANN REARRANGEMENT OF THE E ISOMER OF CIS-4,6,6-TRIMETHYLBICYCLO-HEPTAN-2-ONE OXIME

The individual E isomer of 4,6,6-trimethylbicycloheptan-2-one oxime has been obtained, and its transformations under the conditions of acid catalysis have been studied.The action of sulfuric acid on a solution of the oxime in acetonitrile leads to the selective formation of 5,7,7-trimethyl-2-azabicyclooctan-3-one, while the action of hydrochloric acid with heating gives 4-isopropyl-3-methylaniline.

2,6-Dinitroaniline herbicides

The invention is substituted 2,6-dinitroaniline compounds and preemergence herbicidal methods and compositions employing the substituted 2,6-dinitroaniline compounds.