6375-75-3

Basic information

• Product Name: 3-chloro-N,N-diethylaniline
• Synonyms: 3-Chloro-N,N-diethylaniline; Aniline, m-chloro-N,N-diethyl-; Aniline, m-chloro-N,N-diethyl-,; benzenamine, 3-chloro-N,N-diethyl-
• CAS NO: 6375-75-3
• Molecular Formula: C₁₀H₁₄ClN
• Molecular Weight: 183.6779
• Mol File: 6375-75-3.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 268.1°C at 760 mmHg
• Flash Point: 115.9°C
• Density: 1.065g/cm³
• Vapor Pressure: 0.00784mmHg at 25°C
• Refractive Index: 1.547
• CAS DataBase Reference: 3-chloro-N,N-diethylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 3-chloro-N,N-diethylaniline(6375-75-3)
• EPA Substance Registry System: 3-chloro-N,N-diethylaniline(6375-75-3)

Safety Data

• Hazardous Substances Data: 6375-75-3(Hazardous Substances Data)

Usage

General Description

3-Chloro-N,N-diethylaniline is a chemical compound, typically present as a liquid. It belongs to the class of organic compounds known as N-alkylanilines, which are characterized by containing an aniline moiety that is N-alkylated. Its molecular formula is C10H14ClN and its molecular weight is 185.68 g/mol. It features an aniline group - a benzene ring with an amine group attached - substituted with two ethyl groups and a chlorine atom. 3-chloro-N,N-diethylaniline is chemically reactive and it's often used as a precursor or intermediate in numerous chemical preparations and organic syntheses in several industrial applications. The potential risks and safety measures should always be considered while handling this chemical, especially in its liquid form.

Upstream product

• 75-03-6 ethyl iodide 
• 108-42-9 3-chloro-aniline 
• 74-96-4 ethyl bromide 
• 78-40-0 triethyl phosphate 
• 588-07-8 3-Chloroacetanilide 
• 64-19-7 acetic acid 
• 64-17-5 ethanol 
• 121-73-3 3-Nitrochlorobenzene 
• 15258-44-3 N-ethyl-3-chloroaniline 
• 857948-33-5 N-(3-Chloro-phenyl)-N-ethyl-acetamide 

Downstream Products

• 1424-67-5 2-chloro-4-diethylaminobenzaldehyde 
• 133387-29-8 N,N-diethyl-5-chloro-2-nitro-aniline 
• 1234421-76-1 2-{2-[3-(diethylamino)phenyl]phenyl}pyridine 
• 1234421-79-4 2-{2,6-bis[3-(diethylamino)phenyl]phenyl}pyridine 
• 1234421-81-8 2-{6-methyl-2-[3-(diethylamino)phenyl]phenyl}pyridine 
• 72375-44-1 [3-Chloro-4-(4-nitro-phenylazo)-phenyl]-diethyl-amine 
• 52830-78-1 2-(2-chloro-4-(diethylamino)-benzoyl)benzoic acid 
• 859330-26-0 bis-(2-chloro-4-diethylamino-6-nitro-phenyl)-methane 
• 2359-58-2 N⁴,N⁴-diethyl-2-chloro-p-phenylenediamine 
• 145022-20-4 N,N,N',N'-Tetraethyl-phenanthrene-3,6-diamine 
• 52131-99-4 3-chloro-4-nitroso-N,N-diethylaniline 

Relevant articles and documents

AZO COMPOUND AND TEXTILE PRINTING METHOD

To provide a dye having good light fastness and used for various recording media, preferably for fiber, and further preferably for polyester fiber.SOLUTION: The present invention provides a compound represented by the formula (1) in the figure. (In the formula (1), R1 represents a hydrogen atom or nitro group; R2 and R3 each independently represent a C1-C4 alkyl group optionally substituted with a C1-C4 alkoxy group or phenyl group; R4 represents a halogen atom; and R2 and R3 may be linked to each other to form a ring.)SELECTED DRAWING: None

COLORED DISPERSION, INK COMPOSITION USING THE SAME, AND DISPERSION STABILITY IMPROVEMENT METHOD THEREWITH AND PRINTING METHOD OF HYDROPHOBIC FIBER

PROBLEM TO BE SOLVED: To provide dispersion liquid for inkjet printing ink that can manufacture a dyed thing excellent in color rendering, can obtain the dyeing having high sublimation transfer efficiency, high concentration and high quality, in sublimation transfer dying using inkjet printing, furthermore, excellent in storage stability. SOLUTION: A colorant dispersion comprises (A) a compound expressed by a formula (1), (B) C.I. Disperse Blue 360, and (C) a dispersant, in which when a total content of (A) and (B) is set to 100, a content of (B) is 10 or larger and 90 or smaller, (C) the dispersant contains at least any one selected from the group consisting of polyoxyethylene aryl phenyl ether-based dispersant, and polyoxyethylene arylphenyl ether sulfate-based dispersant. (R1 is H or a nitro group; R2 and R3 may be independently substituted with C1-C4 alkoxy group or C1-C4 alkyl groups that may be substituted with phenyl group; R4 is halogen atom; and R2 and R3 may be mutually coupling to form a ring.) SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Catalytic N-Alkylation of Amines Using Carboxylic Acids and Molecular Hydrogen

A convenient, practical and green N-alkylation of amines has been accomplished by applying readily available carboxylic acids in the presence of molecular hydrogen. Applying an in situ formed ruthenium/triphos complex and an organic acid as cocatalyst, a broad range of alkylated secondary and tertiary amines are obtained in good to excellent yields. This novel method is also successfully applied for the synthesis of unsymmetrically substituted N-methyl/alkyl anilines through a direct three-component coupling reaction of the corresponding amines, carboxylic acids, and CO2 as a C1 source.