2955-67-1

Basic information

• Product Name: N-N-BUTYLPROPIONAMIDE
• Synonyms: N-N-BUTYLPROPIONAMIDE;N-BUTYLPROPIONAMIDE;butylpropionamide;N-Butylpropanamide;N-Butylpropionamide
• CAS NO: 2955-67-1
• Molecular Formula: C₇H₁₅NO
• Molecular Weight: 129.2
• Mol File: 2955-67-1.mol
• Article Data: 4

Chemical Properties

• Melting Point: 80 °C
• Boiling Point: 237 °C
• Flash Point: 122.3°C
• Appearance: /
• Density: 0,89 g/cm3
• Refractive Index: 1.4400-1.4430
• PKA: 16.61±0.46(Predicted)
• CAS DataBase Reference: N-N-BUTYLPROPIONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-N-BUTYLPROPIONAMIDE(2955-67-1)
• EPA Substance Registry System: N-N-BUTYLPROPIONAMIDE(2955-67-1)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 2955-67-1(Hazardous Substances Data)

Usage

General Description

N-N-butylpropionamide is a chemical compound with the molecular formula C7H15NO. It belongs to the class of amides, which are organic compounds derived from carboxylic acids. N-N-butylpropionamide is commonly used as a solvent in industrial applications, such as in the manufacturing of plastics, resins, and coatings. It is also used as a lubricant and as an intermediate in the synthesis of pharmaceuticals and agrochemicals. This chemical is known for its low toxicity and relatively low volatility, making it a safer alternative to other solvents. Additionally, N-N-butylpropionamide is biodegradable and has low environmental impact, making it an attractive choice for various industrial processes.

Upstream product

• 105-37-3 Ethyl propionate 
• 109-73-9 N-butylamine 
• 1956-06-5 4-nitrophenyl propionate 
• 107-10-8 propylamine 
• 764-85-2 Nonanoyl chloride 
• 10431-98-8 2-ethyl-4,5-dihydrooxazole 

Downstream Products

• 32796-69-3 N-propionylbutyramide 
• 20193-21-9 N-propyl-1-butylamine 

Relevant articles and documents

PRODUCTION METHOD OF AMIDE COMPOUND

PROBLEM TO BE SOLVED: To provide a production method of an amide compound, which can use a variety of carboxylic acid halides and can produce a desired amide compound at a yield higher than a batch process by suppressing a side reaction. SOLUTION: Provided is a production method of an amide compound using a flow type reactor, in which the flow type reactor includes: a first flow path; a second flow path; a first mixing means provided at a confluent part of the first flow path and the second flow path; and a third flow path that is connected to the first mixing means and arranged on a down stream side of the first mixing means, the production method comprising: a mixing step of obtaining a mixed liquid by circulating a first liquid containing the carboxylic acid halide in the first flow path, circulating a second liquid containing an amine compound having a molecular weight of 1,000 or less, an inorganic alkali and water in the second flow path, and mixing the first liquid and the second liquid by the first mixing means to obtain a mixture; and a reaction step of obtaining an amide compound by circulating the mixed liquid in the third flow path and reacting the carboxylic acid halide and the amine compound in the third flow path. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2020,JPO&INPIT

Nucleophilic Ring Opening of 2-Oxazolines with Amines: A Convenient Synthesis for Unsymmetrically Substituted Ethylenediamines

The reaction of 2-alkyl-2-oxazolines with alkyl- and arylamines was investigated.The acid-catalyzed nucleophilic ring opening of the 2-oxazolines yields N-(2-aminoethyl)carboxamides in good to excellent yields with secondary amines and hindered primary amines.The N-(2-aminoethyl)carboxamides were hydrolyzed under acidic or basic conditions to selectively yield unsymmetrically substituted ethylenediamines.