5831-87-8

Basic information

• Product Name: N,N-dibutylhexadecanamide
• CAS NO: 5831-87-8
• Molecular Formula: C₂₄H₄₉NO
• Molecular Weight: 367.652
• Mol File: 5831-87-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 399.4°C at 760 mmHg
• Flash Point: 142.7°C
• Density: 0.856g/cm³
• Vapor Pressure: 1.37E-06mmHg at 25°C
• Refractive Index: 1.457
• CAS DataBase Reference: N,N-dibutylhexadecanamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dibutylhexadecanamide(5831-87-8)
• EPA Substance Registry System: N,N-dibutylhexadecanamide(5831-87-8)

Safety Data

• Hazardous Substances Data: 5831-87-8(Hazardous Substances Data)

Upstream product

• 74058-64-3 1-(2-Thioxo-thiazolidin-3-yl)-hexadecan-1-one 
• 111-92-2 dibutylamine 
• 100663-86-3 C₂₈H₄₀N₂O₂ 
• 57-10-3 1-hexadecylcarboxylic acid 
• 112-67-4 n-hexadecanoyl chloride 

Relevant articles and documents

Compositions comprising N,N-dialkylalkanamides

This invention provides compositions comprising a physiologically-active agent and a compound represented by the general formula STR1 wherein R1 and R2 are independently selected from the group consisting of alkyl radicals and cycloalkyl radicals comprising from 1 to 10 carbon atoms and R is selected from the group consisting of alkyl radicals and cycloalkyl radicals comprising from 1 to 30 carbon atoms; provided, however, that the total number of carbon atoms in said compound is 15 or more and the total number of carbon atoms in R1 and R2 is 5 or more.

Monitored Aminolysis of 3-Acyl-1,3-thiazolidine-2-thiones: Synthesis of Amides and Amide Alkaloids

A functional heterocycle, 3-acyl-1,3-thiazolidine-2-thione has been shown to be effective as an acylating reagent for the amino group.ATT (1) was readily prepared by several methods, and reacted with various amino compounds in CHCl3, CH2Cl2, THF, EtOH, THF-H2O, or sulfolane to afford the corresponding amides, 2a-w and 3-10 in very high yields within a short time.This reagent exhibits high chemo-selectivity.Its reaction with the diamines 13 and 15 and the triamine 29, which include a primary amino group(s) and a secondary amino group, gave the products acylated only at the primary amino group(s), 14, 16, and 30, respectively, in high yields.Aminoalcohols and aminophenols were chemoselectively converted into acylaminoalcohols and acylaminophenols, respectively, by ATT (1).By utilizing this method, several amide alkaloids (26, 28, 30, and 34) were efficiently synthesized.This new aminolysis can be monitored by the disappearance of the yellow color of the starting materials, ATT (1); it is remarkably characteristic of this reaction. Keywords - monitored aminolysis; 3-acyl-1,3-thiazolidine-2-thione; high chemo-selectivity; amide synthesis; fagaramide; dolicotheline; spermidine; maytenine; N-ferulyltryptamine