7726-08-1

Basic information

• Product Name: N-Caprinoylethanolamide
• Synonyms: N-(2-Hydroxyethyl)capric acid amide;N-(2-Hydroxyethyl)capric amide;N-(2-Hydroxyethyl)caprinamide;N-(2-Hydroxyethyl)decanamide;N-Caprinoylethanolamide
• CAS NO: 7726-08-1
• Molecular Formula: C₁₂H₂₅NO₂
• Molecular Weight: 215.33
• Mol File: 7726-08-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 78-80 °C(Solv: water (7732-18-5))
• Boiling Point: 384.9±25.0 °C(Predicted)
• Appearance: /
• Density: 0.935±0.06 g/cm3(Predicted)
• PKA: 14.49±0.10(Predicted)
• CAS DataBase Reference: N-Caprinoylethanolamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Caprinoylethanolamide(7726-08-1)
• EPA Substance Registry System: N-Caprinoylethanolamide(7726-08-1)

Safety Data

• Hazardous Substances Data: 7726-08-1(Hazardous Substances Data)

Upstream product

• 110-38-3 decanoic acid ethyl ester 
• 141-43-5 ethanolamine 
• 334-48-5 1-decanoic acid 
• 112-13-0 n-decanoyl chloride 

Downstream Products

• 7596-88-5 N-dodecanoylglycine 
• 14246-55-0 N-myristoylglycine 
• 2441-41-0 N-palmitoyl glycine 
• 6333-54-6 N-stearoylglycine 
• 14305-32-9 N-n-decanoylglycine 
• 14246-53-8 N-(1-oxooctyl)glycine 

Relevant articles and documents

Poly-2-oxazoline-derived polyurethanes: A versatile synthetic approach to renewable polyurethane thermosets

2-Nonyl-2-oxazoline and 2-(9-decenyl)-2-oxazoline have been copolymerized in different proportions by cationic ring-opening polymerization to obtain a series of random linear copolymers with tailored molecular weight and double bond functionality in the side chains. Thiol-ene addition of 2-mercaptoethanol has been used to produce a set of polyoxazoline-polyols under mild conditions and with quantitative double bond transformation. The polyols obtained in this way were reacted with methylene-bis(phenylisocyanate) to yield a series of amorphous and semicrystalline polyurethane networks. The thermal stability and the thermomechanical properties of these thermosets have been studied and related with the structure of the parent polyols.

N-acylation of ethanolamine using lipase: A chemoselective catalyst

The N-acylation of ethanolamine (2) with various fatty acids 1a-d and esters of fatty acids 1e-h using Candida antarctica B lipase (Novozym 435) are described and optimum conditions for selective N-acylation rather than O-acylation are also discussed. Microwave assisted solution phase, solid supported and conventional methods were investigated and results were compared. There is a synergy between the enzyme catalysis and microwave irradiation.

USE OF CERTAIN N-ACYLETHANOLAMINES TO ACHIEVE ETHYLENE- AND CYTOKININ-LIKE EFFECTS IN PLANTS AND FUNGI

N-acylethanolamines (NAEs) that can deliver an ethylene- or cytokinin-like effects to a plant, plant part or fungus are disclosed. Also disclosed are methods of using the NAES.