40716-42-5

Basic information

• Product Name: [R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide
• Synonyms: [R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide;RICINOLEAMIDE DEA;9-Octadecenamide, 12-hydroxy-N,N-bis(2-hydroxyethyl)-, (9Z,12R)-;(Z,12R)-12-hydroxy-N,N-bis(2-hydroxyethyl)octadec-9-enamide;(12R,9Z)-12-Hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide
• CAS NO: 40716-42-5
• Molecular Formula: C22H43NO4
• Molecular Weight: 385.58112
• EINECS: 255-051-3
• Mol File: 40716-42-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 560.5°Cat760mmHg
• Flash Point: 292.8°C
• Appearance: /
• Density: 1.007g/cm³
• Vapor Pressure: 6.76E-15mmHg at 25°C
• Refractive Index: 1.499
• CAS DataBase Reference: [R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide(CAS DataBase Reference)
• NIST Chemistry Reference: [R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide(40716-42-5)
• EPA Substance Registry System: [R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide(40716-42-5)

Safety Data

• Hazardous Substances Data: 40716-42-5(Hazardous Substances Data)

Usage

Uses

ricinoleamide DEA is an emulsifier with lubricity, and good wetting and softening properties. It can also serve as a foam booster and formula stabilizer when blended with anionic surfactants such as lauryl sulfates.

InChI:InChI=1/C22H43NO4/c1-2-3-4-11-14-21(26)15-12-9-7-5-6-8-10-13-16-22(27)23(17-19-24)18-20-25/h9,12,21,24-26H,2-8,10-11,13-20H2,1H3/b12-9-/t21-/m1/s1

Upstream product

• 111-42-2 2,2'-iminobis[ethanol] 
• 141-22-0 Ricinoleic acid 

Relevant articles and documents

Synthesis and characterization of ricinoleamide-based polyurethane

Ricinus communis (RC) oil-based materials are currently receiving increasing attention because of economic and environmental concerns. In the present work, RC oil - a natural triol has been utilized for the development of an advanced polymeric material - poly(urethanericinoleamide) (PUR) through very simple synthesis and curing strategy, omitting derivatization steps or side reactions, chain extenders and crosslinkers. The synthesis of PUR was carried out in two steps. The first step is the introduction of an amide group in the RC oil (89.5% ricinoleic acid) via base catalyzed amidation, which results in N, N-bis (2-hydroxyethyl) ricinoleamide (HERA). The second step is urethanation of HERA by the reaction of toluene-2,4-diisocyanate (TDI) in minimal possible organic solvent by one-shot technique, which results in the formation of polyurethane along with amide linkages. The physico-chemical and spectral studies (FT-IR, 1H-NMR and 13C-NMR techniques) confirm these two reactions and the structure of PUR. The resin was cured at ambient temperature without any cross linker. Solubility of the resin was investigated in different polar and non-polar solvents. Thermo-gravimetric analysis (TGA)/differential thermal analysis (DTA) and Differential Scanning Calorimetry (DSC) were used to determine the thermal stability and curing behavior of PUR. An ambient cured ricinoleamide modified polyurethane resin exhibited thermal resistance up to 200-220 °C. AOCS 2011.