97605-97-5

Basic information

• Product Name: 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl oleate
• Synonyms: 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl oleate;(Z)-9-Octadecenoic acid 2-hydroxy-3-(2,3-dihydroxypropoxy)propyl ester;(Z)-9-Octadecenoic acid 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl ester;Oleic acid 2,6,7-trihydroxy-4-oxaheptan-1-yl ester;Oleic acid 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl ester
• CAS NO: 97605-97-5
• Molecular Formula: C₂₄H₄₆O₆
• Molecular Weight: 430.61844
• EINECS: 307-368-4
• Mol File: 97605-97-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 560.3°Cat760mmHg
• Flash Point: 176.6°C
• Appearance: /
• Density: 1.02g/cm³
• Vapor Pressure: 6.9E-15mmHg at 25°C
• Refractive Index: 1.486
• CAS DataBase Reference: 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl oleate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl oleate(97605-97-5)
• EPA Substance Registry System: 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl oleate(97605-97-5)

Safety Data

• Hazardous Substances Data: 97605-97-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C24H46O6/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-23(29-20-22(27)18-25)17-24(28)30-19-21(2)26/h10-11,21-23,25-27H,3-9,12-20H2,1-2H3/b11-10-

Upstream product

• 122-32-7 trioleoylglycerol 
• 627-82-7 diglycerol 

Relevant articles and documents

1-O-Alkyl (di)glycerol ethers synthesis from methyl esters and triglycerides by two pathways: Catalytic reductive alkylation and transesterification/reduction

From available and bio-sourced methyl esters, monoglycerides or oleic sunflower refined oil, the corresponding 1-O-alkyl (di)glycerol ethers were obtained in both high yields and selectivity by two different pathways. With methyl esters, a reductive alkylation with (di)glycerol was realized under 50 bar hydrogen pressure in the presence of 1 mol% of Pd/C and an acid co-catalyst. A second two step procedure was evaluated from methyl esters or triolein and consisted of a first transesterification to the corresponding monoglyceride with a BaO/Al2O3 catalyst, then its reduction to the desired glycerol monoether with a recyclable heterogeneous catalytic system Pd/C and Amberlyst 35 under H2 pressure. In addition, a mechanism for the reaction was also proposed.