60501-41-9

Basic information

• Product Name: (Z)-[(octadec-9-enyloxy)methyl]oxirane
• Synonyms: (Z)-[(octadec-9-enyloxy)methyl]oxirane;OLEYLGLYCIDYLETHER;(Oleyloxymethyl)oxirane;[(9-octadecenyloxy)methyl]-, (Z)-Oxirane;[[[(Z)-9-Octadecenyl]oxy]methyl]oxirane
• CAS NO: 60501-41-9
• Molecular Formula: C₂₁H₄₀O₂
• Molecular Weight: 324.5411
• EINECS: 262-268-7
• Mol File: 60501-41-9.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 417.9°C at 760 mmHg
• Flash Point: 131.7°C
• Appearance: /
• Density: 0.895g/cm³
• Vapor Pressure: 8.29E-07mmHg at 25°C
• Refractive Index: 1.467
• CAS DataBase Reference: (Z)-[(octadec-9-enyloxy)methyl]oxirane(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-[(octadec-9-enyloxy)methyl]oxirane(60501-41-9)
• EPA Substance Registry System: (Z)-[(octadec-9-enyloxy)methyl]oxirane(60501-41-9)

Safety Data

• Hazardous Substances Data: 60501-41-9(Hazardous Substances Data)

Usage

General Description

(Z)-[(octadec-9-enyloxy)methyl]oxirane, also known as oxirane, is a chemical compound that belongs to the family of ethers and epoxy compounds. Its molecular structure consists of an oxirane ring attached to a long hydrocarbon chain, making it a fatty acid ester derivative. (Z)-[(octadec-9-enyloxy)methyl]oxirane is used in various industries, such as in the production of adhesives, coatings, and plastics. It is known for its ability to form strong and flexible bonds, as well as its resistance to corrosion and chemicals. Additionally, (Z)-[(octadec-9-enyloxy)methyl]oxirane has potential applications in the field of pharmaceuticals and biotechnology as a building block for the synthesis of bioactive molecules. However, it is important to handle and use this compound with care as it may be toxic and harmful if not properly managed.

InChI:InChI=1/C21H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-22-19-21-20-23-21/h9-10,21H,2-8,11-20H2,1H3/b10-9-

Upstream product

• 143-28-2 oleoyl alcohol 
• 106-89-8 epichlorohydrin 
• 213738-39-7 1-O-oleyl-rac-glycero-3-p-toluenesulfonate 
• 118712-54-2 glycidyl p-toluenesulfonate 
• 3132-64-7 1,2-Epoxy-3-bromopropane 

Downstream Products

• 593-31-7 rac-1-(Z-9-octadecenyl)glycerol 
• 13051-29-1 monoacetyl pentaerythritol 

Relevant articles and documents

Synthesis of new deuterated lipid probes for membrane fluidity measurements

New phosphatidylcholine analogs have been synthesized in order to be used as probes for membrane fluidity measurements in 2H-NMR experiments. A 1,3-asymmetrical diether glycerophosphatidylcholine pentadeuterated at the glycerol moiety is elaborated starting from propiolic acid in a 8-steps procedure whereas the corresponding monodeuterated compound is prepared from epibromohydrin.

Synthesis of natural 1- O -alkylglycerols: A study on the chemoselective opening of the epoxide ring by onium quaternary salts (N and P) and ionic liquids

A chemoselective route for the synthesis of 1-O-alkylglycerols chimyl (1), batyl (2), and selachyl (3) is reported. These compounds can be naturally isolated from shark liver oil and the skin of animals such as stingrays and chimeras and exhibit potential anti-fouling activity. The synthetic approach developed in this work included two distinct methods of preparation. The first was based on solvent-free reactions catalyzed by onium quaternary salts (N and P) and ionic liquids; the second methodology was based on a series of one-pot reactions.

LIPID COMPOUNDS FOR SUPRESSION OF TUMORIGENESIS

The present invention provides compounds, or pharmaceutically acceptable salts or analogs thereof, which exhibit anti-tumor activity. The present invention also includes methods for inhibiting the growth of cancer cells by contacting an effective amount of a compound of the present invention with the cancer cells in vitro or in vivo.