2190-30-9

Basic information

• Product Name: 1,2-dioleoyl-3-palmitoylglycerol
• Synonyms: 1,2-dioleoyl-3-palmitoylglycerol
• CAS NO: 2190-30-9
• Molecular Weight: 859.411
• Mol File: 2190-30-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 18-19 °C
• Boiling Point: 802.2±45.0 °C(Predicted)
• Density: 0.9027 g/cm3(Temp: 24 °C)
• CAS DataBase Reference: 1,2-dioleoyl-3-palmitoylglycerol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-dioleoyl-3-palmitoylglycerol(2190-30-9)
• EPA Substance Registry System: 1,2-dioleoyl-3-palmitoylglycerol(2190-30-9)

Safety Data

• Hazardous Substances Data: 2190-30-9(Hazardous Substances Data)

Upstream product

• 112-77-6 (Z)-9-octadecenoyl chloride 
• 305847-08-9 rac-1-monopalmitoylglycerol 
• 112-80-1 cis-Octadecenoic acid 
• 555-44-2 glyceroltripalmitate 
• 542-44-9 (S)-2,3-dihydroxypropyl hexadecanoic acid ester 
• 112-39-0 hexadecanoic acid methyl ester 
• 18418-21-8 1,2-O-isopropylidene-3-O-palmitoylglycerine 
• 122-32-7 trioleoylglycerol 
• 14465-68-0 trilinolenin 

Downstream Products

• 14960-35-1 1,2-dioleoyl-3-palmitoylglycerol 
• 65390-75-2 sn-1,2-dioleoyl-3-palmitoylglycerol 

Relevant articles and documents

Regioisomeric characterization of triacylglycerols using silver-ion HPLC/MS and randomization synthesis of standards

Silver-ion normal-phase high-performance liquid chromatography (HPLC) provides a superior separation selectivity for lipids differing in the number and position of double bonds in fatty acid chains including the resolution of triacylglycerol (TG) regioiso

Synthesis of the racemic analog of a honeybee (Apis mellifera) breeding pheromone component

The synthesis of 1-palmitoyl-2,3-dioleoylglycerine, the racemic analog of a honeybee breeding pheromone component, from 1,2-O-isopropylideneglycerine was proposed. 2004 Springer Science + Business Media, Inc.

Host-recognizing kairomones for parasitic wasp, Anisopteromalus calandrae, from larvae of azuki bean weevil, Callosobruchus chinensis.

Host-recognizing kairomones for the stinging behavior of the parasitic wasp, Anisopteromalus calandrae, were identified on host azuki bean weevil larvae, Callosobruchus chinensis (L.). The kairomones were extracted with acetone from Chinese green beans, from which emerged wasps and host weevils had been removed. The kairomones are a mixture of triacylglycerols and fatty acids, each of which is separately active, and with no observable synergistic effect between them. These compounds are known to be constituents of an oviposition-marking pheromone of host azuki bean weevils. However, they differ from the previously reported saturated hydrocarbons and diacylglycerols of the kairomone that another parasitic wasp, Dinarmus basalis, uses for the host recognition of C. chinensis. Thus, A. calandrae and D. basalis selectively utilize different constituents of the oviposition-marking pheromone of C. chinensis as host-recognizing kairomones.