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ChemicalBook--->CAS DataBase List--->3443-82-1

3443-82-1

3443-82-1 Structure

3443-82-1 Structure
IdentificationBack Directory
[Name]

2-LINOLEOYL-RAC-GLYCEROL
[CAS]

3443-82-1
[Synonyms]

2-LG
2-Monolinolein
Glycerol 2-linolate
2-LINOLEOYL GLYCEROL
2-O-Linoleoylglycerol
2-Monolinoleoylglycerol
2-O-Linoleoyl-L-glycerol
2-LINOLEOYL-RAC-GLYCEROL
2-Linoleoylglycerol solution
9Z,12Z-OCTADECADIENOIC ACID, 2-GLYCERYL ESTER
(9Z,12Z)-9,12-Octadecadienoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester
[Molecular Formula]

C21H38O4
[MDL Number]

MFCD05863969
[MOL File]

3443-82-1.mol
[Molecular Weight]

354.52
Chemical PropertiesBack Directory
[Appearance]

Colourless Oil
[Melting point ]

9°C
[Boiling point ]

485.0±40.0 °C(Predicted)
[density ]

0.981±0.06 g/cm3(Predicted)
[Fp ]

2℃
[storage temp. ]

?20°C
[solubility ]

Chloroform (Slightly), DMF (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly)
[form ]

Oil
[pka]

13.54±0.10(Predicted)
[color ]

Colourless to Pale Yellow
[BRN ]

1715064
[Stability:]

Temperature Sensitive
[CAS DataBase Reference]

3443-82-1
Hazard InformationBack Directory
[Chemical Properties]

Colourless Oil
[Uses]

A fatty acid
[Definition]

ChEBI: A 2-monoglyceride where linoleoyl forms the 2-acyl group.
[Uses]

2-Arachidonoyl glycerol (2-AG) has been isolated from porcine brain, and has been characterized as the natural endocannabinoid ligand for the CB1 receptor. The congener of 2-AG in which a linoleoyl group replaces the arachidonoyl group is 2-linoleoyl glycerol (2-LG), and this compound also appears in vivo in conjunction with 2-AG. Although the intrinsic activity of 2-LG is low, it potentiates the activity of other endocannabinoids, including 2-AG. This “entourage” effect has been attributed to blockade of the breakdown and reuptake pathways that normally function to reduce endocannabinoid levels rapidly upon release.
Safety DataBack Directory
[Hazard Codes ]

F,Xn
[Risk Statements ]

11-20/21/22-36
[Safety Statements ]

16-36/37
[RIDADR ]

UN 1648 3 / PGII
[WGK Germany ]

3
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