| Identification | Back 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 Properties | Back 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 Information | Back 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. |
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Energy Chemical
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