Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C27H52O5 |
| Molecular Weight | 456.6988 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCCC
InChI
InChIKey=OQQOAWVKVDAJOI-UHFFFAOYSA-N
InChI=1S/C27H52O5/c1-3-5-7-9-11-13-15-17-19-21-26(29)31-24-25(23-28)32-27(30)22-20-18-16-14-12-10-8-6-4-2/h25,28H,3-24H2,1-2H3
| Molecular Formula | C27H52O5 |
| Molecular Weight | 456.6988 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Glyceryl 1,2-dilaurate is the fatty acid diester of glycerol. Glyceryl diesters, on a whole, are FDA and CIR approved and are given the GRAS rating. It is used as an emollient (skin conditioning agent) in cosmetics for increasing the "body" and viscosity of emulsions and improving the elegance of low-cost formulations. In addition, it may be used for the preparation of nanolipid carriers for drug delivery.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Parasite impairment by targeting Plasmodium-infected RBCs using glyceryl-dilaurate nanostructured lipid carriers. | 2014-08 |
|
| Amended final report on the safety assessment of glyceryl dilaurate, glyceryl diarachidate, glyceryl dibehenate, glyceryl dierucate, glyceryl dihydroxystearate, glyceryl diisopalmitate, glyceryl diisostearate, glyceryl dilinoleate, glyceryl dimyristate, glyceryl dioleate, glyceryl diricinoleate, glyceryl dipalmitate, glyceryl dipalmitoleate, glyceryl distearate, glyceryl palmitate lactate, glyceryl stearate citrate, glyceryl stearate lactate, and glyceryl stearate succinate. | 2007 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:50:53 GMT 2025
by
admin
on
Mon Mar 31 17:50:53 GMT 2025
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| Record UNII |
9S1016G3A2
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| Record Status |
Validated (UNII)
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9S1016G3A2
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DTXSID30880897
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33979
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