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D8394

Sigma-Aldrich

1,2-Dioleoyl-rac-glycerol

≥97%

Synonym(s):

(9Z)-9-Octadecenoic acid 1,1′-[1-(hydroxymethyl)-1,2-ethanediyl] ester, (±)-1,2-Diolein, 1,2-Di(cis-9-octadecenoyl)-rac-glycerol, rac-1,2-Dioleoylglycerol, rac-Glycerol 1,2-dioleate, DG(18:1(9Z)/18:1(9Z)/0:0)[rac]

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About This Item

Empirical Formula (Hill Notation):
C39H72O5
CAS Number:
Molecular Weight:
620.99
Beilstein/REAXYS Number:
1917687
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic (organic)

Quality Level

assay

≥97%

form

liquid

impurities

≤3% 1,3-isomer

functional group

ester

lipid type

neutral glycerides

shipped in

dry ice

storage temp.

−20°C

SMILES string

CCCCCCCC\C=C/CCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCC\C=C/CCCCCCCC

InChI

1S/C39H72O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(41)43-36-37(35-40)44-39(42)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h17-20,37,40H,3-16,21-36H2,1-2H3/b19-17-,20-18-

InChI key

AFSHUZFNMVJNKX-CLFAGFIQSA-N

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Related Categories

Application


  • Diacylglycerol acyltransferases from Vernonia and Stokesia prefer substrates with vernolic acid.: Studies enzyme preferences for 1,2-Dioleoyl-rac-glycerol in the biosynthesis of industrially important oils, offering pathways to enhance bio-oil production using specific enzymatic processes (Yu et al., 2006).

Caution

Some isomerization may occur in storage or in solution.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Lipids, components of the plasma and intracellular membranes as well as of droplets, provide different biological functions related to energy, carbon storage, and stress responses. Bacterial species display diverse membrane composition that changes in response to the different environmental conditions.
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Journal of oleo science, 70(2), 227-236 (2021-01-19)
n-3 polyunsaturated fatty acids (PUFA)-rich triacylglycerols (TAG) with many beneficial effects are still difficult to be synthesized efficiently and rapidly by current synthetic techniques. This study reports the fatty acid specificity of immobilized MAS1 lipase and its efficient synthesis of
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SLAS discovery : advancing life sciences R & D, 22(4), 360-365 (2017-03-23)
Monoacylglycerol acyltransferase (MGAT) activity catalyzes the synthesis of diacylglycerol (DAG) from fatty acyl-CoA and monoacylglycerol as substrates. It is important for the resynthesis of triacylglycerol (TAG) in the intestine. In the present study, we developed a MGAT enzymatic assay of
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