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D8394

Sigma-Aldrich

1,2-Dioleoyl-rac-glycerol

≥97%

Sinônimo(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

Fórmula empírica (Notação de Hill):
C39H72O5
Número CAS:
2442-61-7
Peso molecular:
620.99
Beilstein:
1917687
Número MDL:
MFCD00043031
Código UNSPSC:
12352211
ID de substância PubChem:
24894210
NACRES:
NA.25

fonte biológica

synthetic (organic)

Ensaio

≥97%

Formulário

liquid

Impurezas

≤3% 1,3-isomer

grupo funcional

ester

tipo de lipídio

neutral glycerides

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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-

chave InChI

AFSHUZFNMVJNKX-CLFAGFIQSA-N

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Aplicação


  • 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).

Atenção

Some isomerization may occur in storage or in solution.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
SLCG9973
SLCC4100
SLBZ6366
SLBX1007
SLBV4825

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rac-Glyceryl-1,1,2,3,3-d5-1,2-dioleate 98 atom % D, 95% (CP)

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Sigma-Aldrich

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Trioleato de glicerila

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Sigma-Aldrich

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1-Oleoyl-2-acetyl-sn-glycerol

Valeria Scala et al.
Frontiers in microbiology, 9, 1839-1839 (2018-08-30)
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.
Xiumei Wang et al.
Bioprocess and biosystems engineering, 44(3), 575-584 (2020-11-21)
This study reports the properties of immobilized MAS1-H108A lipase from marine Streptomyces sp. strain W007 on XAD1180 resin and its application in the synthesis of n-3 polyunsaturated fatty acids (PUFA)-rich triacylglycerols (TAG) for the first time. It was found that
Xiumei Wang et al.
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
Ryutaro Adachi et al.
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
Konglong Feng et al.
Bioresource technology, 298, 122553-122553 (2019-12-18)
Deacidification of high-acid soy sauce residue (SSR) oil is crucial to utilization of SSR oil. Aspergillus niger lipase (ANL) has been widely applied for such purpose while its immobilization still has large room for improvement. ANL was immobilized onto six
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