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D1639

Sigma-Aldrich

1,3-Dipalmitoylglycerin

≥99%

Synonym(e):

α,γ-Dipalmitin, Glycerin-1,3-Dipalmitat

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About This Item

Empirische Formel (Hill-System):
C35H68O5
CAS-Nummer:
502-52-3
Molekulargewicht:
568.91
Beilstein:
1809772
EG-Nummer:
207-942-3
MDL-Nummer:
MFCD00042877
UNSPSC-Code:
12352211
PubChem Substanz-ID:
24893503
NACRES:
NA.25

Biologische Quelle

synthetic (organic)

Qualitätsniveau

200

Assay

≥99%

Form

powder

Verunreinigungen

≤1% 1,2-isomer

Funktionelle Gruppe

ester

Lipid-Typ

neutral glycerides

Versandbedingung

ambient

Lagertemp.

−20°C

SMILES String

CCCCCCCCCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCCCCCCCCC

InChI

1S/C35H68O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-34(37)39-31-33(36)32-40-35(38)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h33,36H,3-32H2,1-2H3

InChIKey

GFAZGHREJPXDMH-UHFFFAOYSA-N

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Anwendung

Glyceryl 1,3-dipalmitate has been used as a standard in lipid analysis of feeds and omasal digesta. It has also been used as a standard in identifying sn-1,3 diacylglycerol (DAG) in skeletal muscles.

Biochem./physiol. Wirkung

Glyceryl 1,3-dipalmitate from Lactobacillus paracasei subsp. possesses neuroprotective effects.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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Annette Karen Serup et al.
Diabetes, 65(10), 2932-2942 (2016-08-05)
Type 2 diabetes and skeletal muscle insulin resistance have been linked to accumulation of the intramyocellular lipid-intermediate diacylglycerol (DAG). However, recent animal and human studies have questioned such an association. Given that DAG appears in different stereoisomers and has different
A Halmemies-Beauchet-Filleau et al.
Journal of dairy science, 96(9), 5882-5900 (2013-07-16)
Diets based on red clover silage (RCS) typically increase the concentration of polyunsaturated fatty acids (PUFA) in ruminant milk and meat compared with grass silages (GS), an effect that has been attributed to higher activity of polyphenol oxidase in red
Mari Merce Cascant et al.
Analytical and bioanalytical chemistry, 409(14), 3527-3539 (2017-04-09)
There is a great interest in finding alternatives and green solvents in extraction processes to replace petroleum based solvents. In order to investigate these possibilities, computational methods, as Hansen solubility parameters (HSP) and conductor-like screening model for real solvent (COSMO-RS)
Raquel B Gómez-Coca et al.
Food chemistry, 330, 127226-127226 (2020-06-17)
The detection of soft deodorized olive oils in extra virgin olive oil (EVOO) has become a challenging task ever since it was demonstrated that: 1. The process does not form the typical refining markers, e.g. stigmastadienes, and 2. The determination
Xiuwen Wang et al.
Biotechnology letters, 41(6-7), 789-799 (2019-05-10)
To investigate the lipase-catalyzed synthesis of high purity sn-1/3 and sn-2 monoacylglycerols (1/3-MAG and 2-MAG) of different fatty acids (FAs). The 1/3-MAGs of three FAs (16:0, 17:0, 16:1) were synthesized using lipase-catalyzed esterification of glycerol with FAs. The 2-MAGs were
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