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75614

Supelco

2-Palmitoylglycerol

analytical standard

Sinonimo/i:

β-Monopalmitin, 2-Hexadecanoylglycerol, 2-Monohexadecanoylglycerol, 2-Monopalmitin, 2-Monopalmitoylglycerol, Hexadecanoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester

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About This Item

Formula empirica (notazione di Hill):
C19H38O4
Numero CAS:
23470-00-0
Peso molecolare:
330.50
Beilstein:
1796692
Numero MDL:
MFCD00058513
Codice UNSPSC:
85151701
ID PubChem:
329766169
NACRES:
NA.24

Origine biologica

synthetic

Livello qualitativo

100

Grado

analytical standard

Saggio

≥95% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

food and beverages

Formato

neat

Gruppo funzionale

ester

Temperatura di conservazione

−70°C

Stringa SMILE

O=C(CCCCCCCCCCCCCCC)OC(CO)CO

InChI

1S/C19H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(22)23-18(16-20)17-21/h18,20-21H,2-17H2,1H3
BBNYCLAREVXOSG-UHFFFAOYSA-N

Applicazioni

2-Palmitoylglycerol may be used as a reference standard for the separation and determination of the analyte in partial glyceride mixtures using thin layer chromatography with flame ionization detection (TLC-FID).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG9086
BCCG2931
BCCD5519
BCCD1561
BCCC0600

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USP

USP

1446000

Monoglycerides

1,2-Dipalmitoyl-rac-glycerol ≥99%

Sigma-Aldrich

D2135

1,2-Dipalmitoyl-rac-glycerol

Hexacosane analytical standard

Supelco

52183

Hexacosane

1,2-Dipalmitoyl-sn-glycerol ≥99%

Sigma-Aldrich

D9135

1,2-Dipalmitoyl-sn-glycerol

Quantitative determination of isomeric glycerides, free fatty acids and triglycerides by thin layer chromatography-flame ionization detector system.
Tanaka M, et al.
Methods, 15(10), 872-875 (1980)
Elizabeth J Judge et al.
Rapid communications in mass spectrometry : RCM, 31(20), 1690-1698 (2017-08-10)
Positional analysis of intact triglycerides could provide greater insights into the link between fatty acid position and lipotoxic diseases. However, this methodology has been impeded by lack of commercial availability of positionally pure triglycerides. This work reports on a strategy
Biswajit Khatua et al.
Science advances, 7(5) (2021-01-31)
Obesity sometimes seems protective in disease. This obesity paradox is predominantly described in reports from the Western Hemisphere during acute illnesses. Since adipose triglyceride composition corresponds to long-term dietary patterns, we performed a meta-analysis modeling the effect of obesity on
Caroline Turcotte et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 34(3), 4253-4265 (2020-02-06)
The endocannabinoid (eCB) 2-arachidonoyl-gycerol (2-AG) modulates immune responses by activating cannabinoid receptors or through its multiple metabolites, notably eicosanoids. Thus, 2-AG hydrolysis inhibition might represent an interesting anti-inflammatory strategy that would simultaneously increase the levels of 2-AG and decrease those
Benjamin Jenkins et al.
Metabolites, 10(7) (2020-07-28)
Typical lipidomics methods incorporate a liquid-liquid extraction with LC-MS quantitation; however, the classic sample extraction methods are not high-throughput and do not perform well at extracting the full range of lipids especially, the relatively polar species (e.g., acyl-carnitines and glycosphingolipids).
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