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Key Documents

700186M

Avanti

17:0 cholesteryl ester

cholest-5-en-3β-yl heptadecanoate, methylene chloride solution

Sinónimos:

cholesteryl heptadecanoate; 110864

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About This Item

Fórmula empírica (notación de Hill):
C44H78O2
Número de CAS:
Peso molecular:
639.09
UNSPSC Code:
12352211
NACRES:
NA.25

assay

>99% (TLC)

form

methylene chloride solution

packaging

pkg of 1 × 1 mL (700186M-1mg)

manufacturer/tradename

Avanti Research - A Croda Brand 700186M

concentration

1 mg/mL (700186M-1mg)

shipped in

dry ice

storage temp.

−20°C

InChI

1S/C44H78O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-24-42(45)46-37-29-31-43(5)36(33-37)25-26-38-40-28-27-39(35(4)23-21-22-34(2)3)44(40,6)32-30-41(38)43/h25,34-35,37-41H,7-24,26-33H2,1-6H3/t35-,37+,38+,39-,40+,41+,43+,44-/m1/s1

InChI key

PPQNZVDOBYGOLY-BFGJSWSOSA-N

General description

17:0 cholesteryl ester (cholesteryl heptadecanoate) is a lipid present in the seeds of Persea grattisima and Chrysophyllum albidum.

Application

17:0 cholesteryl ester (cholesteryl heptadecanoate) has been used as an internal standard in mass spectrometry imaging (MSI). It may be used:
  • in the egg yolk lipid extraction as an internal standard for mass spectroscopy analysis
  • as a reference internal standard for plasma lipid determination using thin layer chromatography (TLC)
  • as an external standard in liquid chromatography-tandem mass spectrometry

Packaging

5 mL Clear Glass Sealed Ampule (700186M-1mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

also commonly purchased with this product

Referencia del producto
Descripción
Precios

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 2


Certificados de análisis (COA)

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FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 32(6), 2966-2978 (2018-02-07)
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This study aimed to compare eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA) and docosahexaenoic acid (DHA) incorporated into red blood cells (RBC) phospholipids (PL), plasma PL, plasma triglyceride (TAG), and plasma cholesteryl ester (CE) fractions, and the metabolomics profiles in a

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