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840505C

Avanti

18:0-20:4 PG

1-stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1′-rac-glycerol) (sodium salt), chloroform

Synonym(s):

1-octadecanoyl-2-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phospho-(1′racglycerol) (sodium salt); SAPG; PG(18:0/20:4(5Z,8Z,11Z,14Z)); 110653

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About This Item

Empirical Formula (Hill Notation):
C44H78O10PNa
CAS Number:
322647-50-7
Molecular Weight:
821.05
UNSPSC Code:
51191904
NACRES:
NA.25

Assay

>99% (TLC)

form

liquid

packaging

pkg of 1 × 2.5 mL (840505C-25mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 840505C

concentration

10 mg/mL (840505C-25mg)

lipid type

phospholipids
cardiolipins

shipped in

dry ice

storage temp.

−20°C

InChI

1S/C44H79O10P.Na/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-36-44(48)54-42(40-53-55(49,50)52-38-41(46)37-45)39-51-43(47)35-33-31-29-27-25-23-21-18-16-14-12-10-8-6-4-2;/h11,13,17,19,22,24,28,30,41-42,45-46H,3-10,12,14-16,18,20-21,23,25-27,29,31-40H2,1-2H3,(H,49,50);/q;+1/p-1/b13-11-,19-17-,24-22-,30-28-;/t41?,42-;/m1./s1

InChI key

XLHSHRIGGNFBGF-PYXSUFCTSA-M

General description

18:0-20:4 PG or 1-stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1′-rac-glycerol) is a sodium salt of glycerophospholipid, with substitution of stearic acid, arachidonic acid and phospho-rac-(1-glycerol) at the sn-1, sn-2 and sn-3 positions respectively, in the glycerol backbone.

Application

18:0-20:4 PG or 1-stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1′-rac-glycerol) (sodium salt) has been used as a standard in liquid chromatography tandem mass spectrometry (LC?MS/MS) method for lipid quantification.

Packaging

5 mL Clear Glass Sealed Ampule (840505C-25mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

Target Organs

Central nervous system

WGK

WGK 3

Certificates of Analysis (COA)

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Max Scherer et al.
Analytical chemistry, 82(21), 8794-8799 (2010-10-16)
Cardiolipin (CL) and bis(monoacylglycero)phosphate (BMP) are unique lipid structures with important biological roles for mitochondrial integrity and endolysosomal degradation, respectively. They are synthesized from common precursors, phosphatidylglycerol (PG) and phosphatidic acid (PA). Here we present a rapid method for the

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