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安全信息

840505C

Avanti

18:0-20:4 PG

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

别名:

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

经验公式（希尔记法）:
C44H78O10PNa
CAS号:
322647-50-7
分子量:
821.05
MDL编号:
MFCD00674297
UNSPSC代码:
51191904
NACRES:
NA.25

方案

>99% (TLC)

表单

liquid

包装

pkg of 1 × 2.5 mL (840505C-25mg)

制造商/商品名称

Avanti Research™ - A Croda Brand 840505C

浓度

10 mg/mL (840505C-25mg)

脂质类型

phospholipids
cardiolipins

运输

dry ice

储存温度

−20°C

SMILES字符串

[Na+].[P](=O)([O-])(OC[C@H](OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC)COC(=O)CCCCCCCCCCCCCCCCC)OCC(O)CO

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

相关类别

一般描述

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.

应用

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.

包装

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

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形图

Skull and crossbonesHealth hazard
GHS06,GHS08

警示用语：

Danger

危险分类

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

靶器官

Central nervous system

WGK

WGK 3

法规信息

危险化学品
易制毒化学品（2类）

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分析证书(COA)

Lot/Batch Number

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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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