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840862C

Avanti

18:0-18:2 PA

1-stearoyl-2-linoleoyl-sn-glycero-3-phosphate (sodium salt), chloroform

Synonym(s):

1-octadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphate (sodium salt); PA(18:0/18:2(9Z,12Z))

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About This Item

Empirical Formula (Hill Notation):
C39H72O8PNa
CAS Number:
Molecular Weight:
722.95
UNSPSC Code:
51191904
NACRES:
NA.25

assay

>99% (TLC)

form

liquid

packaging

pkg of 1 × 2.5 mL (840862C-25mg)

manufacturer/tradename

Avanti Research - A Croda Brand 840862C

concentration

10 mg/mL (840862C-25mg)

lipid type

phospholipids
cardiolipins

shipped in

dry ice

storage temp.

−20°C

InChI

1S/C39H73O8P.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(40)45-35-37(36-46-48(42,43)44)47-39(41)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2;/h12,14,18,20,37H,3-11,13,15-17,19,21-36H2,1-2H3,(H2,42,43,44);/q;+1/p-1/b14-12-,20-18-;/t37-;/m1./s1

InChI key

QCCKEVYCMGRONT-ZNKFQGFOSA-M

General description

Phosphatidic acid (PA) is an amphipathic lipid, containing a polar head group and two long hydrophobic acyl chains. PA is anionic in nature and a membrane structural lipid. It acts as a parent compound for more complex membrane phospholipids.

Biochem/physiol Actions

Phosphatidic acid (PA) is a bioactive lipid and a secondary messenger. PA reacts with water and other phospholipids to produce lipid bilayers and multicomponent bilayers respectively.

Packaging

5 mL Clear Glass Sealed Ampule (840862C-25mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

pictograms

Skull and crossbonesHealth hazard

signalword

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_germany

WGK 3


Certificates of Analysis (COA)

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Bioactive Lipids
An Introduction to Biological Membranes, 453-478 (2016)
Lipid second messengers and Receptors
Encyclopedia of Endocrine Diseases, 77(3), 329-334 (2004)

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