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Key Documents

790427C

Avanti

06:0 PC-d22

Avanti Research - A Croda Brand 790427C

Synonyme(s) :

1,2-dihexanoyl-d22-sn-glycero-3-phosphocholine

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About This Item

Formule empirique (notation de Hill):
C20H18NO8PD22
Numéro CAS:
Poids moléculaire :
475.64
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.12

Pureté

>99% (TLC)

Forme

liquid

Conditionnement

pkg of 1 × 1 mL (790427C-10mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand 790427C

Concentration

10 mg/mL (790427C-10mg)

Conditions d'expédition

dry ice

Température de stockage

−20°C

Description générale

Deuterated fatty acids experience exchange of the deuteriums on the alpha carbon to the carbonyl, i.e., C2 position, and will therefore be a mixture of compounds that are fully deuterated and partially deuterated at that position.
Phosphatidylcholine is a zwitterionic glycerophospholipid, containing choline. It consists of a head and two tails. Head group contains choline and phosphate. Head is polar and water soluble. The tail group contains two fatty acyl chains esterified with glycerol. Tail group is non-polar and water-insoluble. Phosphatidylcholine is synthesized in the liver by phosphatidylethanolamine methyltransferase (PEMT) pathway. It is also synthesized by the Kennedy pathway and the Lands cycle.

Application

06:0 PC-d22 (1,2-dihexanoyl-d22-sn-glycero-3-phosphocholine) has been used:
  • as bicelles for lipid in HN-HN nuclear overhauser enhancement (NOE) detection
  • as an internal standard in residual algal suspension for liquid chromatography-mass spectrometry analysis (LC-MS/MS)
  • to produce bicelles to investigate C-peptide and membrane interaction by diffusion nuclear magnetic resonance (NMR) and 2D total correlation spectroscopy (TOCSY)

Actions biochimiques/physiologiques

Phosphatidylcholine (PC) is a major component of the membrane bilayer. It is involved in the synthesis of signaling molecules. PC is the precursor for the synthesis of sphingomyelin and phosphatidylserine.

Conditionnement

5 mL Clear Glass Sealed Ampule (790427C-10mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictogrammes

Skull and crossbonesHealth hazard

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Central nervous system

Classe de danger pour l'eau (WGK)

WGK 3


Certificats d'analyse (COA)

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Biochemistry of Lipids, Lipoproteins and Membranes (2015)
pH-dependent interaction between C-peptide and phospholipid bicelles
Unnerstaale S and Maler L
Journal of biophysics (Hindawi Publishing Corporation : Online), 2012(1), 43-43 (2012)
Two different pathways of phosphatidylcholine synthesis, the Kennedy Pathway and the Lands Cycle, differentially regulate cellular triacylglycerol storage
Moessinger C, et al.
BMC Cell Biology, 15(1), 43-43 (2014)
Metabolic and morphological changes of an oil accumulating trebouxiophycean alga in nitrogen-deficient conditions
Ito T, et al.
Metabolomics, 9(1), 178-187 (2013)
Membrane lipids:phospholipids
General, Organic, and Biological Chemistry, 581-581 (2006)

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