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Key Documents

850358C

Avanti

16:1 (Δ9-Cis) PC

1,2-dipalmitoleoyl-sn-glycero-3-phosphocholine, chloroform

Synonyme(s) :

1,2-di-(9Z-hexadecenoyl)-sn-glycero-3-phosphocholine; PC(16:1(9Z)/16:1(9Z))

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About This Item

Formule empirique (notation de Hill):
C40H76NO8P
Numéro CAS:
Poids moléculaire :
730.01
Code UNSPSC :
51191904
Nomenclature NACRES :
NA.25

Pureté

>99% (TLC)

Forme

liquid

Conditionnement

pkg of 1 × 2.5 mL (850358C-25mg)
pkg of 2 × 4 mL (850358C-200mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand 850358C

Concentration

10 mg/mL (850358C-25mg)
25 mg/mL (850358C-200mg)

Type de lipide

phospholipids
cardiolipins

Conditions d'expédition

dry ice

Température de stockage

−20°C

Description générale

16:1 (Δ9-Cis) PC (1,2-dipalmitoleoyl-sn-glycero-3-phosphocholine) is a lipid derivative having a phosphocholine backbone. It also has two palmitic acid chains each having one cis double bond at 9th carbon. It is a double mono-unsaturated lipid.
The list of Phosphatidylcholine products offered by Avanti is designed to provide compounds having a variety of physical properties. Products available include short chain (C3-C8 are water soluble and hygroscopic), saturated, multi-unsaturated and mixed acid PC′s. All of the products are purified by HPLC, and special precautions are taken to protect the products for oxidization and hydrolysis.

Application

16:1 (Δ9-Cis) PC (1,2-dipalmitoleoyl-sn-glycero-3-phosphocholine) has been used in liposome preparation. It may be used to prepare giant unilamellar vesicles (GUVs) and multilamellar vesicles (MLVs).

Actions biochimiques/physiologiques

Phosphatidylcholine (PC) forms a hydrophobic surface in the mucus by acting as a surfactant resulting in the inhibition of penetrance of bacteria.

Conditionnement

5 mL Clear Glass Sealed Ampule (850358C-200mg)
5 mL Clear Glass Sealed Ampule (850358C-25mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Souvent commandé avec ce produit

Réf. du produit
Description
Tarif

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 Oral - STOT SE 3

Organes cibles

Liver,Kidney, Respiratory system

Code de la classe de stockage

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

does not flash

Point d'éclair (°C)

does not flash


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

Bilayer thickness and curvature influence binding and insertion of a pHLIP peptide
Karabadzhak AG, et al
Biophysical Journal (2018)
Parian AM
Integrative Medicine (2018)
Solubilization of lipids and lipid phases by the styrene-maleic acid copolymer
<BIG><BIG>Pardo JJD, et al</BIG></BIG>
European Biophysics Journal (2017)
Łukasz Syga et al.
Chembiochem : a European journal of chemical biology, 21(9), 1320-1328 (2019-12-10)
Attachment of lipophilic groups is an important post-translational modification of proteins, which involves the coupling of one or more anchors such as fatty acids, isoprenoids, phospholipids, or glycosylphosphatidyl inositols. To study its impact on the membrane partitioning of hydrophobic peptides
Miranda L Schmidt et al.
Biochimica et biophysica acta. Biomembranes, 1862(5), 183196-183196 (2020-01-21)
Lipid bilayers form the basis of cell membranes and the phase behaviour of the membrane has been linked to proper cell function. Model membranes composed of relatively simple mixtures of phospholipids and cholesterol can already exhibit complex phase behaviour. Specifically

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