790146P
Avanti
16:0-23:2 Diyne PC
1-palmitoyl-2-(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine, powder
Synonym(s):
PTPC
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About This Item
Recommended Products
Assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 25 mg (790146P-25mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 790146P
shipped in
dry ice
storage temp.
−20°C
Application
16:0-23:2 Diyne PC or 1-palmitoyl-2-(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine has been used in lipid-monolayer interface of nanoparticles (NPs) to modify the drug diffusion across the layer.
Biochem/physiol Actions
16:0-23:2 Diyne PC or 1-palmitoyl-2-(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (PTPC) is a polymerizable lipid that can cross-link with adjacent PTPC molecules under ultraviolet light (UV)-irradiation.
Packaging
5 mL Amber Glass Screw Cap Vial (790146P-25mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class Code
11 - Combustible Solids
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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British journal of pharmacology, 163(7), 1402-1410 (2011-03-23)
Traumatic brain injury (TBI) represents the leading cause of death in young individuals. It triggers the accumulation of harmful mediators, leading to secondary damage, yet protective mechanisms are also set in motion. The endocannabinoid (eCB) system consists of ligands, such
Langmuir : the ACS journal of surfaces and colloids, 28(20), 7657-7664 (2012-05-03)
A combination of nonpolymerizable phospholipids (DPPC or DPhPC) and a smaller amount of cross-linking photopolymerizable phospholipids (23:2 DiynePC) is incorporated in an unsupported artificial lipid bilayer formed using the droplet interface bilayer (DIB) approach. The DIB is formed by contacting
Nanoscale, 6(4), 2321-2327 (2014-01-15)
The effects of nanoparticle (NP) properties, such as size, shape and surface charge, on their efficacy and toxicity have been studied extensively. However, the effect of controlled drug release on NP efficacy and toxicity has not been thoroughly evaluated in
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