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790147P

Avanti

16:0-23:2 Diyne PE

1-palmitoyl-2-(10,12-tricosadiynoyl)-sn-glycero-3-phosphoethanolamine, powder

Synonym(s):

PTPE

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About This Item

Empirical Formula (Hill Notation):
C44H80NO8P
CAS Number:
328946-17-4
Molecular Weight:
782.08
MDL number:
MFCD16661190
UNSPSC Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

form

powder

packaging

pkg of 2 × 100 mg (790147P-200mg)
pkg of 1 × 25 mg (790147P-25mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 790147P

shipped in

dry ice

storage temp.

−20°C

General description

16:0-23:2 Diyne PE or 1-palmitoyl-2-(10,12-tricosadiynoyl)-sn-glycero-3-phosphoethanolamine is an ultraviolet (UV)-polymerizable phospholipid.

Application

16:0-23:2 Diyne PE or 1-palmitoyl-2-(10,12-tricosadiynoyl)-sn-glycero-3-phosphoethanolamine has been used in the preparation of:
  • 2-dimensional phospholipid and copolymer nanomembranes
  • planar polymerizable phospholipid membranes for reconstitution of protein ion channels formed by the bacterial toxins
  • mixed monolayers at the air-water interface on a Langmuir-Blodgett (LB) trough

Packaging

5 mL Amber Glass Screw Cap Vial (790147P-200mg)
5 mL Amber Glass Screw Cap Vial (790147P-25mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

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Susan M Daly et al.
Langmuir : the ACS journal of surfaces and colloids, 22(3), 1215-1222 (2006-01-25)
We formed monolayers and black lipid membranes (BLMs) of photopolymerizable lipids mixed with the channel-forming protein gramicidin A to evaluate their miscibility and the potential for improved stability of the BLM scaffold through polymerization. Analyses of surface pressure vs area
S Punnamaraju et al.
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

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