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Merck

810610P

Avanti

4-palmitamido-TEMPO

N-tempoyl palmitamide, powder

Synonym(e):

4-Palmitamido-2,2,6,6-tetramethylpiperidine-1-oxyl; 2,2,6,6-Tetramethyl-4-[(1-oxohexadecyl)amino]-1-piperidinyloxy; 2,2,6,6-tetramethyl-4-palmitamidopiperidinooxy; 2,2,6,6-Tetramethylpalmitoylamidopiperidine-1-oxyl; 4-(Palmitylimino)-2,2,6,6-tetramethyl-1

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About This Item

Empirische Formel (Hill-System):
C25H49N2O2
CAS-Nummer:
Molekulargewicht:
409.67
UNSPSC-Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

Form

powder

Verpackung

pkg of 1 × 1 mg (810610P-1mg)

Hersteller/Markenname

Avanti Research - A Croda Brand 810610P

Lipid-Typ

ESR probes

Versandbedingung

dry ice

Lagertemp.

−20°C

Allgemeine Beschreibung

4-palmitamido-TEMPO/N-tempoyl-palmitamide is a spin label, that is present in the polar head-group region of the membrane.
This amphiphilic compound binds strongly to membranes by virture of its long hydrocarbon chain, but the polarity of the amide linkage is expected to localize the nitroxide function in the aqueous phase adjacent to the membrane surface. The location of the nitroxide function allows one to investigate electrostatic potentials and lipid-protein interactions at the membrane surface.

Anwendung

4-palmitamido-TEMPO/N-tempoyl palmitamide (N-TP) may be used:
  • to enrich rod outer segment (ROS) membranes
  • as a spin probe in vesicles/bilayer to prepare samples for electron spin resonance (ESR) experiments
  • as a component in liposomes to assess the mobility of lipid headgroups

Verpackung

5 mL Amber Glass Screw Cap Vial (810610P-1mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Lagerklassenschlüssel

11 - Combustible Solids


Analysenzertifikate (COA)

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Shani Ben-Zichri et al.
Biochimica et biophysica acta. Biomembranes, 1861(1), 75-82 (2018-11-06)
Curcumin, the main molecular ingredient of the turmeric spice, has been reported to exhibit therapeutic properties for varied diseases and pathological conditions. While curcumin appears to trigger multiple signaling pathways, the precise mechanisms accounting for its therapeutic activity have not
Y K Shin et al.
Biophysical journal, 61(6), 1443-1453 (1992-06-01)
A new general method for the determination of electrostatic potentials at biological surfaces is presented. The approach is based on measurement of the collision frequency of a charged nitroxide in solution with a nitroxide fixed to the surface at the

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