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850705P

Avanti

16:0 PE

Avanti Research™ - A Croda Brand

Synonym(s):

1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine; DPPE; PE(16:0/16:0); 110633

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0.4 ML
CN¥1,578.88

CN¥1,578.88

Estimated to ship onMay 20, 2025Details

Request a Bulk Order
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0.4 ML
CN¥1,578.88

About This Item

Empirical Formula (Hill Notation):
C37H74NO8P
CAS Number:
923-61-5
Molecular Weight:
691.96
MDL number:
MFCD00036776
UNSPSC Code:
51191904
NACRES:
NA.25

CN¥1,578.88

Estimated to ship onMay 20, 2025Details

Request a Bulk Order

description

1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine

Assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 1 g (850705P-1g)
pkg of 1 × 200 mg (850705P-200mg)
pkg of 1 × 25 mg (850705P-25mg)
pkg of 1 × 500 mg (850705P-500mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand

lipid type

phospholipids
cardiolipins

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@@](COP([O-])(OCC[NH3+])=O)(OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O

InChI

1S/C37H74NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-36(39)43-33-35(34-45-47(41,42)44-32-31-38)46-37(40)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h35H,3-34,38H2,1-2H3,(H,41,42)/t35-/m1/s1

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technique(s)

microbiological culture: suitable

technique(s)

microbiological culture: suitable

technique(s)

microbiological culture: suitable

technique(s)

microbiological culture: suitable

biological source

Escherichia coli

biological source

Escherichia coli

biological source

Escherichia coli

biological source

Escherichia coli

morphology

rod shaped

morphology

rod shaped

morphology

rod shaped

morphology

rod shaped

shipped in

wet ice

shipped in

dry ice, wet ice

shipped in

dry ice

shipped in

dry ice

storage temp.

−70°C

storage temp.

−70°C

storage temp.

−70°C

storage temp.

−70°C

General description

Phosphatidylethanolamine is an aminophospholipid. It is present in eukaryotic and prokaryotic cells.[1] Phosphatidylethanolamine is one of the most abundant glycerophospholipids in biological membranes.[2] It is found in nervous tissue.[3]

Application

16:0 PE has been used:
  • for the preparation of perfluorocarbon (PFC) nanoparticles[4]
  • for lipid binding by liposome flotation assays[5]
  • to characterize the metabolic fate of synaptamide in a dopaminergic cell line[6]

Biochem/physiol Actions

Phosphatidylethanolamine forms pure lipid structures.[7] It plays a vital role in autophagy, cell division and protein folding. Phosphatidylethanolamine functions as a precursor for the synthesis of various protein modifications.[2] It controls membrane fluidity in eukaryotic cells.[8] Phosphatidylethanolamine behaves as an intermediate for the synthesis of glycerophospholipid classes.[2]

Packaging

20 mL Clear Glass Screw Cap Vial (850705P-1g)
20 mL Clear Glass Screw Cap Vial (850705P-500mg)
5 mL Amber Glass Screw Cap Vial (850705P-200mg)
5 mL Amber Glass Screw Cap Vial (850705P-25mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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    An Introduction to Biological Membranes: Composition, Structure and Function (2016)
    Anti-JNK2 peptide-siRNA nanostructures improve plaque endothelium and reduce thrombotic risk in atherosclerotic mice
    Pan H, et al.
    International journal of nanomedicine, 13, 5187-5187 (2018)
    The Membranes of Cells (2016)
    Metabolic studies of synaptamide in an immortalized dopaminergic cell line
    Sonti S, et al.
    Prostaglandins & other lipid mediators, 141, 25-33 (2019)
    Benjamin J Peters et al.
    Langmuir : the ACS journal of surfaces and colloids, 34(30), 8939-8951 (2018-07-01)
    Pyridine-based small-molecule drugs, vitamins, and cofactors are vital for many cellular processes, but little is known about their interactions with membrane interfaces. These specific membrane interactions of these small molecules or ions can assist in diffusion across membranes or reach
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