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Safety Information

P3275

Sigma-Aldrich

1,2-Dipalmitoyl-rac-glycero-3-phosphoethanolamine

synthetic, ≥98%

Synonym(s):

1,2-Dihexadecanoyl-rac-glycero-3-phosphoethanolamine, rac-Phosphatidylethanolamine, 1,2-dipalmitoyl, DL-β,γ-Dipalmitoyl-α-cephalin

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About This Item

Empirical Formula (Hill Notation):
C37H74NO8P
CAS Number:
Molecular Weight:
691.96
Beilstein:
1730602
EC Number:
MDL number:
UNSPSC Code:
51191904
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic

Quality Level

Assay

≥98%

form

powder

functional group

phospholipid

lipid type

phosphoglycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCCN)OC(=O)CCCCCCCCCCCCCCC

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)

InChI key

SLKDGVPOSSLUAI-UHFFFAOYSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

P3275-1G:
P3275-BULK:
P3275-500MG:
P3275-VAR:
P3275-100MG:
P3275-250MG:


Certificates of Analysis (COA)

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Sathiah Thennarasu et al.
Biochemistry, 49(50), 10595-10605 (2010-11-11)
In a minimalist design approach, a synthetic peptide MSI-367 [(KFAKKFA)(3)-NH(2)] was designed and synthesized with the objective of generating cell-selective nonlytic peptides, which have a significant bearing on cell targeting. The peptide exhibited potent activity against both bacteria and fungi
Christopher F Monson et al.
Analytical chemistry, 83(6), 2090-2096 (2011-02-16)
A pH controlled flow cell device was constructed to allow electrophoretic movement of charged lipids and membrane associated proteins in supported phospholipid bilayers. The device isolated electrolysis products near the electrodes from the electrophoresis process within the bilayer. This allowed
Siyuan Han et al.
Small (Weinheim an der Bergstrasse, Germany), 8(10), 1596-1606 (2012-03-14)
The use of biodegradable polymeric nanoparticles (NPs) for controlled drug delivery has shown significant therapeutic potential. Polyaspartic acid and polylactic acid are the most intensively studied biodegradable polymers. In the present study, novel amphiphilic biodegradable co-polymer NPs, poly(L-aspartic acid-co-lactic acid)
Xiaowei Ma et al.
International journal of nanomedicine, 7, 1313-1328 (2012-03-16)
There is an urgent need to develop drug-loaded biocompatible nanoscale packages with improved therapeutic efficacy for effective clinical treatment. To address this need, a novel poly (2-hydroxyethyl methacrylate)-poly (lactide)-1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine [PHEMA-g-(PLA-DPPE)] copolymer was designed and synthesized to enable these nanoparticles to
Curt M DeCaro et al.
Physical review. E, Statistical, nonlinear, and soft matter physics, 84(4 Pt 1), 041914-041914 (2011-12-21)
We have fabricated a stack of five 1,2-dipalmitoyl-sn-3-phosphatidylethanolamine (DPPE) bilayers supported on a polished silicon substrate in excess water. The density profile of these stacks normal to the substrate was obtained through analysis of x-ray reflectivity. Near the substrate, we

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