Molecular structure of 1,2-Dipalmitoyl-sn-glycero-3-phosphocholine, CAS Number: 63-89-8
1,2-Dipalmitoyl-sn-glycero-3-phosphocholine (CAS 63-89-8)
See product citations (9)
Alternate Names:
1,2-Dihexadecanoyl-sn-glycero-3-phosphocholine; 1,2-Dihexadecanoyl-sn-glycero-3-phosphorylcholine; DPPC; PC(16:0/16:0)
Application:
1,2-Dipalmitoyl-sn-glycero-3-phosphocholine is a phosphoglyceride that has been used for preparation of liposomal monolayers/bilayers
CAS Number:
63-89-8
Purity:
≥98%
Molecular Weight:
734.04
Molecular Formula:
C40H80NO8P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Product Citations
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
1,2-dipalmitoyl-sn-glycero-3-Phosphatidylcholine (L-DPPC) is a zwitterionic phosphoglyceride that has been used for the preparation of liposomal monolayers. Preparation of proteoliposomes formed with 1,2-dipalmitoyl-sn-glycero-3-Phosphatidylcholine exhibited a five-fold increase in gamma-glutamyl transpeptidase incorporation into erythrocyte membranes, as compared to control membranes. Research has also indicated that DPPC-liposomes could serve effectively as a delivery vehicle for inducing immune responses against glycosphingolipid antigens.
1,2-Dipalmitoyl-sn-glycero-3-phosphocholine (CAS 63-89-8) References
- Effect of Polyvinyl Pyrrolidone on the Thermal Phase Transition of 1,2 Dipalmitoyl-sn-glycero-3-phosphocholine Bilayer. | Savva, M., et al. 1999. J Colloid Interface Sci. 217: 160-165. PMID: 10441424
- Induction of immune responses against glycosphingolipid antigens: comparison of antibody responses in mice immunized with antigen associated with liposomes prepared from various phospholipids. | Uemura, A., et al. 2005. J Vet Med Sci. 67: 1197-201. PMID: 16397376
- The phase transition behavior of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) model membrane influenced by 2,4-dichlorophenol--an FT-Raman spectroscopy study. | Csiszár, A., et al. 2006. Chem Phys Lipids. 139: 115-24. PMID: 16413520
- Isovaleric, methylmalonic, and propionic acid decrease anesthetic EC50 in tadpoles, modulate glycine receptor function, and interact with the lipid 1,2-dipalmitoyl-Sn-glycero-3-phosphocholine. | Weng, Y., et al. 2009. Anesth Analg. 108: 1538-45. PMID: 19372333
- Curcumin disorders 1,2-dipalmitoyl-sn-glycero-3-phosphocholine membranes and favors the formation of nonlamellar structures by 1,2-dielaidoyl-sn-glycero-3-phosphoethanolamine. | Pérez-Lara, A., et al. 2010. J Phys Chem B. 114: 9778-86. PMID: 20666521
- Generation of fatty acids from 1,2-dipalmitoyl-sn-glycero-3-phosphocholine/cardiolipin liposomes that stabilize recombinant human serum albumin. | Frahm, GE., et al. 2013. J Liposome Res. 23: 101-9. PMID: 23294393
- A study of the antibacterial activity of L-phenylalanine and L-tyrosine esters in relation to their CMCs and their interactions with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine, DPPC as model membrane. | Joondan, N., et al. 2014. Microbiol Res. 169: 675-85. PMID: 24667307
- 1,2-Dipalmitoyl-sn-glycero-3-phosphocholine (DPPC)-rich domain formation in binary phospholipid vesicle membranes: two-dimensional nucleation and growth. | Chen, D. and Santore, MM. 2014. Langmuir. 30: 9484-93. PMID: 25084141
- Synthesis, micellisation and interaction of novel quaternary ammonium compounds derived from l-Phenylalanine with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine as model membrane in relation to their antibacterial activity, and their selectivity over human red blood cells. | Joondan, N., et al. 2015. Bioorg Chem. 58: 117-29. PMID: 25618736
- Lyoprotective Effect of Alkyl Sulfobetaines for Freeze-drying 1,2-Dipalmitoyl-sn-glycero-3-phosphocholine Liposomes. | Aikawa, T., et al. 2017. J Oleo Sci. 66: 1277-1284. PMID: 29021493
- Transport of amino acids in gamma-glutamyl transpeptidase-implanted human erythrocytes. | Kalra, VK., et al. 1981. J Biol Chem. 256: 5567-71. PMID: 6113238
- Characterization of the pretransition in 1,2-dipalmitoyl-sn-glycero-3-phosphocholine by Fourier transform infrared spectroscopy. | Cameron, DG., et al. 1980. Biochemistry. 19: 3665-72. PMID: 6893274
- A Fourier transform infrared spectroscopic study of the molecular interaction of cholesterol with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine. | Umemura, J., et al. 1980. Biochim Biophys Acta. 602: 32-44. PMID: 6893416
- Synthesis of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine with labeled acyl groups. | Brimble, PD. and Choy, PC. 1981. Prep Biochem. 11: 525-33. PMID: 6896091
- Synthesis and properties of dimeric glycerophospholipid: 2,2'-dotriacontanedioylbis(1-palmitoyl-sn-glycero-3-phosphocholine). | Yamauchi, K., et al. 1996. J Biochem. 119: 115-9. PMID: 8907184
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,2-Dipalmitoyl-sn-glycero-3-phosphocholine, 50 mg | sc-203458 | 50 mg | $151.00 | |||
1,2-Dipalmitoyl-sn-glycero-3-phosphocholine, 250 mg | sc-203458A | 250 mg | $204.00 |