| Identification | More | [Name]
1,2-DIMYRISTOYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE | [CAS]
998-07-2 | [Synonyms]
1,2-DIMYRISTOYL-SN-GLYCERO-3-PHOSPHATIDYLETHANOLAMINE
1,2-DIMYRISTOYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE
1,2-DIMYRISTOYL-SN-GLYCERO-3-PHOSPHORYLETHANOLAMINE
1,2-DITETRADECANOYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE
14:0 PE
3-SN-PHOSPHATIDYLETHANOLAMINE, 1,2-DIMYRISTOYL
DMPE
L-ALPHA-PHOSPHATIDYLETHANOLAMINE, DIMYRISTOYL
L-ALPHA-PHOSPHATIDYLETHANOLAMINE, DIMYRISTOYL (C14:0)
L-BETA,GAMMA-DIMYRISTOYL-ALPHA-CEPHALIN
L-A-PHOSPHATIDYL-ETHANOLAMINE,*DIMYRISTO YL
L-A-PHOSPHATIDYLETHANOLAMINE,*DIMYRISTOY
1,2-Ditetradecanoyl-sn-glycero-3-phosphoethanolamine, 3-sn-Phosphatidylethanolamine, 1,2-dimyristoyl, L-β,γ-Dimyristoyl-α-cephalin, Dimyristoyl-L-α-phosphatidylethanolamine | [Molecular Formula]
C33H66NO8P | [MDL Number]
MFCD00036775 | [Molecular Weight]
635.85 | [MOL File]
998-07-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
191.0 to 195.0 °C | [Boiling point ]
685.6±65.0 °C(Predicted) | [density ]
1.027±0.06 g/cm3(Predicted) | [storage temp. ]
−20°C
| [solubility ]
Chloroform: 3 mg/ml | [form ]
powder to crystal | [pka]
1.17±0.50(Predicted) | [color ]
White to Almost white | [biological source]
synthetic | [BRN ]
1730529 | [InChIKey]
NEZDNQCXEZDCBI-WJOKGBTCSA-N | [CAS DataBase Reference]
998-07-2(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Description]
Phosphatidylethanolamines (PEs) are phospholipids found in biological membranes, serving both structural and functional roles.1,2 Different types of PEs are commonly used in the generation of micelles, liposomes, and other types of artificial membranes.3,4 1,2-Dimyristoyl-sn-glycero-3-PE (DMPE) is a phospholipid containing the long-chain (14:0) myristic acid inserted at the sn-1 and sn-2 positions. | [Uses]
Tetradecanoic Acid (1R)-1-[[[(2-Aminoethoxy)hydroxyphosphinyl]oxy]methyl]-1,2-ethanediyl Ester is a phospholipid serving both structural and functional roles in biological membranes. | [storage]
Store at -20°C | [Purification Methods]
Recrystallise the kephalin from EtOH [Bevan & Malkin J Chem Soc 2667 1951]. The R-isomer has m 195-196o (sintering at 130-135o) after recrystallisation from CHCl3/MeOH, and [] D 26 +6.7o (c 8.5, CHCl3/AcOH 9:1). [Baer Can J Biochem Physiol 35 239 1957, Baer et al. J Am Chem Soc 74 152 1952, Beilstein 4 IV 1463.] |
|
|