1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE manufacturers
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| | 1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE Basic information |
| Product Name: | 1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE | | Synonyms: | 1,2-DIOCTADECANOYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE;18:0 PE;(R)-1-[[[(2-aminoethoxy)hydroxyphosphinyl]oxy]methyl]ethane-1,2-diyl distearate;L-A-PHOSPHATIDYLETHANOLAMINE,DISTEAROYL;DSPE;L-ALPHA-PHOSPHATIDYLETHANOLAMINE, DISTEAROYL;L-BETA,GAMMA-DISTEAROYL-ALPHA-CEPHALIN;1,2-Distearoyl-sn-glycero-3-phosphoethan | | CAS: | 1069-79-0 | | MF: | C41H82NO8P | | MW: | 748.07 | | EINECS: | 213-963-9 | | Product Categories: | | | Mol File: | 1069-79-0.mol |  |
| | 1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE Chemical Properties |
| Melting point | 172-173℃ | | Boiling point | 760.2±70.0 °C(Predicted) | | density | 0.996 | | storage temp. | -20°C | | solubility | Chloroform (Slightly, Heated, Sonicated) | | form | Solid | | pka | 1.17±0.50(Predicted) | | color | White to Off-White | | BRN | 1730641 | | InChIKey | LVNGJLRDBYCPGB-UHFFFAOYSA-N | | SMILES | C(OC(=O)CCCCCCCCCCCCCCCCC)(COP(OCCN)(O)=O)COC(=O)CCCCCCCCCCCCCCCCC |
| Safety Statements | 24/25 | | WGK Germany | 3 | | F | 10-21 | | HS Code | 29232000 |
| | 1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE Usage And Synthesis |
| Chemical Properties | White powder | | Uses | 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine is used in the generation of micelles and liposomes. | | Definition | ChEBI: (R)-1,2-distearoylphosphatidylethanolamine is an optically active form of 1,2-distearoylphosphatidylethanolamine having (R)-configuration. It has a role as a mouse metabolite. It is an enantiomer of a (S)-1,2-distearoylphosphatidylethanolamine. It is a tautomer of a (R)-1,2-distearoylphosphatidylethanolamine zwitterion. | | General Description | Phosphatidylethanolamine is an aminophospholipid, which is found in eukaryotic and prokaryotic cells. It is one of the most abundant glycerophospholipids in biological membranes. Phosphatidylethanolamine is found in nervous tissue. | | Biochem/physiol Actions | Phosphatidylethanolamine forms pure lipid structures. It modulates membrane fluidity in eukaryotic cells. Phosphatidylethanolamine plays an important role in autophagy, cell division and protein folding. It acts as a precursor for the synthesis of various protein modifications. Phosphatidylethanolamine functions as an intermediate for the synthesis of glycerophospholipid classes. | | Purification Methods | The R-form is recrystallised from CHCl3/MeOH, and the ±-form is recrystallised from EtOH. [Bevan & Malkin J Chem Soc 2667 1951, Baer Can J Biochem Physiol 81 1758 1959, Beilstein 4 IV 1420.] |
| | 1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE Preparation Products And Raw materials |
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