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1-Palmitoyl-2-<12-(methacryloyloxy)dodecanoyl>-L-α-phosphatidylcholine is a complex lipid molecule that belongs to the class of phospholipids. It is composed of a glycerol backbone, with one fatty acid chain (palmitoyl) attached to the first carbon and a second fatty acid chain (12-(methacryloyloxy)dodecanoyl) attached to the second carbon. The methacryloyloxy group in the second fatty acid chain introduces a reactive double bond, which can be used in polymerization reactions. The L-α-phosphatidylcholine part of the molecule consists of a phosphatidyl group linked to a choline moiety, which is a common structural feature in many phospholipids and plays a crucial role in the formation of cell membranes. This specific phospholipid is of interest in the field of biomaterials and drug delivery due to its potential to form stable structures and its ability to be functionalized for various applications.

79481-27-9

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79481-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79481-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,8 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79481-27:
(7*7)+(6*9)+(5*4)+(4*8)+(3*1)+(2*2)+(1*7)=169
169 % 10 = 9
So 79481-27-9 is a valid CAS Registry Number.

79481-27-9Downstream Products

79481-27-9Relevant academic research and scientific papers

Polymerized Phosphatidylcholine Vesicles. Synthesis and Characterization

Regen, Steven L.,Singh, Alok,Oehme, Guenter,Singh, Maninder

, p. 791 - 795 (2007/10/02)

The synthesis and characterization of photopolymerized vesicles derived from bis-L-α-phosphatidylcholine (3) 1--2-palmitoyl-L-α-phosphatidylcholine (4), and 1-palmitoyl-2--L-α-phosphatidylcholine (5) are described.Ultrasonic irradiation of 3, 4, 5, 20percent 3 + 80percent 4, and 20percent 3 + 80percent 5 in water at 50 deg C yields opalescent to optically clear dispersions.Electron microscopy, entrapment of sucrose, and permeability measurements provide strong evidence for closed multilamellar vesicles having diameters ranging between 350 and 1400 Angstroem.Fourier transform 1H NMR spectra of the aqueous dispersions as well as IR spectra of chloroform extracts establish that no significant lipid decomposition occurs during vesicle preparation.Direct UV irradiation (254 nm) produces polymerized analogues of similar size and shape which (1) entrap sucrose, (2) show reduced permeability, and (3) exhibit enchanced stability.

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