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4235-95-4

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  • China Biggest factory Supply High Quality 1,2-DIOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE CAS 4235-95-4

    Cas No: 4235-95-4

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  • 3,5,9-Trioxa-4-phosphaheptacos-18-en-1-aminium,4-hydroxy-N,N,N-trimethyl-10-oxo-7-[[(9Z)-1-oxo-9-octadecen-1-yl]oxy]-, innersalt, 4-oxide, (7R,18Z)- 4235-95-4

    Cas No: 4235-95-4

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4235-95-4 Usage

Uses

Used in Pharmaceutical Applications:
1,2-Dioleoyl-sn-glycero-3-phosphocholine is used as a component in the generation of liposomes for drug delivery systems. It aids in the encapsulation and controlled release of therapeutic agents, enhancing their bioavailability and targeting specific tissues or cells.
Used in Biochemical Research:
DOPC is used as a reconstitution material for proteoliposomes (PL), which are essential tools in the study of membrane proteins and their functions. It helps researchers understand the interactions between proteins and lipids within biological membranes.
Used in the Preparation of Lipid Vesicles:
1,2-Dioleoyl-sn-glycero-3-phosphocholine is used as a primary component in the preparation of lipid vesicles, which serve as models for biological membranes. These vesicles are crucial in studying membrane-related processes, such as membrane fusion, protein-lipid interactions, and the transport of molecules across membranes.
Used in the Replication of Synovial Fluid Structure:
DOPC has been employed in reproducing the supramolecular structure of synovial fluid, which is vital for lubricating and nourishing the joints. This application aids in the development of treatments for joint-related conditions and the study of joint lubrication mechanisms.
Used in the Preparation of Planar Supported Membranes:
1,2-Dioleoyl-sn-glycero-3-phosphocholine is used in the preparation of planar supported membranes, which are essential in the study of membrane biophysics and the development of biosensors and other diagnostic tools.

Biochem/physiol Actions

18:1 (Δ9-Cis) PC (DOPC) shows high resistance to the toxic effects of dimethyl sulfoxide (DMSO).

Check Digit Verification of cas no

The CAS Registry Mumber 4235-95-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4235-95:
(6*4)+(5*2)+(4*3)+(3*5)+(2*9)+(1*5)=84
84 % 10 = 4
So 4235-95-4 is a valid CAS Registry Number.
InChI:InChI=1/C44H84NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h20-23,42H,6-19,24-41H2,1-5H3/b22-20-,23-21-/t42-/m1/s1

4235-95-4 Well-known Company Product Price

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  • TCI America

  • (D4250)  1,2-Dioleoyl-sn-glycero-3-phosphocholine  >97.0%(HPLC)(T)

  • 4235-95-4

  • 250mg

  • 580.00CNY

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  • Sigma

  • (P6354)  1,2-Dioleoyl-sn-glycero-3-phosphocholine  lyophilized powder

  • 4235-95-4

  • P6354-25MG

  • 452.79CNY

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  • Sigma

  • (P6354)  1,2-Dioleoyl-sn-glycero-3-phosphocholine  lyophilized powder

  • 4235-95-4

  • P6354-100MG

  • 964.08CNY

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  • Sigma

  • (P6354)  1,2-Dioleoyl-sn-glycero-3-phosphocholine  lyophilized powder

  • 4235-95-4

  • P6354-1G

  • 4,821.57CNY

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4235-95-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dioleoyl-sn-glycero-3-phosphocholine

1.2 Other means of identification

Product number -
Other names 1,2-Dioleoyl-sn-glycero-3-phosphocholine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4235-95-4 SDS

4235-95-4Relevant articles and documents

Synthesis of phosphatidylcholine: An improved method without using the cadmium chloride complex of sn-glycero-3-phosphocholine

Ichihara, Ken'ichi,Iwasaki, Hitomi,Ueda, Kaori,Takizawa, Ryoko,Naito, Hideko,Tomosugi, Mitsuhiro

, p. 94 - 99 (2005)

An improved safe method that does not contaminate the environment with cadmium chloride, a toxic heavy metal salt, was developed for the synthesis of phosphatidylcholine (PC). PC was synthesized from sn-glycero-3-phosphocholine (GPC) and fatty acid in one step under mild conditions without the use of cadmium chloride. GPC was prepared from egg yolk PC and adsorbed by kieselguhr in a Teflon vessel. The GPC on kieselguhr was acylated with fatty acid in the presence of two reagents, dicyclohexylcarbodiimide for synthesis of fatty acid anhydride and 4-dimethylaminopyridine as an acylating catalyst, at 30°C overnight. The PC thus produced was purified by silica gel column chromatography. The yield of dioleoyl PC was 90% based on the starting material, GPC.

cis-trans Isomerization of monounsaturated fatty acid residues in phospholipids by thiyl radicals

Chatgilialoglu, Chryssostomos,Ferreri, Carla,Ballestri, Marco,Mulazzani, Quinto G.,Landi, Laura

, p. 4593 - 4601 (2007/10/03)

Thiyl radicals reversibly attack the double bonds of methyl oleate and dioleoyl phosphatidyl choline (DOPC), thus producing methyl elaidate and the corresponding phospholipids containing trans-fatty acid residues in high yield. These processes are radical chain reactions with relatively long chain lengths. The rate constant for the β-elimination of a thiyl radical from the adduct radical has been estimated to be 6 x 106 s-1 at ambient temperature. The cis-trans isomerization of fatty acid residues in DOPC vesicles (multilamellar vesicles and large unilamellar vesicles made by the extrusion technique) by a thiyl radical, generated from biologically relevant thiols, has also been studied in detail. The presence of 0.2 mM oxygen does not influence the effectiveness of cis-trans isomerization in both homogeneous solution and lipid vesicles. This process, which does not cause lipid degradation but permanent modification of the membrane constituents, ultimately influences the barrier properties and functions of biological membranes.

The development of improved cationic lipids for gene transfer into cystic fibrosis airway epithelial cells

Harris,Marshall,Lee,Siegel,Mcneilly,Yew,Nietupski,Nichols,Cherry,Wan,Jiang,Lane,Rowe,Scheule,Smith,Cheng

, p. 289 - 292 (2007/10/03)

In an effort to improve the efficiency of cationic lipid mediated gene transfer, over 90 novel cationic lipids of diverse structural types were synthesized and evaluated in vitro. Four cationic lipids derived from phospholipids were examined. The most promising cationic lipid formulations were tested in vivo by intranasal or transtracheal instillation into the lungs of BALB/c mice. The most active formulations gave CAT reporter gene expression levels which are greater than 500 fold over that which could be attained using free DNA alone. Certain cationic lipid formulations have been shown to facilitate substantial expression of the CFTR (cystic fibrosis transmembrane conductance regulator) gene in vitro as determined by the SPQ and Ussing Chamber assays.

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